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Experimental Gerontology|May 1, 1995
Mitochondrial DNA mutations associated with aging and degenerative diseasesT OzawaBiochemistry and Molecular Biology International|April 1, 1996
Mitochondrial DNA mutations associated with the 11778 mutation in Leber's diseaseT Sawano, M Tanaka, K Ohno, et al.Biochemical and Biophysical Research Communications|August 16, 1990
Increase of deleted mitochondrial DNA in the striatum in Parkinson's disease and senescenceS Ikebe, M Tanaka, K Ohno, et al.Biochemical and Biophysical Research Communications|May 29, 1987
Isolation of a cDNA clone for human cytochrome c1 from a lambda gt11 expression libraryM Nishikimi, H Suzuki, S Ohta, et al.The Journal of Clinical Endocrinology and Metabolism|January 1, 1994
Identification of two point mutations in the gene coding luteinizing hormone (LH) beta-subunit, associated with immunologically anomalous LH variantsK Furui, N Suganuma, S Tsukahara, et al.Rinsho Byori. the Japanese Journal of Clinical Pathology|February 1, 1991
[Myoglobinuria caused by multiple deletions of mitochondrial DNA]M Tanaka, K Ohno, K Sahashi, et al.Annals of Neurology|April 1, 1991
Mitochondrial DNA deletions in inherited recurrent myoglobinuriaK Ohno, M Tanaka, K Sahashi, et al.Biochemistry International|October 1, 1987
Characterization of histamine H1-receptor on rat hepatocytesK Tsuchie, M Imoto, M Tanaka, et al.Cancer Research|September 1, 1989
Stimulated rat liver mitochondrial biogenesis after partial hepatectomyM Nagino, M Tanaka, M Nishikimi, et al.Pageof 534