Jean-Vianney Barnier
Overview
Explore the profile of Jean-Vianney Barnier including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
26
Citations
432
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
11.
Baudouin L, Ades N, Kante K, Czarnecki A, Bachelin C, Baskaran A, et al.
Glia
. 2021 Apr;
69(8):1916-1931.
PMID: 33811384
Common in vitro models used to study the mechanisms regulating myelination rely on co-cultures of oligodendrocyte precursor cells (OPCs) and neurons. In such models, myelination occurs in an environment that...
12.
Belmaati Cherkaoui M, Vacca O, Izabelle C, Boulay A, Boulogne C, Gillet C, et al.
Glia
. 2020 Nov;
69(4):954-970.
PMID: 33247858
Intellectual disability in Duchenne muscular dystrophy has been associated with the loss of dystrophin-protein 71, Dp71, the main dystrophin-gene product in the adult brain. Dp71 shows major expression in perivascular...
13.
Castillon C, Gonzalez L, Domenichini F, Guyon S, Da Silva K, Durand C, et al.
Hum Mol Genet
. 2020 Jan;
29(12):1950-1968.
PMID: 31943058
The link between mutations associated with intellectual disability (ID) and the mechanisms underlying cognitive dysfunctions remains largely unknown. Here, we focused on PAK3, a serine/threonine kinase whose gene mutations cause...
14.
Duarte K, Heide S, Poea-Guyon S, Rousseau V, Depienne C, Rastetter A, et al.
Neurobiol Dis
. 2019 Dec;
136:104709.
PMID: 31843706
Corpus callosum agenesis (CCA) is a brain malformation associated with a wide clinical spectrum including intellectual disability (ID) and an etiopathological complexity. We identified a novel missense G424R mutation in...
15.
Franchi S, Astro V, Macco R, Tonoli D, Barnier J, Botta M, et al.
Front Cell Neurosci
. 2017 Jan;
10:289.
PMID: 28066185
Interneurons are essential modulators of brain activity and their abnormal maturation may lead to neural and intellectual disabilities. Here we show that cultures derived from murine medial ganglionic eminences (MGEs)...
16.
Maglorius Renkilaraj M, Baudouin L, Wells C, Doulazmi M, Wehrle R, Cannaya V, et al.
Neurobiol Dis
. 2016 Dec;
98:137-148.
PMID: 27940202
Oligodendrocyte and myelin deficits have been reported in mental/psychiatric diseases. The p21-activated kinase 3 (PAK3), a serine/threonine kinase, whose activity is stimulated by the binding of active Rac and Cdc42...
17.
Perez-Nunez R, Barraza N, Gonzalez-Jamett A, Cardenas A, Barnier J, Caviedes P
Neurotox Res
. 2016 Mar;
30(1):76-87.
PMID: 26966010
In humans, Down syndrome (DS) is caused by the presence of an extra copy of autosome 21. The most striking finding in DS patients is intellectual disability and the onset...
18.
Piccand J, Meunier A, Merle C, Jia Z, Barnier J, Gradwohl G
Diabetes
. 2013 Oct;
63(1):203-15.
PMID: 24163148
The transcription factor neurogenin3 (Ngn3) triggers islet cell differentiation in the developing pancreas. However, little is known about the molecular mechanisms coupling cell cycle exit and differentiation in Ngn3(+) islet...
19.
Combeau G, Kreis P, Domenichini F, Amar M, Fossier P, Rousseau V, et al.
J Biol Chem
. 2012 Jul;
287(36):30084-96.
PMID: 22815483
p21-activated kinase 1 (PAK1) and PAK3 belong to group I of the PAK family and control cell movement and division. They also regulate dendritic spine formation and maturation in the...
20.
Dubos A, Combeau G, Bernardinelli Y, Barnier J, Hartley O, Gaertner H, et al.
J Neurosci
. 2012 Jan;
32(2):519-27.
PMID: 22238087
Several gene mutations linked to intellectual disability in humans code for synaptic molecules implicated in small GTPase signaling. This is the case of the Rac/Cdc42 effector p21-activated kinase 3 (PAK3)....