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Molecular Biology Reports|July 1, 1975
Evidence for a functional association of DNA synthesis with the membrane in mitochondria of Saccharomyces cerevisiaeR M Hall, J S Mattick, S Marzuki, et al.American Journal of Hematology|September 1, 1999
Phenotypic variability of Filipino beta(o)-thalassemia/HbE patients in IndonesiaI Setianingsih, R Williamson, D Daud, et al.Journal of Immunology (Baltimore, Md. : 1950)|September 1, 1985
Reactivity of anti-mitochondrial autoantibodies in primary biliary cirrhosis: definition of two novel mitochondrial polypeptide autoantigensI H Frazer, I R Mackay, T W Jordan, et al.Australian and New Zealand Journal of Medicine|December 1, 1991
Biochemical and molecular investigation of mitochondrial disease: an illustrative case showing the value of a multifaceted approachE Byrne, B Jean-Francois, D Thyagarajan, et al.Biochimica Et Biophysica Acta|September 23, 1991
The human pyruvate dehydrogenase complex: a polymorphic region of the lipoate acetyl transferase (E2) subunit geneL H Moehario, L Wang, R J Devenish, et al.Alcohol (Fayetteville, N.Y.)|May 1, 1984
Alteration of alcohol drinking in the rat by peripherally self-administered acetaldehydeW D Myers, K T Ng, S Marzuki, et al.Journal of the Neurological Sciences|December 1, 1988
Progression from MERRF to MELAS phenotype in a patient with combined respiratory complex I and IV deficienciesE Byrne, I Trounce, X Dennett, et al.Journal of Interferon Research|June 1, 1988
Production of subtype-specific antipeptide antibodies to human interferon-alpha 1 and -alpha 4N Sattayasai, A R Hibbs, G L McMullen, et al.Journal of Medical Genetics|August 27, 1998
Meiotic breakpoint mapping of a proposed X linked visual loss susceptibility locus in Leber's hereditary optic neuropathyH Y Handoko, P J Wirapati, H A Sudoyo, et al.Acta Neurologica Scandinavica|January 1, 1993
Significance of mitochondrial DNA deletions in myotonic dystrophyD Thyagarajan, E Byrne, S Noer, et al.Pageof 9