Bourg N - Search Results

1

Beta-sarcoglycan: genomic analysis and identification of a novel missense mutation in the LGMD2E Amish isolate.

Duclos F, Broux O, Bourg N, Straub V, Feldman GL, Sunada Y, Lim LE, Piccolo F, Cutshall S, Gary F, Quetier F, Kaplan JC, Jackson CE, Beckmann JS, Campbell KP. Duclos F, et al. Among authors: bourg n. Neuromuscul Disord. 1998 Feb;8(1):30-8. doi: 10.1016/s0960-8966(97)00135-1. Neuromuscul Disord. 1998. PMID: 9565988

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: bourg n. Nat Genet. 1995 Nov;11(3):257-65. doi: 10.1038/ng1195-257. Nat Genet. 1995. PMID: 7581448

3

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: bourg n. Neuromuscul Disord. 1996 Dec;6(6):455-62. doi: 10.1016/s0960-8966(96)00386-0. Neuromuscul Disord. 1996. PMID: 9027855

4

Genetic heterogeneity of autosomal recessive limb-girdle muscular dystrophy in a genetic isolate (Amish) and evidence for a new locus.

Allamand V, Broux O, Bourg N, Richard I, Tischfield JA, Hodes ME, Conneally PM, Fardeau M, Jackson CE, Beckmann JS. Allamand V, et al. Among authors: bourg n. Hum Mol Genet. 1995 Mar;4(3):459-63. doi: 10.1093/hmg/4.3.459. Hum Mol Genet. 1995. PMID: 7795603

5

A diagnostic fluorescent marker kit for six limb girdle muscular dystrophies.

Richard I, Bourg N, Marchand S, Alibert O, Eymard B, van der Kooi AJ, Jackson CE, Garcia C, Burgunder JM, Legum C, de Visser M, Fardeau M, Beckmann JS. Richard I, et al. Among authors: bourg n. Neuromuscul Disord. 1999 Dec;9(8):555-63. doi: 10.1016/s0960-8966(99)00037-1. Neuromuscul Disord. 1999. PMID: 10619713

6

Dinucleotide repeat at the D15S129 locus.

Richard I, Bourg N, Beckmann JS. Richard I, et al. Among authors: bourg n. Hum Mol Genet. 1993 Dec;2(12):2199. doi: 10.1093/hmg/2.12.2199-a. Hum Mol Genet. 1993. PMID: 8111397 No abstract available.

7

Genomic organization of the dysferlin gene and novel mutations in Miyoshi myopathy.

Aoki M, Liu J, Richard I, Bashir R, Britton S, Keers SM, Oeltjen J, Brown HE, Marchand S, Bourg N, Beley C, McKenna-Yasek D, Arahata K, Bohlega S, Cupler E, Illa I, Majneh I, Barohn RJ, Urtizberea JA, Fardeau M, Amato A, Angelini C, Bushby K, Beckmann JS, Brown RH Jr. Aoki M, et al. Among authors: bourg n. Neurology. 2001 Jul 24;57(2):271-8. doi: 10.1212/wnl.57.2.271. Neurology. 2001. PMID: 11468312

8

Mapping of a chromosome 15 region involved in limb girdle muscular dystrophy.

Fougerousse F, Broux O, Richard I, Allamand V, de Souza AP, Bourg N, Brenguier L, Devaud C, Pasturaud P, Roudaut C, et al. Fougerousse F, et al. Among authors: bourg n. Hum Mol Genet. 1994 Feb;3(2):285-93. doi: 10.1093/hmg/3.2.285. Hum Mol Genet. 1994. PMID: 8004096

9

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: bourg n. Cell. 1995 Apr 7;81(1):27-40. doi: 10.1016/0092-8674(95)90368-2. Cell. 1995. PMID: 7720071 Free article.

10

Preferential localization of the limb-girdle muscular dystrophy type 2A gene in the proximal part of a 1-cM 15q15.1-q15.3 interval.

Allamand V, Broux O, Richard I, Fougerousse F, Chiannilkulchai N, Bourg N, Brenguier L, Devaud C, Pasturaud P, Pereira de Souza A, et al. Allamand V, et al. Among authors: bourg n. Am J Hum Genet. 1995 Jun;56(6):1417-30. Am J Hum Genet. 1995. PMID: 7762565 Free PMC article.

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