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Behavioural Brain Research
|
January 1, 1996
5-HT1B receptor knock out--behavioral consequences
S Ramboz, F Saudou, D A Amara, et al.
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.
Molecular and Cellular Biology
|
August 26, 1998
Fos family members induce cell cycle entry by activating cyclin D1
J R Brown, E Nigh, R J Lee, 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.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
August 26, 1998
Essential role of the fosB gene in molecular, cellular, and behavioral actions of chronic electroconvulsive seizures
N Hiroi, G J Marek, J R Brown, 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.
Nature Genetics
|
November 1, 1996
Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats
G Imbert, F Saudou, G Yvert, et al.
Nature Genetics
|
September 1, 1997
Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion
G David, N Abbas, G Stevanin, et al.
Human Molecular Genetics
|
December 1, 1996
Screening for proteins with polyglutamine expansions in autosomal dominant cerebellar ataxias
G Stevanin, Y Trottier, G Cancel, et al.
Human Molecular Genetics
|
May 1, 1997
Molecular and clinical correlations in spinocerebellar ataxia 2: a study of 32 families
G Cancel, A Dürr, O Didierjean, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 20) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 20 results.
Behavioural Brain Research
|
January 1, 1996
5-HT1B receptor knock out--behavioral consequences
S Ramboz, F Saudou, D A Amara, et al.
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.
Molecular and Cellular Biology
|
August 26, 1998
Fos family members induce cell cycle entry by activating cyclin D1
J R Brown, E Nigh, R J Lee, 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.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
August 26, 1998
Essential role of the fosB gene in molecular, cellular, and behavioral actions of chronic electroconvulsive seizures
N Hiroi, G J Marek, J R Brown, 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.
Nature Genetics
|
November 1, 1996
Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats
G Imbert, F Saudou, G Yvert, et al.
Nature Genetics
|
September 1, 1997
Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion
G David, N Abbas, G Stevanin, et al.
Human Molecular Genetics
|
December 1, 1996
Screening for proteins with polyglutamine expansions in autosomal dominant cerebellar ataxias
G Stevanin, Y Trottier, G Cancel, et al.
Human Molecular Genetics
|
May 1, 1997
Molecular and clinical correlations in spinocerebellar ataxia 2: a study of 32 families
G Cancel, A Dürr, O Didierjean, et al.
Page
of 2