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Journal Abstract Search
258 related items for PubMed ID: 23544880
1. The distribution and functional properties of Pelizaeus-Merzbacher-like disease-linked Cx47 mutations on Cx47/Cx47 homotypic and Cx47/Cx43 heterotypic gap junctions. Kim MS, Gloor GB, Bai D. Biochem J; 2013 Jun 01; 452(2):249-58. PubMed ID: 23544880 [Abstract] [Full Text] [Related]
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. PubMed ID: 18094232 [Abstract] [Full Text] [Related]
3. Mechanisms of Diseases Associated with Mutation in GJC2/Connexin 47. Abrams CK. Biomolecules; 2023 Apr 21; 13(4):. PubMed ID: 37189458 [Abstract] [Full Text] [Related]
8. 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 21; 90():11-20. PubMed ID: 26625713 [Abstract] [Full Text] [Related]
9. 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 21; 28(8):1503-17. PubMed ID: 18973575 [Abstract] [Full Text] [Related]
11. 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 21; 132(Pt 2):426-38. PubMed ID: 19056803 [Abstract] [Full Text] [Related]
12. Gap junction disorders of myelinating cells. Kleopa KA, Orthmann-Murphy J, Sargiannidou I. Rev Neurosci; 2010 Feb 21; 21(5):397-419. PubMed ID: 21280457 [Abstract] [Full Text] [Related]