Cellular and Deafness Mechanisms Underlying Connexin Mutation-Induced Hearing Loss - A Common Hereditary Deafness.
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Hypothesis of K+-Recycling Defect Is Not a Primary Deafness Mechanism for Cx26 (GJB2) DeficiencyA connexin30 mutation rescues hearing and reveals roles for gap junctions in cochlear amplification and micromechanicsPannexin 1 deficiency can induce hearing lossCharacterization of a knock-in mouse model of the homozygous p.V37I variant in Gjb2.Amplification mode differs along the length of the mouse cochlea as revealed by connexin 26 deletion from specific gap junctionsConnexinopathies: a structural and functional glimpseExpression and function of pannexins in the inner ear and hearing.Connexin-Mediated Signaling in Nonsensory Cells Is Crucial for the Development of Sensory Inner Hair Cells in the Mouse Cochlea.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.Progressive age-dependence and frequency difference in the effect of gap junctions on active cochlear amplification and hearing.Gap junction mediated miRNA intercellular transfer and gene regulation: A novel mechanism for intercellular genetic communication.Signaling in the Auditory System: Implications in Hair Cell Regeneration and Hearing Function.Connexin26 gap junction mediates miRNA intercellular genetic communication in the cochlea and is required for inner ear development.Whole-exome sequencing to identify the cause of congenital sensorineural hearing loss in carriers of a heterozygous GJB2 mutation.Mind the Gaps in Tumor Immunity: Impact of Connexin-Mediated Intercellular Connections.Design and Characterization of a Human Monoclonal Antibody that Modulates Mutant Connexin 26 Hemichannels Implicated in Deafness and Skin DisordersHair Cell Transduction, Tuning, and Synaptic Transmission in the Mammalian Cochlea.c.464A>G variation in the GJB2 gene is detected in a Han Chinese family.Connexin43 Mutant Patient-Derived Induced Pluripotent Stem Cells Exhibit Altered Differentiation Potential.Connexin hemichannels and cochlear function.Gap-junctional channel and hemichannel activity of two recently identified connexin 26 mutants associated with deafness.Gap junction gene and protein families: Connexins, innexins, and pannexins.Knockout of Pannexin-1 Induces Hearing Loss.Genes important for otoneurological diagnostic purposes - current status and future prospectsConnexin 26 Expression in Mammalian Cardiomyocytes
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P2860
Cellular and Deafness Mechanisms Underlying Connexin Mutation-Induced Hearing Loss - A Common Hereditary Deafness.
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2015 nî lūn-bûn
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2015 թուականի Մայիսին հրատարակուած գիտական յօդուած
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2015 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2015年の論文
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2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
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name
Cellular and Deafness Mechanis ...... - A Common Hereditary Deafness
@nl
Cellular and Deafness Mechanis ...... A Common Hereditary Deafness.
@ast
Cellular and Deafness Mechanis ...... A Common Hereditary Deafness.
@en
type
label
Cellular and Deafness Mechanis ...... - A Common Hereditary Deafness
@nl
Cellular and Deafness Mechanis ...... A Common Hereditary Deafness.
@ast
Cellular and Deafness Mechanis ...... A Common Hereditary Deafness.
@en
prefLabel
Cellular and Deafness Mechanis ...... - A Common Hereditary Deafness
@nl
Cellular and Deafness Mechanis ...... A Common Hereditary Deafness.
@ast
Cellular and Deafness Mechanis ...... A Common Hereditary Deafness.
@en
P2860
P3181
P356
P1476
Cellular and Deafness Mechanis ...... A Common Hereditary Deafness.
@en
P2093
Hong-Bo Zhao
Jeffrey C Wingard
P2860
P3181
P356
10.3389/FNCEL.2015.00202
P407
P577
2015-05-29T00:00:00Z