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Genomics
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October 1, 1992
The telomeric 60 kb of chromosome arm 4p is homologous to telomeric regions on 13p, 15p, 21p, and 22p
S Youngman, G P Bates, S Williams, et al.
Genomics
|
January 1, 1991
Increased recombination adjacent to the Huntington disease-linked D4S10 marker
B A Allitto, M E MacDonald, M Bucan, et al.
Journal of Medical Genetics
|
December 1, 1993
Gametic but not somatic instability of CAG repeat length in Huntington's disease
M E MacDonald, G Barnes, J Srinidhi, et al.
Cell
|
August 9, 1996
Homozygous defect in HIV-1 coreceptor accounts for resistance of some multiply-exposed individuals to HIV-1 infection
R Liu, W A Paxton, S Choe, et al.
The Journal of Clinical Investigation
|
September 1, 1989
Clustering of multiallele DNA markers near the Huntington's disease gene
M E MacDonald, S V Cheng, M Zimmer, et al.
Neuron
|
August 1, 1989
Recombination events suggest potential sites for the Huntington's disease gene
M E MacDonald, J L Haines, M Zimmer, et al.
Human Molecular Genetics
|
November 16, 2001
The HD mutation causes progressive lethal neurological disease in mice expressing reduced levels of huntingtin
W Auerbach, M S Hurlbert, P Hilditch-Maguire, et al.
Neurobiology of Disease
|
June 1, 1996
Differential expression of normal and mutant Huntington's disease gene alleles
F Persichetti, L Carlee, P W Faber, et al.
Journal of Medical Genetics
|
July 31, 2007
Factors associated with HD CAG repeat instability in Huntington disease
V C Wheeler, F Persichetti, S M McNeil, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
May 1, 1997
Heterogeneous topographic and cellular distribution of huntingtin expression in the normal human neostriatum
R J Ferrante, C A Gutekunst, F Persichetti, et al.
Page
of 12
Search research articles
Search
Showing results (81-90 of 118) with videos related to
Sort By:
Page
of 12
Genomics
|
October 1, 1992
The telomeric 60 kb of chromosome arm 4p is homologous to telomeric regions on 13p, 15p, 21p, and 22p
S Youngman, G P Bates, S Williams, et al.
Genomics
|
January 1, 1991
Increased recombination adjacent to the Huntington disease-linked D4S10 marker
B A Allitto, M E MacDonald, M Bucan, et al.
Journal of Medical Genetics
|
December 1, 1993
Gametic but not somatic instability of CAG repeat length in Huntington's disease
M E MacDonald, G Barnes, J Srinidhi, et al.
Cell
|
August 9, 1996
Homozygous defect in HIV-1 coreceptor accounts for resistance of some multiply-exposed individuals to HIV-1 infection
R Liu, W A Paxton, S Choe, et al.
The Journal of Clinical Investigation
|
September 1, 1989
Clustering of multiallele DNA markers near the Huntington's disease gene
M E MacDonald, S V Cheng, M Zimmer, et al.
Neuron
|
August 1, 1989
Recombination events suggest potential sites for the Huntington's disease gene
M E MacDonald, J L Haines, M Zimmer, et al.
Human Molecular Genetics
|
November 16, 2001
The HD mutation causes progressive lethal neurological disease in mice expressing reduced levels of huntingtin
W Auerbach, M S Hurlbert, P Hilditch-Maguire, et al.
Neurobiology of Disease
|
June 1, 1996
Differential expression of normal and mutant Huntington's disease gene alleles
F Persichetti, L Carlee, P W Faber, et al.
Journal of Medical Genetics
|
July 31, 2007
Factors associated with HD CAG repeat instability in Huntington disease
V C Wheeler, F Persichetti, S M McNeil, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
May 1, 1997
Heterogeneous topographic and cellular distribution of huntingtin expression in the normal human neostriatum
R J Ferrante, C A Gutekunst, F Persichetti, et al.
Page
of 12