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Showing results (21-30 of 70) with videos related to

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American Journal of Human Genetics|November 1, 1995
Linkage disequilibrium at the Machado-Joseph disease/spinal cerebellar ataxia 3 locus: evidence for a common founder effect in French and Portuguese-Brazilian families as well as a second ancestral Portuguese-Azorean mutationG Stevanin, G Cancel, O Didierjean, et al.
Neurobiology of Disease|March 9, 1999
Heterogeneous intracellular localization and expression of ataxin-3Y Trottier, G Cancel, I An-Gourfinkel, et al.
Annals of Neurology|March 20, 1998
Eye movement abnormalities correlate with genotype in autosomal dominant cerebellar ataxia type IS Rivaud-Pechoux, A Dürr, B Gaymard, et al.
American Journal of Human Genetics|January 1, 1995
The gene for spinal cerebellar ataxia 3 (SCA3) is located in a region of approximately 3 cM on chromosome 14q24.3-q32.2G Stevanin, G Cancel, A Dürr, et al.
Nature Genetics|January 1, 1994
Is DRPLA also linked to 14q?G Cancel, A Dürr, G Stevanin, et al.
Journal of Medical Genetics|October 1, 1995
Characterisation of the unstable expanded CAG repeat in the MJD1 gene in four Brazilian families of Portuguese descent with Machado-Joseph diseaseG Stevanin, E Cassa, G Cancel, et al.
Brain : a Journal of Neurology|February 4, 1998
Autosomal dominant cerebellar ataxia type I. Nerve conduction and evoked potential studies in families with SCA1, SCA2 and SCA3M Abele, K Bürk, F Andres, et al.
Nature|November 23, 1995
Polyglutamine expansion as a pathological epitope in Huntington's disease and four dominant cerebellar ataxiasY Trottier, Y Lutz, G Stevanin, 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.
Nature Genetics|May 1, 1995
The gene for autosomal dominant cerebellar ataxia with pigmentary macular dystrophy maps to chromosome 3p12-p21.1A Benomar, L Krols, G Stevanin, et al.
Pageof 7

Showing results (21-30 of 70) with videos related to

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Pageof 7
American Journal of Human Genetics|November 1, 1995
Linkage disequilibrium at the Machado-Joseph disease/spinal cerebellar ataxia 3 locus: evidence for a common founder effect in French and Portuguese-Brazilian families as well as a second ancestral Portuguese-Azorean mutationG Stevanin, G Cancel, O Didierjean, et al.
Neurobiology of Disease|March 9, 1999
Heterogeneous intracellular localization and expression of ataxin-3Y Trottier, G Cancel, I An-Gourfinkel, et al.
Annals of Neurology|March 20, 1998
Eye movement abnormalities correlate with genotype in autosomal dominant cerebellar ataxia type IS Rivaud-Pechoux, A Dürr, B Gaymard, et al.
American Journal of Human Genetics|January 1, 1995
The gene for spinal cerebellar ataxia 3 (SCA3) is located in a region of approximately 3 cM on chromosome 14q24.3-q32.2G Stevanin, G Cancel, A Dürr, et al.
Nature Genetics|January 1, 1994
Is DRPLA also linked to 14q?G Cancel, A Dürr, G Stevanin, et al.
Journal of Medical Genetics|October 1, 1995
Characterisation of the unstable expanded CAG repeat in the MJD1 gene in four Brazilian families of Portuguese descent with Machado-Joseph diseaseG Stevanin, E Cassa, G Cancel, et al.
Brain : a Journal of Neurology|February 4, 1998
Autosomal dominant cerebellar ataxia type I. Nerve conduction and evoked potential studies in families with SCA1, SCA2 and SCA3M Abele, K Bürk, F Andres, et al.
Nature|November 23, 1995
Polyglutamine expansion as a pathological epitope in Huntington's disease and four dominant cerebellar ataxiasY Trottier, Y Lutz, G Stevanin, 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.
Nature Genetics|May 1, 1995
The gene for autosomal dominant cerebellar ataxia with pigmentary macular dystrophy maps to chromosome 3p12-p21.1A Benomar, L Krols, G Stevanin, et al.
Pageof 7