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G Stevanin

Showing results (71-80 of 81) with videos related to

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Human Molecular Genetics|March 21, 1998
Molecular and clinical correlations in autosomal dominant cerebellar ataxia with progressive macular dystrophy (SCA7)G David, A Dürr, G Stevanin, et al.
Neurology|November 4, 2011
Pentanucleotide repeats at the spinocerebellar ataxia type 31 (SCA31) locus in CaucasiansK Ishikawa, A Dürr, T Klopstock, et al.
Cerebellum (London, England)|December 6, 2013
Consensus paper: pathological mechanisms underlying neurodegeneration in spinocerebellar ataxiasA Matilla-Dueñas, T Ashizawa, A Brice, et al.
Human Molecular Genetics|December 1, 1996
Screening for proteins with polyglutamine expansions in autosomal dominant cerebellar ataxiasG Stevanin, Y Trottier, G Cancel, et al.
Nature Genetics|September 1, 1997
Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansionG David, N Abbas, G Stevanin, et al.
American Journal of Human Genetics|October 3, 1998
Close associations between prevalences of dominantly inherited spinocerebellar ataxias with CAG-repeat expansions and frequencies of large normal CAG alleles in Japanese and Caucasian populationsH Takano, G Cancel, T Ikeuchi, et al.
Human Molecular Genetics|May 1, 1997
Molecular and clinical correlations in spinocerebellar ataxia 2: a study of 32 familiesG Cancel, A Dürr, O Didierjean, et al.
Neurology|October 7, 2009
SPG15 is the second most common cause of hereditary spastic paraplegia with thin corpus callosumC Goizet, A Boukhris, D Maltete, et al.
Journal of Internal Medicine|October 27, 2020
Pseudoxanthoma elasticum overlaps hereditary spastic paraplegia type 56A Legrand, C Pujol, C M Durand, et al.
Human Molecular Genetics|July 1, 1996
Intergenerational instability of the CAG repeat of the gene for Machado-Joseph disease (MJD1) is affected by the genotype of the normal chromosome: implications for the molecular mechanisms of the instability of the CAG repeatS Igarashi, Y Takiyama, G Cancel, et al.
Pageof 9

Showing results (71-80 of 81) with videos related to

Sort By:
Pageof 9
Human Molecular Genetics|March 21, 1998
Molecular and clinical correlations in autosomal dominant cerebellar ataxia with progressive macular dystrophy (SCA7)G David, A Dürr, G Stevanin, et al.
Neurology|November 4, 2011
Pentanucleotide repeats at the spinocerebellar ataxia type 31 (SCA31) locus in CaucasiansK Ishikawa, A Dürr, T Klopstock, et al.
Cerebellum (London, England)|December 6, 2013
Consensus paper: pathological mechanisms underlying neurodegeneration in spinocerebellar ataxiasA Matilla-Dueñas, T Ashizawa, A Brice, et al.
Human Molecular Genetics|December 1, 1996
Screening for proteins with polyglutamine expansions in autosomal dominant cerebellar ataxiasG Stevanin, Y Trottier, G Cancel, et al.
Nature Genetics|September 1, 1997
Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansionG David, N Abbas, G Stevanin, et al.
American Journal of Human Genetics|October 3, 1998
Close associations between prevalences of dominantly inherited spinocerebellar ataxias with CAG-repeat expansions and frequencies of large normal CAG alleles in Japanese and Caucasian populationsH Takano, G Cancel, T Ikeuchi, et al.
Human Molecular Genetics|May 1, 1997
Molecular and clinical correlations in spinocerebellar ataxia 2: a study of 32 familiesG Cancel, A Dürr, O Didierjean, et al.
Neurology|October 7, 2009
SPG15 is the second most common cause of hereditary spastic paraplegia with thin corpus callosumC Goizet, A Boukhris, D Maltete, et al.
Journal of Internal Medicine|October 27, 2020
Pseudoxanthoma elasticum overlaps hereditary spastic paraplegia type 56A Legrand, C Pujol, C M Durand, et al.
Human Molecular Genetics|July 1, 1996
Intergenerational instability of the CAG repeat of the gene for Machado-Joseph disease (MJD1) is affected by the genotype of the normal chromosome: implications for the molecular mechanisms of the instability of the CAG repeatS Igarashi, Y Takiyama, G Cancel, et al.
Pageof 9