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M E MacDonald

Showing results (81-90 of 118) with videos related to

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Genomics|October 1, 1992
The telomeric 60 kb of chromosome arm 4p is homologous to telomeric regions on 13p, 15p, 21p, and 22pS Youngman, G P Bates, S Williams, et al.
Genomics|January 1, 1991
Increased recombination adjacent to the Huntington disease-linked D4S10 markerB 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 diseaseM 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 infectionR 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 geneM E MacDonald, S V Cheng, M Zimmer, et al.
Neuron|August 1, 1989
Recombination events suggest potential sites for the Huntington's disease geneM 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 huntingtinW 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 allelesF Persichetti, L Carlee, P W Faber, et al.
Journal of Medical Genetics|July 31, 2007
Factors associated with HD CAG repeat instability in Huntington diseaseV 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 neostriatumR J Ferrante, C A Gutekunst, F Persichetti, et al.
Pageof 12

Showing results (81-90 of 118) with videos related to

Sort By:
Pageof 12
Genomics|October 1, 1992
The telomeric 60 kb of chromosome arm 4p is homologous to telomeric regions on 13p, 15p, 21p, and 22pS Youngman, G P Bates, S Williams, et al.
Genomics|January 1, 1991
Increased recombination adjacent to the Huntington disease-linked D4S10 markerB 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 diseaseM 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 infectionR 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 geneM E MacDonald, S V Cheng, M Zimmer, et al.
Neuron|August 1, 1989
Recombination events suggest potential sites for the Huntington's disease geneM 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 huntingtinW 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 allelesF Persichetti, L Carlee, P W Faber, et al.
Journal of Medical Genetics|July 31, 2007
Factors associated with HD CAG repeat instability in Huntington diseaseV 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 neostriatumR J Ferrante, C A Gutekunst, F Persichetti, et al.
Pageof 12