Papers associated with kidney (and slc3a1)

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	HNF1B Alters an Evolutionarily Conserved Nephrogenic Program of Target Genes., Grand K., J Am Soc Nephrol. March 1, 2023; 34 (3): 412-432.
	Modeling congenital kidney diseases in Xenopus laevis., Blackburn ATM., Dis Model Mech. April 9, 2019; 12 (4):
	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.
	Heat-shock mediated overexpression of HNF1β mutations has differential effects on gene expression in the Xenopus pronephric kidney., Sauert K., PLoS One. January 1, 2012; 7 (3): e33522.
	Characteristics of transport of selenoamino acids by epithelial amino acid transporters., Nickel A., Chem Biol Interact. February 12, 2009; 177 (3): 234-41.
	Organization of the pronephric kidney revealed by large-scale gene expression mapping., Raciti D., Genome Biol. January 1, 2008; 9 (5): R84.
	Aminoaciduria and altered renal expression of luminal amino acid transporters in mice lacking novel gene collectrin., Malakauskas SM., Am J Physiol Renal Physiol. February 1, 2007; 292 (2): F533-44.
	Cystine and glutamate transport in renal epithelial cells transfected with human system x(-) (c)., Bridges CC., Kidney Int. August 1, 2005; 68 (2): 653-64.
	The dopamine precursor L-dihydroxyphenylalanine is transported by the amino acid transporters rBAT and LAT2 in renal cortex., Quiñones H., Am J Physiol Renal Physiol. July 1, 2004; 287 (1): F74-80.
	Cystinuria-specific rBAT(R365W) mutation reveals two translocation pathways in the amino acid transporter rBAT-b0,+AT., Pineda M., Biochem J. February 1, 2004; 377 (Pt 3): 665-74.
	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 of a novel Na+-independent acidic amino acid transporter with structural similarity to the member of a heterodimeric amino acid transporter family associated with unknown heavy chains., Matsuo H., J Biol Chem. June 7, 2002; 277 (23): 21017-26.
	Identification and characterization of a novel member of the heterodimeric amino acid transporter family presumed to be associated with an unknown heavy chain., Chairoungdua A., J Biol Chem. December 28, 2001; 276 (52): 49390-9.
	Effects of gallium and mercury ions on transport systems., Moschèn., J Dent Res. August 1, 2001; 80 (8): 1753-7.
	Human cystinuria-related transporter: localization and functional characterization., Mizoguchi K., Kidney Int. May 1, 2001; 59 (5): 1821-33.
	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.
	Progressive C-terminal deletions of the renal cystine transporter, NBAT, reveal a novel bimodal pattern of functional expression., Deora AB., J Biol Chem. December 4, 1998; 273 (49): 32980-7.
	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.
	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., J Biol Chem. July 26, 1996; 271 (30): 17761-70.
	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.
	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.
	rBAT, related to L-cysteine transport, is localized to the microvilli of proximal straight tubules, and its expression is regulated in kidney by development., Furriols M., J Biol Chem. December 25, 1993; 268 (36): 27060-8.
	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.
	Two mRNA transcripts (rBAT-1 and rBAT-2) are involved in system b0,(+)-related amino acid transport., Markovich D., J Biol Chem. January 15, 1993; 268 (2): 1362-7.
	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.
	Stimulation of system y(+)-like amino acid transport by the heavy chain of human 4F2 surface antigen in Xenopus laevis oocytes., Bertran J., Proc Natl Acad Sci U S A. June 15, 1992; 89 (12): 5606-10.
	Expression cloning of a cDNA from rabbit kidney cortex that induces a single transport system for cystine and dibasic and neutral amino acids., Bertran J., Proc Natl Acad Sci U S A. June 15, 1992; 89 (12): 5601-5.

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