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Journal of Magnetic Resonance (San Diego, Calif. : 1997)|September 25, 1999
Manifestations of slow site exchange processes in solution NMR: a continuous Gaussian exchange modelJ M Schurr, B S Fujimoto, R Diaz, et al.
American Journal of Human Genetics|October 1, 1987
Abnormal kinetic behavior of cytochrome oxidase in a case of Leigh diseaseM Glerum, B H Robinson, C Spratt, et al.
Genomics|November 1, 1996
Assignment of the PSST subunit gene of human mitochondrial complex I to chromosome 19p13S J Hyslop, A M Duncan, S Pitkänen, et al.
The Journal of Biological Chemistry|February 7, 2001
Structure, functioning, and assembly of the ATP synthase in cells from patients with the T8993G mitochondrial DNA mutation. Comparison with the enzyme in Rho(0) cells completely lacking mtdnaJ J García, I Ogilvie, B H Robinson, et al.
Molecular Aspects of Medicine|January 1, 1995
Self and non-self antigen in diabetic autoimmunity: molecules and mechanismsW J Karges, J Ilonen, B H Robinson, et al.
FEBS Letters|August 15, 1988
Characterization of cytochrome-c oxidase mutants in human fibroblastsD M Glerum, W Yanamura, R A Capaldi, et al.
Biotechnology and Bioengineering|June 5, 1997
Kinetic studies of Chromobacterium viscosum lipase in AOT water in oil microemulsions and gelatin microemulsion-based organogelsT R Jenta, G Batts, G D Rees, et al.
Pediatric Research|January 1, 1990
Effect of lipoic acid in a patient with defective activity of pyruvate dehydrogenase, 2-oxoglutarate dehydrogenase, and branched-chain keto acid dehydrogenaseI Yoshida, L Sweetman, S Kulovich, et al.
Muscle & Nerve|January 14, 1998
Clinical, physiological, and histological features in a kindred with the T3271C melas mutationM A Tarnopolsky, J Maguire, T Myint, et al.
Genome|June 1, 1997
Cloning, characterization, and chromosomal localization of human liver form cytochrome c oxidase subunit VIa related genesF Merante, M Ling, A M Duncan, et al.
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