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Human Molecular Genetics
|
January 1, 1994
Distribution of trinucleotide repeat sequences across a 2 Mbp region containing the Huntington's disease gene
H Hummerich, S Baxendale, R Mott, et al.
The Journal of Comparative Neurology
|
February 13, 2001
Loss of cortical and thalamic neuronal tenascin-C expression in a transgenic mouse expressing exon 1 of the human Huntington disease gene
M Kusakabe, L Mangiarini, E D Laywell, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 14, 1999
Self-assembly of polyglutamine-containing huntingtin fragments into amyloid-like fibrils: implications for Huntington's disease pathology
E Scherzinger, A Sittler, K Schweiger, et al.
Molecular Cell
|
November 11, 1998
SH3GL3 associates with the Huntingtin exon 1 protein and promotes the formation of polygln-containing protein aggregates
A Sittler, S Wälter, N Wedemeyer, et al.
Neurobiology of Disease
|
July 17, 1998
Intranuclear neuronal inclusions in Huntington's disease and dentatorubral and pallidoluysian atrophy: correlation between the density of inclusions and IT15 CAG triplet repeat length
M W Becher, J A Kotzuk, A H Sharp, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
April 7, 1999
Characterization of progressive motor deficits in mice transgenic for the human Huntington's disease mutation
R J Carter, L A Lione, T Humby, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
June 24, 2000
Abnormal synaptic plasticity and impaired spatial cognition in mice transgenic for exon 1 of the human Huntington's disease mutation
K P Murphy, R J Carter, L A Lione, et al.
Somatic Cell and Molecular Genetics
|
January 1, 1991
Mapping of cosmid clones in Huntington's disease region of chromosome 4
W L Whaley, G P Bates, A Novelletto, et al.
Human Molecular Genetics
|
August 1, 1997
Sequence comparison of human and yeast telomeres identifies structurally distinct subtelomeric domains
J Flint, G P Bates, K Clark, et al.
Neuroscience
|
October 19, 2000
Amyloid-like inclusions in Huntington's disease
D P McGowan, W van Roon-Mom, H Holloway, et al.
Page
of 7
Search research articles
Search
Showing results (41-50 of 68) with videos related to
Sort By:
Page
of 7
Human Molecular Genetics
|
January 1, 1994
Distribution of trinucleotide repeat sequences across a 2 Mbp region containing the Huntington's disease gene
H Hummerich, S Baxendale, R Mott, et al.
The Journal of Comparative Neurology
|
February 13, 2001
Loss of cortical and thalamic neuronal tenascin-C expression in a transgenic mouse expressing exon 1 of the human Huntington disease gene
M Kusakabe, L Mangiarini, E D Laywell, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 14, 1999
Self-assembly of polyglutamine-containing huntingtin fragments into amyloid-like fibrils: implications for Huntington's disease pathology
E Scherzinger, A Sittler, K Schweiger, et al.
Molecular Cell
|
November 11, 1998
SH3GL3 associates with the Huntingtin exon 1 protein and promotes the formation of polygln-containing protein aggregates
A Sittler, S Wälter, N Wedemeyer, et al.
Neurobiology of Disease
|
July 17, 1998
Intranuclear neuronal inclusions in Huntington's disease and dentatorubral and pallidoluysian atrophy: correlation between the density of inclusions and IT15 CAG triplet repeat length
M W Becher, J A Kotzuk, A H Sharp, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
April 7, 1999
Characterization of progressive motor deficits in mice transgenic for the human Huntington's disease mutation
R J Carter, L A Lione, T Humby, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
June 24, 2000
Abnormal synaptic plasticity and impaired spatial cognition in mice transgenic for exon 1 of the human Huntington's disease mutation
K P Murphy, R J Carter, L A Lione, et al.
Somatic Cell and Molecular Genetics
|
January 1, 1991
Mapping of cosmid clones in Huntington's disease region of chromosome 4
W L Whaley, G P Bates, A Novelletto, et al.
Human Molecular Genetics
|
August 1, 1997
Sequence comparison of human and yeast telomeres identifies structurally distinct subtelomeric domains
J Flint, G P Bates, K Clark, et al.
Neuroscience
|
October 19, 2000
Amyloid-like inclusions in Huntington's disease
D P McGowan, W van Roon-Mom, H Holloway, et al.
Page
of 7