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Jamel Chelly

Showing results (21-30 of 226) with videos related to

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Neuromuscular Disorders : NMD|September 7, 2014
When a mid-intronic variation of DMD gene creates an ESE siteMadiha Trabelsi, Caroline Beugnet, Nathalie Deburgrave, et al.
Communicative & Integrative Biology|August 18, 2010
Neuronal JNK pathway activation by IL-1 is mediated through IL1RAPL1, a protein required for development of cognitive functionsAlice Pavlowsky, Alice Zanchi, Marta Pallotto, et al.
Molecular Cell|June 18, 2004
Mechanism of microtubule stabilization by doublecortinCarolyn A Moores, Mylène Perderiset, Fiona Francis, et al.
Neuromolecular Medicine|July 26, 2015
Astrocyte Transcriptome from the Mecp2(308)-Truncated Mouse Model of Rett SyndromeChloé Delépine, Juliette Nectoux, Franck Letourneur, et al.
European Journal of Human Genetics : EJHG|May 28, 2009
Mutation in the SLC9A6 gene is not a frequent cause of sporadic Angelman-like syndromeYann Fichou, Nadia Bahi-Buisson, Juliette Nectoux, et al.
Human Molecular Genetics|July 7, 2010
Disease-associated mutations in TUBA1A result in a spectrum of defects in the tubulin folding and heterodimer assembly pathwayGuoling Tian, Xavier H Jaglin, David A Keays, et al.
Molecular Biology of the Cell|January 18, 2008
A pachygyria-causing alpha-tubulin mutation results in inefficient cycling with CCT and a deficient interaction with TBCBGuoling Tian, Xiang-Peng Kong, Xavier H Jaglin, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|December 27, 2005
Calpain 10 and development of diabetes mellitus in cystic fibrosisSalma Derbel, Celine Doumaguet, Dominique Hubert, et al.
European Journal of Medical Genetics|August 2, 2005
X-linked mental retardation, short stature, microcephaly and hypogonadism maps to Xp22.1-p21.3 in a Belgian familyHilde Van Esch, Ginevra Zanni, Maureen Holvoet, et al.
Neurogenetics|November 27, 2008
The first missense mutation causing Rett syndrome specifically affecting the MeCP2_e1 isoformYann Fichou, Juliette Nectoux, Nadia Bahi-Buisson, et al.
Pageof 23

Showing results (21-30 of 226) with videos related to

Sort By:
Pageof 23
Neuromuscular Disorders : NMD|September 7, 2014
When a mid-intronic variation of DMD gene creates an ESE siteMadiha Trabelsi, Caroline Beugnet, Nathalie Deburgrave, et al.
Communicative & Integrative Biology|August 18, 2010
Neuronal JNK pathway activation by IL-1 is mediated through IL1RAPL1, a protein required for development of cognitive functionsAlice Pavlowsky, Alice Zanchi, Marta Pallotto, et al.
Molecular Cell|June 18, 2004
Mechanism of microtubule stabilization by doublecortinCarolyn A Moores, Mylène Perderiset, Fiona Francis, et al.
Neuromolecular Medicine|July 26, 2015
Astrocyte Transcriptome from the Mecp2(308)-Truncated Mouse Model of Rett SyndromeChloé Delépine, Juliette Nectoux, Franck Letourneur, et al.
European Journal of Human Genetics : EJHG|May 28, 2009
Mutation in the SLC9A6 gene is not a frequent cause of sporadic Angelman-like syndromeYann Fichou, Nadia Bahi-Buisson, Juliette Nectoux, et al.
Human Molecular Genetics|July 7, 2010
Disease-associated mutations in TUBA1A result in a spectrum of defects in the tubulin folding and heterodimer assembly pathwayGuoling Tian, Xavier H Jaglin, David A Keays, et al.
Molecular Biology of the Cell|January 18, 2008
A pachygyria-causing alpha-tubulin mutation results in inefficient cycling with CCT and a deficient interaction with TBCBGuoling Tian, Xiang-Peng Kong, Xavier H Jaglin, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|December 27, 2005
Calpain 10 and development of diabetes mellitus in cystic fibrosisSalma Derbel, Celine Doumaguet, Dominique Hubert, et al.
European Journal of Medical Genetics|August 2, 2005
X-linked mental retardation, short stature, microcephaly and hypogonadism maps to Xp22.1-p21.3 in a Belgian familyHilde Van Esch, Ginevra Zanni, Maureen Holvoet, et al.
Neurogenetics|November 27, 2008
The first missense mutation causing Rett syndrome specifically affecting the MeCP2_e1 isoformYann Fichou, Juliette Nectoux, Nadia Bahi-Buisson, et al.
Pageof 23