| scholarly article | Q13442814 |
| P50 | author | Charles K. Abrams | Q87969760 |
| Steven S. Scherer | Q109937193 | ||
| P2093 | author name string | Richard Reynolds | |
| Kleopas A Kleopa | |||
| Meejin Ahn | |||
| Irene Sargiannidou | |||
| Alan D Enriquez | |||
| Alejandro Peinado | |||
| P2860 | cites work | The CNS phenotype of X-linked Charcot-Marie-Tooth disease: more than a peripheral problem | Q48122134 |
| Transient, recurrent, white matter lesions in X-linked Charcot-Marie-Tooth disease with novel connexin 32 mutation | Q48329111 | ||
| Transient central nervous system white matter abnormality in X-linked Charcot-Marie-Tooth disease. | Q48480609 | ||
| Connexin32 in oligodendrocytes and association with myelinated fibers in mouse and rat brain | Q48761472 | ||
| trans-dominant inhibition of connexin-43 by mutant connexin-26: implications for dominant connexin disorders affecting epidermal differentiation | Q48881472 | ||
| Relation between axons and oligodendroglial cells during initial myelination. I. The glial unit | Q48953673 | ||
| Species specificity of mammalian connexin-26 to form open voltage-gated hemichannels. | Q50460921 | ||
| Functional defects of Cx26 resulting from a heterozygous missense mutation in a family with dominant deaf-mutism and palmoplantar keratoderma. | Q50502976 | ||
| The effects of a dominant connexin32 mutant in myelinating Schwann cells. | Q52571597 | ||
| Connexin32 is a myelin-related protein in the PNS and CNS | Q71038789 | ||
| Clinical and pathological observations in men lacking the gap junction protein connexin 32 | Q73339087 | ||
| Altered trafficking of mutant connexin32 | Q73863874 | ||
| Electrical properties of gap junction hemichannels identified in transfected HeLa cells | Q74211772 | ||
| Diverse trafficking abnormalities of connexin32 mutants causing CMTX | Q78597337 | ||
| Genetic and physiological evidence that oligodendrocyte gap junctions contribute to spatial buffering of potassium released during neuronal activity | Q79301429 | ||
| Phylogenetic analysis of three complete gap junction gene families reveals lineage-specific duplications and highly supported gene classes | Q81595526 | ||
| Connexin mutations in X-linked Charcot-Marie-Tooth disease | Q24323296 | ||
| Cell-specific expression of connexins and evidence of restricted gap junctional coupling between glial cells and between neurons | Q24669745 | ||
| 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 | Q24674144 | ||
| Loss-of-function GJA12/Connexin47 mutations cause Pelizaeus-Merzbacher-like disease | Q24682835 | ||
| The mouse gap junction gene connexin29 is highly expressed in sciatic nerve and regulated during brain development | Q28585793 | ||
| Gating and regulation of connexin 43 (Cx43) hemichannels | Q30480722 | ||
| Coupling of astrocyte connexins Cx26, Cx30, Cx43 to oligodendrocyte Cx29, Cx32, Cx47: Implications from normal and connexin32 knockout mice | Q30499066 | ||
| Connexin47, connexin29 and connexin32 co-expression in oligodendrocytes and Cx47 association with zonula occludens-1 (ZO-1) in mouse brain | Q30499651 | ||
| Defective N-acetylaspartate catabolism reduces brain acetate levels and myelin lipid synthesis in Canavan's disease. | Q33933163 | ||
| Structural and functional diversity of connexin genes in the mouse and human genome | Q34137753 | ||
| Connexin29 is uniquely distributed within myelinating glial cells of the central and peripheral nervous systems. | Q34142186 | ||
| Connexin 47 (Cx47)-deficient mice with enhanced green fluorescent protein reporter gene reveal predominant oligodendrocytic expression of Cx47 and display vacuolized myelin in the CNS. | Q34205721 | ||
| Connexins are critical for normal myelination in the CNS. | Q34211666 | ||
| Unique distributions of the gap junction proteins connexin29, connexin32, and connexin47 in oligodendrocytes | Q34338568 | ||
| Intracellular transport, assembly, and degradation of wild-type and disease-linked mutant gap junction proteins | Q34719366 | ||
| Connexin29 and connexin32 at oligodendrocyte and astrocyte gap junctions and in myelin of the mouse central nervous system | Q35768258 | ||
| Pathogenesis of X-linked Charcot-Marie-Tooth disease: differential effects of two mutations in connexin 32 | Q35885518 | ||
| Sensitivity of the brain transcriptome to connexin ablation. | Q36162598 | ||
| Connexin-based gap junction hemichannels: gating mechanisms | Q36162607 | ||
| The vertebrate connexin family | Q36433664 | ||
| Biophysical properties of connexin-45 gap junction hemichannels studied in vertebrate cells | Q36445082 | ||
| Molecular genetics of X-linked Charcot-Marie-Tooth disease | Q36507155 | ||
| Voltage gating and permeation in a gap junction hemichannel | Q37558064 | ||
| Connexin 32 mutations from X-linked Charcot-Marie-Tooth disease patients: functional defects and dominant negative effects | Q40242690 | ||
| Changes in permeability caused by connexin 32 mutations underlie X-linked Charcot-Marie-Tooth disease | Q41082001 | ||
| Cx29 and Cx32, two connexins expressed by myelinating glia, do not interact and are functionally distinct | Q42089141 | ||
| Scrape-loading and dye transfer. A rapid and simple technique to study gap junctional intercellular communication | Q43521106 | ||
| Cellular mechanisms of connexin32 mutations associated with CNS manifestations | Q44059866 | ||
| Corticospinal tract MRI hyperintensity in X-linked Charcot-Marie-Tooth Disease | Q46623941 | ||
| Phenotypic and cellular expression of two novel connexin32 mutations causing CMT1X. | Q46943270 | ||
| Four classes of intercellular channels between glial cells in the CNS. | Q47643765 | ||
| Connexin32-null mice develop demyelinating peripheral neuropathy | Q47700279 | ||
| Axon-myelin sheath relations of oligodendrocyte unit phenotypes in the adult rat anterior medullary velum | Q47901295 | ||
| P4510 | describes a project that uses | ImageJ | Q1659584 |
| P433 | issue | 2 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | oligodendrocyte | Q916698 |
| P304 | page(s) | 221-33 | |
| P577 | publication date | 2008-05-01 | |
| P1433 | published in | Neurobiology of Disease | Q15716606 |
| P1476 | title | Human oligodendrocytes express Cx31.3: function and interactions with Cx32 mutants | |
| P478 | volume | 30 |
| Q61806966 | Connexin and Pannexin-Based Channels in Oligodendrocytes: Implications in Brain Health and Disease |
| Q30485962 | Connexin32 mutations cause loss of function in Schwann cells and oligodendrocytes leading to PNS and CNS myelination defects |
| Q83770907 | Disruption of oligodendrocyte gap junctions in experimental autoimmune encephalomyelitis |
| Q38265030 | GJB1-associated X-linked Charcot-Marie-Tooth disease, a disorder affecting the central and peripheral nervous systems |
| Q48579102 | Gap junction pathology in multiple sclerosis lesions and normal-appearing white matter |
| Q37689002 | Gap junctions in inherited human disease |
| Q26823332 | Gap junctions in inherited human disorders of the central nervous system |
| Q40374604 | Gene therapy targeting oligodendrocytes provides therapeutic benefit in a leukodystrophy model. |
| Q36368553 | How do mutations in GJB1 cause X-linked Charcot-Marie-Tooth disease? |
| Q50523078 | Human connexin30.2/31.3 (GJC3) does not form functional gap junction channels but causes enhanced ATP release in HeLa cells. |
| Q36942808 | Molecular mechanisms of inherited demyelinating neuropathies |
| Q53084843 | Recurrent central nervous system white matter changes in charcot-Marie-tooth type X disease. |
| Q28550067 | Simvastatin Sodium Salt and Fluvastatin Interact with Human Gap Junction Gamma-3 Protein |
| Q60046937 | Synaptic Functions of Hemichannels and Pannexons: A Double-Edged Sword |
| Q39130684 | The oligodendroglial precursor cell line Oli-neu represents a cell culture system to examine functional expression of the mouse gap junction gene connexin29 (Cx29). |
| Q34262821 | The role of gap junction channels during physiologic and pathologic conditions of the human central nervous system |
| Q53809193 | The role of gap junctions in Charcot-Marie-Tooth disease. |
| Q92975668 | The role of oligodendrocyte gap junctions in neuroinflammation |
| Q57176565 | What's the Function of Connexin 32 in the Peripheral Nervous System? |
| Q37188598 | X-linked Charcot-Marie-Tooth disease |
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