Papers associated with osseous labyrinth

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	Identification of a hydrophobic residue as a key determinant of fructose transport by the facilitative hexose transporter SLC2A7 (GLUT7)., Manolescu A., J Biol Chem. December 30, 2005; 280 (52): 42978-83.
	Electrostatics in the cytoplasmic pore produce intrinsic inward rectification in kir2.1 channels., Yeh SH., J Gen Physiol. December 1, 2005; 126 (6): 551-62.
	An inhibitor of TRPV1 channels isolated from funnel Web spider venom., Kitaguchi T., Biochemistry. November 29, 2005; 44 (47): 15544-9.
	Stoichiometry of the alpha9alpha10 nicotinic cholinergic receptor., Plazas PV., J Neurosci. November 23, 2005; 25 (47): 10905-12.
	EYA1 expression in the developing inner ear., Bane BC., Ann Otol Rhinol Laryngol. November 1, 2005; 114 (11): 853-8.
	Inner ear formation during the early larval development of Xenopus laevis., Quick QA., Dev Dyn. November 1, 2005; 234 (3): 791-801.
	Expression and functional phenotype of mouse ERG K+ channels in the inner ear: potential role in K+ regulation in the inner ear., Nie L., J Neurosci. September 21, 2005; 25 (38): 8671-9.
	Pharmacological implications of two distinct mechanisms of interaction of memantine with N-methyl-D-aspartate-gated channels., Chen HS., J Pharmacol Exp Ther. September 1, 2005; 314 (3): 961-71.
	A novel alpha-conotoxin, PeIA, cloned from Conus pergrandis, discriminates between rat alpha9alpha10 and alpha7 nicotinic cholinergic receptors., McIntosh JM., J Biol Chem. August 26, 2005; 280 (34): 30107-12.
	Probing the geometry of the inner vestibule of BK channels with sugars., Brelidze TI., J Gen Physiol. August 1, 2005; 126 (2): 105-21.
	Slow inactivation in voltage gated potassium channels is insensitive to the binding of pore occluding peptide toxins., Oliva C., Biophys J. August 1, 2005; 89 (2): 1009-19.
	Cysteine accessibility in ClC-0 supports conservation of the ClC intracellular vestibule., Engh AM., J Gen Physiol. June 1, 2005; 125 (6): 601-17.
	Pharmacology of acetylcholine-mediated cell signaling in the lateral line organ following efferent stimulation., Dawkins R., J Neurophysiol. May 1, 2005; 93 (5): 2541-51.
	Small-scale molecular motions accomplish glutamate uptake in human glutamate transporters., Koch HP., J Neurosci. February 16, 2005; 25 (7): 1730-6.
	A multifunctional aromatic residue in the external pore vestibule of Na+ channels contributes to the local anesthetic receptor., Tsang SY., Mol Pharmacol. February 1, 2005; 67 (2): 424-34.
	State-dependent changes in the electrostatic potential in the pore of a GluR channel., Sobolevsky AI., Biophys J. January 1, 2005; 88 (1): 235-42.
	A ring of negative charges in the intracellular vestibule of Kir2.1 channel modulates K+ permeation., Chang HK., Biophys J. January 1, 2005; 88 (1): 243-54.
	Molecular basis of inward rectification: polyamine interaction sites located by combined channel and ligand mutagenesis., Kurata HT., J Gen Physiol. November 1, 2004; 124 (5): 541-54.
	Inhibition of CFTR channels by a peptide toxin of scorpion venom., Fuller MD., Am J Physiol Cell Physiol. November 1, 2004; 287 (5): C1328-41.
	Three mechanisms underlie KCNQ2/3 heteromeric potassium M-channel potentiation., Etxeberria A., J Neurosci. October 13, 2004; 24 (41): 9146-52.
	Lidocaine: a foot in the door of the inner vestibule prevents ultra-slow inactivation of a voltage-gated sodium channel., Sandtner W., Mol Pharmacol. September 1, 2004; 66 (3): 648-57.
	Regulation of K+ flow by a ring of negative charges in the outer pore of BKCa channels. Part I: Aspartate 292 modulates K+ conduction by external surface charge effect., Haug T., J Gen Physiol. August 1, 2004; 124 (2): 173-84.
	The role of Pax2 in mouse inner ear development., Burton Q., Dev Biol. August 1, 2004; 272 (1): 161-75.
	Anthraquinone polyamines: novel channel blockers to study N-methyl-D-aspartate receptors., Kashiwagi K., J Pharmacol Exp Ther. June 1, 2004; 309 (3): 884-93.
	Molecular basis of pH and Ca2+ regulation of aquaporin water permeability., Németh-Cahalan KL., J Gen Physiol. May 1, 2004; 123 (5): 573-80.
	Cloning and expression of a small-conductance Ca(2+)-activated K+ channel from the mouse cochlea: coexpression with alpha9/alpha10 acetylcholine receptors., Nie L., J Neurophysiol. April 1, 2004; 91 (4): 1536-44.
	Protons block BK channels by competitive inhibition with K+ and contribute to the limits of unitary currents at high voltages., Brelidze TI., J Gen Physiol. March 1, 2004; 123 (3): 305-19.
	Outer pore topology of the ECaC-TRPV5 channel by cysteine scan mutagenesis., Dodier Y., J Biol Chem. February 20, 2004; 279 (8): 6853-62.
	Molecular basis of calcium regulation in connexin-32 hemichannels., Gómez-Hernández JM., Proc Natl Acad Sci U S A. December 23, 2003; 100 (26): 16030-5.
	Agonist-induced conformational changes in the extracellular domain of alpha 7 nicotinic acetylcholine receptors., Lyford LK., Mol Pharmacol. September 1, 2003; 64 (3): 650-8.
	Gating competence of constitutively open CLC-0 mutants revealed by the interaction with a small organic Inhibitor., Traverso S., J Gen Physiol. September 1, 2003; 122 (3): 295-306.
	Beta1 subunits facilitate gating of BK channels by acting through the Ca2+, but not the Mg2+, activating mechanisms., Qian X., Proc Natl Acad Sci U S A. August 19, 2003; 100 (17): 10061-6.
	External TEA block of shaker K+ channels is coupled to the movement of K+ ions within the selectivity filter., Thompson J., J Gen Physiol. August 1, 2003; 122 (2): 239-46.
	A ring of eight conserved negatively charged amino acids doubles the conductance of BK channels and prevents inward rectification., Brelidze TI., Proc Natl Acad Sci U S A. July 22, 2003; 100 (15): 9017-22.
	Three-dimensional morphology of inner ear development in Xenopus laevis., Bever MM., Dev Dyn. July 1, 2003; 227 (3): 422-30.
	Local anesthetic block of Kv channels: role of the S6 helix and the S5-S6 linker for bupivacaine action., Nilsson J., Mol Pharmacol. June 1, 2003; 63 (6): 1417-29.
	BeKm-1 is a HERG-specific toxin that shares the structure with ChTx but the mechanism of action with ErgTx1., Zhang M., Biophys J. May 1, 2003; 84 (5): 3022-36.
	[K(+)](o)-dependent change in conformation of the HERG1 long QT mutation N629D channel results in partial reversal of the in vitro disease phenotype., Teng GQ., Cardiovasc Res. March 1, 2003; 57 (3): 642-50.
	Molecular site of action of the antiarrhythmic drug propafenone at the voltage-operated potassium channel Kv2.1., Madeja M., Mol Pharmacol. March 1, 2003; 63 (3): 547-56.
	The link between ion permeation and inactivation gating of Kv4 potassium channels., Shahidullah M., Biophys J. February 1, 2003; 84 (2 Pt 1): 928-41.
	Direct interaction with a nuclear protein and regulation of gene silencing by a variant of the Ca2+-channel beta 4 subunit., Hibino H., Proc Natl Acad Sci U S A. January 7, 2003; 100 (1): 307-12.
	Loss-of-function and residual channel activity of connexin26 mutations associated with non-syndromic deafness., Bruzzone R., FEBS Lett. January 2, 2003; 533 (1-3): 79-88.
	Interactions of the C-11 hydroxyl of tetrodotoxin with the sodium channel outer vestibule., Choudhary G., Biophys J. January 1, 2003; 84 (1): 287-94.
	Staggering of subunits in NMDAR channels., Sobolevsky AI., Biophys J. December 1, 2002; 83 (6): 3304-14.
	DRPEER: a motif in the extracellular vestibule conferring high Ca2+ flux rates in NMDA receptor channels., Watanabe J., J Neurosci. December 1, 2002; 22 (23): 10209-16.
	Binding symmetry of extracellular divalent cations to conduction pore studied using tandem dimers of a CNG channel., Kwon RJ., Biochem Biophys Res Commun. November 8, 2002; 298 (4): 478-85.
	Structural and functional role of the extracellular s5-p linker in the HERG potassium channel., Liu J., J Gen Physiol. November 1, 2002; 120 (5): 723-37.
	The transmembrane serine protease (TMPRSS3) mutated in deafness DFNB8/10 activates the epithelial sodium channel (ENaC) in vitro., Guipponi M., Hum Mol Genet. November 1, 2002; 11 (23): 2829-36.
	Glutamate 172, essential for modulation of L247T alpha7 ACh receptors by Ca2+, lines the extracellular vestibule., Eddins D., Am J Physiol Cell Physiol. November 1, 2002; 283 (5): C1454-60.
	Interaction between fast and ultra-slow inactivation in the voltage-gated sodium channel. Does the inactivation gate stabilize the channel structure?, Hilber K., J Biol Chem. October 4, 2002; 277 (40): 37105-15.

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