Published in Biochim Biophys Acta on July 13, 2012
The human Cx26-D50A and Cx26-A88V mutations causing keratitis-ichthyosis-deafness syndrome display increased hemichannel activity. Am J Physiol Cell Physiol (2013) 1.12
Connexin mutants and cataracts. Front Pharmacol (2013) 1.11
Insights on the mechanisms of Ca(2+) regulation of connexin26 hemichannels revealed by human pathogenic mutations (D50N/Y). J Gen Physiol (2013) 1.06
Mix and match: investigating heteromeric and heterotypic gap junction channels in model systems and native tissues. FEBS Lett (2014) 1.04
Altered inhibition of Cx26 hemichannels by pH and Zn2+ in the A40V mutation associated with keratitis-ichthyosis-deafness syndrome. J Biol Chem (2014) 0.90
Cataract-causing mutation of human connexin 46 impairs gap junction, but increases hemichannel function and cell death. PLoS One (2013) 0.90
An electrostatic mechanism for Ca(2+)-mediated regulation of gap junction channels. Nat Commun (2016) 0.89
Palmoplantar keratoderma along with neuromuscular and metabolic phenotypes in Slurp1-deficient mice. J Invest Dermatol (2014) 0.88
Two tyrosine-based sorting signals in the Cx43 C-terminus cooperate to mediate gap junction endocytosis. Mol Biol Cell (2013) 0.87
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Motifs in the permeation pathway of connexin channels mediate voltage and Ca (2+) sensing. Front Physiol (2014) 0.83
Dominant negative connexin26 mutation R75W causing severe hearing loss influences normal programmed cell death in postnatal organ of Corti. BMC Genet (2014) 0.83
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Phenotypic variability in gap junction syndromic skin disorders: experience from KID and Clouston syndromes' clinical diagnostics. J Appl Genet (2015) 0.81
Connexins and gap junctions in the inner ear--it's not just about K⁺ recycling. Cell Tissue Res (2014) 0.80
Characterization of a novel water pocket inside the human Cx26 hemichannel structure. Biophys J (2014) 0.80
Vitamin D3 regulates the formation and degradation of gap junctions in androgen-responsive human prostate cancer cells. PLoS One (2014) 0.80
Connexin hemichannels influence genetically determined inflammatory and hyperproliferative skin diseases. Pharmacol Res (2015) 0.79
Syndromic deafness mutations at Asn 14 differentially alter the open stability of Cx26 hemichannels. J Gen Physiol (2016) 0.78
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Altered CO2 sensitivity of connexin26 mutant hemichannels in vitro. Physiol Rep (2016) 0.77
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Accessing gap-junction channel structure-function relationships through molecular modeling and simulations. BMC Cell Biol (2017) 0.75
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