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Nippon Ganka Gakkai Zasshi|August 1, 1991
[Detection of deletions in platelet mitochondrial DNA in Kearns-Sayre syndrome using polymerase chain reaction]Y Ota, S Awaya, M Tanaka, et al.Journal of the Neurological Sciences|January 1, 1990
Progressive cytochrome c oxidase deficiency in a case of Leigh's encephalomyelopathyY Koga, I Nonaka, M Nakao, et al.Human Mutation|January 1, 1997
Method for in situ investigation of mitochondrial DNA deletionsS A Kovalenko, P J Harms, M Tanaka, et al.Acta Neuropathologica|January 1, 1991
Functional respiratory chain studies in mitochondrial cytopathies. Support for mitochondrial DNA heteroplasmy in myoclonus epilepsy and ragged red fibers (MERRF) syndromeE Byrne, I Trounce, S Marzuki, et al.Biochemical and Biophysical Research Communications|February 15, 1995
Genotype and phenotype of severe mitochondrial cardiomyopathy: a recipient of heart transplantation and the genetic controlT Ozawa, K Katsumata, M Hayakawa, et al.Internal Medicine (Tokyo, Japan)|July 1, 1995
Mitochondrial encephalomyopathy with A to G transition of mitochondrial transfer RNA(Leu(UUR)) 3,243 presenting hypertrophic cardiomyopathyY Hiruta, K Chin, K Shitomi, et al.Journal of the Neurological Sciences|September 1, 1988
Familial mitochondrial myopathy associated with peripheral neuropathy: partial deficiencies of complex I and complex IVH Mizusawa, M Watanabe, I Kanazawa, et al.Journal of the Neurological Sciences|November 1, 1990
Cytoplasmic body and mitochondrial DNA deletionK Sahashi, K Ohno, M Tanaka, et al.Biochimica Et Biophysica Acta|August 27, 1991
Direct DNA sequencing from colony: analysis of multiple deletions of mitochondrial genomeK Ohno, M Tanaka, H Ino, et al.Biochemical and Biophysical Research Communications|September 29, 1989
Deficiencies in complex I subunits of the respiratory chain in Parkinson's diseaseY Mizuno, S Ohta, M Tanaka, et al.Pageof 534