Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Robert, Kilker"'
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
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