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American Journal of Perinatology|May 1, 1995
Congenital myotonic dystrophy: molecular diagnosis and clinical studyK Hojo, H Yamagata, H Moji, et al.Journal of the Neurological Sciences|July 1, 1996
An intergenerational contraction of the CTG repeat in Japanese myotonic dystrophyR Matsumura, T Namikawa, T Miki, et al.Nihon Ronen Igakkai Zasshi. Japanese Journal of Geriatrics|May 19, 1998
[A case of mild-type myotonic dystrophy with dementia and severe arteriosclerosis obliterans]M Horiki, A Morishima, H Yamagata, et al.Dementia and Geriatric Cognitive Disorders|February 15, 2001
Genetic association between Alzheimer disease and the alpha-synuclein geneM Matsubara, H Yamagata, K Kamino, et al.Nihon Ronen Igakkai Zasshi. Japanese Journal of Geriatrics|October 14, 2000
[A very elderly autopsy case of cecal cancer with pulmonary lymphangitis carcinomatosa]M Matsubara, K Kohara, K Uemura, et al.Neurology|October 1, 1994
Congenital myotonic dystrophy transmitted from an asymptomatic father with a DM-specific geneK Ohya, N Tachi, S Chiba, et al.Journal of Biochemistry|June 1, 1983
Temperature-sensitive prolipoprotein signal peptidase in an Escherichia coli mutant: use of the mutant for an efficient and convenient assay systemH YamagataJournal of Medical Genetics|November 1, 1992
Comparison of the myotonic dystrophy associated CTG repeat in European and Japanese populationsJ Davies, H Yamagata, P Shelbourne, et al.The Japanese Journal of Human Genetics|September 1, 1994
Characteristics of dynamic mutation in Japanese myotonic dystrophyH Yamagata, T Miki, N Yamanaka, et al.Bioscience, Biotechnology, and Biochemistry|January 24, 1998
Molecular cloning and characterization of a cDNA encoding early light-inducible protein from soybean (Glycine max L.)H Yamagata, C BowlerPageof 105