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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.

Abstract
摘要

引用本文的文献

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本文引用的文献

1
The intestinal absorption defect in cystinuria.
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.
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.
Science. 1964 Jan 31;143(3605):482-4. doi: 10.1126/science.143.3605.482.
5
Stature and nutrition in cystinuria and Hartnup disease.
Br Med J. 1963 Mar 2;1(5330):590-2. doi: 10.1136/bmj.1.5330.590.
6
Aminoacid metabolism in cystinuria.
Clin Sci. 1962 Oct;23:285-304.
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.

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