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P Pasturaud

Showing results (1-10 of 11) with videos related to

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Human Molecular Genetics|December 1, 1993
Dinucleotide repeat polymorphism at the locus D15S222F Fougerousse, P Pasturaud, J S Beckmann
Human Molecular Genetics|April 1, 1995
A primary expression map of the chromosome 15q15 region containing the recessive form of limb-girdle muscular dystrophy (LGMD2A) geneN Chiannilkulchai, P Pasturaud, I Richard, et al.
Cell|April 7, 1995
Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2AI Richard, O Broux, V Allamand, et al.
Genomics|October 1, 1994
Regional localization of human chromosome 15 lociI Richard, O Broux, N Chiannilkulchai, et al.
Human Molecular Genetics|February 1, 1994
Mapping of a chromosome 15 region involved in limb girdle muscular dystrophyF Fougerousse, O Broux, I Richard, et al.
American Journal of Human Genetics|June 1, 1995
Preferential localization of the limb-girdle muscular dystrophy type 2A gene in the proximal part of a 1-cM 15q15.1-q15.3 intervalV Allamand, O Broux, I Richard, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 8, 1999
SIAH-1 promotes apoptosis and tumor suppression through a network involving the regulation of protein folding, unfolding, and trafficking: identification of common effectors with p53 and p21(Waf1)J P Roperch, F Lethrone, S Prieur, et al.
Leukemia|October 6, 2001
A new recurrent and specific cryptic translocation, t(5;14)(q35;q32), is associated with expression of the Hox11L2 gene in T acute lymphoblastic leukemiaO A Bernard, M Busson-LeConiat, P Ballerini, et al.
Neuromuscular Disorders : NMD|December 1, 1996
Identification of muscle-specific calpain and beta-sarcoglycan genes in progressive autosomal recessive muscular dystrophiesJ S Beckmann, I Richard, O Broux, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 20, 1996
Activation of the human homologue of the Drosophila sina gene in apoptosis and tumor suppressionM Nemani, G Linares-Cruz, H Bruzzoni-Giovanelli, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Human Molecular Genetics|December 1, 1993
Dinucleotide repeat polymorphism at the locus D15S222F Fougerousse, P Pasturaud, J S Beckmann
Human Molecular Genetics|April 1, 1995
A primary expression map of the chromosome 15q15 region containing the recessive form of limb-girdle muscular dystrophy (LGMD2A) geneN Chiannilkulchai, P Pasturaud, I Richard, et al.
Cell|April 7, 1995
Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2AI Richard, O Broux, V Allamand, et al.
Genomics|October 1, 1994
Regional localization of human chromosome 15 lociI Richard, O Broux, N Chiannilkulchai, et al.
Human Molecular Genetics|February 1, 1994
Mapping of a chromosome 15 region involved in limb girdle muscular dystrophyF Fougerousse, O Broux, I Richard, et al.
American Journal of Human Genetics|June 1, 1995
Preferential localization of the limb-girdle muscular dystrophy type 2A gene in the proximal part of a 1-cM 15q15.1-q15.3 intervalV Allamand, O Broux, I Richard, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 8, 1999
SIAH-1 promotes apoptosis and tumor suppression through a network involving the regulation of protein folding, unfolding, and trafficking: identification of common effectors with p53 and p21(Waf1)J P Roperch, F Lethrone, S Prieur, et al.
Leukemia|October 6, 2001
A new recurrent and specific cryptic translocation, t(5;14)(q35;q32), is associated with expression of the Hox11L2 gene in T acute lymphoblastic leukemiaO A Bernard, M Busson-LeConiat, P Ballerini, et al.
Neuromuscular Disorders : NMD|December 1, 1996
Identification of muscle-specific calpain and beta-sarcoglycan genes in progressive autosomal recessive muscular dystrophiesJ S Beckmann, I Richard, O Broux, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 20, 1996
Activation of the human homologue of the Drosophila sina gene in apoptosis and tumor suppressionM Nemani, G Linares-Cruz, H Bruzzoni-Giovanelli, et al.
Pageof 2