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Journal Abstract Search
223 related items for PubMed ID: 1222373
1. Experimental cystinuria: the cycloleucine model. I. Amino acid interactions in renal and intestinal epithelia. Craan AG, Bergeron M. Can J Physiol Pharmacol; 1975 Dec; 53(6):1027-36. PubMed ID: 1222373 [Abstract] [Full Text] [Related]
2. Experimental cystinuria: the cycloleucine model. II. Amino acid efflux from intestinal and renal tissues. Craan AG, Bergeron M. Metabolism; 1978 Nov; 27(11):1613-25. PubMed ID: 703604 [Abstract] [Full Text] [Related]
3. [Effect of cycloleucine on renal uptake of dibasic amino acids and cystine]. Moatti N, Lemonnier A, Barthon F. Biomedicine; 1976 Feb 10; 25(1):18-22. PubMed ID: 963187 [Abstract] [Full Text] [Related]
4. Renal handling of dibasic amino acids and cystine in cystinuria. Kato T. Clin Sci Mol Med; 1977 Jul 10; 53(1):9-15. PubMed ID: 872525 [Abstract] [Full Text] [Related]
5. Biochemical and genetic studies in cystinuria: observations on double heterozygotes of genotype I-II. Morin CL, Thompson MW, Jackson SH, Sass-Kortsak A. J Clin Invest; 1971 Sep 10; 50(9):1961-76. PubMed ID: 5564399 [Abstract] [Full Text] [Related]
6. Tissue transport defects of dibasic amino acids. Segal S. Bibl Paediatr; 1968 Sep 10; 87():56-71. PubMed ID: 4888869 [No Abstract] [Full Text] [Related]
7. Transport interactions of cystine and dibasic amino acids in isolated rat renal tubules. Foreman JW, Hwang SM, Segal S. Metabolism; 1980 Jan 10; 29(1):53-61. PubMed ID: 7351876 [Abstract] [Full Text] [Related]
8. Transport of dibasic amino acids, cystine, and tryptophan by cultured human fibroblasts: absence of a defect in cystinuria and Hartnup disease. Groth U, Rosenberg LE. J Clin Invest; 1972 Aug 10; 51(8):2130-42. PubMed ID: 5054467 [Abstract] [Full Text] [Related]
9. Amino acid uptake by kidney and jejunal tissue from dogs with cystine stones. Holtzapple PG, Bovee K, Rea CF. Science; 1969 Dec 19; 166(3912):1525-7. PubMed ID: 17655050 [Abstract] [Full Text] [Related]
11. Differential cystine and dibasic amino acid handling after loss of function of the amino acid transporter b0,+AT (Slc7a9) in mice. Di Giacopo A, Rubio-Aliaga I, Cantone A, Artunc F, Rexhepaj R, Frey-Wagner I, Font-Llitjós M, Gehring N, Stange G, Jaenecke I, Mohebbi N, Closs EI, Palacín M, Nunes V, Daniel H, Lang F, Capasso G, Wagner CA. Am J Physiol Renal Physiol; 2013 Dec 15; 305(12):F1645-55. PubMed ID: 24107421 [Abstract] [Full Text] [Related]
12. Cystinuria caused by mutations in rBAT, a gene involved in the transport of cystine. Calonge MJ, Gasparini P, Chillarón J, Chillón M, Gallucci M, Rousaud F, Zelante L, Testar X, Dallapiccola B, Di Silverio F. Nat Genet; 1994 Apr 15; 6(4):420-5. PubMed ID: 8054986 [Abstract] [Full Text] [Related]
13. Renal transport of lysine and arginine in cystinuria. Kato T. Tohoku J Exp Med; 1983 Jan 15; 139(1):9-16. PubMed ID: 6404004 [Abstract] [Full Text] [Related]
14. The molecular basis of cystinuria: the role of the rBAT gene. Palacín M, Mora C, Chillarón J, Calonge MJ, Estévez R, Torrents D, Testar X, Zorzano A, Nunes V, Purroy J, Estivill X, Gasparini P, Bisceglia L, Zelante L. Amino Acids; 1996 Jun 15; 11(2):225-46. PubMed ID: 24178689 [Abstract] [Full Text] [Related]
15. Novel cystine transporter in renal proximal tubule identified as a missing partner of cystinuria-related plasma membrane protein rBAT/SLC3A1. Nagamori S, Wiriyasermkul P, Guarch ME, Okuyama H, Nakagomi S, Tadagaki K, Nishinaka Y, Bodoy S, Takafuji K, Okuda S, Kurokawa J, Ohgaki R, Nunes V, Palacín M, Kanai Y. Proc Natl Acad Sci U S A; 2016 Jan 19; 113(3):775-80. PubMed ID: 26739563 [Abstract] [Full Text] [Related]
16. CYSTINURIA: IN VITRO DEMONSTRATION OF AN INTESTINAL TRANSPORT DEFECT. THIER S, FOX M, SEGAL S, ROSENBERG LE. Science; 1964 Jan 31; 143(3605):482-4. PubMed ID: 14080318 [Abstract] [Full Text] [Related]
17. Cycloleucine inhibition of amino acid transport in human and rat kidney cortex. Holtzapple P, Rea C, Genel M, Segal S. J Lab Clin Med; 1970 May 31; 75(5):818-25. PubMed ID: 5439680 [No Abstract] [Full Text] [Related]
18. Aminoaciduria resulting from cycloleucine administration in man. Brown RR. Science; 1967 Jul 28; 157(3787):432-4. PubMed ID: 6028026 [Abstract] [Full Text] [Related]
19. 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. Fjellstedt E, Harnevik L, Jeppsson JO, Tiselius HG, Söderkvist P, Denneberg T. Urol Res; 2003 Dec 28; 31(6):417-25. PubMed ID: 14586528 [Abstract] [Full Text] [Related]