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Current Opinion in Neurobiology|October 1, 1996
Huntington's disease: translating a CAG repeat into a pathogenic mechanismM E MacDonald, J F GusellaNature Reviews. Neuroscience|March 17, 2001
Molecular genetics: unmasking polyglutamine triggers in neurodegenerative diseaseJ F Gusella, M E MacDonaldAnnual Review of Medicine|January 1, 1996
Trinucleotide instability: a repeating theme in human inherited disordersJ F Gusella, M E MacDonaldCurrent Opinion in Neurobiology|October 1, 1995
Huntington's disease: CAG genetics expands neurobiologyJ F Gusella, M E MacDonaldCurrent Opinion in Neurobiology|August 4, 1998
Huntingtin: a single bait hooks many speciesJ F Gusella, M E MacDonaldArchives of Neurology|November 1, 1993
Molecular genetics of Huntington's diseaseJ F Gusella, M E MacDonald, C M Ambrose, et al.Annals of Neurology|May 1, 1997
CAG repeat number governs the development rate of pathology in Huntington's diseaseJ B Penney, J P Vonsattel, M E MacDonald, et al.Human Molecular Genetics|August 13, 1998
Huntingtin interacts with a family of WW domain proteinsP W Faber, G T Barnes, J Srinidhi, et al.The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|November 1, 1984
Genetic linkage of the Huntington's disease gene to a DNA markerJ F GusellaPageof 29