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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.