KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL DOMINANT; KIDAD

Literature (4)

Literature for OMIM 148210: KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL DOMINANT; KIDAD

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Connexins in epidermal homeostasis and skin disease., Scott CA,Tattersall D,O'Toole EA,Kelsell DP, Biochim Biophys Acta. August 1, 2012; 1818(8):0006-3002.
Aberrant connexin26 hemichannels underlying keratitis-ichthyosis-deafness syndrome are potently inhibited by mefloquine., Wang HZ,Li L,Srinivas M,White TW,Sellitto C,Brink PR,Levit NA, J Invest Dermatol. April 1, 2015; 135(4):1523-1747.
Insights on the mechanisms of Ca(2+) regulation of connexin26 hemichannels revealed by human pathogenic mutations (D50N/Y)., Lopez W,Gonzalez J,Liu Y,Harris AL,Contreras JE, J Gen Physiol. July 1, 2013; 142(1):1540-7748.
The connexin26 human mutation N14K disrupts cytosolic intersubunit interactions and promotes channel opening., Valdez Capuccino JM,Chatterjee P,García IE,Botello-Smith WM,Zhang H,Harris AL,Luo Y,Contreras JE, J Gen Physiol. March 4, 2019; 151(3):1540-7748.

Connexins in epidermal homeostasis and skin disease., Scott CA,Tattersall D,O'Toole EA,Kelsell DP, Biochim Biophys Acta. August 1, 2012; 1818(8):0006-3002.

Aberrant connexin26 hemichannels underlying keratitis-ichthyosis-deafness syndrome are potently inhibited by mefloquine., Wang HZ,Li L,Srinivas M,White TW,Sellitto C,Brink PR,Levit NA, J Invest Dermatol. April 1, 2015; 135(4):1523-1747.

The connexin26 human mutation N14K disrupts cytosolic intersubunit interactions and promotes channel opening., Valdez Capuccino JM,Chatterjee P,García IE,Botello-Smith WM,Zhang H,Harris AL,Luo Y,Contreras JE, J Gen Physiol. March 4, 2019; 151(3):1540-7748.