Showing results (121-130 of 430) with videos related to
Sort By:
Pageof 43
Nature Genetics|April 1, 1992
Mutant prion proteins in Gerstmann-Sträussler-Scheinker disease with neurofibrillary tanglesK Hsiao, S R Dlouhy, M R Farlow, et al.Neurology|November 1, 1989
Gerstmann-Sträussler-Scheinker disease. II. Neurofibrillary tangles and plaques with PrP-amyloid coexist in an affected familyB Ghetti, F Tagliavini, C L Masters, et al.Journal of Medical Genetics|December 1, 1993
Gametic but not somatic instability of CAG repeat length in Huntington's diseaseM E MacDonald, G Barnes, J Srinidhi, et al.Human Molecular Genetics|March 1, 1995
Genetic heterogeneity of autosomal recessive limb-girdle muscular dystrophy in a genetic isolate (Amish) and evidence for a new locusV Allamand, O Broux, N Bourg, et al.Cold Spring Harbor Symposia on Quantitative Biology|January 1, 1986
Molecular genetics of Huntington's diseaseJ F Gusella, T C Gilliam, R E Tanzi, et al.Annals of the New York Academy of Sciences|January 1, 1991
Genetic heterogeneity in tuberous sclerosis. Study of a large collaborative datasetJ L Haines, J Amos, J Attwood, et al.Biodegradation|April 12, 2003
Reduction of Np(V) and precipitation of Np(IV) by an anaerobic microbial consortiumBruce E Rittmann, James E Banaszak, Donald T ReedThe Journal of Biological Chemistry|March 8, 1996
Multiple Sp1 binding sites in the cardiac/slow twitch muscle sarcoplasmic reticulum Ca2+-ATPase gene promoter are required for expression in Sol8 muscle cellsD L Baker, V Dave, T Reed, et al.Environmental Science & Technology|February 18, 2014
Quantifying export flows of used electronics: advanced methods to resolve used goods within trade dataHuabo Duan, T Reed Miller, Jeremy Gregory, et al.Human Genetics|February 29, 1976
Partial trisomy 11,46,XX,-3,-20, + der3, + der20,t(3:11:20), resulting from a complex maternal rearrangement of chromosomes 3, 11, 20C G Palmer, C Poland, T Reed, et al.Pageof 43