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E R McCabe

Showing results (111-120 of 160) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|January 1, 1992
Targeting of hexokinase 1 to liver and hepatoma mitochondriaB D Gelb, V Adams, S N Jones, et al.
Human Genetics|September 1, 1989
Characterization of patients with glycerol kinase deficiency utilizing cDNA probes for the Duchenne muscular dystrophy locusJ A Towbin, D R Wu, J Chamberlain, et al.
Biochemical Medicine and Metabolic Biology|June 1, 1986
Measurement of adenosine triphosphate and 2,3-diphosphoglycerate in stored blood with 31P nuclear magnetic resonance spectroscopyD R Ambruso, B Hawkins, D L Johnson, et al.
Pediatric Research|March 11, 1992
Genotypic confirmation from the original dried blood specimens in a neonatal hemoglobinopathy screening programM Descartes, Y Huang, Y H Zhang, et al.
American Journal of Diseases of Children (1960)|September 1, 1987
Lack of effect of lithium carbonate in patients with glycogenosis IbD H Mahoney, D R Ambruso, E R McCabe, et al.
Biochemical Medicine and Metabolic Biology|August 1, 1991
Screening for cystic fibrosis: feasibility of molecular genetic analysis of dried blood specimensW K Seltzer, F Accurso, M Z Fall, et al.
Progress in Clinical and Biological Research|January 1, 1992
Prevalence of K329E mutation in the medium-chain acyl-CoA dehydrogenase gene determined from Guthrie cardsY Matsubara, K Narisawa, K Tada, et al.
The Journal of Clinical Investigation|April 1, 1988
Perinatal hypophosphatasia: tissue levels of vitamin B6 are unremarkable despite markedly increased circulating concentrations of pyridoxal-5'-phosphate. Evidence for an ectoenzyme role for tissue-nonspecific alkaline phosphataseM P Whyte, J D Mahuren, K N Fedde, et al.
Genomics|July 1, 1990
DXS28 (C7) maps centromeric to DXS68 (L1-4) and DXS67 (B24) by deletion analysisJ A Towbin, J S Chamberlain, D R Wu, et al.
Lancet (London, England)|August 31, 1991
Prevalence of K329E mutation in medium-chain acyl-CoA dehydrogenase gene determined from Guthrie cardsY Matsubara, K Narisawa, K Tada, et al.
Pageof 16

Showing results (111-120 of 160) with videos related to

Sort By:
Pageof 16
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1992
Targeting of hexokinase 1 to liver and hepatoma mitochondriaB D Gelb, V Adams, S N Jones, et al.
Human Genetics|September 1, 1989
Characterization of patients with glycerol kinase deficiency utilizing cDNA probes for the Duchenne muscular dystrophy locusJ A Towbin, D R Wu, J Chamberlain, et al.
Biochemical Medicine and Metabolic Biology|June 1, 1986
Measurement of adenosine triphosphate and 2,3-diphosphoglycerate in stored blood with 31P nuclear magnetic resonance spectroscopyD R Ambruso, B Hawkins, D L Johnson, et al.
Pediatric Research|March 11, 1992
Genotypic confirmation from the original dried blood specimens in a neonatal hemoglobinopathy screening programM Descartes, Y Huang, Y H Zhang, et al.
American Journal of Diseases of Children (1960)|September 1, 1987
Lack of effect of lithium carbonate in patients with glycogenosis IbD H Mahoney, D R Ambruso, E R McCabe, et al.
Biochemical Medicine and Metabolic Biology|August 1, 1991
Screening for cystic fibrosis: feasibility of molecular genetic analysis of dried blood specimensW K Seltzer, F Accurso, M Z Fall, et al.
Progress in Clinical and Biological Research|January 1, 1992
Prevalence of K329E mutation in the medium-chain acyl-CoA dehydrogenase gene determined from Guthrie cardsY Matsubara, K Narisawa, K Tada, et al.
The Journal of Clinical Investigation|April 1, 1988
Perinatal hypophosphatasia: tissue levels of vitamin B6 are unremarkable despite markedly increased circulating concentrations of pyridoxal-5'-phosphate. Evidence for an ectoenzyme role for tissue-nonspecific alkaline phosphataseM P Whyte, J D Mahuren, K N Fedde, et al.
Genomics|July 1, 1990
DXS28 (C7) maps centromeric to DXS68 (L1-4) and DXS67 (B24) by deletion analysisJ A Towbin, J S Chamberlain, D R Wu, et al.
Lancet (London, England)|August 31, 1991
Prevalence of K329E mutation in medium-chain acyl-CoA dehydrogenase gene determined from Guthrie cardsY Matsubara, K Narisawa, K Tada, et al.
Pageof 16