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Journal Abstract Search

229 related items for PubMed ID: 25449862

  • 1. Connexins, gap junctions and peripheral neuropathy.
    Kleopa KA, Sargiannidou I.
    Neurosci Lett; 2015 Jun 02; 596():27-32. PubMed ID: 25449862
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  • 2. Molecular genetics of X-linked Charcot-Marie-Tooth disease.
    Kleopa KA, Scherer SS.
    Neuromolecular Med; 2006 Jun 02; 8(1-2):107-22. PubMed ID: 16775370
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  • 3. Gap junction disorders of myelinating cells.
    Kleopa KA, Orthmann-Murphy J, Sargiannidou I.
    Rev Neurosci; 2010 Jun 02; 21(5):397-419. PubMed ID: 21280457
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  • 4. Intrathecal gene therapy in mouse models expressing CMT1X mutations.
    Kagiava A, Karaiskos C, Richter J, Tryfonos C, Lapathitis G, Sargiannidou I, Christodoulou C, Kleopa KA.
    Hum Mol Genet; 2018 Apr 15; 27(8):1460-1473. PubMed ID: 29462293
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  • 5. Intraneural GJB1 gene delivery improves nerve pathology in a model of X-linked Charcot-Marie-Tooth disease.
    Sargiannidou I, Kagiava A, Bashiardes S, Richter J, Christodoulou C, Scherer SS, Kleopa KA.
    Ann Neurol; 2015 Aug 15; 78(2):303-16. PubMed ID: 26010264
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  • 6. Functional analysis of connexin-32 mutants associated with X-linked dominant Charcot-Marie-Tooth disease.
    Wang HL, Chang WT, Yeh TH, Wu T, Chen MS, Wu CY.
    Neurobiol Dis; 2004 Mar 15; 15(2):361-70. PubMed ID: 15006706
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  • 7. X-linked Charcot-Marie-Tooth disease.
    Scherer SS, Kleopa KA.
    J Peripher Nerv Syst; 2012 Dec 15; 17 Suppl 3(0 3):9-13. PubMed ID: 23279425
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  • 14. Golgi-retained Cx32 mutants interfere with gene addition therapy for CMT1X.
    Kyriakoudi S, Sargiannidou I, Kagiava A, Olympiou M, Kleopa KA.
    Hum Mol Genet; 2017 May 01; 26(9):1622-1633. PubMed ID: 28334782
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  • 15. Transgenic expression of human connexin32 in myelinating Schwann cells prevents demyelination in connexin32-null mice.
    Scherer SS, Xu YT, Messing A, Willecke K, Fischbeck KH, Jeng LJ.
    J Neurosci; 2005 Feb 09; 25(6):1550-9. PubMed ID: 15703409
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  • 16. Gene expression profiling studies in regenerating nerves in a mouse model for CMT1X: uninjured Cx32-knockout peripheral nerves display expression profile of injured wild type nerves.
    Freidin M, Asche-Godin S, Abrams CK.
    Exp Neurol; 2015 Jan 09; 263():339-49. PubMed ID: 25447941
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  • 17. [Two novel mutations of GJB1 gene associated with typical X-linked Charcot-Marie-Tooth disease].
    Qiao XH, Li YX, Chang XZ, Luan XH, Chen B, Bu DF, Yuan Y.
    Zhonghua Yi Xue Za Zhi; 2009 Dec 22; 89(47):3328-31. PubMed ID: 20193560
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  • 19. Connexin channels in Schwann cells and the development of the X-linked form of Charcot-Marie-Tooth disease.
    Ressot C, Bruzzone R.
    Brain Res Brain Res Rev; 2000 Apr 22; 32(1):192-202. PubMed ID: 10751670
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  • 20. Voltage opens unopposed gap junction hemichannels formed by a connexin 32 mutant associated with X-linked Charcot-Marie-Tooth disease.
    Abrams CK, Bennett MV, Verselis VK, Bargiello TA.
    Proc Natl Acad Sci U S A; 2002 Mar 19; 99(6):3980-4. PubMed ID: 11891346
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