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Science Advances
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July 30, 2025
GPR161 mechanosensitivity at the primary cilium drives neuronal saltatory migration
Théo Paillard, Ada Allam, Mohamed Doulazmi, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
October 10, 2003
The transmembrane semaphorin Sema4D/CD100, an inhibitor of axonal growth, is expressed on oligodendrocytes and upregulated after CNS lesion
Caroline Moreau-Fauvarque, Atsushi Kumanogoh, Emeline Camand, et al.
BMC Genomics
|
April 1, 2009
Gene expression signature of cerebellar hypoplasia in a mouse model of Down syndrome during postnatal development
Julien Laffaire, Isabelle Rivals, Luce Dauphinot, et al.
Neurobiology of Disease
|
December 13, 2016
The intellectual disability protein PAK3 regulates oligodendrocyte precursor cell differentiation
Majistor Raj Luxman Maglorius Renkilaraj, Lucas Baudouin, Claire M Wells, et al.
Cell Reports
|
January 20, 2021
Loss of floor plate Netrin-1 impairs midline crossing of corticospinal axons and leads to mirror movements
Oriane Pourchet, Marie-Pierre Morel, Quentin Welniarz, et al.
Scientific Reports
|
March 26, 2017
Non cell-autonomous role of DCC in the guidance of the corticospinal tract at the midline
Quentin Welniarz, Marie-Pierre Morel, Oriane Pourchet, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
May 31, 2013
Mature Purkinje cells require the retinoic acid-related orphan receptor-α (RORα) to maintain climbing fiber mono-innervation and other adult characteristics
Xiao Ru Chen, Nicolas Heck, Ann M Lohof, et al.
Journal of Medical Genetics
|
June 12, 2023
Congenital mirror movements are associated with defective polymerisation of RAD51
Oriane Trouillard, Pauline Dupaigne, Margaux Dunoyer, et al.
Human Brain Mapping
|
January 18, 2019
The supplementary motor area modulates interhemispheric interactions during movement preparation
Quentin Welniarz, Cécile Gallea, Jean-Charles Lamy, et al.
American Journal of Human Genetics
|
February 7, 2012
RAD51 haploinsufficiency causes congenital mirror movements in humans
Christel Depienne, Delphine Bouteiller, Aurélie Méneret, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 42) with videos related to
Sort By:
Page
of 5
Science Advances
|
July 30, 2025
GPR161 mechanosensitivity at the primary cilium drives neuronal saltatory migration
Théo Paillard, Ada Allam, Mohamed Doulazmi, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
October 10, 2003
The transmembrane semaphorin Sema4D/CD100, an inhibitor of axonal growth, is expressed on oligodendrocytes and upregulated after CNS lesion
Caroline Moreau-Fauvarque, Atsushi Kumanogoh, Emeline Camand, et al.
BMC Genomics
|
April 1, 2009
Gene expression signature of cerebellar hypoplasia in a mouse model of Down syndrome during postnatal development
Julien Laffaire, Isabelle Rivals, Luce Dauphinot, et al.
Neurobiology of Disease
|
December 13, 2016
The intellectual disability protein PAK3 regulates oligodendrocyte precursor cell differentiation
Majistor Raj Luxman Maglorius Renkilaraj, Lucas Baudouin, Claire M Wells, et al.
Cell Reports
|
January 20, 2021
Loss of floor plate Netrin-1 impairs midline crossing of corticospinal axons and leads to mirror movements
Oriane Pourchet, Marie-Pierre Morel, Quentin Welniarz, et al.
Scientific Reports
|
March 26, 2017
Non cell-autonomous role of DCC in the guidance of the corticospinal tract at the midline
Quentin Welniarz, Marie-Pierre Morel, Oriane Pourchet, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
May 31, 2013
Mature Purkinje cells require the retinoic acid-related orphan receptor-α (RORα) to maintain climbing fiber mono-innervation and other adult characteristics
Xiao Ru Chen, Nicolas Heck, Ann M Lohof, et al.
Journal of Medical Genetics
|
June 12, 2023
Congenital mirror movements are associated with defective polymerisation of RAD51
Oriane Trouillard, Pauline Dupaigne, Margaux Dunoyer, et al.
Human Brain Mapping
|
January 18, 2019
The supplementary motor area modulates interhemispheric interactions during movement preparation
Quentin Welniarz, Cécile Gallea, Jean-Charles Lamy, et al.
American Journal of Human Genetics
|
February 7, 2012
RAD51 haploinsufficiency causes congenital mirror movements in humans
Christel Depienne, Delphine Bouteiller, Aurélie Méneret, et al.
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of 5