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Article

Differential susceptibility of Cx26 mutations associated with epidermal dysplasias to peptidoglycan derived from Staphylococcus aureus and Staphylococcus epidermidis.

Experimental dermatology - 1 Aug 2012

Donnelly Steven, English Grant, de Zwart-Storm Eugene A, Lang Sue, van Steensel Maurice A M, Martin Patricia E

Abstract excerpt

Mutations in Connexin26 (Cx26) give rise to a spectrum of dominantly inherited hyperproliferating skin disorders, the severest being keratitis-ichthyosis-deafness (KID) syndrome, an inflammatory skin disorder, with patients prone to opportunistic infections. We compared the effects of peptidoglyc...

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Source

Identifiers

PMID: 22643125
DOI: 10.1111/j.1600-0625.2012.01521.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-22643125-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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