Potassium ion movement in the inner ear: insights from genetic disease and mouse models
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EAST syndrome: Clinical, pathophysiological, and genetic aspects of mutations in KCNJ10Aberrant Cx26 hemichannels and keratitis-ichthyosis-deafness syndrome: insights into syndromic hearing lossMice with conditional deletion of Cx26 exhibit no vestibular phenotype despite secondary loss of Cx30 in the vestibular end organsLead roles for supporting actors: critical functions of inner ear supporting cellsGenetic Polymorphisms Associated with Hearing Threshold Shift in Subjects during First Encounter with Occupational Impulse Noise.The human deafness-associated connexin 30 T5M mutation causes mild hearing loss and reduces biochemical coupling among cochlear non-sensory cells in knock-in mice.Drug-induced ototoxicity: Mechanisms, Pharmacogenetics, and protective strategies.Organ of Corti and Stria Vascularis: Is there an Interdependence for Survival?Electrogenic transport and K(+) ion channel expression by the human endolymphatic sac epithelium.KCNK5 channels mostly expressed in cochlear outer sulcus cells are indispensable for hearingGenetics of peripheral vestibular dysfunction: lessons from mutant mouse strains.Integration of human and mouse genetics reveals pendrin function in hearing and deafnessComputational model of a circulation current that controls electrochemical properties in the mammalian cochlea.TAK1 expression in the cochlea: a specific marker for adult supporting cells.Calcium signaling in the cochlea - Molecular mechanisms and physiopathological implications.Ion homeostasis in the ear: mechanisms, maladies, and management.ATP-mediated cell-cell signaling in the organ of Corti: the role of connexin channels.Jervell and Lange-Nielsen syndrome in a father and daughter from a large highly inbred family: a 16-year follow-up of 59 living members.Mouse middle ear ion homeostasis channels and intercellular junctions.Molecular aspects of structure, gating, and physiology of pH-sensitive background K2P and Kir K+-transport channels.Molecular architecture of the stria vascularis membrane transport system, which is essential for physiological functions of the mammalian cochlea.Kv1 channels and neural processing in vestibular calyx afferents.Intercellular Ca(2+) waves: mechanisms and function.Specific expression of Kcna10, Pxn and Odf2 in the organ of Corti.Impaired surface expression and conductance of the KCNQ4 channel lead to sensorineural hearing lossDevelopment of the stria vascularis and potassium regulation in the human fetal cochlea: Insights into hereditary sensorineural hearing lossPhysiology and pathophysiology of SLC12A1/2 transporters.Human fetal inner ear involvement in congenital cytomegalovirus infection.Connexin-Mediated Signaling in Nonsensory Cells Is Crucial for the Development of Sensory Inner Hair Cells in the Mouse Cochlea.Claudins: unlocking the code to tight junction function during embryogenesis and in disease.The salt-wasting phenotype of EAST syndrome, a disease with multifaceted symptoms linked to the KCNJ10 K+ channel.Maintenance and regulation of extracellular volume and the ion environment in Drosophila larval nerves.Regulation of sodium transport in the inner ear.Ca2+ homeostasis defects and hereditary hearing loss.Cell biology and physiology of CLC chloride channels and transporters.Regulatory-auxiliary subunits of CLC chloride channel-transport proteins.Gene expression profiles of the cochlea and vestibular endorgans: localization and function of genes causing deafness.Gene expression profiling of the inner ear.Claudins: vital partners in transcellular and paracellular transport coupling.Upregulation of the Nr2f1-A830082K12Rik gene pair in murine neural crest cells results in a complex phenotype reminiscent of Waardenburg syndrome type 4
P2860
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P2860
Potassium ion movement in the inner ear: insights from genetic disease and mouse models
description
2009 nî lūn-bûn
@nan
2009 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Potassium ion movement in the inner ear: insights from genetic disease and mouse models
@ast
Potassium ion movement in the inner ear: insights from genetic disease and mouse models
@en
type
label
Potassium ion movement in the inner ear: insights from genetic disease and mouse models
@ast
Potassium ion movement in the inner ear: insights from genetic disease and mouse models
@en
prefLabel
Potassium ion movement in the inner ear: insights from genetic disease and mouse models
@ast
Potassium ion movement in the inner ear: insights from genetic disease and mouse models
@en
P2860
P1433
P1476
Potassium ion movement in the inner ear: insights from genetic disease and mouse models
@en
P2093
Anselm A Zdebik
Philine Wangemann
P2860
P304
P356
10.1152/PHYSIOL.00018.2009
P577
2009-10-01T00:00:00Z