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The Journal of Clinical Investigation|July 1, 1986
Biochemical and molecular genetic characterization of a new variant prealbumin associated with hereditary amyloidosisM R Wallace, F E Dwulet, P M Conneally, et al.Neuroscience|June 1, 2000
Reversal of presynaptic deficits of apolipoprotein E-deficient mice in human apolipoprotein E transgenic miceS Chapman, T Sabo, A D Roses, et al.American Journal of Human Genetics|March 1, 1992
A test of the hypothesis that age at onset in Huntington disease is controlled by an X-linked recessive modifierR M Ridley, L A Farrer, C D Frith, et al.Genetic Epidemiology|January 1, 1984
Huntington disease: estimation of heterozygote status using linked genetic markersP M Conneally, M R Wallace, J F Gusella, et al.Journal of Medical Genetics|September 1, 1988
Anticipation in Huntington's disease is inherited through the male line but may originate in the femaleR M Ridley, C D Frith, T J Crow, et al.Experimental Gerontology|December 13, 2000
Identification of novel genes in late-onset Alzheimer's diseaseM A Pericak-Vance, J Grubber, L R Bailey, et al.Journal of the Neurological Sciences|November 1, 1976
Increased phosphorylated components of erythrocyte membrane spectrin band II with reference to Duchenne muscular dystrophyA D Roses, M Herbstreith, B Metcalf, et al.Neurobiology of Disease|August 9, 2001
Impaired neuronal plasticity in transgenic mice expressing human apolipoprotein E4 compared to E3 in a model of entorhinal cortex lesionF White, J A Nicoll, A D Roses, et al.JAMA|October 23, 1997
Complete genomic screen in late-onset familial Alzheimer disease. Evidence for a new locus on chromosome 12M A Pericak-Vance, M P Bass, L H Yamaoka, et al.Genetic Epidemiology|January 1, 1997
No association or linkage between an intronic polymorphism of presenilin-1 and sporadic or late-onset familial Alzheimer diseaseW K Scott, L H Yamaoka, P A Locke, et al.Pageof 37