Pages that link to "Q42515610"
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The following pages link to KCNJ10 (Kir4.1) potassium channel knockout abolishes endocochlear potential (Q42515610):
Displaying 50 items.
- Inwardly rectifying potassium channels: their structure, function, and physiological roles (Q24296441) (← links)
- Epilepsy, ataxia, sensorineural deafness, tubulopathy, and KCNJ10 mutations (Q24631051) (← links)
- The endocochlear potential depends on two K+ diffusion potentials and an electrical barrier in the stria vascularis of the inner ear (Q24652355) (← links)
- Loss of KCNJ10 protein expression abolishes endocochlear potential and causes deafness in Pendred syndrome mouse model (Q24805411) (← links)
- EAST syndrome: Clinical, pathophysiological, and genetic aspects of mutations in KCNJ10 (Q26738592) (← links)
- The role of connexins in ear and skin physiology - functional insights from disease-associated mutations (Q26827294) (← links)
- Mice with conditional deletion of Cx26 exhibit no vestibular phenotype despite secondary loss of Cx30 in the vestibular end organs (Q27311137) (← links)
- The unique electrical properties in an extracellular fluid of the mammalian cochlea; their functional roles, homeostatic processes, and pathological significance. (Q28076301) (← links)
- LIMP-2/LGP85 deficiency causes ureteric pelvic junction obstruction, deafness and peripheral neuropathy in mice (Q28181137) (← links)
- K+ cycling and the endocochlear potential (Q28198160) (← links)
- Impaired stria vascularis integrity upon loss of E-cadherin in basal cells (Q28506436) (← links)
- Conditional knock-out of Kir4.1 leads to glial membrane depolarization, inhibition of potassium and glutamate uptake, and enhanced short-term synaptic potentiation (Q28508728) (← links)
- Postnatal developmental expression of the PDZ scaffolds Na+ -H+ exchanger regulatory factors 1 and 2 in the rat cochlea (Q28577406) (← links)
- Organ of Corti and Stria Vascularis: Is there an Interdependence for Survival? (Q30365442) (← links)
- Characterization of Lgr5+ progenitor cell transcriptomes in the apical and basal turns of the mouse cochlea. (Q30367432) (← links)
- KCNK5 channels mostly expressed in cochlear outer sulcus cells are indispensable for hearing (Q30396787) (← links)
- Slc26a4-insufficiency causes fluctuating hearing loss and stria vascularis dysfunction (Q30410497) (← links)
- Free radical stress-mediated loss of Kcnj10 protein expression in stria vascularis contributes to deafness in Pendred syndrome mouse model (Q30413304) (← links)
- Potassium ion movement in the inner ear: insights from genetic disease and mouse models (Q30413390) (← links)
- The role of an inwardly rectifying K(+) channel (Kir4.1) in the inner ear and hearing loss (Q30414096) (← links)
- Genetics of auditory mechano-electrical transduction (Q30421422) (← links)
- Potassium currents in isolated deiters' cells of Guinea pig. (Q30445278) (← links)
- Deafness and permanently reduced potassium channel gene expression and function in hypothyroid Pit1dw mutants. (Q30445850) (← links)
- Feline deafness (Q30447868) (← links)
- Mice deficient in H+-ATPase a4 subunit have severe hearing impairment associated with enlarged endolymphatic compartments within the inner ear. (Q30453338) (← links)
- Physiopathology of the cochlear microcirculation (Q30456047) (← links)
- Genetic background of Prop1(df) mutants provides remarkable protection against hypothyroidism-induced hearing impairment (Q30469465) (← links)
- Localization and functional studies of pendrin in the mouse inner ear provide insight about the etiology of deafness in pendred syndrome (Q30473447) (← links)
- Age-related changes in cochlear endolymphatic potassium and potential in CD-1 and CBA/CaJ mice (Q30473450) (← links)
- The Membrane Properties of Cochlear Root Cells are Consistent with Roles in Potassium Recirculation and Spatial Buffering (Q30474322) (← links)
- Supporting cell characteristics in long-deafened aged mouse ears (Q30478412) (← links)
- Connexin30 deficiency causes instrastrial fluid-blood barrier disruption within the cochlear stria vascularis (Q30479250) (← links)
- Endocochlear potential depends on Cl- channels: mechanism underlying deafness in Bartter syndrome IV. (Q30484470) (← links)
- Mice lacking ganglioside GM3 synthase exhibit complete hearing loss due to selective degeneration of the organ of Corti (Q30484717) (← links)
- Analysis of the mouse mutant Cloth-ears shows a role for the voltage-gated sodium channel Scn8a in peripheral neural hearing loss (Q30485081) (← links)
- A zebrafish model for Waardenburg syndrome type IV reveals diverse roles for Sox10 in the otic vesicle (Q30485384) (← links)
- A systemic gentamicin pathway across the stria vascularis (Q30488731) (← links)
- Conservation of hearing by simultaneous mutation of Na,K-ATPase and NKCC1. (Q30492373) (← links)
- Loss of cochlear HCO3- secretion causes deafness via endolymphatic acidification and inhibition of Ca2+ reabsorption in a Pendred syndrome mouse model (Q30494661) (← links)
- The ATP-sensitive K(+)-channel (K(ATP)) controls early left-right patterning in Xenopus and chick embryos. (Q30496547) (← links)
- Orphan glutamate receptor delta1 subunit required for high-frequency hearing (Q30500847) (← links)
- Neurological features of epilepsy, ataxia, sensorineural deafness, tubulopathy syndrome. (Q30616239) (← links)
- C-Raf deficiency leads to hearing loss and increased noise susceptibility (Q30664961) (← links)
- Immunoreactivities for glutathione S-transferases and glutathione peroxidase in the lateral wall of pigmented and albino guinea pig cochlea (Q33370963) (← links)
- The color loci of mice--a genetic century (Q34214082) (← links)
- Varitint-waddler: a double whammy for hearing. (Q34275022) (← links)
- Endogenous retrovirus insertion in the KIT oncogene determines white and white spotting in domestic cats (Q34352040) (← links)
- Kcnj10 is a major type of K+ channel in mouse corneal epithelial cells and plays a role in initiating EGFR signaling (Q34354013) (← links)
- Molecular basis of decreased Kir4.1 function in SeSAME/EAST syndrome (Q34457174) (← links)
- The contribution of genes involved in potassium-recycling in the inner ear to noise-induced hearing loss (Q34545156) (← links)