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E R McCabe

Showing results (101-110 of 160) with videos related to

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Human Genetics|March 1, 1989
Molecular genetic diagnosis of sickle cell disease using dried blood specimens on blotters used for newborn screeningD C Jinks, M Minter, D A Tarver, et al.
Pediatrics|April 1, 1990
Transient organic aciduria and methemoglobinemia with acute gastroenteritisM A Kay, W O'Brien, B Kessler, et al.
Biochemical Medicine|October 1, 1982
Glutaric, 3-hydroxypropionic, and lactic aciduria with metabolic acidemia, following extensive small bowel resectionE R McCabe, S I Goodman, P V Fennessey, et al.
Genomics|December 1, 1991
Mammalian hexokinase 1: evolutionary conservation and structure to function analysisL D Griffin, B D Gelb, D A Wheeler, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 1, 1978
Methylmalonic/beta-hydroxy-n-valeric aciduria due to methylmalonyl-CoA mutase deficiencyS I Goodman, E R McCabe, P V Fennessey, et al.
Biochemical Medicine and Metabolic Biology|April 1, 1989
Synthesis and characterization of a bovine hexokinase 1 cDNA probe by mixed oligonucleotide primed amplification of cDNA using high complexity primer mixturesL D Griffin, G R MacGregor, D M Muzny, et al.
The Journal of Clinical Endocrinology and Metabolism|December 22, 1999
IMAGe, a new clinical association of intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomaliesE Vilain, M Le Merrer, C Lecointre, et al.
Biochemical Medicine and Metabolic Biology|June 1, 1992
Characterization of human genomic yeast artificial chromosome inserts containing hexokinase 1 coding information on chromosome 10B D Gelb, K C Worley, L D Griffin, et al.
Journal of Inherited Metabolic Disease|January 1, 1982
Human glycerol kinase deficiency: enzyme kinetics and fibroblast hybridizationE R McCabe, D Sadava, W W Bullen, et al.
Biochemical Medicine and Metabolic Biology|October 1, 1989
Demonstration and characterization of human cardiac porin: a voltage-dependent channel involved in adenine nucleotide movement across the outer mitochondrial membraneJ A Towbin, M Minter, D Brdiczka, et al.
Pageof 16

Showing results (101-110 of 160) with videos related to

Sort By:
Pageof 16
Human Genetics|March 1, 1989
Molecular genetic diagnosis of sickle cell disease using dried blood specimens on blotters used for newborn screeningD C Jinks, M Minter, D A Tarver, et al.
Pediatrics|April 1, 1990
Transient organic aciduria and methemoglobinemia with acute gastroenteritisM A Kay, W O'Brien, B Kessler, et al.
Biochemical Medicine|October 1, 1982
Glutaric, 3-hydroxypropionic, and lactic aciduria with metabolic acidemia, following extensive small bowel resectionE R McCabe, S I Goodman, P V Fennessey, et al.
Genomics|December 1, 1991
Mammalian hexokinase 1: evolutionary conservation and structure to function analysisL D Griffin, B D Gelb, D A Wheeler, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 1, 1978
Methylmalonic/beta-hydroxy-n-valeric aciduria due to methylmalonyl-CoA mutase deficiencyS I Goodman, E R McCabe, P V Fennessey, et al.
Biochemical Medicine and Metabolic Biology|April 1, 1989
Synthesis and characterization of a bovine hexokinase 1 cDNA probe by mixed oligonucleotide primed amplification of cDNA using high complexity primer mixturesL D Griffin, G R MacGregor, D M Muzny, et al.
The Journal of Clinical Endocrinology and Metabolism|December 22, 1999
IMAGe, a new clinical association of intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomaliesE Vilain, M Le Merrer, C Lecointre, et al.
Biochemical Medicine and Metabolic Biology|June 1, 1992
Characterization of human genomic yeast artificial chromosome inserts containing hexokinase 1 coding information on chromosome 10B D Gelb, K C Worley, L D Griffin, et al.
Journal of Inherited Metabolic Disease|January 1, 1982
Human glycerol kinase deficiency: enzyme kinetics and fibroblast hybridizationE R McCabe, D Sadava, W W Bullen, et al.
Biochemical Medicine and Metabolic Biology|October 1, 1989
Demonstration and characterization of human cardiac porin: a voltage-dependent channel involved in adenine nucleotide movement across the outer mitochondrial membraneJ A Towbin, M Minter, D Brdiczka, et al.
Pageof 16