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DEFECTIVE UPTAKE OF BASIC AMINO ACIDS AND L-CYSTINE BY INTESTINAL MUCOSA OF PATIENTS WITH CYSTINURIA.

作者信息

MCCARTHY C F, BORLAND J L, LYNCH H J, OWEN E E, TYOR M P

出版信息

J Clin Invest. 1964 Aug;43(8):1518-24. doi: 10.1172/JCI105028.

DOI:10.1172/JCI105028
PMID:14201536
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC441952/
Abstract
摘要

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DEFECTIVE UPTAKE OF BASIC AMINO ACIDS AND L-CYSTINE BY INTESTINAL MUCOSA OF PATIENTS WITH CYSTINURIA.胱氨酸尿症患者肠黏膜对碱性氨基酸和L-胱氨酸的摄取缺陷
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2
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Urinary excretion of total cystine and the dibasic amino acids arginine, lysine and ornithine in relation to genetic findings in patients with cystinuria treated with sulfhydryl compounds.胱氨酸尿症患者使用巯基化合物治疗时，总胱氨酸以及二元氨基酸精氨酸、赖氨酸和鸟氨酸的尿排泄量与基因检测结果的关系。
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EVIDENCE AGAINST A SINGLE RENAL TRANSPORT DEFECT IN CYSTINURIA.胱氨酸尿症单一肾脏转运缺陷的反证
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Some factors affecting amino acid absorption.
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Chloride dependent amino acid transport in the human small intestine.人类小肠中氯离子依赖型氨基酸转运
Gut. 1995 Feb;36(2):215-9. doi: 10.1136/gut.36.2.215.
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Lysine fluxes across the jejunal epithelium in lysinuric protein intolerance.赖氨酸尿性蛋白不耐受症中赖氨酸穿过空肠上皮的通量
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Modelling of electrolyte transport in renal and intestinal epithelia. Implications for transport defects.肾和肠上皮细胞中电解质转运的建模。对转运缺陷的影响。
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[An isolated defect of the tubular cystine reabsorption in a family with idiopathic hypoparathyroidism].[一家特发性甲状旁腺功能减退症患者中肾小管胱氨酸重吸收的孤立性缺陷]
Klin Wochenschr. 1967 Jan 1;45(1):38-40. doi: 10.1007/BF01745737.
10
Intestinal transport of cystine and cysteine in man: evidence for separate mechanisms.人体中胱氨酸和半胱氨酸的肠道转运：存在不同机制的证据。
J Clin Invest. 1967 Jan;46(1):30-4. doi: 10.1172/JCI105508.

本文引用的文献

1
The intestinal absorption defect in cystinuria.胱氨酸尿症中的肠道吸收缺陷。
Gut. 1961 Dec;2(4):323-37. doi: 10.1136/gut.2.4.323.
2
Excretion of amino acids in cystinuria.
Proc Soc Exp Biol Med. 1951 Dec;78(3):705-8. doi: 10.3181/00379727-78-19189.
3
The pattern of amino-acid excretion in cystinuria.胱氨酸尿症中氨基酸的排泄模式。
Ann Hum Genet. 1955 Feb;19(3):196-208. doi: 10.1111/j.1469-1809.1955.tb01344.x.
4
CYSTINURIA: IN VITRO DEMONSTRATION OF AN INTESTINAL TRANSPORT DEFECT.胱氨酸尿症：肠道转运缺陷的体外证明
Science. 1964 Jan 31;143(3605):482-4. doi: 10.1126/science.143.3605.482.
5
Stature and nutrition in cystinuria and Hartnup disease.胱氨酸尿症和哈特纳普病中的身高与营养状况。
Br Med J. 1963 Mar 2;1(5330):590-2. doi: 10.1136/bmj.1.5330.590.
6
Aminoacid metabolism in cystinuria.胱氨酸尿症中的氨基酸代谢
Clin Sci. 1962 Oct;23:285-304.
7
Inulin and endogenous amino acid renal clearances in cystinuria: evidence for tubular secretion.胱氨酸尿症中菊粉和内源性氨基酸的肾脏清除率：肾小管分泌的证据。
J Clin Invest. 1962 Feb;41(2):281-8. doi: 10.1172/JCI104481.
8
Active transport of lysine, ornithine, arginine and cystine by the intestine.
Biochem Biophys Res Commun. 1961 Apr 28;4:478-81. doi: 10.1016/0006-291x(61)90312-6.
9
A peroral hydraulic biopsy tube for multiple sampling at any level of the gastro-intestinal tract.一种用于在胃肠道任何水平进行多次采样的经口液压活检管。
Gastroenterology. 1961 Jan;40:120-6.
10
The uptake of amino acids by isolated segments of rat intestine. I. A survey of factors affecting the measurement of uptake.大鼠肠道分离段对氨基酸的摄取。I. 影响摄取量测量的因素综述。
Biochim Biophys Acta. 1960 Sep 23;43:268-77. doi: 10.1016/0006-3002(60)90437-6.