Analysis of maple syrup urine disease in cell culture: Use of substrates
- 1 September 1989
- journal article
- research article
- Published by Elsevier in Clinica Chimica Acta; International Journal of Clinical Chemistry
- Vol. 184 (1) , 47-56
- https://doi.org/10.1016/0009-8981(89)90255-6
Abstract
No abstract availableKeywords
This publication has 31 references indexed in Scilit:
- Functional differences in the catabolism of branched-chain l-amino acids in cultured normal and maple syrup urine disease fibroblastsBiochemical Medicine and Metabolic Biology, 1989
- Purification and characterization of human liver branched-chain α-keto acid dehydrogenase complexBiochemical Medicine and Metabolic Biology, 1987
- Intracellular levels and metabolism of leucine and α-ketoisocaproate in normal and maple syrup urine disease fibroblastsBiochemical Medicine, 1984
- Degradation of branched-chain amino acids and their derived 2-oxo acids and fatty acids in human and rat heart and skeletal muscleBiochemical Medicine, 1982
- Maple syrup urine disease: α-Ketoisocaproate decarboxylation activity in different types of cultured amniotic fluid cellsPrenatal Diagnosis, 1981
- ANTENATAL DIAGNOSIS OF MAPLE-SYRUP-URINE DISEASEThe Lancet, 1978
- Heterogeneity in maple syrup urine disease: Aspects of cofactor requirement and complementation in cultured fibroblastsClinical Genetics, 1977
- Enzyme activity in classical and variant forms of maple syrup urine diseasePublished by Elsevier ,1972
- Metabolism of the white blood cells in maple-syrup-urine diseaseBiochimica et Biophysica Acta, 1960
- PLAQUE FORMATION AND ISOLATION OF PURE LINES WITH POLIOMYELITIS VIRUSESThe Journal of Experimental Medicine, 1954