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Jamel Chelly

Showing results (11-20 of 226) with videos related to

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Annals of Clinical and Translational Neurology|August 9, 2019
Impaired glycinergic transmission in hyperekplexia: a model of parasomnia overlap disorderRégis Lopez, François Rivier, Jamel Chelly, et al.
European Journal of Human Genetics : EJHG|May 25, 2006
Genetics and pathophysiology of mental retardationJamel Chelly, Malik Khelfaoui, Fiona Francis, et al.
Journal of Human Genetics|December 3, 2010
An isoform of the severe encephalopathy-related CDKL5 gene, including a novel exon with extremely high sequence conservation, is specifically expressed in brainYann Fichou, Juliette Nectoux, Nadia Bahi-Buisson, et al.
FEBS Letters|December 15, 2012
MeCP2 deficiency is associated with impaired microtubule stabilityChloé Delépine, Juliette Nectoux, Nadia Bahi-Buisson, et al.
The European Journal of Neuroscience|March 8, 2006
The role of ARX in cortical developmentGaëlle Friocourt, Karine Poirier, Sonja Rakić, et al.
Developmental Neuroscience|December 14, 2007
Alternative transcripts of Dclk1 and Dclk2 and their expression in doublecortin knockout miceFrançoise Phan Dinh Tuy, Yoann Saillour, Caroline Kappeler, et al.
Plos One|July 14, 2010
Synaptic maturation at cortical projections to the lateral amygdala in a mouse model of Rett syndromeFrédéric Gambino, Malik Khelfaoui, Bernard Poulain, et al.
Journal of the Neurological Sciences|June 23, 2019
A novel heterozygous ANO3 mutation responsible for myoclonic dystoniaChloé Laurencin, Emmanuel Broussolle, Teodor Danaila, et al.
American Journal of Medical Genetics. Part A|July 6, 2010
Somatic mosaicism for a CDKL5 mutation as an epileptic encephalopathy in malesJulien Masliah-Plachon, Stéphane Auvin, Juliette Nectoux, et al.
Cerebral Cortex (New York, N.Y. : 1991)|May 24, 2003
Doublecortin functions at the extremities of growing neuronal processesGaëlle Friocourt, Annette Koulakoff, Philippe Chafey, et al.
Pageof 23

Showing results (11-20 of 226) with videos related to

Sort By:
Pageof 23
Annals of Clinical and Translational Neurology|August 9, 2019
Impaired glycinergic transmission in hyperekplexia: a model of parasomnia overlap disorderRégis Lopez, François Rivier, Jamel Chelly, et al.
European Journal of Human Genetics : EJHG|May 25, 2006
Genetics and pathophysiology of mental retardationJamel Chelly, Malik Khelfaoui, Fiona Francis, et al.
Journal of Human Genetics|December 3, 2010
An isoform of the severe encephalopathy-related CDKL5 gene, including a novel exon with extremely high sequence conservation, is specifically expressed in brainYann Fichou, Juliette Nectoux, Nadia Bahi-Buisson, et al.
FEBS Letters|December 15, 2012
MeCP2 deficiency is associated with impaired microtubule stabilityChloé Delépine, Juliette Nectoux, Nadia Bahi-Buisson, et al.
The European Journal of Neuroscience|March 8, 2006
The role of ARX in cortical developmentGaëlle Friocourt, Karine Poirier, Sonja Rakić, et al.
Developmental Neuroscience|December 14, 2007
Alternative transcripts of Dclk1 and Dclk2 and their expression in doublecortin knockout miceFrançoise Phan Dinh Tuy, Yoann Saillour, Caroline Kappeler, et al.
Plos One|July 14, 2010
Synaptic maturation at cortical projections to the lateral amygdala in a mouse model of Rett syndromeFrédéric Gambino, Malik Khelfaoui, Bernard Poulain, et al.
Journal of the Neurological Sciences|June 23, 2019
A novel heterozygous ANO3 mutation responsible for myoclonic dystoniaChloé Laurencin, Emmanuel Broussolle, Teodor Danaila, et al.
American Journal of Medical Genetics. Part A|July 6, 2010
Somatic mosaicism for a CDKL5 mutation as an epileptic encephalopathy in malesJulien Masliah-Plachon, Stéphane Auvin, Juliette Nectoux, et al.
Cerebral Cortex (New York, N.Y. : 1991)|May 24, 2003
Doublecortin functions at the extremities of growing neuronal processesGaëlle Friocourt, Annette Koulakoff, Philippe Chafey, et al.
Pageof 23