Showing results (11-20 of 301) with videos related to
Sort By:
Pageof 31
Neurobiology of Disease|December 1, 1994
Huntington's disease CAG trinucleotide repeats in pathologically confirmed post-mortem brainsF Persichetti, J Srinidhi, L Kanaley, 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.Archives 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.Human Molecular Genetics|November 25, 2000
Huntingtin: an iron-regulated protein essential for normal nuclear and perinuclear organellesP Hilditch-Maguire, F Trettel, L A Passani, 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 GusellaFASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|July 1, 1989
Location cloning strategy for characterizing genetic defects in Huntington's disease and Alzheimer's diseaseJ F GusellaPageof 31