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Jamel Chelly

Showing results (1-10 of 226) with videos related to

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Handbook of Clinical Neurology|April 30, 2013
Progressive muscular dystrophiesJamel Chelly, Isabelle Desguerre
Nature Reviews. Genetics|May 19, 2006
Molecular genetics of Rett syndrome: when DNA methylation goes unrecognizedThierry Bienvenu, Jamel Chelly
Neuron|June 24, 2003
From fragile X mental retardation protein to Rac1 GTPase: new insights from Fly CYFIPPierre Billuart, Jamel Chelly
European Journal of Human Genetics : EJHG|August 21, 2004
Monogenic X-linked mental retardation: is it as frequent as currently estimated? The paradox of the ARX (Aristaless X) mutationsJean-Louis Mandel, Jamel Chelly
Journal of Neuropathology and Experimental Neurology|May 3, 2006
Pitfalls of the morphologic approachFerechte Encha-Razavi, Jamel Chelly
Trends in Genetics : TIG|October 30, 2009
Tubulin-related cortical dysgeneses: microtubule dysfunction underlying neuronal migration defectsXavier H Jaglin, Jamel Chelly
Medecine Sciences : M/S|November 9, 2005
[X-linked mental retardation]Pierre Billuart, Jamel Chelly, Simone Gilgenkrantz
Medecine Sciences : M/S|February 15, 2008
[Effective exon skipping in humans: a symbolic but promising jump into DMD therapy]Jean-Claude Kaplan, Jamel Chelly, Luis Garcia
Journal of Neurochemistry|February 3, 2009
X-linked mental retardation: focus on synaptic function and plasticityYann Humeau, Frédéric Gambino, Jamel Chelly, et al.
Neurogenetics|September 25, 2012
Refining the phenotype associated with MEF2C point mutationsThierry Bienvenu, Bertrand Diebold, Jamel Chelly, et al.
Pageof 23

Showing results (1-10 of 226) with videos related to

Sort By:
Pageof 23
Handbook of Clinical Neurology|April 30, 2013
Progressive muscular dystrophiesJamel Chelly, Isabelle Desguerre
Nature Reviews. Genetics|May 19, 2006
Molecular genetics of Rett syndrome: when DNA methylation goes unrecognizedThierry Bienvenu, Jamel Chelly
Neuron|June 24, 2003
From fragile X mental retardation protein to Rac1 GTPase: new insights from Fly CYFIPPierre Billuart, Jamel Chelly
European Journal of Human Genetics : EJHG|August 21, 2004
Monogenic X-linked mental retardation: is it as frequent as currently estimated? The paradox of the ARX (Aristaless X) mutationsJean-Louis Mandel, Jamel Chelly
Journal of Neuropathology and Experimental Neurology|May 3, 2006
Pitfalls of the morphologic approachFerechte Encha-Razavi, Jamel Chelly
Trends in Genetics : TIG|October 30, 2009
Tubulin-related cortical dysgeneses: microtubule dysfunction underlying neuronal migration defectsXavier H Jaglin, Jamel Chelly
Medecine Sciences : M/S|November 9, 2005
[X-linked mental retardation]Pierre Billuart, Jamel Chelly, Simone Gilgenkrantz
Medecine Sciences : M/S|February 15, 2008
[Effective exon skipping in humans: a symbolic but promising jump into DMD therapy]Jean-Claude Kaplan, Jamel Chelly, Luis Garcia
Journal of Neurochemistry|February 3, 2009
X-linked mental retardation: focus on synaptic function and plasticityYann Humeau, Frédéric Gambino, Jamel Chelly, et al.
Neurogenetics|September 25, 2012
Refining the phenotype associated with MEF2C point mutationsThierry Bienvenu, Bertrand Diebold, Jamel Chelly, et al.
Pageof 23