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 D Cederbaum

Showing results (81-90 of 93) with videos related to

Pageof 10
Sort By:
Gene Therapy|December 5, 2014
Minimal ureagenesis is necessary for survival in the murine model of hyperargininemia treated by AAV-based gene therapyC Hu, D S Tai, H Park, et al.
The Journal of Clinical Investigation|February 1, 1989
Differential expression of the two human arginase genes in hyperargininemia. Enzymatic, pathologic, and molecular analysisW W Grody, C Argyle, R M Kern, et al.
Biochemical Genetics|December 1, 1988
Effects of deletions in mouse chromosome 7 on expression of genes encoding the urea-cycle enzymes and phosphoenolpyruvate carboxykinase (GTP) in liver, kidney, and intestineS M Morris, C L Moncman, D M Kepka, et al.
The Journal of Pediatrics|August 1, 1989
Parenteral nutrition in propionic and methylmalonic acidemiaS G Kahler, D S Millington, S D Cederbaum, et al.
American Journal of Human Genetics|August 1, 1986
The gene for human liver arginase (ARG1) is assigned to chromosome band 6q23R S Sparkes, G J Dizikes, I Klisak, et al.
Biochemical and Biophysical Research Communications|May 25, 1995
Co-induction of arginase and nitric oxide synthase in murine macrophages activated by lipopolysaccharideW W Wang, C P Jenkinson, J M Griscavage, et al.
Human Mutation|January 1, 1994
Identification of mutations (D128G, H141L) in the liver arginase gene of patients with hyperargininemiaJ G Vockley, D E Tabor, R M Kern, et al.
Molecular Genetics and Metabolism|June 3, 1998
Cloning and characterization of the mouse and rat type II arginase genesR K Iyer, J M Bando, C P Jenkinson, et al.
Pediatric Research|March 1, 1990
Guanidino compound analysis as a complementary diagnostic parameter for hyperargininemia: follow-up of guanidino compound levels during therapyB Marescau, P P De Deyn, A Lowenthal, et al.
Neurology|December 31, 1997
Outcome of pyruvate dehydrogenase deficiency treated with ketogenic diets. Studies in patients with identical mutationsI D Wexler, S G Hemalatha, J McConnell, et al.
Pageof 10

Showing results (81-90 of 93) with videos related to

Sort By:
Pageof 10
Gene Therapy|December 5, 2014
Minimal ureagenesis is necessary for survival in the murine model of hyperargininemia treated by AAV-based gene therapyC Hu, D S Tai, H Park, et al.
The Journal of Clinical Investigation|February 1, 1989
Differential expression of the two human arginase genes in hyperargininemia. Enzymatic, pathologic, and molecular analysisW W Grody, C Argyle, R M Kern, et al.
Biochemical Genetics|December 1, 1988
Effects of deletions in mouse chromosome 7 on expression of genes encoding the urea-cycle enzymes and phosphoenolpyruvate carboxykinase (GTP) in liver, kidney, and intestineS M Morris, C L Moncman, D M Kepka, et al.
The Journal of Pediatrics|August 1, 1989
Parenteral nutrition in propionic and methylmalonic acidemiaS G Kahler, D S Millington, S D Cederbaum, et al.
American Journal of Human Genetics|August 1, 1986
The gene for human liver arginase (ARG1) is assigned to chromosome band 6q23R S Sparkes, G J Dizikes, I Klisak, et al.
Biochemical and Biophysical Research Communications|May 25, 1995
Co-induction of arginase and nitric oxide synthase in murine macrophages activated by lipopolysaccharideW W Wang, C P Jenkinson, J M Griscavage, et al.
Human Mutation|January 1, 1994
Identification of mutations (D128G, H141L) in the liver arginase gene of patients with hyperargininemiaJ G Vockley, D E Tabor, R M Kern, et al.
Molecular Genetics and Metabolism|June 3, 1998
Cloning and characterization of the mouse and rat type II arginase genesR K Iyer, J M Bando, C P Jenkinson, et al.
Pediatric Research|March 1, 1990
Guanidino compound analysis as a complementary diagnostic parameter for hyperargininemia: follow-up of guanidino compound levels during therapyB Marescau, P P De Deyn, A Lowenthal, et al.
Neurology|December 31, 1997
Outcome of pyruvate dehydrogenase deficiency treated with ketogenic diets. Studies in patients with identical mutationsI D Wexler, S G Hemalatha, J McConnell, et al.
Pageof 10