Papers associated with inner ear

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	Conserved dimeric subunit stoichiometry of SLC26 multifunctional anion exchangers., Detro-Dassen S., J Biol Chem. February 15, 2008; 283 (7): 4177-88.
	Mutations at arginine 352 alter the pore architecture of CFTR., Cui G., J Membr Biol. March 1, 2008; 222 (2): 91-106.
	Molecular determinants of the anticonvulsant felbamate binding site in the N-methyl-D-aspartate receptor., Chang HR., J Med Chem. March 27, 2008; 51 (6): 1534-45.
	Sox9 is required for invagination of the otic placode in mice., Barrionuevo F., Dev Biol. May 1, 2008; 317 (1): 213-24.
	Mechanics of the exceptional anuran ear., Schoffelen RL., J Comp Physiol A Neuroethol Sens Neural Behav Physiol. May 1, 2008; 194 (5): 417-28.
	Probing the binding sites and mechanisms of action of two human ether-a-go-go-related gene channel activators, 1,3-bis-(2-hydroxy-5-trifluoromethyl-phenyl)-urea (NS1643) and 2-[2-(3,4-dichloro-phenyl)-2,3-dihydro-1H-isoindol-5-ylamino]-nicotinic acid (PD307243)., Xu X., Mol Pharmacol. June 1, 2008; 73 (6): 1709-21.
	An ontology for Xenopus anatomy and development., Segerdell E., BMC Dev Biol. June 23, 2008; 8 92.
	Differential effects of linear and cyclic polyamines on NMDA receptor activities., Masuko T., Neurochem Int. July 1, 2008; 53 (1-2): 38-44.
	Is TEA an inhibitor for human Aquaporin-1?, Müller EM., Pflugers Arch. July 1, 2008; 456 (4): 663-9.
	A cytoplasmic domain mutation in ClC-Kb affects long-distance communication across the membrane., Martinez GQ., PLoS One. July 23, 2008; 3 (7): e2746.
	Timeline and distribution of melanocyte precursors in the mouse heart., Brito FC., Pigment Cell Melanoma Res. August 1, 2008; 21 (4): 464-70.
	Semicircular canal size determines the developmental onset of angular vestibuloocular reflexes in larval Xenopus., Lambert FM., J Neurosci. August 6, 2008; 28 (32): 8086-95.
	Molecular identity and functional properties of a novel T-type Ca2+ channel cloned from the sensory epithelia of the mouse inner ear., Nie L., J Neurophysiol. October 1, 2008; 100 (4): 2287-99.
	Zebrafish TRPA1 channels are required for chemosensation but not for thermosensation or mechanosensory hair cell function., Prober DA., J Neurosci. October 1, 2008; 28 (40): 10102-10.
	Localization of Kv2.2 protein in Xenopus laevis embryos and tadpoles., Gravagna NG., J Comp Neurol. October 10, 2008; 510 (5): 508-24.
	The ion pathway through the opened Na(+),K(+)-ATPase pump., Takeuchi A., Nature. November 20, 2008; 456 (7220): 413-6.
	Hindbrain-derived Wnt and Fgf signals cooperate to specify the otic placode in Xenopus., Park BY., Dev Biol. December 1, 2008; 324 (1): 108-21.
	PTK7 recruits dsh to regulate neural crest migration., Shnitsar I., Development. December 1, 2008; 135 (24): 4015-24.
	RNA isolation from Xenopus inner ear sensory endorgans for transcriptional profiling and molecular cloning., Trujillo-Provencio C., Methods Mol Biol. January 1, 2009; 493 3-20.
	STRUCTURE AND FUNCTION OF THE MIDDLE EAR APPARATUS OF THE AQUATIC FROG, XENOPUS LAEVIS., Mason M., Proc Inst Acoust. January 1, 2009; 31 13-21.
	Four Ca2+ ions activate TRPM2 channels by binding in deep crevices near the pore but intracellularly of the gate., Csanády L., J Gen Physiol. February 1, 2009; 133 (2): 189-203.
	K+ binding in the G-loop and water cavity facilitates Ba2+ movement in the Kir2.1 channel., Chang HK., Biochim Biophys Acta. February 1, 2009; 1788 (2): 500-6.
	Hypo-functional SLC26A4 variants associated with nonsyndromic hearing loss and enlargement of the vestibular aqueduct: genotype-phenotype correlation or coincidental polymorphisms?, Choi BY., Hum Mutat. April 1, 2009; 30 (4): 599-608.
	The analysis of desensitizing CNGA1 channels reveals molecular interactions essential for normal gating., Mazzolini M., J Gen Physiol. April 1, 2009; 133 (4): 375-86.
	Mutations of KCNJ10 together with mutations of SLC26A4 cause digenic nonsyndromic hearing loss associated with enlarged vestibular aqueduct syndrome., Yang T., Am J Hum Genet. May 1, 2009; 84 (5): 651-7.
	Epilepsy, ataxia, sensorineural deafness, tubulopathy, and KCNJ10 mutations., Bockenhauer D., N Engl J Med. May 7, 2009; 360 (19): 1960-70.
	The evolutionarily conserved residue A653 plays a key role in HERG channel closing., Stepanovic SZ., J Physiol. June 1, 2009; 587 (Pt 11): 2555-66.
	Efficient molecular genetic diagnosis of enlarged vestibular aqueducts in East Asians., Choi BY., Genet Test Mol Biomarkers. October 1, 2009; 13 (5): 679-87.
	Vestibular asymmetry as the cause of idiopathic scoliosis: a possible answer from Xenopus., Lambert FM., J Neurosci. October 7, 2009; 29 (40): 12477-83.
	An electrostatic interaction between TEA and an introduced pore aromatic drives spring-in-the-door inactivation in Shaker potassium channels., Ahern CA., J Gen Physiol. December 1, 2009; 134 (6): 461-9.
	Conformational changes associated with proton-dependent gating of ASIC1a., Passero CJ., J Biol Chem. December 25, 2009; 284 (52): 36473-36481.
	Transplantation of Xenopus laevis ears reveals the ability to form afferent and efferent connections with the spinal cord., Elliott KL., Int J Dev Biol. January 1, 2010; 54 (10): 1443-51.
	Diffusion of a soluble protein, photoactivatable GFP, through a sensory cilium., Calvert PD., J Gen Physiol. March 1, 2010; 135 (3): 173-96.
	GJB2 mutations in Mongolia: complex alleles, low frequency, and reduced fitness of the deaf., Tekin M., Ann Hum Genet. March 1, 2010; 74 (2): 155-64.
	Long-term consequences of Sox9 depletion on inner ear development., Park BY., Dev Dyn. April 1, 2010; 239 (4): 1102-12.
	The N terminus of monoamine transporters is a lever required for the action of amphetamines., Sucic S., J Biol Chem. April 2, 2010; 285 (14): 10924-38.
	Cooccupancy of the outer vestibule of voltage-gated sodium channels by micro-conotoxin KIIIA and saxitoxin or tetrodotoxin., Zhang MM., J Neurophysiol. July 1, 2010; 104 (1): 88-97.
	Fast and slow voltage sensor rearrangements during activation gating in Kv1.2 channels detected using tetramethylrhodamine fluorescence., Horne AJ., J Gen Physiol. July 1, 2010; 136 (1): 83-99.
	A pore residue of the KCNQ3 potassium M-channel subunit controls surface expression., Gómez-Posada JC., J Neurosci. July 7, 2010; 30 (27): 9316-23.
	The R109H variant of fascin-2, a developmentally regulated actin crosslinker in hair-cell stereocilia, underlies early-onset hearing loss of DBA/2J mice., Shin JB., J Neurosci. July 21, 2010; 30 (29): 9683-94.
	Identification of sites responsible for the potentiating effect of niflumic acid on ClC-Ka kidney chloride channels., Zifarelli G., Br J Pharmacol. August 1, 2010; 160 (7): 1652-61.
	A regulatory calcium-binding site at the subunit interface of CLC-K kidney chloride channels., Gradogna A., J Gen Physiol. September 1, 2010; 136 (3): 311-23.
	Zebrafish cx30.3: identification and characterization of a gap junction gene highly expressed in the skin., Tao L., Dev Dyn. October 1, 2010; 239 (10): 2627-36.
	Multiple enhancers located in a 1-Mb region upstream of POU3F4 promote expression during inner ear development and may be required for hearing., Naranjo S., Hum Genet. October 1, 2010; 128 (4): 411-9.
	A molecular switch between the outer and the inner vestibules of the voltage-gated Na+ channel., Zarrabi T., J Biol Chem. December 10, 2010; 285 (50): 39458-70.
	Characterization of new otic enhancers of the pou3f4 gene reveal distinct signaling pathway regulation and spatio-temporal patterns., Robert-Moreno À., PLoS One. December 31, 2010; 5 (12): e15907.
	Generation of knockout mice expressing a GFP-reporter under the control of the Lmx1a locus., Griesel G., Gene Expr Patterns. January 1, 2011; 11 (5-6): 345-8.
	CXCL14 expression during chick embryonic development., Gordon CT., Int J Dev Biol. January 1, 2011; 55 (3): 335-40.
	Asymmetric configurations and N-terminal rearrangements in connexin26 gap junction channels., Oshima A., J Mol Biol. January 21, 2011; 405 (3): 724-35.
	Lineage-specific evolution of the vertebrate Otopetrin gene family revealed by comparative genomic analyses., Hurle B., BMC Evol Biol. January 24, 2011; 11 23.

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