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Jamel Chelly

Showing results (41-50 of 226) with videos related to

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European Journal of Human Genetics : EJHG|June 26, 2003
In vitro follicular growth affects oocyte imprinting establishment in miceAntoine Kerjean, Philippe Couvert, Thomas Heams, et al.
European Journal of Human Genetics : EJHG|March 17, 2005
Mutations in exon 1 of MECP2B are not a common cause of X-linked mental retardation in malesKarine Poirier, Fiona Francis, Ben Hamel, et al.
American Journal of Medical Genetics. Part A|November 18, 2008
Novel mutation of IL1RAPL1 gene in a nonspecific X-linked mental retardation (MRX) familyMagdalena Nawara, Jakub Klapecki, Katarzyna Borg, et al.
Pediatric Neurology|October 2, 2007
Netrin G1 mutations are an uncommon cause of atypical Rett syndrome with or without epilepsyJuliette Nectoux, Benoit Girard, Nadia Bahi-Buisson, et al.
The Journal of Physiology|November 30, 2011
Rapid reversal of impaired inhibitory and excitatory transmission but not spine dysgenesis in a mouse model of mental retardationAndrew D Powell, Kalbinder K Gill, Pierre-Philippe Saintot, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 21, 2009
Epileptic encephalopathy in a girl with an interstitial deletion of Xp22 comprising promoter and exon 1 of the CDKL5 geneNadia Bahi-Buisson, Benoit Girard, Agnes Gautier, et al.
Genetic Testing|August 16, 2002
Spectrum of MECP2 mutations in Rett syndromeThierry Bienvenu, Laurent Villard, Nicolas De Roux, et al.
The Journal of Biological Chemistry|June 18, 2002
Active caspase-8 translocates into the nucleus of apoptotic cells to inactivate poly(ADP-ribose) polymerase-2Alexandra Benchoua, Cécile Couriaud, Christelle Guégan, et al.
BMC Neurology|November 25, 2016
A step toward essential tremor gene discovery: identification of extreme phenotype and screening of HTRA2 and ANO3Mathilde Renaud, Christophe Marcel, Gabrielle Rudolf, et al.
Molecular and Cellular Neurosciences|August 23, 2003
The RhoGAP activity of OPHN1, a new F-actin-binding protein, is negatively controlled by its amino-terminal domainFabien Fauchereau, Ulrike Herbrand, Philippe Chafey, et al.
Pageof 23

Showing results (41-50 of 226) with videos related to

Sort By:
Pageof 23
European Journal of Human Genetics : EJHG|June 26, 2003
In vitro follicular growth affects oocyte imprinting establishment in miceAntoine Kerjean, Philippe Couvert, Thomas Heams, et al.
European Journal of Human Genetics : EJHG|March 17, 2005
Mutations in exon 1 of MECP2B are not a common cause of X-linked mental retardation in malesKarine Poirier, Fiona Francis, Ben Hamel, et al.
American Journal of Medical Genetics. Part A|November 18, 2008
Novel mutation of IL1RAPL1 gene in a nonspecific X-linked mental retardation (MRX) familyMagdalena Nawara, Jakub Klapecki, Katarzyna Borg, et al.
Pediatric Neurology|October 2, 2007
Netrin G1 mutations are an uncommon cause of atypical Rett syndrome with or without epilepsyJuliette Nectoux, Benoit Girard, Nadia Bahi-Buisson, et al.
The Journal of Physiology|November 30, 2011
Rapid reversal of impaired inhibitory and excitatory transmission but not spine dysgenesis in a mouse model of mental retardationAndrew D Powell, Kalbinder K Gill, Pierre-Philippe Saintot, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 21, 2009
Epileptic encephalopathy in a girl with an interstitial deletion of Xp22 comprising promoter and exon 1 of the CDKL5 geneNadia Bahi-Buisson, Benoit Girard, Agnes Gautier, et al.
Genetic Testing|August 16, 2002
Spectrum of MECP2 mutations in Rett syndromeThierry Bienvenu, Laurent Villard, Nicolas De Roux, et al.
The Journal of Biological Chemistry|June 18, 2002
Active caspase-8 translocates into the nucleus of apoptotic cells to inactivate poly(ADP-ribose) polymerase-2Alexandra Benchoua, Cécile Couriaud, Christelle Guégan, et al.
BMC Neurology|November 25, 2016
A step toward essential tremor gene discovery: identification of extreme phenotype and screening of HTRA2 and ANO3Mathilde Renaud, Christophe Marcel, Gabrielle Rudolf, et al.
Molecular and Cellular Neurosciences|August 23, 2003
The RhoGAP activity of OPHN1, a new F-actin-binding protein, is negatively controlled by its amino-terminal domainFabien Fauchereau, Ulrike Herbrand, Philippe Chafey, et al.
Pageof 23