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E R McCabe

Showing results (131-140 of 160) with videos related to

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The Journal of Biological Chemistry|January 25, 1993
Cloning and functional expression in yeast of two human isoforms of the outer mitochondrial membrane channel, the voltage-dependent anion channelE Blachly-Dyson, E B Zambronicz, W H Yu, et al.
Annals of Neurology|May 1, 1980
Glycerol kinase deficiency with neuromuscular, skeletal, and adrenal abnormalitiesM A Guggenheim, E R McCabe, M Roig, et al.
Journal of Bacteriology|October 1, 1990
Mutational analysis of the Escherichia coli glpFK region with Tn5 mutagenesis and the polymerase chain reactionJ R Lupski, Y H Zhang, M Rieger, et al.
Biochemical and Biophysical Research Communications|October 24, 1977
Human glycerol kinase deficiency with hyperglycerolemia and glyceroluriaE R McCabe, P V Fennessey, M A Guggenheim, et al.
The Journal of Pediatrics|August 1, 1984
Nutritional deficits exist before 2 months of age in some infants with cystic fibrosis identified by screening testM C Reardon, K B Hammond, F J Accurso, et al.
Circulation|June 1, 1993
X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locusJ A Towbin, J F Hejtmancik, P Brink, et al.
The Journal of Pediatrics|May 1, 1984
A juvenile form of glycerol kinase deficiency with episodic vomiting, acidemia, and stuporE I Ginns, J A Barranger, S W McClean, et al.
Pediatric Research|August 1, 1986
Pancytopenia in propionic acidemia: hematologic evaluation and studies of hematopoiesis in vitroL C Stork, D R Ambruso, S F Wallner, et al.
The Journal of Pediatrics|June 1, 1982
Glutaric acidemia type II: clinical, biochemical, and morphologic considerationsS I Goodman, D O Stene, E R McCabe, et al.
Neurology|November 1, 1980
Glutaric acidemia: a metabolic disorder causing progressive choreoathetosisR L Leibel, V E Shih, S I Goodman, et al.
Pageof 16

Showing results (131-140 of 160) with videos related to

Sort By:
Pageof 16
The Journal of Biological Chemistry|January 25, 1993
Cloning and functional expression in yeast of two human isoforms of the outer mitochondrial membrane channel, the voltage-dependent anion channelE Blachly-Dyson, E B Zambronicz, W H Yu, et al.
Annals of Neurology|May 1, 1980
Glycerol kinase deficiency with neuromuscular, skeletal, and adrenal abnormalitiesM A Guggenheim, E R McCabe, M Roig, et al.
Journal of Bacteriology|October 1, 1990
Mutational analysis of the Escherichia coli glpFK region with Tn5 mutagenesis and the polymerase chain reactionJ R Lupski, Y H Zhang, M Rieger, et al.
Biochemical and Biophysical Research Communications|October 24, 1977
Human glycerol kinase deficiency with hyperglycerolemia and glyceroluriaE R McCabe, P V Fennessey, M A Guggenheim, et al.
The Journal of Pediatrics|August 1, 1984
Nutritional deficits exist before 2 months of age in some infants with cystic fibrosis identified by screening testM C Reardon, K B Hammond, F J Accurso, et al.
Circulation|June 1, 1993
X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locusJ A Towbin, J F Hejtmancik, P Brink, et al.
The Journal of Pediatrics|May 1, 1984
A juvenile form of glycerol kinase deficiency with episodic vomiting, acidemia, and stuporE I Ginns, J A Barranger, S W McClean, et al.
Pediatric Research|August 1, 1986
Pancytopenia in propionic acidemia: hematologic evaluation and studies of hematopoiesis in vitroL C Stork, D R Ambruso, S F Wallner, et al.
The Journal of Pediatrics|June 1, 1982
Glutaric acidemia type II: clinical, biochemical, and morphologic considerationsS I Goodman, D O Stene, E R McCabe, et al.
Neurology|November 1, 1980
Glutaric acidemia: a metabolic disorder causing progressive choreoathetosisR L Leibel, V E Shih, S I Goodman, et al.
Pageof 16