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Nature Reviews. Genetics|February 2, 2002
No post-genetics era in human disease researchJames Gusella, Marcy MacDonaldBrain Research Bulletin|March 14, 2007
Genetic criteria for Huntington's disease pathogenesisJames F Gusella, Marcy MacdonaldJournal of Huntington'S Disease|December 17, 2016
Important but not Enough - Information about HD Related Topics and Peer and Professional Support for Young Adults from HD FamiliesUlrike Braisch, Saul Martinez-Horta, Marcy MacDonald, et al.The Journal of Neuroscience Nursing : Journal of the American Association of Neuroscience Nurses|January 28, 2009
Patient and physician attitudes regarding clinical trials in neurofibromatosis 1Mary McQueen, Mia MacCollin, James Gusella, et al.The American Journal of Psychiatry|April 3, 2010
Prevalence of incompletely penetrant Huntington's disease alleles among individuals with major depressive disorderRoy H Perlis, Jordan W Smoller, Jayalakshmi Mysore, et al.International Journal of Molecular Medicine|January 5, 2006
Late-onset and typical Huntington disease families from Crete have distinct genetic originsEleonora Kartsaki, Cleanthe Spanaki, Minas Tzagournissakis, et al.Human Molecular Genetics|May 28, 2004
Mutant huntingtin directly increases susceptibility of mitochondria to the calcium-induced permeability transition and cytochrome c releaseYeun Su Choo, Gail V W Johnson, Marcy MacDonald, et al.The Journal of Biological Chemistry|March 9, 2006
Regulation of intracellular accumulation of mutant Huntingtin by Beclin 1Mamoru Shibata, Tao Lu, Tsuyoshi Furuya, et al.European Journal of Human Genetics : EJHG|June 23, 2016
A novel neurodevelopmental disorder associated with compound heterozygous variants in the huntingtin geneLance H Rodan, Julie Cohen, Ali Fatemi, et al.Cancer Genetics and Cytogenetics|October 11, 2005
Inactivation patterns of NF2 and DAL-1/4.1B (EPB41L3) in sporadic meningiomaFabio Nunes, Yiping Shen, Yo Niida, et al.Pageof 3