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88 results

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Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
An expanded CAG repeat sequence in spinocerebellar ataxia type 7.
Lindblad K, Savontaus ML, Stevanin G, Holmberg M, Digre K, Zander C, Ehrsson H, David G, Benomar A, Nikoskelainen E, Trottier Y, Holmgren G, Ptacek LJ, Anttinen A, Brice A, Schalling M. Lindblad K, et al. Among authors: trottier y. Genome Res. 1996 Oct;6(10):965-71. doi: 10.1101/gr.6.10.965. Genome Res. 1996. PMID: 8908515 Free article.
Screening for proteins with polyglutamine expansions in autosomal dominant cerebellar ataxias.
Stevanin G, Trottier Y, Cancel G, Dürr A, David G, Didierjean O, Bürk K, Imbert G, Saudou F, Abada-Bendib M, Gourfinkel-An I, Benomar A, Abbas N, Klockgether T, Grid D, Agid Y, Mandel JL, Brice A. Stevanin G, et al. Among authors: trottier y. Hum Mol Genet. 1996 Dec;5(12):1887-92. doi: 10.1093/hmg/5.12.1887. Hum Mol Genet. 1996. PMID: 8968739
Linkage disequilibrium between the spinocerebellar ataxia 3/Machado-Joseph disease mutation and two intragenic polymorphisms, one of which, X359Y, affects the stop codon.
Stevanin G, Lebre AS, Mathieux C, Cancel G, Abbas N, Didierjean O, Dürr A, Trottier Y, Agid Y, Brice A. Stevanin G, et al. Among authors: trottier y. Am J Hum Genet. 1997 Jun;60(6):1548-52. doi: 10.1016/S0002-9297(07)64251-7. Am J Hum Genet. 1997. PMID: 9199580 Free PMC article. No abstract available.
Polyglutamine expansions and neurodegenerative diseases.
Saudou F, Devys D, Trottier Y, Imbert G, Stoeckel ME, Brice A, Mandel JL. Saudou F, et al. Among authors: trottier y. Cold Spring Harb Symp Quant Biol. 1996;61:639-47. Cold Spring Harb Symp Quant Biol. 1996. PMID: 9246490 Review. No abstract available.
88 results