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Showing results (41-50 of 59) with videos related to

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Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|September 8, 2021
Dichorionic twin pregnancy complicated by duodenal atresia and umbilical cord ulceration with intrauterine fetal demiseE Krispin, D J Danner, R Donepudi, et al.
Metabolism: Clinical and Experimental|June 1, 1974
Maple syrup urine disease: coenzyme function and prenatal monitoringL J Elsas, J H Priest, F B Wheeler, et al.
The Journal of Biological Chemistry|May 5, 1988
Nucleotide sequence of a cDNA for branched chain acyltransferase with analysis of the deduced protein structureK B Hummel, S Litwer, A P Bradford, et al.
Developmental Biology|November 1, 1978
Developmental control of 2-aminoisobutyric acid transport by 7-and 14-day chick heart cell aggregates. Roles of insulin and amino acidsF B Wheeler, A C Santora, D J Danner, et al.
The Journal of Clinical Investigation|March 1, 1985
Absence of branched chain acyl-transferase as a cause of maple syrup urine diseaseD J Danner, N Armstrong, S C Heffelfinger, et al.
Lancet (London, England)|May 14, 1988
Primary biliary cirrhosis: identification of two major M2 mitochondrial autoantigensS J Yeaman, S P Fussey, D J Danner, et al.
Biochemical Medicine and Metabolic Biology|June 1, 1993
Thiamin-responsive maple syrup urine disease in a patient antigenically missing dihydrolipoamide acyltransferaseN P Ellerine, W J Herring, L J Elsas, et al.
Biochimica Et Biophysica Acta|October 20, 1992
The complete cDNA sequence for dihydrolipoyl transacylase (E2) of human branched-chain alpha-keto acid dehydrogenase complexK S Lau, J L Chuang, W J Herring, et al.
The Journal of Biological Chemistry|November 25, 1992
Structure of the gene encoding dihydrolipoyl transacylase (E2) component of human branched chain alpha-keto acid dehydrogenase complex and characterization of an E2 pseudogeneK S Lau, W J Herring, J L Chuang, et al.
Hepatology (Baltimore, Md.)|January 1, 1989
Reactivity of primary biliary cirrhosis sera with a human fetal liver cDNA clone of branched-chain alpha-keto acid dehydrogenase dihydrolipoamide acyltransferase, the 52 kD mitochondrial autoantigenC D Surh, D J Danner, A Ahmed, et al.
Pageof 6

Showing results (41-50 of 59) with videos related to

Sort By:
Pageof 6
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|September 8, 2021
Dichorionic twin pregnancy complicated by duodenal atresia and umbilical cord ulceration with intrauterine fetal demiseE Krispin, D J Danner, R Donepudi, et al.
Metabolism: Clinical and Experimental|June 1, 1974
Maple syrup urine disease: coenzyme function and prenatal monitoringL J Elsas, J H Priest, F B Wheeler, et al.
The Journal of Biological Chemistry|May 5, 1988
Nucleotide sequence of a cDNA for branched chain acyltransferase with analysis of the deduced protein structureK B Hummel, S Litwer, A P Bradford, et al.
Developmental Biology|November 1, 1978
Developmental control of 2-aminoisobutyric acid transport by 7-and 14-day chick heart cell aggregates. Roles of insulin and amino acidsF B Wheeler, A C Santora, D J Danner, et al.
The Journal of Clinical Investigation|March 1, 1985
Absence of branched chain acyl-transferase as a cause of maple syrup urine diseaseD J Danner, N Armstrong, S C Heffelfinger, et al.
Lancet (London, England)|May 14, 1988
Primary biliary cirrhosis: identification of two major M2 mitochondrial autoantigensS J Yeaman, S P Fussey, D J Danner, et al.
Biochemical Medicine and Metabolic Biology|June 1, 1993
Thiamin-responsive maple syrup urine disease in a patient antigenically missing dihydrolipoamide acyltransferaseN P Ellerine, W J Herring, L J Elsas, et al.
Biochimica Et Biophysica Acta|October 20, 1992
The complete cDNA sequence for dihydrolipoyl transacylase (E2) of human branched-chain alpha-keto acid dehydrogenase complexK S Lau, J L Chuang, W J Herring, et al.
The Journal of Biological Chemistry|November 25, 1992
Structure of the gene encoding dihydrolipoyl transacylase (E2) component of human branched chain alpha-keto acid dehydrogenase complex and characterization of an E2 pseudogeneK S Lau, W J Herring, J L Chuang, et al.
Hepatology (Baltimore, Md.)|January 1, 1989
Reactivity of primary biliary cirrhosis sera with a human fetal liver cDNA clone of branched-chain alpha-keto acid dehydrogenase dihydrolipoamide acyltransferase, the 52 kD mitochondrial autoantigenC D Surh, D J Danner, A Ahmed, et al.
Pageof 6