Allamand V - Search Results

1

Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophy.

Roberds SL, Leturcq F, Allamand V, Piccolo F, Jeanpierre M, Anderson RD, Lim LE, Lee JC, Tomé FM, Romero NB, et al. Roberds SL, et al. Among authors: allamand v. Cell. 1994 Aug 26;78(4):625-33. doi: 10.1016/0092-8674(94)90527-4. Cell. 1994. PMID: 8069911

2

Beta-sarcoglycan: characterization and role in limb-girdle muscular dystrophy linked to 4q12.

Lim LE, Duclos F, Broux O, Bourg N, Sunada Y, Allamand V, Meyer J, Richard I, Moomaw C, Slaughter C, et al. Lim LE, et al. Among authors: allamand v. Nat Genet. 1995 Nov;11(3):257-65. doi: 10.1038/ng1195-257. Nat Genet. 1995. PMID: 7581448

3

Adhalin gene polymorphism.

Allamand V, Leturcq F, Piccolo F, Jeanpierre M, Azibi K, Roberds SL, Lim LE, Campbell KP, Beckmann JS, Kaplan JC. Allamand V, et al. Hum Mol Genet. 1994 Dec;3(12):2269. doi: 10.1093/hmg/3.12.2269. Hum Mol Genet. 1994. PMID: 7881446 No abstract available.

4

Characterization of delta-sarcoglycan, a novel component of the oligomeric sarcoglycan complex involved in limb-girdle muscular dystrophy.

Jung D, Duclos F, Apostol B, Straub V, Lee JC, Allamand V, Venzke DP, Sunada Y, Moomaw CR, Leveille CJ, Slaughter CA, Crawford TO, McPherson JD, Campbell KP. Jung D, et al. Among authors: allamand v. J Biol Chem. 1996 Dec 13;271(50):32321-9. doi: 10.1074/jbc.271.50.32321. J Biol Chem. 1996. PMID: 8943294 Free article.

5

Identification of muscle-specific calpain and beta-sarcoglycan genes in progressive autosomal recessive muscular dystrophies.

Beckmann JS, Richard I, Broux O, Fougerousse F, Allamand V, Chiannilkulchai N, Lim LE, Duclos F, Bourg N, Brenguier L, Pasturaud P, Quétier F, Roudaut C, Sunada Y, Meyer J, Dinçer P, Lefranc G, Merlini L, Topaloglu H, Tomé FM, Cohen D, Jackson CE, Campbell KP, Fardeau M. Beckmann JS, et al. Among authors: allamand v. Neuromuscul Disord. 1996 Dec;6(6):455-62. doi: 10.1016/s0960-8966(96)00386-0. Neuromuscul Disord. 1996. PMID: 9027855

6

Disruption of the beta-sarcoglycan gene reveals pathogenetic complexity of limb-girdle muscular dystrophy type 2E.

Durbeej M, Cohn RD, Hrstka RF, Moore SA, Allamand V, Davidson BL, Williamson RA, Campbell KP. Durbeej M, et al. Among authors: allamand v. Mol Cell. 2000 Jan;5(1):141-51. doi: 10.1016/s1097-2765(00)80410-4. Mol Cell. 2000. PMID: 10678176 Free article.

7

Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A.

Richard I, Broux O, Allamand V, Fougerousse F, Chiannilkulchai N, Bourg N, Brenguier L, Devaud C, Pasturaud P, Roudaut C, et al. Richard I, et al. Among authors: allamand v. Cell. 1995 Apr 7;81(1):27-40. doi: 10.1016/0092-8674(95)90368-2. Cell. 1995. PMID: 7720071 Free article.

8

Early adenovirus-mediated gene transfer effectively prevents muscular dystrophy in alpha-sarcoglycan-deficient mice.

Allamand V, Donahue KM, Straub V, Davisson RL, Davidson BL, Campbell KP. Allamand V, et al. Gene Ther. 2000 Aug;7(16):1385-91. doi: 10.1038/sj.gt.3301247. Gene Ther. 2000. PMID: 10981665

9

Animal models for muscular dystrophy: valuable tools for the development of therapies.

Allamand V, Campbell KP. Allamand V, et al. Hum Mol Genet. 2000 Oct;9(16):2459-67. doi: 10.1093/hmg/9.16.2459. Hum Mol Genet. 2000. PMID: 11005802 Review.

10

Gene transfer establishes primacy of striated vs. smooth muscle sarcoglycan complex in limb-girdle muscular dystrophy.

Durbeej M, Sawatzki SM, Barresi R, Schmainda KM, Allamand V, Michele DE, Campbell KP. Durbeej M, et al. Among authors: allamand v. Proc Natl Acad Sci U S A. 2003 Jul 22;100(15):8910-5. doi: 10.1073/pnas.1537554100. Epub 2003 Jul 8. Proc Natl Acad Sci U S A. 2003. PMID: 12851463 Free PMC article.

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