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3. Identification of five novel SLC3A1 (rBAT) gene mutations in Japanese cystinuria. Egoshi KI; Akakura K; Kodama T; Ito H Kidney Int; 2000 Jan; 57(1):25-32. PubMed ID: 10620184 [TBL] [Abstract][Full Text] [Related]
4. Assignment of the gene responsible for cystinuria (rBAT) and of markers D2S119 and D2S177 to 2p16 by fluorescence in situ hybridization. Calonge MJ; Nadal M; Calvano S; Testar X; Zelante L; Zorzano A; Estivill X; Gasparini P; Palacín M; Nunes V Hum Genet; 1995 Jun; 95(6):633-6. PubMed ID: 7789946 [TBL] [Abstract][Full Text] [Related]
5. Analysis of the genes SLC7A9 and SLC3A1 in unclassified cystinurics: mutation detection rates and association between variants in SLC7A9 and the disease. Schmidt C; Albers A; Tomiuk J; Eggermann K; Wagner C; Capasso G; Lahme S; Hesse A; Lang F; Zerres K; Eggermann T Clin Nephrol; 2002 May; 57(5):342-8. PubMed ID: 12036192 [TBL] [Abstract][Full Text] [Related]
6. Genomic structure and organization of the human rBAT gene (SLC3A1). Purroy J; Bisceglia L; Calonge MJ; Zelante L; Testar X; Zorzano A; Estivill X; Palacín M; Nunes V; Gasparini P Genomics; 1996 Oct; 37(2):249-52. PubMed ID: 8921402 [TBL] [Abstract][Full Text] [Related]
7. Molecular genetic analysis of SLC3A1 and SLC7A9 genes in Czech and Slovak cystinuric patients. Skopková Z; Hrabincová E; Stástná S; Kozák L; Adam T Ann Hum Genet; 2005 Sep; 69(Pt 5):501-7. PubMed ID: 16138908 [TBL] [Abstract][Full Text] [Related]
8. Molecular genetics of cystinuria: mutation analysis of SLC3A1 and evidence for another gene in type I (silent) phenotype. Saadi I; Chen XZ; Hediger M; Ong P; Pereira P; Goodyer P; Rozen R Kidney Int; 1998 Jul; 54(1):48-55. PubMed ID: 9648062 [TBL] [Abstract][Full Text] [Related]
9. Significant contribution of genomic rearrangements in SLC3A1 and SLC7A9 to the etiology of cystinuria. Schmidt C; Vester U; Wagner CA; Lahme S; Hesse A; Hoyer P; Lang F; Zerres K; Eggermann T; Kidney Int; 2003 Nov; 64(5):1564-72. PubMed ID: 14531788 [TBL] [Abstract][Full Text] [Related]
10. Identification of 12 novel mutations in the SLC3A1 gene in Swedish cystinuria patients. Harnevik L; Fjellstedt E; Molbaek A; Tiselius HG; Denneberg T; Söderkvist P Hum Mutat; 2001 Dec; 18(6):516-25. PubMed ID: 11748844 [TBL] [Abstract][Full Text] [Related]
11. Mutation analysis of SLC7A9 in cystinuria patients in Sweden. Harnevik L; Fjellstedt E; Molbaek A; Denneberg T; Söderkvist P Genet Test; 2003; 7(1):13-20. PubMed ID: 12820697 [TBL] [Abstract][Full Text] [Related]
12. Cystinuria in children: distribution and frequencies of mutations in the SLC3A1 and SLC7A9 genes. Botzenhart E; Vester U; Schmidt C; Hesse A; Halber M; Wagner C; Lang F; Hoyer P; Zerres K; Eggermann T; Kidney Int; 2002 Oct; 62(4):1136-42. PubMed ID: 12234283 [TBL] [Abstract][Full Text] [Related]
13. Functional analysis of mutations in SLC7A9, and genotype-phenotype correlation in non-Type I cystinuria. Font MA; Feliubadaló L; Estivill X; Nunes V; Golomb E; Kreiss Y; Pras E; Bisceglia L; d'Adamo AP; Zelante L; Gasparini P; Bassi MT; George AL; Manzoni M; Riboni M; Ballabio A; Borsani G; Reig N; Fernández E; Zorzano A; Bertran J; Palacín M; Hum Mol Genet; 2001 Feb; 10(4):305-16. PubMed ID: 11157794 [TBL] [Abstract][Full Text] [Related]
14. A recessive contiguous gene deletion of chromosome 2p16 associated with cystinuria and a mitochondrial disease. Parvari R; Brodyansky I; Elpeleg O; Moses S; Landau D; Hershkovitz E Am J Hum Genet; 2001 Oct; 69(4):869-75. PubMed ID: 11524703 [TBL] [Abstract][Full Text] [Related]
15. Mutations in the SLC3A1 transporter gene in cystinuria. Pras E; Raben N; Golomb E; Arber N; Aksentijevich I; Schapiro JM; Harel D; Katz G; Liberman U; Pras M Am J Hum Genet; 1995 Jun; 56(6):1297-303. PubMed ID: 7539209 [TBL] [Abstract][Full Text] [Related]
16. Canine cystinuria: polymorphism in the canine SLC3A1 gene and identification of a nonsense mutation in cystinuric Newfoundland dogs. Henthorn PS; Liu J; Gidalevich T; Fang J; Casal ML; Patterson DF; Giger U Hum Genet; 2000 Oct; 107(4):295-303. PubMed ID: 11129328 [TBL] [Abstract][Full Text] [Related]
17. Identification of two novel mutations [P122S (364C>T) and 1601delAC] in the SLC3A1 gene in type I cystinurics. Gitomer WL; Reed BY; Pak CY Hum Mutat; 2000 Apr; 15(4):390. PubMed ID: 10738006 [No Abstract] [Full Text] [Related]
18. A splicing mutation (891+4A-->G) in SLC3A1 leads to exon 4 skipping and causes cystinuria in a Moslem Arab family. Pras E; Golomb E; Drake C; Aksentijevich I; Katz G; Kastner DL Hum Mutat; 1998; Suppl 1():S28-30. PubMed ID: 9452031 [No Abstract] [Full Text] [Related]
19. Genetic heterogeneity in cystinuria: the SLC3A1 gene is linked to type I but not to type III cystinuria. Calonge MJ; Volpini V; Bisceglia L; Rousaud F; de Sanctis L; Beccia E; Zelante L; Testar X; Zorzano A; Estivill X Proc Natl Acad Sci U S A; 1995 Oct; 92(21):9667-71. PubMed ID: 7568194 [TBL] [Abstract][Full Text] [Related]
20. [From gene to disease; SLC3A1, SLC7A9 and cystinuria]. Breuning MH; Hamdy NA Ned Tijdschr Geneeskd; 2003 Feb; 147(6):245-7. PubMed ID: 12621979 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]