The Inner Ear Contains Heteromeric Channels Composed of Cx26 and Cx30 and Deafness-Related Mutations in Cx26 Have a Dominant Negative Effect on Cx30
Author:
Publisher
Informa UK Limited
Subject
Cell Biology,Clinical Biochemistry,General Medicine
Link
http://www.tandfonline.com/doi/pdf/10.1080/cac.10.4-6.341.346
Reference11 articles.
1. Hereditary deafness and phenotyping in humans
2. Targeted Ablation of Connexin26 in the Inner Ear Epithelial Gap Junction Network Causes Hearing Impairment and Cell Death
3. Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus
4. A technique for slicing the rat cochlea around the onset of hearing
5. De novo mutation of the connexin 26 gene associated with dominant non-syndromic sensorineural hearing loss
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1. Functional Consequences of Pathogenic Variants of the GJB2 Gene (Cx26) Localized in Different Cx26 Domains;Biomolecules;2023-10-13
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3. Recent insights into gap junction biogenesis in the cochlea;Developmental Dynamics;2022-09-26
4. GJB2 and GJB6 gene transcripts in the human cochlea: A study using RNAscope, confocal, and super-resolution structured illumination microscopy;Frontiers in Molecular Neuroscience;2022-09-20
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