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Journal Abstract Search

143 related items for PubMed ID: 37551045

  • 1. Two new mouse models of Gjb1-associated Charcot-Marie-Tooth disease type 1X.
    Tadenev ALD, Hatton CL, Pattavina B, Mullins T, Schneider R, Bogdanik LP, Burgess RW.
    J Peripher Nerv Syst; 2023 Sep; 28(3):317-328. PubMed ID: 37551045
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  • 2. 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; 78(2):303-16. PubMed ID: 26010264
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  • 4. How do mutations in GJB1 cause X-linked Charcot-Marie-Tooth disease?
    Kleopa KA, Abrams CK, Scherer SS.
    Brain Res; 2012 Dec 03; 1487():198-205. PubMed ID: 22771394
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  • 5. Axonal pathology precedes demyelination in a mouse model of X-linked demyelinating/type I Charcot-Marie Tooth neuropathy.
    Vavlitou N, Sargiannidou I, Markoullis K, Kyriacou K, Scherer SS, Kleopa KA.
    J Neuropathol Exp Neurol; 2010 Sep 03; 69(9):945-58. PubMed ID: 20720503
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  • 6. Gene replacement therapy after neuropathy onset provides therapeutic benefit in a model of CMT1X.
    Kagiava A, Richter J, Tryfonos C, Karaiskos C, Heslegrave AJ, Sargiannidou I, Rossor AM, Zetterberg H, Reilly MM, Christodoulou C, Kleopa KA.
    Hum Mol Genet; 2019 Nov 01; 28(21):3528-3542. PubMed ID: 31411673
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  • 7. 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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  • 8. 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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  • 9. Molecular genetics of X-linked Charcot-Marie-Tooth disease.
    Kleopa KA, Scherer SS.
    Neuromolecular Med; 2006 Jan 09; 8(1-2):107-22. PubMed ID: 16775370
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  • 12. [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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  • 13. GJB1 mutations c.212T>G and c.311A>C induce apoptosis and inwardly rectifying potassium current changes in X-linked Charcot-Marie-Tooth type 1.
    Guo H, Liu Y, Gu J, Luo J, Ma Y, Xiao F.
    Biochem Biophys Res Commun; 2021 Dec 10; 582():8-15. PubMed ID: 34678594
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  • 16. AAV9-mediated Schwann cell-targeted gene therapy rescues a model of demyelinating neuropathy.
    Kagiava A, Karaiskos C, Richter J, Tryfonos C, Jennings MJ, Heslegrave AJ, Sargiannidou I, Stavrou M, Zetterberg H, Reilly MM, Christodoulou C, Horvath R, Kleopa KA.
    Gene Ther; 2021 Nov 10; 28(10-11):659-675. PubMed ID: 33692503
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  • 17. 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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  • 20. Targeting the colony stimulating factor 1 receptor alleviates two forms of Charcot-Marie-Tooth disease in mice.
    Klein D, Patzkó Á, Schreiber D, van Hauwermeiren A, Baier M, Groh J, West BL, Martini R.
    Brain; 2015 Nov 02; 138(Pt 11):3193-205. PubMed ID: 26297559
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