Gap junction-mediated intercellular biochemical coupling in cochlear supporting cells is required for normal cochlear functions. - Wikidata - wikimedia - TriplyDB

Gap junction-mediated intercellular biochemical coupling in cochlear supporting cells is required for normal cochlear functions.

Gap junction-mediated intercellular biochemical coupling in cochlear supporting cells is required for normal cochlear functions.

http://www.wikidata.org/entity/Q34084948

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Gap junction mediated intercellular metabolite transfer in the cochlea is compromised in connexin30 null mice The role of connexins in ear and skin physiology - functional insights from disease-associated mutations Gap junctions The cochlea as an independent neuroendocrine organ: expression and possible roles of a local hypothalamic-pituitary-adrenal axis-equivalent signaling system Cellular and Deafness Mechanisms Underlying Connexin Mutation-Induced Hearing Loss - A Common Hereditary Deafness.Human connexin26 and connexin30 form functional heteromeric and heterotypic channels Gap junctions and cochlear homeostasis A fully atomistic model of the Cx32 connexon Assembly of the cochlear gap junction macromolecular complex requires connexin 26.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.Noise-Induced Loss of Hair Cells and Cochlear Synaptopathy Are Mediated by the Activation of AMPK.Quantitative High-Resolution Cellular Map of the Organ of Corti.Developmental expression of inositol 1, 4, 5-trisphosphate receptor in the post-natal rat cochlea.Permeation of fluorophore-conjugated phalloidin into live hair cells of the inner ear is modulated by P2Y receptors.Potassium ion movement in the inner ear: insights from genetic disease and mouse models Inner ear supporting cells: rethinking the silent majority.ATP activates P2X receptors to mediate gap junctional coupling in the cochlea.The cochlear CRF signaling systems and their mechanisms of action in modulating cochlear sensitivity and protection against trauma.BAAV mediated GJB2 gene transfer restores gap junction coupling in cochlear organotypic cultures from deaf Cx26Sox10Cre mice.A mutation in synaptojanin 2 causes progressive hearing loss in the ENU-mutagenised mouse strain Mozart.Functional consequences of novel connexin 26 mutations associated with hereditary hearing loss A mouse model for degeneration of the spiral ligament.Recent findings and emerging questions in cochlear noise injury.Gap-junction channels dysfunction in deafness and hearing loss.Peptide- and collagen-based hydrogel substrates for in vitro culture of chick cochleae.Post-translational modifications of connexin26 revealed by mass spectrometry.Differentially altered Ca2+ regulation and Ca2+ permeability in Cx26 hemichannels formed by the A40V and G45E mutations that cause keratitis ichthyosis deafness syndrome Adenosine triphosphate acts as a paracrine signaling molecule to reduce the motility of T cells.Eeyore: a novel mouse model of hereditary deafness.Hearing loss associated with enlargement of the vestibular aqueduct: mechanistic insights from clinical phenotypes, genotypes, and mouse models.Connexinopathies: a structural and functional glimpse Critical role of the first transmembrane domain of Cx26 in regulating oligomerization and function Hereditary sensorineural hearing loss: advances in molecular genetics and mutation analysis.Supporting sensory transduction: cochlear fluid homeostasis and the endocochlear potential.Ca2+ signaling in the inner ear.Connexin channel permeability to cytoplasmic molecules.Connexin26 deafness associated mutations show altered permeability to large cationic molecules Targeted connexin26 ablation arrests postnatal development of the organ of Corti.Diverse deafness mechanisms of connexin mutations revealed by studies using in vitro approaches and mouse models.The M34A mutant of Connexin26 reveals active conductance states in pore-suspending membranes

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P2860

Gap junction-mediated intercellular biochemical coupling in cochlear supporting cells is required for normal cochlear functions.

http://www.wikidata.org/entity/Q34084948

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James A Sipp

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Ping Chen

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Shoab Ahmad

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Wenxue Tang

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Xi Lin

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Yanping Zhang

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P2860

A new generation of Ca2+ indicators with greatly improved fluorescence properties

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus

Calcium waves propagate through radial glial cells and modulate proliferation in the developing neocortex

Gap junctions in the rat cochlea: immunohistochemical and ultrastructural analysis

Gap junctions in the inner ear: comparison of distribution patterns in different vertebrates and assessement of connexin composition in mammals

Unique and redundant connexin contributions to lens development

Developmental expression patterns of connexin26 and -30 in the rat cochlea

Connexin30 (Gjb6)-deficiency causes severe hearing impairment and lack of endocochlear potential

Novel mutations in the connexin 26 gene (GJB2) that cause autosomal recessive (DFNB1) hearing loss.

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