---
_id: '6793'
abstract:
- lang: eng
text: The Regge symmetry is a set of remarkable relations between two tetrahedra
whose edge lengths are related in a simple fashion. It was first discovered as
a consequence of an asymptotic formula in mathematical physics. Here, we give
a simple geometric proof of Regge symmetries in Euclidean, spherical, and hyperbolic
geometry.
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Arseniy
full_name: Akopyan, Arseniy
id: 430D2C90-F248-11E8-B48F-1D18A9856A87
last_name: Akopyan
orcid: 0000-0002-2548-617X
- first_name: Ivan
full_name: Izmestiev, Ivan
last_name: Izmestiev
citation:
ama: Akopyan A, Izmestiev I. The Regge symmetry, confocal conics, and the Schläfli
formula. Bulletin of the London Mathematical Society. 2019;51(5):765-775.
doi:10.1112/blms.12276
apa: Akopyan, A., & Izmestiev, I. (2019). The Regge symmetry, confocal conics,
and the Schläfli formula. Bulletin of the London Mathematical Society.
London Mathematical Society. https://doi.org/10.1112/blms.12276
chicago: Akopyan, Arseniy, and Ivan Izmestiev. “The Regge Symmetry, Confocal Conics,
and the Schläfli Formula.” Bulletin of the London Mathematical Society.
London Mathematical Society, 2019. https://doi.org/10.1112/blms.12276.
ieee: A. Akopyan and I. Izmestiev, “The Regge symmetry, confocal conics, and the
Schläfli formula,” Bulletin of the London Mathematical Society, vol. 51,
no. 5. London Mathematical Society, pp. 765–775, 2019.
ista: Akopyan A, Izmestiev I. 2019. The Regge symmetry, confocal conics, and the
Schläfli formula. Bulletin of the London Mathematical Society. 51(5), 765–775.
mla: Akopyan, Arseniy, and Ivan Izmestiev. “The Regge Symmetry, Confocal Conics,
and the Schläfli Formula.” Bulletin of the London Mathematical Society,
vol. 51, no. 5, London Mathematical Society, 2019, pp. 765–75, doi:10.1112/blms.12276.
short: A. Akopyan, I. Izmestiev, Bulletin of the London Mathematical Society 51
(2019) 765–775.
date_created: 2019-08-11T21:59:23Z
date_published: 2019-10-01T00:00:00Z
date_updated: 2025-07-10T11:53:52Z
day: '01'
department:
- _id: HeEd
doi: 10.1112/blms.12276
ec_funded: 1
external_id:
arxiv:
- '1903.04929'
isi:
- '000478560200001'
intvolume: ' 51'
isi: 1
issue: '5'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/1903.04929
month: '10'
oa: 1
oa_version: Preprint
page: 765-775
project:
- _id: 266A2E9E-B435-11E9-9278-68D0E5697425
call_identifier: H2020
grant_number: '788183'
name: Alpha Shape Theory Extended
publication: Bulletin of the London Mathematical Society
publication_identifier:
eissn:
- 1469-2120
issn:
- 0024-6093
publication_status: published
publisher: London Mathematical Society
quality_controlled: '1'
scopus_import: '1'
status: public
title: The Regge symmetry, confocal conics, and the Schläfli formula
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 51
year: '2019'
...
---
_id: '6795'
abstract:
- lang: eng
text: The green‐beard effect is one proposed mechanism predicted to underpin the
evolu‐tion of altruistic behavior. It relies on the recognition and the selective
help of altruists to each other in order to promote and sustain altruistic behavior.
However, this mechanism has often been dismissed as unlikely or uncommon, as it
is assumed that both the signaling trait and altruistic trait need to be encoded
by the same gene or through tightly linked genes. Here, we use models of indirect
genetic effects (IGEs) to find the minimum correlation between the signaling and
altruistic trait required for the evolution of the latter. We show that this correlation
threshold depends on the strength of the interaction (influence of the green beard
on the expression of the altruistic trait), as well as the costs and benefits
of the altruistic behavior. We further show that this correlation does not necessarily
have to be high and support our analytical results by simulations.
article_processing_charge: No
article_type: original
author:
- first_name: Barbora
full_name: Trubenova, Barbora
id: 42302D54-F248-11E8-B48F-1D18A9856A87
last_name: Trubenova
orcid: 0000-0002-6873-2967
- first_name: Reinmar
full_name: Hager, Reinmar
last_name: Hager
citation:
ama: Trubenova B, Hager R. Green beards in the light of indirect genetic effects.
Ecology and Evolution. 2019;9(17):9597-9608. doi:10.1002/ece3.5484
apa: Trubenova, B., & Hager, R. (2019). Green beards in the light of indirect
genetic effects. Ecology and Evolution. Wiley. https://doi.org/10.1002/ece3.5484
chicago: Trubenova, Barbora, and Reinmar Hager. “Green Beards in the Light of Indirect
Genetic Effects.” Ecology and Evolution. Wiley, 2019. https://doi.org/10.1002/ece3.5484.
ieee: B. Trubenova and R. Hager, “Green beards in the light of indirect genetic
effects,” Ecology and Evolution, vol. 9, no. 17. Wiley, pp. 9597–9608,
2019.
ista: Trubenova B, Hager R. 2019. Green beards in the light of indirect genetic
effects. Ecology and Evolution. 9(17), 9597–9608.
mla: Trubenova, Barbora, and Reinmar Hager. “Green Beards in the Light of Indirect
Genetic Effects.” Ecology and Evolution, vol. 9, no. 17, Wiley, 2019, pp.
9597–608, doi:10.1002/ece3.5484.
short: B. Trubenova, R. Hager, Ecology and Evolution 9 (2019) 9597–9608.
date_created: 2019-08-11T21:59:24Z
date_published: 2019-09-01T00:00:00Z
date_updated: 2026-04-03T09:50:31Z
day: '01'
ddc:
- '576'
department:
- _id: NiBa
doi: 10.1002/ece3.5484
ec_funded: 1
external_id:
isi:
- '000479973400001'
file:
- access_level: open_access
checksum: adcb70af4901977d95b8747eeee01bd7
content_type: application/pdf
creator: dernst
date_created: 2019-08-12T07:30:30Z
date_updated: 2020-07-14T12:47:40Z
file_id: '6799'
file_name: 2019_EcologyEvolution_Trubenova.pdf
file_size: 2839636
relation: main_file
file_date_updated: 2020-07-14T12:47:40Z
has_accepted_license: '1'
intvolume: ' 9'
isi: 1
issue: '17'
language:
- iso: eng
month: '09'
oa: 1
oa_version: Published Version
page: 9597-9608
project:
- _id: 25AEDD42-B435-11E9-9278-68D0E5697425
call_identifier: H2020
grant_number: '704172'
name: Rate of Adaptation in Changing Environment
publication: Ecology and Evolution
publication_identifier:
eissn:
- 2045-7758
publication_status: published
publisher: Wiley
quality_controlled: '1'
scopus_import: '1'
status: public
title: Green beards in the light of indirect genetic effects
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: 9
year: '2019'
...
---
_id: '6818'
abstract:
- lang: eng
text: Indigoidine is a blue natural pigment, which can be efficiently synthetized
in E. coli. In addition to its antioxidant and antimicrobial activities indigoidine
due to its stability and deep blue color can find an application as an industrial,
environmentally friendly dye. Moreover, similarly to its counterpart regular indigo
dye, due to its molecular structure, indigoidine is an organic semiconductor.
Fully conjugated aromatic moiety and intermolecular hydrogen bonding of indigoidine
result in an unusually narrow bandgap for such a small molecule. This, in its
turn, result is tight molecular packing in the solid state and opens a path for
a wide range of application in organic and bio-electronics, such as electrochemical
and field effect transistors, organic solar cells, light and bio-sensors etc.
article_number: '107768'
article_processing_charge: No
article_type: original
author:
- first_name: Cigdem
full_name: Yumusak, Cigdem
last_name: Yumusak
- first_name: Anna Jancik
full_name: Prochazkova, Anna Jancik
last_name: Prochazkova
- first_name: Dogukan H
full_name: Apaydin, Dogukan H
id: 2FF891BC-F248-11E8-B48F-1D18A9856A87
last_name: Apaydin
orcid: 0000-0002-1075-8857
- first_name: Hathaichanok
full_name: Seelajaroen, Hathaichanok
last_name: Seelajaroen
- first_name: Niyazi Serdar
full_name: Sariciftci, Niyazi Serdar
last_name: Sariciftci
- first_name: Martin
full_name: Weiter, Martin
last_name: Weiter
- first_name: Jozef
full_name: Krajcovic, Jozef
last_name: Krajcovic
- first_name: Yong
full_name: Qin, Yong
last_name: Qin
- first_name: Wei
full_name: Zhang, Wei
last_name: Zhang
- first_name: Jixun
full_name: Zhan, Jixun
last_name: Zhan
- first_name: Alexander
full_name: Kovalenko, Alexander
last_name: Kovalenko
citation:
ama: Yumusak C, Prochazkova AJ, Apaydin DH, et al. Indigoidine - Biosynthesized
organic semiconductor. Dyes and Pigments. 2019;171. doi:10.1016/j.dyepig.2019.107768
apa: Yumusak, C., Prochazkova, A. J., Apaydin, D. H., Seelajaroen, H., Sariciftci,
N. S., Weiter, M., … Kovalenko, A. (2019). Indigoidine - Biosynthesized organic
semiconductor. Dyes and Pigments. Elsevier. https://doi.org/10.1016/j.dyepig.2019.107768
chicago: Yumusak, Cigdem, Anna Jancik Prochazkova, Dogukan H Apaydin, Hathaichanok
Seelajaroen, Niyazi Serdar Sariciftci, Martin Weiter, Jozef Krajcovic, et al.
“Indigoidine - Biosynthesized Organic Semiconductor.” Dyes and Pigments.
Elsevier, 2019. https://doi.org/10.1016/j.dyepig.2019.107768.
ieee: C. Yumusak et al., “Indigoidine - Biosynthesized organic semiconductor,”
Dyes and Pigments, vol. 171. Elsevier, 2019.
ista: Yumusak C, Prochazkova AJ, Apaydin DH, Seelajaroen H, Sariciftci NS, Weiter
M, Krajcovic J, Qin Y, Zhang W, Zhan J, Kovalenko A. 2019. Indigoidine - Biosynthesized
organic semiconductor. Dyes and Pigments. 171, 107768.
mla: Yumusak, Cigdem, et al. “Indigoidine - Biosynthesized Organic Semiconductor.”
Dyes and Pigments, vol. 171, 107768, Elsevier, 2019, doi:10.1016/j.dyepig.2019.107768.
short: C. Yumusak, A.J. Prochazkova, D.H. Apaydin, H. Seelajaroen, N.S. Sariciftci,
M. Weiter, J. Krajcovic, Y. Qin, W. Zhang, J. Zhan, A. Kovalenko, Dyes and Pigments
171 (2019).
date_created: 2019-08-18T22:00:39Z
date_published: 2019-12-01T00:00:00Z
date_updated: 2023-08-29T07:11:09Z
day: '01'
department:
- _id: MaIb
doi: 10.1016/j.dyepig.2019.107768
external_id:
isi:
- '000484870700099'
intvolume: ' 171'
isi: 1
language:
- iso: eng
month: '12'
oa_version: None
publication: Dyes and Pigments
publication_identifier:
issn:
- 0143-7208
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: Indigoidine - Biosynthesized organic semiconductor
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 171
year: '2019'
...
---
_id: '6819'
abstract:
- lang: eng
text: Glyphosate (N-phosphonomethyl glycine) and its commercial herbicide formulations
have been shown to exert toxicity via various mechanisms. It has been asserted
that glyphosate substitutes for glycine in polypeptide chains leading to protein
misfolding and toxicity. However, as no direct evidence exists for glycine to
glyphosate substitution in proteins, including in mammalian organisms, we tested
this claim by conducting a proteomics analysis of MDA-MB-231 human breast cancer
cells grown in the presence of 100 mg/L glyphosate for 6 days. Protein extracts
from three treated and three untreated cell cultures were analysed as one TMT-6plex
labelled sample, to highlight a specific pattern (+/+/+/−/−/−) of reporter intensities
for peptides bearing true glyphosate treatment induced-post translational modifications
as well as allowing an investigation of the total proteome.
article_number: '494'
article_processing_charge: No
author:
- first_name: Michael N.
full_name: Antoniou, Michael N.
last_name: Antoniou
- first_name: Armel
full_name: Nicolas, Armel
id: 2A103192-F248-11E8-B48F-1D18A9856A87
last_name: Nicolas
- first_name: Robin
full_name: Mesnage, Robin
last_name: Mesnage
- first_name: Martina
full_name: Biserni, Martina
last_name: Biserni
- first_name: Francesco V.
full_name: Rao, Francesco V.
last_name: Rao
- first_name: Cristina Vazquez
full_name: Martin, Cristina Vazquez
last_name: Martin
citation:
ama: Antoniou MN, Nicolas A, Mesnage R, Biserni M, Rao FV, Martin CV. Glyphosate
does not substitute for glycine in proteins of actively dividing mammalian cells.
BMC Research Notes. 2019;12. doi:10.1186/s13104-019-4534-3
apa: Antoniou, M. N., Nicolas, A., Mesnage, R., Biserni, M., Rao, F. V., & Martin,
C. V. (2019). Glyphosate does not substitute for glycine in proteins of actively
dividing mammalian cells. BMC Research Notes. BioMed Central. https://doi.org/10.1186/s13104-019-4534-3
chicago: Antoniou, Michael N., Armel Nicolas, Robin Mesnage, Martina Biserni, Francesco
V. Rao, and Cristina Vazquez Martin. “Glyphosate Does Not Substitute for Glycine
in Proteins of Actively Dividing Mammalian Cells.” BMC Research Notes.
BioMed Central, 2019. https://doi.org/10.1186/s13104-019-4534-3.
ieee: M. N. Antoniou, A. Nicolas, R. Mesnage, M. Biserni, F. V. Rao, and C. V. Martin,
“Glyphosate does not substitute for glycine in proteins of actively dividing mammalian
cells,” BMC Research Notes, vol. 12. BioMed Central, 2019.
ista: Antoniou MN, Nicolas A, Mesnage R, Biserni M, Rao FV, Martin CV. 2019. Glyphosate
does not substitute for glycine in proteins of actively dividing mammalian cells.
BMC Research Notes. 12, 494.
mla: Antoniou, Michael N., et al. “Glyphosate Does Not Substitute for Glycine in
Proteins of Actively Dividing Mammalian Cells.” BMC Research Notes, vol.
12, 494, BioMed Central, 2019, doi:10.1186/s13104-019-4534-3.
short: M.N. Antoniou, A. Nicolas, R. Mesnage, M. Biserni, F.V. Rao, C.V. Martin,
BMC Research Notes 12 (2019).
date_created: 2019-08-18T22:00:39Z
date_published: 2019-08-08T00:00:00Z
date_updated: 2023-02-23T14:08:14Z
day: '08'
ddc:
- '570'
department:
- _id: LifeSc
doi: 10.1186/s13104-019-4534-3
external_id:
pmid:
- '31395095'
file:
- access_level: open_access
checksum: 4a2bb7994b7f2c432bf44f5127ea3102
content_type: application/pdf
creator: dernst
date_created: 2019-08-23T11:10:35Z
date_updated: 2020-07-14T12:47:40Z
file_id: '6829'
file_name: 2019_BMC_Antoniou.pdf
file_size: 1177482
relation: main_file
file_date_updated: 2020-07-14T12:47:40Z
has_accepted_license: '1'
intvolume: ' 12'
language:
- iso: eng
month: '08'
oa: 1
oa_version: Published Version
pmid: 1
publication: BMC Research Notes
publication_identifier:
eissn:
- 1756-0500
publication_status: published
publisher: BioMed Central
quality_controlled: '1'
related_material:
record:
- id: '9784'
relation: research_data
status: public
scopus_import: 1
status: public
title: Glyphosate does not substitute for glycine in proteins of actively dividing
mammalian cells
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: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 12
year: '2019'
...
---
_id: '6821'
abstract:
- lang: eng
text: To determine the visual sensitivities of an organism of interest, quantitative
reverse transcription–polymerase chain reaction (qRT–PCR) is often used to quantify
expression of the light‐sensitive opsins in the retina. While qRT–PCR is an affordable,
high‐throughput method for measuring expression, it comes with inherent normalization
issues that affect the interpretation of results, especially as opsin expression
can vary greatly based on developmental stage, light environment or diurnal cycles.
We tested for diurnal cycles of opsin expression over a period of 24 hr at 1‐hr
increments and examined how normalization affects a data set with fluctuating
expression levels using qRT–PCR and transcriptome data from the retinae of the
cichlid Pelmatolapia mariae. We compared five methods of normalizing opsin expression
relative to (a) the average of three stably expressed housekeeping genes (Ube2z,
EF1‐α and β‐actin), (b) total RNA concentration, (c) GNAT2, (the cone‐specific
subunit of transducin), (d) total opsin expression and (e) only opsins expressed
in the same cone type. Normalizing by proportion of cone type produced the least
variation and would be best for removing time‐of‐day variation. In contrast, normalizing
by housekeeping genes produced the highest daily variation in expression and demonstrated
that the peak of cone opsin expression was in the late afternoon. A weighted correlation
network analysis showed that the expression of different cone opsins follows a
very similar daily cycle. With the knowledge of how these normalization methods
affect opsin expression data, we make recommendations for designing sampling approaches
and quantification methods based upon the scientific question being examined.
article_processing_charge: No
article_type: original
author:
- first_name: Miranda R.
full_name: Yourick, Miranda R.
last_name: Yourick
- first_name: Benjamin A.
full_name: Sandkam, Benjamin A.
last_name: Sandkam
- first_name: William J
full_name: Gammerdinger, William J
id: 3A7E01BC-F248-11E8-B48F-1D18A9856A87
last_name: Gammerdinger
orcid: 0000-0001-9638-1220
- first_name: Daniel
full_name: Escobar-Camacho, Daniel
last_name: Escobar-Camacho
- first_name: Sri Pratima
full_name: Nandamuri, Sri Pratima
last_name: Nandamuri
- first_name: Frances E.
full_name: Clark, Frances E.
last_name: Clark
- first_name: Brendan
full_name: Joyce, Brendan
last_name: Joyce
- first_name: Matthew A.
full_name: Conte, Matthew A.
last_name: Conte
- first_name: Thomas D.
full_name: Kocher, Thomas D.
last_name: Kocher
- first_name: Karen L.
full_name: Carleton, Karen L.
last_name: Carleton
citation:
ama: Yourick MR, Sandkam BA, Gammerdinger WJ, et al. Diurnal variation in opsin
expression and common housekeeping genes necessitates comprehensive normalization
methods for quantitative real-time PCR analyses. Molecular Ecology Resources.
2019;19(6):1447-1460. doi:10.1111/1755-0998.13062
apa: Yourick, M. R., Sandkam, B. A., Gammerdinger, W. J., Escobar-Camacho, D., Nandamuri,
S. P., Clark, F. E., … Carleton, K. L. (2019). Diurnal variation in opsin expression
and common housekeeping genes necessitates comprehensive normalization methods
for quantitative real-time PCR analyses. Molecular Ecology Resources. Wiley.
https://doi.org/10.1111/1755-0998.13062
chicago: Yourick, Miranda R., Benjamin A. Sandkam, William J Gammerdinger, Daniel
Escobar-Camacho, Sri Pratima Nandamuri, Frances E. Clark, Brendan Joyce, Matthew
A. Conte, Thomas D. Kocher, and Karen L. Carleton. “Diurnal Variation in Opsin
Expression and Common Housekeeping Genes Necessitates Comprehensive Normalization
Methods for Quantitative Real-Time PCR Analyses.” Molecular Ecology Resources.
Wiley, 2019. https://doi.org/10.1111/1755-0998.13062.
ieee: M. R. Yourick et al., “Diurnal variation in opsin expression and common
housekeeping genes necessitates comprehensive normalization methods for quantitative
real-time PCR analyses,” Molecular Ecology Resources, vol. 19, no. 6. Wiley,
pp. 1447–1460, 2019.
ista: Yourick MR, Sandkam BA, Gammerdinger WJ, Escobar-Camacho D, Nandamuri SP,
Clark FE, Joyce B, Conte MA, Kocher TD, Carleton KL. 2019. Diurnal variation in
opsin expression and common housekeeping genes necessitates comprehensive normalization
methods for quantitative real-time PCR analyses. Molecular Ecology Resources.
19(6), 1447–1460.
mla: Yourick, Miranda R., et al. “Diurnal Variation in Opsin Expression and Common
Housekeeping Genes Necessitates Comprehensive Normalization Methods for Quantitative
Real-Time PCR Analyses.” Molecular Ecology Resources, vol. 19, no. 6, Wiley,
2019, pp. 1447–60, doi:10.1111/1755-0998.13062.
short: M.R. Yourick, B.A. Sandkam, W.J. Gammerdinger, D. Escobar-Camacho, S.P. Nandamuri,
F.E. Clark, B. Joyce, M.A. Conte, T.D. Kocher, K.L. Carleton, Molecular Ecology
Resources 19 (2019) 1447–1460.
date_created: 2019-08-18T22:00:41Z
date_published: 2019-11-01T00:00:00Z
date_updated: 2023-08-29T07:10:44Z
day: '01'
department:
- _id: BeVi
doi: 10.1111/1755-0998.13062
external_id:
isi:
- '000480196800001'
pmid:
- '31325910'
intvolume: ' 19'
isi: 1
issue: '6'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6995727
month: '11'
oa: 1
oa_version: Submitted Version
page: 1447-1460
pmid: 1
publication: Molecular Ecology Resources
publication_identifier:
eissn:
- 1755-0998
publication_status: published
publisher: Wiley
quality_controlled: '1'
scopus_import: '1'
status: public
title: Diurnal variation in opsin expression and common housekeeping genes necessitates
comprehensive normalization methods for quantitative real-time PCR analyses
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 19
year: '2019'
...
---
_id: '6824'
abstract:
- lang: eng
text: Platelets are small anucleate cellular fragments that are released by megakaryocytes
and safeguard vascular integrity through a process termed ‘haemostasis’. However,
platelets have important roles beyond haemostasis as they contribute to the initiation
and coordination of intravascular immune responses. They continuously monitor
blood vessel integrity and tightly coordinate vascular trafficking and functions
of multiple cell types. In this way platelets act as ‘patrolling officers of the
vascular highway’ that help to establish effective immune responses to infections
and cancer. Here we discuss the distinct biological features of platelets that
allow them to shape immune responses to pathogens and tumour cells, highlighting
the parallels between these responses.
article_processing_charge: No
article_type: original
author:
- 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: Steffen
full_name: Massberg, Steffen
last_name: Massberg
citation:
ama: 'Gärtner FR, Massberg S. Patrolling the vascular borders: Platelets in immunity
to infection and cancer. Nature Reviews Immunology. 2019;19(12):747–760.
doi:10.1038/s41577-019-0202-z'
apa: 'Gärtner, F. R., & Massberg, S. (2019). Patrolling the vascular borders:
Platelets in immunity to infection and cancer. Nature Reviews Immunology.
Springer Nature. https://doi.org/10.1038/s41577-019-0202-z'
chicago: 'Gärtner, Florian R, and Steffen Massberg. “Patrolling the Vascular Borders:
Platelets in Immunity to Infection and Cancer.” Nature Reviews Immunology.
Springer Nature, 2019. https://doi.org/10.1038/s41577-019-0202-z.'
ieee: 'F. R. Gärtner and S. Massberg, “Patrolling the vascular borders: Platelets
in immunity to infection and cancer,” Nature Reviews Immunology, vol. 19,
no. 12. Springer Nature, pp. 747–760, 2019.'
ista: 'Gärtner FR, Massberg S. 2019. Patrolling the vascular borders: Platelets
in immunity to infection and cancer. Nature Reviews Immunology. 19(12), 747–760.'
mla: 'Gärtner, Florian R., and Steffen Massberg. “Patrolling the Vascular Borders:
Platelets in Immunity to Infection and Cancer.” Nature Reviews Immunology,
vol. 19, no. 12, Springer Nature, 2019, pp. 747–760, doi:10.1038/s41577-019-0202-z.'
short: F.R. Gärtner, S. Massberg, Nature Reviews Immunology 19 (2019) 747–760.
date_created: 2019-08-20T17:24:32Z
date_published: 2019-12-01T00:00:00Z
date_updated: 2025-04-14T07:43:17Z
day: '01'
department:
- _id: MiSi
doi: 10.1038/s41577-019-0202-z
ec_funded: 1
external_id:
isi:
- '000499090600011'
pmid:
- '31409920'
intvolume: ' 19'
isi: 1
issue: '12'
language:
- iso: eng
month: '12'
oa_version: None
page: 747–760
pmid: 1
project:
- _id: 260AA4E2-B435-11E9-9278-68D0E5697425
call_identifier: H2020
grant_number: '747687'
name: Mechanical Adaptation of Lamellipodial Actin Networks in Migrating Cells
publication: Nature Reviews Immunology
publication_identifier:
eissn:
- 1474-1741
issn:
- 1474-1733
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'Patrolling the vascular borders: Platelets in immunity to infection and cancer'
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 19
year: '2019'
...
---
_id: '6828'
abstract:
- lang: eng
text: In this paper we construct a family of exact functors from the category of
Whittaker modules of the simple complex Lie algebra of type to the category of
finite-dimensional modules of the graded affine Hecke algebra of type . Using
results of Backelin [2] and of Arakawa-Suzuki [1], we prove that these functors
map standard modules to standard modules (or zero) and simple modules to simple
modules (or zero). Moreover, we show that each simple module of the graded affine
Hecke algebra appears as the image of a simple Whittaker module. Since the Whittaker
category contains the BGG category as a full subcategory, our results generalize
results of Arakawa-Suzuki [1], which in turn generalize Schur-Weyl duality between
finite-dimensional representations of and representations of the symmetric group
.
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Adam
full_name: Brown, Adam
id: 70B7FDF6-608D-11E9-9333-8535E6697425
last_name: Brown
citation:
ama: Brown A. Arakawa-Suzuki functors for Whittaker modules. Journal of Algebra.
2019;538:261-289. doi:10.1016/j.jalgebra.2019.07.027
apa: Brown, A. (2019). Arakawa-Suzuki functors for Whittaker modules. Journal
of Algebra. Elsevier. https://doi.org/10.1016/j.jalgebra.2019.07.027
chicago: Brown, Adam. “Arakawa-Suzuki Functors for Whittaker Modules.” Journal
of Algebra. Elsevier, 2019. https://doi.org/10.1016/j.jalgebra.2019.07.027.
ieee: A. Brown, “Arakawa-Suzuki functors for Whittaker modules,” Journal of Algebra,
vol. 538. Elsevier, pp. 261–289, 2019.
ista: Brown A. 2019. Arakawa-Suzuki functors for Whittaker modules. Journal of Algebra.
538, 261–289.
mla: Brown, Adam. “Arakawa-Suzuki Functors for Whittaker Modules.” Journal of
Algebra, vol. 538, Elsevier, 2019, pp. 261–89, doi:10.1016/j.jalgebra.2019.07.027.
short: A. Brown, Journal of Algebra 538 (2019) 261–289.
date_created: 2019-08-22T07:54:13Z
date_published: 2019-11-15T00:00:00Z
date_updated: 2023-08-29T07:11:47Z
day: '15'
department:
- _id: HeEd
doi: 10.1016/j.jalgebra.2019.07.027
external_id:
arxiv:
- '1805.04676'
isi:
- '000487176300011'
intvolume: ' 538'
isi: 1
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/1805.04676
month: '11'
oa: 1
oa_version: Preprint
page: 261-289
publication: Journal of Algebra
publication_identifier:
issn:
- 0021-8693
publication_status: published
publisher: Elsevier
quality_controlled: '1'
status: public
title: Arakawa-Suzuki functors for Whittaker modules
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 538
year: '2019'
...
---
_id: '6831'
abstract:
- lang: eng
text: "* Understanding the mechanisms causing phenotypic differences between females
and males has long fascinated evolutionary biologists. An extensive literature
exists on animal sexual dimorphism but less information is known about sex differences
in plants, particularly the extent of geographical variation in sexual dimorphism
and its life‐cycle dynamics.\r\n* Here, we investigated patterns of genetically
based sexual dimorphism in vegetative and reproductive traits of a wind‐pollinated
dioecious plant, Rumex hastatulus, across three life‐cycle stages using open‐pollinated
families from 30 populations spanning the geographic range and chromosomal variation
(XY and XY1Y2) of the species.\r\n* The direction and degree of sexual dimorphism
was highly variable among populations and life‐cycle stages. Sex‐specific differences
in reproductive function explained a significant amount of temporal change in
sexual dimorphism. For several traits, geographical variation in sexual dimorphism
was associated with bioclimatic parameters, likely due to the differential responses
of the sexes to climate. We found no systematic differences in sexual dimorphism
between chromosome races.\r\n* Sex‐specific trait differences in dioecious plants
largely result from a balance between sexual and natural selection on resource
allocation. Our results indicate that abiotic factors associated with geographical
context also play a role in modifying sexual dimorphism during the plant life‐cycle."
article_processing_charge: Yes (via OA deal)
article_type: original
author:
- first_name: Gemma
full_name: Puixeu Sala, Gemma
id: 33AB266C-F248-11E8-B48F-1D18A9856A87
last_name: Puixeu Sala
orcid: 0000-0001-8330-1754
- first_name: Melinda
full_name: Pickup, Melinda
id: 2C78037E-F248-11E8-B48F-1D18A9856A87
last_name: Pickup
orcid: 0000-0001-6118-0541
- first_name: David
full_name: Field, David
last_name: Field
orcid: 0000-0002-4014-8478
- first_name: Spencer C.H.
full_name: Barrett, Spencer C.H.
last_name: Barrett
citation:
ama: 'Puixeu Sala G, Pickup M, Field D, Barrett SCH. Variation in sexual dimorphism
in a wind-pollinated plant: The influence of geographical context and life-cycle
dynamics. New Phytologist. 2019;224(3):1108-1120. doi:10.1111/nph.16050'
apa: 'Puixeu Sala, G., Pickup, M., Field, D., & Barrett, S. C. H. (2019). Variation
in sexual dimorphism in a wind-pollinated plant: The influence of geographical
context and life-cycle dynamics. New Phytologist. Wiley. https://doi.org/10.1111/nph.16050'
chicago: 'Puixeu Sala, Gemma, Melinda Pickup, David Field, and Spencer C.H. Barrett.
“Variation in Sexual Dimorphism in a Wind-Pollinated Plant: The Influence of Geographical
Context and Life-Cycle Dynamics.” New Phytologist. Wiley, 2019. https://doi.org/10.1111/nph.16050.'
ieee: 'G. Puixeu Sala, M. Pickup, D. Field, and S. C. H. Barrett, “Variation in
sexual dimorphism in a wind-pollinated plant: The influence of geographical context
and life-cycle dynamics,” New Phytologist, vol. 224, no. 3. Wiley, pp.
1108–1120, 2019.'
ista: 'Puixeu Sala G, Pickup M, Field D, Barrett SCH. 2019. Variation in sexual
dimorphism in a wind-pollinated plant: The influence of geographical context and
life-cycle dynamics. New Phytologist. 224(3), 1108–1120.'
mla: 'Puixeu Sala, Gemma, et al. “Variation in Sexual Dimorphism in a Wind-Pollinated
Plant: The Influence of Geographical Context and Life-Cycle Dynamics.” New
Phytologist, vol. 224, no. 3, Wiley, 2019, pp. 1108–20, doi:10.1111/nph.16050.'
short: G. Puixeu Sala, M. Pickup, D. Field, S.C.H. Barrett, New Phytologist 224
(2019) 1108–1120.
corr_author: '1'
date_created: 2019-08-25T22:00:51Z
date_published: 2019-11-01T00:00:00Z
date_updated: 2026-04-07T13:25:33Z
day: '01'
ddc:
- '570'
department:
- _id: NiBa
- _id: BeVi
doi: 10.1111/nph.16050
ec_funded: 1
external_id:
isi:
- '000481376500001'
file:
- access_level: open_access
checksum: 6370e7567d96b7b562e77d8b89653f80
content_type: application/pdf
creator: apreinsp
date_created: 2019-08-27T12:44:54Z
date_updated: 2020-07-14T12:47:42Z
file_id: '6833'
file_name: 2019_NewPhytologist_Puixeu.pdf
file_size: 2314016
relation: main_file
file_date_updated: 2020-07-14T12:47:42Z
has_accepted_license: '1'
intvolume: ' 224'
isi: 1
issue: '3'
language:
- iso: eng
month: '11'
oa: 1
oa_version: Published Version
page: 1108-1120
project:
- _id: 2564DBCA-B435-11E9-9278-68D0E5697425
call_identifier: H2020
grant_number: '665385'
name: International IST Doctoral Program
publication: New Phytologist
publication_identifier:
eissn:
- 1469-8137
publication_status: published
publisher: Wiley
quality_controlled: '1'
related_material:
record:
- id: '9803'
relation: research_data
status: public
- id: '14058'
relation: dissertation_contains
status: public
scopus_import: '1'
status: public
title: 'Variation in sexual dimorphism in a wind-pollinated plant: The influence of
geographical context and life-cycle dynamics'
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: 224
year: '2019'
...
---
_id: '6832'
abstract:
- lang: eng
text: Steady-state turnover is a hallmark of epithelial tissues throughout adult
life. Intestinal epithelial turnover is marked by continuous cell migration, which
is assumed to be driven by mitotic pressure from the crypts. However, the balance
of forces in renewal remains ill-defined. Combining biophysical modeling and quantitative
three-dimensional tissue imaging with genetic and physical manipulations, we revealed
the existence of an actin-related protein 2/3 complex–dependent active migratory
force, which explains quantitatively the profiles of cell speed, density, and
tissue tension along the villi. Cells migrate collectively with minimal rearrangements
while displaying dual—apicobasal and front-back—polarity characterized by actin-rich
basal protrusions oriented in the direction of migration. We propose that active
migration is a critical component of gut epithelial turnover.
article_processing_charge: No
author:
- first_name: Denis
full_name: Krndija, Denis
last_name: Krndija
- first_name: Fatima El
full_name: Marjou, Fatima El
last_name: Marjou
- first_name: Boris
full_name: Guirao, Boris
last_name: Guirao
- first_name: Sophie
full_name: Richon, Sophie
last_name: Richon
- first_name: Olivier
full_name: Leroy, Olivier
last_name: Leroy
- first_name: Yohanns
full_name: Bellaiche, Yohanns
last_name: Bellaiche
- first_name: Edouard B
full_name: Hannezo, Edouard B
id: 3A9DB764-F248-11E8-B48F-1D18A9856A87
last_name: Hannezo
orcid: 0000-0001-6005-1561
- first_name: Danijela Matic
full_name: Vignjevic, Danijela Matic
last_name: Vignjevic
citation:
ama: Krndija D, Marjou FE, Guirao B, et al. Active cell migration is critical for
steady-state epithelial turnover in the gut. Science. 2019;365(6454):705-710.
doi:10.1126/science.aau3429
apa: Krndija, D., Marjou, F. E., Guirao, B., Richon, S., Leroy, O., Bellaiche, Y.,
… Vignjevic, D. M. (2019). Active cell migration is critical for steady-state
epithelial turnover in the gut. Science. American Association for the Advancement
of Science. https://doi.org/10.1126/science.aau3429
chicago: Krndija, Denis, Fatima El Marjou, Boris Guirao, Sophie Richon, Olivier
Leroy, Yohanns Bellaiche, Edouard B Hannezo, and Danijela Matic Vignjevic. “Active
Cell Migration Is Critical for Steady-State Epithelial Turnover in the Gut.” Science.
American Association for the Advancement of Science, 2019. https://doi.org/10.1126/science.aau3429.
ieee: D. Krndija et al., “Active cell migration is critical for steady-state
epithelial turnover in the gut,” Science, vol. 365, no. 6454. American
Association for the Advancement of Science, pp. 705–710, 2019.
ista: Krndija D, Marjou FE, Guirao B, Richon S, Leroy O, Bellaiche Y, Hannezo EB,
Vignjevic DM. 2019. Active cell migration is critical for steady-state epithelial
turnover in the gut. Science. 365(6454), 705–710.
mla: Krndija, Denis, et al. “Active Cell Migration Is Critical for Steady-State
Epithelial Turnover in the Gut.” Science, vol. 365, no. 6454, American
Association for the Advancement of Science, 2019, pp. 705–10, doi:10.1126/science.aau3429.
short: D. Krndija, F.E. Marjou, B. Guirao, S. Richon, O. Leroy, Y. Bellaiche, E.B.
Hannezo, D.M. Vignjevic, Science 365 (2019) 705–710.
date_created: 2019-08-25T22:00:51Z
date_published: 2019-08-16T00:00:00Z
date_updated: 2023-08-29T07:16:40Z
day: '16'
department:
- _id: EdHa
doi: 10.1126/science.aau3429
external_id:
isi:
- '000481688700050'
pmid:
- '31416964'
intvolume: ' 365'
isi: 1
issue: '6454'
language:
- iso: eng
month: '08'
oa_version: None
page: 705-710
pmid: 1
publication: Science
publication_status: published
publisher: American Association for the Advancement of Science
quality_controlled: '1'
scopus_import: '1'
status: public
title: Active cell migration is critical for steady-state epithelial turnover in the
gut
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 365
year: '2019'
...
---
_id: '6835'
abstract:
- lang: eng
text: We derive the Hasse principle and weak approximation for fibrations of certain
varieties in the spirit of work by Colliot-Thélène–Sansuc and Harpaz–Skorobogatov–Wittenberg.
Our varieties are defined through polynomials in many variables and part of our
work is devoted to establishing Schinzel's hypothesis for polynomials of this
kind. This last part is achieved by using arguments behind Birch's well-known
result regarding the Hasse principle for complete intersections with the notable
difference that we prove our result in 50% fewer variables than in the classical
Birch setting. We also study the problem of square-free values of an integer polynomial
with 66.6% fewer variables than in the Birch setting.
article_number: '102794'
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Kevin N
full_name: Destagnol, Kevin N
id: 44DDECBC-F248-11E8-B48F-1D18A9856A87
last_name: Destagnol
- first_name: Efthymios
full_name: Sofos, Efthymios
last_name: Sofos
citation:
ama: Destagnol KN, Sofos E. Rational points and prime values of polynomials in moderately
many variables. Bulletin des Sciences Mathematiques. 2019;156(11). doi:10.1016/j.bulsci.2019.102794
apa: Destagnol, K. N., & Sofos, E. (2019). Rational points and prime values
of polynomials in moderately many variables. Bulletin Des Sciences Mathematiques.
Elsevier. https://doi.org/10.1016/j.bulsci.2019.102794
chicago: Destagnol, Kevin N, and Efthymios Sofos. “Rational Points and Prime Values
of Polynomials in Moderately Many Variables.” Bulletin Des Sciences Mathematiques.
Elsevier, 2019. https://doi.org/10.1016/j.bulsci.2019.102794.
ieee: K. N. Destagnol and E. Sofos, “Rational points and prime values of polynomials
in moderately many variables,” Bulletin des Sciences Mathematiques, vol.
156, no. 11. Elsevier, 2019.
ista: Destagnol KN, Sofos E. 2019. Rational points and prime values of polynomials
in moderately many variables. Bulletin des Sciences Mathematiques. 156(11), 102794.
mla: Destagnol, Kevin N., and Efthymios Sofos. “Rational Points and Prime Values
of Polynomials in Moderately Many Variables.” Bulletin Des Sciences Mathematiques,
vol. 156, no. 11, 102794, Elsevier, 2019, doi:10.1016/j.bulsci.2019.102794.
short: K.N. Destagnol, E. Sofos, Bulletin Des Sciences Mathematiques 156 (2019).
date_created: 2019-09-01T22:00:55Z
date_published: 2019-11-01T00:00:00Z
date_updated: 2023-08-29T07:18:02Z
day: '01'
department:
- _id: TiBr
doi: 10.1016/j.bulsci.2019.102794
external_id:
arxiv:
- '1801.03082'
isi:
- '000496342100002'
intvolume: ' 156'
isi: 1
issue: '11'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/1801.03082
month: '11'
oa: 1
oa_version: Preprint
publication: Bulletin des Sciences Mathematiques
publication_identifier:
issn:
- 0007-4497
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: Rational points and prime values of polynomials in moderately many variables
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 156
year: '2019'
...
---
_id: '6836'
abstract:
- lang: eng
text: Direct reciprocity is a powerful mechanism for the evolution of cooperation
on the basis of repeated interactions1,2,3,4. It requires that interacting individuals
are sufficiently equal, such that everyone faces similar consequences when they
cooperate or defect. Yet inequality is ubiquitous among humans5,6 and is generally
considered to undermine cooperation and welfare7,8,9,10. Most previous models
of reciprocity do not include inequality11,12,13,14,15. These models assume that
individuals are the same in all relevant aspects. Here we introduce a general
framework to study direct reciprocity among unequal individuals. Our model allows
for multiple sources of inequality. Subjects can differ in their endowments, their
productivities and in how much they benefit from public goods. We find that extreme
inequality prevents cooperation. But if subjects differ in productivity, some
endowment inequality can be necessary for cooperation to prevail. Our mathematical
predictions are supported by a behavioural experiment in which we vary the endowments
and productivities of the subjects. We observe that overall welfare is maximized
when the two sources of heterogeneity are aligned, such that more productive individuals
receive higher endowments. By contrast, when endowments and productivities are
misaligned, cooperation quickly breaks down. Our findings have implications for
policy-makers concerned with equity, efficiency and the provisioning of public
goods.
article_processing_charge: No
article_type: letter_note
author:
- first_name: Oliver P.
full_name: Hauser, Oliver P.
last_name: Hauser
- first_name: Christian
full_name: Hilbe, Christian
id: 2FDF8F3C-F248-11E8-B48F-1D18A9856A87
last_name: Hilbe
orcid: 0000-0001-5116-955X
- first_name: Krishnendu
full_name: Chatterjee, Krishnendu
id: 2E5DCA20-F248-11E8-B48F-1D18A9856A87
last_name: Chatterjee
orcid: 0000-0002-4561-241X
- first_name: Martin A.
full_name: Nowak, Martin A.
last_name: Nowak
citation:
ama: Hauser OP, Hilbe C, Chatterjee K, Nowak MA. Social dilemmas among unequals.
Nature. 2019;572(7770):524-527. doi:10.1038/s41586-019-1488-5
apa: Hauser, O. P., Hilbe, C., Chatterjee, K., & Nowak, M. A. (2019). Social
dilemmas among unequals. Nature. Springer Nature. https://doi.org/10.1038/s41586-019-1488-5
chicago: Hauser, Oliver P., Christian Hilbe, Krishnendu Chatterjee, and Martin A.
Nowak. “Social Dilemmas among Unequals.” Nature. Springer Nature, 2019.
https://doi.org/10.1038/s41586-019-1488-5.
ieee: O. P. Hauser, C. Hilbe, K. Chatterjee, and M. A. Nowak, “Social dilemmas among
unequals,” Nature, vol. 572, no. 7770. Springer Nature, pp. 524–527, 2019.
ista: Hauser OP, Hilbe C, Chatterjee K, Nowak MA. 2019. Social dilemmas among unequals.
Nature. 572(7770), 524–527.
mla: Hauser, Oliver P., et al. “Social Dilemmas among Unequals.” Nature,
vol. 572, no. 7770, Springer Nature, 2019, pp. 524–27, doi:10.1038/s41586-019-1488-5.
short: O.P. Hauser, C. Hilbe, K. Chatterjee, M.A. Nowak, Nature 572 (2019) 524–527.
date_created: 2019-09-01T22:00:56Z
date_published: 2019-08-22T00:00:00Z
date_updated: 2025-07-10T11:53:55Z
day: '22'
ddc:
- '000'
department:
- _id: KrCh
doi: 10.1038/s41586-019-1488-5
ec_funded: 1
external_id:
isi:
- '000482219600045'
file:
- access_level: open_access
checksum: a6e0e3168bf62de624e7772cdfaeb26f
content_type: application/pdf
creator: dernst
date_created: 2020-05-14T10:00:32Z
date_updated: 2020-07-14T12:47:42Z
file_id: '7828'
file_name: 2019_Nature_Hauser.pdf
file_size: 18577756
relation: main_file
file_date_updated: 2020-07-14T12:47:42Z
has_accepted_license: '1'
intvolume: ' 572'
isi: 1
issue: '7770'
language:
- iso: eng
month: '08'
oa: 1
oa_version: Submitted Version
page: 524-527
project:
- _id: 2581B60A-B435-11E9-9278-68D0E5697425
call_identifier: FP7
grant_number: '279307'
name: 'Quantitative Graph Games: Theory and Applications'
- _id: 25832EC2-B435-11E9-9278-68D0E5697425
call_identifier: FWF
grant_number: S 11407_N23
name: Rigorous Systems Engineering
- _id: 25681D80-B435-11E9-9278-68D0E5697425
call_identifier: FP7
grant_number: '291734'
name: International IST Postdoc Fellowship Programme
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/too-much-inequality-impedes-support-for-public-goods-according-to-research-published-in-nature/
scopus_import: '1'
status: public
title: Social dilemmas among unequals
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 572
year: '2019'
...
---
_id: '6837'
abstract:
- lang: eng
text: Migrasomes are a recently discovered type of extracellular vesicles that are
characteristically generated along retraction fibers in migrating cells. Two studies
now show how migrasomes are formed and how they function in the physiologically
relevant context of the developing zebrafish embryo.
article_processing_charge: No
author:
- first_name: Ste
full_name: Tavano, Ste
id: 2F162F0C-F248-11E8-B48F-1D18A9856A87
last_name: Tavano
orcid: 0000-0001-9970-7804
- 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: Tavano S, Heisenberg C-PJ. Migrasomes take center stage. Nature Cell Biology.
2019;21(8):918-920. doi:10.1038/s41556-019-0369-3
apa: Tavano, S., & Heisenberg, C.-P. J. (2019). Migrasomes take center stage.
Nature Cell Biology. Springer Nature. https://doi.org/10.1038/s41556-019-0369-3
chicago: Tavano, Ste, and Carl-Philipp J Heisenberg. “Migrasomes Take Center Stage.”
Nature Cell Biology. Springer Nature, 2019. https://doi.org/10.1038/s41556-019-0369-3.
ieee: S. Tavano and C.-P. J. Heisenberg, “Migrasomes take center stage,” Nature
Cell Biology, vol. 21, no. 8. Springer Nature, pp. 918–920, 2019.
ista: Tavano S, Heisenberg C-PJ. 2019. Migrasomes take center stage. Nature Cell
Biology. 21(8), 918–920.
mla: Tavano, Ste, and Carl-Philipp J. Heisenberg. “Migrasomes Take Center Stage.”
Nature Cell Biology, vol. 21, no. 8, Springer Nature, 2019, pp. 918–20,
doi:10.1038/s41556-019-0369-3.
short: S. Tavano, C.-P.J. Heisenberg, Nature Cell Biology 21 (2019) 918–920.
date_created: 2019-09-01T22:00:57Z
date_published: 2019-08-01T00:00:00Z
date_updated: 2023-08-29T07:42:20Z
day: '01'
department:
- _id: CaHe
doi: 10.1038/s41556-019-0369-3
external_id:
isi:
- '000478029000003'
pmid:
- '31371826'
intvolume: ' 21'
isi: 1
issue: '8'
language:
- iso: eng
month: '08'
oa_version: None
page: 918-920
pmid: 1
publication: Nature Cell Biology
publication_identifier:
eissn:
- 1476-4679
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: Migrasomes take center stage
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 21
year: '2019'
...
---
_id: '6840'
abstract:
- lang: eng
text: "We discuss thermodynamic properties of harmonically trapped\r\nimperfect
quantum gases. The spatial inhomogeneity of these systems imposes\r\na redefinition
of the mean-field interparticle potential energy as compared\r\nto the homogeneous
case. In our approach, it takes the form a\r\n2N2 ωd, where\r\nN is the number
of particles, ω—the harmonic trap frequency, d—system’s\r\ndimensionality, and
a is a parameter characterizing the interparticle interaction.\r\nWe provide arguments
that this model corresponds to the limiting case of\r\na long-ranged interparticle
potential of vanishingly small amplitude. This\r\nconclusion is drawn from a computation
similar to the well-known Kac scaling\r\nprocedure, which is presented here in
a form adapted to the case of an isotropic\r\nharmonic trap. We show that within
the model, the imperfect gas of trapped\r\nrepulsive bosons undergoes the Bose–Einstein
condensation provided d > 1.\r\nThe main result of our analysis is that in d =
1 the gas of attractive imperfect\r\nfermions with a = −aF < 0 is thermodynamically
equivalent to the gas of\r\nrepulsive bosons with a = aB > 0 provided the parameters
aF and aB fulfill\r\nthe relation aB + aF = \x1F. This result supplements similar
recent conclusion\r\nabout thermodynamic equivalence of two-dimensional (2D) uniform
imperfect\r\nrepulsive Bose and attractive Fermi gases."
article_number: '063101'
article_processing_charge: No
arxiv: 1
author:
- first_name: Krzysztof
full_name: Mysliwy, Krzysztof
id: 316457FC-F248-11E8-B48F-1D18A9856A87
last_name: Mysliwy
- first_name: Marek
full_name: Napiórkowski, Marek
last_name: Napiórkowski
citation:
ama: 'Mysliwy K, Napiórkowski M. Thermodynamics of inhomogeneous imperfect quantum
gases in harmonic traps. Journal of Statistical Mechanics: Theory and Experiment.
2019;2019(6). doi:10.1088/1742-5468/ab190d'
apa: 'Mysliwy, K., & Napiórkowski, M. (2019). Thermodynamics of inhomogeneous
imperfect quantum gases in harmonic traps. Journal of Statistical Mechanics:
Theory and Experiment. IOP Publishing. https://doi.org/10.1088/1742-5468/ab190d'
chicago: 'Mysliwy, Krzysztof, and Marek Napiórkowski. “Thermodynamics of Inhomogeneous
Imperfect Quantum Gases in Harmonic Traps.” Journal of Statistical Mechanics:
Theory and Experiment. IOP Publishing, 2019. https://doi.org/10.1088/1742-5468/ab190d.'
ieee: 'K. Mysliwy and M. Napiórkowski, “Thermodynamics of inhomogeneous imperfect
quantum gases in harmonic traps,” Journal of Statistical Mechanics: Theory
and Experiment, vol. 2019, no. 6. IOP Publishing, 2019.'
ista: 'Mysliwy K, Napiórkowski M. 2019. Thermodynamics of inhomogeneous imperfect
quantum gases in harmonic traps. Journal of Statistical Mechanics: Theory and
Experiment. 2019(6), 063101.'
mla: 'Mysliwy, Krzysztof, and Marek Napiórkowski. “Thermodynamics of Inhomogeneous
Imperfect Quantum Gases in Harmonic Traps.” Journal of Statistical Mechanics:
Theory and Experiment, vol. 2019, no. 6, 063101, IOP Publishing, 2019, doi:10.1088/1742-5468/ab190d.'
short: 'K. Mysliwy, M. Napiórkowski, Journal of Statistical Mechanics: Theory and
Experiment 2019 (2019).'
date_created: 2019-09-01T22:00:59Z
date_published: 2019-06-13T00:00:00Z
date_updated: 2025-03-31T16:01:18Z
day: '13'
department:
- _id: RoSe
doi: 10.1088/1742-5468/ab190d
ec_funded: 1
external_id:
arxiv:
- '1810.02209'
isi:
- '000471650100001'
intvolume: ' 2019'
isi: 1
issue: '6'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/1810.02209
month: '06'
oa: 1
oa_version: Preprint
project:
- _id: 2564DBCA-B435-11E9-9278-68D0E5697425
call_identifier: H2020
grant_number: '665385'
name: International IST Doctoral Program
publication: 'Journal of Statistical Mechanics: Theory and Experiment'
publication_identifier:
eissn:
- 1742-5468
publication_status: published
publisher: IOP Publishing
quality_controlled: '1'
scopus_import: '1'
status: public
title: Thermodynamics of inhomogeneous imperfect quantum gases in harmonic traps
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 2019
year: '2019'
...
---
_id: '6843'
abstract:
- lang: eng
text: The aim of this short paper is to offer a complete characterization of all
(not necessarily surjective) isometric embeddings of the Wasserstein space Wp(X),
where S is a countable discrete metric space and 0Journal of Mathematical Analysis and Applications.
2019;480(2). doi:10.1016/j.jmaa.2019.123435
apa: Gehér, G. P., Titkos, T., & Virosztek, D. (2019). On isometric embeddings
of Wasserstein spaces – the discrete case. Journal of Mathematical Analysis
and Applications. Elsevier. https://doi.org/10.1016/j.jmaa.2019.123435
chicago: Gehér, György Pál, Tamás Titkos, and Daniel Virosztek. “On Isometric Embeddings
of Wasserstein Spaces – the Discrete Case.” Journal of Mathematical Analysis
and Applications. Elsevier, 2019. https://doi.org/10.1016/j.jmaa.2019.123435.
ieee: G. P. Gehér, T. Titkos, and D. Virosztek, “On isometric embeddings of Wasserstein
spaces – the discrete case,” Journal of Mathematical Analysis and Applications,
vol. 480, no. 2. Elsevier, 2019.
ista: Gehér GP, Titkos T, Virosztek D. 2019. On isometric embeddings of Wasserstein
spaces – the discrete case. Journal of Mathematical Analysis and Applications.
480(2), 123435.
mla: Gehér, György Pál, et al. “On Isometric Embeddings of Wasserstein Spaces –
the Discrete Case.” Journal of Mathematical Analysis and Applications,
vol. 480, no. 2, 123435, Elsevier, 2019, doi:10.1016/j.jmaa.2019.123435.
short: G.P. Gehér, T. Titkos, D. Virosztek, Journal of Mathematical Analysis and
Applications 480 (2019).
date_created: 2019-09-01T22:01:01Z
date_published: 2019-12-15T00:00:00Z
date_updated: 2025-07-10T11:53:55Z
day: '15'
department:
- _id: LaEr
doi: 10.1016/j.jmaa.2019.123435
ec_funded: 1
external_id:
arxiv:
- '1809.01101'
isi:
- '000486563900031'
intvolume: ' 480'
isi: 1
issue: '2'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/1809.01101
month: '12'
oa: 1
oa_version: Preprint
project:
- _id: 25681D80-B435-11E9-9278-68D0E5697425
call_identifier: FP7
grant_number: '291734'
name: International IST Postdoc Fellowship Programme
publication: Journal of Mathematical Analysis and Applications
publication_identifier:
eissn:
- 1096-0813
issn:
- 0022-247X
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: On isometric embeddings of Wasserstein spaces – the discrete case
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 480
year: '2019'
...
---
_id: '6844'
abstract:
- lang: eng
text: Studying the progression of the proliferative and differentiative patterns
of neural stem cells at the individual cell level is crucial to the understanding
of cortex development and how the disruption of such patterns can lead to malformations
and neurodevelopmental diseases. However, our understanding of the precise lineage
progression programme at single-cell resolution is still incomplete due to the
technical variations in lineage- tracing approaches. One of the key challenges
involves developing a robust theoretical framework in which we can integrate experimental
observations and introduce correction factors to obtain a reliable and representative
description of the temporal modulation of proliferation and differentiation. In
order to obtain more conclusive insights, we carry out virtual clonal analysis
using mathematical modelling and compare our results against experimental data.
Using a dataset obtained with Mosaic Analysis with Double Markers, we illustrate
how the theoretical description can be exploited to interpret and reconcile the
disparity between virtual and experimental results.
article_processing_charge: No
article_type: original
author:
- first_name: Noemi
full_name: Picco, Noemi
last_name: Picco
- first_name: Simon
full_name: Hippenmeyer, Simon
id: 37B36620-F248-11E8-B48F-1D18A9856A87
last_name: Hippenmeyer
orcid: 0000-0003-2279-1061
- first_name: Julio
full_name: Rodarte, Julio
id: 3C70A038-F248-11E8-B48F-1D18A9856A87
last_name: Rodarte
- first_name: Carmen
full_name: Streicher, Carmen
id: 36BCB99C-F248-11E8-B48F-1D18A9856A87
last_name: Streicher
- first_name: Zoltán
full_name: Molnár, Zoltán
last_name: Molnár
- first_name: Philip K.
full_name: Maini, Philip K.
last_name: Maini
- first_name: Thomas E.
full_name: Woolley, Thomas E.
last_name: Woolley
citation:
ama: Picco N, Hippenmeyer S, Rodarte J, et al. A mathematical insight into cell
labelling experiments for clonal analysis. Journal of Anatomy. 2019;235(3):686-696.
doi:10.1111/joa.13001
apa: Picco, N., Hippenmeyer, S., Rodarte, J., Streicher, C., Molnár, Z., Maini,
P. K., & Woolley, T. E. (2019). A mathematical insight into cell labelling
experiments for clonal analysis. Journal of Anatomy. Wiley. https://doi.org/10.1111/joa.13001
chicago: Picco, Noemi, Simon Hippenmeyer, Julio Rodarte, Carmen Streicher, Zoltán
Molnár, Philip K. Maini, and Thomas E. Woolley. “A Mathematical Insight into Cell
Labelling Experiments for Clonal Analysis.” Journal of Anatomy. Wiley,
2019. https://doi.org/10.1111/joa.13001.
ieee: N. Picco et al., “A mathematical insight into cell labelling experiments
for clonal analysis,” Journal of Anatomy, vol. 235, no. 3. Wiley, pp. 686–696,
2019.
ista: Picco N, Hippenmeyer S, Rodarte J, Streicher C, Molnár Z, Maini PK, Woolley
TE. 2019. A mathematical insight into cell labelling experiments for clonal analysis.
Journal of Anatomy. 235(3), 686–696.
mla: Picco, Noemi, et al. “A Mathematical Insight into Cell Labelling Experiments
for Clonal Analysis.” Journal of Anatomy, vol. 235, no. 3, Wiley, 2019,
pp. 686–96, doi:10.1111/joa.13001.
short: N. Picco, S. Hippenmeyer, J. Rodarte, C. Streicher, Z. Molnár, P.K. Maini,
T.E. Woolley, Journal of Anatomy 235 (2019) 686–696.
date_created: 2019-09-02T11:57:28Z
date_published: 2019-09-01T00:00:00Z
date_updated: 2025-04-14T07:43:05Z
day: '01'
ddc:
- '570'
department:
- _id: SiHi
doi: 10.1111/joa.13001
ec_funded: 1
external_id:
isi:
- '000482426800017'
file:
- access_level: open_access
checksum: 160f960844b204057f20896e0e1f8ee7
content_type: application/pdf
creator: dernst
date_created: 2019-09-02T12:05:18Z
date_updated: 2020-07-14T12:47:42Z
file_id: '6845'
file_name: 2019_JournalAnatomy_Picco.pdf
file_size: 1192994
relation: main_file
file_date_updated: 2020-07-14T12:47:42Z
has_accepted_license: '1'
intvolume: ' 235'
isi: 1
issue: '3'
language:
- iso: eng
month: '09'
oa: 1
oa_version: Published Version
page: 686-696
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: Journal of Anatomy
publication_identifier:
eissn:
- 1469-7580
issn:
- 0021-8782
publication_status: published
publisher: Wiley
quality_controlled: '1'
scopus_import: '1'
status: public
title: A mathematical insight into cell labelling experiments for clonal analysis
tmp:
image: /images/cc_by_nc.png
legal_code_url: https://creativecommons.org/licenses/by-nc/4.0/legalcode
name: Creative Commons Attribution-NonCommercial 4.0 International (CC BY-NC 4.0)
short: CC BY-NC (4.0)
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 235
year: '2019'
...
---
_id: '6855'
abstract:
- lang: eng
text: Many traits of interest are highly heritable and genetically complex, meaning
that much of the variation they exhibit arises from differences at numerous loci
in the genome. Complex traits and their evolution have been studied for more than
a century, but only in the last decade have genome-wide association studies (GWASs)
in humans begun to reveal their genetic basis. Here, we bring these threads of
research together to ask how findings from GWASs can further our understanding
of the processes that give rise to heritable variation in complex traits and of
the genetic basis of complex trait evolution in response to changing selection
pressures (i.e., of polygenic adaptation). Conversely, we ask how evolutionary
thinking helps us to interpret findings from GWASs and informs related efforts
of practical importance.
article_processing_charge: No
author:
- first_name: Guy
full_name: Sella, Guy
last_name: Sella
- first_name: Nicholas H
full_name: Barton, Nicholas H
id: 4880FE40-F248-11E8-B48F-1D18A9856A87
last_name: Barton
orcid: 0000-0002-8548-5240
citation:
ama: Sella G, Barton NH. Thinking about the evolution of complex traits in the era
of genome-wide association studies. Annual Review of Genomics and Human Genetics.
2019;20:461-493. doi:10.1146/annurev-genom-083115-022316
apa: Sella, G., & Barton, N. H. (2019). Thinking about the evolution of complex
traits in the era of genome-wide association studies. Annual Review of Genomics
and Human Genetics. Annual Reviews. https://doi.org/10.1146/annurev-genom-083115-022316
chicago: Sella, Guy, and Nicholas H Barton. “Thinking about the Evolution of Complex
Traits in the Era of Genome-Wide Association Studies.” Annual Review of Genomics
and Human Genetics. Annual Reviews, 2019. https://doi.org/10.1146/annurev-genom-083115-022316.
ieee: G. Sella and N. H. Barton, “Thinking about the evolution of complex traits
in the era of genome-wide association studies,” Annual Review of Genomics and
Human Genetics, vol. 20. Annual Reviews, pp. 461–493, 2019.
ista: Sella G, Barton NH. 2019. Thinking about the evolution of complex traits in
the era of genome-wide association studies. Annual Review of Genomics and Human
Genetics. 20, 461–493.
mla: Sella, Guy, and Nicholas H. Barton. “Thinking about the Evolution of Complex
Traits in the Era of Genome-Wide Association Studies.” Annual Review of Genomics
and Human Genetics, vol. 20, Annual Reviews, 2019, pp. 461–93, doi:10.1146/annurev-genom-083115-022316.
short: G. Sella, N.H. Barton, Annual Review of Genomics and Human Genetics 20 (2019)
461–493.
corr_author: '1'
date_created: 2019-09-07T14:28:29Z
date_published: 2019-07-05T00:00:00Z
date_updated: 2024-10-09T20:58:59Z
day: '05'
ddc:
- '576'
department:
- _id: NiBa
doi: 10.1146/annurev-genom-083115-022316
external_id:
isi:
- '000485148400020'
pmid:
- '31283361'
file:
- access_level: open_access
checksum: 23d3978cf4739a89ce2c3e779f9305ca
content_type: application/pdf
creator: dernst
date_created: 2019-09-09T07:22:12Z
date_updated: 2020-07-14T12:47:42Z
file_id: '6862'
file_name: 2019_AnnualReview_Sella.pdf
file_size: 411491
relation: main_file
file_date_updated: 2020-07-14T12:47:42Z
has_accepted_license: '1'
intvolume: ' 20'
isi: 1
language:
- iso: eng
month: '07'
oa: 1
oa_version: Published Version
page: 461-493
pmid: 1
publication: Annual Review of Genomics and Human Genetics
publication_identifier:
eissn:
- 1545-293X
issn:
- 1527-8204
publication_status: published
publisher: Annual Reviews
quality_controlled: '1'
scopus_import: '1'
status: public
title: Thinking about the evolution of complex traits in the era of genome-wide association
studies
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: 20
year: '2019'
...
---
_id: '6857'
abstract:
- lang: eng
text: "Gene Drives are regarded as future tools with a high potential for population
control. Due to their inherent ability to overcome the rules of Mendelian inheritance,
gene drives (GD) may spread genes rapidly through populations of sexually reproducing
organisms. A release of organisms carrying a GD would constitute a paradigm shift
in the handling of genetically modified organisms because gene drive organisms
(GDO) are designed to drive their transgenes into wild populations and thereby
increase the number of GDOs. The rapid development in this field and its focus
on wild populations demand a prospective risk assessment with a focus on exposure
related aspects. Presently, it is unclear how adequate risk management could be
guaranteed to limit the spread of GDs in time and space, in order to avoid potential
adverse effects in socio‐ecological systems.\r\n\r\nThe recent workshop on the
“Evaluation of Spatial and Temporal Control of Gene Drives” hosted by the Institute
of Safety/Security and Risk Sciences (ISR) in Vienna aimed at gaining some insight
into the potential population dynamic behavior of GDs and appropriate measures
of control. Scientists from France, Germany, England, and the USA discussed both
topics in this meeting on April 4–5, 2019. This article summarizes results of
the workshop."
article_number: '1900151'
article_processing_charge: No
article_type: original
author:
- first_name: B
full_name: Giese, B
last_name: Giese
- first_name: J L
full_name: Friess, J L
last_name: Friess
- first_name: 'M F '
full_name: 'Schetelig, M F '
last_name: Schetelig
- first_name: Nicholas H
full_name: Barton, Nicholas H
id: 4880FE40-F248-11E8-B48F-1D18A9856A87
last_name: Barton
orcid: 0000-0002-8548-5240
- first_name: Philip
full_name: Messer, Philip
last_name: Messer
- first_name: Florence
full_name: Debarre, Florence
last_name: Debarre
- first_name: H
full_name: Meimberg, H
last_name: Meimberg
- first_name: N
full_name: Windbichler, N
last_name: Windbichler
- first_name: C
full_name: Boete, C
last_name: Boete
citation:
ama: 'Giese B, Friess JL, Schetelig MF, et al. Gene Drives: Dynamics and regulatory
matters – A report from the workshop “Evaluation of spatial and temporal control
of Gene Drives”, 4 – 5 April 2019, Vienna. BioEssays. 2019;41(11). doi:10.1002/bies.201900151'
apa: 'Giese, B., Friess, J. L., Schetelig, M. F., Barton, N. H., Messer, P., Debarre,
F., … Boete, C. (2019). Gene Drives: Dynamics and regulatory matters – A report
from the workshop “Evaluation of spatial and temporal control of Gene Drives”,
4 – 5 April 2019, Vienna. BioEssays. Wiley. https://doi.org/10.1002/bies.201900151'
chicago: 'Giese, B, J L Friess, M F Schetelig, Nicholas H Barton, Philip Messer,
Florence Debarre, H Meimberg, N Windbichler, and C Boete. “Gene Drives: Dynamics
and Regulatory Matters – A Report from the Workshop ‘Evaluation of Spatial and
Temporal Control of Gene Drives’, 4 – 5 April 2019, Vienna.” BioEssays.
Wiley, 2019. https://doi.org/10.1002/bies.201900151.'
ieee: 'B. Giese et al., “Gene Drives: Dynamics and regulatory matters – A
report from the workshop ‘Evaluation of spatial and temporal control of Gene Drives’,
4 – 5 April 2019, Vienna,” BioEssays, vol. 41, no. 11. Wiley, 2019.'
ista: 'Giese B, Friess JL, Schetelig MF, Barton NH, Messer P, Debarre F, Meimberg
H, Windbichler N, Boete C. 2019. Gene Drives: Dynamics and regulatory matters
– A report from the workshop “Evaluation of spatial and temporal control of Gene
Drives”, 4 – 5 April 2019, Vienna. BioEssays. 41(11), 1900151.'
mla: 'Giese, B., et al. “Gene Drives: Dynamics and Regulatory Matters – A Report
from the Workshop ‘Evaluation of Spatial and Temporal Control of Gene Drives’,
4 – 5 April 2019, Vienna.” BioEssays, vol. 41, no. 11, 1900151, Wiley,
2019, doi:10.1002/bies.201900151.'
short: B. Giese, J.L. Friess, M.F. Schetelig, N.H. Barton, P. Messer, F. Debarre,
H. Meimberg, N. Windbichler, C. Boete, BioEssays 41 (2019).
date_created: 2019-09-07T14:40:03Z
date_published: 2019-11-01T00:00:00Z
date_updated: 2023-08-30T06:56:26Z
day: '01'
ddc:
- '570'
department:
- _id: NiBa
doi: 10.1002/bies.201900151
external_id:
isi:
- '000489502000001'
file:
- access_level: open_access
checksum: 8cc7551bff70b2658f8d5630f228ee12
content_type: application/pdf
creator: dernst
date_created: 2019-10-11T06:59:26Z
date_updated: 2020-07-14T12:47:42Z
file_id: '6939'
file_name: 2019_BioEssays_Giese.pdf
file_size: 193248
relation: main_file
file_date_updated: 2020-07-14T12:47:42Z
has_accepted_license: '1'
intvolume: ' 41'
isi: 1
issue: '11'
language:
- iso: eng
month: '11'
oa: 1
oa_version: Published Version
publication: BioEssays
publication_identifier:
eissn:
- 1521-1878
publication_status: published
publisher: Wiley
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'Gene Drives: Dynamics and regulatory matters – A report from the workshop
“Evaluation of spatial and temporal control of Gene Drives”, 4 – 5 April 2019, Vienna'
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: 41
year: '2019'
...
---
_id: '6858'
article_processing_charge: No
article_type: review
author:
- first_name: Nicholas H
full_name: Barton, Nicholas H
id: 4880FE40-F248-11E8-B48F-1D18A9856A87
last_name: Barton
orcid: 0000-0002-8548-5240
citation:
ama: Barton NH. Is speciation driven by cycles of mixing and isolation? National
Science Review. 2019;6(2):291-292. doi:10.1093/nsr/nwy113
apa: Barton, N. H. (2019). Is speciation driven by cycles of mixing and isolation?
National Science Review. Oxford University Press. https://doi.org/10.1093/nsr/nwy113
chicago: Barton, Nicholas H. “Is Speciation Driven by Cycles of Mixing and Isolation?”
National Science Review. Oxford University Press, 2019. https://doi.org/10.1093/nsr/nwy113.
ieee: N. H. Barton, “Is speciation driven by cycles of mixing and isolation?,” National
Science Review, vol. 6, no. 2. Oxford University Press, pp. 291–292, 2019.
ista: Barton NH. 2019. Is speciation driven by cycles of mixing and isolation? National
Science Review. 6(2), 291–292.
mla: Barton, Nicholas H. “Is Speciation Driven by Cycles of Mixing and Isolation?”
National Science Review, vol. 6, no. 2, Oxford University Press, 2019,
pp. 291–92, doi:10.1093/nsr/nwy113.
short: N.H. Barton, National Science Review 6 (2019) 291–292.
date_created: 2019-09-07T14:43:02Z
date_published: 2019-03-01T00:00:00Z
date_updated: 2023-08-29T07:51:09Z
day: '01'
ddc:
- '570'
department:
- _id: NiBa
doi: 10.1093/nsr/nwy113
external_id:
isi:
- '000467957400025'
file:
- access_level: open_access
checksum: 571d60fa21a568607d1fd04e119da88c
content_type: application/pdf
creator: dernst
date_created: 2020-10-02T09:16:44Z
date_updated: 2020-10-02T09:16:44Z
file_id: '8595'
file_name: 2019_NSR_Barton.pdf
file_size: 106463
relation: main_file
success: 1
file_date_updated: 2020-10-02T09:16:44Z
has_accepted_license: '1'
intvolume: ' 6'
isi: 1
issue: '2'
language:
- iso: eng
month: '03'
oa: 1
oa_version: Published Version
page: 291-292
publication: National Science Review
publication_identifier:
eissn:
- 2053-714X
issn:
- 2095-5138
publication_status: published
publisher: Oxford University Press
quality_controlled: '1'
scopus_import: '1'
status: public
title: Is speciation driven by cycles of mixing and isolation?
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: 6
year: '2019'
...
---
_id: '6859'
abstract:
- lang: eng
text: V (vacuolar)/A (archaeal)-type adenosine triphosphatases (ATPases), found
in archaeaand eubacteria, couple ATP hydrolysis or synthesis to proton translocation
across theplasma membrane using the rotary-catalysis mechanism. They belong to
the V-typeATPase family, which differs from the mitochondrial/chloroplast F-type
ATP synthasesin overall architecture. We solved cryo–electron microscopy structures
of the intactThermus thermophilusV/A-ATPase, reconstituted into lipid nanodiscs,
in three rotationalstates and two substates. These structures indicate substantial
flexibility betweenV1and Voin a working enzyme, which results from mechanical
competition between centralshaft rotation and resistance from the peripheral stalks.
We also describedetails of adenosine diphosphate inhibition release, V1-Votorque
transmission, andproton translocation, which are relevant for the entire V-type
ATPase family.
acknowledged_ssus:
- _id: ScienComp
article_number: eaaw9144
article_processing_charge: No
author:
- first_name: Long
full_name: Zhou, Long
id: 3E751364-F248-11E8-B48F-1D18A9856A87
last_name: Zhou
orcid: 0000-0002-1864-8951
- first_name: Leonid A
full_name: Sazanov, Leonid A
id: 338D39FE-F248-11E8-B48F-1D18A9856A87
last_name: Sazanov
orcid: 0000-0002-0977-7989
citation:
ama: Zhou L, Sazanov LA. Structure and conformational plasticity of the intact Thermus
thermophilus V/A-type ATPase. Science. 2019;365(6455). doi:10.1126/science.aaw9144
apa: Zhou, L., & Sazanov, L. A. (2019). Structure and conformational plasticity
of the intact Thermus thermophilus V/A-type ATPase. Science. AAAS. https://doi.org/10.1126/science.aaw9144
chicago: Zhou, Long, and Leonid A Sazanov. “Structure and Conformational Plasticity
of the Intact Thermus Thermophilus V/A-Type ATPase.” Science. AAAS, 2019.
https://doi.org/10.1126/science.aaw9144.
ieee: L. Zhou and L. A. Sazanov, “Structure and conformational plasticity of the
intact Thermus thermophilus V/A-type ATPase,” Science, vol. 365, no. 6455.
AAAS, 2019.
ista: Zhou L, Sazanov LA. 2019. Structure and conformational plasticity of the intact
Thermus thermophilus V/A-type ATPase. Science. 365(6455), eaaw9144.
mla: Zhou, Long, and Leonid A. Sazanov. “Structure and Conformational Plasticity
of the Intact Thermus Thermophilus V/A-Type ATPase.” Science, vol. 365,
no. 6455, eaaw9144, AAAS, 2019, doi:10.1126/science.aaw9144.
short: L. Zhou, L.A. Sazanov, Science 365 (2019).
date_created: 2019-09-07T19:04:45Z
date_published: 2019-08-23T00:00:00Z
date_updated: 2023-08-29T07:52:02Z
day: '23'
department:
- _id: LeSa
doi: 10.1126/science.aaw9144
external_id:
isi:
- '000482464000043'
pmid:
- '31439765'
intvolume: ' 365'
isi: 1
issue: '6455'
language:
- iso: eng
month: '08'
oa_version: None
pmid: 1
publication: Science
publication_identifier:
eissn:
- 1095-9203
issn:
- 0036-8075
publication_status: published
publisher: AAAS
quality_controlled: '1'
related_material:
link:
- description: News on IST Website
relation: press_release
url: https://ist.ac.at/en/news/structure-of-protein-nano-turbine-revealed/
scopus_import: '1'
status: public
title: Structure and conformational plasticity of the intact Thermus thermophilus
V/A-type ATPase
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 365
year: '2019'
...
---
_id: '6867'
abstract:
- lang: eng
text: A novel magnetic scratch method achieves repeatability, reproducibility and
geometric control greater than pipette scratch assays and closely approximating
the precision of cell exclusion assays while inducing the cell injury inherently
necessary for wound healing assays. The magnetic scratch is affordable, easily
implemented and standardisable and thus may contribute toward better comparability
of data generated in different studies and laboratories.
article_number: '12625'
article_processing_charge: No
author:
- first_name: M.
full_name: Fenu, M.
last_name: Fenu
- first_name: T.
full_name: Bettermann, T.
last_name: Bettermann
- first_name: C.
full_name: Vogl, C.
last_name: Vogl
- first_name: Nasser
full_name: Darwish-Miranda, Nasser
id: 39CD9926-F248-11E8-B48F-1D18A9856A87
last_name: Darwish-Miranda
orcid: 0000-0002-8821-8236
- first_name: J.
full_name: Schramel, J.
last_name: Schramel
- first_name: F.
full_name: Jenner, F.
last_name: Jenner
- first_name: I.
full_name: Ribitsch, I.
last_name: Ribitsch
citation:
ama: Fenu M, Bettermann T, Vogl C, et al. A novel magnet-based scratch method for
standardisation of wound-healing assays. Scientific Reports. 2019;9(1).
doi:10.1038/s41598-019-48930-7
apa: Fenu, M., Bettermann, T., Vogl, C., Darwish-Miranda, N., Schramel, J., Jenner,
F., & Ribitsch, I. (2019). A novel magnet-based scratch method for standardisation
of wound-healing assays. Scientific Reports. Springer Nature. https://doi.org/10.1038/s41598-019-48930-7
chicago: Fenu, M., T. Bettermann, C. Vogl, Nasser Darwish-Miranda, J. Schramel,
F. Jenner, and I. Ribitsch. “A Novel Magnet-Based Scratch Method for Standardisation
of Wound-Healing Assays.” Scientific Reports. Springer Nature, 2019. https://doi.org/10.1038/s41598-019-48930-7.
ieee: M. Fenu et al., “A novel magnet-based scratch method for standardisation
of wound-healing assays,” Scientific Reports, vol. 9, no. 1. Springer Nature,
2019.
ista: Fenu M, Bettermann T, Vogl C, Darwish-Miranda N, Schramel J, Jenner F, Ribitsch
I. 2019. A novel magnet-based scratch method for standardisation of wound-healing
assays. Scientific Reports. 9(1), 12625.
mla: Fenu, M., et al. “A Novel Magnet-Based Scratch Method for Standardisation of
Wound-Healing Assays.” Scientific Reports, vol. 9, no. 1, 12625, Springer
Nature, 2019, doi:10.1038/s41598-019-48930-7.
short: M. Fenu, T. Bettermann, C. Vogl, N. Darwish-Miranda, J. Schramel, F. Jenner,
I. Ribitsch, Scientific Reports 9 (2019).
date_created: 2019-09-15T22:00:42Z
date_published: 2019-09-02T00:00:00Z
date_updated: 2026-04-03T09:39:11Z
day: '02'
ddc:
- '570'
department:
- _id: Bio
doi: 10.1038/s41598-019-48930-7
external_id:
isi:
- '000483697800007'
pmid:
- '31477739'
file:
- access_level: open_access
checksum: 9cfd986d4108e288cc72276ef047ab0c
content_type: application/pdf
creator: dernst
date_created: 2019-09-16T12:42:40Z
date_updated: 2020-07-14T12:47:42Z
file_id: '6879'
file_name: 2019_ScientificReports_Fenu.pdf
file_size: 3523795
relation: main_file
file_date_updated: 2020-07-14T12:47:42Z
has_accepted_license: '1'
intvolume: ' 9'
isi: 1
issue: '1'
language:
- iso: eng
month: '09'
oa: 1
oa_version: Published Version
pmid: 1
publication: Scientific Reports
publication_identifier:
eissn:
- 2045-2322
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: A novel magnet-based scratch method for standardisation of wound-healing assays
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: 9
year: '2019'
...