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S D Cederbaum

Showing results (71-80 of 93) with videos related to

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Pediatrics|November 1, 1976
Ketonic diet in the management of pyruvate dehydrogenase deficiencyR E Falk, S D Cederbaum, J P Blass, et al.
Pediatric Research|June 11, 1992
Deletion in blood mitochondrial DNA in Kearns-Sayre syndromeN Fischel-Ghodsian, M C Bohlman, T R Prezant, et al.
Molecular Genetics and Metabolism|October 6, 1998
Molecular basis of hyperargininemia: structure-function consequences of mutations in human liver arginaseD E Ash, L R Scolnick, Z F Kanyo, et al.
Archives of Biochemistry and Biophysics|July 1, 1987
Regulation of mRNA levels for five urea cycle enzymes in rat liver by diet, cyclic AMP, and glucocorticoidsS M Morris, C L Moncman, K D Rand, et al.
Pediatric Research|July 1, 1979
Hyperargininemia with arginase deficiencyS D Cederbaum, K N Shaw, E B Spector, et al.
The New England Journal of Medicine|July 2, 1992
Brief report: renal tubular acidosis in carnitine palmitoyltransferase type 1 deficiencyZ C Falik-Borenstein, S C Jordan, J M Saudubray, et al.
Gene Therapy|February 6, 2015
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.
Human Genetics|March 1, 1993
Arginase deficiency manifesting delayed clinical sequelae and induction of a kidney arginase isozymeW W Grody, R M Kern, D Klein, et al.
Biochemical and Molecular Medicine|October 1, 1996
Loss of function mutations in conserved regions of the human arginase I geneJ G Vockley, B K Goodman, D E Tabor, et al.
The American Journal of Physiology|November 1, 1996
Arginase activity in endothelial cells: inhibition by NG-hydroxy-L-arginine during high-output NO productionG M Buga, R Singh, S Pervin, et al.
Pageof 10

Showing results (71-80 of 93) with videos related to

Sort By:
Pageof 10
Pediatrics|November 1, 1976
Ketonic diet in the management of pyruvate dehydrogenase deficiencyR E Falk, S D Cederbaum, J P Blass, et al.
Pediatric Research|June 11, 1992
Deletion in blood mitochondrial DNA in Kearns-Sayre syndromeN Fischel-Ghodsian, M C Bohlman, T R Prezant, et al.
Molecular Genetics and Metabolism|October 6, 1998
Molecular basis of hyperargininemia: structure-function consequences of mutations in human liver arginaseD E Ash, L R Scolnick, Z F Kanyo, et al.
Archives of Biochemistry and Biophysics|July 1, 1987
Regulation of mRNA levels for five urea cycle enzymes in rat liver by diet, cyclic AMP, and glucocorticoidsS M Morris, C L Moncman, K D Rand, et al.
Pediatric Research|July 1, 1979
Hyperargininemia with arginase deficiencyS D Cederbaum, K N Shaw, E B Spector, et al.
The New England Journal of Medicine|July 2, 1992
Brief report: renal tubular acidosis in carnitine palmitoyltransferase type 1 deficiencyZ C Falik-Borenstein, S C Jordan, J M Saudubray, et al.
Gene Therapy|February 6, 2015
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.
Human Genetics|March 1, 1993
Arginase deficiency manifesting delayed clinical sequelae and induction of a kidney arginase isozymeW W Grody, R M Kern, D Klein, et al.
Biochemical and Molecular Medicine|October 1, 1996
Loss of function mutations in conserved regions of the human arginase I geneJ G Vockley, B K Goodman, D E Tabor, et al.
The American Journal of Physiology|November 1, 1996
Arginase activity in endothelial cells: inhibition by NG-hydroxy-L-arginine during high-output NO productionG M Buga, R Singh, S Pervin, et al.
Pageof 10