Coupling of astrocyte connexins Cx26, Cx30, Cx43 to oligodendrocyte Cx29, Cx32, Cx47: Implications from normal and connexin32 knockout mice. - Wikidata - awgldk - TriplyDB

Coupling of astrocyte connexins Cx26, Cx30, Cx43 to oligodendrocyte Cx29, Cx32, Cx47: Implications from normal and connexin32 knockout mice.

Coupling of astrocyte connexins Cx26, Cx30, Cx43 to oligodendrocyte Cx29, Cx32, Cx47: Implications from normal and connexin32 knockout mice.

http://www.wikidata.org/entity/Q30499066

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GJC2 missense mutations cause human lymphedema Mutations in the gene encoding gap junction protein alpha 12 (connexin 46.6) cause Pelizaeus-Merzbacher-like disease Evidence for a role of connexin 43 in trigeminal pain using RNA interference in vivo Gap junctions couple astrocytes and oligodendrocytes Hereditary spastic paraplegia is a novel phenotype for GJA12/GJC2 mutations Human oligodendrocytes express Cx31.3: function and interactions with Cx32 mutants Connexin-47 and connexin-32 in gap junctions of oligodendrocyte somata, myelin sheaths, paranodal loops and Schmidt-Lanterman incisures: implications for ionic homeostasis and potassium siphoning.Loss-of-function GJA12/Connexin47 mutations cause Pelizaeus-Merzbacher-like disease Myelin damage and repair in pathologic CNS: challenges and prospects Gap junctions in inherited human disorders of the central nervous system.Transplantation of stem cell-derived astrocytes for the treatment of amyotrophic lateral sclerosis and spinal cord injury Gap junctions and hemichannels composed of connexins: potential therapeutic targets for neurodegenerative diseases Enhanced neurite outgrowth in PC12 cells mediated by connexin hemichannels and ATP Localization of connexin 30 in the luminal membrane of cells in the distal nephron Cx32 and Cx47 mediate oligodendrocyte:astrocyte and oligodendrocyte:oligodendrocyte gap junction coupling.Connexin26 expression in brain parenchymal cells demonstrated by targeted connexin ablation in transgenic mice.Molecular disruptions of the panglial syncytium block potassium siphoning and axonal saltatory conduction: pertinence to neuromyelitis optica and other demyelinating diseases of the central nervous system.Astrocytic connexin distributions and rapid, extensive dye transfer via gap junctions in the inferior colliculus: implications for [(14)C]glucose metabolite trafficking.Connexin32 mutations cause loss of function in Schwann cells and oligodendrocytes leading to PNS and CNS myelination defects Ablation of Cx47 in transgenic mice leads to the loss of MUPP1, ZONAB and multiple connexins at oligodendrocyte-astrocyte gap junctions Identification of connexin36 in gap junctions between neurons in rodent locus coeruleus Connexin47, connexin29 and connexin32 co-expression in oligodendrocytes and Cx47 association with zonula occludens-1 (ZO-1) in mouse brain.Activated microglia do not form functional gap junctions in vivo.Pathologic and phenotypic alterations in a mouse expressing a connexin47 missense mutation that causes Pelizaeus-Merzbacher-like disease in humans.Gap junctions.The role of gap junction channels during physiologic and pathologic conditions of the human central nervous system Mutations in cardiovascular connexin genes.Early disruption of glial communication via connexin gap junction in multiple sclerosis, Baló's disease and neuromyelitis optica.Re-evaluation of connexins associated with motoneurons in rodent spinal cord, sexually dimorphic motor nuclei and trigeminal motor nucleus.Reduction and redistribution of gap and adherens junction proteins after ischemia and reperfusion Freeze-fracture and immunogold analysis of aquaporin-4 (AQP4) square arrays, with models of AQP4 lattice assembly.Connexin29 and connexin32 at oligodendrocyte and astrocyte gap junctions and in myelin of the mouse central nervous system.Synergy between electrical coupling and membrane properties promotes strong synchronization of neurons of the mesencephalic trigeminal nucleus.Mixed Electrical-Chemical Synapses in Adult Rat Hippocampus are Primarily Glutamatergic and Coupled by Connexin-36 Connexin composition in apposed gap junction hemiplaques revealed by matched double-replica freeze-fracture replica immunogold labeling Connexin36 vs. connexin32, "miniature" neuronal gap junctions, and limited electrotonic coupling in rodent suprachiasmatic nucleus.Molecular genetics of X-linked Charcot-Marie-Tooth disease.Modulation of connexin expression and gap junction communication in astrocytes by the gram-positive bacterium S. aureus.Possible involvement of TLRs and hemichannels in stress-induced CNS dysfunction via mastocytes, and glia activation.Connexin and pannexin mediated cell-cell communication.

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P2860

Coupling of astrocyte connexins Cx26, Cx30, Cx43 to oligodendrocyte Cx29, Cx32, Cx47: Implications from normal and connexin32 knockout mice.

http://www.wikidata.org/entity/Q30499066

description

2003 nî lūn-bûn

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2003 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

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2003 թվականի դեկտեմբերին հրատարակված գիտական հոդված

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2003年の論文

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2003年論文

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2003年論文

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2003年論文

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2003年論文

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2003年論文

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2003年论文

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name

Coupling of astrocyte connexin ...... and connexin32 knockout mice.

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Coupling of astrocyte connexin ...... and connexin32 knockout mice.

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Coupling of astrocyte connexin ...... and connexin32 knockout mice.

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Coupling of astrocyte connexin ...... and connexin32 knockout mice.

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Coupling of astrocyte connexin ...... and connexin32 knockout mice.

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A-V Ionescu

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B D Lynn

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J E Rash

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P2860

Connexin mutations in X-linked Charcot-Marie-Tooth disease

Cell-specific expression of connexins and evidence of restricted gap junctional coupling between glial cells and between neurons

Connexin29 expression, immunocytochemistry and freeze-fracture replica immunogold labelling (FRIL) in sciatic nerve

Connexin32 and X-linked Charcot-Marie-Tooth disease

Connexin30 in rodent, cat and human brain: selective expression in gray matter astrocytes, co-localization with connexin43 at gap junctions and late developmental appearance

Connexin 26 and basic fibroblast growth factor are expressed primarily in the subpial and subependymal layers in adult brain parenchyma: roles in stem cell proliferation and morphological plasticity?

Central visual, acoustic, and motor pathway involvement in a Charcot-Marie-Tooth family with an Asn205Ser mutation in the connexin 32 gene.

Structural and functional diversity of connexin genes in the mouse and human genome.

Connexin29 is uniquely distributed within myelinating glial cells of the central and peripheral nervous systems.

Formation of hybrid cell-cell channels.

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10.1002/GLIA.10278

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3

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44

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14603462

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oligodendrocyte

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1852517

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