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American Journal of Human Genetics|December 12, 2000
Gene preference in maple syrup urine diseaseM M Nellis, D J DannerAmerican Journal of Human Genetics|November 1, 1988
Mitochondrial import and processing of an in vitro synthesized human prebranched chain acyltransferase fragmentS Litwer, D J DannerBiochemical and Biophysical Research Communications|September 16, 1985
Identification of a cDNA clone in lambda gt11 for the transacylase component of branched chain ketoacid dehydrogenaseS Litwer, D J DannerBiochemical Genetics|October 1, 1983
Branched-chain ketoacid dehydrogenase activity and growth of normal and mutant human fibroblasts: the effect of branched-chain amino acid concentration in culture mediumD J Danner, J H PriestFrontiers in Bioscience : a Journal and Virtual Library|June 4, 1998
Human mutations affecting branched chain alpha-ketoacid dehydrogenaseD J Danner, C B DoeringAmerican Journal of Physiology. Cell Physiology|October 13, 2000
Amino acid deprivation induces translation of branched-chain alpha-ketoacid dehydrogenase kinaseC B Doering, D J DannerBiochemical Medicine and Metabolic Biology|December 1, 1993
Molecular genetic characterization of maple syrup urine disease in European familiesF Peinemann, U Wendel, D J DannerBiochimica Et Biophysica Acta|December 31, 1997
Two new mutations in the human E1 beta subunit of branched chain alpha-ketoacid dehydrogenase associated with maple syrup urine diseaseB B McConnell, B Burkholder, D J DannerThe Journal of Biological Chemistry|September 5, 1989
Reversion of the maple syrup urine disease phenotype of impaired branched chain alpha-ketoacid dehydrogenase complex activity in fibroblasts from an affected childS Litwer, W J Herring, D J DannerJournal of Cellular Biochemistry|April 1, 1996
Influence of subunit transcript and protein levels on formation of a mitochondrial multienzyme complexB B McConnell, M C McKean, D J DannerPageof 5