174 related articles for article (PubMed ID: 12053065)
1. Cystine transport activity of heterozygous rBAT mutants expressed in Xenopus oocytes.
Ishihara M; Ogura T; Akakura K; Egoshi K; Mikami K; Nakaya H; Ito H
Nephron; 2002 Jun; 91(2):276-80. PubMed ID: 12053065
[TBL] [Abstract][Full Text] [Related]
2. Mutations of the basic amino acid transporter gene associated with cystinuria.
Miyamoto K; Katai K; Tatsumi S; Sone K; Segawa H; Yamamoto H; Taketani Y; Takada K; Morita K; Kanayama H
Biochem J; 1995 Sep; 310 ( Pt 3)(Pt 3):951-5. PubMed ID: 7575432
[TBL] [Abstract][Full Text] [Related]
3. An intracellular trafficking defect in type I cystinuria rBAT mutants M467T and M467K.
Chillarón J; Estévez R; Samarzija I; Waldegger S; Testar X; Lang F; Zorzano A; Busch A; Palacín M
J Biol Chem; 1997 Apr; 272(14):9543-9. PubMed ID: 9083097
[TBL] [Abstract][Full Text] [Related]
4. 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; 6(4):420-5. PubMed ID: 8054986
[TBL] [Abstract][Full Text] [Related]
5. Expression cloning of a human renal cDNA that induces high affinity transport of L-cystine shared with dibasic amino acids in Xenopus oocytes.
Bertran J; Werner A; Chillarón J; Nunes V; Biber J; Testar X; Zorzano A; Estivill X; Murer H; Palacín M
J Biol Chem; 1993 Jul; 268(20):14842-9. PubMed ID: 7686906
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Slc7a9-deficient mice develop cystinuria non-I and cystine urolithiasis.
Feliubadaló L; Arbonés ML; Mañas S; Chillarón J; Visa J; Rodés M; Rousaud F; Zorzano A; Palacín M; Nunes V
Hum Mol Genet; 2003 Sep; 12(17):2097-108. PubMed ID: 12915471
[TBL] [Abstract][Full Text] [Related]
8. Expression of the activity of cystine/glutamate exchange transporter, system x(c)(-), by xCT and rBAT.
Wang H; Tamba M; Kimata M; Sakamoto K; Bannai S; Sato H
Biochem Biophys Res Commun; 2003 Jun; 305(3):611-8. PubMed ID: 12763038
[TBL] [Abstract][Full Text] [Related]
9. Role of rBAT gene products in cystinuria.
Miyamoto K; Katai K; Tatsumi S; Sone K; Segawa H; Takada K; Yamamoto H; Taketani Y; Morita K; Kanayama H; Kagawa S; Takeda E
Int J Urol; 1996 Jan; 3(1 Suppl):S92-4. PubMed ID: 24449952
[TBL] [Abstract][Full Text] [Related]
10. A new family of proteins (rBAT and 4F2hc) involved in cationic and zwitterionic amino acid transport: a tale of two proteins in search of a transport function.
Palacín M
J Exp Biol; 1994 Nov; 196():123-37. PubMed ID: 7823016
[TBL] [Abstract][Full Text] [Related]
11. Obligatory amino acid exchange via systems bo,+-like and y+L-like. A tertiary active transport mechanism for renal reabsorption of cystine and dibasic amino acids.
Chillarón J; Estévez R; Mora C; Wagner CA; Suessbrich H; Lang F; Gelpí JL; Testar X; Busch AE; Zorzano A; Palacín M
J Biol Chem; 1996 Jul; 271(30):17761-70. PubMed ID: 8663357
[TBL] [Abstract][Full Text] [Related]
12. Cystinuria-specific rBAT(R365W) mutation reveals two translocation pathways in the amino acid transporter rBAT-b0,+AT.
Pineda M; Wagner CA; Bröer A; Stehberger PA; Kaltenbach S; Gelpí JL; Martín Del Río R; Zorzano A; Palacín M; Lang F; Bröer S
Biochem J; 2004 Feb; 377(Pt 3):665-74. PubMed ID: 14561219
[TBL] [Abstract][Full Text] [Related]
13. The rBAT gene is responsible for L-cystine uptake via the b0,(+)-like amino acid transport system in a "renal proximal tubular" cell line (OK cells).
Mora C; Chillarón J; Calonge MJ; Forgo J; Testar X; Nunes V; Murer H; Zorzano A; Palacín M
J Biol Chem; 1996 May; 271(18):10569-76. PubMed ID: 8631857
[TBL] [Abstract][Full Text] [Related]
14. The molecular basis of cystinuria: an update.
Goodyer P; Boutros M; Rozen R
Exp Nephrol; 2000; 8(3):123-7. PubMed ID: 10810228
[TBL] [Abstract][Full Text] [Related]
15. Cystinuria phenotyping by oral lysine and arginine loading.
de Sanctis L; Bonetti G; Bruno M; De Luca F; Bisceglia L; Palacin M; Dianzani I; Ponzone A
Clin Nephrol; 2001 Dec; 56(6):467-74. PubMed ID: 11770798
[TBL] [Abstract][Full Text] [Related]
16. Cloning and expression of a b(0,+)-like amino acid transporter functioning as a heterodimer with 4F2hc instead of rBAT. A new candidate gene for cystinuria.
Rajan DP; Kekuda R; Huang W; Wang H; Devoe LD; Leibach FH; Prasad PD; Ganapathy V
J Biol Chem; 1999 Oct; 274(41):29005-10. PubMed ID: 10506149
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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; 11(2):225-46. PubMed ID: 24178689
[TBL] [Abstract][Full Text] [Related]
19. Luminal heterodimeric amino acid transporter defective in cystinuria.
Pfeiffer R; Loffing J; Rossier G; Bauch C; Meier C; Eggermann T; Loffing-Cueni D; Kühn LC; Verrey F
Mol Biol Cell; 1999 Dec; 10(12):4135-47. PubMed ID: 10588648
[TBL] [Abstract][Full Text] [Related]
20. rBAT-b(0,+)AT heterodimer is the main apical reabsorption system for cystine in the kidney.
Fernández E; Carrascal M; Rousaud F; Abián J; Zorzano A; Palacín M; Chillarón J
Am J Physiol Renal Physiol; 2002 Sep; 283(3):F540-8. PubMed ID: 12167606
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]