Role of argininosuccinate synthetase in the regulation of urea synthesis in the rat and argininosuccinate synthetase-associated metabolic disorder in man.
作者信息
Saheki T, Tsuda M, Takada S, Kusumi K, Katsunuma T
出版信息
Adv Enzyme Regul. 1980;18:221-38. doi: 10.1016/0065-2571(80)90017-5.
PMID:7446299
Abstract
摘要
相似文献
1
Role of argininosuccinate synthetase in the regulation of urea synthesis in the rat and argininosuccinate synthetase-associated metabolic disorder in man.精氨琥珀酸合成酶在大鼠尿素合成调节中的作用及人类精氨琥珀酸合成酶相关代谢紊乱
Adv Enzyme Regul. 1980;18:221-38. doi: 10.1016/0065-2571(80)90017-5.
2
[A case of citrullinemia with cluster type distribution of argininosuccinate synthetase in the liver].[1例肝脏中精氨琥珀酸合成酶呈簇状分布的瓜氨酸血症]
Rinsho Shinkeigaku. 1987 Jul;27(7):931-5.
3
Qualitative abnormality of liver argininosuccinate synthetase in a patient with citrullinemia.一名瓜氨酸血症患者肝脏中精氨琥珀酸合成酶的定性异常。
Adv Exp Med Biol. 1982;153:77-82. doi: 10.1007/978-1-4757-6903-6_10.
4
Argininosuccinate synthetase activity in cultured skin fibroblasts of citrullinemic patients.瓜氨酸血症患者培养的皮肤成纤维细胞中的精氨琥珀酸合成酶活性。
Clin Chim Acta. 1982 Jan 5;118(1):93-7. doi: 10.1016/0009-8981(82)90230-3.
5
Enzymatic analysis of citrullinemia (12 cases) in Japan.日本瓜氨酸血症的酶学分析（12例）
Adv Exp Med Biol. 1982;153:63-76. doi: 10.1007/978-1-4757-6903-6_9.
6
7
Qualitative and quantitative abnormalities of argininosuccinate synthetase in citrullinemia.瓜氨酸血症中精氨琥珀酸合成酶的定性和定量异常
Clin Chim Acta. 1981 Feb 5;109(3):325-35. doi: 10.1016/0009-8981(81)90318-1.
8
Argininosuccinate synthetase activity in cultured human lymphocytes.培养的人淋巴细胞中的精氨琥珀酸合成酶活性
Biochem Genet. 1977 Apr;15(3-4):395-407. doi: 10.1007/BF00484469.
9
Studies on liver argininosuccinate synthetase in a patient with citrullinemia and in normal subjects.瓜氨酸血症患者及正常受试者肝脏精氨琥珀酸合成酶的研究。
J Biochem. 1979 Jan;85(1):191-5. doi: 10.1093/oxfordjournals.jbchem.a132309.
10
Regulation of urea synthesis: changes in the concentration of ornithine in the liver corresponding to changes in urea synthesis.尿素合成的调节：肝脏中鸟氨酸浓度的变化与尿素合成的变化相对应。
Adv Exp Med Biol. 1982;153:255-63. doi: 10.1007/978-1-4757-6903-6_32.
引用本文的文献
1
Pathogenesis and pathophysiology of citrin (a mitochondrial aspartate glutamate carrier) deficiency.柠烯（一种线粒体天冬氨酸谷氨酸载体）缺乏症的发病机制和病理生理学
Metab Brain Dis. 2002 Dec;17(4):335-46. doi: 10.1023/a:1021961919148.
2
Identification of two novel mutations in the SLC25A13 gene and detection of seven mutations in 102 patients with adult-onset type II citrullinemia.成人型II型瓜氨酸血症102例患者中SLC25A13基因两个新突变的鉴定及七个突变的检测
Hum Genet. 2000 Dec;107(6):537-45. doi: 10.1007/s004390000430.
Zotero 插件