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N Bourg

Showing results (1-10 of 14) with videos related to

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Human Molecular Genetics|December 1, 1993
Dinucleotide repeat at the D15S129 locusI Richard, N Bourg, J S Beckmann
Genomics|October 1, 1994
Regional localization of human chromosome 15 lociI Richard, O Broux, N Chiannilkulchai, 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.
Nature Genetics|November 1, 1995
Beta-sarcoglycan: characterization and role in limb-girdle muscular dystrophy linked to 4q12L E Lim, F Duclos, O Broux, 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.
Human Molecular Genetics|March 1, 1995
Genetic heterogeneity of autosomal recessive limb-girdle muscular dystrophy in a genetic isolate (Amish) and evidence for a new locusV Allamand, O Broux, N Bourg, et al.
The Journal of Cell Biology|January 3, 2001
Loss of calpain 3 proteolytic activity leads to muscular dystrophy and to apoptosis-associated IkappaBalpha/nuclear factor kappaB pathway perturbation in miceI Richard, C Roudaut, S Marchand, et al.
Neuromuscular Disorders : NMD|January 5, 2000
A diagnostic fluorescent marker kit for six limb girdle muscular dystrophiesI Richard, N Bourg, S Marchand, et al.
Neuromuscular Disorders : NMD|May 5, 1998
Beta-sarcoglycan: genomic analysis and identification of a novel missense mutation in the LGMD2E Amish isolateF Duclos, O Broux, N Bourg, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Human Molecular Genetics|December 1, 1993
Dinucleotide repeat at the D15S129 locusI Richard, N Bourg, J S Beckmann
Genomics|October 1, 1994
Regional localization of human chromosome 15 lociI Richard, O Broux, N Chiannilkulchai, 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.
Nature Genetics|November 1, 1995
Beta-sarcoglycan: characterization and role in limb-girdle muscular dystrophy linked to 4q12L E Lim, F Duclos, O Broux, 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.
Human Molecular Genetics|March 1, 1995
Genetic heterogeneity of autosomal recessive limb-girdle muscular dystrophy in a genetic isolate (Amish) and evidence for a new locusV Allamand, O Broux, N Bourg, et al.
The Journal of Cell Biology|January 3, 2001
Loss of calpain 3 proteolytic activity leads to muscular dystrophy and to apoptosis-associated IkappaBalpha/nuclear factor kappaB pathway perturbation in miceI Richard, C Roudaut, S Marchand, et al.
Neuromuscular Disorders : NMD|January 5, 2000
A diagnostic fluorescent marker kit for six limb girdle muscular dystrophiesI Richard, N Bourg, S Marchand, et al.
Neuromuscular Disorders : NMD|May 5, 1998
Beta-sarcoglycan: genomic analysis and identification of a novel missense mutation in the LGMD2E Amish isolateF Duclos, O Broux, N Bourg, et al.
Pageof 2