Connexin - Wikipedia
PDF) Six New Gap Junction Beta 1 Gene Mutations and Their Phenotypic Expression in Czech Patients with Charcot-Marie-Tooth Disease
Mutagenetix/Phenotypic Mutations/L - M/L1 - LabArchives, Your Electronic Lab Notebook (ELN)
122 Mendelian Disorders of Cornification (MEDOC): the Erythrokeratodermas | Plastic Surgery Key
Table 1 from Gap junction beta 1 (GJB1) gene mutations in Italian patients with X-linked Charcot-Marie-Tooth disease | Semantic Scholar
In Vitro Models of GJB2-Related Hearing Loss Recapitulate Ca2+ Transients via a Gap Junction Characteristic of Developing Cochlea - ScienceDirect
Sorting-motif mutant YA/VD-Cx43 restores defective gap junction... | Download Scientific Diagram
Emerging roles of gap junction proteins connexins in cancer metastasis, chemoresistance and clinical application | Journal of Biomedical Science | Full Text
Connexins in health and disease - Yamasaki - 2018 - Clinical and Experimental Neuroimmunology - Wiley Online Library
The sorting-motif mutant YA/VD-Cx43 restores gap junction assembly. (A)... | Download Scientific Diagram
Gap junctional signaling in pattern regulation: Physiological network connectivity instructs growth and form - Mathews - 2017 - Developmental Neurobiology - Wiley Online Library
Regulation of gap junction intercellular communication by connexin ubiquitination: physiological and pathophysiological implications | SpringerLink
PLOS ONE: Cataract-Causing Mutation of Human Connexin 46 Impairs Gap Junction, but Increases Hemichannel Function and Cell Death
Phosphorylation of Ser-395 by PKA increases Cx50 gap junction coupling... | Download Scientific Diagram
Cells | Free Full-Text | Gap Junction Intercellular Communication in the Carcinogenesis Hallmarks: Is This a Phenomenon or Epiphenomenon? | HTML
Connexin43 mutations linked to skin disease have augmented hemichannel activity | Scientific Reports
Diverse pattern of gap junction beta-2 and gap junction beta-4 genes mutations and lack of contribution of DFNB21, DFNB24, DFNB29, and DFNB42 loci in autosomal recessive nonsyndromic hearing loss patients in Hormozgan,
chCx50(E48K) mutant cannot mediate gap junction dye coupling in CEF... | Download Scientific Diagram
Effects of S279 or S282 mutation on Cx43 expression and gap junction... | Download Scientific Diagram
Gap junction modulation - Wikipedia
Frontiers | Role of Connexin-Based Gap Junction Channels in Communication of Myelin Sheath in Schwann Cells | Cellular Neuroscience
Frontiers | Cancer Connectors: Connexins, Gap Junctions, and Communication | Oncology
A mechanism of gap junction docking revealed by functional rescue of a human-disease-linked connexin mutant | Journal of Cell Science
Mutations in the gene encoding gap junction protein β-3 associated with autosomal dominant hearing impairment | Nature Genetics
The role of the gap junction perinexus in cardiac conduction: Potential as a novel anti-arrhythmic drug target - ScienceDirect
Role of connexin 43 in different forms of intercellular communication – gap junctions, extracellular vesicles and tunnelling nanotubes | Journal of Cell Science
