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Year | Number of Results |
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2008 | 2 |
2009 | 1 |
2010 | 1 |
2024 | 0 |
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Human oligodendrocytes express Cx31.3: function and interactions with Cx32 mutants.
Neurobiol Dis. 2008 May;30(2):221-33. doi: 10.1016/j.nbd.2008.01.009. Epub 2008 Feb 15.
Neurobiol Dis. 2008.
PMID: 18353664
Free PMC article.
A dominant connexin43 mutant does not have dominant effects on gap junction coupling in astrocytes.
Wasseff S, Abrams CK, Scherer SS.
Wasseff S, et al.
Neuron Glia Biol. 2010 Nov;6(4):213-23. doi: 10.1017/S1740925X11000019. Epub 2011 Mar 4.
Neuron Glia Biol. 2010.
PMID: 21375791
Free PMC article.
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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.
Orthmann-Murphy JL, et al.
Brain. 2009 Feb;132(Pt 2):426-38. doi: 10.1093/brain/awn328. Epub 2008 Dec 4.
Brain. 2009.
PMID: 19056803
Free PMC article.
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