---
_id: '10699'
abstract:
- lang: eng
text: This is the third of three talks describing the observation and characterization
of a ferromagnetic moiré heterostructure based on twisted bilayer graphene aligned
to hexagonal boron nitride. In this segment I will present scanning probe magnetometry
data acquired using a nanoSQUID-on-tip microscope, which provides ~150 nm spatial
resolution and a field sensitivity of ~10 nT/rtHz. We study the distribution of
magnetic domains within the device as a function of density, magnetic field training,
and DC current. Our data allow us to constrain the magnitude of the orbital magnetic
moment of the electrons in the QAH state. Comparison with simultaneously acquired
transport data allows us to precisely correlate single domain dynamics with discrete
jumps in the observed anomalous Hall signal.
acknowledgement: I would like to thank the MURI program, Sloan foundation, AFOSR,
and ARO for their generous support of this work. I would also like to thank the
NSF GRFP and the Hertz foundation for their generous support of my graduate studies.
alternative_title:
- Bulletin of the American Physical Society
article_number: B59.00013
article_processing_charge: No
author:
- first_name: Charles
full_name: Tschirhart, Charles
last_name: Tschirhart
- first_name: Marec
full_name: Serlin, Marec
last_name: Serlin
- first_name: Hryhoriy
full_name: Polshyn, Hryhoriy
id: edfc7cb1-526e-11ec-b05a-e6ecc27e4e48
last_name: Polshyn
orcid: 0000-0001-8223-8896
- first_name: Yuxuan
full_name: Zhang, Yuxuan
last_name: Zhang
- first_name: Jiacheng
full_name: Zhu, Jiacheng
last_name: Zhu
- first_name: Leon
full_name: Balents, Leon
last_name: Balents
- first_name: Martin E.
full_name: Huber, Martin E.
last_name: Huber
- first_name: Kenji
full_name: Watanabe, Kenji
last_name: Watanabe
- first_name: Takashi
full_name: Tanaguchi, Takashi
last_name: Tanaguchi
- first_name: Andrea
full_name: Young, Andrea
last_name: Young
citation:
ama: 'Tschirhart C, Serlin M, Polshyn H, et al. Intrinsic quantized anomalous Hall
effect in a moiré heterostructure, part III: Scanning probe magnetometry. In:
APS March Meeting 2020. Vol 65. American Physical Society; 2020.'
apa: 'Tschirhart, C., Serlin, M., Polshyn, H., Zhang, Y., Zhu, J., Balents, L.,
… Young, A. (2020). Intrinsic quantized anomalous Hall effect in a moiré heterostructure,
part III: Scanning probe magnetometry. In APS March Meeting 2020 (Vol.
65). Denver, CO, United States: American Physical Society.'
chicago: 'Tschirhart, Charles, Marec Serlin, Hryhoriy Polshyn, Yuxuan Zhang, Jiacheng
Zhu, Leon Balents, Martin E. Huber, Kenji Watanabe, Takashi Tanaguchi, and Andrea
Young. “Intrinsic Quantized Anomalous Hall Effect in a Moiré Heterostructure,
Part III: Scanning Probe Magnetometry.” In APS March Meeting 2020, Vol.
65. American Physical Society, 2020.'
ieee: 'C. Tschirhart et al., “Intrinsic quantized anomalous Hall effect in
a moiré heterostructure, part III: Scanning probe magnetometry,” in APS March
Meeting 2020, Denver, CO, United States, 2020, vol. 65, no. 1.'
ista: 'Tschirhart C, Serlin M, Polshyn H, Zhang Y, Zhu J, Balents L, Huber ME, Watanabe
K, Tanaguchi T, Young A. 2020. Intrinsic quantized anomalous Hall effect in a
moiré heterostructure, part III: Scanning probe magnetometry. APS March Meeting
2020. APS: American Physical Society, Bulletin of the American Physical Society,
vol. 65, B59.00013.'
mla: 'Tschirhart, Charles, et al. “Intrinsic Quantized Anomalous Hall Effect in
a Moiré Heterostructure, Part III: Scanning Probe Magnetometry.” APS March
Meeting 2020, vol. 65, no. 1, B59.00013, American Physical Society, 2020.'
short: C. Tschirhart, M. Serlin, H. Polshyn, Y. Zhang, J. Zhu, L. Balents, M.E.
Huber, K. Watanabe, T. Tanaguchi, A. Young, in:, APS March Meeting 2020, American
Physical Society, 2020.
conference:
end_date: 2020-03-06
location: Denver, CO, United States
name: 'APS: American Physical Society'
start_date: 2020-03-02
date_created: 2022-01-28T10:57:49Z
date_published: 2020-03-01T00:00:00Z
date_updated: 2023-02-21T15:57:52Z
day: '01'
extern: '1'
external_id:
arxiv:
- '1907.00261'
intvolume: ' 65'
issue: '1'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://meetings.aps.org/Meeting/MAR20/Session/B59.13
month: '03'
oa: 1
oa_version: Published Version
publication: APS March Meeting 2020
publication_identifier:
issn:
- 0003-0503
publication_status: published
publisher: American Physical Society
quality_controlled: '1'
related_material:
record:
- id: '10619'
relation: other
status: public
status: public
title: 'Intrinsic quantized anomalous Hall effect in a moiré heterostructure, part
III: Scanning probe magnetometry'
type: conference
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
volume: 65
year: '2020'
...
---
_id: '10697'
abstract:
- lang: eng
text: We report the observation of a quantized anomalous Hall effect in a moiré
heterostructure consisting of twisted bilayer graphene aligned to an encapsulating
hBN substrate. The effect occurs at a density of 3 electrons per superlattice
unit cell, where we observe magnetic hysteresis and a Hall resistance quantized
to within 0.1% of the resistance quantum at temperatures as high as 3K. In this
first of 3 talks, I will describe the fabrication procedure for our device as
well as basic transport characterization measurements. I will introduce the phenomenology
of twisted bilayer graphene and present evidence for hBN alignment as manifested
in the hierarchy of symmetry-breaking gaps and anomalous magnetoresistance.
acknowledgement: I would like to thank the MURI program, Sloan foundation, AFOSR,
and ARO for their generous support of this work.
alternative_title:
- Bulletin of the American Physical Society
article_number: B59.00012
article_processing_charge: No
author:
- first_name: Yuxuan
full_name: Zhang, Yuxuan
last_name: Zhang
- first_name: Marec
full_name: Serlin, Marec
last_name: Serlin
- first_name: Charles
full_name: Tschirhart, Charles
last_name: Tschirhart
- first_name: Hryhoriy
full_name: Polshyn, Hryhoriy
id: edfc7cb1-526e-11ec-b05a-e6ecc27e4e48
last_name: Polshyn
orcid: 0000-0001-8223-8896
- first_name: Jiacheng
full_name: Zhu, Jiacheng
last_name: Zhu
- first_name: Leon
full_name: Balents, Leon
last_name: Balents
- first_name: Martin E.
full_name: Huber, Martin E.
last_name: Huber
- first_name: Takashi
full_name: Taniguchi, Takashi
last_name: Taniguchi
- first_name: Kenji
full_name: Watanabe, Kenji
last_name: Watanabe
- first_name: Andrea
full_name: Young, Andrea
last_name: Young
citation:
ama: 'Zhang Y, Serlin M, Tschirhart C, et al. Intrinsic quantized anomalous Hall
effect in a moiré heterostructure, part I: Device fabrication and transport. In:
APS March Meeting 2020. Vol 65. American Physical Society; 2020.'
apa: 'Zhang, Y., Serlin, M., Tschirhart, C., Polshyn, H., Zhu, J., Balents, L.,
… Young, A. (2020). Intrinsic quantized anomalous Hall effect in a moiré heterostructure,
part I: Device fabrication and transport. In APS March Meeting 2020 (Vol.
65). Denver, CO, United States: American Physical Society.'
chicago: 'Zhang, Yuxuan, Marec Serlin, Charles Tschirhart, Hryhoriy Polshyn, Jiacheng
Zhu, Leon Balents, Martin E. Huber, Takashi Taniguchi, Kenji Watanabe, and Andrea
Young. “Intrinsic Quantized Anomalous Hall Effect in a Moiré Heterostructure,
Part I: Device Fabrication and Transport.” In APS March Meeting 2020, Vol.
65. American Physical Society, 2020.'
ieee: 'Y. Zhang et al., “Intrinsic quantized anomalous Hall effect in a moiré
heterostructure, part I: Device fabrication and transport,” in APS March Meeting
2020, Denver, CO, United States, 2020, vol. 65, no. 1.'
ista: 'Zhang Y, Serlin M, Tschirhart C, Polshyn H, Zhu J, Balents L, Huber ME, Taniguchi
T, Watanabe K, Young A. 2020. Intrinsic quantized anomalous Hall effect in a moiré
heterostructure, part I: Device fabrication and transport. APS March Meeting 2020.
APS: American Physical Society, Bulletin of the American Physical Society, vol.
65, B59.00012.'
mla: 'Zhang, Yuxuan, et al. “Intrinsic Quantized Anomalous Hall Effect in a Moiré
Heterostructure, Part I: Device Fabrication and Transport.” APS March Meeting
2020, vol. 65, no. 1, B59.00012, American Physical Society, 2020.'
short: Y. Zhang, M. Serlin, C. Tschirhart, H. Polshyn, J. Zhu, L. Balents, M.E.
Huber, T. Taniguchi, K. Watanabe, A. Young, in:, APS March Meeting 2020, American
Physical Society, 2020.
conference:
end_date: 2020-03-06
location: Denver, CO, United States
name: 'APS: American Physical Society'
start_date: 2020-03-02
date_created: 2022-01-28T10:28:35Z
date_published: 2020-03-01T00:00:00Z
date_updated: 2023-02-21T15:57:52Z
day: '01'
extern: '1'
external_id:
arxiv:
- '1907.00261'
intvolume: ' 65'
issue: '1'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://meetings.aps.org/Meeting/MAR20/Session/B59.12
month: '03'
oa: 1
oa_version: Published Version
publication: APS March Meeting 2020
publication_status: published
publisher: American Physical Society
quality_controlled: '1'
related_material:
record:
- id: '10619'
relation: other
status: public
status: public
title: 'Intrinsic quantized anomalous Hall effect in a moiré heterostructure, part
I: Device fabrication and transport'
type: conference
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
volume: 65
year: '2020'
...
---
_id: '10696'
abstract:
- lang: eng
text: We experimentally investigate twisted van der Waals heterostructures of monolayer
graphene rotated with respect to a bernal stacked graphene bilayer. We report
transport measurements for devices with twist angles between 0.9 and 1.4°. The
electric field allows efficient tuning of the width, isolation and the topology
of the moiré bands in this system. By comparing magnetoresistance measurements
to numerical simulations, we develop an understanding of the band structure. Finally,
we observe correlated states at half- and quarter-fillings, which arise when narrow
moire sublattice band is isolated by energy gaps from dispersive bands. We investigate
the effects of in-plane and out-of-plane magnetic field on these states and discuss
the implication for their spin- and valley- polarization.
alternative_title:
- Bulletin of the American Physical Society
article_number: B51.00005
article_processing_charge: No
author:
- first_name: Hryhoriy
full_name: Polshyn, Hryhoriy
id: edfc7cb1-526e-11ec-b05a-e6ecc27e4e48
last_name: Polshyn
orcid: 0000-0001-8223-8896
- first_name: Jihang
full_name: Zhu, Jihang
last_name: Zhu
- first_name: Manish
full_name: Kumar, Manish
last_name: Kumar
- first_name: Takashi
full_name: Taniguchi, Takashi
last_name: Taniguchi
- first_name: Kenji
full_name: Watanabe, Kenji
last_name: Watanabe
- first_name: Allan
full_name: MacDonald, Allan
last_name: MacDonald
- first_name: Andrea
full_name: Young, Andrea
last_name: Young
citation:
ama: 'Polshyn H, Zhu J, Kumar M, et al. Correlated states and tunable topological
bands in twisted monolayer-bilayer graphene heterostructures. In: APS March
Meeting 2020. Vol 65. American Physical Society; 2020.'
apa: 'Polshyn, H., Zhu, J., Kumar, M., Taniguchi, T., Watanabe, K., MacDonald, A.,
& Young, A. (2020). Correlated states and tunable topological bands in twisted
monolayer-bilayer graphene heterostructures. In APS March Meeting 2020
(Vol. 65). Denver, CO, United States: American Physical Society.'
chicago: Polshyn, Hryhoriy, Jihang Zhu, Manish Kumar, Takashi Taniguchi, Kenji Watanabe,
Allan MacDonald, and Andrea Young. “Correlated States and Tunable Topological
Bands in Twisted Monolayer-Bilayer Graphene Heterostructures.” In APS March
Meeting 2020, Vol. 65. American Physical Society, 2020.
ieee: H. Polshyn et al., “Correlated states and tunable topological bands
in twisted monolayer-bilayer graphene heterostructures,” in APS March Meeting
2020, Denver, CO, United States, 2020, vol. 65, no. 1.
ista: 'Polshyn H, Zhu J, Kumar M, Taniguchi T, Watanabe K, MacDonald A, Young A.
2020. Correlated states and tunable topological bands in twisted monolayer-bilayer
graphene heterostructures. APS March Meeting 2020. APS: American Physical Society,
Bulletin of the American Physical Society, vol. 65, B51.00005.'
mla: Polshyn, Hryhoriy, et al. “Correlated States and Tunable Topological Bands
in Twisted Monolayer-Bilayer Graphene Heterostructures.” APS March Meeting
2020, vol. 65, no. 1, B51.00005, American Physical Society, 2020.
short: H. Polshyn, J. Zhu, M. Kumar, T. Taniguchi, K. Watanabe, A. MacDonald, A.
Young, in:, APS March Meeting 2020, American Physical Society, 2020.
conference:
end_date: 2020-03-06
location: Denver, CO, United States
name: 'APS: American Physical Society'
start_date: 2020-03-02
date_created: 2022-01-28T10:09:19Z
date_published: 2020-03-01T00:00:00Z
date_updated: 2022-02-08T10:22:08Z
day: '01'
extern: '1'
intvolume: ' 65'
issue: '1'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://meetings.aps.org/Meeting/MAR20/Session/B51.5
month: '03'
oa: 1
oa_version: Published Version
publication: APS March Meeting 2020
publication_identifier:
issn:
- 0003-0503
publication_status: published
publisher: American Physical Society
quality_controlled: '1'
status: public
title: Correlated states and tunable topological bands in twisted monolayer-bilayer
graphene heterostructures
type: conference
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
volume: 65
year: '2020'
...
---
_id: '10701'
abstract:
- lang: eng
text: Partially filled Landau levels host competing electronic orders. For example,
electron solids may prevail close to integer filling of the Landau levels before
giving way to fractional quantum Hall liquids at higher carrier density1,2. Here,
we report the observation of an electron solid with non-collinear spin texture
in monolayer graphene, consistent with solidification of skyrmions3—topological
spin textures characterized by quantized electrical charge4,5. We probe the spin
texture of the solids using a modified Corbino geometry that allows ferromagnetic
magnons to be launched and detected6,7. We find that magnon transport is highly
efficient when one Landau level is filled (ν=1), consistent with quantum Hall
ferromagnetic spin polarization. However, even minimal doping immediately quenches
the magnon signal while leaving the vanishing low-temperature charge conductivity
unchanged. Our results can be understood by the formation of a solid of charged
skyrmions near ν=1, whose non-collinear spin texture leads to rapid magnon decay.
Data near fractional fillings show evidence of several fractional skyrmion solids,
suggesting that graphene hosts a highly tunable landscape of coupled spin and
charge orders.
acknowledgement: We acknowledge discussions with B. Halperin, C. Huang, A. Macdonald
and M. Zalatel. Experimental work at UCSB was supported by the Army Research Office
under awards nos. MURI W911NF-16-1-0361 and W911NF-16-1-0482. K.W. and T.T. acknowledge
support from the Elemental Strategy Initiative conducted by MEXT (Japan) and CREST
(JPMJCR15F3), JST. A.F.Y. acknowledges the support of the David and Lucile Packard
Foundation and and Alfred. P. Sloan Foundation.
article_processing_charge: No
article_type: original
author:
- first_name: Haoxin
full_name: Zhou, Haoxin
last_name: Zhou
- first_name: Hryhoriy
full_name: Polshyn, Hryhoriy
id: edfc7cb1-526e-11ec-b05a-e6ecc27e4e48
last_name: Polshyn
orcid: 0000-0001-8223-8896
- first_name: Takashi
full_name: Taniguchi, Takashi
last_name: Taniguchi
- first_name: Kenji
full_name: Watanabe, Kenji
last_name: Watanabe
- first_name: Andrea F.
full_name: Young, Andrea F.
last_name: Young
citation:
ama: Zhou H, Polshyn H, Taniguchi T, Watanabe K, Young AF. Skyrmion solids in monolayer
graphene. Nature Physics. 2020;16(2):154-158. doi:10.1038/s41567-019-0729-8
apa: Zhou, H., Polshyn, H., Taniguchi, T., Watanabe, K., & Young, A. F. (2020).
Skyrmion solids in monolayer graphene. Nature Physics. Springer Nature.
https://doi.org/10.1038/s41567-019-0729-8
chicago: Zhou, Haoxin, Hryhoriy Polshyn, Takashi Taniguchi, Kenji Watanabe, and
Andrea F. Young. “Skyrmion Solids in Monolayer Graphene.” Nature Physics.
Springer Nature, 2020. https://doi.org/10.1038/s41567-019-0729-8.
ieee: H. Zhou, H. Polshyn, T. Taniguchi, K. Watanabe, and A. F. Young, “Skyrmion
solids in monolayer graphene,” Nature Physics, vol. 16, no. 2. Springer
Nature, pp. 154–158, 2020.
ista: Zhou H, Polshyn H, Taniguchi T, Watanabe K, Young AF. 2020. Skyrmion solids
in monolayer graphene. Nature Physics. 16(2), 154–158.
mla: Zhou, Haoxin, et al. “Skyrmion Solids in Monolayer Graphene.” Nature Physics,
vol. 16, no. 2, Springer Nature, 2020, pp. 154–58, doi:10.1038/s41567-019-0729-8.
short: H. Zhou, H. Polshyn, T. Taniguchi, K. Watanabe, A.F. Young, Nature Physics
16 (2020) 154–158.
date_created: 2022-01-28T12:04:09Z
date_published: 2020-02-01T00:00:00Z
date_updated: 2022-01-31T07:10:07Z
day: '01'
doi: 10.1038/s41567-019-0729-8
extern: '1'
external_id:
arxiv:
- '1904.11485'
intvolume: ' 16'
issue: '2'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/1904.11485
month: '02'
oa: 1
oa_version: Preprint
page: 154-158
publication: Nature Physics
publication_identifier:
eissn:
- 1745-2481
issn:
- 1745-2473
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
status: public
title: Skyrmion solids in monolayer graphene
type: journal_article
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
volume: 16
year: '2020'
...
---
_id: '11056'
abstract:
- lang: eng
text: Aging of the circulatory system correlates with the pathogenesis of a large
spectrum of diseases. However, it is largely unknown which factors drive the age-dependent
or pathological decline of the vasculature and how vascular defects relate to
tissue aging. The goal of the study is to design a multianalytical approach to
identify how the cellular microenvironment (i.e., fibroblasts) and serum from
healthy donors of different ages or Alzheimer disease (AD) patients can modulate
the functionality of organ-specific vascular endothelial cells (VECs). Long-living
human microvascular networks embedding VECs and fibroblasts from skin biopsies
are generated. RNA-seq, secretome analyses, and microfluidic assays demonstrate
that fibroblasts from young donors restore the functionality of aged endothelial
cells, an effect also achieved by serum from young donors. New biomarkers of vascular
aging are validated in human biopsies and it is shown that young serum induces
angiopoietin-like-4, which can restore compromised vascular barriers. This strategy
is then employed to characterize transcriptional/functional changes induced on
the blood–brain barrier by AD serum, demonstrating the importance of PTP4A3 in
the regulation of permeability. Features of vascular degeneration during aging
and AD are recapitulated, and a tool to identify novel biomarkers that can be
exploited to develop future therapeutics modulating vascular function is established.
article_number: '2000044'
article_processing_charge: No
article_type: original
author:
- first_name: Simone
full_name: Bersini, Simone
last_name: Bersini
- first_name: Rafael
full_name: Arrojo e Drigo, Rafael
last_name: Arrojo e Drigo
- first_name: Ling
full_name: Huang, Ling
last_name: Huang
- first_name: Maxim N.
full_name: Shokhirev, Maxim N.
last_name: Shokhirev
- first_name: Martin W
full_name: HETZER, Martin W
id: 86c0d31b-b4eb-11ec-ac5a-eae7b2e135ed
last_name: HETZER
orcid: 0000-0002-2111-992X
citation:
ama: Bersini S, Arrojo e Drigo R, Huang L, Shokhirev MN, Hetzer M. Transcriptional
and functional changes of the human microvasculature during physiological aging
and Alzheimer disease. Advanced Biosystems. 2020;4(5). doi:10.1002/adbi.202000044
apa: Bersini, S., Arrojo e Drigo, R., Huang, L., Shokhirev, M. N., & Hetzer,
M. (2020). Transcriptional and functional changes of the human microvasculature
during physiological aging and Alzheimer disease. Advanced Biosystems.
Wiley. https://doi.org/10.1002/adbi.202000044
chicago: Bersini, Simone, Rafael Arrojo e Drigo, Ling Huang, Maxim N. Shokhirev,
and Martin Hetzer. “Transcriptional and Functional Changes of the Human Microvasculature
during Physiological Aging and Alzheimer Disease.” Advanced Biosystems.
Wiley, 2020. https://doi.org/10.1002/adbi.202000044.
ieee: S. Bersini, R. Arrojo e Drigo, L. Huang, M. N. Shokhirev, and M. Hetzer, “Transcriptional
and functional changes of the human microvasculature during physiological aging
and Alzheimer disease,” Advanced Biosystems, vol. 4, no. 5. Wiley, 2020.
ista: Bersini S, Arrojo e Drigo R, Huang L, Shokhirev MN, Hetzer M. 2020. Transcriptional
and functional changes of the human microvasculature during physiological aging
and Alzheimer disease. Advanced Biosystems. 4(5), 2000044.
mla: Bersini, Simone, et al. “Transcriptional and Functional Changes of the Human
Microvasculature during Physiological Aging and Alzheimer Disease.” Advanced
Biosystems, vol. 4, no. 5, 2000044, Wiley, 2020, doi:10.1002/adbi.202000044.
short: S. Bersini, R. Arrojo e Drigo, L. Huang, M.N. Shokhirev, M. Hetzer, Advanced
Biosystems 4 (2020).
date_created: 2022-04-07T07:43:57Z
date_published: 2020-05-01T00:00:00Z
date_updated: 2022-07-18T08:30:48Z
day: '01'
ddc:
- '570'
doi: 10.1002/adbi.202000044
extern: '1'
external_id:
pmid:
- '32402127'
file:
- access_level: open_access
checksum: 5584d9a1609812dc75c02ce1e35d2ec0
content_type: application/pdf
creator: dernst
date_created: 2022-04-08T07:06:05Z
date_updated: 2022-04-08T07:06:05Z
file_id: '11134'
file_name: 2020_AdvancedBiosystems_Bersini.pdf
file_size: 2490829
relation: main_file
success: 1
file_date_updated: 2022-04-08T07:06:05Z
has_accepted_license: '1'
intvolume: ' 4'
issue: '5'
keyword:
- General Biochemistry
- Genetics and Molecular Biology
- Biomedical Engineering
- Biomaterials
language:
- iso: eng
license: https://creativecommons.org/licenses/by-nc-nd/4.0/
month: '05'
oa: 1
oa_version: Published Version
pmid: 1
publication: Advanced Biosystems
publication_identifier:
issn:
- 2366-7478
- 2366-7478
publication_status: published
publisher: Wiley
quality_controlled: '1'
scopus_import: '1'
status: public
title: Transcriptional and functional changes of the human microvasculature during
physiological aging and Alzheimer disease
tmp:
image: /images/cc_by_nc_nd.png
legal_code_url: https://creativecommons.org/licenses/by-nc-nd/4.0/legalcode
name: Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International
(CC BY-NC-ND 4.0)
short: CC BY-NC-ND (4.0)
type: journal_article
user_id: 72615eeb-f1f3-11ec-aa25-d4573ddc34fd
volume: 4
year: '2020'
...
---
_id: '11055'
abstract:
- lang: eng
text: Vascular dysfunctions are a common feature of multiple age-related diseases.
However, modeling healthy and pathological aging of the human vasculature represents
an unresolved experimental challenge. Here, we generated induced vascular endothelial
cells (iVECs) and smooth muscle cells (iSMCs) by direct reprogramming of healthy
human fibroblasts from donors of different ages and Hutchinson-Gilford Progeria
Syndrome (HGPS) patients. iVECs induced from old donors revealed upregulation
of GSTM1 and PALD1, genes linked to oxidative stress, inflammation and endothelial
junction stability, as vascular aging markers. A functional assay performed on
PALD1 KD VECs demonstrated a recovery in vascular permeability. We found that
iSMCs from HGPS donors overexpressed bone morphogenetic protein (BMP)−4, which
plays a key role in both vascular calcification and endothelial barrier damage
observed in HGPS. Strikingly, BMP4 concentrations are higher in serum from HGPS
vs. age-matched mice. Furthermore, targeting BMP4 with blocking antibody recovered
the functionality of the vascular barrier in vitro, hence representing a potential
future therapeutic strategy to limit cardiovascular dysfunction in HGPS. These
results show that iVECs and iSMCs retain disease-related signatures, allowing
modeling of vascular aging and HGPS in vitro.
article_number: e54383
article_processing_charge: No
article_type: original
author:
- first_name: Simone
full_name: Bersini, Simone
last_name: Bersini
- first_name: Roberta
full_name: Schulte, Roberta
last_name: Schulte
- first_name: Ling
full_name: Huang, Ling
last_name: Huang
- first_name: Hannah
full_name: Tsai, Hannah
last_name: Tsai
- first_name: Martin W
full_name: HETZER, Martin W
id: 86c0d31b-b4eb-11ec-ac5a-eae7b2e135ed
last_name: HETZER
orcid: 0000-0002-2111-992X
citation:
ama: Bersini S, Schulte R, Huang L, Tsai H, Hetzer M. Direct reprogramming of human
smooth muscle and vascular endothelial cells reveals defects associated with aging
and Hutchinson-Gilford progeria syndrome. eLife. 2020;9. doi:10.7554/elife.54383
apa: Bersini, S., Schulte, R., Huang, L., Tsai, H., & Hetzer, M. (2020). Direct
reprogramming of human smooth muscle and vascular endothelial cells reveals defects
associated with aging and Hutchinson-Gilford progeria syndrome. ELife.
eLife Sciences Publications. https://doi.org/10.7554/elife.54383
chicago: Bersini, Simone, Roberta Schulte, Ling Huang, Hannah Tsai, and Martin Hetzer.
“Direct Reprogramming of Human Smooth Muscle and Vascular Endothelial Cells Reveals
Defects Associated with Aging and Hutchinson-Gilford Progeria Syndrome.” ELife.
eLife Sciences Publications, 2020. https://doi.org/10.7554/elife.54383.
ieee: S. Bersini, R. Schulte, L. Huang, H. Tsai, and M. Hetzer, “Direct reprogramming
of human smooth muscle and vascular endothelial cells reveals defects associated
with aging and Hutchinson-Gilford progeria syndrome,” eLife, vol. 9. eLife
Sciences Publications, 2020.
ista: Bersini S, Schulte R, Huang L, Tsai H, Hetzer M. 2020. Direct reprogramming
of human smooth muscle and vascular endothelial cells reveals defects associated
with aging and Hutchinson-Gilford progeria syndrome. eLife. 9, e54383.
mla: Bersini, Simone, et al. “Direct Reprogramming of Human Smooth Muscle and Vascular
Endothelial Cells Reveals Defects Associated with Aging and Hutchinson-Gilford
Progeria Syndrome.” ELife, vol. 9, e54383, eLife Sciences Publications,
2020, doi:10.7554/elife.54383.
short: S. Bersini, R. Schulte, L. Huang, H. Tsai, M. Hetzer, ELife 9 (2020).
date_created: 2022-04-07T07:43:48Z
date_published: 2020-09-08T00:00:00Z
date_updated: 2022-07-18T08:30:37Z
day: '08'
ddc:
- '570'
doi: 10.7554/elife.54383
extern: '1'
external_id:
pmid:
- '32896271'
file:
- access_level: open_access
checksum: f8b3821349a194050be02570d8fe7d4b
content_type: application/pdf
creator: dernst
date_created: 2022-04-08T06:53:10Z
date_updated: 2022-04-08T06:53:10Z
file_id: '11132'
file_name: 2020_eLife_Bersini.pdf
file_size: 4399825
relation: main_file
success: 1
file_date_updated: 2022-04-08T06:53:10Z
has_accepted_license: '1'
intvolume: ' 9'
keyword:
- General Immunology and Microbiology
- General Biochemistry
- Genetics and Molecular Biology
- General Medicine
- General Neuroscience
language:
- iso: eng
license: https://creativecommons.org/licenses/by/4.0/
month: '09'
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'
scopus_import: '1'
status: public
title: Direct reprogramming of human smooth muscle and vascular endothelial cells
reveals defects associated with aging and Hutchinson-Gilford progeria syndrome
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: 72615eeb-f1f3-11ec-aa25-d4573ddc34fd
volume: 9
year: '2020'
...
---
_id: '11054'
abstract:
- lang: eng
text: In recent years, the nuclear pore complex (NPC) has emerged as a key player
in genome regulation and cellular homeostasis. New discoveries have revealed that
the NPC has multiple cellular functions besides mediating the molecular exchange
between the nucleus and the cytoplasm. In this review, we discuss non-transport
aspects of the NPC focusing on the NPC-genome interaction, the extreme longevity
of the NPC proteins, and NPC dysfunction in age-related diseases. The examples
summarized herein demonstrate that the NPC, which first evolved to enable the
biochemical communication between the nucleus and the cytoplasm, now doubles as
the gatekeeper of cellular identity and aging.
article_processing_charge: No
article_type: review
author:
- first_name: Ukrae H.
full_name: Cho, Ukrae H.
last_name: Cho
- first_name: Martin W
full_name: HETZER, Martin W
id: 86c0d31b-b4eb-11ec-ac5a-eae7b2e135ed
last_name: HETZER
orcid: 0000-0002-2111-992X
citation:
ama: 'Cho UH, Hetzer M. Nuclear periphery takes center stage: The role of nuclear
pore complexes in cell identity and aging. Neuron. 2020;106(6):899-911.
doi:10.1016/j.neuron.2020.05.031'
apa: 'Cho, U. H., & Hetzer, M. (2020). Nuclear periphery takes center stage:
The role of nuclear pore complexes in cell identity and aging. Neuron.
Elsevier. https://doi.org/10.1016/j.neuron.2020.05.031'
chicago: 'Cho, Ukrae H., and Martin Hetzer. “Nuclear Periphery Takes Center Stage:
The Role of Nuclear Pore Complexes in Cell Identity and Aging.” Neuron.
Elsevier, 2020. https://doi.org/10.1016/j.neuron.2020.05.031.'
ieee: 'U. H. Cho and M. Hetzer, “Nuclear periphery takes center stage: The role
of nuclear pore complexes in cell identity and aging,” Neuron, vol. 106,
no. 6. Elsevier, pp. 899–911, 2020.'
ista: 'Cho UH, Hetzer M. 2020. Nuclear periphery takes center stage: The role of
nuclear pore complexes in cell identity and aging. Neuron. 106(6), 899–911.'
mla: 'Cho, Ukrae H., and Martin Hetzer. “Nuclear Periphery Takes Center Stage: The
Role of Nuclear Pore Complexes in Cell Identity and Aging.” Neuron, vol.
106, no. 6, Elsevier, 2020, pp. 899–911, doi:10.1016/j.neuron.2020.05.031.'
short: U.H. Cho, M. Hetzer, Neuron 106 (2020) 899–911.
date_created: 2022-04-07T07:43:36Z
date_published: 2020-06-17T00:00:00Z
date_updated: 2022-07-18T08:29:35Z
day: '17'
doi: 10.1016/j.neuron.2020.05.031
extern: '1'
external_id:
pmid:
- '32553207'
intvolume: ' 106'
issue: '6'
keyword:
- General Neuroscience
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://doi.org/10.1016/j.neuron.2020.05.031
month: '06'
oa: 1
oa_version: Published Version
page: 899-911
pmid: 1
publication: Neuron
publication_identifier:
issn:
- 0896-6273
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'Nuclear periphery takes center stage: The role of nuclear pore complexes in
cell identity and aging'
type: journal_article
user_id: 72615eeb-f1f3-11ec-aa25-d4573ddc34fd
volume: 106
year: '2020'
...
---
_id: '11057'
abstract:
- lang: eng
text: During mitosis, transcription of genomic DNA is dramatically reduced, before
it is reactivated during nuclear reformation in anaphase/telophase. Many aspects
of the underlying principles that mediate transcriptional memory and reactivation
in the daughter cells remain unclear. Here, we used ChIP-seq on synchronized cells
at different stages after mitosis to generate genome-wide maps of histone modifications.
Combined with EU-RNA-seq and Hi-C analyses, we found that during prometaphase,
promoters, enhancers, and insulators retain H3K4me3 and H3K4me1, while losing
H3K27ac. Enhancers globally retaining mitotic H3K4me1 or locally retaining mitotic
H3K27ac are associated with cell type-specific genes and their transcription factors
for rapid transcriptional activation. As cells exit mitosis, promoters regain
H3K27ac, which correlates with transcriptional reactivation. Insulators also gain
H3K27ac and CCCTC-binding factor (CTCF) in anaphase/telophase. This increase of
H3K27ac in anaphase/telophase is required for posttranscriptional activation and
may play a role in the establishment of topologically associating domains (TADs).
Together, our results suggest that the genome is reorganized in a sequential order,
in which histone methylations occur first in prometaphase, histone acetylation,
and CTCF in anaphase/telophase, transcription in cytokinesis, and long-range chromatin
interactions in early G1. We thus provide insights into the histone modification
landscape that allows faithful reestablishment of the transcriptional program
and TADs during cell division.
article_processing_charge: No
article_type: original
author:
- first_name: Hyeseon
full_name: Kang, Hyeseon
last_name: Kang
- first_name: Maxim N.
full_name: Shokhirev, Maxim N.
last_name: Shokhirev
- first_name: Zhichao
full_name: Xu, Zhichao
last_name: Xu
- first_name: Sahaana
full_name: Chandran, Sahaana
last_name: Chandran
- first_name: Jesse R.
full_name: Dixon, Jesse R.
last_name: Dixon
- first_name: Martin W
full_name: HETZER, Martin W
id: 86c0d31b-b4eb-11ec-ac5a-eae7b2e135ed
last_name: HETZER
orcid: 0000-0002-2111-992X
citation:
ama: Kang H, Shokhirev MN, Xu Z, Chandran S, Dixon JR, Hetzer M. Dynamic regulation
of histone modifications and long-range chromosomal interactions during postmitotic
transcriptional reactivation. Genes & Development. 2020;34(13-14):913-930.
doi:10.1101/gad.335794.119
apa: Kang, H., Shokhirev, M. N., Xu, Z., Chandran, S., Dixon, J. R., & Hetzer,
M. (2020). Dynamic regulation of histone modifications and long-range chromosomal
interactions during postmitotic transcriptional reactivation. Genes & Development.
Cold Spring Harbor Laboratory Press. https://doi.org/10.1101/gad.335794.119
chicago: Kang, Hyeseon, Maxim N. Shokhirev, Zhichao Xu, Sahaana Chandran, Jesse
R. Dixon, and Martin Hetzer. “Dynamic Regulation of Histone Modifications and
Long-Range Chromosomal Interactions during Postmitotic Transcriptional Reactivation.”
Genes & Development. Cold Spring Harbor Laboratory Press, 2020. https://doi.org/10.1101/gad.335794.119.
ieee: H. Kang, M. N. Shokhirev, Z. Xu, S. Chandran, J. R. Dixon, and M. Hetzer,
“Dynamic regulation of histone modifications and long-range chromosomal interactions
during postmitotic transcriptional reactivation,” Genes & Development,
vol. 34, no. 13–14. Cold Spring Harbor Laboratory Press, pp. 913–930, 2020.
ista: Kang H, Shokhirev MN, Xu Z, Chandran S, Dixon JR, Hetzer M. 2020. Dynamic
regulation of histone modifications and long-range chromosomal interactions during
postmitotic transcriptional reactivation. Genes & Development. 34(13–14),
913–930.
mla: Kang, Hyeseon, et al. “Dynamic Regulation of Histone Modifications and Long-Range
Chromosomal Interactions during Postmitotic Transcriptional Reactivation.” Genes
& Development, vol. 34, no. 13–14, Cold Spring Harbor Laboratory Press,
2020, pp. 913–30, doi:10.1101/gad.335794.119.
short: H. Kang, M.N. Shokhirev, Z. Xu, S. Chandran, J.R. Dixon, M. Hetzer, Genes
& Development 34 (2020) 913–930.
date_created: 2022-04-07T07:44:09Z
date_published: 2020-04-28T00:00:00Z
date_updated: 2022-07-18T08:31:08Z
day: '28'
ddc:
- '570'
doi: 10.1101/gad.335794.119
extern: '1'
external_id:
pmid:
- '32499403'
file:
- access_level: open_access
checksum: 84e92d40e67936c739628315c238daf9
content_type: application/pdf
creator: dernst
date_created: 2022-04-08T07:12:33Z
date_updated: 2022-04-08T07:12:33Z
file_id: '11136'
file_name: 2020_GenesDevelopment_Kang.pdf
file_size: 4406772
relation: main_file
success: 1
file_date_updated: 2022-04-08T07:12:33Z
has_accepted_license: '1'
intvolume: ' 34'
issue: 13-14
keyword:
- Developmental Biology
- Genetics
language:
- iso: eng
month: '04'
oa: 1
oa_version: Published Version
page: 913-930
pmid: 1
publication: Genes & Development
publication_identifier:
issn:
- 0890-9369
- 1549-5477
publication_status: published
publisher: Cold Spring Harbor Laboratory Press
quality_controlled: '1'
scopus_import: '1'
status: public
title: Dynamic regulation of histone modifications and long-range chromosomal interactions
during postmitotic transcriptional reactivation
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: 72615eeb-f1f3-11ec-aa25-d4573ddc34fd
volume: 34
year: '2020'
...
---
_id: '11058'
abstract:
- lang: eng
text: Nucleoporin 93 (Nup93) expression inversely correlates with the survival of
triple-negative breast cancer patients. However, our knowledge of Nup93 function
in breast cancer besides its role as structural component of the nuclear pore
complex is not understood. Combination of functional assays and genetic analyses
suggested that chromatin interaction of Nup93 partially modulates the expression
of genes associated with actin cytoskeleton remodeling and epithelial to mesenchymal
transition, resulting in impaired invasion of triple-negative, claudin-low breast
cancer cells. Nup93 depletion induced stress fiber formation associated with reduced
cell migration/proliferation and impaired expression of mesenchymal-like genes.
Silencing LIMCH1, a gene responsible for actin cytoskeleton remodeling and up-regulated
upon Nup93 depletion, partially restored the invasive phenotype of cancer cells.
Loss of Nup93 led to significant defects in tumor establishment/propagation in
vivo, whereas patient samples revealed that high Nup93 and low LIMCH1 expression
correlate with late tumor stage. Our approach identified Nup93 as contributor
of triple-negative, claudin-low breast cancer cell invasion and paves the way
to study the role of nuclear envelope proteins during breast cancer tumorigenesis.
article_number: e201900623
article_processing_charge: No
article_type: original
author:
- first_name: Simone
full_name: Bersini, Simone
last_name: Bersini
- first_name: Nikki K
full_name: Lytle, Nikki K
last_name: Lytle
- first_name: Roberta
full_name: Schulte, Roberta
last_name: Schulte
- first_name: Ling
full_name: Huang, Ling
last_name: Huang
- first_name: Geoffrey M
full_name: Wahl, Geoffrey M
last_name: Wahl
- first_name: Martin W
full_name: HETZER, Martin W
id: 86c0d31b-b4eb-11ec-ac5a-eae7b2e135ed
last_name: HETZER
orcid: 0000-0002-2111-992X
citation:
ama: Bersini S, Lytle NK, Schulte R, Huang L, Wahl GM, Hetzer M. Nup93 regulates
breast tumor growth by modulating cell proliferation and actin cytoskeleton remodeling.
Life Science Alliance. 2020;3(1). doi:10.26508/lsa.201900623
apa: Bersini, S., Lytle, N. K., Schulte, R., Huang, L., Wahl, G. M., & Hetzer,
M. (2020). Nup93 regulates breast tumor growth by modulating cell proliferation
and actin cytoskeleton remodeling. Life Science Alliance. Life Science
Alliance. https://doi.org/10.26508/lsa.201900623
chicago: Bersini, Simone, Nikki K Lytle, Roberta Schulte, Ling Huang, Geoffrey M
Wahl, and Martin Hetzer. “Nup93 Regulates Breast Tumor Growth by Modulating Cell
Proliferation and Actin Cytoskeleton Remodeling.” Life Science Alliance.
Life Science Alliance, 2020. https://doi.org/10.26508/lsa.201900623.
ieee: S. Bersini, N. K. Lytle, R. Schulte, L. Huang, G. M. Wahl, and M. Hetzer,
“Nup93 regulates breast tumor growth by modulating cell proliferation and actin
cytoskeleton remodeling,” Life Science Alliance, vol. 3, no. 1. Life Science
Alliance, 2020.
ista: Bersini S, Lytle NK, Schulte R, Huang L, Wahl GM, Hetzer M. 2020. Nup93 regulates
breast tumor growth by modulating cell proliferation and actin cytoskeleton remodeling.
Life Science Alliance. 3(1), e201900623.
mla: Bersini, Simone, et al. “Nup93 Regulates Breast Tumor Growth by Modulating
Cell Proliferation and Actin Cytoskeleton Remodeling.” Life Science Alliance,
vol. 3, no. 1, e201900623, Life Science Alliance, 2020, doi:10.26508/lsa.201900623.
short: S. Bersini, N.K. Lytle, R. Schulte, L. Huang, G.M. Wahl, M. Hetzer, Life
Science Alliance 3 (2020).
date_created: 2022-04-07T07:44:18Z
date_published: 2020-01-01T00:00:00Z
date_updated: 2022-07-18T08:31:20Z
day: '01'
ddc:
- '570'
doi: 10.26508/lsa.201900623
extern: '1'
external_id:
pmid:
- '31959624'
file:
- access_level: open_access
checksum: 3bf33e7e93bef7823287807206b69b38
content_type: application/pdf
creator: dernst
date_created: 2022-04-08T07:33:01Z
date_updated: 2022-04-08T07:33:01Z
file_id: '11137'
file_name: 2020_LifeScienceAlliance_Bersini.pdf
file_size: 2653960
relation: main_file
success: 1
file_date_updated: 2022-04-08T07:33:01Z
has_accepted_license: '1'
intvolume: ' 3'
issue: '1'
keyword:
- Health
- Toxicology and Mutagenesis
- Plant Science
- Biochemistry
- Genetics and Molecular Biology (miscellaneous)
- Ecology
language:
- iso: eng
month: '01'
oa: 1
oa_version: Published Version
pmid: 1
publication: Life Science Alliance
publication_identifier:
issn:
- 2575-1077
publication_status: published
publisher: Life Science Alliance
quality_controlled: '1'
scopus_import: '1'
status: public
title: Nup93 regulates breast tumor growth by modulating cell proliferation and actin
cytoskeleton remodeling
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: 72615eeb-f1f3-11ec-aa25-d4573ddc34fd
volume: 3
year: '2020'
...
---
_id: '11503'
abstract:
- lang: eng
text: "Context. The Lyα emitter (LAE) fraction, XLAE, is a potentially powerful
probe of the evolution of the intergalactic neutral hydrogen gas fraction. However,
uncertainties in the measurement of XLAE are still under debate.\r\nAims. Thanks
to deep data obtained with the integral field spectrograph Multi Unit Spectroscopic
Explorer (MUSE), we can measure the evolution of the LAE fraction homogeneously
over a wide redshift range of z ≈ 3–6 for UV-faint galaxies (down to UV magnitudes
of M1500 ≈ −17.75). This is a significantly fainter range than in former studies
(M1500 ≤ −18.75) and it allows us to probe the bulk of the population of high-redshift
star-forming galaxies.\r\nMethods. We constructed a UV-complete photometric-redshift
sample following UV luminosity functions and measured the Lyα emission with MUSE
using the latest (second) data release from the MUSE Hubble Ultra Deep Field Survey.\r\nResults.
We derived the redshift evolution of XLAE for M1500 ∈ [ − 21.75; −17.75] for the
first time with a equivalent width range EW(Lyα) ≥ 65 Å and found low values of
XLAE ≲ 30% at z ≲ 6. The best-fit linear relation is XLAE = 0.07+0.06−0.03z −
0.22+0.12−0.24. For M1500 ∈ [ − 20.25; −18.75] and EW(Lyα) ≥ 25 Å, our XLAE values
are consistent with those in the literature within 1σ at z ≲ 5, but our median
values are systematically lower than reported values over the whole redshift range.
In addition, we do not find a significant dependence of XLAE on M1500 for EW(Lyα)
≥ 50 Å at z ≈ 3–4, in contrast with previous work. The differences in XLAE mainly
arise from selection biases for Lyman Break Galaxies (LBGs) in the literature:
UV-faint LBGs are more easily selected if they have strong Lyα emission, hence
XLAE is biased towards higher values when those samples are used.\r\nConclusions.
Our results suggest either a lower increase of XLAE towards z ≈ 6 than previously
suggested, or even a turnover of XLAE at z ≈ 5.5, which may be the signature of
a late or patchy reionization process. We compared our results with predictions
from a cosmological galaxy evolution model. We find that a model with a bursty
star formation (SF) can reproduce our observed LAE fractions much better than
models where SF is a smooth function of time."
acknowledgement: We thank the anonymous referee for constructive comments and suggestions.
We would like to express our gratitude to Stephane De Barros and Pablo Arrabal Haro
for kindly providing their data plotted in Figs. 1, 2, and 8. We are grateful to
Kazuhiro Shimasaku, Masami Ouchi, Rieko Momose, Daniel Schaerer, Hidenobu Yajima,
Taku Okamura, Makoto Ando, and Hinako Goto for giving insightful comments and suggestions.
This work is based on observations taken by VLT, which is operated by European Southern
Observatory. This research made use of Astropy (http://www.astropy.org), which is
a community-developed core Python package for Astronomy (Astropy Collaboration 2013,
2018), MARZ, MPDAF, and matplotlib (Hunter 2007). H.K. acknowledges support from
Japan Society for the Promotion of Science (JSPS) through the JSPS Research Fellowship
for Young Scientists and Overseas Challenge Program for Young Researchers. AV acknowledges
support from the ERC starting grant 757258-TRIPLE and the SNF Professorship 176808-TRIPLE.
This work was supported by the project FOGHAR (Agence Nationale de la Recherche,
ANR-13-BS05-0010-02). JB acknowledges support from the ORAGE project from the Agence
Nationale de la Recherche under grant ANR-14-CE33-0016-03. JR acknowledges support
from the ERC starting grant 336736-CALENDS. T. H. acknowledges supports by the Grant-inAid
for Scientic Research 19J01620.
article_number: A12
article_processing_charge: No
article_type: original
author:
- first_name: Haruka
full_name: Kusakabe, Haruka
last_name: Kusakabe
- first_name: Jérémy
full_name: Blaizot, Jérémy
last_name: Blaizot
- first_name: Thibault
full_name: Garel, Thibault
last_name: Garel
- first_name: Anne
full_name: Verhamme, Anne
last_name: Verhamme
- first_name: Roland
full_name: Bacon, Roland
last_name: Bacon
- first_name: Johan
full_name: Richard, Johan
last_name: Richard
- first_name: Takuya
full_name: Hashimoto, Takuya
last_name: Hashimoto
- first_name: Hanae
full_name: Inami, Hanae
last_name: Inami
- first_name: Simon
full_name: Conseil, Simon
last_name: Conseil
- first_name: Bruno
full_name: Guiderdoni, Bruno
last_name: Guiderdoni
- first_name: Alyssa B.
full_name: Drake, Alyssa B.
last_name: Drake
- first_name: Edmund
full_name: Christian Herenz, Edmund
last_name: Christian Herenz
- first_name: Joop
full_name: Schaye, Joop
last_name: Schaye
- first_name: Pascal
full_name: Oesch, Pascal
last_name: Oesch
- first_name: Jorryt J
full_name: Matthee, Jorryt J
id: 7439a258-f3c0-11ec-9501-9df22fe06720
last_name: Matthee
orcid: 0000-0003-2871-127X
- first_name: Raffaella
full_name: Anna Marino, Raffaella
last_name: Anna Marino
- first_name: Kasper
full_name: Borello Schmidt, Kasper
last_name: Borello Schmidt
- first_name: Roser
full_name: Pelló, Roser
last_name: Pelló
- first_name: Michael
full_name: Maseda, Michael
last_name: Maseda
- first_name: Floriane
full_name: Leclercq, Floriane
last_name: Leclercq
- first_name: Josephine
full_name: Kerutt, Josephine
last_name: Kerutt
- first_name: Guillaume
full_name: Mahler, Guillaume
last_name: Mahler
citation:
ama: 'Kusakabe H, Blaizot J, Garel T, et al. The MUSE Hubble Ultra Deep Field Survey:
XIV. Evolution of the Lyα emitter fraction from z = 3 to z = 6. Astronomy &
Astrophysics. 2020;638. doi:10.1051/0004-6361/201937340'
apa: 'Kusakabe, H., Blaizot, J., Garel, T., Verhamme, A., Bacon, R., Richard, J.,
… Mahler, G. (2020). The MUSE Hubble Ultra Deep Field Survey: XIV. Evolution of
the Lyα emitter fraction from z = 3 to z = 6. Astronomy & Astrophysics.
EDP Sciences. https://doi.org/10.1051/0004-6361/201937340'
chicago: 'Kusakabe, Haruka, Jérémy Blaizot, Thibault Garel, Anne Verhamme, Roland
Bacon, Johan Richard, Takuya Hashimoto, et al. “The MUSE Hubble Ultra Deep Field
Survey: XIV. Evolution of the Lyα Emitter Fraction from z = 3 to z = 6.” Astronomy
& Astrophysics. EDP Sciences, 2020. https://doi.org/10.1051/0004-6361/201937340.'
ieee: 'H. Kusakabe et al., “The MUSE Hubble Ultra Deep Field Survey: XIV.
Evolution of the Lyα emitter fraction from z = 3 to z = 6,” Astronomy &
Astrophysics, vol. 638. EDP Sciences, 2020.'
ista: 'Kusakabe H, Blaizot J, Garel T, Verhamme A, Bacon R, Richard J, Hashimoto
T, Inami H, Conseil S, Guiderdoni B, Drake AB, Christian Herenz E, Schaye J, Oesch
P, Matthee JJ, Anna Marino R, Borello Schmidt K, Pelló R, Maseda M, Leclercq F,
Kerutt J, Mahler G. 2020. The MUSE Hubble Ultra Deep Field Survey: XIV. Evolution
of the Lyα emitter fraction from z = 3 to z = 6. Astronomy & Astrophysics.
638, A12.'
mla: 'Kusakabe, Haruka, et al. “The MUSE Hubble Ultra Deep Field Survey: XIV. Evolution
of the Lyα Emitter Fraction from z = 3 to z = 6.” Astronomy & Astrophysics,
vol. 638, A12, EDP Sciences, 2020, doi:10.1051/0004-6361/201937340.'
short: H. Kusakabe, J. Blaizot, T. Garel, A. Verhamme, R. Bacon, J. Richard, T.
Hashimoto, H. Inami, S. Conseil, B. Guiderdoni, A.B. Drake, E. Christian Herenz,
J. Schaye, P. Oesch, J.J. Matthee, R. Anna Marino, K. Borello Schmidt, R. Pelló,
M. Maseda, F. Leclercq, J. Kerutt, G. Mahler, Astronomy & Astrophysics 638
(2020).
date_created: 2022-07-06T09:50:48Z
date_published: 2020-06-03T00:00:00Z
date_updated: 2022-07-19T09:35:20Z
day: '03'
doi: 10.1051/0004-6361/201937340
extern: '1'
external_id:
arxiv:
- '2003.12083'
intvolume: ' 638'
keyword:
- Space and Planetary Science
- Astronomy and Astrophysics
- 'dark ages / reionization / first stars / early Universe / cosmology: observations
/ galaxies: evolution / galaxies: high-redshift / intergalactic medium'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/2003.12083
month: '06'
oa: 1
oa_version: Published Version
publication: Astronomy & Astrophysics
publication_identifier:
eissn:
- 1432-0746
issn:
- 0004-6361
publication_status: published
publisher: EDP Sciences
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'The MUSE Hubble Ultra Deep Field Survey: XIV. Evolution of the Lyα emitter
fraction from z = 3 to z = 6'
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 638
year: '2020'
...