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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 cells
R 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 patients
E 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 fibroblasts
W 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 mouse
B 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 deficiency
M Duran, M Hofkamp, W J Rhead, et al.
The Journal of Biological Chemistry
|
January 13, 1995
Evidence for intermediate channeling in mitochondrial beta-oxidation
M 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 dichloroacetate
P 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 peroxisomes
J 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 syndrome
W 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 sibling
M D Medlock, W J Rhead, L Pollack, et al.
Page
of 7
Search research articles
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Showing results (31-40 of 65) with videos related to
Sort By:
Page
of 7
The Journal of Biological Chemistry
|
July 25, 1976
Cystine metabolism in human fibroblasts. Comparison of normal, cystinotic, and gamma-glutamylcysteine synethetase-deficient cells
R 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 patients
E 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 fibroblasts
W 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 mouse
B 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 deficiency
M Duran, M Hofkamp, W J Rhead, et al.
The Journal of Biological Chemistry
|
January 13, 1995
Evidence for intermediate channeling in mitochondrial beta-oxidation
M 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 dichloroacetate
P 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 peroxisomes
J 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 syndrome
W 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 sibling
M D Medlock, W J Rhead, L Pollack, et al.
Page
of 7