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P M Coates

Showing results (11-20 of 86) with videos related to

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Atherosclerosis|October 1, 1986
Genetic variation of human mononuclear leukocyte lysosomal acid lipase activity. Relationship to atherosclerosisP M Coates, T Langer, J A Cortner
The Journal of Clinical Investigation|September 1, 1990
Molecular basis of medium chain acyl-coenzyme A dehydrogenase deficiency. An A to G transition at position 985 that causes a lysine-304 to glutamate substitution in the mature protein is the single prevalent mutationI Yokota, Y Indo, P M Coates, et al.
Pediatric Research|January 1, 1978
Acid and neutral lipases of cultured adipocytes of infants and childrenF O Adebonojo, P M Coates, J A Cortner
Progress in Clinical and Biological Research|January 1, 1990
Genetic defects of acyl-CoA dehydrogenases: studies using an electron transfer flavoprotein reduction assayD E Hale, C A Stanley, P M Coates
Progress in Clinical and Biological Research|January 1, 1990
Medium-chain acyl-CoA dehydrogenase deficiencyC A Stanley, D E Hale, P M Coates
Biochimica Et Biophysica Acta|January 4, 1979
I-cell disease: intracellular desialylation of lysosomal enzymes using an influenza virus vectorR A Spritz, P M Coates, F S Lief
Annual Review of Nutrition|January 1, 1989
Gene polymorphisms and variability of human apolipoproteinsE A Fisher, P M Coates, J A Cortner
Progress in Clinical and Biological Research|January 1, 1990
The long-chain acyl-CoA dehydrogenase deficiencyD E Hale, C A Stanley, P M Coates
The Journal of Pediatrics|April 1, 1990
Prevalence and expression of familial combined hyperlipidemia in childhoodJ A Cortner, P M Coates, P R Gallagher
Annals of Human Genetics|July 1, 1975
A preliminary genetic interpretation of the esterase isozymes of human tissuesP M Coates, M A Mestriner, D A Hopkinson
Pageof 9

Showing results (11-20 of 86) with videos related to

Sort By:
Pageof 9
Atherosclerosis|October 1, 1986
Genetic variation of human mononuclear leukocyte lysosomal acid lipase activity. Relationship to atherosclerosisP M Coates, T Langer, J A Cortner
The Journal of Clinical Investigation|September 1, 1990
Molecular basis of medium chain acyl-coenzyme A dehydrogenase deficiency. An A to G transition at position 985 that causes a lysine-304 to glutamate substitution in the mature protein is the single prevalent mutationI Yokota, Y Indo, P M Coates, et al.
Pediatric Research|January 1, 1978
Acid and neutral lipases of cultured adipocytes of infants and childrenF O Adebonojo, P M Coates, J A Cortner
Progress in Clinical and Biological Research|January 1, 1990
Genetic defects of acyl-CoA dehydrogenases: studies using an electron transfer flavoprotein reduction assayD E Hale, C A Stanley, P M Coates
Progress in Clinical and Biological Research|January 1, 1990
Medium-chain acyl-CoA dehydrogenase deficiencyC A Stanley, D E Hale, P M Coates
Biochimica Et Biophysica Acta|January 4, 1979
I-cell disease: intracellular desialylation of lysosomal enzymes using an influenza virus vectorR A Spritz, P M Coates, F S Lief
Annual Review of Nutrition|January 1, 1989
Gene polymorphisms and variability of human apolipoproteinsE A Fisher, P M Coates, J A Cortner
Progress in Clinical and Biological Research|January 1, 1990
The long-chain acyl-CoA dehydrogenase deficiencyD E Hale, C A Stanley, P M Coates
The Journal of Pediatrics|April 1, 1990
Prevalence and expression of familial combined hyperlipidemia in childhoodJ A Cortner, P M Coates, P R Gallagher
Annals of Human Genetics|July 1, 1975
A preliminary genetic interpretation of the esterase isozymes of human tissuesP M Coates, M A Mestriner, D A Hopkinson
Pageof 9