Zobrazeno 1 - 10
of 162
pro vyhledávání: '"Arie, Horowitz"'
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 12 (2024)
Externí odkaz:
https://doaj.org/article/15bc0096e6e64a9480b55feb7681328a
Autor:
Florent Marguet, Myriam Vezain, Pascale Marcorelles, Séverine Audebert-Bellanger, Kévin Cassinari, Nathalie Drouot, Pascal Chambon, Bruno J. Gonzalez, Arie Horowitz, Annie Laquerriere, Pascale Saugier-Veber
Publikováno v:
Acta Neuropathologica Communications, Vol 9, Iss 1, Pp 1-7 (2021)
Abstract The prevalence of congenital hydrocephalus has been estimated at 1.1 per 1000 infants when including cases diagnosed before 1 year of age after exclusion of neural tube defects. Classification criteria are based either on CSF dynamics, patho
Externí odkaz:
https://doaj.org/article/a05c3f30da5b41a0a0d5ebe0f0978624
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 14 (2020)
Externí odkaz:
https://doaj.org/article/5f979bc0ebed485db6fb5c7bfb33abb2
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:
Patrick Lüningschrör, Beyenech Binotti, Benjamin Dombert, Peter Heimann, Angel Perez-Lara, Carsten Slotta, Nadine Thau-Habermann, Cora R. von Collenberg, Franziska Karl, Markus Damme, Arie Horowitz, Isabelle Maystadt, Annette Füchtbauer, Ernst-Martin Füchtbauer, Sibylle Jablonka, Robert Blum, Nurcan Üçeyler, Susanne Petri, Barbara Kaltschmidt, Reinhard Jahn, Christian Kaltschmidt, Michael Sendtner
Publikováno v:
Nature Communications, Vol 8, Iss 1, Pp 1-17 (2017)
Accumulating evidence suggests that disruption of autophagy is associated with neurodegeneration. Here the authors show that Plekhg5 acts as a GEF for Rab26, a small GTPase that promotes the autophagy of synaptic vesicles in neurons; mice lacking Ple
Externí odkaz:
https://doaj.org/article/ba7baaeefffb431d9f931d09c46a1a22
Publikováno v:
Nature Reviews Gastroenterology & Hepatology.
Autor:
Myriam Vezain, Bruno J. Gonzalez, Florent Marguet, Annie Laquerrière, Nathalie Drouot, Arie Horowitz, Pascale Saugier-Veber, Kévin Cassinari, Pascale Marcorelles, Séverine Audebert-Bellanger, Pascal Chambon
Publikováno v:
Acta Neuropathologica Communications
Acta Neuropathologica Communications, Vol 9, Iss 1, Pp 1-7 (2021)
Acta Neuropathologica Communications, Vol 9, Iss 1, Pp 1-7 (2021)
The prevalence of congenital hydrocephalus has been estimated at 1.1 per 1000 infants when including cases diagnosed before 1 year of age after exclusion of neural tube defects. Classification criteria are based either on CSF dynamics, pathophysiolog
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 14 (2020)
Frontiers in Cellular Neuroscience
Frontiers in Cellular Neuroscience
The purpose of this mini-review is to examine if publicly available cerebrospinal fluid (CSF) proteomics data sets can be exploited to provide insight into the etiology of hydrocephalus, into the character of the injury inflicted on the parenchyma by
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
Autor:
Arie Horowitz
Publikováno v:
EMBO Rep
Comment on "Close loop peer review" by Michael Hill.