GJB2 Promotes HCC Progression by Activating Glycolysis Through Cytoplasmic Translocation and Generating a Suppressive Tumor Microenvironment Based on Single Cell RNA Sequencing., PMID:39162005
IgM Deficiency Associated With Connexin Mutation in an 18-Year-old Male., PMID:36968253
Antibody gene transfer treatment drastically improves epidermal pathology in a keratitis ichthyosis deafness syndrome model using male mice., PMID:36736132
Unusual cutaneous manifestations and congenital hearing loss in a patient with GJB2 (F142L) mutation., PMID:33914937
Vitamin D receptor and metabolite effects on corneal epithelial cell gap junction proteins., PMID:31465769
Roles of aberrant hemichannel activities due to mutant connexin26 in the pathogenesis of KID syndrome., PMID:30150638
Depolarized Hepatocytes Express the Stem/Progenitor Cell Marker Neighbor of Punc E11 After Bile Duct Ligation in Mice., PMID:29624127
Hidradenitis suppurativa in association with keratitis-ichthyosis-deafness syndrome treated with adalimumab., PMID:29570225
A deafness mechanism of digenic Cx26 (GJB2) and Cx30 (GJB6) mutations: Reduction of endocochlear potential by impairment of heterogeneous gap junctional function in the cochlear lateral wall., PMID:28823936
The Complex Structure of the Mouse Placental Labyrinth Revealed by Double Immunofluorescence Labeling of Slc2a1 and Gjb2., PMID:28724843
Deformation of the Outer Hair Cells and the Accumulation of Caveolin-2 in Connexin 26 Deficient Mice., PMID:26492081
Cx26 knockout predisposes the mammary gland to primary mammary tumors in a DMBA-induced mouse model of breast cancer., PMID:26439696
Anti-angiogenesis therapy and gap junction inhibition reduce MDA-MB-231 breast cancer cell invasion and metastasis in vitro and in vivo., PMID:26218768
A Convenient and Efficient Method to Enrich and Maintain Highly Proliferative Human Fetal Liver Stem Cells., PMID:25556695
Connexin26 (GJB2) deficiency reduces active cochlear amplification leading to late-onset hearing loss., PMID:25451287
Visfatin reduces gap junction mediated cell-to-cell communication in proximal tubule-derived epithelial cells., PMID:24335170
Ultrastructural pathological changes in the cochlear cells of connexin 26 conditional knockout mice., PMID:23917463
Importance of Connexin-43 based gap junction in cirrhosis and acute-on-chronic liver failure., PMID:23376361
Melanocytic tumors express connexin 43 but not 26: immunohistochemical analysis with potential significance in melanocytic oncogenesis., PMID:23344009
Connexin 36 is expressed in beta and connexins 26 and 32 in acinar cells at the end of the secondary transition of mouse pancreatic development and increase during fetal and perinatal life., PMID:22505190
Paris polyphylla Smith extract induces apoptosis and activates cancer suppressor gene connexin26 expression., PMID:22502669
Ablation of connexin30 in transgenic mice alters expression patterns of connexin26 and connexin32 in glial cells and leptomeninges., PMID:22098503
Connexin26 expression in brain parenchymal cells demonstrated by targeted connexin ablation in transgenic mice., PMID:21714813
Different domains are critical for oligomerization compatibility of different connexins., PMID:21348854
The human deafness-associated connexin 30 T5M mutation causes mild hearing loss and reduces biochemical coupling among cochlear non-sensory cells in knock-in mice., PMID:20858605
Clinical significance of the expression of connexin26 in colorectal cancer., PMID:20565955
The potency of the fs260 connexin43 mutant to impair keratinocyte differentiation is distinct from other disease-linked connexin43 mutants., PMID:20515445
Unique expression of connexins in the human cochlea., PMID:19450429
Clinical and molecular genetic analysis of a family with macrothrombocytopenia and early onset sensorineural hearing loss., PMID:19285578
Differential expression and localization of connexins 26 and 43 in the rat gingival epithelium., PMID:19194037
Perturbing plasma membrane hemichannels attenuates calcium signalling in cardiac cells and HeLa cells expressing connexins., PMID:18951659
Cellular characterization of Connexin26 and Connnexin30 expression in the cochlear lateral wall., PMID:18581144
Extracellular-loop peptide antibodies reveal a predominant hemichannel organization of connexins in polarized intestinal cells., PMID:18267319
The protective effect of functional connexin43 channels on a human epithelial cell line exposed to oxidative stress., PMID:18235030
Tissue microarray analysis of connexin expression and its prognostic significance in human breast cancer., PMID:17583422
A deafness-associated mutant human connexin 26 improves the epithelial barrier in vitro., PMID:17581693
A case of keratitis-ichthyosis-deafness (KID) syndrome., PMID:17442083
Connexin26 expression is associated with lymphatic vessel invasion and poor prognosis in human breast cancer., PMID:17203385
Connexins act as tumor suppressors in three-dimensional mammary cell organoids by regulating differentiation and angiogenesis., PMID:17047050
Differential induction of connexins 26 and 30 in skin tumors and their adjacent epidermis., PMID:16046668
Alterations in connexin26 expression during colorectal carcinogenesis., PMID:16015037
In vivo and in vitro expression of connexins in the human corneal epithelium., PMID:15914609
Connexin 26 correlates with Bcl-xL and Bax proteins expression in colorectal cancer., PMID:15770735
Expression of connexins 26, 32 and 43 in the human colon--an immunohistochemical study., PMID:15704645
Expression of connexin 26 in the lateral wall of the rat cochlea after acoustic trauma., PMID:15224875
Connexin47, connexin29 and connexin32 co-expression in oligodendrocytes and Cx47 association with zonula occludens-1 (ZO-1) in mouse brain., PMID:15183511
Connexins 26, 30, and 43: differences among spontaneous, chronic, and accelerated human wound healing., PMID:15140236
Gap junction development in the human fetal hair follicle and bulge region., PMID:15030324
Transport and function of cx26 mutants involved in skin and deafness disorders., PMID:14681041
The inner ear contains heteromeric channels composed of cx26 and cx30 and deafness-related mutations in cx26 have a dominant negative effect on cx30., PMID:14681039
For research use only. Not for human or drug use.
