scholarly article | Q13442814 |
P50 | author | Michael Koval | Q41130425 |
P2093 | author name string | Michael Koval | |
P2860 | cites work | An investigation of the role of transmembrane domains in Golgi protein retention | Q24598282 |
Complete predicted three-dimensional structure of the facilitator transmembrane protein and hepatitis C virus receptor CD81: conserved and variable structural domains in the tetraspanin superfamily | Q27472918 | ||
ERGIC-53 and traffic in the secretory pathway | Q28143617 | ||
Multimeric connexin interactions prior to the trans-Golgi network | Q28210082 | ||
Connexin family members target to lipid raft domains and interact with caveolin-1 | Q28216028 | ||
Tetraspanin functions and associated microdomains | Q28284176 | ||
Differential phosphorylation of connexin46 and connexin50 by H2O2 activation of protein kinase Cgamma | Q28286350 | ||
Female infertility in mice lacking connexin 37 | Q28302927 | ||
Defining a minimal motif required to prevent connexin oligomerization in the endoplasmic reticulum | Q28564736 | ||
Connexin46 is retained as monomers in a trans-Golgi compartment of osteoblastic cells | Q28564999 | ||
Connexin 43 interacts with zona occludens-1 and -2 proteins in a cell cycle stage-specific manner | Q28582860 | ||
BI-1 regulates an apoptosis pathway linked to endoplasmic reticulum stress | Q28592598 | ||
Human diseases: clues to cracking the connexin code? | Q28645800 | ||
Diverse functions of vertebrate gap junctions | Q28645877 | ||
Analysis of gap junction assembly using mutated connexins detected in Charcot-Marie-Tooth X-linked disease | Q28646227 | ||
Using CLUSTAL for multiple sequence alignments | Q29547794 | ||
Quality control in the endoplasmic reticulum | Q29619929 | ||
Emerging issues of connexin channels: biophysics fills the gap. | Q30167614 | ||
Heterocellular contact at the myoendothelial junction influences gap junction organization | Q30437155 | ||
Beyond the gap: functions of unpaired connexon channels | Q33186594 | ||
Heteromeric connexons in lens gap junction channels | Q33555084 | ||
Cell-free synthesis and assembly of connexins into functional gap junction membrane channels | Q33886651 | ||
Assembly of urothelial plaques: tetraspanin function in membrane protein trafficking. | Q33938319 | ||
The state of lipid rafts: from model membranes to cells | Q33963927 | ||
Palmitoylation of tetraspanin proteins: modulation of CD151 lateral interactions, subcellular distribution, and integrin-dependent cell morphology | Q34011703 | ||
Connexin29 is uniquely distributed within myelinating glial cells of the central and peripheral nervous systems. | Q34142186 | ||
Zonula occludens-1 alters connexin43 gap junction size and organization by influencing channel accretion | Q34148181 | ||
Multisubunit assembly of an integral plasma membrane channel protein, gap junction connexin43, occurs after exit from the ER | Q34306752 | ||
Functional analysis of selective interactions among rodent connexins | Q34448036 | ||
Mechanisms of Cx43 and Cx26 transport to the plasma membrane and gap junction regeneration | Q34450643 | ||
Increased gap junction assembly between cultured cells upon cholesterol supplementation | Q34567479 | ||
Intracellular transport, assembly, and degradation of wild-type and disease-linked mutant gap junction proteins | Q34719366 | ||
Secretory pathway quality control operating in Golgi, plasmalemmal, and endosomal systems | Q34970141 | ||
Plasma membrane channels formed by connexins: their regulation and functions. | Q35541877 | ||
Noncoordinate regulation of ENaC: paradigm lost? | Q35553555 | ||
The Birth of a Channel | Q35558419 | ||
Quality Control and Protein Folding in the Secretory Pathway | Q35564863 | ||
An update on connexin genes and their nomenclature in mouse and man. | Q35609932 | ||
Regulation of connexin biosynthesis, assembly, gap junction formation, and removal | Q35700076 | ||
Selective permeability of gap junction channels | Q35700130 | ||
Predicting function from structure: 3D structure studies of the mammalian Golgi complex | Q35746733 | ||
Molecular basis for Golgi maintenance and biogenesis | Q35840114 | ||
Membrane lipids and vesicular traffic. | Q35840118 | ||
Polarized sorting in epithelial cells: raft clustering and the biogenesis of the apical membrane | Q35963496 | ||
Evolution of gap junction proteins--the pannexin alternative. | Q36085400 | ||
Structural organization of gap junction channels | Q36144636 | ||
Functional consequences of heterogeneous gap junction channel formation and its influence in health and disease | Q36162581 | ||
Connexin phosphorylation as a regulatory event linked to gap junction channel assembly | Q36162583 | ||
Connexin phosphorylation as a regulatory event linked to gap junction internalization and degradation | Q36162592 | ||
Protein-protein interactions in the tetraspanin web. | Q36197803 | ||
Oligomerization of a membrane protein correlates with its retention in the Golgi complex | Q36233449 | ||
The alpha and beta subunits of the Na,K-ATPase can assemble at the plasma membrane into functional enzyme | Q36234677 | ||
Targeting of protein ERGIC-53 to the ER/ERGIC/cis-Golgi recycling pathway | Q36236056 | ||
The Pattern of Disulfide Linkages in the Extracellular Loop Regions of Connexin 32 Suggests a Model for the Docking Interface of Gap Junctions | Q36255213 | ||
Palmitoylation supports assembly and function of integrin-tetraspanin complexes | Q36322840 | ||
Transfected connexin45 alters gap junction permeability in cells expressing endogenous connexin43 | Q36382669 | ||
Functional expression of the murine connexin 36 gene coding for a neuron-specific gap junctional protein | Q36861898 | ||
Membrane integration of in vitro-translated gap junctional proteins: co- and post-translational mechanisms | Q37380207 | ||
Incompatibility of connexin 40 and 43 Hemichannels in gap junctions between mammalian cells is determined by intracellular domains | Q37383889 | ||
Distribution of caveolin-1 and connexin43 in normal and injured alveolar epithelial R3/1 cells | Q40430244 | ||
ZO-1 alters the plasma membrane localization and function of Cx43 in osteoblastic cells | Q40430394 | ||
Functional expression in Xenopus oocytes of gap-junctional hemichannels formed by a cysteine-less connexin 43. | Q40542865 | ||
Selective assembly of connexin37 into heterocellular gap junctions at the oocyte/granulosa cell interface | Q40557070 | ||
Connexin43 and connexin26 form gap junctions, but not heteromeric channels in co-expressing cells | Q40558677 | ||
Loss of function and impaired degradation of a cataract-associated mutant connexin50. | Q40640625 | ||
Connexin-specific distribution within gap junctions revealed in living cells. | Q40845302 | ||
Phenotypic control of gap junctional communication by cultured alveolar epithelial cells | Q40954064 | ||
Protein targeting to endoplasmic reticulum by dilysine signals involves direct retention in addition to retrieval | Q40954125 | ||
Three-dimensional structure of a recombinant gap junction membrane channel | Q40972332 | ||
Connexins, connexons, and intercellular communication | Q41114815 | ||
Synthesis and assembly of human beta 1 gap junctions in BHK cells by DNA transfection with the human beta 1 cDNA. | Q41262887 | ||
Specific permeability and selective formation of gap junction channels in connexin-transfected HeLa cells | Q41665390 | ||
Synthesis and assembly of connexins in vitro into homomeric and heteromeric functional gap junction hemichannels. | Q41897817 | ||
Targeted gap junction protein constructs reveal connexin-specific differences in oligomerization | Q43945269 | ||
Impaired permeability to Ins(1,4,5)P3 in a mutant connexin underlies recessive hereditary deafness | Q45183609 | ||
Assembly of heteromeric connexons in guinea-pig liver en route to the Golgi apparatus, plasma membrane and gap junctions | Q45345949 | ||
Specific amino-acid residues in the N-terminus and TM3 implicated in channel function and oligomerization compatibility of connexin43. | Q45345951 | ||
Lipid rafts prepared by different methods contain different connexin channels, but gap junctions are not lipid rafts | Q46721269 | ||
Regulation of connexin43 oligomerization is saturable | Q46986527 | ||
Four classes of intercellular channels between glial cells in the CNS. | Q47643765 | ||
Aberrant gating, but a normal expression pattern, underlies the recessive phenotype of the deafness mutant Connexin26M34T. | Q47915800 | ||
trans-dominant inhibition of connexin-43 by mutant connexin-26: implications for dominant connexin disorders affecting epidermal differentiation | Q48881472 | ||
Oculodentodigital dysplasia-causing connexin43 mutants are non-functional and exhibit dominant effects on wild-type connexin43. | Q50781208 | ||
Isozymes of the Na-K-ATPase: heterogeneity in structure, diversity in function. | Q52182292 | ||
A Cα Model for the Transmembrane α Helices of Gap Junction Intercellular Channels | Q57207119 | ||
Connexins and gap junctions of astrocytes and oligodendrocytes in the CNS | Q58493657 | ||
The recycling pathway of protein ERGIC-53 and dynamics of the ER-Golgi intermediate compartment | Q77465529 | ||
Diverse trafficking abnormalities of connexin32 mutants causing CMTX | Q78597337 | ||
P433 | issue | 3 | |
P304 | page(s) | 159-166 | |
P577 | publication date | 2006-02-21 | |
P13046 | publication type of scholarly work | review article | Q7318358 |
P1433 | published in | Trends in Cell Biology | Q1573994 |
P1476 | title | Pathways and control of connexin oligomerization | |
P478 | volume | 16 |
Q39269380 | Alveolocapillary model system to study alveolar re-epithelialization |
Q81166280 | Beta cells preferentially exchange cationic molecules via connexin 36 gap junction channels |
Q30436052 | Biological and biophysical properties of vascular connexin channels |
Q36260704 | Cardiac Cx43, Cx40 and Cx45 co-assembling: involvement of connexins epitopes in formation of hemichannels and Gap junction channels |
Q33569405 | Cellular mechanisms of tissue fibrosis. 6. Purinergic signaling and response in fibroblasts and tissue fibrosis |
Q35375452 | Characterization of novel Pannexin 1 isoforms from rat pituitary cells and their association with ATP-gated P2X channels |
Q27657704 | Characterization of the Structure and Intermolecular Interactions between the Connexin40 and Connexin43 Carboxyl-terminal and Cytoplasmic Loop Domains |
Q94585924 | Choroid plexus and the blood-cerebrospinal fluid barrier in disease |
Q35130231 | Claudins: control of barrier function and regulation in response to oxidant stress. |
Q37175399 | Conformational maturation and post-ER multisubunit assembly of gap junction proteins |
Q34888171 | Connexin 43 connexon to gap junction transition is regulated by zonula occludens-1 |
Q36743696 | Connexin37: a potential modifier gene of inflammatory disease. |
Q37526742 | Connexins, cell motility, and the cytoskeleton |
Q37947566 | Connexins: Key Mediators of Endocrine Function |
Q52716310 | Connexins: Synthesis, Post-Translational Modifications, and Trafficking in Health and Disease. |
Q21245510 | Connexins: a myriad of functions extending beyond assembly of gap junction channels |
Q34103139 | Cross-talk between pulmonary injury, oxidant stress, and gap junctional communication. |
Q33856632 | Cx43 associates with Na(v)1.5 in the cardiomyocyte perinexus. |
Q35579792 | Cx50 requires an intact PDZ-binding motif and ZO-1 for the formation of functional intercellular channels |
Q36410614 | Cytoplasmic amino acids within the membrane interface region influence connexin oligomerization |
Q38024660 | Degradation of Connexins Through the Proteasomal, Endolysosomal and Phagolysosomal Pathways |
Q37707273 | Degradation of connexins and gap junctions |
Q37402174 | Differential pathways of claudin oligomerization and integration into tight junctions |
Q37193492 | ERp29 restricts Connexin43 oligomerization in the endoplasmic reticulum |
Q46149428 | Functional differences between human Cx37 polymorphic hemichannels |
Q38006692 | GJB2 Gene Mutations in Syndromic Skin Diseases with Sensorineural Hearing Loss |
Q93006776 | Gap Junctions in the Bone Marrow Lympho-Hematopoietic Stem Cell Niche, Leukemia Progression, and Chemoresistance |
Q33941978 | Gap junctions and blood-tissue barriers |
Q37689002 | Gap junctions in inherited human disease |
Q91395198 | Generation of Functional CX26-Gap-Junction-Plaque-Forming Cells with Spontaneous Ca2+ Transients via a Gap Junction Characteristic of Developing Cochlea |
Q37388212 | Glycosylation regulates pannexin intermixing and cellular localization |
Q37858330 | Golgi Bypass: Skirting Around the Heart of Classical Secretion |
Q33354230 | Identification of rab20 as a potential regulator of connexin 43 trafficking |
Q39521011 | Impact of Microarray Preprocessing Techniques in Unraveling Biological Pathways |
Q54565145 | Increased interaction of connexin43 with zonula occludens-1 during inhibition of gap junctions by G protein-coupled receptor agonists |
Q42747495 | Intercellular diffusion of a fluorescent sucrose analog via the septal junctions in a filamentous cyanobacterium |
Q36017752 | Junctional abnormalities in human airway epithelial cells expressing F508del CFTR. |
Q30437824 | Localized expression of an Ins(1,4,5)P3 receptor at the myoendothelial junction selectively regulates heterocellular Ca2+ communication |
Q37576096 | Loss of Coupling Distinguishes GJB1 Mutations Associated with CNS Manifestations of CMT1X from Those Without CNS Manifestations |
Q38268356 | Mechanisms linking connexin mutations to human diseases |
Q30417856 | Mechanisms of ATP release and signalling in the blood vessel wall |
Q34017761 | Mechanisms of gap junction traffic in health and disease |
Q38190331 | Mix and match: investigating heteromeric and heterotypic gap junction channels in model systems and native tissues |
Q36942808 | Molecular mechanisms of inherited demyelinating neuropathies |
Q36031604 | Molecular mechanisms regulating formation, trafficking and processing of annular gap junctions |
Q34137935 | Mutations in connexin genes and disease |
Q26825229 | Posttranslational modifications in connexins and pannexins |
Q37158482 | Proteins and Mechanisms Regulating Gap-Junction Assembly, Internalization, and Degradation |
Q57823583 | Proteoliposome Engineering with Cell-Free Membrane Protein Synthesis: Control of Membrane Protein Sorting into Liposomes by Chaperoning Systems |
Q90007845 | Regulation of gap junction intercellular communication by connexin ubiquitination: physiological and pathophysiological implications |
Q36659412 | Role of gap junction, hemichannels, and connexin 43 in mineralizing in response to intermittent and continuous application of parathyroid hormone |
Q85948282 | Role of gap junctions in the contractile response to agonists in the mesenteric artery of spontaneously hypertensive rats |
Q30426561 | Spontaneous lung dysfunction and fibrosis in mice lacking connexin 40 and endothelial cell connexin 43 |
Q30157630 | Structural changes in the carboxyl terminus of the gap junction protein connexin 40 caused by the interaction with c-Src and zonula occludens-1. |
Q37801564 | Structure of the gap junction channel and its implications for its biological functions |
Q50530039 | Subcellular distribution of connexin45 in OFF bipolar cells of the mouse retina |
Q34398416 | Syndromic and non-syndromic disease-linked Cx43 mutations |
Q35939846 | The Gap Junction Channel Protein Connexin 43 Is Covalently Modified and Regulated by SUMOylation |
Q38177259 | The emerging Pannexin 1 signalome: a new nexus revealed? |
Q50317243 | The pathological effects of connexin 26 variants related to hearing loss by in silico and in vitro analysis |
Q48638047 | The role of the C-terminus in functional expression and internalization of rat connexin46 (rCx46). |
Q83693363 | The role of the Cx43 C-terminus in GJ plaque formation and internalization |
Q57471977 | Therapeutic strategies targeting connexins |
Q45318452 | Transport of connexins along the secretory pathway |
Q36035273 | Ubiquitination, intracellular trafficking, and degradation of connexins |
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