Results 21 to 30 of about 5,562,313 (185)

Connexin-43 hemichannels orchestrate NOD-like receptor protein-3 (NLRP3) inflammasome activation and sterile inflammation in tubular injury.

open access: yes, 2023
Background: Without aviable cure, chronic kidney disease is a global health concern. Inflammatory damagein and around the renal tubules dictates disease severity and is contributed to by multiple cell types.
Christos Chadjichristos (17752530)   +8 more
core   +5 more sources

SUPPLEMENTARY MATERIALS: A microtubule-Connexin-43 regulatory link suppresses arrhythmias and cardiac fibrosis in Duchenne muscular dystrophy mice.

open access: yes, 2022
This is supplementary material of the manuscript entitled: Microtubule-Connexin-43 regulation suppresses arrhythmias and fibrosis in Duchenne muscular dystrophy mice.
Lai-hua Xie (12361865)   +10 more
core   +1 more source

Visfatin reduces gap junction mediated cell-to-cell communication in proximal tubule-derived epithelial cells [PDF]

open access: yes, 2013
Background/Aims: In the current study we examined if the adipocytokine, visfatin, alters connexinmediated intercellular communication in proximal tubule-derived epithelial cells.
Mark J. Wall   +7 more
core   +1 more source

Mechanistic effect of the human GJB6 gene and its mutations in HaCaT cell proliferation and apoptosis

open access: yesBrazilian Journal of Medical and Biological Research, 2018
We constructed lentiviral vectors containing the human wild-type GJB6 gene and the mutant variants A88V and G11R. The three proteins were stably expressed by the Tet-on system in the HaCaT cell line and used to study the functional effect of the variants.
Yuting Lu   +10 more
doaj   +1 more source

Frequency of GJB2 mutations, GJB6‐D13S1830 and GJB6‐D13S1854 deletions among patients with non‐syndromic hearing loss from the central region of Iran

open access: yesMolecular Genetics & Genomic Medicine, 2019
Background In the present study, we investigate the prevalence of the GJB2 gene mutations, and deletions in the GJB6 gene, namely del (GJB6‐D13S1830) and del (GJB6‐D13S1854), in patients with autosomal recessive non‐syndromic hearing loss (ARNSHL) from ...
Hossein Naddafnia   +3 more
doaj   +1 more source

Connexin30-Deficiency Causes Mild Hearing Loss With the Reduction of Endocochlear Potential and ATP Release

open access: yesFrontiers in Cellular Neuroscience, 2022
GJB2 and GJB6 are adjacent genes encoding connexin 26 (Cx26) and connexin 30 (Cx30), respectively, with overlapping expressions in the inner ear. Both genes are associated with the commonest monogenic hearing disorder, recessive isolated deafness DFNB1 ...
Junmin Chen   +28 more
doaj   +1 more source

Upregulation of Connexin 30 in Intestinal Phenotype Gastric Cancer and Its Reduction during Tumor Progression [PDF]

open access: yes, 2010
Aims: The mucin phenotype is associated with clinicopathological findings and tumorigenesis in gastric cancer (GC). The aim was to search for a novel marker regulating the intestinal phenotype of GC. Methods and Results: We performed microarray analyses,
Naoya Sakamoto   +15 more
core   +1 more source

A Human-Derived Monoclonal Antibody Targeting Extracellular Connexin Domain Selectively Modulates Hemichannel Function

open access: yesFrontiers in Physiology, 2019
Connexin hemichannels, which are plasma membrane hexameric channels (connexons) composed of connexin protein protomers, have been implicated in a host of physiological processes and pathological conditions. A number of single point pathological mutations
Gaia Ziraldo   +18 more
doaj   +1 more source

In vivo genetic manipulation of inner ear connexin expression by bovine adeno-associated viral vectors

open access: yesScientific Reports, 2017
We have previously shown that in vitro transduction with bovine adeno–associated viral (BAAV) vectors restores connexin expression and rescues gap junction coupling in cochlear organotypic cultures from connexin–deficient mice that are models DFNB1 ...
Giulia Crispino   +7 more
doaj   +1 more source

Molecular composition and distribution of gap junctions in the sensory epithelium of the human cochlea—a super-resolution structured illumination microscopy (SR-SIM) study

open access: yesUpsala Journal of Medical Sciences, 2017
Background: Mutations in the GJB2 gene, which encodes the Connexin26 (Cx26) protein, are the most common cause of childhood hearing loss in American and European populations.
Wei Liu   +9 more
doaj   +1 more source

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