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Y Trottier

Showing results (11-20 of 34) with videos related to

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Genomics|June 1, 1994
The gene for the TATA binding protein (TBP) that contains a highly polymorphic protein coding CAG repeat maps to 6q27G Imbert, Y Trottier, J Beckmann, et al.
Advances in Experimental Medicine and Biology|June 14, 2001
Pathological mechanisms in polyglutamine expansion diseasesD Devys, G Yvert, A Lunkes, et al.
American Journal of Medical Genetics|July 15, 1994
Male with typical fragile X phenotype is deleted for part of the FMR1 gene and for about 100 kb of upstream regionY Trottier, G Imbert, A Poustka, et al.
EXS|January 1, 1993
Microsatellites and disease: a new paradigmK Wrogemann, V Biancalana, D Devys, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|August 6, 1999
Properties of polyglutamine expansion in vitro and in a cellular model for Huntington's diseaseA Lunkes, Y Trottier, J Fagart, et al.
Cold Spring Harbor Symposia on Quantitative Biology|January 1, 1996
Polyglutamine expansions and neurodegenerative diseasesF Saudou, D Devys, Y Trottier, et al.
Psychiatry Research|October 23, 1997
A preliminary study on early onset schizophrenia and bipolar disorder: large polyglutamine expansions are not involvedF Schürhoff, G Stevanin, Y Trottier, et al.
Neurobiology of Disease|March 9, 1999
Heterogeneous intracellular localization and expression of ataxin-3Y Trottier, G Cancel, I An-Gourfinkel, et al.
Human Molecular Genetics|June 17, 1999
High level expression of expanded full-length ataxin-3 in vitro causes cell death and formation of intranuclear inclusions in neuronal cellsB O Evert, U Wüllner, J B Schulz, et al.
Journal of Neurology|April 1, 1997
Clinical and genetic analysis of three German kindreds with autosomal dominant cerebellar ataxia type I linked to the SCA2 locusK Bürk, G Stevanin, O Didierjean, et al.
Pageof 4

Showing results (11-20 of 34) with videos related to

Sort By:
Pageof 4
Genomics|June 1, 1994
The gene for the TATA binding protein (TBP) that contains a highly polymorphic protein coding CAG repeat maps to 6q27G Imbert, Y Trottier, J Beckmann, et al.
Advances in Experimental Medicine and Biology|June 14, 2001
Pathological mechanisms in polyglutamine expansion diseasesD Devys, G Yvert, A Lunkes, et al.
American Journal of Medical Genetics|July 15, 1994
Male with typical fragile X phenotype is deleted for part of the FMR1 gene and for about 100 kb of upstream regionY Trottier, G Imbert, A Poustka, et al.
EXS|January 1, 1993
Microsatellites and disease: a new paradigmK Wrogemann, V Biancalana, D Devys, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|August 6, 1999
Properties of polyglutamine expansion in vitro and in a cellular model for Huntington's diseaseA Lunkes, Y Trottier, J Fagart, et al.
Cold Spring Harbor Symposia on Quantitative Biology|January 1, 1996
Polyglutamine expansions and neurodegenerative diseasesF Saudou, D Devys, Y Trottier, et al.
Psychiatry Research|October 23, 1997
A preliminary study on early onset schizophrenia and bipolar disorder: large polyglutamine expansions are not involvedF Schürhoff, G Stevanin, Y Trottier, et al.
Neurobiology of Disease|March 9, 1999
Heterogeneous intracellular localization and expression of ataxin-3Y Trottier, G Cancel, I An-Gourfinkel, et al.
Human Molecular Genetics|June 17, 1999
High level expression of expanded full-length ataxin-3 in vitro causes cell death and formation of intranuclear inclusions in neuronal cellsB O Evert, U Wüllner, J B Schulz, et al.
Journal of Neurology|April 1, 1997
Clinical and genetic analysis of three German kindreds with autosomal dominant cerebellar ataxia type I linked to the SCA2 locusK Bürk, G Stevanin, O Didierjean, et al.
Pageof 4