Papers associated with intestine (and slc3a1)

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	The molecular mechanism of intestinal levodopa absorption and its possible implications for the treatment of Parkinson's disease., Camargo SM., J Pharmacol Exp Ther. October 1, 2014; 351 (1): 114-23.
	Characteristics of transport of selenoamino acids by epithelial amino acid transporters., Nickel A., Chem Biol Interact. February 12, 2009; 177 (3): 234-41.
	Apical heterodimeric cystine and cationic amino acid transporter expressed in MDCK cells., Bauch C., Am J Physiol Renal Physiol. July 1, 2002; 283 (1): F181-9.
	Identification and characterization of a Na(+)-independent neutral amino acid transporter that associates with the 4F2 heavy chain and exhibits substrate selectivity for small neutral D- and L-amino acids., Fukasawa Y., J Biol Chem. March 31, 2000; 275 (13): 9690-8.
	The molecular basis of cystinuria: an update., Goodyer P., Exp Nephrol. January 1, 2000; 8 (3): 123-7.
	LAT2, a new basolateral 4F2hc/CD98-associated amino acid transporter of kidney and intestine., Rossier G., J Biol Chem. December 3, 1999; 274 (49): 34948-54.
	Luminal heterodimeric amino acid transporter defective in cystinuria., Pfeiffer R., Mol Biol Cell. December 1, 1999; 10 (12): 4135-47.
	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., J Biol Chem. October 8, 1999; 274 (41): 29005-10.
	Molecular genetics of cystinuria: mutation analysis of SLC3A1 and evidence for another gene in type I (silent) phenotype., Saadi I., Kidney Int. July 1, 1998; 54 (1): 48-55.
	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., J Biol Chem. May 3, 1996; 271 (18): 10569-76.
	Heavy metal mediated inhibition of rBAT-induced amino acid transport., Waldegger S., Kidney Int. June 1, 1995; 47 (6): 1677-81.
	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. November 1, 1994; 196 123-37.
	Cystinuria caused by mutations in rBAT, a gene involved in the transport of cystine., Calonge MJ., Nat Genet. April 1, 1994; 6 (4): 420-5.
	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., J Biol Chem. July 15, 1993; 268 (20): 14842-9.
	Cloning and chromosomal localization of a human kidney cDNA involved in cystine, dibasic, and neutral amino acid transport., Lee WS., J Clin Invest. May 1, 1993; 91 (5): 1959-63.
	Poly(A)+ RNA from rabbit intestinal mucosa induces b0,+ and y+ amino acid transport activities in Xenopus laevis oocytes., Magagnin S., J Biol Chem. August 5, 1992; 267 (22): 15384-90.

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