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Characterization of neutral and cationic amino acid transport in Xenopus oocytes. , Campa MJ, Kilberg MS., J Cell Physiol. December 1, 1989; 141 (3): 645-52.
Mechanism of polyamine spermidine uptake by Xenopus laevis oocytes. , Khan NA, Quemener V, Havouis R, Moulinoux JP., Biochem Int. January 1, 1990; 21 (4): 607-13.
Expression of rat liver Na+/L-alanine co-transport in Xenopus laevis oocytes. Effect of glucagon in vivo. , Palacin M, Werner A, Dittmer J, Murer H, Biber J., Biochem J. August 15, 1990; 270 (1): 189-95.
Expression of rat liver glutamine transporters in Xenopus laevis oocytes. , Taylor PM, Mackenzie B, Low SY, Rennie MJ., J Biol Chem. February 25, 1992; 267 (6): 3873-7.
Genetic transfer of a nonpeptide antagonist binding site to a previously unresponsive angiotensin receptor. , Ji H, Zheng W, Zhang Y , Catt KJ, Sandberg K., Proc Natl Acad Sci U S A. September 26, 1995; 92 (20): 9240-4.
Cloning and functional characterization of a system ASC-like Na+-dependent neutral amino acid transporter. , Utsunomiya-Tate N, Endou H, Kanai Y., J Biol Chem. June 21, 1996; 271 (25): 14883-90.
ASCT-1 is a neutral amino acid exchanger with chloride channel activity. , Zerangue N, Kavanaugh MP., J Biol Chem. November 8, 1996; 271 (45): 27991-4.
Cloning, functional expression and brain localization of a novel unconventional outward rectifier K+ channel. , Fink M, Duprat F, Lesage F , Reyes R, Romey G, Heurteaux C, Lazdunski M., EMBO J. December 16, 1996; 15 (24): 6854-62.
Mechanism of enhancement of slow delayed rectifier current by extracellular sulfhydryl modification. , Yao JA, Jiang M, Tseng GN., Am J Physiol. July 1, 1997; 273 (1 Pt 2): H208-19.
Cystic fibrosis transmembrane conductance regulator ( CFTR) anion binding as a probe of the pore. , Mansoura MK, Smith SS, Choi AD, Richards NW, Strong TV, Drumm ML, Collins FS, Dawson DC., Biophys J. March 1, 1998; 74 (3): 1320-32.
Cysteine-scanning mutagenesis of flanking regions at the boundary between external loop I or IV and transmembrane segment II or VII in the GLUT1 glucose transporter. , Olsowski A, Monden I, Keller K., Biochemistry. July 28, 1998; 37 (30): 10738-45.
Chimeric constructs between human and rat equilibrative nucleoside transporters (hENT1 and rENT1) reveal hENT1 structural domains interacting with coronary vasoactive drugs. , Sundaram M, Yao SY, Ng AM, Griffiths M, Cass CE, Baldwin SA, Young JD., J Biol Chem. August 21, 1998; 273 (34): 21519-25.
Identification of the high-affinity tolbutamide site on the SUR1 subunit of the K(ATP) channel. , Ashfield R, Gribble FM, Ashcroft SJ, Ashcroft FM., Diabetes. June 1, 1999; 48 (6): 1341-7.
Identification of amino acid residues responsible for the pyrimidine and purine nucleoside specificities of human concentrative Na(+) nucleoside cotransporters hCNT1 and hCNT2. , Loewen SK, Ng AM, Yao SY, Cass CE, Baldwin SA, Young JD., J Biol Chem. August 27, 1999; 274 (35): 24475-84.
The astroglial ASCT2 amino acid transporter as a mediator of glutamine efflux. , Bröer A, Brookes N, Ganapathy V, Dimmer KS, Wagner CA, Lang F , Bröer S., J Neurochem. November 1, 1999; 73 (5): 2184-94.
A nuclear factor, ASC-2, as a cancer-amplified transcriptional coactivator essential for ligand-dependent transactivation by nuclear receptors in vivo. , Lee SK, Anzick SL, Choi JE, Bubendorf L, Guan XY, Jung YK, Kallioniemi OP, Kononen J, Trent JM, Azorsa D, Jhun BH, Cheong JH, Lee YC , Meltzer PS, Lee JW , Lee JW ., J Biol Chem. November 26, 1999; 274 (48): 34283-93.
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, Segawa H, Kim JY , Chairoungdua A, Kim DK, Matsuo H, Cha SH , Endou H, Kanai Y., J Biol Chem. March 31, 2000; 275 (13): 9690-8.
Reorientation of aquaporin-1 topology during maturation in the endoplasmic reticulum. , Lu Y, Turnbull IR, Bragin A, Carveth K, Verkman AS, Skach WR., Mol Biol Cell. September 1, 2000; 11 (9): 2973-85.
Helix packing of functionally important regions of the cardiac Na(+)-Ca(2+) exchanger. , Qiu Z, Nicoll DA, Philipson KD., J Biol Chem. January 5, 2001; 276 (1): 194-9.
Equilibrative nucleoside transporters: mapping regions of interaction for the substrate analogue nitrobenzylthioinosine (NBMPR) using rat chimeric proteins. , Sundaram M, Yao SY, Ng AM, Cass CE, Baldwin SA, Young JD., Biochemistry. July 10, 2001; 40 (27): 8146-51.
Structural basis for the interference between nicorandil and sulfonylurea action. , Reimann F, Ashcroft FM, Gribble FM., Diabetes. October 1, 2001; 50 (10): 2253-9.
A disulfide bond is required for functional assembly of NCX1 from complementary fragments. , Qiu Z, Chen J , Nicoll DA, Philipson KD., Biochem Biophys Res Commun. October 5, 2001; 287 (4): 825-8.
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, Kanai Y, Matsuo H, Inatomi J, Kim DK, Endou H., J Biol Chem. December 28, 2001; 276 (52): 49390-9.
The oxidant thimerosal modulates gating behavior of KCNQ1 by interaction with the channel outer shell. , Kerst G, Brousos H, Schreiber R, Nitschke R, Hug MJ, Greger R, Bleich M., J Membr Biol. March 15, 2002; 186 (2): 89-100.
Characterisation and cloning of a Na(+)-dependent broad-specificity neutral amino acid transporter from NBL-1 cells: a novel member of the ASC/B(0) transporter family. , Pollard M, Meredith D, McGivan JD., Biochim Biophys Acta. April 12, 2002; 1561 (2): 202-8.
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, Kanai Y, Kim JY , Chairoungdua A, Kim DK, Inatomi J, Shigeta Y, Ishimine H, Chaekuntode S, Tachampa K, Choi HW, Babu E, Fukuda J, Endou H., J Biol Chem. June 7, 2002; 277 (23): 21017-26.
Functional and molecular characterization of nucleobase transport by recombinant human and rat equilibrative nucleoside transporters 1 and 2. Chimeric constructs reveal a role for the ENT2 helix 5-6 region in nucleobase translocation. , Yao SY, Ng AM, Vickers MF, Sundaram M, Cass CE, Baldwin SA, Young JD., J Biol Chem. July 12, 2002; 277 (28): 24938-48.
Cooperativity and flexibility of cystic fibrosis transmembrane conductance regulator transmembrane segments participate in membrane localization of a charged residue. , Carveth K, Buck T, Anthony V, Skach WR., J Biol Chem. October 18, 2002; 277 (42): 39507-14.
Analysis of the differential modulation of sulphonylurea block of beta-cell and cardiac ATP-sensitive K+ (K(ATP)) channels by Mg-nucleotides. , Reimann F, Dabrowski M, Jones P, Gribble FM, Ashcroft FM., J Physiol. February 15, 2003; 547 (Pt 1): 159-68.
Cation stoichiometry and cation pathway in the Na, K-ATPase and nongastric H, K-ATPase. , Horisberger JD, Guennoun S, Burnay M, Geering K., Ann N Y Acad Sci. April 1, 2003; 986 127-32.
Cross-linking of glycine receptor transmembrane segments two and three alters coupling of ligand binding with channel opening. , Lobo IA, Trudell JR, Harris RA., J Neurochem. August 1, 2004; 90 (4): 962-9.
The amino acid transporter asc-1 is not involved in cystinuria. , Pineda M, Font M, Bassi MT, Manzoni M, Borsani G, Marigo V, Fernández E, Río RM, Purroy J, Zorzano A, Nunes V, Palacín M., Kidney Int. October 1, 2004; 66 (4): 1453-64.
Mutational analysis of the alpha-1 repeat of the cardiac Na(+)-Ca2+ exchanger. , Ottolia M, Nicoll DA, Philipson KD., J Biol Chem. January 14, 2005; 280 (2): 1061-9.
Secondary structure and gating rearrangements of transmembrane segments in rat P2X4 receptor channels. , Silberberg SD, Chang TH, Swartz KJ., J Gen Physiol. April 1, 2005; 125 (4): 347-59.
Recent progress in structure-function analyses of Nramp proton-dependent metal-ion transporters. , Courville P, Chaloupka R, Cellier MF., Biochem Cell Biol. December 1, 2006; 84 (6): 960-78.
Specific mutations in transmembrane helix 8 of human concentrative Na+/nucleoside cotransporter hCNT1 affect permeant selectivity and cation coupling. , Slugoski MD, Loewen SK, Ng AM, Smith KM, Yao SY, Karpinski E, Cass CE, Baldwin SA, Young JD., Biochemistry. February 13, 2007; 46 (6): 1684-93.
Ivermectin Interaction with transmembrane helices reveals widespread rearrangements during opening of P2X receptor channels. , Silberberg SD, Li M, Swartz KJ., Neuron. April 19, 2007; 54 (2): 263-74.
A conductive pathway generated from fragments of the human red cell anion exchanger AE1. , Parker MD , Young MT, Daly CM, Meech RW, Boron WF, Tanner MJ., J Physiol. May 15, 2007; 581 (Pt 1): 33-50.
The Xenopus FcR family demonstrates continually high diversification of paired receptors in vertebrate evolution. , Guselnikov SV , Ramanayake T, Erilova AY, Mechetina LV, Najakshin AM, Robert J , Taranin AV., BMC Evol Biol. February 8, 2008; 8 148.
Presence of aquaporin and V-ATPase on the contractile vacuole of Amoeba proteus. , Nishihara E, Yokota E, Tazaki A , Orii H, Katsuhara M, Kataoka K, Igarashi H, Moriyama Y , Shimmen T, Sonobe S., Biol Cell. March 1, 2008; 100 (3): 179-88.
Structural signatures and membrane helix 4 in GLUT1: inferences from human blood- brain glucose transport mutants. , Pascual JM, Wang D, Yang R, Shi L, Yang H, De Vivo DC., J Biol Chem. June 13, 2008; 283 (24): 16732-42.
Roles of ectodomain and transmembrane regions in ethanol and agonist action in purinergic P2X2 and P2X3 receptors. , Asatryan L, Popova M, Woodward JJ, King BF , Alkana RL, Davies DL., Neuropharmacology. October 1, 2008; 55 (5): 835-43.
Cystic fibrosis transmembrane conductance regulator: using differential reactivity toward channel-permeant and channel-impermeant thiol-reactive probes to test a molecular model for the pore. , Alexander C, Ivetac A, Liu X, Norimatsu Y, Serrano JR, Landstrom A, Sansom M, Dawson DC., Biochemistry. October 27, 2009; 48 (42): 10078-88.
AR-C155858 is a potent inhibitor of monocarboxylate transporters MCT1 and MCT2 that binds to an intracellular site involving transmembrane helices 7-10. , Ovens MJ, Davies AJ, Wilson MC, Murray CM, Halestrap AP., Biochem J. January 15, 2010; 425 (3): 523-30.
The inhibition of monocarboxylate transporter 2 ( MCT2) by AR-C155858 is modulated by the associated ancillary protein. , Ovens MJ, Manoharan C, Wilson MC, Murray CM, Halestrap AP., Biochem J. October 15, 2010; 431 (2): 217-25.
The intracellular amino terminus plays a dominant role in desensitization of ATP-gated P2X receptor ion channels. , Allsopp RC, Evans RJ., J Biol Chem. December 30, 2011; 286 (52): 44691-701.
Effect of simultaneously replacing putative TM6 and TM12 of human NBCe1-A with those from NBCn1 on surface abundance in Xenopus oocytes. , Chen LM, Qin X, Moss FJ, Liu Y , Boron WF., J Membr Biol. March 1, 2012; 245 (3): 131-40.
Arg188 in rice sucrose transporter OsSUT1 is crucial for substrate transport. , Sun Y, Ward JM., BMC Biochem. November 21, 2012; 13 26.
The SLC16 gene family - structure, role and regulation in health and disease. , Halestrap AP., Mol Aspects Med. January 1, 2013; 34 (2-3): 337-49.
Both transmembrane domains of BK β1 subunits are essential to confer the normal phenotype of β1-containing BK channels. , Kuntamallappanavar G, Toro L, Dopico AM., PLoS One. January 1, 2014; 9 (10): e109306.