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The Inner Nuclear Membrane Protein Nemp1 Is a New Type of RanGTP-Binding Protein in Eukaryotes. , Shibano T., PLoS One. May 6, 2015; 10 (5): e0127271.
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.
The intracellular amino terminus plays a dominant role in desensitization of ATP-gated P2X receptor ion channels. , Allsopp RC., J Biol Chem. December 30, 2011; 286 (52): 44691-701.
The inhibition of monocarboxylate transporter 2 ( MCT2) by AR-C155858 is modulated by the associated ancillary protein. , Ovens MJ., Biochem J. October 15, 2010; 431 (2): 217-25.
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., Biochem J. January 15, 2010; 425 (3): 523-30.
Roles of ectodomain and transmembrane regions in ethanol and agonist action in purinergic P2X2 and P2X3 receptors. , Asatryan L., Neuropharmacology. October 1, 2008; 55 (5): 835-43.
Structural signatures and membrane helix 4 in GLUT1: inferences from human blood- brain glucose transport mutants. , Pascual JM., J Biol Chem. June 13, 2008; 283 (24): 16732-42.
The Xenopus FcR family demonstrates continually high diversification of paired receptors in vertebrate evolution. , Guselnikov SV ., BMC Evol Biol. February 8, 2008; 8 148.
Ivermectin Interaction with transmembrane helices reveals widespread rearrangements during opening of P2X receptor channels. , Silberberg SD., Neuron. April 19, 2007; 54 (2): 263-74.
Specific mutations in transmembrane helix 8 of human concentrative Na+/nucleoside cotransporter hCNT1 affect permeant selectivity and cation coupling. , Slugoski MD., Biochemistry. February 13, 2007; 46 (6): 1684-93.
Cooperativity and flexibility of cystic fibrosis transmembrane conductance regulator transmembrane segments participate in membrane localization of a charged residue. , Carveth K., J Biol Chem. October 18, 2002; 277 (42): 39507-14.
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., J Biol Chem. July 12, 2002; 277 (28): 24938-48.
Structural basis for the interference between nicorandil and sulfonylurea action. , Reimann F., Diabetes. October 1, 2001; 50 (10): 2253-9.
Equilibrative nucleoside transporters: mapping regions of interaction for the substrate analogue nitrobenzylthioinosine (NBMPR) using rat chimeric proteins. , Sundaram M., Biochemistry. July 10, 2001; 40 (27): 8146-51.
Reorientation of aquaporin-1 topology during maturation in the endoplasmic reticulum. , Lu Y., Mol Biol Cell. September 1, 2000; 11 (9): 2973-85.
Identification of amino acid residues responsible for the pyrimidine and purine nucleoside specificities of human concentrative Na(+) nucleoside cotransporters hCNT1 and hCNT2. , Loewen SK., J Biol Chem. August 27, 1999; 274 (35): 24475-84.
Chimeric constructs between human and rat equilibrative nucleoside transporters (hENT1 and rENT1) reveal hENT1 structural domains interacting with coronary vasoactive drugs. , Sundaram M., J Biol Chem. August 21, 1998; 273 (34): 21519-25.
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., Biochemistry. July 28, 1998; 37 (30): 10738-45.
Cystic fibrosis transmembrane conductance regulator ( CFTR) anion binding as a probe of the pore. , Mansoura MK., Biophys J. March 1, 1998; 74 (3): 1320-32.
Genetic transfer of a nonpeptide antagonist binding site to a previously unresponsive angiotensin receptor. , Ji H., Proc Natl Acad Sci U S A. September 26, 1995; 92 (20): 9240-4.