The potency of the fs260 connexin43 mutant to impair keratinocyte differentiation is distinct from other disease-linked connexin43 mutants

Oculo-dento-digital dysplasia: Lack of genotype–phenotype correlation for GJA1 mutations and usefulness of neuro-imaging

(2009) M.J. Alao et al.   European Journal of Medical Genetics

GJA1mutations, variants, and connexin 43 dysfunction as it relates to the oculodentodigital dysplasia phenotype

(2009) William A. Paznekas et al.   HUMAN MUTATION

Cx43 has distinct mobility within plasma-membrane domains, indicative of progressive formation of gap-junction plaques

(2009) J. Simek et al.   JOURNAL OF CELL SCIENCE

ERp29 Restricts Connexin43 Oligomerization in the Endoplasmic Reticulum

(2009) Shamie Das et al.   MOLECULAR BIOLOGY OF THE CELL

Conformational Maturation and Post-ER Multisubunit Assembly of Gap Junction Proteins

(2009) Judy K. VanSlyke et al.   MOLECULAR BIOLOGY OF THE CELL

Connexin 43 and plakophilin-2 as a protein complex that regulates blood-testis barrier dynamics

(2009) M. W. M. Li et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

New evidence for the correlation of the p.G130V mutation in the GJB2 gene and syndromic hearing loss with palmoplantar keratoderma

(2008) Sandra Iossa et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A