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P M Coates

Showing results (51-60 of 86) with videos related to

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FEBS Letters|February 1, 1978
Effect of thyroxine on acid lipase activity of adult rat liverP M Coates, S A Brown, H Lau, et al.
American Journal of Human Genetics|December 1, 1991
Molecular survey of a prevalent mutation, 985A-to-G transition, and identification of five infrequent mutations in the medium-chain Acyl-CoA dehydrogenase (MCAD) gene in 55 patients with MCAD deficiencyI Yokota, P M Coates, D E Hale, et al.
Biochimica Et Biophysica Acta|February 26, 1979
Acid lipase activity of human lymphocytesP M Coates, J A Cortner, G M Hoffman, et al.
The International Journal of Biochemistry|January 1, 1979
Heat and thyroxine sensitive isozymes of rat liver N-acetyl-beta-glucosaminidaseL V Oberkotter, C Horowitz, P M Coates, et al.
Pediatric Research|September 1, 1986
Biosynthesis of variant medium chain acyl-CoA dehydrogenase in cultured fibroblasts from patients with medium chain acyl-CoA dehydrogenase deficiencyY Ikeda, D E Hale, S M Keese, et al.
The Journal of Clinical Investigation|January 1, 1988
Genetic deficiency of short-chain acyl-coenzyme A dehydrogenase in cultured fibroblasts from a patient with muscle carnitine deficiency and severe skeletal muscle weaknessP M Coates, D E Hale, G Finocchiaro, et al.
American Family Physician|May 1, 1989
Medium-chain acyl-CoA dehydrogenase deficiencyR J Egidio, G L Francis, P M Coates, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Familial combined hyperlipidaemia: use of stable isotopes to demonstrate overproduction of very low-density lipoprotein apolipoprotein B by the liverJ A Cortner, P M Coates, M J Bennett, et al.
Pediatric Pathology|November 1, 1991
Medium-chain acyl-CoA dehydrogenase deficiency: postmortem diagnosis in a case of sudden infant death and neonatal diagnosis of an affected siblingM J Bennett, P Rinaldo, D S Millington, et al.
Genetic Epidemiology|January 1, 1993
Genotype at a major locus with large effects on apolipoprotein B levels predicts familial combined hyperlipidemiaG P Jarvik, T H Beaty, P R Gallagher, et al.
Pageof 9

Showing results (51-60 of 86) with videos related to

Sort By:
Pageof 9
FEBS Letters|February 1, 1978
Effect of thyroxine on acid lipase activity of adult rat liverP M Coates, S A Brown, H Lau, et al.
American Journal of Human Genetics|December 1, 1991
Molecular survey of a prevalent mutation, 985A-to-G transition, and identification of five infrequent mutations in the medium-chain Acyl-CoA dehydrogenase (MCAD) gene in 55 patients with MCAD deficiencyI Yokota, P M Coates, D E Hale, et al.
Biochimica Et Biophysica Acta|February 26, 1979
Acid lipase activity of human lymphocytesP M Coates, J A Cortner, G M Hoffman, et al.
The International Journal of Biochemistry|January 1, 1979
Heat and thyroxine sensitive isozymes of rat liver N-acetyl-beta-glucosaminidaseL V Oberkotter, C Horowitz, P M Coates, et al.
Pediatric Research|September 1, 1986
Biosynthesis of variant medium chain acyl-CoA dehydrogenase in cultured fibroblasts from patients with medium chain acyl-CoA dehydrogenase deficiencyY Ikeda, D E Hale, S M Keese, et al.
The Journal of Clinical Investigation|January 1, 1988
Genetic deficiency of short-chain acyl-coenzyme A dehydrogenase in cultured fibroblasts from a patient with muscle carnitine deficiency and severe skeletal muscle weaknessP M Coates, D E Hale, G Finocchiaro, et al.
American Family Physician|May 1, 1989
Medium-chain acyl-CoA dehydrogenase deficiencyR J Egidio, G L Francis, P M Coates, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Familial combined hyperlipidaemia: use of stable isotopes to demonstrate overproduction of very low-density lipoprotein apolipoprotein B by the liverJ A Cortner, P M Coates, M J Bennett, et al.
Pediatric Pathology|November 1, 1991
Medium-chain acyl-CoA dehydrogenase deficiency: postmortem diagnosis in a case of sudden infant death and neonatal diagnosis of an affected siblingM J Bennett, P Rinaldo, D S Millington, et al.
Genetic Epidemiology|January 1, 1993
Genotype at a major locus with large effects on apolipoprotein B levels predicts familial combined hyperlipidemiaG P Jarvik, T H Beaty, P R Gallagher, et al.
Pageof 9