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A mutation linked to retinitis pigmentosa in HPRP31 causes protein instability and impairs its interactions with spliceosomal snRNPs

    1.
    SYSNO0334100
    TitleA mutation linked to retinitis pigmentosa in HPRP31 causes protein instability and impairs its interactions with spliceosomal snRNPs
    Author(s) Huranová, Martina (UMG-J) ORCID
    Hnilicová, Jarmila (UMG-J)
    Fleischer, Branislav (UMG-J)
    Cvačková, Zuzana (UMG-J) RID
    Staněk, David (UMG-J) RID
    Source Title Human Molecular Genetics. Roč. 18, č. 11 (2009), s. 2014-2023. - : Oxford University Press
    Document TypeČlánek v odborném periodiku
    Grant KAN200520801 GA AV ČR - Academy of Sciences of the Czech Republic (AV ČR)
    Partner group program, DE - Germany
    CEZAV0Z50520514 - UMG-J (2005-2011)
    Languageeng
    CountryGB
    Keywords retinitis pigmentosa * snRNP * splicing
    Permanent Linkhttp://hdl.handle.net/11104/0178923
     
Number of the records: 1  

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