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J-GLOBAL ID：200902202471681214   Reference number：09A1163737

Assay of alanine:glyoxylate aminotransferase in human liver by its serine: glyoxylate aminotransferase activity

セリン:グリオキシル酸アミノトランスフェラーゼ活性による,ヒト肝臓のアラニン:グリオキシル酸アミノトランスフェラーゼ分析

Author (6)： NAGATA Masao (Dep. of Urology, Hamamatsu Univ. School of Medicine) ,  ICHIYAMA Arata (First Dep. of Biochemistry, Hamamatsu Univ. School of Medicine) ,  TAKAYAMA Tatsuya (Dep. of Urology, Hamamatsu Univ. School of Medicine) ,  ODA Toshiaki (First Dep. of Biochemistry, Hamamatsu Univ. School of Medicine) ,  MUGIYA Soichi (Dep. of Urology, Hamamatsu Univ. School of Medicine) ,  OZONO Seiichiro (Dep. of Urology, Hamamatsu Univ. School of Medicine)
Material： Biomedical Research  (Biomed Res)
Volume： 30  Issue： 5  Page： 295-301 (J-STAGE)  Publication year： 2009 
JST Material Number： Z0236B  ISSN： 0388-6107  Document type： Article
Article type： 原著論文  Country of issue： Japan (JPN)  Language： ENGLISH (EN)

Thesaurus term： *transaminase ,...
Semi thesaurus term： *アラニン:グリオキシル酸アミノトランスフェラーゼ ,...

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JST classification (3)： Diagnostics of metabolic diseases,nutritional diseases.  (GD05020U) ,  Enzyme in general  (EB09010D) ,  Liver  (EJ06060J)

Substance index (2)： Hydroxypyruvic acid ,  Pyridoxal Phosphate

Reference (19)：

• 1. Cramer SD and Takayama T (2009) Primary hyperoxaluria, Chapter 33. In: Genetic Diseases of the Kidney (Richard L, Stefan S, Gerhard G and Donald S, eds.), pp 571-586, Elsevier Inc., San Diego, CA
• 2. Danpure CJ, Cooper PJ, Wise PJ and Jennings PR (1989) An enzyme trafficking defect in two patients with primary hyperoxaluria type 1: Peroxisomal alanine:glyoxylate aminotransferase rerouted to mitochondria. J Cell Biol 108, 1345-1352.
• 3. Danpure CJ and Jennings PR (1986) Peroxisomal alanine: glyoxylate aminotransferase deficiency in primary hyperoxaluria type 1. FEBS Lett 201, 20-24.
• 4. Danpure CJ and Jennings PR (1988) Further studies on the activity and subcellular distribution of alanine:glyoxylate aminotransferase in the livers of patients with primary hyperoxaluria type 1. Clin Sci 75, 315-322.
• 5. Danpure CJ and Purdue PE (1995) Primary hyperoxaluria. In: The Metabolic and Molecular Bases of Inherited Disease. Vol. 2, 7th Ed. (Scriver CR, Beauded AL, Sly WS and Valle D, eds.), pp 2385-2424, McGraw-Hill, New York

Terms in the title (8)： セリン ,  グリオキシル酸 ,  アミノトランスフェラーゼ ,  活性 ,  ヒト ,  肝臓 ,  アラニン ,  分析