PEROXISOMAL ALANINE - GLYOXYLATE AMINOTRANSFERASE DEFICIENCY IN PRIMARY HYPEROXALURIA TYPE-I

被引：321

作者：

DANPURE, CJ

JENNINGS, PR

机构：

来源：

FEBS LETTERS | 1986年 / 201卷 / 01期

关键词：

D O I：

10.1016/0014-5793(86)80563-4

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

引用

页码：20 / 24

页数：5

共 29 条

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[8] METABOLISM OF [1-14C]GLYOXYLATE [1-14C]GLYCOLLATE [1-14C]GLYCINE AND [2-14C]GLYCINE BY HOMOGENATES OF KIDNEY AND LIVER TISSUE FROM HYPEROXALURIC AND CONTROL SUBJECTS [J].

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[9] STUDIES ON PRIMARY HYPEROXALURIA .1. IN VIVO DEMONSTRATION OF A DEFECT IN GLYOXYLATE METABOLISM [J].

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[10] IDENTIFICATION OF ENZYMES THAT CATALYZE OXIDATION OF GLYOXYLATE TO OXALATE IN 100000 G SUPERNATANT FRACTION OF HUMAN HYPEROXALURIC AND CONTROL LIVER AND HEART TISSUE [J].

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CLINICAL SCIENCE, 1973, 44 (03) :227-+

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