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A connexin30 mutation rescues hearing and reveals roles for gap junctions in cochlear amplification and micromechanics | Nature Communications
PLOS ONE: Cataract-Causing Mutation of Human Connexin 46 Impairs Gap Junction, but Increases Hemichannel Function and Cell Death
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The p.Tyr136X mutation confines the effect of the pGly45Glu mutation.... | Download Scientific Diagram
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Effects of S279 or S282 mutation on Cx43 expression and gap junction... | Download Scientific Diagram
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Connexins in health and disease - Yamasaki - 2018 - Clinical and Experimental Neuroimmunology - Wiley Online Library
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Regulation of gap junction intercellular communication by connexin ubiquitination: physiological and pathophysiological implications | SpringerLink
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Connexin43 mutations linked to skin disease have augmented hemichannel activity | Scientific Reports
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Frontiers | Role of Connexin-Based Gap Junction Channels in Communication of Myelin Sheath in Schwann Cells | Cellular Neuroscience
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The sorting-motif mutant YA/VD-Cx43 restores gap junction assembly. (A)... | Download Scientific Diagram
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Mutations in the gene encoding gap junction protein β-3 associated with autosomal dominant hearing impairment | Nature Genetics
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PDF) Six New Gap Junction Beta 1 Gene Mutations and Their Phenotypic Expression in Czech Patients with Charcot-Marie-Tooth Disease
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In Vitro Models of GJB2-Related Hearing Loss Recapitulate Ca2+ Transients via a Gap Junction Characteristic of Developing Cochlea - ScienceDirect
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