Human Connexin30.2/31.3 (GJC3) does not Form Functional Gap Junction Channels but Causes Enhanced ATP Release in HeLa Cells

Mutation R184Q of connexin 26 in hearing loss patients has a dominant-negative effect on connexin 26 and connexin 30

(2010) Ching-Chyuan Su et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Prospective variants screening of connexin genes in children with hearing impairment: genotype/phenotype correlation

(2010) Jiann-Jou Yang et al.   HUMAN GENETICS

Identification of Novel Variants in the Cx29 Gene of Nonsyndromic Hearing Loss Patients Using Buccal Cells and Restriction Fragment Length Polymorphism Method

(2009) Wen-Hung Wang et al.   AUDIOLOGY AND NEURO-OTOLOGY

A novel mutation in the connexin 29 gene may contribute to nonsyndromic hearing loss

(2009) Hui-Mei Hong et al.   HUMAN GENETICS

Mouse lens connexin23 (Gje1) does not form functional gap junction channels but causes enhanced ATP release from HeLa cells

(2008) Stephan Sonntag et al.   EUROPEAN JOURNAL OF CELL BIOLOGY

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

(2008) Irene Sargiannidou et al.   NEUROBIOLOGY OF DISEASE

ATP release through connexin hemichannels and gap junction transfer of second messengers propagate Ca2+ signals across the inner ear

(2008) F. Anselmi et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA