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W J Rhead

Showing results (31-40 of 65) with videos related to

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The Journal of Biological Chemistry|July 25, 1976
Cystine metabolism in human fibroblasts. Comparison of normal, cystinotic, and gamma-glutamylcysteine synethetase-deficient cellsR G Oshima, W J Rhead, J G Thoene, et al.
The Journal of Clinical Investigation|November 1, 1992
Glutaric acidemia type II. Heterogeneity in beta-oxidation flux, polypeptide synthesis, and complementary DNA mutations in the alpha subunit of electron transfer flavoprotein in eight patientsE Freneaux, V C Sheffield, L Molin, et al.
Science (New York, N.Y.)|July 1, 1983
Dicarboxylic aciduria: deficient [1-14C]octanoate oxidation and medium-chain acyl-CoA dehydrogenase in fibroblastsW J Rhead, B A Amendt, K S Fritchman, et al.
Pediatric Research|June 1, 1992
Short-chain acyl-coenzyme A dehydrogenase activity, antigen, and biosynthesis are absent in the BALB/cByJ mouseB A Amendt, E Freneaux, C Reece, et al.
Pediatrics|December 1, 1986
Sudden child death and 'healthy' affected family members with medium-chain acyl-coenzyme A dehydrogenase deficiencyM Duran, M Hofkamp, W J Rhead, et al.
The Journal of Biological Chemistry|January 13, 1995
Evidence for intermediate channeling in mitochondrial beta-oxidationM A Nada, W J Rhead, H Sprecher, et al.
The Journal of Pediatrics|September 1, 1993
Transient improvement of congenital lactic acidosis in a male infant with pyruvate decarboxylase deficiency treated with dichloroacetateP P Tóth, H el-Shanti, S Eivins, et al.
Prostaglandins, Leukotrienes, and Essential Fatty Acids|February 1, 1995
Formation of a novel arachidonic acid metabolite in peroxisomesJ A Gordon, S K Heller, W J Rhead, et al.
The Journal of Pediatrics|August 1, 1972
Vitamin E, selenium, and the sudden infant death syndromeW J Rhead, G N Schrauzer, S L Saltzstein, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association|September 1, 1991
A case of glutaric acidemia type II (severe multiple acyl-CoA dehydrogenation disorder) with subsequent prenatal exclusion in a siblingM D Medlock, W J Rhead, L Pollack, et al.
Pageof 7

Showing results (31-40 of 65) with videos related to

Sort By:
Pageof 7
The Journal of Biological Chemistry|July 25, 1976
Cystine metabolism in human fibroblasts. Comparison of normal, cystinotic, and gamma-glutamylcysteine synethetase-deficient cellsR G Oshima, W J Rhead, J G Thoene, et al.
The Journal of Clinical Investigation|November 1, 1992
Glutaric acidemia type II. Heterogeneity in beta-oxidation flux, polypeptide synthesis, and complementary DNA mutations in the alpha subunit of electron transfer flavoprotein in eight patientsE Freneaux, V C Sheffield, L Molin, et al.
Science (New York, N.Y.)|July 1, 1983
Dicarboxylic aciduria: deficient [1-14C]octanoate oxidation and medium-chain acyl-CoA dehydrogenase in fibroblastsW J Rhead, B A Amendt, K S Fritchman, et al.
Pediatric Research|June 1, 1992
Short-chain acyl-coenzyme A dehydrogenase activity, antigen, and biosynthesis are absent in the BALB/cByJ mouseB A Amendt, E Freneaux, C Reece, et al.
Pediatrics|December 1, 1986
Sudden child death and 'healthy' affected family members with medium-chain acyl-coenzyme A dehydrogenase deficiencyM Duran, M Hofkamp, W J Rhead, et al.
The Journal of Biological Chemistry|January 13, 1995
Evidence for intermediate channeling in mitochondrial beta-oxidationM A Nada, W J Rhead, H Sprecher, et al.
The Journal of Pediatrics|September 1, 1993
Transient improvement of congenital lactic acidosis in a male infant with pyruvate decarboxylase deficiency treated with dichloroacetateP P Tóth, H el-Shanti, S Eivins, et al.
Prostaglandins, Leukotrienes, and Essential Fatty Acids|February 1, 1995
Formation of a novel arachidonic acid metabolite in peroxisomesJ A Gordon, S K Heller, W J Rhead, et al.
The Journal of Pediatrics|August 1, 1972
Vitamin E, selenium, and the sudden infant death syndromeW J Rhead, G N Schrauzer, S L Saltzstein, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association|September 1, 1991
A case of glutaric acidemia type II (severe multiple acyl-CoA dehydrogenation disorder) with subsequent prenatal exclusion in a siblingM D Medlock, W J Rhead, L Pollack, et al.
Pageof 7