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Jamel Chelly

Showing results (81-90 of 226) with videos related to

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Brain Research. Molecular Brain Research|March 3, 2004
Neuroanatomical distribution of ARX in brain and its localisation in GABAergic neuronsKarine Poirier, Hilde Van Esch, Gaëlle Friocourt, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 15, 2017
Protein Kinase A Deregulation in the Medial Prefrontal Cortex Impairs Working Memory in Murine Oligophrenin-1 DeficiencyChun-Lei Zhang, Mattia Aime, Emilie Laheranne, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 23, 2012
Mutation of plasma membrane Ca2+ ATPase isoform 3 in a family with X-linked congenital cerebellar ataxia impairs Ca2+ homeostasisGinevra Zanni, Tito Calì, Vera M Kalscheuer, et al.
Human Mutation|March 17, 2006
Novel JARID1C/SMCX mutations in patients with X-linked mental retardationAndreas Tzschach, Steffen Lenzner, Bettina Moser, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 16, 2007
IL1-receptor accessory protein-like 1 (IL1RAPL1), a protein involved in cognitive functions, regulates N-type Ca2+-channel and neurite elongationFrédéric Gambino, Alice Pavlowsky, Aurélie Béglé, et al.
American Journal of Medical Genetics. Part A|January 22, 2004
Specific clinical and brain MRI features in mentally retarded patients with mutations in the Oligophrenin-1 geneVincent des Portes, Nathalie Boddaert, Silvia Sacco, et al.
American Journal of Medical Genetics|October 12, 2002
TM4SF2 gene involvement reconsidered in an XLMR family after neuropsychological assessmentMarie Gomot, Nathalie Ronce, Sabine Dessay, et al.
Neurogenetics|September 28, 2013
Homozygous truncating mutation of the KBP gene, encoding a KIF1B-binding protein, in a familial case of fetal polymicrogyriaStéphanie Valence, Karine Poirier, Nicolas Lebrun, et al.
The Journal of Molecular Diagnostics : JMD|September 26, 2009
A new chromosome x exon-specific microarray platform for screening of patients with X-linked disordersStavros Bashiardes, Ludmila Kousoulidou, Hans van Bokhoven, et al.
Stem Cells (Dayton, Ohio)|November 22, 2012
Differentially activated macrophages orchestrate myogenic precursor cell fate during human skeletal muscle regenerationMarielle Saclier, Houda Yacoub-Youssef, Abigail L Mackey, et al.
Pageof 23

Showing results (81-90 of 226) with videos related to

Sort By:
Pageof 23
Brain Research. Molecular Brain Research|March 3, 2004
Neuroanatomical distribution of ARX in brain and its localisation in GABAergic neuronsKarine Poirier, Hilde Van Esch, Gaëlle Friocourt, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 15, 2017
Protein Kinase A Deregulation in the Medial Prefrontal Cortex Impairs Working Memory in Murine Oligophrenin-1 DeficiencyChun-Lei Zhang, Mattia Aime, Emilie Laheranne, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 23, 2012
Mutation of plasma membrane Ca2+ ATPase isoform 3 in a family with X-linked congenital cerebellar ataxia impairs Ca2+ homeostasisGinevra Zanni, Tito Calì, Vera M Kalscheuer, et al.
Human Mutation|March 17, 2006
Novel JARID1C/SMCX mutations in patients with X-linked mental retardationAndreas Tzschach, Steffen Lenzner, Bettina Moser, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 16, 2007
IL1-receptor accessory protein-like 1 (IL1RAPL1), a protein involved in cognitive functions, regulates N-type Ca2+-channel and neurite elongationFrédéric Gambino, Alice Pavlowsky, Aurélie Béglé, et al.
American Journal of Medical Genetics. Part A|January 22, 2004
Specific clinical and brain MRI features in mentally retarded patients with mutations in the Oligophrenin-1 geneVincent des Portes, Nathalie Boddaert, Silvia Sacco, et al.
American Journal of Medical Genetics|October 12, 2002
TM4SF2 gene involvement reconsidered in an XLMR family after neuropsychological assessmentMarie Gomot, Nathalie Ronce, Sabine Dessay, et al.
Neurogenetics|September 28, 2013
Homozygous truncating mutation of the KBP gene, encoding a KIF1B-binding protein, in a familial case of fetal polymicrogyriaStéphanie Valence, Karine Poirier, Nicolas Lebrun, et al.
The Journal of Molecular Diagnostics : JMD|September 26, 2009
A new chromosome x exon-specific microarray platform for screening of patients with X-linked disordersStavros Bashiardes, Ludmila Kousoulidou, Hans van Bokhoven, et al.
Stem Cells (Dayton, Ohio)|November 22, 2012
Differentially activated macrophages orchestrate myogenic precursor cell fate during human skeletal muscle regenerationMarielle Saclier, Houda Yacoub-Youssef, Abigail L Mackey, et al.
Pageof 23