---
DOAJ_listed: '1'
OA_place: publisher
OA_type: gold
_id: '22520'
abstract:
- lang: eng
  text: Increasing urbanization is likely to intensify the urban heat island effect,
    decrease outdoor thermal comfort, and enhance runoff generation in cities. Urban
    green spaces are often proposed as a mitigation strategy to counteract these adverse
    effects, and many recent developments of urban climate models focus on the inclusion
    of green and blue infrastructure to inform urban planning. However, many models
    still lack the ability to account for different plant types and oversimplify the
    interactions between the built environment, vegetation, and hydrology. In this
    study, we present an urban ecohydrological model, Urban Tethys-Chloris (UT&C),
    that combines principles of ecosystem modelling with an urban canopy scheme accounting
    for the biophysical and ecophysiological characteristics of roof vegetation, ground
    vegetation, and urban trees. UT&C is a fully coupled energy and water balance
    model that calculates 2 m air temperature, 2 m humidity, and surface temperatures
    based on the infinite urban canyon approach. It further calculates the urban hydrological
    fluxes in the absence of snow, including transpiration as a function of plant
    photosynthesis. Hence, UT&C accounts for the effects of different plant types
    on the urban climate and hydrology, as well as the effects of the urban environment
    on plant well-being and performance. UT&C performs well when compared against
    energy flux measurements of eddy-covariance towers located in three cities in
    different climates (Singapore, Melbourne, and Phoenix). A sensitivity analysis,
    performed as a proof of concept for the city of Singapore, shows a mean decrease
    in 2 m air temperature of 1.1 ∘C for fully grass-covered ground, 0.2 ∘C for high
    values of leaf area index (LAI), and 0.3 ∘C for high values of Vc,max (an expression
    of photosynthetic capacity). These reductions in temperature were combined with
    a simultaneous increase in relative humidity by 6.5 %, 2.1 %, and 1.6 %, for fully
    grass-covered ground, high values of LAI, and high values of Vc,max, respectively.
    Furthermore, the increase of pervious vegetated ground is able to significantly
    reduce surface runoff.
article_processing_charge: No
article_type: original
author:
- first_name: Naika
  full_name: Meili, Naika
  last_name: Meili
- first_name: Gabriele
  full_name: Manoli, Gabriele
  last_name: Manoli
- first_name: Paolo
  full_name: Burlando, Paolo
  last_name: Burlando
- first_name: Elie
  full_name: Bou-Zeid, Elie
  last_name: Bou-Zeid
- first_name: Winston T. L.
  full_name: Chow, Winston T. L.
  last_name: Chow
- first_name: Andrew M.
  full_name: Coutts, Andrew M.
  last_name: Coutts
- first_name: Edoardo
  full_name: Daly, Edoardo
  last_name: Daly
- first_name: Kerry A.
  full_name: Nice, Kerry A.
  last_name: Nice
- first_name: Matthias
  full_name: Roth, Matthias
  last_name: Roth
- first_name: Nigel J.
  full_name: Tapper, Nigel J.
  last_name: Tapper
- first_name: Erik
  full_name: Velasco, Erik
  last_name: Velasco
- first_name: Enrique R.
  full_name: Vivoni, Enrique R.
  last_name: Vivoni
- first_name: Simone
  full_name: Fatichi, Simone
  id: cf8e546b-a9b0-11f0-a43b-aa89ed1b56d6
  last_name: Fatichi
citation:
  ama: Meili N, Manoli G, Burlando P, et al. An urban ecohydrological model to quantify
    the effect of vegetation on urban climate and hydrology (UT&#38;C v1.0). <i>Geoscientific
    Model Development</i>. 2020;13(1):335-362. doi:<a href="https://doi.org/10.5194/gmd-13-335-2020">10.5194/gmd-13-335-2020</a>
  apa: Meili, N., Manoli, G., Burlando, P., Bou-Zeid, E., Chow, W. T. L., Coutts,
    A. M., … Fatichi, S. (2020). An urban ecohydrological model to quantify the effect
    of vegetation on urban climate and hydrology (UT&#38;C v1.0). <i>Geoscientific
    Model Development</i>. Copernicus Publications. <a href="https://doi.org/10.5194/gmd-13-335-2020">https://doi.org/10.5194/gmd-13-335-2020</a>
  chicago: Meili, Naika, Gabriele Manoli, Paolo Burlando, Elie Bou-Zeid, Winston T.
    L. Chow, Andrew M. Coutts, Edoardo Daly, et al. “An Urban Ecohydrological Model
    to Quantify the Effect of Vegetation on Urban Climate and Hydrology (UT&#38;C
    v1.0).” <i>Geoscientific Model Development</i>. Copernicus Publications, 2020.
    <a href="https://doi.org/10.5194/gmd-13-335-2020">https://doi.org/10.5194/gmd-13-335-2020</a>.
  ieee: N. Meili <i>et al.</i>, “An urban ecohydrological model to quantify the effect
    of vegetation on urban climate and hydrology (UT&#38;C v1.0),” <i>Geoscientific
    Model Development</i>, vol. 13, no. 1. Copernicus Publications, pp. 335–362, 2020.
  ista: Meili N, Manoli G, Burlando P, Bou-Zeid E, Chow WTL, Coutts AM, Daly E, Nice
    KA, Roth M, Tapper NJ, Velasco E, Vivoni ER, Fatichi S. 2020. An urban ecohydrological
    model to quantify the effect of vegetation on urban climate and hydrology (UT&#38;C
    v1.0). Geoscientific Model Development. 13(1), 335–362.
  mla: Meili, Naika, et al. “An Urban Ecohydrological Model to Quantify the Effect
    of Vegetation on Urban Climate and Hydrology (UT&#38;C v1.0).” <i>Geoscientific
    Model Development</i>, vol. 13, no. 1, Copernicus Publications, 2020, pp. 335–62,
    doi:<a href="https://doi.org/10.5194/gmd-13-335-2020">10.5194/gmd-13-335-2020</a>.
  short: N. Meili, G. Manoli, P. Burlando, E. Bou-Zeid, W.T.L. Chow, A.M. Coutts,
    E. Daly, K.A. Nice, M. Roth, N.J. Tapper, E. Velasco, E.R. Vivoni, S. Fatichi,
    Geoscientific Model Development 13 (2020) 335–362.
das_tickbox: '1'
date_created: 2026-07-27T12:30:24Z
date_published: 2020-01-31T00:00:00Z
date_updated: 2026-08-07T09:11:10Z
day: '31'
doi: 10.5194/gmd-13-335-2020
extern: '1'
intvolume: '        13'
issue: '1'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.5194/gmd-13-335-2020
month: '01'
oa: 1
oa_version: Published Version
page: 335-362
publication: Geoscientific Model Development
publication_identifier:
  eissn:
  - 1991-9603
  issn:
  - 1991-959X
publication_status: published
publisher: Copernicus Publications
quality_controlled: '1'
scopus_import: '1'
status: public
title: An urban ecohydrological model to quantify the effect of vegetation on urban
  climate and hydrology (UT&C v1.0)
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
volume: 13
year: '2020'
...
---
OA_type: closed access
_id: '22526'
abstract:
- lang: eng
  text: Climate change can reduce surface-water supply by enhancing evapotranspiration
    in forested mountains, especially during heatwaves. We investigate this ‘drought
    paradox’ for the European Alps using a 1,212-station database and hyper-resolution
    ecohydrological simulations to quantify blue (runoff) and green (evapotranspiration)
    water fluxes. During the 2003 heatwave, evapotranspiration in large areas over
    the Alps was above average despite low precipitation, amplifying the runoff deficit
    by 32% in the most runoff-productive areas (1,300–3,000 m above sea level). A
    3 °C air temperature increase could enhance annual evapotranspiration by up to
    100 mm (45 mm on average), which would reduce annual runoff at a rate similar
    to a 3% precipitation decrease. This suggests that green-water feedbacks—which
    are often poorly represented in large-scale model simulations—pose an additional
    threat to water resources, especially in dry summers. Despite uncertainty in the
    validation of the hyper-resolution ecohydrological modelling with observations,
    this approach permits more realistic predictions of mountain region water availability.
article_processing_charge: No
article_type: original
author:
- first_name: Theodoros
  full_name: Mastrotheodoros, Theodoros
  last_name: Mastrotheodoros
- first_name: Christoforos
  full_name: Pappas, Christoforos
  last_name: Pappas
- first_name: Peter
  full_name: Molnar, Peter
  last_name: Molnar
- first_name: Paolo
  full_name: Burlando, Paolo
  last_name: Burlando
- first_name: Gabriele
  full_name: Manoli, Gabriele
  last_name: Manoli
- first_name: Juraj
  full_name: Parajka, Juraj
  last_name: Parajka
- first_name: Riccardo
  full_name: Rigon, Riccardo
  last_name: Rigon
- first_name: Borbala
  full_name: Szeles, Borbala
  last_name: Szeles
- first_name: Michele
  full_name: Bottazzi, Michele
  last_name: Bottazzi
- first_name: Panagiotis
  full_name: Hadjidoukas, Panagiotis
  last_name: Hadjidoukas
- first_name: Simone
  full_name: Fatichi, Simone
  id: cf8e546b-a9b0-11f0-a43b-aa89ed1b56d6
  last_name: Fatichi
citation:
  ama: Mastrotheodoros T, Pappas C, Molnar P, et al. More green and less blue water
    in the Alps during warmer summers. <i>Nature Climate Change</i>. 2020;10:155-161.
    doi:<a href="https://doi.org/10.1038/s41558-019-0676-5">10.1038/s41558-019-0676-5</a>
  apa: Mastrotheodoros, T., Pappas, C., Molnar, P., Burlando, P., Manoli, G., Parajka,
    J., … Fatichi, S. (2020). More green and less blue water in the Alps during warmer
    summers. <i>Nature Climate Change</i>. Springer Nature. <a href="https://doi.org/10.1038/s41558-019-0676-5">https://doi.org/10.1038/s41558-019-0676-5</a>
  chicago: Mastrotheodoros, Theodoros, Christoforos Pappas, Peter Molnar, Paolo Burlando,
    Gabriele Manoli, Juraj Parajka, Riccardo Rigon, et al. “More Green and Less Blue
    Water in the Alps during Warmer Summers.” <i>Nature Climate Change</i>. Springer
    Nature, 2020. <a href="https://doi.org/10.1038/s41558-019-0676-5">https://doi.org/10.1038/s41558-019-0676-5</a>.
  ieee: T. Mastrotheodoros <i>et al.</i>, “More green and less blue water in the Alps
    during warmer summers,” <i>Nature Climate Change</i>, vol. 10. Springer Nature,
    pp. 155–161, 2020.
  ista: Mastrotheodoros T, Pappas C, Molnar P, Burlando P, Manoli G, Parajka J, Rigon
    R, Szeles B, Bottazzi M, Hadjidoukas P, Fatichi S. 2020. More green and less blue
    water in the Alps during warmer summers. Nature Climate Change. 10, 155–161.
  mla: Mastrotheodoros, Theodoros, et al. “More Green and Less Blue Water in the Alps
    during Warmer Summers.” <i>Nature Climate Change</i>, vol. 10, Springer Nature,
    2020, pp. 155–61, doi:<a href="https://doi.org/10.1038/s41558-019-0676-5">10.1038/s41558-019-0676-5</a>.
  short: T. Mastrotheodoros, C. Pappas, P. Molnar, P. Burlando, G. Manoli, J. Parajka,
    R. Rigon, B. Szeles, M. Bottazzi, P. Hadjidoukas, S. Fatichi, Nature Climate Change
    10 (2020) 155–161.
das_tickbox: '1'
date_created: 2026-07-27T12:30:24Z
date_published: 2020-02-01T00:00:00Z
date_updated: 2026-08-07T09:15:51Z
day: '01'
doi: 10.1038/s41558-019-0676-5
extern: '1'
intvolume: '        10'
language:
- iso: eng
month: '02'
oa_version: None
page: 155-161
publication: Nature Climate Change
publication_identifier:
  eissn:
  - 1758-6798
  issn:
  - 1758-678X
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: More green and less blue water in the Alps during warmer summers
type: journal_article
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
volume: 10
year: '2020'
...
---
OA_place: publisher
OA_type: free access
_id: '22542'
abstract:
- lang: eng
  text: Temporal dynamics of urban warming have been extensivelystudied at the diurnal
    scale, but the impact of background cli-mate on the observed seasonality of surface
    urban heat islands(SUHIs) remains largely unexplored. On seasonal time scales,
    theintensity of urban–rural surface temperature differences (∆Ts)exhibits distinctive
    hysteretic cycles whose shape and loopingdirection vary across climatic zones.
    These observations high-light possible delays underlying the dynamics of the coupledurban–biosphere
    system. However, a general argument explain-ing the observed hysteretic patterns
    remains elusive. A coarse-grained model of SUHI coupled with a stochastic soil
    waterbalance is developed to demonstrate that the time lags betweenradiation forcing,
    air temperature, and rainfall generate a rate-dependent hysteresis, explaining
    the observed seasonal varia-tions of ∆Ts. If solar radiation is in phase with
    water availability,summer conditions cause strong SUHI intensities due to highrural
    evaporative cooling. Conversely, cities in seasonally dryregions where evapotranspiration
    is out of phase with radia-tion show a summertime oasis effect controlled by backgroundclimate
    and vegetation properties. These seasonal patterns ofwarming and cooling have
    signiﬁcant implications for heat mit-igation strategies as urban green spaces
    can reduce ∆Ts duringsummertime, while potentially negative effects of albedo
    man-agement during winter are mitigated by the seasonality of solarradiation.
article_processing_charge: No
article_type: original
author:
- first_name: Gabriele
  full_name: Manoli, Gabriele
  last_name: Manoli
- first_name: Simone
  full_name: Fatichi, Simone
  id: cf8e546b-a9b0-11f0-a43b-aa89ed1b56d6
  last_name: Fatichi
- first_name: Elie
  full_name: Bou-Zeid, Elie
  last_name: Bou-Zeid
- first_name: Gabriel G.
  full_name: Katul, Gabriel G.
  last_name: Katul
citation:
  ama: Manoli G, Fatichi S, Bou-Zeid E, Katul GG. Seasonal hysteresis of surface urban
    heat islands. <i>Proceedings of the National Academy of Sciences</i>. 2020;117(13):7082-7089.
    doi:<a href="https://doi.org/10.1073/pnas.1917554117">10.1073/pnas.1917554117</a>
  apa: Manoli, G., Fatichi, S., Bou-Zeid, E., &#38; Katul, G. G. (2020). Seasonal
    hysteresis of surface urban heat islands. <i>Proceedings of the National Academy
    of Sciences</i>. National Academy of Sciences. <a href="https://doi.org/10.1073/pnas.1917554117">https://doi.org/10.1073/pnas.1917554117</a>
  chicago: Manoli, Gabriele, Simone Fatichi, Elie Bou-Zeid, and Gabriel G. Katul.
    “Seasonal Hysteresis of Surface Urban Heat Islands.” <i>Proceedings of the National
    Academy of Sciences</i>. National Academy of Sciences, 2020. <a href="https://doi.org/10.1073/pnas.1917554117">https://doi.org/10.1073/pnas.1917554117</a>.
  ieee: G. Manoli, S. Fatichi, E. Bou-Zeid, and G. G. Katul, “Seasonal hysteresis
    of surface urban heat islands,” <i>Proceedings of the National Academy of Sciences</i>,
    vol. 117, no. 13. National Academy of Sciences, pp. 7082–7089, 2020.
  ista: Manoli G, Fatichi S, Bou-Zeid E, Katul GG. 2020. Seasonal hysteresis of surface
    urban heat islands. Proceedings of the National Academy of Sciences. 117(13),
    7082–7089.
  mla: Manoli, Gabriele, et al. “Seasonal Hysteresis of Surface Urban Heat Islands.”
    <i>Proceedings of the National Academy of Sciences</i>, vol. 117, no. 13, National
    Academy of Sciences, 2020, pp. 7082–89, doi:<a href="https://doi.org/10.1073/pnas.1917554117">10.1073/pnas.1917554117</a>.
  short: G. Manoli, S. Fatichi, E. Bou-Zeid, G.G. Katul, Proceedings of the National
    Academy of Sciences 117 (2020) 7082–7089.
das_tickbox: '1'
date_created: 2026-07-27T12:30:24Z
date_published: 2020-03-31T00:00:00Z
date_updated: 2026-08-07T09:21:58Z
day: '31'
doi: 10.1073/pnas.1917554117
extern: '1'
external_id:
  pmid:
  - '32184330 '
intvolume: '       117'
issue: '13'
keyword:
- Cities
- Hysteresis
- Seasonality
- Surface temperature
- Urban heat island
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1073/pnas.1917554117
month: '03'
oa: 1
oa_version: Published Version
page: 7082-7089
pmid: 1
publication: Proceedings of the National Academy of Sciences
publication_identifier:
  eissn:
  - 1091-6490
  issn:
  - 0027-8424
publication_status: published
publisher: National Academy of Sciences
quality_controlled: '1'
scopus_import: '1'
status: public
title: Seasonal hysteresis of surface urban heat islands
type: journal_article
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
volume: 117
year: '2020'
...
---
_id: '14891'
abstract:
- lang: eng
  text: We give the first mathematically rigorous justification of the local density
    approximation in density functional theory. We provide a quantitative estimate
    on the difference between the grand-canonical Levy–Lieb energy of a given density
    (the lowest possible energy of all quantum states having this density) and the
    integral over the uniform electron gas energy of this density. The error involves
    gradient terms and justifies the use of the local density approximation in the
    situation where the density is very flat on sufficiently large regions in space.
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Mathieu
  full_name: Lewin, Mathieu
  last_name: Lewin
- first_name: Elliott H.
  full_name: Lieb, Elliott H.
  last_name: Lieb
- first_name: Robert
  full_name: Seiringer, Robert
  id: 4AFD0470-F248-11E8-B48F-1D18A9856A87
  last_name: Seiringer
  orcid: 0000-0002-6781-0521
citation:
  ama: Lewin M, Lieb EH, Seiringer R. The local density approximation in density functional
    theory. <i>Pure and Applied Analysis</i>. 2020;2(1):35-73. doi:<a href="https://doi.org/10.2140/paa.2020.2.35">10.2140/paa.2020.2.35</a>
  apa: Lewin, M., Lieb, E. H., &#38; Seiringer, R. (2020). The local density approximation
    in density functional theory. <i>Pure and Applied Analysis</i>. Mathematical Sciences
    Publishers. <a href="https://doi.org/10.2140/paa.2020.2.35">https://doi.org/10.2140/paa.2020.2.35</a>
  chicago: Lewin, Mathieu, Elliott H. Lieb, and Robert Seiringer. “The Local Density
    Approximation in Density Functional Theory.” <i>Pure and Applied Analysis</i>.
    Mathematical Sciences Publishers, 2020. <a href="https://doi.org/10.2140/paa.2020.2.35">https://doi.org/10.2140/paa.2020.2.35</a>.
  ieee: M. Lewin, E. H. Lieb, and R. Seiringer, “The local density approximation in
    density functional theory,” <i>Pure and Applied Analysis</i>, vol. 2, no. 1. Mathematical
    Sciences Publishers, pp. 35–73, 2020.
  ista: Lewin M, Lieb EH, Seiringer R. 2020. The local density approximation in density
    functional theory. Pure and Applied Analysis. 2(1), 35–73.
  mla: Lewin, Mathieu, et al. “The Local Density Approximation in Density Functional
    Theory.” <i>Pure and Applied Analysis</i>, vol. 2, no. 1, Mathematical Sciences
    Publishers, 2020, pp. 35–73, doi:<a href="https://doi.org/10.2140/paa.2020.2.35">10.2140/paa.2020.2.35</a>.
  short: M. Lewin, E.H. Lieb, R. Seiringer, Pure and Applied Analysis 2 (2020) 35–73.
corr_author: '1'
date_created: 2024-01-28T23:01:44Z
date_published: 2020-01-01T00:00:00Z
date_updated: 2026-08-12T08:47:14Z
day: '01'
department:
- _id: RoSe
doi: 10.2140/paa.2020.2.35
external_id:
  arxiv:
  - '1903.04046'
intvolume: '         2'
issue: '1'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.48550/arXiv.1903.04046
month: '01'
oa: 1
oa_version: Preprint
page: 35-73
publication: Pure and Applied Analysis
publication_identifier:
  eissn:
  - 2578-5885
  issn:
  - 2578-5893
publication_status: published
publisher: Mathematical Sciences Publishers
quality_controlled: '1'
scopus_import: '1'
status: public
title: The local density approximation in density functional theory
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 2
year: '2020'
...
---
_id: '7388'
abstract:
- lang: eng
  text: We give a Wong-Zakai type characterisation of the solutions of quasilinear
    heat equations driven by space-time white noise in 1 + 1 dimensions. In order
    to show that the renormalisation counterterms are local in the solution, a careful
    arrangement of a few hundred terms is required. The main tool in this computation
    is a general ‘integration by parts’ formula that provides a number of linear identities
    for the renormalisation constants.
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Mate
  full_name: Gerencser, Mate
  id: 44ECEDF2-F248-11E8-B48F-1D18A9856A87
  last_name: Gerencser
citation:
  ama: Gerencser M. Nondivergence form quasilinear heat equations driven by space-time
    white noise. <i>Annales de l’Institut Henri Poincaré C</i>. 2020;37(3):663-682.
    doi:<a href="https://doi.org/10.1016/j.anihpc.2020.01.003">10.1016/j.anihpc.2020.01.003</a>
  apa: Gerencser, M. (2020). Nondivergence form quasilinear heat equations driven
    by space-time white noise. <i>Annales de l’Institut Henri Poincaré C</i>. Elsevier.
    <a href="https://doi.org/10.1016/j.anihpc.2020.01.003">https://doi.org/10.1016/j.anihpc.2020.01.003</a>
  chicago: Gerencser, Mate. “Nondivergence Form Quasilinear Heat Equations Driven
    by Space-Time White Noise.” <i>Annales de l’Institut Henri Poincaré C</i>. Elsevier,
    2020. <a href="https://doi.org/10.1016/j.anihpc.2020.01.003">https://doi.org/10.1016/j.anihpc.2020.01.003</a>.
  ieee: M. Gerencser, “Nondivergence form quasilinear heat equations driven by space-time
    white noise,” <i>Annales de l’Institut Henri Poincaré C</i>, vol. 37, no. 3. Elsevier,
    pp. 663–682, 2020.
  ista: Gerencser M. 2020. Nondivergence form quasilinear heat equations driven by
    space-time white noise. Annales de l’Institut Henri Poincaré C. 37(3), 663–682.
  mla: Gerencser, Mate. “Nondivergence Form Quasilinear Heat Equations Driven by Space-Time
    White Noise.” <i>Annales de l’Institut Henri Poincaré C</i>, vol. 37, no. 3, Elsevier,
    2020, pp. 663–82, doi:<a href="https://doi.org/10.1016/j.anihpc.2020.01.003">10.1016/j.anihpc.2020.01.003</a>.
  short: M. Gerencser, Annales de l’Institut Henri Poincaré C 37 (2020) 663–682.
date_created: 2020-01-29T09:39:41Z
date_published: 2020-05-01T00:00:00Z
date_updated: 2026-08-12T09:16:09Z
day: '01'
department:
- _id: JaMa
doi: 10.1016/j.anihpc.2020.01.003
external_id:
  arxiv:
  - '1902.07635'
  isi:
  - '000531049800007'
intvolume: '        37'
isi: 1
issue: '3'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1902.07635
month: '05'
oa: 1
oa_version: Preprint
page: 663-682
publication: Annales de l'Institut Henri Poincaré C
publication_identifier:
  issn:
  - 0294-1449
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: Nondivergence form quasilinear heat equations driven by space-time white noise
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 37
year: '2020'
...
---
_id: '8536'
abstract:
- lang: eng
  text: This work analyzes the latency of the simplified successive cancellation (SSC)
    decoding scheme for polar codes proposed by Alamdar-Yazdi and Kschischang. It
    is shown that, unlike conventional successive cancellation decoding, where latency
    is linear in the block length, the latency of SSC decoding is sublinear. More
    specifically, the latency of SSC decoding is O(N 1−1/µ ), where N is the block
    length and µ is the scaling exponent of the channel, which captures the speed
    of convergence of the rate to capacity. Numerical results demonstrate the tightness
    of the bound and show that most of the latency reduction arises from the parallel
    decoding of subcodes of rate 0 and 1.
acknowledgement: M. Mondelli was partially supported by grants NSF DMS-1613091, CCF-1714305,
  IIS-1741162 and ONR N00014-18-1-2729. S. A. Hashemi is supported by a Postdoctoral
  Fellowship from the Natural Sciences and Engineering Research Council of Canada
  (NSERC) and by Huawei.
article_number: 401-406
article_processing_charge: No
arxiv: 1
author:
- first_name: Marco
  full_name: Mondelli, Marco
  id: 27EB676C-8706-11E9-9510-7717E6697425
  last_name: Mondelli
  orcid: 0000-0002-3242-7020
- first_name: Seyyed Ali
  full_name: Hashemi, Seyyed Ali
  last_name: Hashemi
- first_name: John
  full_name: Cioffi, John
  last_name: Cioffi
- first_name: Andrea
  full_name: Goldsmith, Andrea
  last_name: Goldsmith
citation:
  ama: 'Mondelli M, Hashemi SA, Cioffi J, Goldsmith A. Simplified successive cancellation
    decoding of polar codes has sublinear latency. In: <i>IEEE International Symposium
    on Information Theory</i>. Vol 2020-June. IEEE; 2020. doi:<a href="https://doi.org/10.1109/ISIT44484.2020.9174141">10.1109/ISIT44484.2020.9174141</a>'
  apa: 'Mondelli, M., Hashemi, S. A., Cioffi, J., &#38; Goldsmith, A. (2020). Simplified
    successive cancellation decoding of polar codes has sublinear latency. In <i>IEEE
    International Symposium on Information Theory</i> (Vol. 2020–June). Los Angeles,
    CA, United States: IEEE. <a href="https://doi.org/10.1109/ISIT44484.2020.9174141">https://doi.org/10.1109/ISIT44484.2020.9174141</a>'
  chicago: Mondelli, Marco, Seyyed Ali Hashemi, John Cioffi, and Andrea Goldsmith.
    “Simplified Successive Cancellation Decoding of Polar Codes Has Sublinear Latency.”
    In <i>IEEE International Symposium on Information Theory</i>, Vol. 2020–June.
    IEEE, 2020. <a href="https://doi.org/10.1109/ISIT44484.2020.9174141">https://doi.org/10.1109/ISIT44484.2020.9174141</a>.
  ieee: M. Mondelli, S. A. Hashemi, J. Cioffi, and A. Goldsmith, “Simplified successive
    cancellation decoding of polar codes has sublinear latency,” in <i>IEEE International
    Symposium on Information Theory</i>, Los Angeles, CA, United States, 2020, vol.
    2020–June.
  ista: 'Mondelli M, Hashemi SA, Cioffi J, Goldsmith A. 2020. Simplified successive
    cancellation decoding of polar codes has sublinear latency. IEEE International
    Symposium on Information Theory. ISIT: International Symposium on Information
    Theory vol. 2020–June, 401–406.'
  mla: Mondelli, Marco, et al. “Simplified Successive Cancellation Decoding of Polar
    Codes Has Sublinear Latency.” <i>IEEE International Symposium on Information Theory</i>,
    vol. 2020–June, 401–406, IEEE, 2020, doi:<a href="https://doi.org/10.1109/ISIT44484.2020.9174141">10.1109/ISIT44484.2020.9174141</a>.
  short: M. Mondelli, S.A. Hashemi, J. Cioffi, A. Goldsmith, in:, IEEE International
    Symposium on Information Theory, IEEE, 2020.
conference:
  end_date: 2020-06-26
  location: Los Angeles, CA, United States
  name: 'ISIT: International Symposium on Information Theory'
  start_date: 2020-06-21
date_created: 2020-09-20T22:01:37Z
date_published: 2020-06-01T00:00:00Z
date_updated: 2026-08-12T11:12:23Z
day: '01'
department:
- _id: MaMo
doi: 10.1109/ISIT44484.2020.9174141
external_id:
  arxiv:
  - '1909.04892'
  isi:
  - '000714963400069'
isi: 1
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1909.04892
month: '06'
oa: 1
oa_version: Preprint
publication: IEEE International Symposium on Information Theory
publication_identifier:
  isbn:
  - '9781728164328'
  issn:
  - 2157-8095
publication_status: published
publisher: IEEE
quality_controlled: '1'
related_material:
  record:
  - id: '9047'
    relation: later_version
    status: public
scopus_import: '1'
status: public
title: Simplified successive cancellation decoding of polar codes has sublinear latency
type: conference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 2020-June
year: '2020'
...
---
_id: '7651'
abstract:
- lang: eng
  text: The growth of snail shells can be described by simple mathematical rules.
    Variation in a few parameters can explain much of the diversity of shell shapes
    seen in nature. However, empirical studies of gastropod shell shape variation
    typically use geometric morphometric approaches, which do not capture this growth
    pattern. We have developed a way to infer a set of developmentally descriptive
    shape parameters based on three-dimensional logarithmic helicospiral growth and
    using landmarks from two-dimensional shell images as input. We demonstrate the
    utility of this approach, and compare it to the geometric morphometric approach,
    using a large set of Littorina saxatilis shells in which locally adapted populations
    differ in shape. Our method can be modified easily to make it applicable to a
    wide range of shell forms, which would allow for investigations of the similarities
    and differences between and within many different species of gastropods.
article_number: '20190721'
article_processing_charge: No
article_type: original
author:
- first_name: J.
  full_name: Larsson, J.
  last_name: Larsson
- first_name: Anja M
  full_name: Westram, Anja M
  id: 3C147470-F248-11E8-B48F-1D18A9856A87
  last_name: Westram
  orcid: 0000-0003-1050-4969
- first_name: S.
  full_name: Bengmark, S.
  last_name: Bengmark
- first_name: T.
  full_name: Lundh, T.
  last_name: Lundh
- first_name: R. K.
  full_name: Butlin, R. K.
  last_name: Butlin
citation:
  ama: Larsson J, Westram AM, Bengmark S, Lundh T, Butlin RK. A developmentally descriptive
    method for quantifying shape in gastropod shells. <i>Journal of the Royal Society
    Interface</i>. 2020;17(163). doi:<a href="https://doi.org/10.1098/rsif.2019.0721">10.1098/rsif.2019.0721</a>
  apa: Larsson, J., Westram, A. M., Bengmark, S., Lundh, T., &#38; Butlin, R. K. (2020).
    A developmentally descriptive method for quantifying shape in gastropod shells.
    <i>Journal of the Royal Society Interface</i>. Royal Society. <a href="https://doi.org/10.1098/rsif.2019.0721">https://doi.org/10.1098/rsif.2019.0721</a>
  chicago: Larsson, J., Anja M Westram, S. Bengmark, T. Lundh, and R. K. Butlin. “A
    Developmentally Descriptive Method for Quantifying Shape in Gastropod Shells.”
    <i>Journal of the Royal Society Interface</i>. Royal Society, 2020. <a href="https://doi.org/10.1098/rsif.2019.0721">https://doi.org/10.1098/rsif.2019.0721</a>.
  ieee: J. Larsson, A. M. Westram, S. Bengmark, T. Lundh, and R. K. Butlin, “A developmentally
    descriptive method for quantifying shape in gastropod shells,” <i>Journal of the
    Royal Society Interface</i>, vol. 17, no. 163. Royal Society, 2020.
  ista: Larsson J, Westram AM, Bengmark S, Lundh T, Butlin RK. 2020. A developmentally
    descriptive method for quantifying shape in gastropod shells. Journal of the Royal
    Society Interface. 17(163), 20190721.
  mla: Larsson, J., et al. “A Developmentally Descriptive Method for Quantifying Shape
    in Gastropod Shells.” <i>Journal of the Royal Society Interface</i>, vol. 17,
    no. 163, 20190721, Royal Society, 2020, doi:<a href="https://doi.org/10.1098/rsif.2019.0721">10.1098/rsif.2019.0721</a>.
  short: J. Larsson, A.M. Westram, S. Bengmark, T. Lundh, R.K. Butlin, Journal of
    the Royal Society Interface 17 (2020).
date_created: 2020-04-08T15:19:17Z
date_published: 2020-02-01T00:00:00Z
date_updated: 2026-08-12T14:06:19Z
day: '01'
ddc:
- '570'
department:
- _id: NiBa
doi: 10.1098/rsif.2019.0721
file:
- access_level: open_access
  checksum: 4eb102304402f5c56432516b84df86d6
  content_type: application/pdf
  creator: dernst
  date_created: 2020-04-14T12:31:16Z
  date_updated: 2020-07-14T12:48:01Z
  file_id: '7660'
  file_name: 2020_JournRoyalSociety_Larsson.pdf
  file_size: 1556190
  relation: main_file
file_date_updated: 2020-07-14T12:48:01Z
has_accepted_license: '1'
intvolume: '        17'
issue: '163'
language:
- iso: eng
month: '02'
oa: 1
oa_version: Published Version
publication: Journal of the Royal Society Interface
publication_identifier:
  eissn:
  - 1742-5662
  issn:
  - 1742-5689
publication_status: published
publisher: Royal Society
quality_controlled: '1'
scopus_import: '1'
status: public
title: A developmentally descriptive method for quantifying shape in gastropod shells
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 17
year: '2020'
...
---
_id: '7431'
abstract:
- lang: eng
  text: 'In many real-world systems, information can be transmitted in two qualitatively
    different ways: by copying or by transformation. Copying occurs when messages
    are transmitted without modification, e.g. when an offspring receives an unaltered
    copy of a gene from its parent. Transformation occurs when messages are modified
    systematically during transmission, e.g. when mutational biases occur during genetic
    replication. Standard information-theoretic measures do not distinguish these
    two modes of information transfer, although they may reflect different mechanisms
    and have different functional consequences. Starting from a few simple axioms,
    we derive a decomposition of mutual information into the information transmitted
    by copying versus the information transmitted by transformation. We begin with
    a decomposition that applies when the source and destination of the channel have
    the same set of messages and a notion of message identity exists. We then generalize
    our decomposition to other kinds of channels, which can involve different source
    and destination sets and broader notions of similarity. In addition, we show that
    copy information can be interpreted as the minimal work needed by a physical copying
    process, which is relevant for understanding the physics of replication. We use
    the proposed decomposition to explore a model of amino acid substitution rates.
    Our results apply to any system in which the fidelity of copying, rather than
    simple predictability, is of critical relevance.'
acknowledgement: "AK was supported by Grant No. FQXi-RFP-1622 from the FQXi foundation,
  and Grant No. CHE-1648973 from the U.S.\r\nNational Science Foundation. AK would
  like to thank the Santa Fe Institute for supporting this research. The authors\r\nthank
  Jordi Fortuny, Rudolf Hanel, Joshua Garland, and Blai Vidiella for helpful discussions,
  as well as the anonymous\r\nreviewers for their insightful suggestions. "
article_number: '0623'
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Artemy
  full_name: Kolchinsky, Artemy
  last_name: Kolchinsky
- first_name: Bernat
  full_name: Corominas-Murtra, Bernat
  id: 43BE2298-F248-11E8-B48F-1D18A9856A87
  last_name: Corominas-Murtra
  orcid: 0000-0001-9806-5643
citation:
  ama: Kolchinsky A, Corominas-Murtra B. Decomposing information into copying versus
    transformation. <i>Journal of the Royal Society Interface</i>. 2020;17(162). doi:<a
    href="https://doi.org/10.1098/rsif.2019.0623">10.1098/rsif.2019.0623</a>
  apa: Kolchinsky, A., &#38; Corominas-Murtra, B. (2020). Decomposing information
    into copying versus transformation. <i>Journal of the Royal Society Interface</i>.
    Royal Society. <a href="https://doi.org/10.1098/rsif.2019.0623">https://doi.org/10.1098/rsif.2019.0623</a>
  chicago: Kolchinsky, Artemy, and Bernat Corominas-Murtra. “Decomposing Information
    into Copying versus Transformation.” <i>Journal of the Royal Society Interface</i>.
    Royal Society, 2020. <a href="https://doi.org/10.1098/rsif.2019.0623">https://doi.org/10.1098/rsif.2019.0623</a>.
  ieee: A. Kolchinsky and B. Corominas-Murtra, “Decomposing information into copying
    versus transformation,” <i>Journal of the Royal Society Interface</i>, vol. 17,
    no. 162. Royal Society, 2020.
  ista: Kolchinsky A, Corominas-Murtra B. 2020. Decomposing information into copying
    versus transformation. Journal of the Royal Society Interface. 17(162), 0623.
  mla: Kolchinsky, Artemy, and Bernat Corominas-Murtra. “Decomposing Information into
    Copying versus Transformation.” <i>Journal of the Royal Society Interface</i>,
    vol. 17, no. 162, 0623, Royal Society, 2020, doi:<a href="https://doi.org/10.1098/rsif.2019.0623">10.1098/rsif.2019.0623</a>.
  short: A. Kolchinsky, B. Corominas-Murtra, Journal of the Royal Society Interface
    17 (2020).
date_created: 2020-02-02T23:01:03Z
date_published: 2020-01-29T00:00:00Z
date_updated: 2026-08-12T14:08:47Z
day: '29'
department:
- _id: EdHa
doi: 10.1098/rsif.2019.0623
external_id:
  arxiv:
  - '1903.10693'
  isi:
  - '000538369800002'
  pmid:
  - '31964273'
intvolume: '        17'
isi: 1
issue: '162'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1903.10693
month: '01'
oa: 1
oa_version: Preprint
pmid: 1
publication: Journal of the Royal Society Interface
publication_identifier:
  eissn:
  - 1742-5662
publication_status: published
publisher: Royal Society
quality_controlled: '1'
scopus_import: '1'
status: public
title: Decomposing information into copying versus transformation
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 17
year: '2020'
...
---
OA_place: publisher
OA_type: hybrid
_id: '9814'
abstract:
- lang: eng
  text: Data and mathematica notebooks for plotting figures from Language learning
    with communication between learners
article_processing_charge: No
author:
- first_name: Rasmus
  full_name: Ibsen-Jensen, Rasmus
  id: 3B699956-F248-11E8-B48F-1D18A9856A87
  last_name: Ibsen-Jensen
  orcid: 0000-0003-4783-0389
- first_name: Josef
  full_name: Tkadlec, Josef
  id: 3F24CCC8-F248-11E8-B48F-1D18A9856A87
  last_name: Tkadlec
  orcid: 0000-0002-1097-9684
- first_name: Krishnendu
  full_name: Chatterjee, Krishnendu
  id: 2E5DCA20-F248-11E8-B48F-1D18A9856A87
  last_name: Chatterjee
  orcid: 0000-0002-4561-241X
- first_name: Martin
  full_name: Nowak, Martin
  last_name: Nowak
citation:
  ama: Ibsen-Jensen R, Tkadlec J, Chatterjee K, Nowak M. Data and mathematica notebooks
    for plotting figures from language learning with communication between learners
    from language acquisition with communication between learners. 2020. doi:<a href="https://doi.org/10.6084/m9.figshare.5973013.v1">10.6084/m9.figshare.5973013.v1</a>
  apa: Ibsen-Jensen, R., Tkadlec, J., Chatterjee, K., &#38; Nowak, M. (2020). Data
    and mathematica notebooks for plotting figures from language learning with communication
    between learners from language acquisition with communication between learners.
    Royal Society. <a href="https://doi.org/10.6084/m9.figshare.5973013.v1">https://doi.org/10.6084/m9.figshare.5973013.v1</a>
  chicago: Ibsen-Jensen, Rasmus, Josef Tkadlec, Krishnendu Chatterjee, and Martin
    Nowak. “Data and Mathematica Notebooks for Plotting Figures from Language Learning
    with Communication between Learners from Language Acquisition with Communication
    between Learners.” Royal Society, 2020. <a href="https://doi.org/10.6084/m9.figshare.5973013.v1">https://doi.org/10.6084/m9.figshare.5973013.v1</a>.
  ieee: R. Ibsen-Jensen, J. Tkadlec, K. Chatterjee, and M. Nowak, “Data and mathematica
    notebooks for plotting figures from language learning with communication between
    learners from language acquisition with communication between learners.” Royal
    Society, 2020.
  ista: Ibsen-Jensen R, Tkadlec J, Chatterjee K, Nowak M. 2020. Data and mathematica
    notebooks for plotting figures from language learning with communication between
    learners from language acquisition with communication between learners, Royal
    Society, <a href="https://doi.org/10.6084/m9.figshare.5973013.v1">10.6084/m9.figshare.5973013.v1</a>.
  mla: Ibsen-Jensen, Rasmus, et al. <i>Data and Mathematica Notebooks for Plotting
    Figures from Language Learning with Communication between Learners from Language
    Acquisition with Communication between Learners</i>. Royal Society, 2020, doi:<a
    href="https://doi.org/10.6084/m9.figshare.5973013.v1">10.6084/m9.figshare.5973013.v1</a>.
  short: R. Ibsen-Jensen, J. Tkadlec, K. Chatterjee, M. Nowak, (2020).
date_created: 2021-08-06T13:09:57Z
date_published: 2020-10-15T00:00:00Z
date_updated: 2026-08-12T14:08:28Z
day: '15'
department:
- _id: KrCh
doi: 10.6084/m9.figshare.5973013.v1
main_file_link:
- open_access: '1'
  url: https://doi.org/10.6084/m9.figshare.5973013.v1
month: '10'
oa: 1
oa_version: Published Version
publisher: Royal Society
related_material:
  record:
  - id: '198'
    relation: used_in_publication
    status: public
status: public
title: Data and mathematica notebooks for plotting figures from language learning
  with communication between learners from language acquisition with communication
  between learners
type: research_data_reference
user_id: 0043cee0-e5fc-11ee-9736-f83bc23afbf0
year: '2020'
...
---
_id: '7563'
abstract:
- lang: eng
  text: "We introduce “state space persistence analysis” for deducing the symbolic
    dynamics of time series data obtained from high-dimensional chaotic attractors.
    To this end, we adapt a topological data analysis technique known as persistent
    homology for the characterization of state space projections of chaotic trajectories
    and periodic orbits. By comparing the shapes along a chaotic trajectory to those
    of the periodic orbits, state space persistence analysis quantifies the shape
    similarity of chaotic trajectory segments and periodic orbits. We demonstrate
    the method by applying it to the three-dimensional Rössler system and a 30-dimensional
    discretization of the Kuramoto–Sivashinsky partial differential equation in (1+1)
    dimensions.\r\nOne way of studying chaotic attractors systematically is through
    their symbolic dynamics, in which one partitions the state space into qualitatively
    different regions and assigns a symbol to each such region.1–3 This yields a “coarse-grained”
    state space of the system, which can then be reduced to a Markov chain encoding
    all possible transitions between the states of the system. While it is possible
    to obtain the symbolic dynamics of low-dimensional chaotic systems with standard
    tools such as Poincaré maps, when applied to high-dimensional systems such as
    turbulent flows, these tools alone are not sufficient to determine symbolic dynamics.4,5
    In this paper, we develop “state space persistence analysis” and demonstrate that
    it can be utilized to infer the symbolic dynamics in very high-dimensional settings."
article_number: '033109'
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Gökhan
  full_name: Yalniz, Gökhan
  id: 66E74FA2-D8BF-11E9-8249-8DE2E5697425
  last_name: Yalniz
  orcid: 0000-0002-8490-9312
- first_name: Nazmi B
  full_name: Budanur, Nazmi B
  id: 3EA1010E-F248-11E8-B48F-1D18A9856A87
  last_name: Budanur
  orcid: 0000-0003-0423-5010
citation:
  ama: Yalniz G, Budanur NB. Inferring symbolic dynamics of chaotic flows from persistence.
    <i>Chaos</i>. 2020;30(3). doi:<a href="https://doi.org/10.1063/1.5122969">10.1063/1.5122969</a>
  apa: Yalniz, G., &#38; Budanur, N. B. (2020). Inferring symbolic dynamics of chaotic
    flows from persistence. <i>Chaos</i>. AIP Publishing. <a href="https://doi.org/10.1063/1.5122969">https://doi.org/10.1063/1.5122969</a>
  chicago: Yalniz, Gökhan, and Nazmi B Budanur. “Inferring Symbolic Dynamics of Chaotic
    Flows from Persistence.” <i>Chaos</i>. AIP Publishing, 2020. <a href="https://doi.org/10.1063/1.5122969">https://doi.org/10.1063/1.5122969</a>.
  ieee: G. Yalniz and N. B. Budanur, “Inferring symbolic dynamics of chaotic flows
    from persistence,” <i>Chaos</i>, vol. 30, no. 3. AIP Publishing, 2020.
  ista: Yalniz G, Budanur NB. 2020. Inferring symbolic dynamics of chaotic flows from
    persistence. Chaos. 30(3), 033109.
  mla: Yalniz, Gökhan, and Nazmi B. Budanur. “Inferring Symbolic Dynamics of Chaotic
    Flows from Persistence.” <i>Chaos</i>, vol. 30, no. 3, 033109, AIP Publishing,
    2020, doi:<a href="https://doi.org/10.1063/1.5122969">10.1063/1.5122969</a>.
  short: G. Yalniz, N.B. Budanur, Chaos 30 (2020).
corr_author: '1'
date_created: 2020-03-04T08:06:25Z
date_published: 2020-03-03T00:00:00Z
date_updated: 2026-09-02T08:16:31Z
day: '03'
ddc:
- '530'
department:
- _id: BjHo
doi: 10.1063/1.5122969
external_id:
  arxiv:
  - '1910.04584'
  isi:
  - '000519254800002'
intvolume: '        30'
isi: 1
issue: '3'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1063/1.5122969
month: '03'
oa: 1
oa_version: Published Version
publication: Chaos
publication_identifier:
  eissn:
  - 1089-7682
  issn:
  - 1054-1500
publication_status: published
publisher: AIP Publishing
quality_controlled: '1'
related_material:
  record:
  - id: '19684'
    relation: dissertation_contains
    status: public
scopus_import: '1'
status: public
title: Inferring symbolic dynamics of chaotic flows from persistence
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 30
year: '2020'
...
---
_id: '8586'
abstract:
- lang: eng
  text: Cryo-electron microscopy (cryo-EM) of cellular specimens provides insights
    into biological processes and structures within a native context. However, a major
    challenge still lies in the efficient and reproducible preparation of adherent
    cells for subsequent cryo-EM analysis. This is due to the sensitivity of many
    cellular specimens to the varying seeding and culturing conditions required for
    EM experiments, the often limited amount of cellular material and also the fragility
    of EM grids and their substrate. Here, we present low-cost and reusable 3D printed
    grid holders, designed to improve specimen preparation when culturing challenging
    cellular samples directly on grids. The described grid holders increase cell culture
    reproducibility and throughput, and reduce the resources required for cell culturing.
    We show that grid holders can be integrated into various cryo-EM workflows, including
    micro-patterning approaches to control cell seeding on grids, and for generating
    samples for cryo-focused ion beam milling and cryo-electron tomography experiments.
    Their adaptable design allows for the generation of specialized grid holders customized
    to a large variety of applications.
acknowledged_ssus:
- _id: ScienComp
- _id: LifeSc
- _id: Bio
- _id: EM-Fac
acknowledgement: This work was supported by the Austrian Science Fund (FWF, P33367)
  to FKMS. BZ acknowledges support by the Niederösterreich Fond. This research was
  also supported by the Scientific Service Units (SSU) of IST Austria through resources
  provided by Scientific Computing (SciComp), the Life Science Facility (LSF), the
  BioImaging Facility (BIF) and the Electron Microscopy Facility (EMF). We thank Georgi
  Dimchev (IST Austria) and Sonja Jacob (Vienna Biocenter Core Facilities) for testing
  our grid holders in different experimental setups and Daniel Gütl and the Kondrashov
  group (IST Austria) for granting us repeated access to their 3D printers. We also
  thank Jonna Alanko and the Sixt lab (IST Austria) for providing us HeLa cells, primary
  BL6 mouse tail fibroblasts, NIH 3T3 fibroblasts and human telomerase immortalised
  foreskin fibroblasts for our experiments. We are thankful to Ori Avinoam and William
  Wan for helpful comments on the manuscript and also thank Dorotea Fracchiolla (Art&Science)
  for illustrating the graphical abstract.
article_number: '107633'
article_processing_charge: Yes (via OA deal)
article_type: original
author:
- first_name: Florian
  full_name: Fäßler, Florian
  id: 404F5528-F248-11E8-B48F-1D18A9856A87
  last_name: Fäßler
  orcid: 0000-0001-7149-769X
- first_name: Bettina
  full_name: Zens, Bettina
  id: 45FD126C-F248-11E8-B48F-1D18A9856A87
  last_name: Zens
  orcid: 0000-0002-9561-1239
- first_name: Robert
  full_name: Hauschild, Robert
  id: 4E01D6B4-F248-11E8-B48F-1D18A9856A87
  last_name: Hauschild
  orcid: 0000-0001-9843-3522
- first_name: Florian KM
  full_name: Schur, Florian KM
  id: 48AD8942-F248-11E8-B48F-1D18A9856A87
  last_name: Schur
  orcid: 0000-0003-4790-8078
citation:
  ama: Fäßler F, Zens B, Hauschild R, Schur FK. 3D printed cell culture grid holders
    for improved cellular specimen preparation in cryo-electron microscopy. <i>Journal
    of Structural Biology</i>. 2020;212(3). doi:<a href="https://doi.org/10.1016/j.jsb.2020.107633">10.1016/j.jsb.2020.107633</a>
  apa: Fäßler, F., Zens, B., Hauschild, R., &#38; Schur, F. K. (2020). 3D printed
    cell culture grid holders for improved cellular specimen preparation in cryo-electron
    microscopy. <i>Journal of Structural Biology</i>. Elsevier. <a href="https://doi.org/10.1016/j.jsb.2020.107633">https://doi.org/10.1016/j.jsb.2020.107633</a>
  chicago: Fäßler, Florian, Bettina Zens, Robert Hauschild, and Florian KM Schur.
    “3D Printed Cell Culture Grid Holders for Improved Cellular Specimen Preparation
    in Cryo-Electron Microscopy.” <i>Journal of Structural Biology</i>. Elsevier,
    2020. <a href="https://doi.org/10.1016/j.jsb.2020.107633">https://doi.org/10.1016/j.jsb.2020.107633</a>.
  ieee: F. Fäßler, B. Zens, R. Hauschild, and F. K. Schur, “3D printed cell culture
    grid holders for improved cellular specimen preparation in cryo-electron microscopy,”
    <i>Journal of Structural Biology</i>, vol. 212, no. 3. Elsevier, 2020.
  ista: Fäßler F, Zens B, Hauschild R, Schur FK. 2020. 3D printed cell culture grid
    holders for improved cellular specimen preparation in cryo-electron microscopy.
    Journal of Structural Biology. 212(3), 107633.
  mla: Fäßler, Florian, et al. “3D Printed Cell Culture Grid Holders for Improved
    Cellular Specimen Preparation in Cryo-Electron Microscopy.” <i>Journal of Structural
    Biology</i>, vol. 212, no. 3, 107633, Elsevier, 2020, doi:<a href="https://doi.org/10.1016/j.jsb.2020.107633">10.1016/j.jsb.2020.107633</a>.
  short: F. Fäßler, B. Zens, R. Hauschild, F.K. Schur, Journal of Structural Biology
    212 (2020).
corr_author: '1'
date_created: 2020-09-29T13:24:06Z
date_published: 2020-12-01T00:00:00Z
date_updated: 2026-09-04T22:30:02Z
day: '01'
ddc:
- '570'
department:
- _id: FlSc
doi: 10.1016/j.jsb.2020.107633
external_id:
  isi:
  - '000600997800008'
  pmid:
  - '32987119'
file:
- access_level: open_access
  checksum: c48cbf594e84fc2f91966ffaafc0918c
  content_type: application/pdf
  creator: dernst
  date_created: 2020-12-10T14:01:10Z
  date_updated: 2020-12-10T14:01:10Z
  file_id: '8937'
  file_name: 2020_JourStrucBiology_Faessler.pdf
  file_size: 7076870
  relation: main_file
  success: 1
file_date_updated: 2020-12-10T14:01:10Z
has_accepted_license: '1'
intvolume: '       212'
isi: 1
issue: '3'
keyword:
- electron microscopy
- cryo-EM
- EM sample preparation
- 3D printing
- cell culture
language:
- iso: eng
month: '12'
oa: 1
oa_version: Published Version
pmid: 1
project:
- _id: 9B954C5C-BA93-11EA-9121-9846C619BF3A
  grant_number: P33367
  name: Structure and isoform diversity of the Arp2/3 complex
- _id: 059B463C-7A3F-11EA-A408-12923DDC885E
  name: NÖ-Fonds Preis für die Jungforscherin des Jahres am IST Austria
publication: Journal of Structural Biology
publication_identifier:
  issn:
  - 1047-8477
publication_status: published
publisher: Elsevier
quality_controlled: '1'
related_material:
  record:
  - id: '14592'
    relation: used_in_publication
    status: public
  - id: '12491'
    relation: dissertation_contains
    status: public
scopus_import: '1'
status: public
title: 3D printed cell culture grid holders for improved cellular specimen preparation
  in cryo-electron microscopy
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 212
year: '2020'
...
---
_id: '7473'
abstract:
- lang: eng
  text: How structural and functional properties of synapses relate to each other
    is a fundamental question in neuroscience. Electrophysiology has elucidated mechanisms
    of synaptic transmission, and electron microscopy (EM) has provided insight into
    morphological properties of synapses. Here we describe an enhanced method for
    functional EM (“flash and freeze”), combining optogenetic stimulation with high-pressure
    freezing. We demonstrate that the improved method can be applied to intact networks
    in acute brain slices and organotypic slice cultures from mice. As a proof of
    concept, we probed vesicle pool changes during synaptic transmission at the hippocampal
    mossy fiber-CA3 pyramidal neuron synapse. Our findings show overlap of the docked
    vesicle pool and the functionally defined readily releasable pool and provide
    evidence of fast endocytosis at this synapse. Functional EM with acute slices
    and slice cultures has the potential to reveal the structural and functional mechanisms
    of transmission in intact, genetically perturbed, and disease-affected synapses.
acknowledgement: This project has received funding from the European Research Council
  (ERC) and European Commission (EC), under the European Union’s Horizon 2020 research
  and innovation programme (ERC grant agreement No. 692692 and Marie Sklodowska-Curie
  708497) and from Fonds zur Förderung der Wissenschaftlichen Forschung (Z 312-B27
  Wittgenstein award and DK W1205-B09). We thank Johann Danzl and Ryuichi Shigemoto
  for critically reading the manuscript; Walter Kaufmann, Daniel Gutl, and Vanessa
  Zheden for extensive EM training, advice, and experimental assistance; Benjamin
  Suter for substantial help with light stimulation, ImageJ plugins for analysis,
  and manuscript editing; Florian Marr and Christina Altmutter for technical support;
  Eleftheria Kralli-Beller for manuscript editing; Julia König and Paul Wurzinger
  (Leica Microsystems) for helpful technical discussions; and Taija Makinen for providing
  the Prox1-CreERT2 mouse line.
article_processing_charge: No
article_type: original
author:
- first_name: Carolina
  full_name: Borges Merjane, Carolina
  id: 4305C450-F248-11E8-B48F-1D18A9856A87
  last_name: Borges Merjane
  orcid: 0000-0003-0005-401X
- first_name: Olena
  full_name: Kim, Olena
  id: 3F8ABDDA-F248-11E8-B48F-1D18A9856A87
  last_name: Kim
  orcid: 0000-0003-2344-1039
- first_name: Peter M
  full_name: Jonas, Peter M
  id: 353C1B58-F248-11E8-B48F-1D18A9856A87
  last_name: Jonas
  orcid: 0000-0001-5001-4804
citation:
  ama: Borges Merjane C, Kim O, Jonas PM. Functional electron microscopy (“Flash and
    Freeze”) of identified cortical synapses in acute brain slices. <i>Neuron</i>.
    2020;105:992-1006. doi:<a href="https://doi.org/10.1016/j.neuron.2019.12.022">10.1016/j.neuron.2019.12.022</a>
  apa: Borges Merjane, C., Kim, O., &#38; Jonas, P. M. (2020). Functional electron
    microscopy (“Flash and Freeze”) of identified cortical synapses in acute brain
    slices. <i>Neuron</i>. Elsevier. <a href="https://doi.org/10.1016/j.neuron.2019.12.022">https://doi.org/10.1016/j.neuron.2019.12.022</a>
  chicago: Borges Merjane, Carolina, Olena Kim, and Peter M Jonas. “Functional Electron
    Microscopy (‘Flash and Freeze’) of Identified Cortical Synapses in Acute Brain
    Slices.” <i>Neuron</i>. Elsevier, 2020. <a href="https://doi.org/10.1016/j.neuron.2019.12.022">https://doi.org/10.1016/j.neuron.2019.12.022</a>.
  ieee: C. Borges Merjane, O. Kim, and P. M. Jonas, “Functional electron microscopy
    (‘Flash and Freeze’) of identified cortical synapses in acute brain slices,” <i>Neuron</i>,
    vol. 105. Elsevier, pp. 992–1006, 2020.
  ista: Borges Merjane C, Kim O, Jonas PM. 2020. Functional electron microscopy (“Flash
    and Freeze”) of identified cortical synapses in acute brain slices. Neuron. 105,
    992–1006.
  mla: Borges Merjane, Carolina, et al. “Functional Electron Microscopy (‘Flash and
    Freeze’) of Identified Cortical Synapses in Acute Brain Slices.” <i>Neuron</i>,
    vol. 105, Elsevier, 2020, pp. 992–1006, doi:<a href="https://doi.org/10.1016/j.neuron.2019.12.022">10.1016/j.neuron.2019.12.022</a>.
  short: C. Borges Merjane, O. Kim, P.M. Jonas, Neuron 105 (2020) 992–1006.
corr_author: '1'
date_created: 2020-02-10T15:59:45Z
date_published: 2020-03-18T00:00:00Z
date_updated: 2026-09-04T22:30:05Z
day: '18'
ddc:
- '570'
department:
- _id: PeJo
doi: 10.1016/j.neuron.2019.12.022
ec_funded: 1
external_id:
  isi:
  - '000520854700008'
  pmid:
  - '31928842'
file:
- access_level: open_access
  checksum: 3582664addf26859e86ac5bec3e01416
  content_type: application/pdf
  creator: dernst
  date_created: 2020-11-20T08:58:53Z
  date_updated: 2020-11-20T08:58:53Z
  file_id: '8778'
  file_name: 2020_Neuron_BorgesMerjane.pdf
  file_size: 9712957
  relation: main_file
  success: 1
file_date_updated: 2020-11-20T08:58:53Z
has_accepted_license: '1'
intvolume: '       105'
isi: 1
language:
- iso: eng
month: '03'
oa: 1
oa_version: Published Version
page: 992-1006
pmid: 1
project:
- _id: 25B7EB9E-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '692692'
  name: Biophysics and circuit function of a giant cortical glutamatergic synapse
- _id: 25BAF7B2-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '708497'
  name: Presynaptic calcium channels distribution and impact on coupling at the hippocampal
    mossy fiber synapse
- _id: 25C5A090-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: Z00312
  name: Synaptic communication in neuronal microcircuits
- _id: 25C3DBB6-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: W01205
  name: Zellkommunikation in Gesundheit und Krankheit
publication: Neuron
publication_identifier:
  issn:
  - 0896-6273
publication_status: published
publisher: Elsevier
quality_controlled: '1'
related_material:
  link:
  - description: News on IST Homepage
    relation: press_release
    url: https://ist.ac.at/en/news/flash-and-freeze-reveals-dynamics-of-nerve-connections/
  record:
  - id: '11196'
    relation: dissertation_contains
    status: public
scopus_import: '1'
status: public
title: Functional electron microscopy (“Flash and Freeze”) of identified cortical
  synapses in acute brain slices
tmp:
  image: /images/cc_by_nc_nd.png
  legal_code_url: https://creativecommons.org/licenses/by-nc-nd/4.0/legalcode
  name: Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International
    (CC BY-NC-ND 4.0)
  short: CC BY-NC-ND (4.0)
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 105
year: '2020'
...
---
_id: '7387'
abstract:
- lang: eng
  text: Most bacteria accomplish cell division with the help of a dynamic protein
    complex called the divisome, which spans the cell envelope in the plane of division.
    Assembly and activation of this machinery are coordinated by the tubulin-related
    GTPase FtsZ, which was found to form treadmilling filaments on supported bilayers
    in vitro1, as well as in live cells, in which filaments circle around the cell
    division site2,3. Treadmilling of FtsZ is thought to actively move proteins around
    the division septum, thereby distributing peptidoglycan synthesis and coordinating
    the inward growth of the septum to form the new poles of the daughter cells4.
    However, the molecular mechanisms underlying this function are largely unknown.
    Here, to study how FtsZ polymerization dynamics are coupled to downstream proteins,
    we reconstituted part of the bacterial cell division machinery using its purified
    components FtsZ, FtsA and truncated transmembrane proteins essential for cell
    division. We found that the membrane-bound cytosolic peptides of FtsN and FtsQ
    co-migrated with treadmilling FtsZ–FtsA filaments, but despite their directed
    collective behaviour, individual peptides showed random motion and transient confinement.
    Our work suggests that divisome proteins follow treadmilling FtsZ filaments by
    a diffusion-and-capture mechanism, which can give rise to a moving zone of signalling
    activity at the division site.
acknowledgement: We acknowledge members of the Loose laboratory at IST Austria for
  helpful discussions—in particular, P. Caldas for help with the treadmilling analysis,
  M. Jimenez, A. Raso and N. Ropero for providing Alexa Fluor 488- and Alexa Fluor
  647-labelled FtsA for the MST and analytical ultracentrifugation experiments. We
  thank C. You for providing the DODA-tris-NTA phospholipids, as well as J. Piehler
  and C. Richter (Department of Biology, University of Osnabruck, Germany) for the
  SLIMfast single-molecule tracking software and help with the confinement analysis.
  We thank J. Errington and H. Murray (both at Newcastle University, UK) for critical
  reading of the manuscript, and J. Brugués (MPI-CBG and MPI-PKS, Dresden, Germany)
  for help with the MATLAB programming and reading of the manuscript. This work was
  supported by the European Research Council through grant ERC-2015-StG-679239 to
  M.L. and grants HFSP LT 000824/2016-L4 and EMBO ALTF 1163-2015 to N.B., a grant
  from the Ministry of Economy and Competitiveness of the Spanish Government (BFU2016-75471-C2-1-P)
  to C.A. and G.R., and a Wellcome Trust Senior Investigator award (101824/Z/13/Z)
  and a grant from the BBSRC (BB/R017409/1) to W.V.
article_processing_charge: No
article_type: letter_note
author:
- first_name: Natalia S.
  full_name: Baranova, Natalia S.
  id: 38661662-F248-11E8-B48F-1D18A9856A87
  last_name: Baranova
  orcid: 0000-0002-3086-9124
- first_name: Philipp
  full_name: Radler, Philipp
  id: 40136C2A-F248-11E8-B48F-1D18A9856A87
  last_name: Radler
  orcid: '0000-0001-9198-2182 '
- first_name: Víctor M.
  full_name: Hernández-Rocamora, Víctor M.
  last_name: Hernández-Rocamora
- first_name: Carlos
  full_name: Alfonso, Carlos
  last_name: Alfonso
- first_name: Maria D
  full_name: Lopez Pelegrin, Maria D
  id: 319AA9CE-F248-11E8-B48F-1D18A9856A87
  last_name: Lopez Pelegrin
- first_name: Germán
  full_name: Rivas, Germán
  last_name: Rivas
- first_name: Waldemar
  full_name: Vollmer, Waldemar
  last_name: Vollmer
- first_name: Martin
  full_name: Loose, Martin
  id: 462D4284-F248-11E8-B48F-1D18A9856A87
  last_name: Loose
  orcid: 0000-0001-7309-9724
citation:
  ama: Baranova NS, Radler P, Hernández-Rocamora VM, et al. Diffusion and capture
    permits dynamic coupling between treadmilling FtsZ filaments and cell division
    proteins. <i>Nature Microbiology</i>. 2020;5:407-417. doi:<a href="https://doi.org/10.1038/s41564-019-0657-5">10.1038/s41564-019-0657-5</a>
  apa: Baranova, N. S., Radler, P., Hernández-Rocamora, V. M., Alfonso, C., Lopez
    Pelegrin, M. D., Rivas, G., … Loose, M. (2020). Diffusion and capture permits
    dynamic coupling between treadmilling FtsZ filaments and cell division proteins.
    <i>Nature Microbiology</i>. Springer Nature. <a href="https://doi.org/10.1038/s41564-019-0657-5">https://doi.org/10.1038/s41564-019-0657-5</a>
  chicago: Baranova, Natalia S., Philipp Radler, Víctor M. Hernández-Rocamora, Carlos
    Alfonso, Maria D Lopez Pelegrin, Germán Rivas, Waldemar Vollmer, and Martin Loose.
    “Diffusion and Capture Permits Dynamic Coupling between Treadmilling FtsZ Filaments
    and Cell Division Proteins.” <i>Nature Microbiology</i>. Springer Nature, 2020.
    <a href="https://doi.org/10.1038/s41564-019-0657-5">https://doi.org/10.1038/s41564-019-0657-5</a>.
  ieee: N. S. Baranova <i>et al.</i>, “Diffusion and capture permits dynamic coupling
    between treadmilling FtsZ filaments and cell division proteins,” <i>Nature Microbiology</i>,
    vol. 5. Springer Nature, pp. 407–417, 2020.
  ista: Baranova NS, Radler P, Hernández-Rocamora VM, Alfonso C, Lopez Pelegrin MD,
    Rivas G, Vollmer W, Loose M. 2020. Diffusion and capture permits dynamic coupling
    between treadmilling FtsZ filaments and cell division proteins. Nature Microbiology.
    5, 407–417.
  mla: Baranova, Natalia S., et al. “Diffusion and Capture Permits Dynamic Coupling
    between Treadmilling FtsZ Filaments and Cell Division Proteins.” <i>Nature Microbiology</i>,
    vol. 5, Springer Nature, 2020, pp. 407–17, doi:<a href="https://doi.org/10.1038/s41564-019-0657-5">10.1038/s41564-019-0657-5</a>.
  short: N.S. Baranova, P. Radler, V.M. Hernández-Rocamora, C. Alfonso, M.D. Lopez
    Pelegrin, G. Rivas, W. Vollmer, M. Loose, Nature Microbiology 5 (2020) 407–417.
corr_author: '1'
date_created: 2020-01-28T16:14:41Z
date_published: 2020-01-20T00:00:00Z
date_updated: 2026-09-04T22:30:13Z
day: '20'
department:
- _id: MaLo
doi: 10.1038/s41564-019-0657-5
ec_funded: 1
external_id:
  isi:
  - '000508584700007'
  pmid:
  - '31959972'
intvolume: '         5'
isi: 1
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: http://europepmc.org/article/PMC/7048620
month: '01'
oa: 1
oa_version: Submitted Version
page: 407-417
pmid: 1
project:
- _id: 2595697A-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '679239'
  name: Self-Organization of the Bacterial Cell
- _id: 259B655A-B435-11E9-9278-68D0E5697425
  grant_number: LT000824/2016
  name: Reconstitution of bacterial cell wall synthesis
- _id: 2596EAB6-B435-11E9-9278-68D0E5697425
  grant_number: ALTF 2015-1163
  name: Synthesis of bacterial cell wall
publication: Nature Microbiology
publication_identifier:
  issn:
  - 2058-5276
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
related_material:
  link:
  - description: News on IST Homepage
    relation: press_release
    url: https://ist.ac.at/en/news/little-cell-big-cover-story/
  record:
  - id: '14280'
    relation: dissertation_contains
    status: public
scopus_import: '1'
status: public
title: Diffusion and capture permits dynamic coupling between treadmilling FtsZ filaments
  and cell division proteins
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 5
year: '2020'
...
---
_id: '7888'
abstract:
- lang: eng
  text: Embryonic stem cell cultures are thought to self-organize into embryoid bodies,
    able to undergo symmetry-breaking, germ layer specification and even morphogenesis.
    Yet, it is unclear how to reconcile this remarkable self-organization capacity
    with classical experiments demonstrating key roles for extrinsic biases by maternal
    factors and/or extraembryonic tissues in embryogenesis. Here, we show that zebrafish
    embryonic tissue explants, prepared prior to germ layer induction and lacking
    extraembryonic tissues, can specify all germ layers and form a seemingly complete
    mesendoderm anlage. Importantly, explant organization requires polarized inheritance
    of maternal factors from dorsal-marginal regions of the blastoderm. Moreover,
    induction of endoderm and head-mesoderm, which require peak Nodal-signaling levels,
    is highly variable in explants, reminiscent of embryos with reduced Nodal signals
    from the extraembryonic tissues. Together, these data suggest that zebrafish explants
    do not undergo bona fide self-organization, but rather display features of genetically
    encoded self-assembly, where intrinsic genetic programs control the emergence
    of order.
article_number: e55190
article_processing_charge: No
article_type: original
author:
- first_name: Alexandra
  full_name: Schauer, Alexandra
  id: 30A536BA-F248-11E8-B48F-1D18A9856A87
  last_name: Schauer
  orcid: 0000-0001-7659-9142
- first_name: Diana C
  full_name: Nunes Pinheiro, Diana C
  id: 2E839F16-F248-11E8-B48F-1D18A9856A87
  last_name: Nunes Pinheiro
  orcid: 0000-0003-4333-7503
- first_name: Robert
  full_name: Hauschild, Robert
  id: 4E01D6B4-F248-11E8-B48F-1D18A9856A87
  last_name: Hauschild
  orcid: 0000-0001-9843-3522
- first_name: Carl-Philipp J
  full_name: Heisenberg, Carl-Philipp J
  id: 39427864-F248-11E8-B48F-1D18A9856A87
  last_name: Heisenberg
  orcid: 0000-0002-0912-4566
citation:
  ama: Schauer A, Nunes Pinheiro DC, Hauschild R, Heisenberg C-PJ. Zebrafish embryonic
    explants undergo genetically encoded self-assembly. <i>eLife</i>. 2020;9. doi:<a
    href="https://doi.org/10.7554/elife.55190">10.7554/elife.55190</a>
  apa: Schauer, A., Nunes Pinheiro, D. C., Hauschild, R., &#38; Heisenberg, C.-P.
    J. (2020). Zebrafish embryonic explants undergo genetically encoded self-assembly.
    <i>ELife</i>. eLife Sciences Publications. <a href="https://doi.org/10.7554/elife.55190">https://doi.org/10.7554/elife.55190</a>
  chicago: Schauer, Alexandra, Diana C Nunes Pinheiro, Robert Hauschild, and Carl-Philipp
    J Heisenberg. “Zebrafish Embryonic Explants Undergo Genetically Encoded Self-Assembly.”
    <i>ELife</i>. eLife Sciences Publications, 2020. <a href="https://doi.org/10.7554/elife.55190">https://doi.org/10.7554/elife.55190</a>.
  ieee: A. Schauer, D. C. Nunes Pinheiro, R. Hauschild, and C.-P. J. Heisenberg, “Zebrafish
    embryonic explants undergo genetically encoded self-assembly,” <i>eLife</i>, vol.
    9. eLife Sciences Publications, 2020.
  ista: Schauer A, Nunes Pinheiro DC, Hauschild R, Heisenberg C-PJ. 2020. Zebrafish
    embryonic explants undergo genetically encoded self-assembly. eLife. 9, e55190.
  mla: Schauer, Alexandra, et al. “Zebrafish Embryonic Explants Undergo Genetically
    Encoded Self-Assembly.” <i>ELife</i>, vol. 9, e55190, eLife Sciences Publications,
    2020, doi:<a href="https://doi.org/10.7554/elife.55190">10.7554/elife.55190</a>.
  short: A. Schauer, D.C. Nunes Pinheiro, R. Hauschild, C.-P.J. Heisenberg, ELife
    9 (2020).
corr_author: '1'
date_created: 2020-05-25T15:01:40Z
date_published: 2020-04-06T00:00:00Z
date_updated: 2026-09-04T22:30:15Z
day: '06'
ddc:
- '570'
department:
- _id: CaHe
- _id: Bio
doi: 10.7554/elife.55190
ec_funded: 1
external_id:
  isi:
  - '000531544400001'
  pmid:
  - '32250246'
file:
- access_level: open_access
  checksum: f6aad884cf706846ae9357fcd728f8b5
  content_type: application/pdf
  creator: dernst
  date_created: 2020-05-25T15:15:43Z
  date_updated: 2020-07-14T12:48:04Z
  file_id: '7890'
  file_name: 2020_eLife_Schauer.pdf
  file_size: 7744848
  relation: main_file
file_date_updated: 2020-07-14T12:48:04Z
has_accepted_license: '1'
intvolume: '         9'
isi: 1
language:
- iso: eng
month: '04'
oa: 1
oa_version: Published Version
pmid: 1
project:
- _id: 260F1432-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '742573'
  name: Interaction and feedback between cell mechanics and fate specification in
    vertebrate gastrulation
- _id: 26B1E39C-B435-11E9-9278-68D0E5697425
  grant_number: '25239'
  name: 'Mesendoderm specification in zebrafish: The role of extraembryonic tissues'
- _id: 26520D1E-B435-11E9-9278-68D0E5697425
  grant_number: ALTF 850-2017
  name: Coordination of mesendoderm cell fate specification and internalization during
    zebrafish gastrulation
- _id: 266BC5CE-B435-11E9-9278-68D0E5697425
  grant_number: LT000429
  name: Coordination of mesendoderm fate specification and internalization during
    zebrafish gastrulation
publication: eLife
publication_identifier:
  issn:
  - 2050-084X
publication_status: published
publisher: eLife Sciences Publications
quality_controlled: '1'
related_material:
  record:
  - id: '12891'
    relation: dissertation_contains
    status: public
scopus_import: '1'
status: public
title: Zebrafish embryonic explants undergo genetically encoded self-assembly
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 9
year: '2020'
...
---
OA_place: repository
OA_type: green
_id: '7885'
abstract:
- lang: eng
  text: Eukaryotic cells migrate by coupling the intracellular force of the actin
    cytoskeleton to the environment. While force coupling is usually mediated by transmembrane
    adhesion receptors, especially those of the integrin family, amoeboid cells such
    as leukocytes can migrate extremely fast despite very low adhesive forces1. Here
    we show that leukocytes cannot only migrate under low adhesion but can also transmit
    forces in the complete absence of transmembrane force coupling. When confined
    within three-dimensional environments, they use the topographical features of
    the substrate to propel themselves. Here the retrograde flow of the actin cytoskeleton
    follows the texture of the substrate, creating retrograde shear forces that are
    sufficient to drive the cell body forwards. Notably, adhesion-dependent and adhesion-independent
    migration are not mutually exclusive, but rather are variants of the same principle
    of coupling retrograde actin flow to the environment and thus can potentially
    operate interchangeably and simultaneously. As adhesion-free migration is independent
    of the chemical composition of the environment, it renders cells completely autonomous
    in their locomotive behaviour.
acknowledged_ssus:
- _id: Bio
- _id: LifeSc
- _id: M-Shop
acknowledgement: We thank A. Leithner and J. Renkawitz for discussion and critical
  reading of the manuscript; J. Schwarz and M. Mehling for establishing the microfluidic
  setups; the Bioimaging Facility of IST Austria for excellent support, as well as
  the Life Science Facility and the Miba Machine Shop of IST Austria; and F. N. Arslan,
  L. E. Burnett and L. Li for their work during their rotation in the IST PhD programme.
  This work was supported by the European Research Council (ERC StG 281556 and CoG
  724373) to M.S. and grants from the Austrian Science Fund (FWF P29911) and the WWTF
  to M.S. M.H. was supported by the European Regional Development Fund Project (CZ.02.1.01/0.0/0.0/15_003/0000476).
  F.G. received funding from the European Union’s Horizon 2020 research and innovation
  programme under the Marie Skłodowska-Curie grant agreement no. 747687.
article_processing_charge: No
article_type: original
author:
- first_name: Anne
  full_name: Reversat, Anne
  id: 35B76592-F248-11E8-B48F-1D18A9856A87
  last_name: Reversat
  orcid: 0000-0003-0666-8928
- first_name: Florian R
  full_name: Gärtner, Florian R
  id: 397A88EE-F248-11E8-B48F-1D18A9856A87
  last_name: Gärtner
  orcid: 0000-0001-6120-3723
- first_name: Jack
  full_name: Merrin, Jack
  id: 4515C308-F248-11E8-B48F-1D18A9856A87
  last_name: Merrin
  orcid: 0000-0001-5145-4609
- first_name: Julian A
  full_name: Stopp, Julian A
  id: 489E3F00-F248-11E8-B48F-1D18A9856A87
  last_name: Stopp
- first_name: Saren
  full_name: Tasciyan, Saren
  id: 4323B49C-F248-11E8-B48F-1D18A9856A87
  last_name: Tasciyan
  orcid: 0000-0003-1671-393X
- first_name: Juan L
  full_name: Aguilera Servin, Juan L
  id: 2A67C376-F248-11E8-B48F-1D18A9856A87
  last_name: Aguilera Servin
  orcid: 0000-0002-2862-8372
- first_name: Ingrid
  full_name: De Vries, Ingrid
  id: 4C7D837E-F248-11E8-B48F-1D18A9856A87
  last_name: De Vries
- first_name: Robert
  full_name: Hauschild, Robert
  id: 4E01D6B4-F248-11E8-B48F-1D18A9856A87
  last_name: Hauschild
  orcid: 0000-0001-9843-3522
- first_name: Miroslav
  full_name: Hons, Miroslav
  id: 4167FE56-F248-11E8-B48F-1D18A9856A87
  last_name: Hons
  orcid: 0000-0002-6625-3348
- first_name: Matthieu
  full_name: Piel, Matthieu
  last_name: Piel
- first_name: Andrew
  full_name: Callan-Jones, Andrew
  last_name: Callan-Jones
- first_name: Raphael
  full_name: Voituriez, Raphael
  last_name: Voituriez
- first_name: Michael K
  full_name: Sixt, Michael K
  id: 41E9FBEA-F248-11E8-B48F-1D18A9856A87
  last_name: Sixt
  orcid: 0000-0002-6620-9179
citation:
  ama: Reversat A, Gärtner FR, Merrin J, et al. Cellular locomotion using environmental
    topography. <i>Nature</i>. 2020;582:582–585. doi:<a href="https://doi.org/10.1038/s41586-020-2283-z">10.1038/s41586-020-2283-z</a>
  apa: Reversat, A., Gärtner, F. R., Merrin, J., Stopp, J. A., Tasciyan, S., Aguilera
    Servin, J. L., … Sixt, M. K. (2020). Cellular locomotion using environmental topography.
    <i>Nature</i>. Springer Nature. <a href="https://doi.org/10.1038/s41586-020-2283-z">https://doi.org/10.1038/s41586-020-2283-z</a>
  chicago: Reversat, Anne, Florian R Gärtner, Jack Merrin, Julian A Stopp, Saren Tasciyan,
    Juan L Aguilera Servin, Ingrid de Vries, et al. “Cellular Locomotion Using Environmental
    Topography.” <i>Nature</i>. Springer Nature, 2020. <a href="https://doi.org/10.1038/s41586-020-2283-z">https://doi.org/10.1038/s41586-020-2283-z</a>.
  ieee: A. Reversat <i>et al.</i>, “Cellular locomotion using environmental topography,”
    <i>Nature</i>, vol. 582. Springer Nature, pp. 582–585, 2020.
  ista: Reversat A, Gärtner FR, Merrin J, Stopp JA, Tasciyan S, Aguilera Servin JL,
    de Vries I, Hauschild R, Hons M, Piel M, Callan-Jones A, Voituriez R, Sixt MK.
    2020. Cellular locomotion using environmental topography. Nature. 582, 582–585.
  mla: Reversat, Anne, et al. “Cellular Locomotion Using Environmental Topography.”
    <i>Nature</i>, vol. 582, Springer Nature, 2020, pp. 582–585, doi:<a href="https://doi.org/10.1038/s41586-020-2283-z">10.1038/s41586-020-2283-z</a>.
  short: A. Reversat, F.R. Gärtner, J. Merrin, J.A. Stopp, S. Tasciyan, J.L. Aguilera
    Servin, I. de Vries, R. Hauschild, M. Hons, M. Piel, A. Callan-Jones, R. Voituriez,
    M.K. Sixt, Nature 582 (2020) 582–585.
date_created: 2020-05-24T22:01:01Z
date_published: 2020-06-25T00:00:00Z
date_updated: 2026-09-04T22:30:17Z
day: '25'
department:
- _id: NanoFab
- _id: Bio
- _id: MiSi
doi: 10.1038/s41586-020-2283-z
ec_funded: 1
external_id:
  isi:
  - '000532688300008'
  pmid:
  - '32581372'
intvolume: '       582'
isi: 1
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1101/793919
month: '06'
oa: 1
oa_version: Preprint
page: 582–585
pmid: 1
project:
- _id: 25A603A2-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '281556'
  name: Cytoskeletal force generation and force transduction of migrating leukocytes
- _id: 25FE9508-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '724373'
  name: Cellular Navigation Along Spatial Gradients
- _id: 26018E70-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: P29911
  name: Mechanical adaptation of lamellipodial actin
- _id: 260AA4E2-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '747687'
  name: Mechanical Adaptation of Lamellipodial Actin Networks in Migrating Cells
publication: Nature
publication_identifier:
  eissn:
  - 1476-4687
  issn:
  - 0028-0836
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
related_material:
  link:
  - description: News on IST Homepage
    relation: press_release
    url: https://ist.ac.at/en/news/off-road-mode-enables-mobile-cells-to-move-freely/
  record:
  - id: '12401'
    relation: dissertation_contains
    status: public
  - id: '14697'
    relation: dissertation_contains
    status: public
scopus_import: '1'
status: public
title: Cellular locomotion using environmental topography
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 582
year: '2020'
...
---
_id: '9198'
abstract:
- lang: eng
  text: "The optimization of multilayer neural networks typically leads to a solution\r\nwith
    zero training error, yet the landscape can exhibit spurious local minima\r\nand
    the minima can be disconnected. In this paper, we shed light on this\r\nphenomenon:
    we show that the combination of stochastic gradient descent (SGD)\r\nand over-parameterization
    makes the landscape of multilayer neural networks\r\napproximately connected and
    thus more favorable to optimization. More\r\nspecifically, we prove that SGD solutions
    are connected via a piecewise linear\r\npath, and the increase in loss along this
    path vanishes as the number of\r\nneurons grows large. This result is a consequence
    of the fact that the\r\nparameters found by SGD are increasingly dropout stable
    as the network becomes\r\nwider. We show that, if we remove part of the neurons
    (and suitably rescale the\r\nremaining ones), the change in loss is independent
    of the total number of\r\nneurons, and it depends only on how many neurons are
    left. Our results exhibit\r\na mild dependence on the input dimension: they are
    dimension-free for two-layer\r\nnetworks and depend linearly on the dimension
    for multilayer networks. We\r\nvalidate our theoretical findings with numerical
    experiments for different\r\narchitectures and classification tasks."
acknowledgement: M. Mondelli was partially supported by the 2019 LopezLoreta Prize.
  The authors thank Phan-Minh Nguyen for helpful discussions and the IST Distributed
  Algorithms and Systems Lab for providing computational resources.
article_processing_charge: No
arxiv: 1
author:
- first_name: Aleksandr
  full_name: Shevchenko, Aleksandr
  id: F2B06EC2-C99E-11E9-89F0-752EE6697425
  last_name: Shevchenko
- first_name: Marco
  full_name: Mondelli, Marco
  id: 27EB676C-8706-11E9-9510-7717E6697425
  last_name: Mondelli
  orcid: 0000-0002-3242-7020
citation:
  ama: 'Shevchenko A, Mondelli M. Landscape connectivity and dropout stability of
    SGD solutions for over-parameterized neural networks. In: <i>Proceedings of the
    37th International Conference on Machine Learning</i>. Vol 119. ML Research Press;
    2020:8773-8784.'
  apa: Shevchenko, A., &#38; Mondelli, M. (2020). Landscape connectivity and dropout
    stability of SGD solutions for over-parameterized neural networks. In <i>Proceedings
    of the 37th International Conference on Machine Learning</i> (Vol. 119, pp. 8773–8784).
    ML Research Press.
  chicago: Shevchenko, Aleksandr, and Marco Mondelli. “Landscape Connectivity and
    Dropout Stability of SGD Solutions for Over-Parameterized Neural Networks.” In
    <i>Proceedings of the 37th International Conference on Machine Learning</i>, 119:8773–84.
    ML Research Press, 2020.
  ieee: A. Shevchenko and M. Mondelli, “Landscape connectivity and dropout stability
    of SGD solutions for over-parameterized neural networks,” in <i>Proceedings of
    the 37th International Conference on Machine Learning</i>, 2020, vol. 119, pp.
    8773–8784.
  ista: Shevchenko A, Mondelli M. 2020. Landscape connectivity and dropout stability
    of SGD solutions for over-parameterized neural networks. Proceedings of the 37th
    International Conference on Machine Learning. vol. 119, 8773–8784.
  mla: Shevchenko, Aleksandr, and Marco Mondelli. “Landscape Connectivity and Dropout
    Stability of SGD Solutions for Over-Parameterized Neural Networks.” <i>Proceedings
    of the 37th International Conference on Machine Learning</i>, vol. 119, ML Research
    Press, 2020, pp. 8773–84.
  short: A. Shevchenko, M. Mondelli, in:, Proceedings of the 37th International Conference
    on Machine Learning, ML Research Press, 2020, pp. 8773–8784.
date_created: 2021-02-25T09:36:22Z
date_published: 2020-07-13T00:00:00Z
date_updated: 2026-09-04T22:30:18Z
day: '13'
ddc:
- '000'
department:
- _id: MaMo
- _id: DaAl
external_id:
  arxiv:
  - '1912.10095'
file:
- access_level: open_access
  checksum: f042c8d4316bd87c6361aa76f1fbdbbe
  content_type: application/pdf
  creator: dernst
  date_created: 2021-03-02T15:38:14Z
  date_updated: 2021-03-02T15:38:14Z
  file_id: '9217'
  file_name: 2020_PMLR_Shevchenko.pdf
  file_size: 5336380
  relation: main_file
  success: 1
file_date_updated: 2021-03-02T15:38:14Z
has_accepted_license: '1'
intvolume: '       119'
language:
- iso: eng
month: '07'
oa: 1
oa_version: Published Version
page: 8773-8784
project:
- _id: 059876FA-7A3F-11EA-A408-12923DDC885E
  name: Prix Lopez-Loretta 2019 - Marco Mondelli
publication: Proceedings of the 37th International Conference on Machine Learning
publication_status: published
publisher: ML Research Press
quality_controlled: '1'
related_material:
  record:
  - id: '17465'
    relation: dissertation_contains
    status: public
status: public
title: Landscape connectivity and dropout stability of SGD solutions for over-parameterized
  neural networks
type: conference
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
volume: 119
year: '2020'
...
---
_id: '7815'
abstract:
- lang: eng
  text: Beginning from a limited pool of progenitors, the mammalian cerebral cortex
    forms highly organized functional neural circuits. However, the underlying cellular
    and molecular mechanisms regulating lineage transitions of neural stem cells (NSCs)
    and eventual production of neurons and glia in the developing neuroepithelium
    remains unclear. Methods to trace NSC division patterns and map the lineage of
    clonally related cells have advanced dramatically. However, many contemporary
    lineage tracing techniques suffer from the lack of cellular resolution of progeny
    cell fate, which is essential for deciphering progenitor cell division patterns.
    Presented is a protocol using mosaic analysis with double markers (MADM) to perform
    in vivo clonal analysis. MADM concomitantly manipulates individual progenitor
    cells and visualizes precise division patterns and lineage progression at unprecedented
    single cell resolution. MADM-based interchromosomal recombination events during
    the G2-X phase of mitosis, together with temporally inducible CreERT2, provide
    exact information on the birth dates of clones and their division patterns. Thus,
    MADM lineage tracing provides unprecedented qualitative and quantitative optical
    readouts of the proliferation mode of stem cell progenitors at the single cell
    level. MADM also allows for examination of the mechanisms and functional requirements
    of candidate genes in NSC lineage progression. This method is unique in that comparative
    analysis of control and mutant subclones can be performed in the same tissue environment
    in vivo. Here, the protocol is described in detail, and experimental paradigms
    to employ MADM for clonal analysis and lineage tracing in the developing cerebral
    cortex are demonstrated. Importantly, this protocol can be adapted to perform
    MADM clonal analysis in any murine stem cell niche, as long as the CreERT2 driver
    is present.
acknowledged_ssus:
- _id: Bio
- _id: LifeSc
- _id: PreCl
article_number: e61147
article_processing_charge: No
article_type: original
author:
- first_name: Robert J
  full_name: Beattie, Robert J
  id: 2E26DF60-F248-11E8-B48F-1D18A9856A87
  last_name: Beattie
  orcid: 0000-0002-8483-8753
- first_name: Carmen
  full_name: Streicher, Carmen
  id: 36BCB99C-F248-11E8-B48F-1D18A9856A87
  last_name: Streicher
- first_name: Nicole
  full_name: Amberg, Nicole
  id: 4CD6AAC6-F248-11E8-B48F-1D18A9856A87
  last_name: Amberg
  orcid: 0000-0002-3183-8207
- first_name: Giselle T
  full_name: Cheung, Giselle T
  id: 471195F6-F248-11E8-B48F-1D18A9856A87
  last_name: Cheung
  orcid: 0000-0001-8457-2572
- first_name: Ximena
  full_name: Contreras, Ximena
  id: 475990FE-F248-11E8-B48F-1D18A9856A87
  last_name: Contreras
- first_name: Andi H
  full_name: Hansen, Andi H
  id: 38853E16-F248-11E8-B48F-1D18A9856A87
  last_name: Hansen
- first_name: Simon
  full_name: Hippenmeyer, Simon
  id: 37B36620-F248-11E8-B48F-1D18A9856A87
  last_name: Hippenmeyer
  orcid: 0000-0003-2279-1061
citation:
  ama: Beattie RJ, Streicher C, Amberg N, et al. Lineage tracing and clonal analysis
    in developing cerebral cortex using mosaic analysis with double markers (MADM).
    <i>Journal of Visual Experiments</i>. 2020;(159). doi:<a href="https://doi.org/10.3791/61147">10.3791/61147</a>
  apa: Beattie, R. J., Streicher, C., Amberg, N., Cheung, G. T., Contreras, X., Hansen,
    A. H., &#38; Hippenmeyer, S. (2020). Lineage tracing and clonal analysis in developing
    cerebral cortex using mosaic analysis with double markers (MADM). <i>Journal of
    Visual Experiments</i>. MyJove Corporation. <a href="https://doi.org/10.3791/61147">https://doi.org/10.3791/61147</a>
  chicago: Beattie, Robert J, Carmen Streicher, Nicole Amberg, Giselle T Cheung, Ximena
    Contreras, Andi H Hansen, and Simon Hippenmeyer. “Lineage Tracing and Clonal Analysis
    in Developing Cerebral Cortex Using Mosaic Analysis with Double Markers (MADM).”
    <i>Journal of Visual Experiments</i>. MyJove Corporation, 2020. <a href="https://doi.org/10.3791/61147">https://doi.org/10.3791/61147</a>.
  ieee: R. J. Beattie <i>et al.</i>, “Lineage tracing and clonal analysis in developing
    cerebral cortex using mosaic analysis with double markers (MADM),” <i>Journal
    of Visual Experiments</i>, no. 159. MyJove Corporation, 2020.
  ista: Beattie RJ, Streicher C, Amberg N, Cheung GT, Contreras X, Hansen AH, Hippenmeyer
    S. 2020. Lineage tracing and clonal analysis in developing cerebral cortex using
    mosaic analysis with double markers (MADM). Journal of Visual Experiments. (159),
    e61147.
  mla: Beattie, Robert J., et al. “Lineage Tracing and Clonal Analysis in Developing
    Cerebral Cortex Using Mosaic Analysis with Double Markers (MADM).” <i>Journal
    of Visual Experiments</i>, no. 159, e61147, MyJove Corporation, 2020, doi:<a href="https://doi.org/10.3791/61147">10.3791/61147</a>.
  short: R.J. Beattie, C. Streicher, N. Amberg, G.T. Cheung, X. Contreras, A.H. Hansen,
    S. Hippenmeyer, Journal of Visual Experiments (2020).
corr_author: '1'
date_created: 2020-05-11T08:31:20Z
date_published: 2020-05-08T00:00:00Z
date_updated: 2026-09-04T22:30:20Z
day: '08'
ddc:
- '570'
department:
- _id: SiHi
doi: 10.3791/61147
ec_funded: 1
external_id:
  isi:
  - '000546406600043'
  pmid:
  - '32449730'
file:
- access_level: open_access
  checksum: 3154ea7f90b9fb45e084cd1c2770597d
  content_type: application/pdf
  creator: rbeattie
  date_created: 2020-05-11T08:28:38Z
  date_updated: 2020-07-14T12:48:03Z
  file_id: '7816'
  file_name: jove-protocol-61147-lineage-tracing-clonal-analysis-developing-cerebral-cortex-using.pdf
  file_size: 1352186
  relation: main_file
file_date_updated: 2020-07-14T12:48:03Z
has_accepted_license: '1'
isi: 1
issue: '159'
language:
- iso: eng
month: '05'
oa: 1
oa_version: Published Version
pmid: 1
project:
- _id: 264E56E2-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: M02416
  name: Molecular Mechanisms Regulating Gliogenesis in the Neocortex
- _id: 268F8446-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: T01031
  name: Role of Eed in neural stem cell lineage progression
- _id: 260C2330-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '754411'
  name: ISTplus - Postdoctoral Fellowships
- _id: 2625A13E-B435-11E9-9278-68D0E5697425
  grant_number: '24812'
  name: Molecular mechanisms of radial neuronal migration
- _id: 260018B0-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '725780'
  name: Principles of Neural Stem Cell Lineage Progression in Cerebral Cortex Development
publication: Journal of Visual Experiments
publication_identifier:
  issn:
  - 1940-087X
publication_status: published
publisher: MyJove Corporation
quality_controlled: '1'
related_material:
  record:
  - id: '7902'
    relation: part_of_dissertation
    status: public
scopus_import: '1'
status: public
title: Lineage tracing and clonal analysis in developing cerebral cortex using mosaic
  analysis with double markers (MADM)
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2020'
...
---
OA_place: publisher
_id: '7902'
abstract:
- lang: eng
  text: "Mosaic genetic analysis has been widely used in different model organisms
    such as the fruit fly to study gene-function in a cell-autonomous or tissue-specific
    fashion. More recently, and less easily conducted, mosaic genetic analysis in
    mice has also been enabled with the ambition to shed light on human gene function
    and disease. These genetic tools are of particular interest, but not restricted
    to, the study of the brain. Notably, the MADM technology offers a genetic approach
    in mice to visualize and concomitantly manipulate small subsets of genetically
    defined cells at a clonal level and single cell resolution. MADM-based analysis
    has already advanced the study of genetic mechanisms regulating brain development
    and is expected that further MADM-based analysis of genetic alterations will continue
    to reveal important insights on the fundamental principles of development and
    disease to potentially assist in the development of new therapies or treatments.\r\nIn
    summary, this work completed and characterized the necessary genome-wide genetic
    tools to perform MADM-based analysis at single cell level of the vast majority
    of mouse genes in virtually any cell type and provided a protocol to perform lineage
    tracing using the novel MADM resource. Importantly, this work also explored and
    revealed novel aspects of biologically relevant events in an in vivo context,
    such as the chromosome-specific bias of chromatid sister segregation pattern,
    the generation of cell-type diversity in the cerebral cortex and in the cerebellum
    and finally, the relevance of the interplay between the cell-autonomous gene function
    and cell-non-autonomous (community) effects in radial glial progenitor lineage
    progression.\r\nThis work provides a foundation and opens the door to further
    elucidating the molecular mechanisms underlying neuronal diversity and astrocyte
    generation."
acknowledged_ssus:
- _id: PreCl
- _id: Bio
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Ximena
  full_name: Contreras, Ximena
  id: 475990FE-F248-11E8-B48F-1D18A9856A87
  last_name: Contreras
citation:
  ama: Contreras X. Genetic dissection of neural development in health and disease
    at single cell resolution. 2020. doi:<a href="https://doi.org/10.15479/AT:ISTA:7902">10.15479/AT:ISTA:7902</a>
  apa: Contreras, X. (2020). <i>Genetic dissection of neural development in health
    and disease at single cell resolution</i>. Institute of Science and Technology
    Austria. <a href="https://doi.org/10.15479/AT:ISTA:7902">https://doi.org/10.15479/AT:ISTA:7902</a>
  chicago: Contreras, Ximena. “Genetic Dissection of Neural Development in Health
    and Disease at Single Cell Resolution.” Institute of Science and Technology Austria,
    2020. <a href="https://doi.org/10.15479/AT:ISTA:7902">https://doi.org/10.15479/AT:ISTA:7902</a>.
  ieee: X. Contreras, “Genetic dissection of neural development in health and disease
    at single cell resolution,” Institute of Science and Technology Austria, 2020.
  ista: Contreras X. 2020. Genetic dissection of neural development in health and
    disease at single cell resolution. Institute of Science and Technology Austria.
  mla: Contreras, Ximena. <i>Genetic Dissection of Neural Development in Health and
    Disease at Single Cell Resolution</i>. Institute of Science and Technology Austria,
    2020, doi:<a href="https://doi.org/10.15479/AT:ISTA:7902">10.15479/AT:ISTA:7902</a>.
  short: X. Contreras, Genetic Dissection of Neural Development in Health and Disease
    at Single Cell Resolution, Institute of Science and Technology Austria, 2020.
corr_author: '1'
date_created: 2020-05-29T08:27:32Z
date_published: 2020-06-05T00:00:00Z
date_updated: 2026-06-18T19:12:39Z
day: '05'
ddc:
- '570'
degree_awarded: PhD
department:
- _id: SiHi
doi: 10.15479/AT:ISTA:7902
ec_funded: 1
file:
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  checksum: 43c172bf006c95b65992d473c7240d13
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  date_updated: 2021-06-07T22:30:03Z
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  file_name: PhDThesis_Contreras.docx
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  date_created: 2020-06-05T08:18:07Z
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file_date_updated: 2021-06-07T22:30:03Z
has_accepted_license: '1'
language:
- iso: eng
month: '06'
oa: 1
oa_version: Published Version
page: '214'
project:
- _id: 260018B0-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '725780'
  name: Principles of Neural Stem Cell Lineage Progression in Cerebral Cortex Development
publication_identifier:
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
related_material:
  record:
  - id: '28'
    relation: dissertation_contains
    status: public
  - id: '7815'
    relation: dissertation_contains
    status: public
  - id: '6830'
    relation: dissertation_contains
    status: public
status: public
supervisor:
- first_name: Simon
  full_name: Hippenmeyer, Simon
  id: 37B36620-F248-11E8-B48F-1D18A9856A87
  last_name: Hippenmeyer
  orcid: 0000-0003-2279-1061
title: Genetic dissection of neural development in health and disease at single cell
  resolution
type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2020'
...
---
_id: '8190'
article_number: e202007029
article_processing_charge: No
article_type: letter_note
author:
- first_name: Michael K
  full_name: Sixt, Michael K
  id: 41E9FBEA-F248-11E8-B48F-1D18A9856A87
  last_name: Sixt
  orcid: 0000-0002-6620-9179
- first_name: Anna
  full_name: Huttenlocher, Anna
  last_name: Huttenlocher
citation:
  ama: 'Sixt MK, Huttenlocher A. Zena Werb (1945-2020): Cell biology in context. <i>The
    Journal of Cell Biology</i>. 2020;219(8). doi:<a href="https://doi.org/10.1083/jcb.202007029">10.1083/jcb.202007029</a>'
  apa: 'Sixt, M. K., &#38; Huttenlocher, A. (2020). Zena Werb (1945-2020): Cell biology
    in context. <i>The Journal of Cell Biology</i>. Rockefeller University Press.
    <a href="https://doi.org/10.1083/jcb.202007029">https://doi.org/10.1083/jcb.202007029</a>'
  chicago: 'Sixt, Michael K, and Anna Huttenlocher. “Zena Werb (1945-2020): Cell Biology
    in Context.” <i>The Journal of Cell Biology</i>. Rockefeller University Press,
    2020. <a href="https://doi.org/10.1083/jcb.202007029">https://doi.org/10.1083/jcb.202007029</a>.'
  ieee: 'M. K. Sixt and A. Huttenlocher, “Zena Werb (1945-2020): Cell biology in context,”
    <i>The Journal of Cell Biology</i>, vol. 219, no. 8. Rockefeller University Press,
    2020.'
  ista: 'Sixt MK, Huttenlocher A. 2020. Zena Werb (1945-2020): Cell biology in context.
    The Journal of Cell Biology. 219(8), e202007029.'
  mla: 'Sixt, Michael K., and Anna Huttenlocher. “Zena Werb (1945-2020): Cell Biology
    in Context.” <i>The Journal of Cell Biology</i>, vol. 219, no. 8, e202007029,
    Rockefeller University Press, 2020, doi:<a href="https://doi.org/10.1083/jcb.202007029">10.1083/jcb.202007029</a>.'
  short: M.K. Sixt, A. Huttenlocher, The Journal of Cell Biology 219 (2020).
date_created: 2020-08-02T22:00:57Z
date_published: 2020-07-22T00:00:00Z
date_updated: 2025-06-12T07:34:40Z
day: '22'
ddc:
- '570'
department:
- _id: MiSi
doi: 10.1083/jcb.202007029
external_id:
  isi:
  - '000573631000004'
  pmid:
  - '32699885'
file:
- access_level: open_access
  checksum: 30016d778d266b8e17d01094917873b8
  content_type: application/pdf
  creator: dernst
  date_created: 2020-08-04T13:11:52Z
  date_updated: 2021-02-02T23:30:03Z
  embargo: 2021-02-01
  file_id: '8200'
  file_name: 2020_JCB_Sixt.pdf
  file_size: 830725
  relation: main_file
file_date_updated: 2021-02-02T23:30:03Z
has_accepted_license: '1'
intvolume: '       219'
isi: 1
issue: '8'
language:
- iso: eng
month: '07'
oa: 1
oa_version: Published Version
pmid: 1
publication: The Journal of Cell Biology
publication_identifier:
  eissn:
  - 1540-8140
publication_status: published
publisher: Rockefeller University Press
scopus_import: '1'
status: public
title: 'Zena Werb (1945-2020): Cell biology in context'
tmp:
  image: /images/cc_by_nc_sa.png
  legal_code_url: https://creativecommons.org/licenses/by-nc-sa/4.0/legalcode
  name: Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC
    BY-NC-SA 4.0)
  short: CC BY-NC-SA (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 219
year: '2020'
...
---
_id: '8350'
abstract:
- lang: eng
  text: "Cytoplasm is a gel-like crowded environment composed of tens of thousands
    of macromolecules, organelles, cytoskeletal networks and cytosol. The structure
    of the cytoplasm is thought to be highly organized and heterogeneous due to the
    crowding of its constituents and their effective compartmentalization. In such
    an environment, the diffusive dynamics of the molecules is very restricted, an
    effect that is further amplified by clustering and anchoring of molecules. Despite
    the jammed nature of the cytoplasm at the microscopic scale, large-scale reorganization
    of cytoplasm is essential for important cellular functions, such as nuclear positioning
    and cell division. How such mesoscale reorganization of the cytoplasm is achieved,
    especially for very large cells such as oocytes or syncytial tissues that can
    span hundreds of micrometers in size, has only begun to be understood.\r\nIn this
    thesis, I focus on the recent advances in elucidating the molecular, cellular
    and biophysical principles underlying cytoplasmic organization across different
    scales, structures and species. First, I outline which of these principles have
    been identified by reductionist approaches, such as in vitro reconstitution assays,
    where boundary conditions and components can be modulated at ease. I then describe
    how the theoretical and experimental framework established in these reduced systems
    have been applied to their more complex in vivo counterparts, in particular oocytes
    and embryonic syncytial structures, and discuss how such complex biological systems
    can initiate symmetry breaking and establish patterning.\r\nSpecifically, I examine
    an example of large-scale reorganizations taking place in zebrafish embryos, where
    extensive cytoplasmic streaming leads to the segregation of cytoplasm from yolk
    granules along the animal-vegetal axis of the embryo. Using biophysical experimentation
    and theory, I investigate the forces underlying this process, to show that this
    process does not rely on cortical actin reorganization, as previously thought,
    but instead on a cell-cycle-dependent bulk actin polymerization wave traveling
    from the animal to the vegetal pole of the embryo. This wave functions in segregation
    by both pulling cytoplasm animally and pushing yolk granules vegetally. Cytoplasm
    pulling is mediated by bulk actin network flows exerting friction forces on the
    cytoplasm, while yolk granule pushing is achieved by a mechanism closely resembling
    actin comet formation on yolk granules. This study defines a novel role of bulk
    actin polymerization waves in embryo polarization via cytoplasmic segregation.
    Lastly, I describe the cytoplasmic reorganizations taking place during zebrafish
    oocyte maturation, where the initial segregation of the cytoplasm and yolk granules
    occurs. Here, I demonstrate a previously uncharacterized wave of microtubule aster
    formation, traveling the oocyte along the animal-vegetal axis. Further research
    is required to determine the role of such microtubule structures in cytoplasmic
    reorganizations therein.\r\nCollectively, these studies provide further evidence
    for the coupling between cell cytoskeleton and cell cycle machinery, which can
    underlie a core self-organizing mechanism for orchestrating large-scale reorganizations
    in a cell-cycle-tunable manner, where the modulations of the force-generating
    machinery and cytoplasmic mechanics can be harbored to fulfill cellular functions."
acknowledged_ssus:
- _id: PreCl
- _id: Bio
- _id: EM-Fac
acknowledgement: "I would have had no fish and hence no results without our wonderful
  fish facility crew, Verena Mayer, Eva Schlegl, Andreas Mlak and Matthias Nowak.
  Special thanks to Verena for being always happy to help and dealing with our chaotic
  schedules in the lab. Danke auch, Verena, für deine Geduld, mit mir auf Deutsch
  zu sprechen. Das hat mir sehr geholfen.\r\nSpecial thanks to the Bioimaging and
  EM facilities at IST Austria for supporting us every day. Very special thanks would
  go to Robert Hauschild for his continuous support on data analysis and also to Jack
  Merrin for designing and building microfabricated chambers for the project and for
  the various discussions on making zebrafish extracts."
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Shayan
  full_name: Shamipour, Shayan
  id: 40B34FE2-F248-11E8-B48F-1D18A9856A87
  last_name: Shamipour
citation:
  ama: Shamipour S. Bulk actin dynamics drive phase segregation in zebrafish oocytes
    . 2020. doi:<a href="https://doi.org/10.15479/AT:ISTA:8350">10.15479/AT:ISTA:8350</a>
  apa: Shamipour, S. (2020). <i>Bulk actin dynamics drive phase segregation in zebrafish
    oocytes </i>. Institute of Science and Technology Austria. <a href="https://doi.org/10.15479/AT:ISTA:8350">https://doi.org/10.15479/AT:ISTA:8350</a>
  chicago: Shamipour, Shayan. “Bulk Actin Dynamics Drive Phase Segregation in Zebrafish
    Oocytes .” Institute of Science and Technology Austria, 2020. <a href="https://doi.org/10.15479/AT:ISTA:8350">https://doi.org/10.15479/AT:ISTA:8350</a>.
  ieee: S. Shamipour, “Bulk actin dynamics drive phase segregation in zebrafish oocytes
    ,” Institute of Science and Technology Austria, 2020.
  ista: Shamipour S. 2020. Bulk actin dynamics drive phase segregation in zebrafish
    oocytes . Institute of Science and Technology Austria.
  mla: Shamipour, Shayan. <i>Bulk Actin Dynamics Drive Phase Segregation in Zebrafish
    Oocytes </i>. Institute of Science and Technology Austria, 2020, doi:<a href="https://doi.org/10.15479/AT:ISTA:8350">10.15479/AT:ISTA:8350</a>.
  short: S. Shamipour, Bulk Actin Dynamics Drive Phase Segregation in Zebrafish Oocytes
    , Institute of Science and Technology Austria, 2020.
corr_author: '1'
date_created: 2020-09-09T11:12:10Z
date_published: 2020-09-09T00:00:00Z
date_updated: 2025-09-11T07:08:52Z
day: '09'
ddc:
- '570'
degree_awarded: PhD
department:
- _id: BjHo
- _id: CaHe
doi: 10.15479/AT:ISTA:8350
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  date_updated: 2021-09-11T22:30:05Z
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has_accepted_license: '1'
language:
- iso: eng
month: '09'
oa: 1
oa_version: None
page: '107'
publication_identifier:
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
related_material:
  record:
  - id: '7001'
    relation: part_of_dissertation
    status: public
  - id: '6508'
    relation: part_of_dissertation
    status: public
  - id: '735'
    relation: part_of_dissertation
    status: public
  - id: '661'
    relation: part_of_dissertation
    status: public
status: public
supervisor:
- first_name: Carl-Philipp J
  full_name: Heisenberg, Carl-Philipp J
  id: 39427864-F248-11E8-B48F-1D18A9856A87
  last_name: Heisenberg
  orcid: 0000-0002-0912-4566
- first_name: Björn
  full_name: Hof, Björn
  id: 3A374330-F248-11E8-B48F-1D18A9856A87
  last_name: Hof
  orcid: 0000-0003-2057-2754
title: 'Bulk actin dynamics drive phase segregation in zebrafish oocytes '
type: dissertation
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2020'
...
