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CATs and HATs: the SLC7 family of amino acid transporters.
Verrey F, Closs EI, Wagner CA, Palacin M, Endou H, Kanai Y. Verrey F, et al. Among authors: palacin m. Pflugers Arch. 2004 Feb;447(5):532-42. doi: 10.1007/s00424-003-1086-z. Epub 2003 Jun 11. Pflugers Arch. 2004. PMID: 14770310 Free article. Review.
Two mRNA transcripts (rBAT-1 and rBAT-2) are involved in system b0,(+)-related amino acid transport.
Markovich D, Stange G, Bertran J, Palacin M, Werner A, Biber J, Murer H. Markovich D, et al. Among authors: palacin m. J Biol Chem. 1993 Jan 15;268(2):1362-7. J Biol Chem. 1993. PMID: 8419338 Free article.
Previously, we isolated a cDNA clone (rBAT-1) of 2.2 kilobase pairs (kb) from a rabbit kidney cortex cDNA library, encoding a protein involved in sodium-independent transport of L-dibasic amino acids, L-cystine, and some neutral amino acids via a system related to b0,(+)-like act …
Previously, we isolated a cDNA clone (rBAT-1) of 2.2 kilobase pairs (kb) from a rabbit kidney cortex cDNA library, encoding a protein involv …
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. Chillarón J, et al. Among authors: palacin m. J Biol Chem. 1996 Jul 26;271(30):17761-70. doi: 10.1074/jbc.271.30.17761. J Biol Chem. 1996. PMID: 8663357 Free article.
Mutations in the rBAT gene cause type I cystinuria, a common inherited aminoaciduria of cystine and dibasic amino acids due to their defective renal and intestinal reabsorption (Calonge, M. J., Gasparini, P., Chillaron, J., Chillon, M., Gallucci, M., Rousaud, …
Mutations in the rBAT gene cause type I cystinuria, a common inherited aminoaciduria of cystine and dibasic amino acids due to their defecti …
336 results