Beckmann JS - Search Results

1

Functional defects of a muscle-specific calpain, p94, caused by mutations associated with limb-girdle muscular dystrophy type 2A.

Ono Y, Shimada H, Sorimachi H, Richard I, Saido TC, Beckmann JS, Ishiura S, Suzuki K. Ono Y, et al. Among authors: beckmann js. J Biol Chem. 1998 Jul 3;273(27):17073-8. doi: 10.1074/jbc.273.27.17073. J Biol Chem. 1998. PMID: 9642272 Free article.

2

Highly conserved structure in the promoter region of the gene for muscle-specific calpain, p94.

Sorimachi H, Forsberg NE, Lee HJ, Joeng SY, Richard I, Beckmann JS, Ishiura S, Suzuki K. Sorimachi H, et al. Among authors: beckmann js. Biol Chem. 1996 Dec;377(12):859-64. Biol Chem. 1996. PMID: 8997499

3

Molecular cloning of mouse canp3, the gene associated with limb-girdle muscular dystrophy 2A in human.

Richard I, Beckmann JS. Richard I, et al. Among authors: beckmann js. Mamm Genome. 1996 May;7(5):377-9. doi: 10.1007/s003359900108. Mamm Genome. 1996. PMID: 8661728 No abstract available.

4

Clinical, pathological, and genetic features of limb-girdle muscular dystrophy type 2A with new calpain 3 gene mutations in seven patients from three Japanese families.

Kawai H, Akaike M, Kunishige M, Inui T, Adachi K, Kimura C, Kawajiri M, Nishida Y, Endo I, Kashiwagi S, Nishino H, Fujiwara T, Okuno S, Roudaut C, Richard I, Beckmann JS, Miyoshi K, Matsumoto T. Kawai H, et al. Among authors: beckmann js. Muscle Nerve. 1998 Nov;21(11):1493-501. doi: 10.1002/(sici)1097-4598(199811)21:11<1493::aid-mus19>3.0.co;2-1. Muscle Nerve. 1998. PMID: 9771675

5

Expression and functional characteristics of calpain 3 isoforms generated through tissue-specific transcriptional and posttranscriptional events.

Herasse M, Ono Y, Fougerousse F, Kimura E, Stockholm D, Beley C, Montarras D, Pinset C, Sorimachi H, Suzuki K, Beckmann JS, Richard I. Herasse M, et al. Among authors: beckmann js. Mol Cell Biol. 1999 Jun;19(6):4047-55. doi: 10.1128/MCB.19.6.4047. Mol Cell Biol. 1999. PMID: 10330145 Free PMC article.

6

Chromosome 15-linked limb-girdle muscular dystrophy: clinical phenotypes in Reunion Island and French metropolitan communities.

Fardeau M, Eymard B, Mignard C, Tomé FM, Richard I, Beckmann JS. Fardeau M, et al. Among authors: beckmann js. Neuromuscul Disord. 1996 Dec;6(6):447-53. doi: 10.1016/s0960-8966(96)00387-2. Neuromuscul Disord. 1996. PMID: 9027854

7

Characterization of monoclonal antibodies to calpain 3 and protein expression in muscle from patients with limb-girdle muscular dystrophy type 2A.

Anderson LV, Davison K, Moss JA, Richard I, Fardeau M, Tomé FM, Hübner C, Lasa A, Colomer J, Beckmann JS. Anderson LV, et al. Among authors: beckmann js. Am J Pathol. 1998 Oct;153(4):1169-79. doi: 10.1016/S0002-9440(10)65661-1. Am J Pathol. 1998. PMID: 9777948 Free PMC article.

8

Loss of calpain 3 proteolytic activity leads to muscular dystrophy and to apoptosis-associated IkappaBalpha/nuclear factor kappaB pathway perturbation in mice.

Richard I, Roudaut C, Marchand S, Baghdiguian S, Herasse M, Stockholm D, Ono Y, Suel L, Bourg N, Sorimachi H, Lefranc G, Fardeau M, Sébille A, Beckmann JS. Richard I, et al. Among authors: beckmann js. J Cell Biol. 2000 Dec 25;151(7):1583-90. doi: 10.1083/jcb.151.7.1583. J Cell Biol. 2000. PMID: 11134085 Free PMC article.

9

Secondary calpain3 deficiency in 2q-linked muscular dystrophy: titin is the candidate gene.

Haravuori H, Vihola A, Straub V, Auranen M, Richard I, Marchand S, Voit T, Labeit S, Somer H, Peltonen L, Beckmann JS, Udd B. Haravuori H, et al. Among authors: beckmann js. Neurology. 2001 Apr 10;56(7):869-77. doi: 10.1212/wnl.56.7.869. Neurology. 2001. PMID: 11294923

10

Pathophysiology of limb girdle muscular dystrophy type 2A: hypothesis and new insights into the IkappaBalpha/NF-kappaB survival pathway in skeletal muscle.

Baghdiguian S, Richard I, Martin M, Coopman P, Beckmann JS, Mangeat P, Lefranc G. Baghdiguian S, et al. Among authors: beckmann js. J Mol Med (Berl). 2001 Jun;79(5-6):254-61. doi: 10.1007/s001090100225. J Mol Med (Berl). 2001. PMID: 11485017 Review.

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