Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

S Milstien

Showing results (71-80 of 109) with videos related to

Pageof 11
Sort By:
The Journal of Clinical Investigation|November 5, 1999
Bacterial translocation in cirrhotic rats stimulates eNOS-derived NO production and impairs mesenteric vascular contractilityR 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 fibroblastsC 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 reductaseJ Lockyer, R G Cook, S Milstien, et al.
Pediatrics|January 1, 1979
Dihydropteridine reductase deficiency associated with severe neurologic disease and mild hyperphenylalaninemiaT G Brewster, M A Moskowitz, S Kaufman, et al.
Pediatrics|December 1, 1984
Biopterin synthesis defects: problems in diagnosisG 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 geneH 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 activityP 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 metabolismB 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 cellsS 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 cDNAB A Citron, S Milstien, J C Gutierrez, et al.
Pageof 11

Showing results (71-80 of 109) with videos related to

Sort By:
Pageof 11
The Journal of Clinical Investigation|November 5, 1999
Bacterial translocation in cirrhotic rats stimulates eNOS-derived NO production and impairs mesenteric vascular contractilityR 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 fibroblastsC 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 reductaseJ Lockyer, R G Cook, S Milstien, et al.
Pediatrics|January 1, 1979
Dihydropteridine reductase deficiency associated with severe neurologic disease and mild hyperphenylalaninemiaT G Brewster, M A Moskowitz, S Kaufman, et al.
Pediatrics|December 1, 1984
Biopterin synthesis defects: problems in diagnosisG 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 geneH 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 activityP 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 metabolismB 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 cellsS 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 cDNAB A Citron, S Milstien, J C Gutierrez, et al.
Pageof 11