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The Western Journal of Medicine|August 1, 1984
Recombinant DNA in medicineS D Cederbaum, G C Fareed, M A Lovett, et al.Molecular and Cellular Biochemistry|February 1, 1985
Differential expression of multiple forms of arginase in cultured cellsE B Spector, R M Kern, D F Haggerty, et al.Biochemical and Biophysical Research Communications|November 26, 1986
Isolation of human liver arginase cDNA and demonstration of nonhomology between the two human arginase genesG J Dizikes, W W Grody, R M Kern, et al.Journal of Chromatography|May 1, 1979
Measurement of urinary pyrimidine bases and nucleosides by high-performance liquid chromatographyJ E Evans, H Tieckelmann, E W Naylor, et al.Neurology|July 1, 1975
Familial poliodystrophy, mitochondrial myopathy, and lactate acidemiaY Shapira, S D Cederbaum, P A Cancilla, et al.The Journal of Pediatrics|August 1, 1979
Hyperlysinemia with saccharopinuria due to combined lysine-ketoglutarate reductase and saccharopine dehydrogenase deficiencies presenting as cystinuriaS D Cederbaum, K N Shaw, J Dancis, et al.Pediatrics|October 1, 1982
A neonatal screening test for argininosuccinic acid lyase deficiency and other urea cycle disordersH W Talbot, A B Sumlin, E W Naylor, et al.Journal of Medical Genetics|April 1, 1978
Erythropoietic protoporphyria, heterozygous cystinuria, and reduced peptidase A activity in a patient with 46,XX/46,XX,18q--mosaicismE W Naylor, W H Murphey, E I Domoszlai, et al.The Journal of Pediatrics|January 10, 2001
Psychosocial issues and coping strategies in families affected by urea cycle disordersJ A Cederbaum, C LeMons, M Rosen, et al.Biochimica Et Biophysica Acta|July 20, 1981
Microinjection of arginase into enzyme-deficient cells with the isolated glycoproteins of Sendai virus as fusogenC A Kruse, E B Spector, S D Cederbaum, et al.Pageof 11