| scholarly article | Q13442814 |
| P50 | author | Thomas W. White | Q42427523 |
| P2093 | author name string | Steven S Scherer | |
| Peter R Brink | |||
| Junxian Zhang | |||
| Sabrina W Yum | |||
| Virginijus Valiunas | |||
| Giedrius Kanaporis | |||
| P2860 | cites work | Crystal structure of the Aequorea victoria green fluorescent protein | Q27733214 |
| Permeability and gating properties of human connexins 26 and 30 expressed in HeLa cells | Q28206633 | ||
| Functional studies of human skin disease- and deafness-associated connexin 30 mutations | Q28213840 | ||
| Connexin30 (Gjb6)-deficiency causes severe hearing impairment and lack of endocochlear potential | Q28218302 | ||
| Gap junctions and cochlear homeostasis | Q28245955 | ||
| Expression of the gap-junction connexins 26 and 30 in the rat cochlea | Q28287580 | ||
| Gap junctions in the rat cochlea: immunohistochemical and ultrastructural analysis | Q28300307 | ||
| Gating properties of gap junction channels assembled from connexin43 and connexin43 fused with green fluorescent protein | Q28367650 | ||
| Gap junctions in the inner ear: comparison of distribution patterns in different vertebrates and assessement of connexin composition in mammals | Q28508885 | ||
| Gap junction channels formed by coexpressed connexin40 and connexin43 | Q28576324 | ||
| Partitioning of lipid-modified monomeric GFPs into membrane microdomains of live cells | Q29547331 | ||
| Restoration of connexin26 protein level in the cochlea completely rescues hearing in a mouse model of human connexin30-linked deafness | Q30478884 | ||
| Targeted ablation of connexin26 in the inner ear epithelial gap junction network causes hearing impairment and cell death | Q30578611 | ||
| Regulation of epidermal growth factor-induced connexin 43 gap junction communication by big mitogen-activated protein kinase1/ERK5 but not ERK1/2 kinase activation | Q31135115 | ||
| Species-specific voltage-gating properties of connexin-45 junctions expressed in Xenopus oocytes | Q33907175 | ||
| Intracellular domains of mouse connexin26 and -30 affect diffusional and electrical properties of gap junction channels | Q33952503 | ||
| 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 | ||
| Mechanisms of Cx43 and Cx26 transport to the plasma membrane and gap junction regeneration | Q34450643 | ||
| Potassium ion recycling pathway via gap junction systems in the mammalian cochlea and its interruption in hereditary nonsyndromic deafness | Q34505515 | ||
| High-resolution FRET microscopy of cholera toxin B-subunit and GPI-anchored proteins in cell plasma membranes | Q34709520 | ||
| Peering inside lipid rafts and caveolae | Q34825921 | ||
| Nonredundant Gap Junction Functions | Q35128775 | ||
| Connexin gene pathology | Q35161187 | ||
| Functional consequences of heterogeneous gap junction channel formation and its influence in health and disease | Q36162581 | ||
| Distribution of a glycosylphosphatidylinositol-anchored protein at the apical surface of MDCK cells examined at a resolution of <100 A using imaging fluorescence resonance energy transfer | Q36256233 | ||
| Expression of a connexin 43/beta-galactosidase fusion protein inhibits gap junctional communication in NIH3T3 cells | Q36382571 | ||
| Distinct and gradient distributions of connexin26 and connexin30 in the cochlear sensory epithelium of guinea pigs | Q36908171 | ||
| Fluorescence energy transfer reveals microdomain formation at physiological temperatures in lipid mixtures modeling the outer leaflet of the plasma membrane | Q40247658 | ||
| Gap-junctional single-channel permeability for fluorescent tracers in mammalian cell cultures | Q40288658 | ||
| Fluorescence resonance energy transfer | Q40398693 | ||
| Cochlear gap junctions coassembled from Cx26 and 30 show faster intercellular Ca2+ signaling than homomeric counterparts. | Q40461910 | ||
| Quantitative fluorescence resonance energy transfer (FRET) measurement with acceptor photobleaching and spectral unmixing | Q40524681 | ||
| Transport and function of cx26 mutants involved in skin and deafness disorders. | Q40542422 | ||
| Connexin43 and connexin26 form gap junctions, but not heteromeric channels in co-expressing cells | Q40558677 | ||
| Resonance energy transfer: methods and applications | Q40684664 | ||
| The gap junction communication channel | Q40974984 | ||
| Connections with connexins: the molecular basis of direct intercellular signaling | Q41006464 | ||
| Multiple connexin proteins in single intercellular channels: connexin compatibility and functional consequences | Q41141420 | ||
| Specific permeability and selective formation of gap junction channels in connexin-transfected HeLa cells | Q41665390 | ||
| Scrape-loading and dye transfer. A rapid and simple technique to study gap junctional intercellular communication | Q43521106 | ||
| Hydrogen peroxide inhibits gap junctional coupling and modulates intracellular free calcium in cochlear Hensen cells. | Q43649289 | ||
| The effects of cytoplasmic acidification upon electrical coupling in the organ of Corti | Q44968909 | ||
| Altered permeability and modulatory character of connexin channels during mammary gland development | Q44987231 | ||
| Impaired permeability to Ins(1,4,5)P3 in a mutant connexin underlies recessive hereditary deafness | Q45183609 | ||
| Compartmentalized and signal-selective gap junctional coupling in the hearing cochlea. | Q46911582 | ||
| Perspectives: biomedicine. The benefits of recycling | Q48110744 | ||
| Evidence for the co-localization of another connexin with connexin-43 at astrocytic gap junctions in rat brain | Q48720791 | ||
| Species specificity of mammalian connexin-26 to form open voltage-gated hemichannels. | Q50460921 | ||
| Mutations in the gene for connexin 26 (GJB2) that cause hearing loss have a dominant negative effect on connexin 30. | Q50484268 | ||
| Connexin interaction patterns in keratinocytes revealed morphologically and by FRET analysis. | Q50774956 | ||
| Biophysical properties of mouse connexin30 gap junction channels studied in transfected human HeLa cells. | Q53926502 | ||
| Connexin-specific cell-to-cell transfer of short interfering RNA by gap junctions | Q59212248 | ||
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | C1032-48 | |
| P577 | publication date | 2007-09-01 | |
| P1433 | published in | American Journal of Physiology - Cell Physiology | Q2227080 |
| P1476 | title | Human connexin26 and connexin30 form functional heteromeric and heterotypic channels | |
| P478 | volume | 293 |
| Q58700137 | A Cell Junctional Protein Network Associated with Connexin-26 |
| Q37359922 | A dominant connexin43 mutant does not have dominant effects on gap junction coupling in astrocytes |
| Q30557012 | A rapid and sensitive assay of intercellular coupling by voltage imaging of gap junction networks |
| Q30495800 | ATP-mediated cell-cell signaling in the organ of Corti: the role of connexin channels |
| Q58493621 | Ablation of connexin30 in transgenic mice alters expression patterns of connexin26 and connexin32 in glial cells and leptomeninges |
| Q34249054 | Activation, permeability, and inhibition of astrocytic and neuronal large pore (hemi)channels |
| Q39536794 | Applying 3D-FRAP microscopy to analyse gap junction-dependent shuttling of small antisense RNAs between cardiomyocytes |
| Q28507910 | Assembly of the cochlear gap junction macromolecular complex requires connexin 26. |
| Q37678191 | Astroglial networks: a step further in neuroglial and gliovascular interactions. |
| Q42927074 | CO2-dependent opening of connexin 26 and related β connexins |
| Q41892709 | CO₂directly modulates connexin 26 by formation of carbamate bridges between subunits |
| Q37893568 | Ca2+ homeostasis defects and hereditary hearing loss. |
| Q30465350 | Calcium signaling in the cochlea - Molecular mechanisms and physiopathological implications. |
| Q36098727 | Characterization of Panglial Gap Junction Networks in the Thalamus, Neocortex, and Hippocampus Reveals a Unique Population of Glial Cells |
| Q34888171 | Connexin 43 connexon to gap junction transition is regulated by zonula occludens-1. |
| Q37218997 | Connexin and pannexin mediated cell-cell communication. |
| Q50057056 | Connexin hemichannels and cochlear function |
| Q59808649 | Connexin-43 Gap Junctions Are Responsible for the Hypothalamic Tanycyte-Coupled Network |
| Q42951334 | Connexin26 Mutations Causing Palmoplantar Keratoderma and Deafness Interact with Connexin43, Modifying Gap Junction and Hemichannel Properties |
| Q36955841 | Connexin26 deafness associated mutations show altered permeability to large cationic molecules |
| Q30466096 | Connexin26 expression in brain parenchymal cells demonstrated by targeted connexin ablation in transgenic mice |
| Q30485962 | Connexin32 mutations cause loss of function in Schwann cells and oligodendrocytes leading to PNS and CNS myelination defects |
| Q34482866 | Correlations of differentially expressed gap junction connexins Cx26, Cx30, Cx32, Cx43 and Cx46 with breast cancer progression and prognosis |
| Q42089141 | Cx29 and Cx32, two connexins expressed by myelinating glia, do not interact and are functionally distinct |
| Q30449325 | Cx32 and Cx47 mediate oligodendrocyte:astrocyte and oligodendrocyte:oligodendrocyte gap junction coupling |
| Q37332766 | Digenic inheritance of non-syndromic deafness caused by mutations at the gap junction proteins Cx26 and Cx31 |
| Q41084037 | Disease-linked connexin26 S17F promotes volar skin abnormalities and mild wound healing defects in mice |
| Q28581350 | Distinct permeation profiles of the connexin 30 and 43 hemichannels |
| Q37397290 | Diverse deafness mechanisms of connexin mutations revealed by studies using in vitro approaches and mouse models |
| Q42791910 | Dominant Cx26 mutants associated with hearing loss have dominant-negative effects on wild type Cx26 |
| Q40519966 | Dominant connexin26 mutants associated with human hearing loss have trans-dominant effects on connexin30. |
| Q38179504 | Extracellular domains play different roles in gap junction formation and docking compatibility. |
| Q34205765 | Functional interactions between polydnavirus and host cellular innexins |
| Q92002832 | GJB2 Mutations Linked to Hearing Loss Exhibit Differential Trafficking and Functional Defects as Revealed in Cochlear-Relevant Cells |
| Q36517757 | Gap junction channels exhibit connexin-specific permeability to cyclic nucleotides. |
| Q38799237 | Gap junction mediated miRNA intercellular transfer and gene regulation: A novel mechanism for intercellular genetic communication |
| Q33941978 | Gap junctions and blood-tissue barriers |
| Q24645936 | Gap junctions couple astrocytes and oligodendrocytes |
| Q34020827 | Gap junctions. |
| Q30490087 | Gap-junction channels dysfunction in deafness and hearing loss |
| Q91395198 | Generation of Functional CX26-Gap-Junction-Plaque-Forming Cells with Spontaneous Ca2+ Transients via a Gap Junction Characteristic of Developing Cochlea |
| Q50523078 | Human connexin30.2/31.3 (GJC3) does not form functional gap junction channels but causes enhanced ATP release in HeLa cells. |
| Q37468759 | Injury-triggered Akt phosphorylation of Cx43: a ZO-1-driven molecular switch that regulates gap junction size |
| Q58863412 | Inner ear connexins, intercellular signalling and deafness |
| Q37510417 | In Vitro Models of GJB2-Related Hearing Loss Recapitulate Ca2+ Transients via a Gap Junction Characteristic of Developing Cochlea |
| Q36255990 | Low prevalence of GJB2 mutations in non-syndromic hearing loss in Western India |
| Q38190331 | Mix and match: investigating heteromeric and heterotypic gap junction channels in model systems and native tissues |
| Q42292699 | Modulation of Asymmetric Flux in Heterotypic Gap Junctions by Pore Shape, Particle Size and Charge. |
| Q33607444 | Molecular and functional asymmetry at a vertebrate electrical synapse |
| Q38682864 | Molecular composition and distribution of gap junctions in the sensory epithelium of the human cochlea-a super-resolution structured illumination microscopy (SR-SIM) study. |
| Q37383087 | Mouse models for human hereditary deafness |
| Q42695768 | Non-dioxin-like organic toxicant PCB153 modulates sphingolipid metabolism in liver progenitor cells: its role in Cx43-formed gap junction impairment |
| Q42153064 | Perinatal Gjb2 gene transfer rescues hearing in a mouse model of hereditary deafness |
| Q47689866 | Permeant-specific gating of connexin 30 hemichannels |
| Q35232370 | Regulation of cellular function by connexin hemichannels |
| Q36074842 | Structural basis for the selective permeability of channels made of communicating junction proteins |
| Q50101868 | The connexin 46 mutant (V44M) impairs gap junction function causing congenital cataract |
| Q50436327 | The connexin26 S17F mouse mutant represents a model for the human hereditary keratitis-ichthyosis-deafness syndrome |
| Q28748215 | 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 |
| Q26827294 | The role of connexins in ear and skin physiology - functional insights from disease-associated mutations |
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