Literature DB >> 20629838

Severe form of keratitis-ichthyosis-deafness (KID) syndrome associated with septic complications.

Kunitaka Haruna, Yasushi Suga, Ami Oizumi, Yuki Mizuno, Hideharu Endo, Toshiaki Shimizu, Toshio Hasegawa, Shigaku Ikeda.   

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Year:  2010        PMID： 20629838     DOI： 10.1111/j.1346-8138.2010.00839.x

Source DB:  PubMed          Journal:  J Dermatol        ISSN： 0385-2407            Impact factor:   4.005


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  8 in total

Review 1.  Human diseases associated with connexin mutations.

Authors:  Miduturu Srinivas; Vytas K Verselis; Thomas W White
Journal:  Biochim Biophys Acta Biomembr       Date:  2017-04-27       Impact factor: 3.747

2.  The human Cx26-D50A and Cx26-A88V mutations causing keratitis-ichthyosis-deafness syndrome display increased hemichannel activity.

Authors:  Pallavi V Mhaske; Noah A Levit; Leping Li; Hong-Zhan Wang; Jack R Lee; Zunaira Shuja; Peter R Brink; Thomas W White
Journal:  Am J Physiol Cell Physiol       Date:  2013-02-27       Impact factor: 4.249

3.  Connexin hemichannels influence genetically determined inflammatory and hyperproliferative skin diseases.

Authors:  Noah A Levit; Thomas W White
Journal:  Pharmacol Res       Date:  2015-07-23       Impact factor: 7.658

Review 4.  Connexin channels in congenital skin disorders.

Authors:  Evelyn Lilly; Caterina Sellitto; Leonard M Milstone; Thomas W White
Journal:  Semin Cell Dev Biol       Date:  2016-01-13       Impact factor: 7.727

5.  Connexin26 hemichannels with a mutation that causes KID syndrome in humans lack sensitivity to CO2.

Authors:  Louise Meigh; Naveed Hussain; Daniel K Mulkey; Nicholas Dale
Journal:  Elife       Date:  2014-11-25       Impact factor: 8.140

6.  Roles of aberrant hemichannel activities due to mutant connexin26 in the pathogenesis of KID syndrome.

Authors:  T Taki; T Takeichi; K Sugiura; M Akiyama
Journal:  Sci Rep       Date:  2018-08-27       Impact factor: 4.379

7.  Whole-exome sequencing of de novo genetic variants in a Chinese family with a sporadic case of congenital nonsyndromic hearing loss.

Authors:  Sijing Hu; Hao Zhang; Yunqiang Liu; Mohan Liu; Jingjing Li; Shunyao Liao
Journal:  F1000Res       Date:  2021-02-02

8.  Aberrant connexin26 hemichannels underlying keratitis-ichthyosis-deafness syndrome are potently inhibited by mefloquine.

Authors:  Noah A Levit; Caterina Sellitto; Hong-Zhan Wang; Leping Li; Miduturu Srinivas; Peter R Brink; Thomas W White
Journal:  J Invest Dermatol       Date:  2014-09-17       Impact factor: 8.551
  8 in total

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