Blikat Vyroben z Koření mutation of gap junction Zbytečný Povinný Vylepšit
Gap junctional signaling in pattern regulation: Physiological network connectivity instructs growth and form - Mathews - 2017 - Developmental Neurobiology - Wiley Online Library
Mutations in the gene encoding gap junction protein β-3 associated with autosomal dominant hearing impairment | Nature Genetics
The p.Tyr136X mutation confines the effect of the pGly45Glu mutation.... | Download Scientific Diagram
PLOS ONE: Cataract-Causing Mutation of Human Connexin 46 Impairs Gap Junction, but Increases Hemichannel Function and Cell Death
A connexin30 mutation rescues hearing and reveals roles for gap junctions in cochlear amplification and micromechanics | Nature Communications
Mapping Cellular Gap Junctions to Understand Disease | News Article | Lehigh University
Frontiers | Cancer Connectors: Connexins, Gap Junctions, and Communication | Oncology
Association between mutations in the gap junction β4 gene and nonsyndromic hearing loss: Genotype‑phenotype correlation patterns
In Vitro Models of GJB2-Related Hearing Loss Recapitulate Ca2+ Transients via a Gap Junction Characteristic of Developing Cochlea - ScienceDirect
Gap junction-mediated cell-to-cell communication in oral development and oral diseases: a concise review of research progress | International Journal of Oral Science
Effects of S279 or S282 mutation on Cx43 expression and gap junction... | Download Scientific Diagram
chCx50(E48K) mutant cannot mediate gap junction dye coupling in CEF... | Download Scientific Diagram
122 Mendelian Disorders of Cornification (MEDOC): the Erythrokeratodermas | Plastic Surgery Key
Wild-type, not Cx45.6 mutant, proteins form functional gap junction... | Download Scientific Diagram
The role of gap junctions in inflammatory and neoplastic disorders (Review)
The sorting-motif mutant YA/VD-Cx43 restores gap junction assembly. (A)... | Download Scientific Diagram
Gap junction modulation - Wikipedia
Handbook - Gap Junctions
A mechanism of gap junction docking revealed by functional rescue of a human-disease-linked connexin mutant | Journal of Cell Science
Cells | Free Full-Text | Gap Junction Intercellular Communication in the Carcinogenesis Hallmarks: Is This a Phenomenon or Epiphenomenon? | HTML
An atrial-fibrillation-linked connexin40 mutant is retained in the endoplasmic reticulum and impairs the function of atrial gap-junction channels | Disease Models & Mechanisms
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,