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Molecular and Cellular Biology|December 1, 1985
A deletion of the 3' end of the Drosophila melanogaster hsp70 gene increases stability of mutant mRNA during recovery from heat shockA A Simcox, C M Cheney, E P Hoffman, et al.Neurology|December 31, 1997
A new locus for hemiplegic migraine maps to chromosome 1q31K Gardner, M M Barmada, L J Ptacek, et al.Journal of Thrombosis and Haemostasis : JTH|October 25, 2006
Decreased platelet expression of myosin regulatory light chain polypeptide (MYL9) and other genes with platelet dysfunction and CBFA2/RUNX1 mutation: insights from platelet expression profilingL Sun, J R Gorospe, E P Hoffman, et al.Physical Medicine and Rehabilitation Clinics of North America|January 20, 1999
Molecular basis of neuromuscular diseasesP F Chance, T Ashizawa, E P Hoffman, et al.Muscle & Nerve|November 1, 1996
Extensive genetic heterogeneity in the "pure" form of autosomal dominant familial spastic paraplegia (Strümpell's disease)H Kobayashi, C A Garcia, P N Tay, et al.Microscopy Research and Technique|February 19, 2000
Plasma membrane cytoskeleton of muscle: a fine structural analysisS C Watkins, M J Cullen, E P Hoffman, et al.Animal Genetics|January 1, 1992
Linkage of hyperkalaemic periodic paralysis in quarter horses to the horse adult skeletal muscle sodium channel geneJ A Rudolph, S J Spier, G Byrns, et al.Muscle & Nerve|November 1, 1991
Muscle histology in Becker muscular dystrophyM Kaido, K Arahata, E P Hoffman, et al.The Journal of Clinical Endocrinology and Metabolism|November 1, 1996
Phenotypic heterogeneity associated with the splicing mutation in congenital adrenal hyperplasia due to 21-hydroxylase deficiencyS F Witchel, D K Bhamidipati, E P Hoffman, et al.Journal of the Neurological Sciences|October 1, 1990
Somatic reversion/suppression of the mouse mdx phenotype in vivoE P Hoffman, J E Morgan, S C Watkins, et al.Pageof 19