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Nature
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November 23, 1995
Polyglutamine expansion as a pathological epitope in Huntington's disease and four dominant cerebellar ataxias
Y Trottier, Y Lutz, G Stevanin, et al.
Neuroreport
|
July 17, 1998
Neuronal distribution of intranuclear inclusions in Huntington's disease with adult onset
I Gourfinkel-An, G Cancel, C Duyckaerts, et al.
American Journal of Human Genetics
|
June 1, 1997
Linkage disequilibrium between the spinocerebellar ataxia 3/Machado-Joseph disease mutation and two intragenic polymorphisms, one of which, X359Y, affects the stop codon
G Stevanin, A S Lebre, C Mathieux, et al.
DNA and Cell Biology
|
August 1, 1994
Rat liver cytochrome P450 2B3: structure of the CYP2B3 gene and immunological identification of a constitutive P450 2B3-like protein in rat liver
A Jean, A Reiss, M Desrochers, et al.
Nature Genetics
|
May 1, 1995
Cellular localization of the Huntington's disease protein and discrimination of the normal and mutated form
Y Trottier, D Devys, G Imbert, et al.
Cell
|
November 1, 1996
Exon 1 of the HD gene with an expanded CAG repeat is sufficient to cause a progressive neurological phenotype in transgenic mice
L Mangiarini, K Sathasivam, M Seller, et al.
Brain Pathology (Zurich, Switzerland)
|
November 6, 1998
An isoform of ataxin-3 accumulates in the nucleus of neuronal cells in affected brain regions of SCA3 patients
T Schmidt, G B Landwehrmeyer, I Schmitt, et al.
Human Molecular Genetics
|
May 23, 1998
Spinocerebellar ataxia type 7 (SCA7): a neurodegenerative disorder with neuronal intranuclear inclusions
M Holmberg, C Duyckaerts, A Dürr, et al.
Neuron
|
August 1, 1997
Intranuclear inclusions of expanded polyglutamine protein in spinocerebellar ataxia type 3
H L Paulson, M K Perez, Y Trottier, et al.
Annals of Neurology
|
December 10, 1997
Differential distribution of the normal and mutated forms of huntingtin in the human brain
I Gourfinkel-An, G Cancel, Y Trottier, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 34) with videos related to
Sort By:
Page
of 4
Nature
|
November 23, 1995
Polyglutamine expansion as a pathological epitope in Huntington's disease and four dominant cerebellar ataxias
Y Trottier, Y Lutz, G Stevanin, et al.
Neuroreport
|
July 17, 1998
Neuronal distribution of intranuclear inclusions in Huntington's disease with adult onset
I Gourfinkel-An, G Cancel, C Duyckaerts, et al.
American Journal of Human Genetics
|
June 1, 1997
Linkage disequilibrium between the spinocerebellar ataxia 3/Machado-Joseph disease mutation and two intragenic polymorphisms, one of which, X359Y, affects the stop codon
G Stevanin, A S Lebre, C Mathieux, et al.
DNA and Cell Biology
|
August 1, 1994
Rat liver cytochrome P450 2B3: structure of the CYP2B3 gene and immunological identification of a constitutive P450 2B3-like protein in rat liver
A Jean, A Reiss, M Desrochers, et al.
Nature Genetics
|
May 1, 1995
Cellular localization of the Huntington's disease protein and discrimination of the normal and mutated form
Y Trottier, D Devys, G Imbert, et al.
Cell
|
November 1, 1996
Exon 1 of the HD gene with an expanded CAG repeat is sufficient to cause a progressive neurological phenotype in transgenic mice
L Mangiarini, K Sathasivam, M Seller, et al.
Brain Pathology (Zurich, Switzerland)
|
November 6, 1998
An isoform of ataxin-3 accumulates in the nucleus of neuronal cells in affected brain regions of SCA3 patients
T Schmidt, G B Landwehrmeyer, I Schmitt, et al.
Human Molecular Genetics
|
May 23, 1998
Spinocerebellar ataxia type 7 (SCA7): a neurodegenerative disorder with neuronal intranuclear inclusions
M Holmberg, C Duyckaerts, A Dürr, et al.
Neuron
|
August 1, 1997
Intranuclear inclusions of expanded polyglutamine protein in spinocerebellar ataxia type 3
H L Paulson, M K Perez, Y Trottier, et al.
Annals of Neurology
|
December 10, 1997
Differential distribution of the normal and mutated forms of huntingtin in the human brain
I Gourfinkel-An, G Cancel, Y Trottier, et al.
Page
of 4