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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

210 related items for PubMed ID: 29462293

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  • 2. 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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  • 8. 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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  • 14. Cellular mechanisms of connexin32 mutations associated with CNS manifestations.
    Kleopa KA, Yum SW, Scherer SS.
    J Neurosci Res; 2002 Jun 01; 68(5):522-34. PubMed ID: 12111842
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  • 16. 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 01; 28(3):317-328. PubMed ID: 37551045
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  • 20. Phenotypic and cellular expression of two novel connexin32 mutations causing CMT1X.
    Kleopa KA, Zamba-Papanicolaou E, Alevra X, Nicolaou P, Georgiou DM, Hadjisavvas A, Kyriakides T, Christodoulou K.
    Neurology; 2006 Feb 14; 66(3):396-402. PubMed ID: 16476939
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