| scholarly article | Q13442814 |
| P50 | author | Eric C. Beyer | Q37370738 |
| Carlos F. Lagos | Q38546932 | ||
| Tomas Perez-Acle | Q43119293 | ||
| Raul Araya-Secchi | Q48358883 | ||
| P2093 | author name string | Juan C Sáez | |
| Viviana M Berthoud | |||
| Vania Figueroa | |||
| Agustín D Martínez | |||
| Oscar Jara | |||
| Jaime Maripillán | |||
| Rodrigo Acuña | |||
| Isaac E García | |||
| P2860 | cites work | Dimerization of the transmembrane domain of Integrin alphaIIb subunit in cell membranes | Q24324737 |
| Connexin43: a protein from rat heart homologous to a gap junction protein from liver | Q24680192 | ||
| Structure of the connexin 26 gap junction channel at 3.5 A resolution | Q27654539 | ||
| Domain assembly of NAADP-gated two-pore channels | Q28250269 | ||
| Defining a minimal motif required to prevent connexin oligomerization in the endoplasmic reticulum | Q28564736 | ||
| Comparative protein structure modeling using Modeller | Q29615142 | ||
| Emerging issues of connexin channels: biophysics fills the gap. | Q30167614 | ||
| Loss-of-function and residual channel activity of connexin26 mutations associated with non-syndromic deafness | Q48840496 | ||
| Homozygosity for the V37I Connexin 26 mutation in three unrelated children with sensorineural hearing loss. | Q50487258 | ||
| Molecular basis of childhood deafness resulting from mutations in the GJB2 (connexin 26) gene. | Q50494656 | ||
| Distinct structural elements in the first membrane-spanning segment of the epithelial sodium channel. | Q53605087 | ||
| Subunit oligomerization, and topology of the inositol 1,4, 5-trisphosphate receptor | Q73041284 | ||
| Gating and regulation of connexin 43 (Cx43) hemichannels | Q30480722 | ||
| Gap-junction channels dysfunction in deafness and hearing loss | Q30490087 | ||
| TOXCAT: a measure of transmembrane helix association in a biological membrane | Q31917651 | ||
| Heteromeric connexons formed by the lens connexins, connexin43 and connexin56. | Q32043463 | ||
| Mutational analysis of threonine 402 adjacent to the GXXXG dimerization motif in transmembrane segment 1 of ABCG2. | Q33718824 | ||
| Metabolic inhibition induces opening of unapposed connexin 43 gap junction hemichannels and reduces gap junctional communication in cortical astrocytes in culture | Q33898269 | ||
| Gap junction-mediated intercellular biochemical coupling in cochlear supporting cells is required for normal cochlear functions | Q34084948 | ||
| Structural and functional diversity of connexin genes in the mouse and human genome | Q34137753 | ||
| Casein kinase 1 regulates connexin-43 gap junction assembly | Q34150954 | ||
| The biochemistry, ultrastructure, and subunit assembly mechanism of AMPA receptors | Q34351420 | ||
| Molecular dynamics simulations of the Cx26 hemichannel: evaluation of structural models with Brownian dynamics | Q35503280 | ||
| Sequence and tissue distribution of a second protein of hepatic gap junctions, Cx26, as deduced from its cDNA | Q35540725 | ||
| Plasma membrane channels formed by connexins: their regulation and functions. | Q35541877 | ||
| Homo- and hetero-oligomerization of G protein-coupled receptors | Q35579619 | ||
| Different domains are critical for oligomerization compatibility of different connexins. | Q35656804 | ||
| Single-channel SCAM identifies pore-lining residues in the first extracellular loop and first transmembrane domains of Cx46 hemichannels | Q36445008 | ||
| Conformational changes in a pore-forming region underlie voltage-dependent "loop gating" of an unapposed connexin hemichannel | Q37268155 | ||
| An aberrant sequence in a connexin46 mutant underlies congenital cataracts. | Q37288625 | ||
| Dimerization and ligand binding affect the structure network of A(2A) adenosine receptor | Q37780304 | ||
| Assembly of nicotinic and other Cys-loop receptors | Q37826784 | ||
| Structure and mechanism of glutamate receptor ion channel assembly, activation and modulation | Q37846960 | ||
| A modified, dual reporter TOXCAT system for monitoring homodimerization of transmembrane segments of proteins | Q38318639 | ||
| Connexin43 and connexin26 form gap junctions, but not heteromeric channels in co-expressing cells | Q40558677 | ||
| Changes in apparent free energy of helix-helix dimerization in a biological membrane due to point mutations | Q41890424 | ||
| Identification and functional characterization of an N-terminal oligomerization domain for polycystin-2. | Q43233958 | ||
| Assembly of gap junction channels: mechanism, effects of calmodulin antagonists and identification of connexin oligomerization determinants | Q43705169 | ||
| The single transmembrane domains of ErbB receptors self-associate in cell membranes | Q43821697 | ||
| Connexin43 and connexin45 form heteromeric gap junction channels in which individual components determine permeability and regulation | Q44011981 | ||
| Essential role of a GXXXG motif for membrane channel formation by Helicobacter pylori vacuolating toxin | Q44299992 | ||
| Specific amino-acid residues in the N-terminus and TM3 implicated in channel function and oligomerization compatibility of connexin43. | Q45345951 | ||
| P4510 | describes a project that uses | ImageJ | Q1659584 |
| P433 | issue | 17 | |
| P921 | main subject | transmembrane protein | Q424204 |
| P304 | page(s) | 3299-3311 | |
| P577 | publication date | 2012-07-11 | |
| P1433 | published in | Molecular Biology of the Cell | Q2338259 |
| P1476 | title | Critical role of the first transmembrane domain of Cx26 in regulating oligomerization and function | |
| P478 | volume | 23 |
| Q42205663 | Altered cellular localization and hemichannel activities of KID syndrome associated connexin26 I30N and D50Y mutations |
| Q38685620 | Association between the p.V37I variant of GJB2 and hearing loss: a pedigree and meta-analysis |
| Q30810767 | Characterization of a knock-in mouse model of the homozygous p.V37I variant in Gjb2. |
| Q42183057 | Characterization of a novel water pocket inside the human Cx26 hemichannel structure |
| Q58742492 | Concatenation of Human Connexin26 (hCx26) and Human Connexin46 (hCx46) for the Analysis of Heteromeric Gap Junction Hemichannels and Heterotypic Gap Junction Channels |
| Q36031035 | Connexinopathies: a structural and functional glimpse |
| Q52716310 | Connexins: Synthesis, Post-Translational Modifications, and Trafficking in Health and Disease. |
| Q26797404 | Diseases associated with leaky hemichannels |
| Q64270584 | Excess of Rare Missense Variants in Hearing Loss Genes in Sporadic Meniere Disease |
| Q30430702 | Extracellular gentamicin reduces the activity of connexin hemichannels and interferes with purinergic Ca(2+) signaling in HeLa cells |
| Q90339565 | Hearing consequences in Gjb2 knock-in mice: implications for human p.V37I mutation |
| Q27320878 | Keratitis-ichthyosis-deafness syndrome-associated Cx26 mutants produce nonfunctional gap junctions but hyperactive hemichannels when co-expressed with wild type Cx43. |
| Q40698511 | Newborn genetic screening for hearing impairment: a population-based longitudinal study. |
| Q34700455 | Prevalence of p.V37I variant of GJB2 in mild or moderate hearing loss in a pediatric population and the interpretation of its pathogenicity |
| Q37158482 | Proteins and mechanisms regulating gap-junction assembly, internalization, and degradation |
| Q58701520 | Roles of aberrant hemichannel activities due to mutant connexin26 in the pathogenesis of KID syndrome |
| Q42633335 | Screening for transmembrane association in divisome proteins using TOXGREEN, a high-throughput variant of the TOXCAT assay |
| Q37047097 | Syndromic deafness mutations at Asn 14 differentially alter the open stability of Cx26 hemichannels |
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