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The Journal of Clinical Investigation
|
November 5, 1999
Bacterial translocation in cirrhotic rats stimulates eNOS-derived NO production and impairs mesenteric vascular contractility
R Wiest, S Das, G Cadelina, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
July 15, 1996
Double transduction with GTP cyclohydrolase I and tyrosine hydroxylase is necessary for spontaneous synthesis of L-DOPA by primary fibroblasts
C Bencsics, S R Wachtel, S Milstien, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 1, 1987
Structure and expression of human dihydropteridine reductase
J Lockyer, R G Cook, S Milstien, et al.
Pediatrics
|
January 1, 1979
Dihydropteridine reductase deficiency associated with severe neurologic disease and mild hyperphenylalaninemia
T G Brewster, M A Moskowitz, S Kaufman, et al.
Pediatrics
|
December 1, 1984
Biopterin synthesis defects: problems in diagnosis
G Hoganson, S Berlow, S Kaufman, et al.
Archives of Neurology
|
May 18, 2001
Neurologic and psychiatric manifestations in a family with a mutation in exon 2 of the guanosine triphosphate-cyclohydrolase gene
H Hahn, M R Trant, M J Brownstein, et al.
The Journal of Clinical Investigation
|
May 1, 1994
Regulation of nitric oxide synthesis by proinflammatory cytokines in human umbilical vein endothelial cells. Elevations in tetrahydrobiopterin levels enhance endothelial nitric oxide synthase specific activity
P Rosenkranz-Weiss, W C Sessa, S Milstien, et al.
American Journal of Human Genetics
|
September 1, 1993
Mutation in the 4a-carbinolamine dehydratase gene leads to mild hyperphenylalaninemia with defective cofactor metabolism
B A Citron, S Kaufman, S Milstien, et al.
The Journal of Pediatrics
|
November 1, 1976
Hyperphenylalaninemia due to dihydropteridine reductase deficiency. Assay of the enzyme in fibroblasts from affected infants, heterozygotes, and in normal amniotic fluid cells
S Milstien, N A Holtzman, M E O'Flynn, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 1, 1990
Isolation and expression of rat liver sepiapterin reductase cDNA
B A Citron, S Milstien, J C Gutierrez, et al.
Page
of 11
Search research articles
Search
Showing results (71-80 of 109) with videos related to
Sort By:
Page
of 11
The Journal of Clinical Investigation
|
November 5, 1999
Bacterial translocation in cirrhotic rats stimulates eNOS-derived NO production and impairs mesenteric vascular contractility
R Wiest, S Das, G Cadelina, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
July 15, 1996
Double transduction with GTP cyclohydrolase I and tyrosine hydroxylase is necessary for spontaneous synthesis of L-DOPA by primary fibroblasts
C Bencsics, S R Wachtel, S Milstien, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 1, 1987
Structure and expression of human dihydropteridine reductase
J Lockyer, R G Cook, S Milstien, et al.
Pediatrics
|
January 1, 1979
Dihydropteridine reductase deficiency associated with severe neurologic disease and mild hyperphenylalaninemia
T G Brewster, M A Moskowitz, S Kaufman, et al.
Pediatrics
|
December 1, 1984
Biopterin synthesis defects: problems in diagnosis
G Hoganson, S Berlow, S Kaufman, et al.
Archives of Neurology
|
May 18, 2001
Neurologic and psychiatric manifestations in a family with a mutation in exon 2 of the guanosine triphosphate-cyclohydrolase gene
H Hahn, M R Trant, M J Brownstein, et al.
The Journal of Clinical Investigation
|
May 1, 1994
Regulation of nitric oxide synthesis by proinflammatory cytokines in human umbilical vein endothelial cells. Elevations in tetrahydrobiopterin levels enhance endothelial nitric oxide synthase specific activity
P Rosenkranz-Weiss, W C Sessa, S Milstien, et al.
American Journal of Human Genetics
|
September 1, 1993
Mutation in the 4a-carbinolamine dehydratase gene leads to mild hyperphenylalaninemia with defective cofactor metabolism
B A Citron, S Kaufman, S Milstien, et al.
The Journal of Pediatrics
|
November 1, 1976
Hyperphenylalaninemia due to dihydropteridine reductase deficiency. Assay of the enzyme in fibroblasts from affected infants, heterozygotes, and in normal amniotic fluid cells
S Milstien, N A Holtzman, M E O'Flynn, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 1, 1990
Isolation and expression of rat liver sepiapterin reductase cDNA
B A Citron, S Milstien, J C Gutierrez, et al.
Page
of 11