Subcellular distribution and cofactor function of human branched chain α-ketoacid dehydrogenase in normal and mutant cultured skin fibroblasts
- 31 May 1975
- journal article
- Published by Elsevier in Biochemical Medicine
- Vol. 13 (1) , 7-22
- https://doi.org/10.1016/0006-2944(75)90135-0
Abstract
No abstract availableKeywords
This publication has 22 references indexed in Scilit:
- Maple Syrup Urine Disease: Coenzyme function and prenatal monitoringMetabolism, 1974
- Oxidative phosphorylation in mitochondria isolated from human fibroblastsBiochimica et Biophysica Acta (BBA) - Bioenergetics, 1973
- Classical Maple Syrup Urine Disease: Cofactor resistanceMetabolism, 1972
- Function of the nonidentical subunits of mammalian pyruvate dehydrogenaseBiochemical and Biophysical Research Communications, 1972
- Cellular localization and characterization of bovine liver branched-chain α-keto acid dehydrogenasesBiochemistry, 1972
- Lipoic acid dependency of human branched chain α-ketoacid oxidaseBiochimica et Biophysica Acta (BBA) - General Subjects, 1972
- THIAMINE-RESPONSIVE MAPLE-SYRUP-URINE DISEASEThe Lancet, 1971
- ENZYMATIC PROPERTIES OF THE INNER AND OUTER MEMBRANES OF RAT LIVER MITOCHONDRIAThe Journal of cell biology, 1968
- The metabolism of leucine in tissue culture of skin fibroblasts of maple-syrup-urine diseaseBiochimica et Biophysica Acta, 1963
- "Maple Syrup Urine Disease"BMJ, 1959