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Jamel Chelly

Showing results (71-80 of 226) with videos related to

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World Journal of Gastroenterology|September 23, 2008
Liver insulin-like growth factor 2 methylation in hepatitis C virus cirrhosis and further occurrence of hepatocellular carcinomaPhilippe Couvert, Alain Carrié, Jacques Pariès, et al.
Muscle & Nerve|May 15, 2012
A new model of experimental fibrosis in hindlimb skeletal muscle of adult mdx mouse mimicking muscular dystrophyIsabelle Desguerre, Ludovic Arnold, Alban Vignaud, et al.
American Journal of Medical Genetics. Part A|November 29, 2016
A novel recurrent LIS1 splice site mutation in classic lissencephalyMarion Philbert, Camille Maillard, Mara Cavallin, et al.
European Journal of Human Genetics : EJHG|December 21, 2006
Mutation screening of brain-expressed X-chromosomal miRNA genes in 464 patients with nonsyndromic X-linked mental retardationWei Chen, Lars R Jensen, Jozef Gecz, et al.
Neurogenetics|August 25, 2010
A FOXG1 mutation in a boy with congenital variant of Rett syndromeTangui Le Guen, Nadia Bahi-Buisson, Juliette Nectoux, et al.
Clinics and Research in Hepatology and Gastroenterology|August 21, 2012
Insulin-like growth factor 2 gene methylation in peripheral blood mononuclear cells of patients with hepatitis C related cirrhosis or hepatocellular carcinomaPhilippe Couvert, Alain Carrié, Sophie Tezenas du Montcel, et al.
Neurogenetics|October 7, 2009
Revisiting the phenotype associated with FOXG1 mutations: two novel cases of congenital Rett variantNadia Bahi-Buisson, Juliette Nectoux, Benoit Girard, et al.
Human Molecular Genetics|March 31, 2006
Branching and nucleokinesis defects in migrating interneurons derived from doublecortin knockout miceCaroline Kappeler, Yoann Saillour, Jean-Pierre Baudoin, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|August 23, 2013
Target-specific vulnerability of excitatory synapses leads to deficits in associative memory in a model of intellectual disorderXander Houbaert, Chun-Lei Zhang, Frédéric Gambino, et al.
European Journal of Human Genetics : EJHG|February 21, 2008
Revised spectrum of mutations in sarcoglycanopathiesMadiha Trabelsi, Niloufar Kavian, Fatma Daoud, et al.
Pageof 23

Showing results (71-80 of 226) with videos related to

Sort By:
Pageof 23
World Journal of Gastroenterology|September 23, 2008
Liver insulin-like growth factor 2 methylation in hepatitis C virus cirrhosis and further occurrence of hepatocellular carcinomaPhilippe Couvert, Alain Carrié, Jacques Pariès, et al.
Muscle & Nerve|May 15, 2012
A new model of experimental fibrosis in hindlimb skeletal muscle of adult mdx mouse mimicking muscular dystrophyIsabelle Desguerre, Ludovic Arnold, Alban Vignaud, et al.
American Journal of Medical Genetics. Part A|November 29, 2016
A novel recurrent LIS1 splice site mutation in classic lissencephalyMarion Philbert, Camille Maillard, Mara Cavallin, et al.
European Journal of Human Genetics : EJHG|December 21, 2006
Mutation screening of brain-expressed X-chromosomal miRNA genes in 464 patients with nonsyndromic X-linked mental retardationWei Chen, Lars R Jensen, Jozef Gecz, et al.
Neurogenetics|August 25, 2010
A FOXG1 mutation in a boy with congenital variant of Rett syndromeTangui Le Guen, Nadia Bahi-Buisson, Juliette Nectoux, et al.
Clinics and Research in Hepatology and Gastroenterology|August 21, 2012
Insulin-like growth factor 2 gene methylation in peripheral blood mononuclear cells of patients with hepatitis C related cirrhosis or hepatocellular carcinomaPhilippe Couvert, Alain Carrié, Sophie Tezenas du Montcel, et al.
Neurogenetics|October 7, 2009
Revisiting the phenotype associated with FOXG1 mutations: two novel cases of congenital Rett variantNadia Bahi-Buisson, Juliette Nectoux, Benoit Girard, et al.
Human Molecular Genetics|March 31, 2006
Branching and nucleokinesis defects in migrating interneurons derived from doublecortin knockout miceCaroline Kappeler, Yoann Saillour, Jean-Pierre Baudoin, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|August 23, 2013
Target-specific vulnerability of excitatory synapses leads to deficits in associative memory in a model of intellectual disorderXander Houbaert, Chun-Lei Zhang, Frédéric Gambino, et al.
European Journal of Human Genetics : EJHG|February 21, 2008
Revised spectrum of mutations in sarcoglycanopathiesMadiha Trabelsi, Niloufar Kavian, Fatma Daoud, et al.
Pageof 23