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Article: The Double Life of Connexin Channels: Single Is a Treat

TitleThe Double Life of Connexin Channels: Single Is a Treat
Authors
Issue Date2015
Citation
Journal of Investigative Dermatology, 2015, v. 135 n. 4, p. 940-943 How to Cite?
AbstractAlthough several genetic diseases are caused by mutations in channels made by connexin family members, there has been little progress in the development and validation of therapeutic options. An in vitro study in this issue of JID suggests that an anti-malarial drug may be beneficial in keratitis-ichthyosis deafness, a severe conexin channel disease associated with potentially fatal recurrent infections.
Persistent Identifierhttp://hdl.handle.net/10722/216467

 

DC FieldValueLanguage
dc.contributor.authorBruzzone, R-
dc.date.accessioned2015-09-18T05:28:36Z-
dc.date.available2015-09-18T05:28:36Z-
dc.date.issued2015-
dc.identifier.citationJournal of Investigative Dermatology, 2015, v. 135 n. 4, p. 940-943-
dc.identifier.urihttp://hdl.handle.net/10722/216467-
dc.description.abstractAlthough several genetic diseases are caused by mutations in channels made by connexin family members, there has been little progress in the development and validation of therapeutic options. An in vitro study in this issue of JID suggests that an anti-malarial drug may be beneficial in keratitis-ichthyosis deafness, a severe conexin channel disease associated with potentially fatal recurrent infections.-
dc.languageeng-
dc.relation.ispartofJournal of Investigative Dermatology-
dc.titleThe Double Life of Connexin Channels: Single Is a Treat-
dc.typeArticle-
dc.identifier.emailBruzzone, R: bruzzone@hkucc.hku.hk-
dc.identifier.authorityBruzzone, R=rp01442-
dc.identifier.doi10.1038/jid.2014.524-
dc.identifier.hkuros252392-
dc.identifier.volume135-
dc.identifier.issue4-
dc.identifier.spage940-
dc.identifier.epage943-

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