Keers S - Search Results

1

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: keers s. Genomics. 2000 Sep 15;68(3):313-21. doi: 10.1006/geno.2000.6290. Genomics. 2000. PMID: 10995573

2

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: keers s. Genomics. 1996 Apr 1;33(1):46-52. doi: 10.1006/geno.1996.0157. Genomics. 1996. PMID: 8617508

3

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: keers s. Nat Genet. 1998 Sep;20(1):37-42. doi: 10.1038/1689. Nat Genet. 1998. PMID: 9731527

4

Dysferlin is a plasma membrane protein and is expressed early in human development.

Anderson LV, Davison K, Moss JA, Young C, Cullen MJ, Walsh J, Johnson MA, Bashir R, Britton S, Keers S, Argov Z, Mahjneh I, Fougerousse F, Beckmann JS, Bushby KM. Anderson LV, et al. Among authors: keers s. Hum Mol Genet. 1999 May;8(5):855-61. doi: 10.1093/hmg/8.5.855. Hum Mol Genet. 1999. PMID: 10196375

5

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: keers s. Neuroreport. 2001 Mar 5;12(3):625-9. doi: 10.1097/00001756-200103050-00039. Neuroreport. 2001. PMID: 11234777

6

From T-tubule to sarcolemma: damage-induced dysferlin translocation in early myogenesis.

Klinge L, Laval S, Keers S, Haldane F, Straub V, Barresi R, Bushby K. Klinge L, et al. Among authors: keers s. FASEB J. 2007 Jun;21(8):1768-76. doi: 10.1096/fj.06-7659com. Epub 2007 Mar 15. FASEB J. 2007. PMID: 17363620

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

8

Confirmation of the 2p locus for the mild autosomal recessive limb-girdle muscular dystrophy gene (LGMD2B) in three families allows refinement of the candidate region.

Passos-Bueno MR, Bashir R, Moreira ES, Vainzof M, Marie SK, Vasquez L, Iughetti P, Bakker E, Keers S, Stephenson A, et al. Passos-Bueno MR, et al. Among authors: keers s. Genomics. 1995 May 1;27(1):192-5. doi: 10.1006/geno.1995.1024. Genomics. 1995. PMID: 7665169

9

A gene for autosomal recessive limb-girdle muscular dystrophy maps to chromosome 2p.

Bashir R, Strachan T, Keers S, Stephenson A, Mahjneh I, Marconi G, Nashef L, Bushby KM. Bashir R, et al. Among authors: keers s. Hum Mol Genet. 1994 Mar;3(3):455-7. doi: 10.1093/hmg/3.3.455. Hum Mol Genet. 1994. PMID: 8012357

10

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. Among authors: keers s. Neuromuscul Disord. 1996 Dec;6(6):491-2. doi: 10.1016/s0960-8966(96)00393-8. Neuromuscul Disord. 1996. PMID: 9027860 No abstract available.

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