Bushby K - Search Results

1

Cloning of the mouse dysferlin gene and genomic characterization of the SJL-Dysf mutation.

Vafiadaki E, Reis A, Keers S, Harrison R, Anderson LV, Raffelsberger T, Ivanova S, Hoger H, Bittner RE, Bushby K, Bashir R. Vafiadaki E, et al. Among authors: bushby k. Neuroreport. 2001 Mar 5;12(3):625-9. doi: 10.1097/00001756-200103050-00039. Neuroreport. 2001. PMID: 11234777

2

The third human FER-1-like protein is highly similar to dysferlin.

Britton S, Freeman T, Vafiadaki E, Keers S, Harrison R, Bushby K, Bashir R. Britton S, et al. Among authors: bushby k. Genomics. 2000 Sep 15;68(3):313-21. doi: 10.1006/geno.2000.6290. Genomics. 2000. PMID: 10995573

3

The molecular biology of LGMD2B--towards the identification of the LGMD gene on chromosome 2p13.

Bushby K, Bashir R, Keers S, Britton S, Zatz M, Passos-Bueno MR, Lovett M, Mahjneh I, Marconi G, Strachan T. Bushby K, et al. Neuromuscul Disord. 1996 Dec;6(6):491-2. doi: 10.1016/s0960-8966(96)00393-8. Neuromuscul Disord. 1996. PMID: 9027860 No abstract available.

4

Bashir R, Britton S, Strachan T, Keers S, Vafiadaki E, Lako M, Richard I, Marchand S, Bourg N, Argov Z, Sadeh M, Mahjneh I, Marconi G, Passos-Bueno MR, Moreira Ede S, Zatz M, Beckmann JS, Bushby K. Bashir R, et al. Among authors: bushby k. Nat Genet. 1998 Sep;20(1):37-42. doi: 10.1038/1689. Nat Genet. 1998. PMID: 9731527

5

Late onset in dysferlinopathy widens the clinical spectrum.

Klinge L, Dean AF, Kress W, Dixon P, Charlton R, Müller JS, Anderson LV, Straub V, Barresi R, Lochmüller H, Bushby K. Klinge L, et al. Among authors: bushby k. Neuromuscul Disord. 2008 Apr;18(4):288-90. doi: 10.1016/j.nmd.2008.01.004. Neuromuscul Disord. 2008. PMID: 18396043

6

Genetic and physical mapping at the limb-girdle muscular dystrophy locus (LGMD2B) on chromosome 2p.

Bashir R, Keers S, Strachan T, Passos-Bueno R, Zatz M, Weissenbach J, Le Paslier D, Meisler M, Bushby K. Bashir R, et al. Among authors: bushby k. Genomics. 1996 Apr 1;33(1):46-52. doi: 10.1006/geno.1996.0157. Genomics. 1996. PMID: 8617508

7

Abnormal merosin in adults. A new form of late onset muscular dystrophy not linked to chromosome 6q2.

Bushby K, Anderson LV, Pollitt C, Naom I, Muntoni F, Bindoff L. Bushby K, et al. Brain. 1998 Apr;121 ( Pt 4):581-8. doi: 10.1093/brain/121.4.581. Brain. 1998. PMID: 9577386

8

Muscular dystrophy due to dysferlin deficiency in Libyan Jews. Clinical and genetic features.

Argov Z, Sadeh M, Mazor K, Soffer D, Kahana E, Eisenberg I, Mitrani-Rosenbaum S, Richard I, Beckmann J, Keers S, Bashir R, Bushby K, Rosenmann H. Argov Z, et al. Among authors: bushby k. Brain. 2000 Jun;123 ( Pt 6):1229-37. doi: 10.1093/brain/123.6.1229. Brain. 2000. PMID: 10825360

9

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: bushby k. Neurology. 2001 Jul 24;57(2):271-8. doi: 10.1212/wnl.57.2.271. Neurology. 2001. PMID: 11468312

10

Aup1, a novel gene on mouse chromosome 6 and human chromosome 2p13.

Jang W, Weber JS, Bashir R, Bushby K, Meisler MH. Jang W, et al. Among authors: bushby k. Genomics. 1996 Sep 1;36(2):366-8. doi: 10.1006/geno.1996.0477. Genomics. 1996. PMID: 8812468

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