Papers associated with cltrn

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	Identification and Characterization of Inhibitors of a Neutral Amino Acid Transporter, SLC6A19, Using Two Functional Cell-Based Assays., Danthi SJ, Liang B, Smicker O, Coupland B, Gregory J, Gefteas E, Tietz D, Klodnitsky H, Randall K, Belanger A, Kuntzweiler TA., SLAS Discov. February 1, 2019; 24 (2): 111-120.
	Amino acid transporter B(0)AT1 (slc6a19) and ancillary protein: impact on function., Margheritis E, Imperiali FG, Cinquetti R, Vollero A, Terova G, Rimoldi S, Girardello R, Bossi E., Pflugers Arch. August 1, 2016; 468 (8): 1363-74.
	Molecular basis for the interaction of the mammalian amino acid transporters B0AT1 and B0AT3 with their ancillary protein collectrin., Fairweather SJ, Bröer A, Subramanian N, Tumer E, Cheng Q, Schmoll D, O'Mara ML, Bröer S., J Biol Chem. October 2, 2015; 290 (40): 24308-25.
	Intestinal peptidases form functional complexes with the neutral amino acid transporter B(0)AT1., Fairweather SJ, Bröer A, O'Mara ML, Bröer S., Biochem J. August 15, 2012; 446 (1): 135-48.
	Heat-shock mediated overexpression of HNF1β mutations has differential effects on gene expression in the Xenopus pronephric kidney., Sauert K, Kahnert S, Roose M, Gull M, Brändli AW, Ryffel GU, Waldner C., PLoS One. January 1, 2012; 7 (3): e33522.
	The nephrogenic potential of the transcription factors osr1, osr2, hnf1b, lhx1 and pax8 assessed in Xenopus animal caps., Drews C, Senkel S, Ryffel GU., BMC Dev Biol. January 31, 2011; 11 5.
	Renal imino acid and glycine transport system ontogeny and involvement in developmental iminoglycinuria., Vanslambrouck JM, Bröer A, Thavyogarajah T, Holst J, Bailey CG, Bröer S, Rasko JE., Biochem J. May 27, 2010; 428 (3): 397-407.
	Orphan transporter SLC6A18 is renal neutral amino acid transporter B0AT3., Singer D, Camargo SM, Huggel K, Romeo E, Danilczyk U, Kuba K, Chesnov S, Caron MG, Penninger JM, Verrey F., J Biol Chem. July 24, 2009; 284 (30): 19953-60.
	Tissue-specific amino acid transporter partners ACE2 and collectrin differentially interact with hartnup mutations., Camargo SM, Singer D, Makrides V, Huggel K, Pos KM, Wagner CA, Kuba K, Danilczyk U, Skovby F, Kleta R, Penninger JM, Verrey F., Gastroenterology. March 1, 2009; 136 (3): 872-82.
	A protein complex in the brush-border membrane explains a Hartnup disorder allele., Kowalczuk S, Bröer A, Tietze N, Vanslambrouck JM, Rasko JE, Bröer S., FASEB J. August 1, 2008; 22 (8): 2880-7.
	Collectrin/tmem27 is expressed at high levels in all segments of the developing Xenopus pronephric nephron and in the Wolffian duct., McCoy KE, Zhou X, Zhou X, Vize PD., Gene Expr Patterns. April 1, 2008; 8 (4): 271-4.
	Collectrin and the kidney., Mount DB., Curr Opin Nephrol Hypertens. September 1, 2007; 16 (5): 427-9.
	Aminoaciduria and altered renal expression of luminal amino acid transporters in mice lacking novel gene collectrin., Malakauskas SM, Quan H, Fields TA, McCall SJ, Yu MJ, Kourany WM, Frey CW, Le TH., Am J Physiol Renal Physiol. February 1, 2007; 292 (2): F533-44.
	Essential role for collectrin in renal amino acid transport., Danilczyk U, Sarao R, Remy C, Benabbas C, Stange G, Richter A, Arya S, Pospisilik JA, Singer D, Camargo SM, Makrides V, Ramadan T, Verrey F, Wagner CA, Penninger JM., Nature. December 21, 2006; 444 (7122): 1088-91.
	Collectrin, a collecting duct-specific transmembrane glycoprotein, is a novel homolog of ACE2 and is developmentally regulated in embryonic kidneys., Zhang H, Wada J, Hida K, Tsuchiyama Y, Hiragushi K, Shikata K, Wang H, Lin S, Kanwar YS, Makino H., J Biol Chem. May 18, 2001; 276 (20): 17132-9.

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