Cellular characterization of Connexin26 and Connnexin30 expression in the cochlear lateral wall.
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Identification and characterization of pannexin expression in the mammalian cochleaAberrant Cx26 hemichannels and keratitis-ichthyosis-deafness syndrome: insights into syndromic hearing lossCellular and Deafness Mechanisms Underlying Connexin Mutation-Induced Hearing Loss - A Common Hereditary Deafness.Hypothesis of K+-Recycling Defect Is Not a Primary Deafness Mechanism for Cx26 (GJB2) DeficiencyPannexin 1 deficiency can induce hearing lossConnexin26 (GJB2) deficiency reduces active cochlear amplification leading to late-onset hearing loss.Pannexin1 channels dominate ATP release in the cochlea ensuring endocochlear potential and auditory receptor potential generation and hearing.The role of an inwardly rectifying K(+) channel (Kir4.1) in the inner ear and hearing loss.The Membrane Properties of Cochlear Root Cells are Consistent with Roles in Potassium Recirculation and Spatial Buffering.ATP-mediated potassium recycling in the cochlear supporting cells.Cell degeneration is not a primary causer for Connexin26 (GJB2) deficiency associated hearing loss.Characterization of a knock-in mouse model of the homozygous p.V37I variant in Gjb2.Diverse deafness mechanisms of connexin mutations revealed by studies using in vitro approaches and mouse models.A deafness mechanism of digenic Cx26 (GJB2) and Cx30 (GJB6) mutations: Reduction of endocochlear potential by impairment of heterogeneous gap junctional function in the cochlear lateral wall.Molecular composition and distribution of gap junctions in the sensory epithelium of the human cochlea-a super-resolution structured illumination microscopy (SR-SIM) study.Endothelin-1 mediated induction of extracellular matrix genes in strial marginal cells underlies strial pathology in Alport mice.Progressive age-dependence and frequency difference in the effect of gap junctions on active cochlear amplification and hearing.Human diseases associated with connexin mutations.Connexin26 gap junction mediates miRNA intercellular genetic communication in the cochlea and is required for inner ear development.Dominant connexin26 mutants associated with human hearing loss have trans-dominant effects on connexin30.Use of self-complementary adeno-associated virus serotype 2 as a tracer for labeling axons: implications for axon regenerationDeafness induced by Connexin 26 (GJB2) deficiency is not determined by endocochlear potential (EP) reduction but is associated with cochlear developmental disorders.Contractility in type III cochlear fibrocytes is dependent on non-muscle myosin II and intercellular gap junctional coupling.Hair Cell Transduction, Tuning, and Synaptic Transmission in the Mammalian Cochlea.Radix astragali inhibits the down-regulation of connexin 26 in the stria vascularis of the guinea pig cochlea after acoustic trauma.
P2860
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P2860
Cellular characterization of Connexin26 and Connnexin30 expression in the cochlear lateral wall.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
2008年论文
@zh
2008年论文
@zh-cn
name
Cellular characterization of C ...... in the cochlear lateral wall.
@en
Cellular characterization of C ...... in the cochlear lateral wall.
@nl
type
label
Cellular characterization of C ...... in the cochlear lateral wall.
@en
Cellular characterization of C ...... in the cochlear lateral wall.
@nl
prefLabel
Cellular characterization of C ...... in the cochlear lateral wall.
@en
Cellular characterization of C ...... in the cochlear lateral wall.
@nl
P2860
P1476
Cellular characterization of C ...... in the cochlear lateral wall.
@en
P2093
Hong-Bo Zhao
Ying-Peng Liu
P2860
P2888
P304
P356
10.1007/S00441-008-0641-5
P577
2008-06-26T00:00:00Z