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Japanese Circulation Journal|October 1, 1992
Mitochondrial DNA mutations in cardiomyopathyT Ito, K Hattori, T Obayashi, et al.Retina (Philadelphia, Pa.)|January 1, 1994
Early retinal involvement in mitochondrial myopathy with mitochondrial DNA deletionY Ota, Y Miyake, S Awaya, et al.Obstetrics and Gynecology|August 1, 1994
Decrease in cytochrome c oxidase and cytochrome oxidase subunit I messenger RNA levels in preeclamptic pregnanciesT Furui, O Kurauchi, M Tanaka, et al.Biochemistry International|March 1, 1987
Partial deficiency of subunits in complex I or IV of patients with mitochondrial myopathiesM Tanaka, M Nishikimi, H Suzuki, et al.Acta Neurologica Scandinavica|December 1, 1989
Mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes with special reference to the mechanism of cerebral manifestationsK Seyama, K Suzuki, Y Mizuno, et al.Biochemical and Biophysical Research Communications|October 24, 1995
Mitochondrial DNA minicircles, lacking replication origins, exist in the cardiac muscle of a young normal subjectM Hayakawa, K Katsumata, M Yoneda, et al.Biochemistry International|September 1, 1991
Deleted mitochondrial DNA in the skeletal muscle of aged individualsM Katayama, M Tanaka, H Yamamoto, et al.Biochemistry International|April 1, 1991
Mechanism of adaptive increase of respiratory enzymes in rat liver mitochondria during obstructive jaundiceM Kanai, M Tanaka, Y Nimura, et al.Biochemical and Biophysical Research Communications|May 15, 1996
Accumulation of somatic nucleotide substitutions in mitochondrial DNA associated with the 3243 A-to-G tRNA(leu)(UUR) mutation in encephalomyopathy and cardiomyopathyS A Kovalenko, M Tanaka, M Yoneda, et al.Biochemistry International|October 1, 1987
In vitro synthesis of L-gulono-gamma-lactone oxidase by rabbit reticulocyte lysateT Koshizaka, M Nishikimi, M Tanaka, et al.Pageof 534