Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 141

1.
2.

Two distinct heterotypic channels mediate gap junction coupling between astrocyte and oligodendrocyte connexins.

Orthmann-Murphy JL, Freidin M, Fischer E, Scherer SS, Abrams CK.

J Neurosci. 2007 Dec 19;27(51):13949-57.

4.

Loss-of-function GJA12/Connexin47 mutations cause Pelizaeus-Merzbacher-like disease.

Orthmann-Murphy JL, Enriquez AD, Abrams CK, Scherer SS.

Mol Cell Neurosci. 2007 Apr;34(4):629-41. Epub 2007 Jan 25.

5.

Four classes of intercellular channels between glial cells in the CNS.

Altevogt BM, Paul DL.

J Neurosci. 2004 May 5;24(18):4313-23.

6.

Engineered Cx40 variants increased docking and function of heterotypic Cx40/Cx43 gap junction channels.

Jassim A, Aoyama H, Ye WG, Chen H, Bai D.

J Mol Cell Cardiol. 2016 Jan;90:11-20. doi: 10.1016/j.yjmcc.2015.11.026. Epub 2015 Dec 2.

PMID:
26625713
7.

Ablation of Cx47 in transgenic mice leads to the loss of MUPP1, ZONAB and multiple connexins at oligodendrocyte-astrocyte gap junctions.

Li X, Penes M, Odermatt B, Willecke K, Nagy JI.

Eur J Neurosci. 2008 Oct;28(8):1503-17. doi: 10.1111/j.1460-9568.2008.06431.x.

8.

Hereditary spastic paraplegia is a novel phenotype for GJA12/GJC2 mutations.

Orthmann-Murphy JL, Salsano E, Abrams CK, Bizzi A, Uziel G, Freidin MM, Lamantea E, Zeviani M, Scherer SS, Pareyson D.

Brain. 2009 Feb;132(Pt 2):426-38. doi: 10.1093/brain/awn328. Epub 2008 Dec 4.

9.

Connexin47, connexin29 and connexin32 co-expression in oligodendrocytes and Cx47 association with zonula occludens-1 (ZO-1) in mouse brain.

Li X, Ionescu AV, Lynn BD, Lu S, Kamasawa N, Morita M, Davidson KG, Yasumura T, Rash JE, Nagy JI.

Neuroscience. 2004;126(3):611-30.

10.

Gap junction disorders of myelinating cells.

Kleopa KA, Orthmann-Murphy J, Sargiannidou I.

Rev Neurosci. 2010;21(5):397-419. Review.

PMID:
21280457
11.

Pelizaeus-Merzbacher-like disease is caused not only by a loss of connexin47 function but also by a hemichannel dysfunction.

Diekmann S, Henneke M, Burckhardt BC, Gärtner J.

Eur J Hum Genet. 2010 Sep;18(9):985-92. doi: 10.1038/ejhg.2010.61. Epub 2010 May 5.

12.

Functional heterotypic interactions between astrocyte and oligodendrocyte connexins.

Magnotti LM, Goodenough DA, Paul DL.

Glia. 2011 Jan;59(1):26-34. doi: 10.1002/glia.21073.

13.

Engineered Cx26 variants established functional heterotypic Cx26/Cx43 and Cx26/Cx40 gap junction channels.

Karademir LB, Aoyama H, Yue B, Chen H, Bai D.

Biochem J. 2016 May 15;473(10):1391-403. doi: 10.1042/BCJ20160200. Epub 2016 Mar 17.

PMID:
26987811
14.

Pathologic and phenotypic alterations in a mouse expressing a connexin47 missense mutation that causes Pelizaeus-Merzbacher-like disease in humans.

Tress O, Maglione M, Zlomuzica A, May D, Dicke N, Degen J, Dere E, Kettenmann H, Hartmann D, Willecke K.

PLoS Genet. 2011 Jul;7(7):e1002146. doi: 10.1371/journal.pgen.1002146. Epub 2011 Jul 7.

15.

Early disruption of glial communication via connexin gap junction in multiple sclerosis, Baló's disease and neuromyelitis optica.

Masaki K.

Neuropathology. 2015 Oct;35(5):469-80. doi: 10.1111/neup.12211. Epub 2015 May 28. Review.

PMID:
26016402
16.
17.

Oligodendrocytes in mouse corpus callosum are coupled via gap junction channels formed by connexin47 and connexin32.

Maglione M, Tress O, Haas B, Karram K, Trotter J, Willecke K, Kettenmann H.

Glia. 2010 Jul;58(9):1104-17. doi: 10.1002/glia.20991.

PMID:
20468052
18.

Transgenic replacement of Cx32 in gap junction-deficient oligodendrocytes rescues the phenotype of a hypomyelinating leukodystrophy model.

Schiza N, Sargiannidou I, Kagiava A, Karaiskos C, Nearchou M, Kleopa KA.

Hum Mol Genet. 2015 Apr 1;24(7):2049-64. doi: 10.1093/hmg/ddu725. Epub 2014 Dec 18.

PMID:
25524707
19.

Identification of cells expressing Cx43, Cx30, Cx26, Cx32 and Cx36 in gap junctions of rat brain and spinal cord.

Rash JE, Yasumura T, Davidson KG, Furman CS, Dudek FE, Nagy JI.

Cell Commun Adhes. 2001;8(4-6):315-20.

20.

Mutations in the gene encoding gap junction protein alpha 12 (connexin 46.6) cause Pelizaeus-Merzbacher-like disease.

Uhlenberg B, Schuelke M, Rüschendorf F, Ruf N, Kaindl AM, Henneke M, Thiele H, Stoltenburg-Didinger G, Aksu F, Topaloğlu H, Nürnberg P, Hübner C, Weschke B, Gärtner J.

Am J Hum Genet. 2004 Aug;75(2):251-60. Epub 2004 Jun 10. Erratum in: Am J Hum Genet. 2004 Oct;5(4):737.

Supplemental Content

Support Center