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Jamel Chelly

Showing results (61-70 of 226) with videos related to

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European Journal of Human Genetics : EJHG|June 5, 2008
A novel splice mutation in PAK3 gene underlying mental retardation with neuropsychiatric featuresImen Rejeb, Yoann Saillour, Laetitia Castelnau, et al.
The EMBO Journal|September 8, 2006
Distinct roles of doublecortin modulating the microtubule cytoskeletonCarolyn A Moores, Mylène Perderiset, Caroline Kappeler, et al.
Neuromuscular Disorders : NMD|March 24, 2009
Use of SNP array analysis to identify a novel TRIM32 mutation in limb-girdle muscular dystrophy type 2HMireille Cossée, Clotilde Lagier-Tourenne, Claire Seguela, et al.
American Journal of Medical Genetics. Part A|March 14, 2007
Sequence variation in ultraconserved and highly conserved elements does not cause X-linked mental retardationArmand Bottani, Jamel Chelly, Arjan P M de Brouwer, et al.
The European Journal of Neuroscience|October 9, 2009
IL1RAPL1 controls inhibitory networks during cerebellar development in miceFrédéric Gambino, Marie Kneib, Alice Pavlowsky, et al.
American Journal of Medical Genetics. Part A|September 2, 2003
A gene for nonsyndromic X-linked mental retardation (MRX77) maps to Xq12-Xq21.33Carolina Sismani, Maria Syrrou, Kyproula Christodoulou, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|May 30, 2008
Cell-autonomous roles of ARX in cell proliferation and neuronal migration during corticogenesisGaëlle Friocourt, Shigeaki Kanatani, Hidenori Tabata, et al.
European Journal of Medical Genetics|November 11, 2008
Impairment of cerebello-thalamo-frontal pathway in Rab-GDI mutated patients with pure mental deficiencyAurore Curie, Silvia Sacco, Gérald Bussy, et al.
Plos One|February 6, 2009
Clinical heterogeneity of duchenne muscular dystrophy (DMD): definition of sub-phenotypes and predictive criteria by long-term follow-upIsabelle Desguerre, Christo Christov, Michele Mayer, et al.
Human Molecular Genetics|April 30, 2009
Inhibition of RhoA pathway rescues the endocytosis defects in Oligophrenin1 mouse model of mental retardationMalik Khelfaoui, Alice Pavlowsky, Andrew D Powell, et al.
Pageof 23

Showing results (61-70 of 226) with videos related to

Sort By:
Pageof 23
European Journal of Human Genetics : EJHG|June 5, 2008
A novel splice mutation in PAK3 gene underlying mental retardation with neuropsychiatric featuresImen Rejeb, Yoann Saillour, Laetitia Castelnau, et al.
The EMBO Journal|September 8, 2006
Distinct roles of doublecortin modulating the microtubule cytoskeletonCarolyn A Moores, Mylène Perderiset, Caroline Kappeler, et al.
Neuromuscular Disorders : NMD|March 24, 2009
Use of SNP array analysis to identify a novel TRIM32 mutation in limb-girdle muscular dystrophy type 2HMireille Cossée, Clotilde Lagier-Tourenne, Claire Seguela, et al.
American Journal of Medical Genetics. Part A|March 14, 2007
Sequence variation in ultraconserved and highly conserved elements does not cause X-linked mental retardationArmand Bottani, Jamel Chelly, Arjan P M de Brouwer, et al.
The European Journal of Neuroscience|October 9, 2009
IL1RAPL1 controls inhibitory networks during cerebellar development in miceFrédéric Gambino, Marie Kneib, Alice Pavlowsky, et al.
American Journal of Medical Genetics. Part A|September 2, 2003
A gene for nonsyndromic X-linked mental retardation (MRX77) maps to Xq12-Xq21.33Carolina Sismani, Maria Syrrou, Kyproula Christodoulou, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|May 30, 2008
Cell-autonomous roles of ARX in cell proliferation and neuronal migration during corticogenesisGaëlle Friocourt, Shigeaki Kanatani, Hidenori Tabata, et al.
European Journal of Medical Genetics|November 11, 2008
Impairment of cerebello-thalamo-frontal pathway in Rab-GDI mutated patients with pure mental deficiencyAurore Curie, Silvia Sacco, Gérald Bussy, et al.
Plos One|February 6, 2009
Clinical heterogeneity of duchenne muscular dystrophy (DMD): definition of sub-phenotypes and predictive criteria by long-term follow-upIsabelle Desguerre, Christo Christov, Michele Mayer, et al.
Human Molecular Genetics|April 30, 2009
Inhibition of RhoA pathway rescues the endocytosis defects in Oligophrenin1 mouse model of mental retardationMalik Khelfaoui, Alice Pavlowsky, Andrew D Powell, et al.
Pageof 23