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The Journal of Biological Chemistry|January 25, 1982
Clofibric acid and phenylpyruvic acid as biochemical probes for studying soluble bovine liver branched chain ketoacid dehydrogenaseD J Danner, E T Sewell, L J Elsas
Metabolic Engineering|December 20, 2000
Controlled overexpression of BCKD kinase expression: metabolic engineering applied to BCAA metabolism in a mammalian systemC B Doering, I R Williams, D J Danner
Human Molecular Genetics|October 1, 1996
Functional analysis in Saccharomyces cerevisiae of naturally occurring amino acid substitutions in human dihydrolipoamide dehydrogenaseM M Lanterman, J R Dickinson, D J Danner
The Biochemical Journal|August 1, 1983
Antibodies to bovine liver branched-chain 2-oxo acid dehydrogenase cross-react with this enzyme complex from other tissues and speciesS C Heffelfinger, E T Sewell, D J Danner
Biochemistry|November 22, 1983
Identification of specific subunits of highly purified bovine liver branched-chain ketoacid dehydrogenaseS C Heffelfinger, E T Sewell, D J Danner
Biochimica Et Biophysica Acta|November 15, 1992
Nucleotide sequence of the 5' end including the initiation codon of cDNA for the E1 alpha subunit of the human branched chain alpha-ketoacid dehydrogenase complexM C McKean, K A Winkeler, D J Danner
Biochimica Et Biophysica Acta|March 20, 1992
Branched chain acyltransferase absence due to an Alu-based genomic deletion allele and an exon skipping allele in a compound heterozygote proband expressing maple syrup urine diseaseW J Herring, M McKean, N Dracopoli, et al.
The Journal of Biological Chemistry|May 5, 1989
Construction and nucleotide sequence of a cDNA encoding the full-length preprotein for human branched chain acyltransferaseD J Danner, S Litwer, W J Herring, et al.
Gene|June 5, 1998
Murine branched chain alpha-ketoacid dehydrogenase kinase; cDNA cloning, tissue distribution, and temporal expression during embryonic developmentC B Doering, C Coursey, W Spangler, et al.
American Journal of Human Genetics|February 1, 1991
Molecular genetic basis of maple syrup urine disease in a family with two defective alleles for branched chain acyltransferase and localization of the gene to human chromosome 1W J Herring, S Litwer, J L Weber, et al.
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