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M E MacDonald

Showing results (51-60 of 118) with videos related to

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Somatic Cell and Molecular Genetics|July 20, 1999
Amyloid formation by mutant huntingtin: threshold, progressivity and recruitment of normal polyglutamine proteinsC C Huang, P W Faber, F Persichetti, et al.
Acta Neuropathologica|October 1, 1996
Coexistence of Huntington's disease and familial amyotrophic lateral sclerosis: case presentationA Rubio, K Steinberg, D A Figlewicz, et al.
Human Molecular Genetics|January 1, 1994
Distribution of trinucleotide repeat sequences across a 2 Mbp region containing the Huntington's disease geneH Hummerich, S Baxendale, R Mott, et al.
The Journal of Experimental Medicine|June 1, 1980
Anemia- and polycythemia-inducing isolates of Friend spleen focus-forming virus. Biological and molecular evidence for two distinct viral genomesM E MacDonald, F H Reynolds, W J Van de Ven, et al.
Human Molecular Genetics|November 25, 2000
Dominant phenotypes produced by the HD mutation in STHdh(Q111) striatal cellsF Trettel, D Rigamonti, P Hilditch-Maguire, et al.
Nature Genetics|December 17, 1997
Huntingtin is required for neurogenesis and is not impaired by the Huntington's disease CAG expansionJ K White, W Auerbach, M P Duyao, et al.
Human Molecular Genetics|April 1, 1993
Dinucleotide repeat polymorphism in the Huntington's disease region at the D4S182 locusD A Tagle, K L Blanchard-McQuate, J Valdes, et al.
Molecular and Cellular Probes|December 1, 1992
Assay by polymerase chain reaction (PCR) of multi-allele polymorphisms in the Huntington's disease region of chromosome 4B A Allitto, A I McClatchey, G Barnes, et al.
Neuron|October 13, 1998
Polyglutamine-expanded human huntingtin transgenes induce degeneration of Drosophila photoreceptor neuronsG R Jackson, I Salecker, X Dong, et al.
Neuroscience|August 5, 2003
Neocortical neurons cultured from mice with expanded CAG repeats in the huntingtin gene: unaltered vulnerability to excitotoxins and other insultsB J Snider, J L Moss, F J Revilla, et al.
Pageof 12

Showing results (51-60 of 118) with videos related to

Sort By:
Pageof 12
Somatic Cell and Molecular Genetics|July 20, 1999
Amyloid formation by mutant huntingtin: threshold, progressivity and recruitment of normal polyglutamine proteinsC C Huang, P W Faber, F Persichetti, et al.
Acta Neuropathologica|October 1, 1996
Coexistence of Huntington's disease and familial amyotrophic lateral sclerosis: case presentationA Rubio, K Steinberg, D A Figlewicz, et al.
Human Molecular Genetics|January 1, 1994
Distribution of trinucleotide repeat sequences across a 2 Mbp region containing the Huntington's disease geneH Hummerich, S Baxendale, R Mott, et al.
The Journal of Experimental Medicine|June 1, 1980
Anemia- and polycythemia-inducing isolates of Friend spleen focus-forming virus. Biological and molecular evidence for two distinct viral genomesM E MacDonald, F H Reynolds, W J Van de Ven, et al.
Human Molecular Genetics|November 25, 2000
Dominant phenotypes produced by the HD mutation in STHdh(Q111) striatal cellsF Trettel, D Rigamonti, P Hilditch-Maguire, et al.
Nature Genetics|December 17, 1997
Huntingtin is required for neurogenesis and is not impaired by the Huntington's disease CAG expansionJ K White, W Auerbach, M P Duyao, et al.
Human Molecular Genetics|April 1, 1993
Dinucleotide repeat polymorphism in the Huntington's disease region at the D4S182 locusD A Tagle, K L Blanchard-McQuate, J Valdes, et al.
Molecular and Cellular Probes|December 1, 1992
Assay by polymerase chain reaction (PCR) of multi-allele polymorphisms in the Huntington's disease region of chromosome 4B A Allitto, A I McClatchey, G Barnes, et al.
Neuron|October 13, 1998
Polyglutamine-expanded human huntingtin transgenes induce degeneration of Drosophila photoreceptor neuronsG R Jackson, I Salecker, X Dong, et al.
Neuroscience|August 5, 2003
Neocortical neurons cultured from mice with expanded CAG repeats in the huntingtin gene: unaltered vulnerability to excitotoxins and other insultsB J Snider, J L Moss, F J Revilla, et al.
Pageof 12