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Showing results (11-20 of 14) with videos related to

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Nature Medicine|May 6, 1999
Calpain 3 deficiency is associated with myonuclear apoptosis and profound perturbation of the IkappaB alpha/NF-kappaB pathway in limb-girdle muscular dystrophy type 2AS Baghdiguian, M Martin, I Richard, et al.
Nature Genetics|September 10, 1998
A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2BR Bashir, S Britton, T Strachan, 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.
Neurology|July 27, 2001
Genomic organization of the dysferlin gene and novel mutations in Miyoshi myopathyM Aoki, J Liu, I Richard, et al.
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Showing results (11-20 of 14) with videos related to

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Pageof 2
You have reached the last page of results.This site can display upto 14 results.
Nature Medicine|May 6, 1999
Calpain 3 deficiency is associated with myonuclear apoptosis and profound perturbation of the IkappaB alpha/NF-kappaB pathway in limb-girdle muscular dystrophy type 2AS Baghdiguian, M Martin, I Richard, et al.
Nature Genetics|September 10, 1998
A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2BR Bashir, S Britton, T Strachan, 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.
Neurology|July 27, 2001
Genomic organization of the dysferlin gene and novel mutations in Miyoshi myopathyM Aoki, J Liu, I Richard, et al.
Pageof 2