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Frontiers 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 DannerMetabolic 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 DannerGene|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|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 DannerAmerican Journal of Human Genetics|December 12, 2000
Gene preference in maple syrup urine diseaseM M Nellis, 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 PriestBiochemical Medicine and Metabolic Biology|December 1, 1993
Molecular genetic characterization of maple syrup urine disease in European familiesF Peinemann, U Wendel, D J DannerHaemophilia : the Official Journal of the World Federation of Hemophilia|July 14, 2016
State of the art: gene therapy of haemophiliaH T Spencer, B E Riley, C B DoeringPageof 5