人类疾病动物模型：遗传性果糖不耐受症。 - Suppr

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超能文献

Animal model of human disease: hereditary fructose intolerance.

作者信息

Phillips M J, Yu D T

出版信息

Am J Pathol. 1974 Jun;75(3):591-4.

PMID:4835994

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1910841/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b2e/1910841/01360f6139e9/amjpathol00476-0188-a.jpg

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Animal model of human disease: hereditary fructose intolerance.人类疾病动物模型：遗传性果糖不耐受症。

Am J Pathol. 1974 Jun;75(3):591-4.

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Hereditary fructose intolerance in parent and child.父母与子女的遗传性果糖不耐受症。

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本文引用的文献

[NEW TECHNIC FOR THE DEMONSTRATION OF INBORN ERRORS OF METABOLISM IN MAN].[用于证明人类先天性代谢缺陷的新技术]

Arq Bras Endocrinol Metabol. 1964 Apr;13:49-56.

Hereditary fructose intolerance. An inborn defect of hepatic fructose-1-phosphate splitting aldolase.遗传性果糖不耐受症。一种肝脏果糖-1-磷酸裂解醛缩酶的先天性缺陷。

Am J Med. 1963 Feb;34:151-67. doi: 10.1016/0002-9343(63)90050-0.

[A biochemical investigation on 2 cases of fructose intolerance].[2例果糖不耐受症的生化研究]

Ann Paediatr Fenn. 1962;8:236-44.

Fructosaemia: an inborn error of fructose metabolism.果糖血症：一种先天性果糖代谢紊乱疾病。

Arch Dis Child. 1963 Jun;38(199):220-30. doi: 10.1136/adc.38.199.220.

[Anomaly of hepatic aldolase in intolerance to fructose].[果糖不耐受时肝脏醛缩酶的异常]

Enzymol Biol Clin (Basel). 1961;1:4-14.

Absence of renal fructose-1-phosphate aldolase activity in hereditary fructose intolerance.

Nature. 1967 May 27;214(5091):920-1. doi: 10.1038/214920b0.

Metabolic intermediates in liver of rats given large amounts of fructose or dihydroxyacetone.给予大量果糖或二羟基丙酮的大鼠肝脏中的代谢中间产物。

Biochem Biophys Res Commun. 1969 Mar 10;34(5):619-26. doi: 10.1016/0006-291x(69)90783-9.

Liver adenine nucleotides: fructose-induced depletion and its effect on protein synthesis.肝脏腺嘌呤核苷酸：果糖诱导的耗竭及其对蛋白质合成的影响。

Science. 1968 Sep 20;161(3847):1253-4. doi: 10.1126/science.161.3847.1253.

Subcellular pathology of hereditary fructose intolerance.遗传性果糖不耐受症的亚细胞病理学

Am J Med. 1968 Jun;44(6):910-21. doi: 10.1016/0002-9343(68)90091-0.

Fructose-1-phosphate aldolase and fructose-1-6-diphosphate aldolase activity in the mucosa of the intestine in hereditary fructose intolerance.遗传性果糖不耐受症患者肠道黏膜中果糖-1-磷酸醛缩酶和果糖-1,6-二磷酸醛缩酶的活性

Scand J Gastroenterol. 1968;3(1):80-2. doi: 10.3109/00365526809180103.

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