The human arginases and arginase deficiency
暂无分享,去创建一个
J. Vockley | W. Grody | S. Cederbaum | C. Jenkinson | R. Iyer | R. Iyer | C. P. Jenkinson | J. G. Vockley | R. M. Kern | W. W. Grody | S. Cederbaum | R. Kern
[1] S. Cederbaum,et al. Molecular basis of hyperargininemia: structure-function consequences of mutations in human liver arginase. , 1998, Molecular genetics and metabolism.
[2] M. Takiguchi,et al. Regulation of the urea cycle enzyme genes in nitric oxide synthesis , 1998, Journal of Inherited Metabolic Disease.
[3] S. Morris,et al. Human type II arginase: sequence analysis and tissue-specific expression. , 1997, Gene.
[4] T. Gotoh,et al. Chromosomal localization of the human arginase II gene and tissue distribution of its mRNA. , 1997, Biochemical and biophysical research communications.
[5] M. Takiguchi,et al. Coinduction of Nitric-oxide Synthase and Arginase I in Cultured Rat Peritoneal Macrophages and Rat Tissues in Vivo by Lipopolysaccharide* , 1997, The Journal of Biological Chemistry.
[6] J. Vockley,et al. Cloning and characterization of the human type II arginase gene. , 1996, Genomics.
[7] L. Ignarro,et al. Arginase activity in endothelial cells: inhibition by NG-hydroxy-L-arginine during high-output NO production. , 1996, The American journal of physiology.
[8] M. Takiguchi,et al. Molecular cloning of cDNA for nonhepatic mitochondrial arginase (arginase II) and comparison of its induction with nitric oxide synthase in a murine macrophage‐like cell line , 1996, FEBS letters.
[9] D. Christianson,et al. Structure of a unique binuclear manganese cluster in arginase , 1996, Nature.
[10] J. Vockley,et al. Loss of function mutations in conserved regions of the human arginase I gene. , 1996, Biochemical and molecular medicine.
[11] W. Grody,et al. Comparative properties of arginases. , 1996, Comparative biochemistry and physiology. Part B, Biochemistry & molecular biology.
[12] I. Matsuda,et al. Molecular basis of phenotypic variation in patients with argininemia , 1995, Human Genetics.
[13] L. Ignarro,et al. Co-induction of arginase and nitric oxide synthase in murine macrophages activated by lipopolysaccharide. , 1995, Biochemical and biophysical research communications.
[14] Y. B. Shi,et al. Thyroid hormone-dependent differential regulation of multiple arginase genes during amphibian metamorphosis. , 1994, The Journal of biological chemistry.
[15] S. Cederbaum,et al. Subcellular location and differential antibody specificity of arginase in tissue culture and whole animals , 1994, International Journal of Developmental Neuroscience.
[16] C. Jenkinson,et al. Rat mammary arginase: isolation and characterization. , 1994, Biochemical medicine and metabolic biology.
[17] A. Nussler,et al. Coinduction of nitric oxide synthase and argininosuccinate synthetase in a murine macrophage cell line. Implications for regulation of nitric oxide production. , 1994, The Journal of biological chemistry.
[18] W. Grody,et al. Arginase deficiency manifesting delayed clinical sequelae and induction of a kidney arginase isozyme , 1993, Human Genetics.
[19] P. D. De Deyn,et al. The pathobiochemistry of uremia and hyperargininemia further demonstrates a metabolic relationship between urea and guanidinosuccinic acid. , 1992, Metabolism: clinical and experimental.
[20] W. Grody,et al. Differential expression of the two human arginase genes in hyperargininemia. Enzymatic, pathologic, and molecular analysis. , 1989, The Journal of clinical investigation.
[21] M. Takiguchi,et al. Human liver-type arginase gene: structure of the gene and analysis of the promoter region. , 1988, Nucleic acids research.
[22] K. Kidd,et al. A PvuII RFLP for the human liver arginase (ARG1) gene. , 1986, Nucleic acids research.
[23] W. Grody,et al. Isolation of human liver arginase cDNA and demonstration of nonhomology between the two human arginase genes. , 1986, Biochemical and biophysical research communications.
[24] T. Mohandas,et al. The gene for human liver arginase (ARG1) is assigned to chromosome band 6q23. , 1986, American journal of human genetics.
[25] S. Cederbaum,et al. Cloning of rat liver arginase cDNA and elucidation of regulation of arginase gene expression in H4 rat hepatoma cells , 1986, Somatic cell and molecular genetics.
[26] S. Cederbaum,et al. Immunologic Studies of Arginase in Tissues of Normal Human Adult and Arginase-Deficient Patients , 1983, Pediatric Research.
[27] S. Cederbaum,et al. Biochemical properties of arginase in human adult and fetal tissues. , 1982, Biochemical medicine.
[28] S. Cederbaum,et al. Treatment of hyperargininaemia due to arginase deficiency with a chemically defined diet , 1982, Journal of Inherited Metabolic Disease.
[29] R. Ouellet,et al. 1174 SODIUM BENZOATE THERAPY AND DIETARY CONTROL IN HYPERARGININEMIA , 1981, Pediatric Research.
[30] C. Sansaricq,et al. Argininemia treated from birth. , 1979, The Journal of pediatrics.
[31] S. Cederbaum,et al. Hyperargininemia with Arginase Deficiency , 1979, Pediatric Research.
[32] W. Knox,et al. Arginase isozymes of rat mammary gland, liver, and other tissues. , 1973, The Journal of biological chemistry.
[33] G. Kaysen,et al. Purification and properties of arginase of rat kidney. , 1973, The Biochemical journal.
[34] P. Hamilton,et al. THE FREE AMINO ACIDS OF HUMAN SPINAL FLUID DETERMINED BY ION EXCHANGE CHROMATOGRAPHY , 1966, Journal of neurochemistry.
[35] A. Peraltaserrano. [Argininuria, convulsions and oligophrenia; a new inborn error of metabolism?]. , 1965 .
[36] S. Brusilow. Urea cycle enzymes , 2001 .
[37] R. C. Green,et al. Hyperargininemia: a treatable inborn error of metabolism? , 1997 .
[38] Roth,et al. Hyperorgininemia: a treatable inborn error of metabolism , 1997 .
[39] M. Zavoral,et al. Arginase Activity Determination A Marker of Large Bowel Mucosa Proliferation , 1996, European journal of clinical chemistry and clinical biochemistry : journal of the Forum of European Clinical Chemistry Societies.
[40] M. Takiguchi,et al. Molecular cloning and nucleotide sequence of cDNA for human liver arginase. , 1987, Proceedings of the National Academy of Sciences of the United States of America.
[41] M. Garstka. [Regulation of the urea cycle]. , 1986, Postepy biochemii.
[42] C. Bourdony,et al. Action of Human Growth Hormone (hGH) on Extrathyroidal Conversion of Thyroxine (T4) to Triiodothyronine (T3) in Children with Hypopituitarism , 1981, Pediatric Research.
[43] S. Cederbaum,et al. Properties of fetal and adult red blood cell arginase: a possible prenatal diagnostic test for arginase deficiency. , 1980, American journal of human genetics.
[44] C. A. Thomas,et al. Molecular cloning. , 1977, Advances in pathobiology.
[45] A. Lowenthal,et al. [Hyperargininemia with arginase deficiency. A new familial metabolic disease. II. Biochemical studies]. , 1970, Zeitschrift fur Kinderheilkunde.
[46] H. Terheggen,et al. Hyperargininmie mit Arginasedefekt Eine neue familire Stoffwechselstrung@@@Hyperargininemia with arginase deficiency a new familial metabolic disease: II. Biochemische Untersuchungen@@@II. biochemical studies , 1970 .