Animal model for hyperprolinaemia: deficiency of mouse proline oxidase activity.
作者信息
Blake R L
出版信息
Biochem J. 1972 Oct;129(4):987-9. doi: 10.1042/bj1290987.
Abstract
摘要
相似文献
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Animal model for hyperprolinaemia: deficiency of mouse proline oxidase activity.高脯氨酸血症的动物模型：小鼠脯氨酸氧化酶活性缺乏
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引用本文的文献
1
Overexpression of proline oxidase induces proline-dependent and mitochondria-mediated apoptosis.脯氨酸氧化酶的过表达诱导脯氨酸依赖性和线粒体介导的细胞凋亡。
Mol Cell Biochem. 2007 Jan;295(1-2):85-92. doi: 10.1007/s11010-006-9276-6. Epub 2006 Jul 28.
2
Inherited metabolic disease in laboratory animals: a review.实验动物中的遗传性代谢疾病：综述
J Inherit Metab Dis. 1980;3(4):133-43. doi: 10.1007/BF02312547.
3
Localization of the membrane defect in transepithelial transport of taurine by parallel studies in vivo and in vitro in hypertaurinuric mice.通过对高牛磺酸尿症小鼠进行体内和体外平行研究，确定牛磺酸跨上皮转运中膜缺陷的定位。
J Clin Invest. 1976 Jan;57(1):183-93. doi: 10.1172/JCI108258.
4
Role of epithelial architecture and intracellular metabolism in proline uptake and transtubular reclamation in PRO/re mouse kidney.上皮结构和细胞内代谢在PRO/re小鼠肾脏脯氨酸摄取和肾小管重吸收中的作用。
Proc Natl Acad Sci U S A. 1975 Apr;72(4):1431-5. doi: 10.1073/pnas.72.4.1431.
5
Mitochondrial proline dehydrogenase deficiency in hyperprolinemic PRO/Re mice: genetic and enzymatic analyses.
Biochem Genet. 1976 Oct;14(9-10):739-57. doi: 10.1007/BF00485338.
6
Altered polyamine metabolism in the PRO/Re strain of inbred mice.近交系小鼠PRO/Re品系中多胺代谢的改变。
Biochem J. 1976 Sep 15;158(3):529-33. doi: 10.1042/bj1580529.
7
Genetic variation in activity of the enzymes of glycolysis and gluconeogenesis between inbred strains of mice.近交系小鼠糖酵解和糖异生酶活性的遗传变异。
Genetics. 1978 Jul;89(3):551-61. doi: 10.1093/genetics/89.3.551.
本文引用的文献
1
Familial hyperprolinemia, cerebral dysfunction and renal anomalies occurring in a family with hereditary nephropathy and deafness.在一个患有遗传性肾病和耳聋的家族中出现的家族性高脯氨酸血症、脑功能障碍和肾脏异常。
N Engl J Med. 1962 Jul 12;267:51-60. doi: 10.1056/NEJM196207122670201.
2
FAMILIAL HYPERPROLINEMIA. REPORT OF A SECOND CASE, ASSOCIATED WITH CONGENITAL RENAL MALFORMATIONS, HEREDITARY HEMATURIA AND MILD MENTAL RETARDATION, WITH DEMONSTRATION OF AN ENZYME DEFECT.家族性高脯氨酸血症。第二例报告，伴有先天性肾畸形、遗传性血尿和轻度智力发育迟缓，并证实存在酶缺陷。
N Engl J Med. 1965 Jun 17;272:1243-54. doi: 10.1056/NEJM196506172722401.
3
Hyperprolinemia and prolinuria in a new inbred strain of mice, PRO-Re.新近交系小鼠PRO-Re中的高脯氨酸血症和脯氨酸尿症
Science. 1972 May 19;176(4036):809-11. doi: 10.1126/science.176.4036.809.
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