Article
Connexin26 hemichannels with a mutation that causes KID syndrome in humans lack sensitivity to CO2.
eLife - 25 Nov 2014
Meigh Louise, Hussain Naveed, Mulkey Daniel K, Dale Nicholas
Abstract excerpt
<title>Abstract</title>Mutations in connexin26 (Cx26) underlie a range of serious human pathologies. Previously we have shown that Cx26 hemichannels are directly opened by CO2 (Meigh et al., 2013). However the effects of human disease-causing mutations on the CO2 sensitivity of Cx26 are entirely unknown. Here, we report the first connection between the CO2 sensitivity of Cx26 and human pathology, by demonstrating...
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