---
_id: '15260'
abstract:
- lang: eng
text: Significant advances in the synthesis and processing of colloidal nanocrystals
have given scientists and engineers access to a vast library of building blocks
with precisely defined size, shape, and composition. These materials have inspired
exciting prospects to enable bottom-up fabrication of programmable materials with
properties by design. Successfully assembling and connecting the building blocks
into superstructures in which constituent nanocrystals can purposefully interact
requires robust understanding of and control over a complex interplay of dynamic
physicochemical processes. Fluid interfaces provide an advantageous experimental
workbench to both probe and control these processes. Despite the ostensible simplicity
of fabricating nanocrystal assemblies at a fluid interface, sensitivity to processing
conditions and limited reproducibility have underscored the complexity of this
process. In situ studies have provided mechanistic insights into the competing
dynamics of key subprocesses including solvent spreading and evaporation, superlattice
formation, ligand detachment kinetics, and nanocrystal attachment. Understanding
how these subprocesses influence the complex choreography of self-assembly, structure
transformation, and oriented attachment processes presents a rich research challenge.
In this context, we present a detailed methodology for self-assembly and attachment
of lead chalcogenide nanocrystals at a liquid–gas interface as a model system
for the fabrication of mono- and multilayer cubic connected superlattices. We
discuss key experimental parameters such as the characteristics of the building
blocks and processing conditions and detailed steps from colloidal nanocrystal
injection to superlattice transfer. We hope that this Methods/Protocols paper
will provide guidance for future advances in the exciting path toward bringing
the prospect of nanocrystal-based programmable materials to fruition.
article_processing_charge: No
article_type: original
author:
- first_name: Jessica
full_name: Cimada daSilva, Jessica
last_name: Cimada daSilva
- first_name: Daniel
full_name: Balazs, Daniel
id: 302BADF6-85FC-11EA-9E3B-B9493DDC885E
last_name: Balazs
orcid: 0000-0001-7597-043X
- first_name: Tyler A.
full_name: Dunbar, Tyler A.
last_name: Dunbar
- first_name: Tobias
full_name: Hanrath, Tobias
last_name: Hanrath
citation:
ama: Cimada daSilva J, Balazs D, Dunbar TA, Hanrath T. Fundamental processes and
practical considerations of lead chalcogenide mesocrystals formed via self-assembly
and directed attachment of nanocrystals at a fluid interface. Chemistry of
Materials. 2021;33(24):9457-9472. doi:10.1021/acs.chemmater.1c02910
apa: Cimada daSilva, J., Balazs, D., Dunbar, T. A., & Hanrath, T. (2021). Fundamental
processes and practical considerations of lead chalcogenide mesocrystals formed
via self-assembly and directed attachment of nanocrystals at a fluid interface.
Chemistry of Materials. American Chemical Society. https://doi.org/10.1021/acs.chemmater.1c02910
chicago: Cimada daSilva, Jessica, Daniel Balazs, Tyler A. Dunbar, and Tobias Hanrath.
“Fundamental Processes and Practical Considerations of Lead Chalcogenide Mesocrystals
Formed via Self-Assembly and Directed Attachment of Nanocrystals at a Fluid Interface.”
Chemistry of Materials. American Chemical Society, 2021. https://doi.org/10.1021/acs.chemmater.1c02910.
ieee: J. Cimada daSilva, D. Balazs, T. A. Dunbar, and T. Hanrath, “Fundamental processes
and practical considerations of lead chalcogenide mesocrystals formed via self-assembly
and directed attachment of nanocrystals at a fluid interface,” Chemistry of
Materials, vol. 33, no. 24. American Chemical Society, pp. 9457–9472, 2021.
ista: Cimada daSilva J, Balazs D, Dunbar TA, Hanrath T. 2021. Fundamental processes
and practical considerations of lead chalcogenide mesocrystals formed via self-assembly
and directed attachment of nanocrystals at a fluid interface. Chemistry of Materials.
33(24), 9457–9472.
mla: Cimada daSilva, Jessica, et al. “Fundamental Processes and Practical Considerations
of Lead Chalcogenide Mesocrystals Formed via Self-Assembly and Directed Attachment
of Nanocrystals at a Fluid Interface.” Chemistry of Materials, vol. 33,
no. 24, American Chemical Society, 2021, pp. 9457–72, doi:10.1021/acs.chemmater.1c02910.
short: J. Cimada daSilva, D. Balazs, T.A. Dunbar, T. Hanrath, Chemistry of Materials
33 (2021) 9457–9472.
date_created: 2024-04-03T07:23:30Z
date_published: 2021-12-16T00:00:00Z
date_updated: 2024-04-03T13:50:53Z
day: '16'
department:
- _id: LifeSc
doi: 10.1021/acs.chemmater.1c02910
intvolume: ' 33'
issue: '24'
keyword:
- Materials Chemistry
- General Chemical Engineering
- General Chemistry
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://www.osti.gov/servlets/purl/1836502
month: '12'
oa: 1
oa_version: Submitted Version
page: 9457-9472
publication: Chemistry of Materials
publication_identifier:
eissn:
- 1520-5002
issn:
- 0897-4756
publication_status: published
publisher: American Chemical Society
quality_controlled: '1'
scopus_import: '1'
status: public
title: Fundamental processes and practical considerations of lead chalcogenide mesocrystals
formed via self-assembly and directed attachment of nanocrystals at a fluid interface
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 33
year: '2021'
...
---
OA_place: publisher
OA_type: free access
_id: '15261'
abstract:
- lang: eng
text: In this article, we study uniqueness of form extensions in a rather general
setting. The method is based on the theory of ordered Hilbert spaces and the concept
of domination of semigroups. Our main abstract result transfers uniqueness of
form extension of a dominating form to that of a dominated form. This result can
be applied to a multitude of examples including various magnetic Schrödinger forms
on graphs and on manifolds.
article_number: '108848'
article_processing_charge: No
article_type: original
author:
- first_name: Daniel
full_name: Lenz, Daniel
last_name: Lenz
- first_name: Marcel
full_name: Schmidt, Marcel
last_name: Schmidt
- first_name: Melchior
full_name: Wirth, Melchior
id: 88644358-0A0E-11EA-8FA5-49A33DDC885E
last_name: Wirth
orcid: 0000-0002-0519-4241
citation:
ama: Lenz D, Schmidt M, Wirth M. Uniqueness of form extensions and domination of
semigroups. Journal of Functional Analysis. 2021;280(6). doi:10.1016/j.jfa.2020.108848
apa: Lenz, D., Schmidt, M., & Wirth, M. (2021). Uniqueness of form extensions
and domination of semigroups. Journal of Functional Analysis. Elsevier.
https://doi.org/10.1016/j.jfa.2020.108848
chicago: Lenz, Daniel, Marcel Schmidt, and Melchior Wirth. “Uniqueness of Form Extensions
and Domination of Semigroups.” Journal of Functional Analysis. Elsevier,
2021. https://doi.org/10.1016/j.jfa.2020.108848.
ieee: D. Lenz, M. Schmidt, and M. Wirth, “Uniqueness of form extensions and domination
of semigroups,” Journal of Functional Analysis, vol. 280, no. 6. Elsevier,
2021.
ista: Lenz D, Schmidt M, Wirth M. 2021. Uniqueness of form extensions and domination
of semigroups. Journal of Functional Analysis. 280(6), 108848.
mla: Lenz, Daniel, et al. “Uniqueness of Form Extensions and Domination of Semigroups.”
Journal of Functional Analysis, vol. 280, no. 6, 108848, Elsevier, 2021,
doi:10.1016/j.jfa.2020.108848.
short: D. Lenz, M. Schmidt, M. Wirth, Journal of Functional Analysis 280 (2021).
corr_author: '1'
date_created: 2024-04-03T07:24:57Z
date_published: 2021-03-15T00:00:00Z
date_updated: 2026-06-18T17:46:54Z
day: '15'
ddc:
- '500'
department:
- _id: JaMa
doi: 10.1016/j.jfa.2020.108848
intvolume: ' 280'
issue: '6'
keyword:
- Analysis
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://doi.org/10.1016/j.jfa.2020.108848
month: '03'
oa: 1
oa_version: Published Version
publication: Journal of Functional Analysis
publication_identifier:
eissn:
- 1096-0783
issn:
- 0022-1236
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: Uniqueness of form extensions and domination of semigroups
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 280
year: '2021'
...
---
_id: '15263'
abstract:
- lang: eng
text: We develop a new Riemannian descent algorithm that relies on momentum to improve
over existing first-order methods for geodesically convex optimization. In contrast,
accelerated convergence rates proved in prior work have only been shown to hold
for geodesically strongly-convex objective functions. We further extend our algorithm
to geodesically weakly-quasi-convex objectives. Our proofs of convergence rely
on a novel estimate sequence that illustrates the dependency of the convergence
rate on the curvature of the manifold. We validate our theoretical results empirically
on several optimization problems defined on the sphere and on the manifold of
positive definite matrices.
acknowledgement: The authors would like to thank professors Nicolas Boumal and Suvrit
Sra for helpful discussions on the content of this paper. Gary Bécigneul was funded
by the Max Planck ETH Center for Learning Systems during the course of this work.
alternative_title:
- PMLR
article_processing_charge: No
arxiv: 1
author:
- first_name: Foivos
full_name: Alimisis, Foivos
id: 19430a34-05f6-11ef-890d-c079cfc60ae2
last_name: Alimisis
- first_name: Antonio
full_name: Orvieto, Antonio
last_name: Orvieto
- first_name: Gary
full_name: Becigneul, Gary
last_name: Becigneul
- first_name: Aurelien
full_name: Lucchi, Aurelien
last_name: Lucchi
citation:
ama: 'Alimisis F, Orvieto A, Becigneul G, Lucchi A. Momentum improves optimization
on Riemannian manifolds. In: Proceedings of the 24th International Conference
on Artificial Intelligence and Statistics. Vol 130. ML Research Press; 2021:1351-1359.'
apa: 'Alimisis, F., Orvieto, A., Becigneul, G., & Lucchi, A. (2021). Momentum
improves optimization on Riemannian manifolds. In Proceedings of the 24th International
Conference on Artificial Intelligence and Statistics (Vol. 130, pp. 1351–1359).
San Diego, CA, United States; Virtual: ML Research Press.'
chicago: Alimisis, Foivos, Antonio Orvieto, Gary Becigneul, and Aurelien Lucchi.
“Momentum Improves Optimization on Riemannian Manifolds.” In Proceedings of
the 24th International Conference on Artificial Intelligence and Statistics,
130:1351–59. ML Research Press, 2021.
ieee: F. Alimisis, A. Orvieto, G. Becigneul, and A. Lucchi, “Momentum improves optimization
on Riemannian manifolds,” in Proceedings of the 24th International Conference
on Artificial Intelligence and Statistics, San Diego, CA, United States; Virtual,
2021, vol. 130, pp. 1351–1359.
ista: 'Alimisis F, Orvieto A, Becigneul G, Lucchi A. 2021. Momentum improves optimization
on Riemannian manifolds. Proceedings of the 24th International Conference on Artificial
Intelligence and Statistics. AISTATS: Conference on Artificial Intelligence and
Statistics, PMLR, vol. 130, 1351–1359.'
mla: Alimisis, Foivos, et al. “Momentum Improves Optimization on Riemannian Manifolds.”
Proceedings of the 24th International Conference on Artificial Intelligence
and Statistics, vol. 130, ML Research Press, 2021, pp. 1351–59.
short: F. Alimisis, A. Orvieto, G. Becigneul, A. Lucchi, in:, Proceedings of the
24th International Conference on Artificial Intelligence and Statistics, ML Research
Press, 2021, pp. 1351–1359.
conference:
end_date: 2021-04-15
location: San Diego, CA, United States; Virtual
name: 'AISTATS: Conference on Artificial Intelligence and Statistics'
start_date: 2021-04-13
date_created: 2024-04-03T07:29:49Z
date_published: 2021-04-15T00:00:00Z
date_updated: 2026-06-18T17:47:19Z
day: '15'
ddc:
- '000'
department:
- _id: DaAl
external_id:
arxiv:
- '2002.04144'
intvolume: ' 130'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://proceedings.mlr.press/v130/alimisis21a.html
month: '04'
oa: 1
oa_version: Published Version
page: 1351-1359
publication: Proceedings of the 24th International Conference on Artificial Intelligence
and Statistics
publication_status: published
publisher: ML Research Press
quality_controlled: '1'
status: public
title: Momentum improves optimization on Riemannian manifolds
type: conference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 130
year: '2021'
...
---
_id: '15264'
abstract:
- lang: eng
text: Signaling by the B cell antigen receptor (BCR) initiates actin remodeling.
The assembly of branched actin networks that are nucleated by the Arp2/3 complex
exert outward force on the plasma membrane, allowing B cells to form membrane
protrusions that can scan the surface of antigen-presenting cells (APCs). The
resulting Arp2/3 complex-dependent actin retrograde flow promotes the centripetal
movement and progressive coalescence of BCR microclusters, which amplifies BCR
signaling. Glia maturation factor γ (GMFγ) is an actin disassembly-protein that
releases Arp2/3 complex-nucleated actin filaments from actin networks. By doing
so, GMFγ could either oppose the actions of the Arp2/3 complex or support Arp2/3
complex-nucleated actin polymerization by contributing to the recycling of actin
monomers and Arp2/3 complexes. We now show that reducing the levels of GMFγ in
human B cell lines via transfection with a specific siRNA impairs the ability
of B cells to spread on antigen-coated surfaces, decreases the velocity of actin
retrograde flow, diminishes the coalescence of BCR microclusters into a central
cluster at the B cell-APC contact site, and decreases APC-induced BCR signaling.
These effects of depleting GMFγ are similar to what occurs when the Arp2/3 complex
is inhibited. This suggests that GMFγ cooperates with the Arp2/3 complex to support
BCR-induced actin remodeling and amplify BCR signaling at the immune synapse.
article_number: '647063'
article_processing_charge: No
article_type: original
author:
- first_name: Nikola
full_name: Deretic, Nikola
last_name: Deretic
- first_name: Madison
full_name: Bolger-Munro, Madison
id: 516F03FA-93A3-11EA-A7C5-D6BE3DDC885E
last_name: Bolger-Munro
orcid: 0000-0002-8176-4824
- first_name: Kate
full_name: Choi, Kate
last_name: Choi
- first_name: Libin
full_name: Abraham, Libin
last_name: Abraham
- first_name: Michael R.
full_name: Gold, Michael R.
last_name: Gold
citation:
ama: Deretic N, Bolger-Munro M, Choi K, Abraham L, Gold MR. The actin-disassembly
protein glia maturation factor γ enhances actin remodeling and B cell antigen
receptor signaling at the immune synapse. Frontiers in Cell and Developmental
Biology. 2021;9. doi:10.3389/fcell.2021.647063
apa: Deretic, N., Bolger-Munro, M., Choi, K., Abraham, L., & Gold, M. R. (2021).
The actin-disassembly protein glia maturation factor γ enhances actin remodeling
and B cell antigen receptor signaling at the immune synapse. Frontiers in Cell
and Developmental Biology. Frontiers Media. https://doi.org/10.3389/fcell.2021.647063
chicago: Deretic, Nikola, Madison Bolger-Munro, Kate Choi, Libin Abraham, and Michael
R. Gold. “The Actin-Disassembly Protein Glia Maturation Factor γ Enhances Actin
Remodeling and B Cell Antigen Receptor Signaling at the Immune Synapse.” Frontiers
in Cell and Developmental Biology. Frontiers Media, 2021. https://doi.org/10.3389/fcell.2021.647063.
ieee: N. Deretic, M. Bolger-Munro, K. Choi, L. Abraham, and M. R. Gold, “The actin-disassembly
protein glia maturation factor γ enhances actin remodeling and B cell antigen
receptor signaling at the immune synapse,” Frontiers in Cell and Developmental
Biology, vol. 9. Frontiers Media, 2021.
ista: Deretic N, Bolger-Munro M, Choi K, Abraham L, Gold MR. 2021. The actin-disassembly
protein glia maturation factor γ enhances actin remodeling and B cell antigen
receptor signaling at the immune synapse. Frontiers in Cell and Developmental
Biology. 9, 647063.
mla: Deretic, Nikola, et al. “The Actin-Disassembly Protein Glia Maturation Factor
γ Enhances Actin Remodeling and B Cell Antigen Receptor Signaling at the Immune
Synapse.” Frontiers in Cell and Developmental Biology, vol. 9, 647063,
Frontiers Media, 2021, doi:10.3389/fcell.2021.647063.
short: N. Deretic, M. Bolger-Munro, K. Choi, L. Abraham, M.R. Gold, Frontiers in
Cell and Developmental Biology 9 (2021).
date_created: 2024-04-03T07:34:08Z
date_published: 2021-07-01T00:00:00Z
date_updated: 2024-04-03T14:10:25Z
day: '01'
ddc:
- '570'
department:
- _id: CaHe
doi: 10.3389/fcell.2021.647063
external_id:
pmid:
- '34336818'
file:
- access_level: open_access
checksum: f6330b5c6718d6780383c0300fd4ef12
content_type: application/pdf
creator: dernst
date_created: 2024-04-03T14:08:05Z
date_updated: 2024-04-03T14:08:05Z
file_id: '15291'
file_name: 2021_Frontiers_Deretic.pdf
file_size: 7430029
relation: main_file
success: 1
file_date_updated: 2024-04-03T14:08:05Z
has_accepted_license: '1'
intvolume: ' 9'
keyword:
- Cell Biology
- Developmental Biology
language:
- iso: eng
month: '07'
oa: 1
oa_version: Published Version
pmid: 1
publication: Frontiers in Cell and Developmental Biology
publication_identifier:
issn:
- 2296-634X
publication_status: published
publisher: Frontiers Media
quality_controlled: '1'
scopus_import: '1'
status: public
title: The actin-disassembly protein glia maturation factor γ enhances actin remodeling
and B cell antigen receptor signaling at the immune synapse
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: 9
year: '2021'
...
---
_id: '15265'
abstract:
- lang: eng
text: 'The highly enhanced thermoelectric figure of merit, zT ≈ 2.6 at 573 K, obtained
recently in Cd-doped polycrystalline AgSbTe2 by Roychowdhury et al. ( Science
2021, 371, 722) brings it to the forefront of thermoelectric and energy materials
research. Ag/Sb cationic ordering in polycrystalline AgSbTe2 was a challenging
issue for a long time: their ordered arrangement in the cationic sublattice in
polycrystalline samples remained elusive despite multiple theoretical predictions
and experimental studies. Recently, selective cation doping has been used to enhance
the Ag/Sb ordering, and cation ordered nanoscale (2–4 nm) domains were observed
in polycrystalline AgSbTe2, which reduce lattice thermal conductivity. The enhanced
cation ordering also delocalizes disorder-induced localized electronic states,
and consequently the electronic transport enhances. In this Focus Review, we provide
the details of the rational design of a high-performance thermoelectric material
using the recently developed atomic order–disorder optimization strategy with
AgSbTe2 as an example. Atomic disorder is ubiquitous in most thermoelectric materials,
and the atomic order–disorder optimization strategy applies to a large variety
of thermoelectric materials.'
article_processing_charge: No
article_type: original
author:
- first_name: Tanmoy
full_name: Ghosh, Tanmoy
id: a5fc9bc3-feff-11ea-93fe-e8015a3c7e9d
last_name: Ghosh
- first_name: Subhajit
full_name: Roychowdhury, Subhajit
last_name: Roychowdhury
- first_name: Moinak
full_name: Dutta, Moinak
last_name: Dutta
- first_name: Kanishka
full_name: Biswas, Kanishka
last_name: Biswas
citation:
ama: 'Ghosh T, Roychowdhury S, Dutta M, Biswas K. High-performance thermoelectric
energy conversion: A tale of atomic ordering in AgSbTe2. ACS Energy Letters.
2021;6(8):2825-2837. doi:10.1021/acsenergylett.1c01184'
apa: 'Ghosh, T., Roychowdhury, S., Dutta, M., & Biswas, K. (2021). High-performance
thermoelectric energy conversion: A tale of atomic ordering in AgSbTe2. ACS
Energy Letters. American Chemical Society. https://doi.org/10.1021/acsenergylett.1c01184'
chicago: 'Ghosh, Tanmoy, Subhajit Roychowdhury, Moinak Dutta, and Kanishka Biswas.
“High-Performance Thermoelectric Energy Conversion: A Tale of Atomic Ordering
in AgSbTe2.” ACS Energy Letters. American Chemical Society, 2021. https://doi.org/10.1021/acsenergylett.1c01184.'
ieee: 'T. Ghosh, S. Roychowdhury, M. Dutta, and K. Biswas, “High-performance thermoelectric
energy conversion: A tale of atomic ordering in AgSbTe2,” ACS Energy Letters,
vol. 6, no. 8. American Chemical Society, pp. 2825–2837, 2021.'
ista: 'Ghosh T, Roychowdhury S, Dutta M, Biswas K. 2021. High-performance thermoelectric
energy conversion: A tale of atomic ordering in AgSbTe2. ACS Energy Letters. 6(8),
2825–2837.'
mla: 'Ghosh, Tanmoy, et al. “High-Performance Thermoelectric Energy Conversion:
A Tale of Atomic Ordering in AgSbTe2.” ACS Energy Letters, vol. 6, no.
8, American Chemical Society, 2021, pp. 2825–37, doi:10.1021/acsenergylett.1c01184.'
short: T. Ghosh, S. Roychowdhury, M. Dutta, K. Biswas, ACS Energy Letters 6 (2021)
2825–2837.
date_created: 2024-04-03T07:36:10Z
date_published: 2021-07-21T00:00:00Z
date_updated: 2024-04-29T06:56:57Z
day: '21'
department:
- _id: MaIb
doi: 10.1021/acsenergylett.1c01184
intvolume: ' 6'
issue: '8'
keyword:
- Materials Chemistry
- Energy Engineering and Power Technology
- Fuel Technology
- Renewable Energy
- Sustainability and the Environment
- Chemistry (miscellaneous)
language:
- iso: eng
month: '07'
oa_version: None
page: 2825-2837
publication: ACS Energy Letters
publication_identifier:
issn:
- 2380-8195
publication_status: published
publisher: American Chemical Society
quality_controlled: '1'
status: public
title: 'High-performance thermoelectric energy conversion: A tale of atomic ordering
in AgSbTe2'
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 6
year: '2021'
...
---
_id: '15266'
abstract:
- lang: eng
text: Plant pathogens often exploit a whole range of effectors to facilitate infection.
The RXLR effector AVR1 produced by the oomycete plant pathogen Phytophthora infestans
suppresses host defense by targeting Sec5. Sec5 is a subunit of the exocyst, a
protein complex that is important for mediating polarized exocytosis during plant
development and defense against pathogens. The mechanism by which AVR1 manipulates
Sec5 functioning is unknown. In this study, we analyzed the effect of AVR1 on
Sec5 localization and functioning in the moss Physcomitrium patens. P. patens
has four Sec5 homologs. Two (PpSec5b and PpSec5d) were found to interact with
AVR1 in yeast-two-hybrid assays while none of the four showed a positive interaction
with AVR1ΔT, a truncated version of AVR1. In P. patens lines carrying β-estradiol
inducible AVR1 or AVR1ΔT transgenes, expression of AVR1 or AVR1ΔT caused defects
in the development of caulonemal protonema cells and abnormal morphology of chloronema
cells. Similar phenotypes were observed in Sec5- or Sec6-silenced P. patens lines,
suggesting that both AVR1 and AVR1ΔT affect exocyst functioning in P. patens.
With respect to Sec5 localization we found no differences between β-estradiol-treated
and untreated transgenic AVR1 lines. Sec5 localizes at the plasma membrane in
growing caulonema cells, also during pathogen attack, and its subcellular localization
is the same, with or without AVR1 in the vicinity.
article_number: e0249637
article_processing_charge: Yes
article_type: original
author:
- first_name: Elysa J. R.
full_name: Overdijk, Elysa J. R.
last_name: Overdijk
- first_name: Vera
full_name: Putker, Vera
last_name: Putker
- first_name: Joep
full_name: Smits, Joep
last_name: Smits
- first_name: Han
full_name: Tang, Han
id: 19BDF720-25A0-11EA-AC6E-928F3DDC885E
last_name: Tang
orcid: 0000-0001-6152-6637
- first_name: Klaas
full_name: Bouwmeester, Klaas
last_name: Bouwmeester
- first_name: Francine
full_name: Govers, Francine
last_name: Govers
- first_name: Tijs
full_name: Ketelaar, Tijs
last_name: Ketelaar
citation:
ama: Overdijk EJR, Putker V, Smits J, et al. Phytophthora infestans RXLR effector
AVR1 disturbs the growth of Physcomitrium patens without affecting Sec5 localization.
PLoS One. 2021;16(4). doi:10.1371/journal.pone.0249637
apa: Overdijk, E. J. R., Putker, V., Smits, J., Tang, H., Bouwmeester, K., Govers,
F., & Ketelaar, T. (2021). Phytophthora infestans RXLR effector AVR1 disturbs
the growth of Physcomitrium patens without affecting Sec5 localization. PLoS
One. Public Library of Science. https://doi.org/10.1371/journal.pone.0249637
chicago: Overdijk, Elysa J. R., Vera Putker, Joep Smits, Han Tang, Klaas Bouwmeester,
Francine Govers, and Tijs Ketelaar. “Phytophthora Infestans RXLR Effector AVR1
Disturbs the Growth of Physcomitrium Patens without Affecting Sec5 Localization.”
PLoS One. Public Library of Science, 2021. https://doi.org/10.1371/journal.pone.0249637.
ieee: E. J. R. Overdijk et al., “Phytophthora infestans RXLR effector AVR1
disturbs the growth of Physcomitrium patens without affecting Sec5 localization,”
PLoS One, vol. 16, no. 4. Public Library of Science, 2021.
ista: Overdijk EJR, Putker V, Smits J, Tang H, Bouwmeester K, Govers F, Ketelaar
T. 2021. Phytophthora infestans RXLR effector AVR1 disturbs the growth of Physcomitrium
patens without affecting Sec5 localization. PLoS One. 16(4), e0249637.
mla: Overdijk, Elysa J. R., et al. “Phytophthora Infestans RXLR Effector AVR1 Disturbs
the Growth of Physcomitrium Patens without Affecting Sec5 Localization.” PLoS
One, vol. 16, no. 4, e0249637, Public Library of Science, 2021, doi:10.1371/journal.pone.0249637.
short: E.J.R. Overdijk, V. Putker, J. Smits, H. Tang, K. Bouwmeester, F. Govers,
T. Ketelaar, PLoS One 16 (2021).
date_created: 2024-04-03T07:38:14Z
date_published: 2021-04-08T00:00:00Z
date_updated: 2024-04-29T06:53:15Z
day: '08'
ddc:
- '580'
department:
- _id: JiFr
doi: 10.1371/journal.pone.0249637
external_id:
pmid:
- '33831039'
file:
- access_level: open_access
checksum: 25b7b329435af57db2c95571a8ef32fe
content_type: application/pdf
creator: dernst
date_created: 2024-04-29T06:51:59Z
date_updated: 2024-04-29T06:51:59Z
file_id: '15349'
file_name: 2021_PlosOne_Overdijk.pdf
file_size: 4738995
relation: main_file
success: 1
file_date_updated: 2024-04-29T06:51:59Z
has_accepted_license: '1'
intvolume: ' 16'
issue: '4'
keyword:
- Multidisciplinary
language:
- iso: eng
month: '04'
oa: 1
oa_version: Published Version
pmid: 1
publication: PLoS One
publication_identifier:
issn:
- 1932-6203
publication_status: published
publisher: Public Library of Science
quality_controlled: '1'
status: public
title: Phytophthora infestans RXLR effector AVR1 disturbs the growth of Physcomitrium
patens without affecting Sec5 localization
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: 16
year: '2021'
...
---
_id: '15269'
abstract:
- lang: eng
text: We study different aspects of quantum field theory at finite density using
methods from quantum information theory. For simplicity we focus on massive Dirac
fermions with nonzero chemical potential, and work in 1 + 1 space-time dimensions.
Using the entanglement entropy on an interval, we construct an entropic c-function
that is finite. Unlike what happens in Lorentz-invariant theories, this c-function
exhibits a strong violation of monotonicity; it also encodes the creation of long-range
entanglement from the Fermi surface. Motivated by previous works on lattice models,
we next calculate numerically the Renyi entropies and find Friedel-type oscillations;
these are understood in terms of a defect operator product expansion. Furthermore,
we consider the mutual information as a measure of correlation functions between
different regions. Using a long-distance expansion previously developed by Cardy,
we argue that the mutual information detects Fermi surface correlations already
at leading order in the expansion. We also analyze the relative entropy and its
Renyi generalizations in order to distinguish states with different charge and/or
mass. In particular, we show that states in different superselection sectors give
rise to a super-extensive behavior in the relative entropy. Finally, we discuss
possible extensions to interacting theories, and argue for the relevance of some
of these measures for probing non-Fermi liquids.
acknowledgement: "We thank H. Casini for many interesting discussions and comments
on the manuscript.\r\nLD is supported by CNEA and UNCuyo, Inst. Balseiro. RM is
supported by IST Austria.\r\nMS is supported by CONICET and UNCuyo, Inst. Balseiro.
GT is supported by CONICET\r\n(PIP grant 11220150100299), ANPCyT (PICT 2018-2517),
CNEA, and UNCuyo,\r\nInst. Balseiro."
article_number: '79'
article_processing_charge: Yes
article_type: original
arxiv: 1
author:
- first_name: Lucas
full_name: Daguerre, Lucas
last_name: Daguerre
- first_name: Raimel A
full_name: Medina Ramos, Raimel A
id: CE680B90-D85A-11E9-B684-C920E6697425
last_name: Medina Ramos
orcid: 0000-0002-5383-2869
- first_name: Mario
full_name: Solís, Mario
last_name: Solís
- first_name: Gonzalo
full_name: Torroba, Gonzalo
last_name: Torroba
citation:
ama: Daguerre L, Medina Ramos RA, Solís M, Torroba G. Aspects of quantum information
in finite density field theory. Journal of High Energy Physics. 2021;2021(3).
doi:10.1007/jhep03(2021)079
apa: Daguerre, L., Medina Ramos, R. A., Solís, M., & Torroba, G. (2021). Aspects
of quantum information in finite density field theory. Journal of High Energy
Physics. Springer Nature. https://doi.org/10.1007/jhep03(2021)079
chicago: Daguerre, Lucas, Raimel A Medina Ramos, Mario Solís, and Gonzalo Torroba.
“Aspects of Quantum Information in Finite Density Field Theory.” Journal of
High Energy Physics. Springer Nature, 2021. https://doi.org/10.1007/jhep03(2021)079.
ieee: L. Daguerre, R. A. Medina Ramos, M. Solís, and G. Torroba, “Aspects of quantum
information in finite density field theory,” Journal of High Energy Physics,
vol. 2021, no. 3. Springer Nature, 2021.
ista: Daguerre L, Medina Ramos RA, Solís M, Torroba G. 2021. Aspects of quantum
information in finite density field theory. Journal of High Energy Physics. 2021(3),
79.
mla: Daguerre, Lucas, et al. “Aspects of Quantum Information in Finite Density Field
Theory.” Journal of High Energy Physics, vol. 2021, no. 3, 79, Springer
Nature, 2021, doi:10.1007/jhep03(2021)079.
short: L. Daguerre, R.A. Medina Ramos, M. Solís, G. Torroba, Journal of High Energy
Physics 2021 (2021).
corr_author: '1'
date_created: 2024-04-03T07:51:06Z
date_published: 2021-03-08T00:00:00Z
date_updated: 2025-09-10T10:15:02Z
day: '08'
ddc:
- '530'
department:
- _id: MaSe
doi: 10.1007/jhep03(2021)079
external_id:
arxiv:
- '2011.01252'
isi:
- '000627376600004'
file:
- access_level: open_access
checksum: 4f540e63988ee87173e02f51a19a6672
content_type: application/pdf
creator: dernst
date_created: 2024-04-10T09:18:38Z
date_updated: 2024-04-10T09:18:38Z
file_id: '15310'
file_name: 2021_JourHighEnergyPhysics_Daguerre.pdf
file_size: 5389195
relation: main_file
success: 1
file_date_updated: 2024-04-10T09:18:38Z
has_accepted_license: '1'
intvolume: ' 2021'
isi: 1
issue: '3'
keyword:
- Nuclear and High Energy Physics
language:
- iso: eng
month: '03'
oa: 1
oa_version: Published Version
publication: Journal of High Energy Physics
publication_identifier:
issn:
- 1029-8479
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: Aspects of quantum information in finite density field theory
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: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 2021
year: '2021'
...
---
_id: '15270'
abstract:
- lang: eng
text: Various toxic compounds disrupt bacterial physiology. While bacteria harbor
defense mechanisms to mitigate the toxicity, these mechanisms are often coupled
to the physiological state of the cells and become ineffective when the physiology
is severely disrupted.
article_number: '676'
article_processing_charge: Yes
article_type: original
author:
- first_name: Dai
full_name: Le, Dai
last_name: Le
- first_name: Ekaterina
full_name: Krasnopeeva, Ekaterina
id: 1F1EE44A-BF83-11EA-B3C1-BB9CC619BF3A
last_name: Krasnopeeva
- first_name: Faris
full_name: Sinjab, Faris
last_name: Sinjab
- first_name: Teuta
full_name: Pilizota, Teuta
last_name: Pilizota
- first_name: Minsu
full_name: Kim, Minsu
last_name: Kim
citation:
ama: Le D, Krasnopeeva E, Sinjab F, Pilizota T, Kim M. Active efflux leads to heterogeneous
dissipation of proton motive force by protonophores in bacteria. mBio.
2021;12(4). doi:10.1128/mbio.00676-21
apa: Le, D., Krasnopeeva, E., Sinjab, F., Pilizota, T., & Kim, M. (2021). Active
efflux leads to heterogeneous dissipation of proton motive force by protonophores
in bacteria. MBio. American Society for Microbiology. https://doi.org/10.1128/mbio.00676-21
chicago: Le, Dai, Ekaterina Krasnopeeva, Faris Sinjab, Teuta Pilizota, and Minsu
Kim. “Active Efflux Leads to Heterogeneous Dissipation of Proton Motive Force
by Protonophores in Bacteria.” MBio. American Society for Microbiology,
2021. https://doi.org/10.1128/mbio.00676-21.
ieee: D. Le, E. Krasnopeeva, F. Sinjab, T. Pilizota, and M. Kim, “Active efflux
leads to heterogeneous dissipation of proton motive force by protonophores in
bacteria,” mBio, vol. 12, no. 4. American Society for Microbiology, 2021.
ista: Le D, Krasnopeeva E, Sinjab F, Pilizota T, Kim M. 2021. Active efflux leads
to heterogeneous dissipation of proton motive force by protonophores in bacteria.
mBio. 12(4), 676.
mla: Le, Dai, et al. “Active Efflux Leads to Heterogeneous Dissipation of Proton
Motive Force by Protonophores in Bacteria.” MBio, vol. 12, no. 4, 676,
American Society for Microbiology, 2021, doi:10.1128/mbio.00676-21.
short: D. Le, E. Krasnopeeva, F. Sinjab, T. Pilizota, M. Kim, MBio 12 (2021).
date_created: 2024-04-03T07:51:57Z
date_published: 2021-08-31T00:00:00Z
date_updated: 2024-04-10T09:13:59Z
day: '31'
ddc:
- '570'
department:
- _id: CaGu
doi: 10.1128/mbio.00676-21
external_id:
pmid:
- '34253054'
file:
- access_level: open_access
checksum: 529e3f97ae5c5f5cc743c4fc130c9440
content_type: application/pdf
creator: dernst
date_created: 2024-04-10T09:05:49Z
date_updated: 2024-04-10T09:05:49Z
file_id: '15309'
file_name: 2021_mBio_Le.pdf
file_size: 1344204
relation: main_file
success: 1
file_date_updated: 2024-04-10T09:05:49Z
has_accepted_license: '1'
intvolume: ' 12'
issue: '4'
keyword:
- Virology
- Microbiology
language:
- iso: eng
month: '08'
oa: 1
oa_version: Published Version
pmid: 1
publication: mBio
publication_identifier:
issn:
- 2150-7511
publication_status: published
publisher: American Society for Microbiology
quality_controlled: '1'
status: public
title: Active efflux leads to heterogeneous dissipation of proton motive force by
protonophores in bacteria
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: 12
year: '2021'
...
---
_id: '15271'
abstract:
- lang: eng
text: 'We settle the complexity of the (∆ + 1)-coloring and (∆ + 1)-list coloring
problems intheCONGESTED CLIQUEmodel by presenting a simpledeterministicalgorithm
for both problemsrunning in a constant number of rounds. This matches the complexity
of the recent breakthroughrandomizedconstant-round (∆ + 1)-list coloring algorithm
due to Chang et al. [Proceedings of the38th ACM Symposium on Principles of Distributed Computing, 2019] and significantly improvesupon
the state-of-the-artO(log ∆)-round deterministic (∆ + 1)-coloring bound of Parter
[Proceed-ings of the 45th Annual International Colloquium on Automata, Languages
and Programming]. Aremarkable property of our algorithm is its simplicity. Whereas
the state-of-the-artrandomizedal-gorithms for this problem are based on the quite
involved local coloring algorithm of Chang, Li, andPettie [Proceedings of the
50th Annual ACM SIGACT Symposium on Theory of Computing, 2018],our algorithm can
be described in just a few lines. At a high level, it applies a careful derandomiza-tion
of a recursive procedure which partitions the nodes and their respective palettes
into separatebins. We show that afterO(1) recursion steps, the remaining uncolored
subgraph within each bin haslinear size and thus can be solved locally by collecting
it to a single node. This algorithm can alsobe implemented in the massively parallel
computation (MPC) model provided that each machine haslinear (inn, the number
of nodes in the input graph) space. We also show an extension of our algo-rithm
to theMPCregime, in which machines havesublinearspace: we present the first deterministic(∆
+ 1)-list coloring algorithm designed for sublinear-spaceMPC, which runs inO(log
∆ + log logn)rounds.'
acknowledgement: The first author was partially supported by the Centre for Discrete Mathematics
and its Applications, by the IBM Faculty Award, and by the EPSRC award EP/N011163/1. The
second author was partially supported by the European Union’s Horizon 2020 research
and innovation program under the Marie Sklodowska-Curie grant agreement 754411. The
first and third authors were partially supported by a Weizmann-UK Making Connections
grant.
article_processing_charge: No
article_type: original
author:
- first_name: Artur
full_name: Czumaj, Artur
last_name: Czumaj
- first_name: Peter
full_name: Davies, Peter
id: 11396234-BB50-11E9-B24C-90FCE5697425
last_name: Davies
orcid: 0000-0002-5646-9524
- first_name: Merav
full_name: Parter, Merav
last_name: Parter
citation:
ama: Czumaj A, Davies P, Parter M. Simple, deterministic, constant-round coloring
in congested clique and MPC. SIAM Journal on Computing. 2021;50(5):1603-1626.
doi:10.1137/20m1366502
apa: Czumaj, A., Davies, P., & Parter, M. (2021). Simple, deterministic, constant-round
coloring in congested clique and MPC. SIAM Journal on Computing. Society
for Industrial and Applied Mathematics. https://doi.org/10.1137/20m1366502
chicago: Czumaj, Artur, Peter Davies, and Merav Parter. “Simple, Deterministic,
Constant-Round Coloring in Congested Clique and MPC.” SIAM Journal on Computing.
Society for Industrial and Applied Mathematics, 2021. https://doi.org/10.1137/20m1366502.
ieee: A. Czumaj, P. Davies, and M. Parter, “Simple, deterministic, constant-round
coloring in congested clique and MPC,” SIAM Journal on Computing, vol.
50, no. 5. Society for Industrial and Applied Mathematics, pp. 1603–1626, 2021.
ista: Czumaj A, Davies P, Parter M. 2021. Simple, deterministic, constant-round
coloring in congested clique and MPC. SIAM Journal on Computing. 50(5), 1603–1626.
mla: Czumaj, Artur, et al. “Simple, Deterministic, Constant-Round Coloring in Congested
Clique and MPC.” SIAM Journal on Computing, vol. 50, no. 5, Society for
Industrial and Applied Mathematics, 2021, pp. 1603–26, doi:10.1137/20m1366502.
short: A. Czumaj, P. Davies, M. Parter, SIAM Journal on Computing 50 (2021) 1603–1626.
date_created: 2024-04-03T07:53:22Z
date_published: 2021-01-01T00:00:00Z
date_updated: 2025-09-10T10:14:11Z
day: '01'
department:
- _id: DaAl
doi: 10.1137/20m1366502
ec_funded: 1
external_id:
isi:
- '000713008600004'
intvolume: ' 50'
isi: 1
issue: '5'
keyword:
- General Mathematics
- General Computer Science
language:
- iso: eng
month: '01'
oa_version: None
page: 1603-1626
project:
- _id: 260C2330-B435-11E9-9278-68D0E5697425
call_identifier: H2020
grant_number: '754411'
name: ISTplus - Postdoctoral Fellowships
publication: SIAM Journal on Computing
publication_identifier:
eissn:
- 1095-7111
issn:
- 0097-5397
publication_status: published
publisher: Society for Industrial and Applied Mathematics
quality_controlled: '1'
scopus_import: '1'
status: public
title: Simple, deterministic, constant-round coloring in congested clique and MPC
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 50
year: '2021'
...
---
_id: '15272'
abstract:
- lang: eng
text: The assembly of neuronal circuits involves the migrations of neurons from
their place of birth to their final location in the nervous system, as well as
the coordinated growth and patterning of axons and dendrites. In screens for genes
required for patterning of the nervous system, we identified the catp-8/P5A-ATPase
as an important regulator of neural patterning. P5A-ATPases are part of the P-type
ATPases, a family of proteins known to serve a conserved function as transporters
of ions, lipids and polyamines in unicellular eukaryotes, plants, and humans.
While the function of many P-type ATPases is relatively well understood, the function
of P5A-ATPases in metazoans remained elusive. We show here, that the Caenorhabditis
elegans ortholog catp-8/P5A-ATPase is
required for defined aspects of nervous system development. Specifically, the
catp-8/P5A-ATPase serves functions in shaping the elaborately
sculpted dendritic trees of somatosensory PVD neurons. Moreover, catp-8/P5A-ATPase
is required for axonal guidance and repulsion at the midline, as well as embryonic
and postembryonic neuronal migrations. Interestingly, not all axons at the midline
require catp-8/P5A-ATPase, although the axons run in
the same fascicles and navigate the same space. Similarly, not all neuronal migrations
require catp-8/P5A-ATPase. A CATP-8/P5A-ATPase reporter
is localized to the ER in most, if not all, tissues and catp-8/P5A-ATPase
can function both cell-autonomously and non-autonomously to regulate neuronal
development. Genetic analyses establish that catp-8/P5A-ATPase
can function in multiple pathways, including the Menorin pathway, previously shown
to control dendritic patterning in PVD, and Wnt signaling, which functions to
control neuronal migrations. Lastly, we show that catp-8/P5A-ATPase
is required for localizing select transmembrane proteins necessary for dendrite
morphogenesis. Collectively, our studies suggest that catp-8/P5A-ATPase
serves diverse, yet specific, roles in different genetic pathways and may be involved
in the regulation or localization of transmembrane and secreted proteins to specific
subcellular compartments.
article_number: e1009475
article_processing_charge: No
article_type: original
author:
- first_name: Leo T. H.
full_name: Tang, Leo T. H.
last_name: Tang
- first_name: Meera
full_name: Trivedi, Meera
last_name: Trivedi
- first_name: Jenna
full_name: Freund, Jenna
last_name: Freund
- first_name: Christopher J.
full_name: Salazar, Christopher J.
last_name: Salazar
- first_name: Maisha
full_name: Rahman, Maisha
last_name: Rahman
- first_name: Nelson
full_name: Ramirez, Nelson
id: 39831956-E4FE-11E9-85DE-0DC7E5697425
last_name: Ramirez
- first_name: Garrett
full_name: Lee, Garrett
last_name: Lee
- first_name: Yu
full_name: Wang, Yu
last_name: Wang
- first_name: Barth D.
full_name: Grant, Barth D.
last_name: Grant
- first_name: Hannes E.
full_name: Bülow, Hannes E.
last_name: Bülow
citation:
ama: Tang LTH, Trivedi M, Freund J, et al. The CATP-8/P5A-type ATPase functions
in multiple pathways during neuronal patterning. PLOS Genetics. 2021;17(7).
doi:10.1371/journal.pgen.1009475
apa: Tang, L. T. H., Trivedi, M., Freund, J., Salazar, C. J., Rahman, M., Ramirez,
N., … Bülow, H. E. (2021). The CATP-8/P5A-type ATPase functions in multiple pathways
during neuronal patterning. PLOS Genetics. Public Library of Science. https://doi.org/10.1371/journal.pgen.1009475
chicago: Tang, Leo T. H., Meera Trivedi, Jenna Freund, Christopher J. Salazar, Maisha
Rahman, Nelson Ramirez, Garrett Lee, Yu Wang, Barth D. Grant, and Hannes E. Bülow.
“The CATP-8/P5A-Type ATPase Functions in Multiple Pathways during Neuronal Patterning.”
PLOS Genetics. Public Library of Science, 2021. https://doi.org/10.1371/journal.pgen.1009475.
ieee: L. T. H. Tang et al., “The CATP-8/P5A-type ATPase functions in multiple
pathways during neuronal patterning,” PLOS Genetics, vol. 17, no. 7. Public
Library of Science, 2021.
ista: Tang LTH, Trivedi M, Freund J, Salazar CJ, Rahman M, Ramirez N, Lee G, Wang
Y, Grant BD, Bülow HE. 2021. The CATP-8/P5A-type ATPase functions in multiple
pathways during neuronal patterning. PLOS Genetics. 17(7), e1009475.
mla: Tang, Leo T. H., et al. “The CATP-8/P5A-Type ATPase Functions in Multiple Pathways
during Neuronal Patterning.” PLOS Genetics, vol. 17, no. 7, e1009475, Public
Library of Science, 2021, doi:10.1371/journal.pgen.1009475.
short: L.T.H. Tang, M. Trivedi, J. Freund, C.J. Salazar, M. Rahman, N. Ramirez,
G. Lee, Y. Wang, B.D. Grant, H.E. Bülow, PLOS Genetics 17 (2021).
date_created: 2024-04-03T07:57:12Z
date_published: 2021-07-01T00:00:00Z
date_updated: 2024-04-10T08:57:16Z
day: '01'
ddc:
- '570'
department:
- _id: MaDe
doi: 10.1371/journal.pgen.1009475
external_id:
pmid:
- '34197450'
file:
- access_level: open_access
checksum: 7352b195e4db6d404f702fe6ad8b55ad
content_type: application/pdf
creator: dernst
date_created: 2024-04-10T08:53:43Z
date_updated: 2024-04-10T08:53:43Z
file_id: '15308'
file_name: 2021_PlosGenetics_Tang.pdf
file_size: 4224934
relation: main_file
success: 1
file_date_updated: 2024-04-10T08:53:43Z
has_accepted_license: '1'
intvolume: ' 17'
issue: '7'
keyword:
- Cancer Research
- Genetics (clinical)
- Genetics
- Molecular Biology
- Ecology
- Evolution
- Behavior and Systematics
language:
- iso: eng
month: '07'
oa: 1
oa_version: Published Version
pmid: 1
publication: PLOS Genetics
publication_identifier:
issn:
- 1553-7404
publication_status: published
publisher: Public Library of Science
quality_controlled: '1'
status: public
title: The CATP-8/P5A-type ATPase functions in multiple pathways during neuronal patterning
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: '2021'
...
---
_id: '15273'
abstract:
- lang: eng
text: Synapses of glutamatergic mossy fibers (MFs) onto cerebellar unipolar brush
cells (UBCs) generate slow excitatory (ON) or inhibitory (OFF) postsynaptic responses
dependent on the complement of glutamate receptors expressed on the UBC’s large
dendritic brush. Using mouse brain slice recording and computational modeling
of synaptic transmission, we found that substantial glutamate is maintained in
the UBC synaptic cleft, sufficient to modify spontaneous firing in OFF UBCs and
tonically desensitize AMPARs of ON UBCs. The source of this ambient glutamate
was spontaneous, spike-independent exocytosis from the MF terminal, and its level
was dependent on activity of glutamate transporters EAAT1–2. Increasing levels
of ambient glutamate shifted the polarity of evoked synaptic responses in ON UBCs
and altered the phase of responses to in vivo-like synaptic activity. Unlike classical
fast synapses, receptors at the UBC synapse are virtually always exposed to a
significant level of glutamate, which varies in a graded manner during transmission.
article_number: e63819
article_processing_charge: Yes
article_type: original
author:
- first_name: Timothy S
full_name: Balmer, Timothy S
last_name: Balmer
- 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: Laurence O
full_name: Trussell, Laurence O
last_name: Trussell
citation:
ama: Balmer TS, Borges Merjane C, Trussell LO. Incomplete removal of extracellular
glutamate controls synaptic transmission and integration at a cerebellar synapse.
eLife. 2021;10. doi:10.7554/elife.63819
apa: Balmer, T. S., Borges Merjane, C., & Trussell, L. O. (2021). Incomplete
removal of extracellular glutamate controls synaptic transmission and integration
at a cerebellar synapse. ELife. eLife Sciences Publications. https://doi.org/10.7554/elife.63819
chicago: Balmer, Timothy S, Carolina Borges Merjane, and Laurence O Trussell. “Incomplete
Removal of Extracellular Glutamate Controls Synaptic Transmission and Integration
at a Cerebellar Synapse.” ELife. eLife Sciences Publications, 2021. https://doi.org/10.7554/elife.63819.
ieee: T. S. Balmer, C. Borges Merjane, and L. O. Trussell, “Incomplete removal of
extracellular glutamate controls synaptic transmission and integration at a cerebellar
synapse,” eLife, vol. 10. eLife Sciences Publications, 2021.
ista: Balmer TS, Borges Merjane C, Trussell LO. 2021. Incomplete removal of extracellular
glutamate controls synaptic transmission and integration at a cerebellar synapse.
eLife. 10, e63819.
mla: Balmer, Timothy S., et al. “Incomplete Removal of Extracellular Glutamate Controls
Synaptic Transmission and Integration at a Cerebellar Synapse.” ELife,
vol. 10, e63819, eLife Sciences Publications, 2021, doi:10.7554/elife.63819.
short: T.S. Balmer, C. Borges Merjane, L.O. Trussell, ELife 10 (2021).
date_created: 2024-04-03T07:58:11Z
date_published: 2021-02-22T00:00:00Z
date_updated: 2024-04-09T11:15:01Z
day: '22'
ddc:
- '570'
department:
- _id: PeJo
doi: 10.7554/elife.63819
external_id:
pmid:
- '33616036'
file:
- access_level: open_access
checksum: bbd4de2e54b7fbc11fba14f59e87fe3f
content_type: application/pdf
creator: dernst
date_created: 2024-04-09T11:13:07Z
date_updated: 2024-04-09T11:13:07Z
file_id: '15307'
file_name: 2021_eLife_Balmer.pdf
file_size: 6997954
relation: main_file
success: 1
file_date_updated: 2024-04-09T11:13:07Z
has_accepted_license: '1'
intvolume: ' 10'
keyword:
- General Immunology and Microbiology
- General Biochemistry
- Genetics and Molecular Biology
- General Medicine
- General Neuroscience
language:
- iso: eng
month: '02'
oa: 1
oa_version: Published Version
pmid: 1
publication: eLife
publication_identifier:
issn:
- 2050-084X
publication_status: published
publisher: eLife Sciences Publications
quality_controlled: '1'
status: public
title: Incomplete removal of extracellular glutamate controls synaptic transmission
and integration at a cerebellar synapse
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: 10
year: '2021'
...
---
_id: '15274'
abstract:
- lang: eng
text: Copper (Cu) is a redox-active micronutrient that is both essential and toxic.
Its cellular homeostasis is critical for supporting cuproprotein maturation while
avoiding excessive oxidative stress. The Cu importer CcoA is the prototype of
the widespread CalT subfamily of the MFS-type transporters. Hence, understanding
its molecular mechanism of function is significant. Here, we show that CcoA undergoes
a thiol:disulfide oxidoreduction cycle, which is important for its Cu import activity.
article_number: e01567
article_processing_charge: No
article_type: original
author:
- first_name: Bahia
full_name: Khalfaoui-Hassani, Bahia
last_name: Khalfaoui-Hassani
- first_name: Petru Iulian
full_name: Trasnea, Petru Iulian
id: D560034C-10C4-11EA-ABF4-A4B43DDC885E
last_name: Trasnea
- first_name: Stefan
full_name: Steimle, Stefan
last_name: Steimle
- first_name: Hans-Georg
full_name: Koch, Hans-Georg
last_name: Koch
- first_name: Fevzi
full_name: Daldal, Fevzi
last_name: Daldal
citation:
ama: Khalfaoui-Hassani B, Trasnea PI, Steimle S, Koch H-G, Daldal F. Cysteine mutants
of the major facilitator superfamily-type transporter CcoA provide insight into
copper import. mBio. 2021;12(4). doi:10.1128/mbio.01567-21
apa: Khalfaoui-Hassani, B., Trasnea, P. I., Steimle, S., Koch, H.-G., & Daldal,
F. (2021). Cysteine mutants of the major facilitator superfamily-type transporter
CcoA provide insight into copper import. MBio. American Society for Microbiology.
https://doi.org/10.1128/mbio.01567-21
chicago: Khalfaoui-Hassani, Bahia, Petru Iulian Trasnea, Stefan Steimle, Hans-Georg
Koch, and Fevzi Daldal. “Cysteine Mutants of the Major Facilitator Superfamily-Type
Transporter CcoA Provide Insight into Copper Import.” MBio. American Society
for Microbiology, 2021. https://doi.org/10.1128/mbio.01567-21.
ieee: B. Khalfaoui-Hassani, P. I. Trasnea, S. Steimle, H.-G. Koch, and F. Daldal,
“Cysteine mutants of the major facilitator superfamily-type transporter CcoA provide
insight into copper import,” mBio, vol. 12, no. 4. American Society for
Microbiology, 2021.
ista: Khalfaoui-Hassani B, Trasnea PI, Steimle S, Koch H-G, Daldal F. 2021. Cysteine
mutants of the major facilitator superfamily-type transporter CcoA provide insight
into copper import. mBio. 12(4), e01567.
mla: Khalfaoui-Hassani, Bahia, et al. “Cysteine Mutants of the Major Facilitator
Superfamily-Type Transporter CcoA Provide Insight into Copper Import.” MBio,
vol. 12, no. 4, e01567, American Society for Microbiology, 2021, doi:10.1128/mbio.01567-21.
short: B. Khalfaoui-Hassani, P.I. Trasnea, S. Steimle, H.-G. Koch, F. Daldal, MBio
12 (2021).
date_created: 2024-04-03T07:59:04Z
date_published: 2021-08-31T00:00:00Z
date_updated: 2024-04-09T10:47:16Z
day: '31'
ddc:
- '570'
department:
- _id: LeSa
doi: 10.1128/mbio.01567-21
external_id:
pmid:
- '34281385'
file:
- access_level: open_access
checksum: 2f6a57637cb3162eaeeb155a5b031e76
content_type: application/pdf
creator: dernst
date_created: 2024-04-09T10:45:11Z
date_updated: 2024-04-09T10:45:11Z
file_id: '15306'
file_name: 2021_mBio_KhalfaouiHassani.pdf
file_size: 3383398
relation: main_file
success: 1
file_date_updated: 2024-04-09T10:45:11Z
has_accepted_license: '1'
intvolume: ' 12'
issue: '4'
keyword:
- Virology
- Microbiology
language:
- iso: eng
month: '08'
oa: 1
oa_version: Published Version
pmid: 1
publication: mBio
publication_identifier:
issn:
- 2150-7511
publication_status: published
publisher: American Society for Microbiology
quality_controlled: '1'
status: public
title: Cysteine mutants of the major facilitator superfamily-type transporter CcoA
provide insight into copper import
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: 12
year: '2021'
...
---
_id: '15275'
abstract:
- lang: eng
text: In 1916, Schur introduced the Ramsey number r(3; m), which is the minimum
integer n > 1 such that for any m-coloring of the edges of the complete graph
Kn, there is a monochromatic copy of K3. He showed that r(3; m) ≤ O(m!), and a
simple construction demonstrates that r(3; m) ≥ 2Ω(m). An old conjecture of Erdős
states that r(3; m) = 2Θ(m). In this note, we prove the conjecture for m-colorings
with bounded VC-dimension, that is, for m-colorings with the property that the
set system induced by the neighborhoods of the vertices with respect to each color
class has bounded VC-dimension.
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Jacob
full_name: Fox, Jacob
last_name: Fox
- first_name: János
full_name: Pach, János
id: E62E3130-B088-11EA-B919-BF823C25FEA4
last_name: Pach
- first_name: Andrew
full_name: Suk, Andrew
last_name: Suk
citation:
ama: Fox J, Pach J, Suk A. Bounded VC-dimension implies the Schur-Erdős conjecture.
Combinatorica. 2021;41(6):803-813. doi:10.1007/s00493-021-4530-9
apa: Fox, J., Pach, J., & Suk, A. (2021). Bounded VC-dimension implies the Schur-Erdős
conjecture. Combinatorica. Springer Nature. https://doi.org/10.1007/s00493-021-4530-9
chicago: Fox, Jacob, János Pach, and Andrew Suk. “Bounded VC-Dimension Implies the
Schur-Erdős Conjecture.” Combinatorica. Springer Nature, 2021. https://doi.org/10.1007/s00493-021-4530-9.
ieee: J. Fox, J. Pach, and A. Suk, “Bounded VC-dimension implies the Schur-Erdős
conjecture,” Combinatorica, vol. 41, no. 6. Springer Nature, pp. 803–813,
2021.
ista: Fox J, Pach J, Suk A. 2021. Bounded VC-dimension implies the Schur-Erdős conjecture.
Combinatorica. 41(6), 803–813.
mla: Fox, Jacob, et al. “Bounded VC-Dimension Implies the Schur-Erdős Conjecture.”
Combinatorica, vol. 41, no. 6, Springer Nature, 2021, pp. 803–13, doi:10.1007/s00493-021-4530-9.
short: J. Fox, J. Pach, A. Suk, Combinatorica 41 (2021) 803–813.
date_created: 2024-04-03T07:59:57Z
date_published: 2021-11-20T00:00:00Z
date_updated: 2024-04-09T10:40:08Z
day: '20'
department:
- _id: HeEd
doi: 10.1007/s00493-021-4530-9
external_id:
arxiv:
- '1912.02342'
intvolume: ' 41'
issue: '6'
keyword:
- Computational Mathematics
- Discrete Mathematics and Combinatorics
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://doi.org/10.48550/arXiv.1912.02342
month: '11'
oa: 1
oa_version: Preprint
page: 803-813
publication: Combinatorica
publication_identifier:
eissn:
- 1439-6912
issn:
- 0209-9683
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
status: public
title: Bounded VC-dimension implies the Schur-Erdős conjecture
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 41
year: '2021'
...
---
_id: '15276'
abstract:
- lang: eng
text: Biotrophic plant pathogens secrete effector proteins to manipulate the host
physiology. Effectors suppress defenses and induce an environment favorable to
disease development. Sequence-based prediction of effector function is impeded
by their rapid evolution rate. In the maize pathogen Ustilago maydis,
effector-coding genes frequently organize in clusters. Here we describe the functional
characterization of the pleiades, a cluster of ten
effector genes, by analyzing the micro- and macroscopic phenotype of the cluster
deletion and expressing these proteins in planta. Deletion
of the pleiades leads to strongly impaired virulence
and accumulation of reactive oxygen species (ROS) in infected tissue. Eight of
the Pleiades suppress the production of ROS upon perception of pathogen associated
molecular patterns (PAMPs). Although functionally redundant, the Pleiades target
different host components. The paralogs Taygeta1 and Merope1 suppress ROS production
in either the cytoplasm or nucleus, respectively. Merope1 targets and promotes
the auto-ubiquitination activity of RFI2, a conserved family of E3 ligases that
regulates the production of PAMP-triggered ROS burst in plants.
article_number: e1009641
article_processing_charge: Yes
article_type: original
author:
- first_name: Fernando
full_name: Navarrete, Fernando
last_name: Navarrete
- first_name: Nenad
full_name: Grujic, Nenad
last_name: Grujic
- first_name: Alexandra
full_name: Stirnberg, Alexandra
last_name: Stirnberg
- first_name: Indira
full_name: Saado, Indira
last_name: Saado
- first_name: David
full_name: Aleksza, David
last_name: Aleksza
- first_name: Michelle C
full_name: Gallei, Michelle C
id: 35A03822-F248-11E8-B48F-1D18A9856A87
last_name: Gallei
orcid: 0000-0003-1286-7368
- first_name: Hazem
full_name: Adi, Hazem
last_name: Adi
- first_name: André
full_name: Alcântara, André
last_name: Alcântara
- first_name: Mamoona
full_name: Khan, Mamoona
last_name: Khan
- first_name: Janos
full_name: Bindics, Janos
last_name: Bindics
- first_name: Marco
full_name: Trujillo, Marco
last_name: Trujillo
- first_name: Armin
full_name: Djamei, Armin
last_name: Djamei
citation:
ama: Navarrete F, Grujic N, Stirnberg A, et al. The Pleiades are a cluster of fungal
effectors that inhibit host defenses. PLOS Pathogens. 2021;17(6). doi:10.1371/journal.ppat.1009641
apa: Navarrete, F., Grujic, N., Stirnberg, A., Saado, I., Aleksza, D., Gallei, M.
C., … Djamei, A. (2021). The Pleiades are a cluster of fungal effectors that inhibit
host defenses. PLOS Pathogens. Public Library of Science. https://doi.org/10.1371/journal.ppat.1009641
chicago: Navarrete, Fernando, Nenad Grujic, Alexandra Stirnberg, Indira Saado, David
Aleksza, Michelle C Gallei, Hazem Adi, et al. “The Pleiades Are a Cluster of Fungal
Effectors That Inhibit Host Defenses.” PLOS Pathogens. Public Library of
Science, 2021. https://doi.org/10.1371/journal.ppat.1009641.
ieee: F. Navarrete et al., “The Pleiades are a cluster of fungal effectors
that inhibit host defenses,” PLOS Pathogens, vol. 17, no. 6. Public Library
of Science, 2021.
ista: Navarrete F, Grujic N, Stirnberg A, Saado I, Aleksza D, Gallei MC, Adi H,
Alcântara A, Khan M, Bindics J, Trujillo M, Djamei A. 2021. The Pleiades are a
cluster of fungal effectors that inhibit host defenses. PLOS Pathogens. 17(6),
e1009641.
mla: Navarrete, Fernando, et al. “The Pleiades Are a Cluster of Fungal Effectors
That Inhibit Host Defenses.” PLOS Pathogens, vol. 17, no. 6, e1009641,
Public Library of Science, 2021, doi:10.1371/journal.ppat.1009641.
short: F. Navarrete, N. Grujic, A. Stirnberg, I. Saado, D. Aleksza, M.C. Gallei,
H. Adi, A. Alcântara, M. Khan, J. Bindics, M. Trujillo, A. Djamei, PLOS Pathogens
17 (2021).
date_created: 2024-04-03T08:00:34Z
date_published: 2021-06-24T00:00:00Z
date_updated: 2024-04-09T10:26:12Z
day: '24'
ddc:
- '580'
department:
- _id: JiFr
doi: 10.1371/journal.ppat.1009641
external_id:
pmid:
- '34166468'
file:
- access_level: open_access
checksum: ab8428291a0c14607c4ea5656c029cff
content_type: application/pdf
creator: dernst
date_created: 2024-04-09T10:24:43Z
date_updated: 2024-04-09T10:24:43Z
file_id: '15305'
file_name: 2021_PlosPathogens_Navarrete.pdf
file_size: 2616563
relation: main_file
success: 1
file_date_updated: 2024-04-09T10:24:43Z
has_accepted_license: '1'
intvolume: ' 17'
issue: '6'
keyword:
- Virology
- Genetics
- Molecular Biology
- Immunology
- Microbiology
- Parasitology
language:
- iso: eng
month: '06'
oa: 1
oa_version: Published Version
pmid: 1
publication: PLOS Pathogens
publication_identifier:
issn:
- 1553-7374
publication_status: published
publisher: Public Library of Science
quality_controlled: '1'
status: public
title: The Pleiades are a cluster of fungal effectors that inhibit host defenses
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: '2021'
...
---
_id: '15277'
abstract:
- lang: eng
text: Alternative splicing generates multiple transcript and protein isoforms from
a single gene and controls transcript intracellular localization and stability
by coupling to mRNA export and nonsense-mediated mRNA decay (NMD). RNA interference
(RNAi) is a potent mechanism to modulate gene expression. However, its interactions
with alternative splicing are poorly understood. We used artificial microRNAs
(amiRNAs, also termed shRNAmiR) to knockdown all splice variants of selected target
genes in Arabidopsis thaliana. We found that splice variants, which vary by their
protein-coding capacity, subcellular localization and sensitivity to NMD, are
affected differentially by an amiRNA, although all of them contain the target
site. Particular transcript isoforms escape amiRNA-mediated degradation due to
their nuclear localization. The nuclear and NMD-sensitive isoforms mask RNAi action
in alternatively spliced genes. Interestingly, Arabidopsis SPL genes, which undergo
alternative splicing and are targets of miR156, are regulated in the same manner.
Moreover, similar results were obtained in mammalian cells using siRNAs, indicating
cross-kingdom conservation of these interactions among RNAi and splicing isoforms.
Furthermore, we report that amiRNA can trigger artificial alternative splicing,
thus expanding the RNAi functional repertoire. Our findings unveil novel interactions
between different post-transcriptional processes in defining transcript fates
and regulating gene expression.
article_processing_charge: No
article_type: original
author:
- first_name: Armin
full_name: Fuchs, Armin
last_name: Fuchs
- first_name: Stefan
full_name: Riegler, Stefan
last_name: Riegler
- first_name: Zahra
full_name: Ayatollahi, Zahra
last_name: Ayatollahi
- first_name: Nicola
full_name: Cavallari, Nicola
id: 457160E6-F248-11E8-B48F-1D18A9856A87
last_name: Cavallari
- first_name: Luciana E
full_name: Giono, Luciana E
last_name: Giono
- first_name: Barbara A
full_name: Nimeth, Barbara A
last_name: Nimeth
- first_name: Krishna V
full_name: Mutanwad, Krishna V
last_name: Mutanwad
- first_name: Alois
full_name: Schweighofer, Alois
last_name: Schweighofer
- first_name: Doris
full_name: Lucyshyn, Doris
last_name: Lucyshyn
- first_name: Andrea
full_name: Barta, Andrea
last_name: Barta
- first_name: Ezequiel
full_name: Petrillo, Ezequiel
last_name: Petrillo
- first_name: Maria
full_name: Kalyna, Maria
last_name: Kalyna
citation:
ama: 'Fuchs A, Riegler S, Ayatollahi Z, et al. Targeting alternative splicing by
RNAi: From the differential impact on splice variants to triggering artificial
pre-mRNA splicing. Nucleic Acids Research. 2021;49(2):1133-1151. doi:10.1093/nar/gkaa1260'
apa: 'Fuchs, A., Riegler, S., Ayatollahi, Z., Cavallari, N., Giono, L. E., Nimeth,
B. A., … Kalyna, M. (2021). Targeting alternative splicing by RNAi: From the differential
impact on splice variants to triggering artificial pre-mRNA splicing. Nucleic
Acids Research. Oxford University Press. https://doi.org/10.1093/nar/gkaa1260'
chicago: 'Fuchs, Armin, Stefan Riegler, Zahra Ayatollahi, Nicola Cavallari, Luciana
E Giono, Barbara A Nimeth, Krishna V Mutanwad, et al. “Targeting Alternative Splicing
by RNAi: From the Differential Impact on Splice Variants to Triggering Artificial
Pre-MRNA Splicing.” Nucleic Acids Research. Oxford University Press, 2021.
https://doi.org/10.1093/nar/gkaa1260.'
ieee: 'A. Fuchs et al., “Targeting alternative splicing by RNAi: From the
differential impact on splice variants to triggering artificial pre-mRNA splicing,”
Nucleic Acids Research, vol. 49, no. 2. Oxford University Press, pp. 1133–1151,
2021.'
ista: 'Fuchs A, Riegler S, Ayatollahi Z, Cavallari N, Giono LE, Nimeth BA, Mutanwad
KV, Schweighofer A, Lucyshyn D, Barta A, Petrillo E, Kalyna M. 2021. Targeting
alternative splicing by RNAi: From the differential impact on splice variants
to triggering artificial pre-mRNA splicing. Nucleic Acids Research. 49(2), 1133–1151.'
mla: 'Fuchs, Armin, et al. “Targeting Alternative Splicing by RNAi: From the Differential
Impact on Splice Variants to Triggering Artificial Pre-MRNA Splicing.” Nucleic
Acids Research, vol. 49, no. 2, Oxford University Press, 2021, pp. 1133–51,
doi:10.1093/nar/gkaa1260.'
short: A. Fuchs, S. Riegler, Z. Ayatollahi, N. Cavallari, L.E. Giono, B.A. Nimeth,
K.V. Mutanwad, A. Schweighofer, D. Lucyshyn, A. Barta, E. Petrillo, M. Kalyna,
Nucleic Acids Research 49 (2021) 1133–1151.
date_created: 2024-04-03T08:02:09Z
date_published: 2021-01-25T00:00:00Z
date_updated: 2024-04-09T10:16:40Z
day: '25'
ddc:
- '570'
department:
- _id: EvBe
doi: 10.1093/nar/gkaa1260
external_id:
pmid:
- '33406240'
file:
- access_level: open_access
checksum: d3c90660759a5d34ad43ba1def130462
content_type: application/pdf
creator: dernst
date_created: 2024-04-09T10:14:39Z
date_updated: 2024-04-09T10:14:39Z
file_id: '15304'
file_name: 2021_NucleicAcidsRes_Fuchs.pdf
file_size: 6539791
relation: main_file
success: 1
file_date_updated: 2024-04-09T10:14:39Z
has_accepted_license: '1'
intvolume: ' 49'
issue: '2'
keyword:
- Genetics
language:
- iso: eng
month: '01'
oa: 1
oa_version: Published Version
page: 1133-1151
pmid: 1
publication: Nucleic Acids Research
publication_identifier:
eissn:
- 1362-4962
issn:
- 0305-1048
publication_status: published
publisher: Oxford University Press
quality_controlled: '1'
status: public
title: 'Targeting alternative splicing by RNAi: From the differential impact on splice
variants to triggering artificial pre-mRNA splicing'
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: 49
year: '2021'
...
---
_id: '15278'
abstract:
- lang: eng
text: ‘Dysbiosis’ of the adult gut microbiota, in response to challenges such as
infection, altered diet, stress, and antibiotics treatment has been recently linked
to pathological alteration of brain function and behavior. Moreover, gut microbiota
composition constantly controls microglia maturation, as revealed by morphological
observations and gene expression analysis. However, it is unclear whether microglia
functional properties and crosstalk with neurons, known to shape and modulate
synaptic development and function, are influenced by the gut microbiota. Here,
we investigated how antibiotic-mediated alteration of the gut microbiota influences
microglial and neuronal functions in adult mice hippocampus. Hippocampal microglia
from adult mice treated with oral antibiotics exhibited increased microglia density,
altered basal patrolling activity, and impaired process rearrangement in response
to damage. Patch clamp recordings at CA3-CA1 synapses revealed that antibiotics
treatment alters neuronal functions, reducing spontaneous postsynaptic glutamatergic
currents and decreasing synaptic connectivity, without reducing dendritic spines
density. Antibiotics treatment was unable to modulate synaptic function in CX3CR1-deficient
mice, pointing to an involvement of microglia–neuron crosstalk through the CX3CL1/CX3CR1
axis in the effect of dysbiosis on neuronal functions. Together, our findings
show that antibiotic alteration of gut microbiota impairs synaptic efficacy, suggesting
that CX3CL1/CX3CR1 signaling supporting microglia is a major player in in the
gut–brain axis, and in particular in the gut microbiota-to-neuron communication
pathway.
article_number: '2648'
article_processing_charge: Yes
article_type: original
author:
- first_name: Federica
full_name: Cordella, Federica
last_name: Cordella
- first_name: Caterina
full_name: Sanchini, Caterina
last_name: Sanchini
- first_name: Maria
full_name: Rosito, Maria
last_name: Rosito
- first_name: Laura
full_name: Ferrucci, Laura
last_name: Ferrucci
- first_name: Natalia
full_name: Pediconi, Natalia
last_name: Pediconi
- first_name: Barbara
full_name: Cortese, Barbara
last_name: Cortese
- first_name: Francesca
full_name: Guerrieri, Francesca
last_name: Guerrieri
- first_name: Giuseppe Rubens
full_name: Pascucci, Giuseppe Rubens
last_name: Pascucci
- first_name: Fabrizio
full_name: Antonangeli, Fabrizio
last_name: Antonangeli
- first_name: Giovanna
full_name: Peruzzi, Giovanna
last_name: Peruzzi
- first_name: Maria
full_name: Giubettini, Maria
last_name: Giubettini
- first_name: Bernadette
full_name: Basilico, Bernadette
id: 36035796-5ACA-11E9-A75E-7AF2E5697425
last_name: Basilico
orcid: 0000-0003-1843-3173
- first_name: Francesca
full_name: Pagani, Francesca
last_name: Pagani
- first_name: Alfonso
full_name: Grimaldi, Alfonso
last_name: Grimaldi
- first_name: Giuseppina
full_name: D’Alessandro, Giuseppina
last_name: D’Alessandro
- first_name: Cristina
full_name: Limatola, Cristina
last_name: Limatola
- first_name: Davide
full_name: Ragozzino, Davide
last_name: Ragozzino
- first_name: Silvia
full_name: Di Angelantonio, Silvia
last_name: Di Angelantonio
citation:
ama: Cordella F, Sanchini C, Rosito M, et al. Antibiotics treatment modulates microglia–synapses
interaction. Cells. 2021;10(10). doi:10.3390/cells10102648
apa: Cordella, F., Sanchini, C., Rosito, M., Ferrucci, L., Pediconi, N., Cortese,
B., … Di Angelantonio, S. (2021). Antibiotics treatment modulates microglia–synapses
interaction. Cells. MDPI. https://doi.org/10.3390/cells10102648
chicago: Cordella, Federica, Caterina Sanchini, Maria Rosito, Laura Ferrucci, Natalia
Pediconi, Barbara Cortese, Francesca Guerrieri, et al. “Antibiotics Treatment
Modulates Microglia–Synapses Interaction.” Cells. MDPI, 2021. https://doi.org/10.3390/cells10102648.
ieee: F. Cordella et al., “Antibiotics treatment modulates microglia–synapses
interaction,” Cells, vol. 10, no. 10. MDPI, 2021.
ista: Cordella F, Sanchini C, Rosito M, Ferrucci L, Pediconi N, Cortese B, Guerrieri
F, Pascucci GR, Antonangeli F, Peruzzi G, Giubettini M, Basilico B, Pagani F,
Grimaldi A, D’Alessandro G, Limatola C, Ragozzino D, Di Angelantonio S. 2021.
Antibiotics treatment modulates microglia–synapses interaction. Cells. 10(10),
2648.
mla: Cordella, Federica, et al. “Antibiotics Treatment Modulates Microglia–Synapses
Interaction.” Cells, vol. 10, no. 10, 2648, MDPI, 2021, doi:10.3390/cells10102648.
short: F. Cordella, C. Sanchini, M. Rosito, L. Ferrucci, N. Pediconi, B. Cortese,
F. Guerrieri, G.R. Pascucci, F. Antonangeli, G. Peruzzi, M. Giubettini, B. Basilico,
F. Pagani, A. Grimaldi, G. D’Alessandro, C. Limatola, D. Ragozzino, S. Di Angelantonio,
Cells 10 (2021).
date_created: 2024-04-03T08:02:52Z
date_published: 2021-10-04T00:00:00Z
date_updated: 2024-04-09T08:53:23Z
day: '04'
ddc:
- '610'
department:
- _id: GaNo
doi: 10.3390/cells10102648
external_id:
pmid:
- '34685628'
file:
- access_level: open_access
checksum: 1a3b251ce82e2b9474b852d2abe5bb03
content_type: application/pdf
creator: dernst
date_created: 2024-04-09T08:51:22Z
date_updated: 2024-04-09T08:51:22Z
file_id: '15303'
file_name: 2021_Cells_Cordella.pdf
file_size: 2196672
relation: main_file
success: 1
file_date_updated: 2024-04-09T08:51:22Z
has_accepted_license: '1'
intvolume: ' 10'
issue: '10'
keyword:
- General Medicine
language:
- iso: eng
month: '10'
oa: 1
oa_version: Published Version
pmid: 1
publication: Cells
publication_identifier:
issn:
- 2073-4409
publication_status: published
publisher: MDPI
quality_controlled: '1'
status: public
title: Antibiotics treatment modulates microglia–synapses interaction
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: 10
year: '2021'
...
---
_id: '15283'
article_processing_charge: No
article_type: original
author:
- first_name: William
full_name: Nicolas, William
last_name: Nicolas
- first_name: Florian
full_name: Fäßler, Florian
id: 404F5528-F248-11E8-B48F-1D18A9856A87
last_name: Fäßler
orcid: 0000-0001-7149-769X
- first_name: Elliot
full_name: Meyerowitz, Elliot
last_name: Meyerowitz
- first_name: Grant
full_name: Jensen, Grant
last_name: Jensen
citation:
ama: Nicolas W, Fäßler F, Meyerowitz E, Jensen G. Peaking into the plant cell wall
using cryo-FIB milling and electron cryo-tomography. Microscopy and Microanalysis.
2021;27(S1):3024-3026. doi:10.1017/s1431927621010503
apa: Nicolas, W., Fäßler, F., Meyerowitz, E., & Jensen, G. (2021). Peaking into
the plant cell wall using cryo-FIB milling and electron cryo-tomography. Microscopy
and Microanalysis. Oxford University Press. https://doi.org/10.1017/s1431927621010503
chicago: Nicolas, William, Florian Fäßler, Elliot Meyerowitz, and Grant Jensen.
“Peaking into the Plant Cell Wall Using Cryo-FIB Milling and Electron Cryo-Tomography.”
Microscopy and Microanalysis. Oxford University Press, 2021. https://doi.org/10.1017/s1431927621010503.
ieee: W. Nicolas, F. Fäßler, E. Meyerowitz, and G. Jensen, “Peaking into the plant
cell wall using cryo-FIB milling and electron cryo-tomography,” Microscopy
and Microanalysis, vol. 27, no. S1. Oxford University Press, pp. 3024–3026,
2021.
ista: Nicolas W, Fäßler F, Meyerowitz E, Jensen G. 2021. Peaking into the plant
cell wall using cryo-FIB milling and electron cryo-tomography. Microscopy and
Microanalysis. 27(S1), 3024–3026.
mla: Nicolas, William, et al. “Peaking into the Plant Cell Wall Using Cryo-FIB Milling
and Electron Cryo-Tomography.” Microscopy and Microanalysis, vol. 27, no.
S1, Oxford University Press, 2021, pp. 3024–26, doi:10.1017/s1431927621010503.
short: W. Nicolas, F. Fäßler, E. Meyerowitz, G. Jensen, Microscopy and Microanalysis
27 (2021) 3024–3026.
date_created: 2024-04-03T08:57:23Z
date_published: 2021-08-01T00:00:00Z
date_updated: 2024-04-09T07:55:56Z
day: '01'
department:
- _id: FlSc
doi: 10.1017/s1431927621010503
intvolume: ' 27'
issue: S1
keyword:
- Instrumentation
language:
- iso: eng
month: '08'
oa_version: None
page: 3024-3026
publication: Microscopy and Microanalysis
publication_identifier:
eissn:
- 1435-8115
issn:
- 1431-9276
publication_status: published
publisher: Oxford University Press
quality_controlled: '1'
status: public
title: Peaking into the plant cell wall using cryo-FIB milling and electron cryo-tomography
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 27
year: '2021'
...
---
_id: '15284'
abstract:
- lang: eng
text: "RevTerm is a static analysis tool for proving non-termination of integer
C programs (possibly with non-determinism). RevTerm is an implementation of our
method for non-termination proving presented in the paper “Proving Non-termination
by Program Reversal”.\r\n\r\n"
article_processing_charge: No
author:
- first_name: Krishnendu
full_name: Chatterjee, Krishnendu
id: 2E5DCA20-F248-11E8-B48F-1D18A9856A87
last_name: Chatterjee
orcid: 0000-0002-4561-241X
- first_name: Ehsan Kafshdar
full_name: Goharshady, Ehsan Kafshdar
last_name: Goharshady
- first_name: Petr
full_name: Novotný, Petr
id: 3CC3B868-F248-11E8-B48F-1D18A9856A87
last_name: Novotný
- first_name: Dorde
full_name: Zikelic, Dorde
id: 294AA7A6-F248-11E8-B48F-1D18A9856A87
last_name: Zikelic
orcid: 0000-0002-4681-1699
citation:
ama: Chatterjee K, Goharshady EK, Novotný P, Zikelic D. RevTerm. 2021. doi:10.1145/3410304
apa: Chatterjee, K., Goharshady, E. K., Novotný, P., & Zikelic, D. (2021). RevTerm.
Association for Computing Machinery. https://doi.org/10.1145/3410304
chicago: Chatterjee, Krishnendu, Ehsan Kafshdar Goharshady, Petr Novotný, and Dorde
Zikelic. “RevTerm.” Association for Computing Machinery, 2021. https://doi.org/10.1145/3410304.
ieee: K. Chatterjee, E. K. Goharshady, P. Novotný, and D. Zikelic, “RevTerm.” Association
for Computing Machinery, 2021.
ista: Chatterjee K, Goharshady EK, Novotný P, Zikelic D. 2021. RevTerm, Association
for Computing Machinery, 10.1145/3410304.
mla: Chatterjee, Krishnendu, et al. RevTerm. Association for Computing Machinery,
2021, doi:10.1145/3410304.
short: K. Chatterjee, E.K. Goharshady, P. Novotný, D. Zikelic, (2021).
corr_author: '1'
date_created: 2024-04-03T09:00:42Z
date_published: 2021-06-01T00:00:00Z
date_updated: 2025-04-15T06:25:30Z
day: '01'
ddc:
- '000'
department:
- _id: KrCh
doi: 10.1145/3410304
has_accepted_license: '1'
main_file_link:
- open_access: '1'
url: https://doi.org/10.1145/3410304
month: '06'
oa: 1
oa_version: Published Version
publisher: Association for Computing Machinery
related_material:
record:
- id: '9644'
relation: used_in_publication
status: public
status: public
title: RevTerm
type: research_data_reference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2021'
...
---
_id: '15285'
abstract:
- lang: eng
text: Ever since the first publication of the standard communication protocol for
computer-assisted electrocardiography (SCP-ECG), prENV 1064, in 1993, by the European
Committee for Standardization (CEN), SCP-ECG has become a leading example in health
informatics, enabling open, secure, and well-documented digital data exchange
at a low cost, for quick and efficient cardiovascular disease detection and management.
Based on the experiences gained, since the 1970s, in computerized electrocardiology,
and on the results achieved by the pioneering, international cooperative research
on common standards for quantitative electrocardiography (CSE), SCP-ECG was designed,
from the beginning, to empower personalized medicine, thanks to serial ECG analysis.
The fundamental concept behind SCP-ECG is to convey the necessary information
for ECG re-analysis, serial comparison, and interpretation, and to structure the
ECG data and metadata in sections that are mostly optional in order to fit all
use cases. SCP-ECG is open to the storage of the ECG signal and ECG measurement
data, whatever the ECG recording modality or computation method, and can store
the over-reading trails and ECG annotations, as well as any computerized or medical
interpretation reports. Only the encoding syntax and the semantics of the ECG
descriptors and of the diagnosis codes are standardized. We present all of the
landmarks in the development and publication of SCP-ECG, from the early 1990s
to the 2009 International Organization for Standardization (ISO) SCP-ECG standards,
including the latest version published by CEN in 2020, which now encompasses rest
and stress ECGs, Holter recordings, and protocol-based trials.
acknowledgement: This research received no external funding. The authors thank the
large number of researchers, engineers, cardiologists, and clinicians from academia,
industry, and normalization organizations who contributed to the development and
testing of the SCP-ECG standards.
article_processing_charge: Yes
article_type: review
author:
- first_name: Paul
full_name: Rubel, Paul
last_name: Rubel
- first_name: Jocelyne
full_name: Fayn, Jocelyne
last_name: Fayn
- first_name: Peter W.
full_name: Macfarlane, Peter W.
last_name: Macfarlane
- first_name: Danilo
full_name: Pani, Danilo
last_name: Pani
- first_name: Alois
full_name: Schlögl, Alois
id: 45BF87EE-F248-11E8-B48F-1D18A9856A87
last_name: Schlögl
orcid: 0000-0002-5621-8100
- first_name: Alpo
full_name: Värri, Alpo
last_name: Värri
citation:
ama: 'Rubel P, Fayn J, Macfarlane PW, Pani D, Schlögl A, Värri A. The history and
challenges of SCP-ECG: The standard communication protocol for computer-assisted
electrocardiography. Hearts. 2021;2(3):384-409. doi:10.3390/hearts2030031'
apa: 'Rubel, P., Fayn, J., Macfarlane, P. W., Pani, D., Schlögl, A., & Värri,
A. (2021). The history and challenges of SCP-ECG: The standard communication protocol
for computer-assisted electrocardiography. Hearts. MDPI. https://doi.org/10.3390/hearts2030031'
chicago: 'Rubel, Paul, Jocelyne Fayn, Peter W. Macfarlane, Danilo Pani, Alois Schlögl,
and Alpo Värri. “The History and Challenges of SCP-ECG: The Standard Communication
Protocol for Computer-Assisted Electrocardiography.” Hearts. MDPI, 2021.
https://doi.org/10.3390/hearts2030031.'
ieee: 'P. Rubel, J. Fayn, P. W. Macfarlane, D. Pani, A. Schlögl, and A. Värri, “The
history and challenges of SCP-ECG: The standard communication protocol for computer-assisted
electrocardiography,” Hearts, vol. 2, no. 3. MDPI, pp. 384–409, 2021.'
ista: 'Rubel P, Fayn J, Macfarlane PW, Pani D, Schlögl A, Värri A. 2021. The history
and challenges of SCP-ECG: The standard communication protocol for computer-assisted
electrocardiography. Hearts. 2(3), 384–409.'
mla: 'Rubel, Paul, et al. “The History and Challenges of SCP-ECG: The Standard Communication
Protocol for Computer-Assisted Electrocardiography.” Hearts, vol. 2, no.
3, MDPI, 2021, pp. 384–409, doi:10.3390/hearts2030031.'
short: P. Rubel, J. Fayn, P.W. Macfarlane, D. Pani, A. Schlögl, A. Värri, Hearts
2 (2021) 384–409.
date_created: 2024-04-03T09:03:31Z
date_published: 2021-08-24T00:00:00Z
date_updated: 2024-04-09T06:51:50Z
day: '24'
ddc:
- '610'
department:
- _id: ScienComp
doi: 10.3390/hearts2030031
file:
- access_level: open_access
checksum: f67142b1e1e8ca5cd7a6a6798f46375e
content_type: application/pdf
creator: dernst
date_created: 2024-04-09T06:49:47Z
date_updated: 2024-04-09T06:49:47Z
file_id: '15302'
file_name: 2021_Hearts_Rubel.pdf
file_size: 3539897
relation: main_file
success: 1
file_date_updated: 2024-04-09T06:49:47Z
has_accepted_license: '1'
intvolume: ' 2'
issue: '3'
keyword:
- General Medicine
language:
- iso: eng
month: '08'
oa: 1
oa_version: Published Version
page: 384-409
publication: Hearts
publication_identifier:
issn:
- 2673-3846
publication_status: published
publisher: MDPI
quality_controlled: '1'
status: public
title: 'The history and challenges of SCP-ECG: The standard communication protocol
for computer-assisted electrocardiography'
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: 2
year: '2021'
...
---
OA_place: publisher
_id: '10007'
abstract:
- lang: eng
text: The present thesis is concerned with the derivation of weak-strong uniqueness
principles for curvature driven interface evolution problems not satisfying a
comparison principle. The specific examples being treated are two-phase Navier-Stokes
flow with surface tension, modeling the evolution of two incompressible, viscous
and immiscible fluids separated by a sharp interface, and multiphase mean curvature
flow, which serves as an idealized model for the motion of grain boundaries in
an annealing polycrystalline material. Our main results - obtained in joint works
with Julian Fischer, Tim Laux and Theresa M. Simon - state that prior to the formation
of geometric singularities due to topology changes, the weak solution concept
of Abels (Interfaces Free Bound. 9, 2007) to two-phase Navier-Stokes flow with
surface tension and the weak solution concept of Laux and Otto (Calc. Var. Partial
Differential Equations 55, 2016) to multiphase mean curvature flow (for networks
in R^2 or double bubbles in R^3) represents the unique solution to these interface
evolution problems within the class of classical solutions, respectively. To the
best of the author's knowledge, for interface evolution problems not admitting
a geometric comparison principle the derivation of a weak-strong uniqueness principle
represented an open problem, so that the works contained in the present thesis
constitute the first positive results in this direction. The key ingredient of
our approach consists of the introduction of a novel concept of relative entropies
for a class of curvature driven interface evolution problems, for which the associated
energy contains an interfacial contribution being proportional to the surface
area of the evolving (network of) interface(s). The interfacial part of the relative
entropy gives sufficient control on the interface error between a weak and a classical
solution, and its time evolution can be computed, at least in principle, for any
energy dissipating weak solution concept. A resulting stability estimate for the
relative entropy essentially entails the above mentioned weak-strong uniqueness
principles. The present thesis contains a detailed introduction to our relative
entropy approach, which in particular highlights potential applications to other
problems in curvature driven interface evolution not treated in this thesis.
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Sebastian
full_name: Hensel, Sebastian
id: 4D23B7DA-F248-11E8-B48F-1D18A9856A87
last_name: Hensel
orcid: 0000-0001-7252-8072
citation:
ama: 'Hensel S. Curvature driven interface evolution: Uniqueness properties of weak
solution concepts. 2021. doi:10.15479/at:ista:10007'
apa: 'Hensel, S. (2021). Curvature driven interface evolution: Uniqueness properties
of weak solution concepts. Institute of Science and Technology Austria. https://doi.org/10.15479/at:ista:10007'
chicago: 'Hensel, Sebastian. “Curvature Driven Interface Evolution: Uniqueness Properties
of Weak Solution Concepts.” Institute of Science and Technology Austria, 2021.
https://doi.org/10.15479/at:ista:10007.'
ieee: 'S. Hensel, “Curvature driven interface evolution: Uniqueness properties of
weak solution concepts,” Institute of Science and Technology Austria, 2021.'
ista: 'Hensel S. 2021. Curvature driven interface evolution: Uniqueness properties
of weak solution concepts. Institute of Science and Technology Austria.'
mla: 'Hensel, Sebastian. Curvature Driven Interface Evolution: Uniqueness Properties
of Weak Solution Concepts. Institute of Science and Technology Austria, 2021,
doi:10.15479/at:ista:10007.'
short: 'S. Hensel, Curvature Driven Interface Evolution: Uniqueness Properties of
Weak Solution Concepts, Institute of Science and Technology Austria, 2021.'
corr_author: '1'
date_created: 2021-09-13T11:12:34Z
date_published: 2021-09-14T00:00:00Z
date_updated: 2026-04-08T07:01:01Z
day: '14'
ddc:
- '515'
degree_awarded: PhD
department:
- _id: GradSch
- _id: JuFi
doi: 10.15479/at:ista:10007
ec_funded: 1
file:
- access_level: closed
checksum: c8475faaf0b680b4971f638f1db16347
content_type: application/x-zip-compressed
creator: shensel
date_created: 2021-09-13T11:03:24Z
date_updated: 2021-09-15T14:37:30Z
file_id: '10008'
file_name: thesis_final_Hensel.zip
file_size: 15022154
relation: source_file
- access_level: open_access
checksum: 1a609937aa5275452822f45f2da17f07
content_type: application/pdf
creator: shensel
date_created: 2021-09-13T14:18:56Z
date_updated: 2021-09-14T09:52:47Z
file_id: '10014'
file_name: thesis_final_Hensel.pdf
file_size: 6583638
relation: main_file
file_date_updated: 2021-09-15T14:37:30Z
has_accepted_license: '1'
language:
- iso: eng
month: '09'
oa: 1
oa_version: Published Version
page: '300'
project:
- _id: 2564DBCA-B435-11E9-9278-68D0E5697425
call_identifier: H2020
grant_number: '665385'
name: International IST Doctoral Program
- _id: 0aa76401-070f-11eb-9043-b5bb049fa26d
call_identifier: H2020
grant_number: '948819'
name: Bridging Scales in Random Materials
publication_identifier:
issn:
- 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
related_material:
record:
- id: '10012'
relation: part_of_dissertation
status: public
- id: '10013'
relation: part_of_dissertation
status: public
- id: '7489'
relation: part_of_dissertation
status: public
status: public
supervisor:
- first_name: Julian L
full_name: Fischer, Julian L
id: 2C12A0B0-F248-11E8-B48F-1D18A9856A87
last_name: Fischer
orcid: 0000-0002-0479-558X
title: 'Curvature driven interface evolution: Uniqueness properties of weak solution
concepts'
type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2021'
...