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2)Turner AJ, Hooper NM. The angiotensin-converting enzyme gene family: genomics and pharmacology. Trends Pharmacol Sci. 2002; 23: 177-83
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3)Danilczyk U, Sarao R, Remy C, et al. Essential role for collectrin in renal amino acid transport. Nature. 2006; 444: 1088-91
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4)Malakauskas SM, Quan H, Fields TA, et al. Aminoaciduria and altered renal expression of luminal amino acid transporters in mice lacking novel gene collectrin. Am J Physiol Renal Physiol. 2007; 292: F533-44
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5)Kleta R, Romeo E, Ristic Z, et al. Mutations in SLC6A19, encoding B0AT1, cause Hartnup disorder. Nat Genet. 2004; 36: 999-1002
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6)Camargo SM, Singer D, Makrides V, et al. Tissue-specific amino acid transporter partners ACE2 and collectrin differentially interact with hartnup mutations. Gastroenterology. 2009; 136: 872-82
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7)Fairweather SJ, Broer A, O’Mara ML, et al. Intestinal peptidases form functional complexes with the neutral amino acid transporter B(0)AT1. Biochem J. 2012; 446: 135-48
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9)Guggino WB, Stanton BA. New insights into cystic fibrosis: molecular switches that regulate CFTR. Nat Rev Mol Cell Biol. 2006; 7: 426-36
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10)Li C, Krishnamurthy PC, Penmatsa H, et al. Spatiotemporal coupling of cAMP transporter to CFTR chloride channel function in the gut epithelia. Cell. 2007; 131: 940-51
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11)Singh AK, Riederer B, Krabbenhoft A, et al. Differential roles of NHERF1, NHERF2, and PDZK1 in regulating CFTR-mediated intestinal anion secretion in mice. J Clin Invest. 2009; 119: 540-50
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12)Enomoto A, Kimura H, Chairoungdua A, et al. Molecular identification of a renal urate anion exchanger that regulates blood urate levels. Nature. 2002; 417: 447-52
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13)Anzai N, Miyazaki H, Noshiro R, et al. The multivalent PDZ domain-containing protein PDZK1 regulates transport activity of renal urate-anion exchanger URAT1 via its C terminus. J Biol Chem. 2004; 279: 45942-50
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14)Ichida K, Hosoyamada M, Hisatome I, et al. Clinical and molecular analysis of patients with renal hypouricemia in Japan-influence of URAT1 gene on urinary urate excretion. J Am Soc Nephrol. 2004; 15: 164-73
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15)Lu Y, Nakanishi T, Tamai I. Functional cooperation of SMCTs and URAT1 for renal reabsorption transport of urate. Drug Metab Pharmacokinet. 2012; in press
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16)Thangaraju M, Ananth S, Martin PM, et al. c/ebpdelta Null mouse as a model for the double knock-out of slc5a8 and slc5a12 in kidney. J Biol Chem. 2006; 281: 26769-73
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17)Kocher O, Pal R, Roberts M, et al. Targeted disruption of the PDZK1 gene by homologous recombination. Mol Cell Biol. 2003; 23: 1175-80
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18)Yesilaltay A, Kocher O, Pal R, et al. PDZK1 is required for maintaining hepatic scavenger receptor, class B, type I (SR-BI) steady state levels but not its surface localization or function. J Biol Chem. 2006; 281: 28975-80
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19)Capuano P, Bacic D, Stange G, et al. Expression and regulation of the renal Na/phosphate cotransporter NaPi-IIa in a mouse model deficient for the PDZ protein PDZK1. Pflugers Arch. 2005; 449: 392-402
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20)Thomson RB, Wang T, Thomson BR, et al. Role of PDZK1 in membrane expression of renal brush border ion exchangers. Proc Natl Acad Sci U S A. 2005; 102: 13331-6
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21)Jiang Z, Asplin JR, Evan AP, et al. Calcium oxalate urolithiasis in mice lacking anion transporter Slc26a6. Nat Genet. 2006; 38: 474-8
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22)Hibino H, Kurachi Y. Distinct detergent-resistant membrane microdomains (lipid rafts) respectively harvest K(+) and water transport systems in brain astroglia. Eur J Neurosci. 2007; 26: 2539-55
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23)Fujii T, Takahashi Y, Ikari A, et al. Functional association between K+-Cl- cotransporter-4 and H+, K+-ATPase in the apical canalicular membrane of gastric parietal cells. J Biol Chem. 2009; 284: 619-29
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24)Fujii T, Fujita K, Takeguchi N, et al. Function of K+-Cl- cotransporters in the acid secretory mechanism of gastric parietal cells. Biol Pharm Bull. 2011; 34: 810-2
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