Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Junning, Yang"'
Autor:
Junning Yang, Claire Simonneau, Robert Kilker, Laura Oakley, Matthew D Byrne, Zuzana Nichtova, Ioana Stefanescu, Fnu Pardeep‐Kumar, Sushil Tripathi, Eric Londin, Pascale Saugier‐Veber, Belinda Willard, Mathew Thakur, Stephen Pickup, Hiroshi Ishikawa, Horst Schroten, Richard Smeyne, Arie Horowitz
Publikováno v:
EMBO Molecular Medicine, Vol 11, Iss 1, Pp 1-19 (2018)
Abstract Though congenital hydrocephalus is heritable, it has been linked only to eight genes, one of which is MPDZ. Humans and mice that carry a truncated version of MPDZ incur severe hydrocephalus resulting in acute morbidity and lethality. We show
Externí odkaz:
https://doaj.org/article/9e7dfd6574c64708bffe246dee632cbb
Publikováno v:
Expert Review of Molecular Diagnostics. 21:723-732
Rapid and accurate diagnostic approaches are essential for impeding the spread of infectious diseases. This review aims to summarize current progress of clustered regularly interspaced short palindromic repeats (CRISPR)-associated (Cas) systems in th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba91742cf4229f45ca0826d6e2ef58e8
https://doi.org/10.1080/14737159.2021.1922080
https://doi.org/10.1080/14737159.2021.1922080
Publikováno v:
Small GTPases. 10:26-32
In this commentary we discuss a paper we published recently on the activities of the GTPase RhoA during neural differentiation of murine embryonic stem cells, and relate our findings to previous studies. We narrate how we found that RhoA impedes neur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97d52a79ed4914d295a0065a6f9bd64f
https://doi.org/10.1080/21541248.2016.1273171
https://doi.org/10.1080/21541248.2016.1273171
Autor:
Junning Yang, Claire Simonneau, Robert Kilker, Laura Oakley, Matthew D Byrne, Zuzana Nichtova, Ioana Stefanescu, Fnu Pardeep‐Kumar, Sushil Tripathi, Eric Londin, Pascale Saugier‐Veber, Belinda Willard, Mathew Thakur, Stephen Pickup, Hiroshi Ishikawa, Horst Schroten, Richard Smeyne, Arie Horowitz
Publikováno v:
EMBO Molecular Medicine, Vol 11, Iss 1, Pp n/a-n/a (2019)
Though congenital hydrocephalus is heritable, it has been linked only to eight genes, one of which is MPDZ. Humans and mice that carry a truncated version of MPDZ incur severe hydrocephalus resulting in acute morbidity and lethality. We show by magne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::d220c04d80925615277c0e17425484f5
https://doaj.org/article/9e7dfd6574c64708bffe246dee632cbb
https://doaj.org/article/9e7dfd6574c64708bffe246dee632cbb
Autor:
Junning, Yang, Claire, Simonneau, Robert, Kilker, Laura, Oakley, Matthew D, Byrne, Zuzana, Nichtova, Ioana, Stefanescu, Fnu, Pardeep-Kumar, Sushil, Tripathi, Eric, Londin, Pascale, Saugier-Veber, Belinda, Willard, Mathew, Thakur, Stephen, Pickup, Hiroshi, Ishikawa, Horst, Schroten, Richard, Smeyne, Arie, Horowitz
Publikováno v:
EMBO Molecular Medicine
Though congenital hydrocephalus is heritable, it has been linked only to eight genes, one of which is MPDZ. Humans and mice that carry a truncated version of MPDZ incur severe hydrocephalus resulting in acute morbidity and lethality. We show by magne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cadab8f6e98b4d2a22f527dfe52aa6d5
https://pubmed.ncbi.nlm.nih.gov/30518636
https://pubmed.ncbi.nlm.nih.gov/30518636
Autor:
Eric Londin, Arie Horowitz, Robert Kilker, Paolo Fortina, Claire Simonneau, Leonard C. Edelstein, Junning Yang, Xianguo Kong
Publikováno v:
Scientific Reports, Vol 9, Iss 1, Pp 1-14 (2019)
Scientific Reports
Scientific Reports
The impermeability of the luminal endothelial cell monolayer is crucial for the normal performance of the vascular and lymphatic systems. A key to this function is the integrity of the monolayer’s intercellular junctions. The known repertoire of ju
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55d0d96ef939f229dae300f0d4818bdc
https://doi.org/10.1101/471854
https://doi.org/10.1101/471854
Autor:
Arie Horowitz, Fnu Pardeep-Kumar, Belinda Willard, Mathew L. Thakur, Junning Yang, Matthew D. Byrne, Robert Kilker, Zuzana Nichtova, Claire Simonneau, Eric Londin, Pascale Saugier-Veber, Stephen Pickup, Richard J. Smeyne, Sushil K. Tripathi, Laura Oakley, Ioana Stefanescu
Though congenital hydrocephalus is heritable, it has been linked only to eight genes, one of which isMPDZ. Humans and mice that carry a truncated version of MPDZ incur severe hydrocephalus resulting in acute morbidity and lethality. We show by magnet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce608700380b4bd4adb8152c26933cfe
Publikováno v:
Science Signaling. 9
Spontaneous neural differentiation of embryonic stem cells is induced by Noggin-mediated inhibition of bone morphogenetic protein 4 (BMP4) signaling. RhoA is a guanosine triphosphatase (GTPase) that regulates cytoskeletal dynamics and gene expression
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f94fe0ca75e1b00d3cb1762885bca0d
https://doi.org/10.1126/scisignal.aaf0791
https://doi.org/10.1126/scisignal.aaf0791
Autor:
Junning Yang, Chuanshen Wu, Stefanescu, Ioana, Jakobsson, Lars, Chervoneva, Inna, Horowitz, Arie
Publikováno v:
Science Signaling; 7/26/2016, Vol. 9 Issue 438, p1-12, 12p