Cystinuria: In vitro Demonstration of an Intestinal Transport Defect

A defect in the transport of L-cystine and L-lysine has been found in the intestinal mucosa of patients with cystinuria. Transport studies in normal intestinal mucosa, in contrast to similar studies in the kidney, show that cystine and lysine are mutually inhibitory.

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Veröffentlicht in:Science (American Association for the Advancement of Science) 1964-01, Vol.143 (3605), p.482-484
Hauptverfasser: Thier, Samuel, Fox, Maurice, Segal, Stanton, Rosenberg, Leon E.
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container_issue 3605
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container_title Science (American Association for the Advancement of Science)
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creator Thier, Samuel
Fox, Maurice
Segal, Stanton
Rosenberg, Leon E.
description A defect in the transport of L-cystine and L-lysine has been found in the intestinal mucosa of patients with cystinuria. Transport studies in normal intestinal mucosa, in contrast to similar studies in the kidney, show that cystine and lysine are mutually inhibitory.
doi_str_mv 10.1126/science.143.3605.482
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subjects Amino acids
Arginine
Biological Transport
Capsules
Cystine
Cystinuria
Electrodes
Excretion
Flasks
Glycine
Humans
In Vitro Techniques
Intestinal Mucosa
Jejunum
Kidney
Kidneys
Lysine
Mucosa
Muscle spindles
Old Medline
Proteins - metabolism
title Cystinuria: In vitro Demonstration of an Intestinal Transport Defect
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