Connexin-caused genetic diseases and corresponding mouse models.
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Connexins: a myriad of functions extending beyond assembly of gap junction channelsGap junction assembly: roles for the formation plaque and regulation by the C-terminus of connexin43Gap junctionsGap junction connexins in female reproductive organs: implications for women's reproductive healthRegulation of neuronal bioenergy homeostasis by glutamateEpithelial barrier assembly requires coordinated activity of multiple domains of the tight junction protein ZO-1Cell degeneration is not a primary causer for Connexin26 (GJB2) deficiency associated hearing loss.A rapid and sensitive assay of intercellular coupling by voltage imaging of gap junction networksMolecular dynamics simulations highlight structural and functional alterations in deafness-related M34T mutation of connexin 26.Cx43 phosphorylation on S279/282 and intercellular communication are regulated by IP3/IP3 receptor signalingKinase programs spatiotemporally regulate gap junction assembly and disassembly: Effects on wound repair.Connexin 30 is expressed in the mouse sino-atrial node and modulates heart rate.Regulation of FAK Activity by Tetraspan Proteins: Potential Clinical Implications in Cancer.Gap junctions in olfactory neurons modulate olfactory sensitivity.Engram formation in psychiatric disorders.Gap junctions.Astroglial Wiring is Adding Complexity to Neuroglial Networking.Zebrafish cx30.3: identification and characterization of a gap junction gene highly expressed in the skinSyndromic and non-syndromic disease-linked Cx43 mutations.Mutations in cardiovascular connexin genes.The gap junction as a "Biological Rosetta Stone": implications of evolution, stem cells to homeostatic regulation of health and disease in the Barker hypothesis.The carboxyl tail of connexin32 regulates gap junction assembly in human prostate and pancreatic cancer cells.Connexin43 phosphorylation in brain, cardiac, endothelial and epithelial tissues.Endothelial Connexin37 and Connexin40 participate in basal but not agonist-induced NO release.Connexin43 mutation causes heterogeneous gap junction loss and sudden infant deathCASK (LIN2) interacts with Cx43 in wounded skin and their coexpression affects cell migration.Gap junctions and hemichannels in signal transmission, function and development of boneVoltage-dependent gating of the Cx32*43E1 hemichannel: conformational changes at the channel entrances.Junctional proteins of the blood-brain barrier: New insights into function and dysfunction.Connexin diversity in the heart: insights from transgenic mouse models.Effects of phosphorylation on the structure and backbone dynamics of the intrinsically disordered connexin43 C-terminal domainA history of gap junction structure: hexagonal arrays to atomic resolution.Metabolic inhibition increases activity of connexin-32 hemichannels permeable to Ca2+ in transfected HeLa cells.Connexin 43 mimetic peptide Gap27 reveals potential differences in the role of Cx43 in wound repair between diabetic and non-diabetic cells.Specific Cx43 phosphorylation events regulate gap junction turnover in vivoConnexins and the gap in context.Connexins: key mediators of endocrine function.Connexins in lymphatic vessel physiology and disease.Cardiac to cancer: connecting connexins to clinical opportunity.Cell communication across gap junctions: a historical perspective and current developments.
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Connexin-caused genetic diseases and corresponding mouse models.
description
article científic
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article scientifique
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articolo scientifico
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artigo científico
@pt
bilimsel makale
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scientific article published on February 2009
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Connexin-caused genetic diseases and corresponding mouse models.
@en
Connexin-caused genetic diseases and corresponding mouse models.
@nl
type
label
Connexin-caused genetic diseases and corresponding mouse models.
@en
Connexin-caused genetic diseases and corresponding mouse models.
@nl
prefLabel
Connexin-caused genetic diseases and corresponding mouse models.
@en
Connexin-caused genetic diseases and corresponding mouse models.
@nl
P356
P1476
Connexin-caused genetic diseases and corresponding mouse models
@en
P2093
Klaus Willecke
P304
P356
10.1089/ARS.2008.2128
P577
2009-02-01T00:00:00Z