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Human Molecular Genetics|December 1, 1995
Mutation analysis of the TSC2 gene in an African-American familyA Kumar, R S Kandt, C Wolpert, et al.Alzheimer Disease and Associated Disorders|January 1, 1988
Cellular localization of messenger RNA encoding amyloid-beta-protein in normal tissue and in Alzheimer diseaseD E Schmechel, D Goldgaber, D S Burkhart, et al.Neurology|May 1, 1983
Radionuclide angiocardiographic analysis of myocardial function in myotonic muscular dystrophyG B Hartwig, K R Rao, F M Radoff, et al.Clinical Genetics|December 1, 1983
Linkage analysis in von Willebrand diseaseM S Verp, R M Radvany, D Green, et al.Journal of Neurochemistry|March 7, 1998
Novel large apolipoprotein E-containing lipoproteins of density 1.006-1.060 g/ml in human cerebrospinal fluidJ R Guyton, S E Miller, M E Martin, et al.Archives of Pathology & Laboratory Medicine|June 1, 1997
Rapid brain autopsy. The Joseph and Kathleen Bryan Alzheimer's Disease Research Center experienceC M Hulette, K A Welsh-Bohmer, B Crain, et al.Neuroscience|March 4, 1998
Age-related congophilic inclusions in the brains of apolipoprotein E-deficient miceT A Robertson, N S Dutton, R N Martins, et al.Biochemical and Biophysical Research Communications|September 23, 1997
Oligomerization of expanded-polyglutamine domain fluorescent fusion proteins in cultured mammalian cellsO Onodera, J R Burke, S E Miller, et al.Biochemical and Biophysical Research Communications|March 15, 1994
A new human slow skeletal troponin T (TnTs) mRNA isoform derived from alternative splicing of a single geneF Samson, L Mesnard, M Mihovilovic, et al.Journal of Cellular Physiology|May 1, 1981
Patients with myotonic dystrophy, a possible segmental progeroid syndrome, and Duchenne muscular dystrophy have fibroblasts with normal limits for in vitro lifespan and growth characteristicsR L Wertz, G B Hartwig, A P Frost, et al.Pageof 37