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Nicolas Lebrun

Showing results (31-40 of 44) with videos related to

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Journal of Immunology (Baltimore, Md. : 1950)|September 9, 2005
Are extensive T cell epitope polymorphisms in the Plasmodium falciparum circumsporozoite antigen, a leading sporozoite vaccine candidate, selected by immune pressure?Chutima Kumkhaek, Kooruethai Phra-Ek, Laurent Rénia, et al.
Plos Genetics|June 23, 2009
Comprehensive linkage and association analyses identify haplotype, near to the TNFSF15 gene, significantly associated with spondyloarthritisElena Zinovieva, Catherine Bourgain, Amir Kadi, et al.
Human Molecular Genetics|September 11, 2010
Mutations in the neuronal ß-tubulin subunit TUBB3 result in malformation of cortical development and neuronal migration defectsKarine Poirier, Yoann Saillour, Nadia Bahi-Buisson, et al.
American Journal of Medical Genetics. Part A|December 21, 2013
Expanding the clinical phenotype of patients with a ZDHHC9 mutationAlice Masurel-Paulet, Vera M Kalscheuer, Nicolas Lebrun, et al.
Human Molecular Genetics|October 12, 2014
Novel IL1RAPL1 mutations associated with intellectual disability impair synaptogenesisMariana Ramos-Brossier, Caterina Montani, Nicolas Lebrun, et al.
Human Molecular Genetics|October 28, 2017
Ciliogenesis and cell cycle alterations contribute to KIF2A-related malformations of cortical developmentLoïc Broix, Laure Asselin, Carla G Silva, et al.
Amino Acids|July 29, 2015
Hypomorphic variants of cationic amino acid transporter 3 in males with autism spectrum disordersCaroline Nava, Johanna Rupp, Jean-Paul Boissel, et al.
Journal of Medical Genetics|November 21, 2014
WWOX-related encephalopathies: delineation of the phenotypical spectrum and emerging genotype-phenotype correlationCyril Mignot, Laetitia Lambert, Laurent Pasquier, et al.
European Journal of Human Genetics : EJHG|September 24, 2015
Mosaic parental germline mutations causing recurrent forms of malformations of cortical developmentJulia Lauer Zillhardt, Karine Poirier, Loïc Broix, et al.
Nature Genetics|April 23, 2013
Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephalyKarine Poirier, Nicolas Lebrun, Loic Broix, et al.
Pageof 5

Showing results (31-40 of 44) with videos related to

Sort By:
Pageof 5
Journal of Immunology (Baltimore, Md. : 1950)|September 9, 2005
Are extensive T cell epitope polymorphisms in the Plasmodium falciparum circumsporozoite antigen, a leading sporozoite vaccine candidate, selected by immune pressure?Chutima Kumkhaek, Kooruethai Phra-Ek, Laurent Rénia, et al.
Plos Genetics|June 23, 2009
Comprehensive linkage and association analyses identify haplotype, near to the TNFSF15 gene, significantly associated with spondyloarthritisElena Zinovieva, Catherine Bourgain, Amir Kadi, et al.
Human Molecular Genetics|September 11, 2010
Mutations in the neuronal ß-tubulin subunit TUBB3 result in malformation of cortical development and neuronal migration defectsKarine Poirier, Yoann Saillour, Nadia Bahi-Buisson, et al.
American Journal of Medical Genetics. Part A|December 21, 2013
Expanding the clinical phenotype of patients with a ZDHHC9 mutationAlice Masurel-Paulet, Vera M Kalscheuer, Nicolas Lebrun, et al.
Human Molecular Genetics|October 12, 2014
Novel IL1RAPL1 mutations associated with intellectual disability impair synaptogenesisMariana Ramos-Brossier, Caterina Montani, Nicolas Lebrun, et al.
Human Molecular Genetics|October 28, 2017
Ciliogenesis and cell cycle alterations contribute to KIF2A-related malformations of cortical developmentLoïc Broix, Laure Asselin, Carla G Silva, et al.
Amino Acids|July 29, 2015
Hypomorphic variants of cationic amino acid transporter 3 in males with autism spectrum disordersCaroline Nava, Johanna Rupp, Jean-Paul Boissel, et al.
Journal of Medical Genetics|November 21, 2014
WWOX-related encephalopathies: delineation of the phenotypical spectrum and emerging genotype-phenotype correlationCyril Mignot, Laetitia Lambert, Laurent Pasquier, et al.
European Journal of Human Genetics : EJHG|September 24, 2015
Mosaic parental germline mutations causing recurrent forms of malformations of cortical developmentJulia Lauer Zillhardt, Karine Poirier, Loïc Broix, et al.
Nature Genetics|April 23, 2013
Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephalyKarine Poirier, Nicolas Lebrun, Loic Broix, et al.
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