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Article

Human oligodendrocytes express Cx31.3: function and interactions with Cx32 mutants.

Neurobiology of disease - 1 May 2008

Sargiannidou Irene, Ahn Meejin, Enriquez Alan D, Peinado Alejandro, Reynolds Richard, Abrams Charles, Scherer Steven S, Kleopa Kleopas A

Abstract excerpt

Murine oligodendrocytes express the gap junction (GJ) proteins connexin32 (Cx32), Cx47, and Cx29. CNS phenotypes in patients with X-linked Charcot-Marie-Tooth disease may be caused by dominant effects of Cx32 mutations on other connexins. Here we examined the expression of Cx31.3 (the human ortholog of murine Cx29) in human brain and its relation to the other oligodendrocyte GJ proteins Cx32 and Cx47....

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Identifiers

PMID: 18353664
DOI: 10.1016/j.nbd.2008.01.009
PMCID: PMC2704064

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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