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ПросмотрНаучные публикации в Scopus по теме "Dysferlinopathy"

ПросмотрНаучные публикации в Scopus по теме "Dysferlinopathy"

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  • Umakhanova Z.; Bardakov S.; Mavlikeev M.; Chernova O.; Magomedova R.; Akhmedova P.; Yakovlev I.; Dalgatov G.; Fedotov V.; Isaev A.; Deev R. (2017)
    The "Funding" section should be: This work was funded by Human Stem Cells Institute PJSC and Roman V. Deev. Theoretical part of this work was supported by Russian Scientific Foundation grant (14-15-00916). Ivan A. Yakovlev ...
  • Starostina I.; Solovyeva V.; Yuryeva K.; Shevchenko K.; Fedotov V.; Rizvanov A.; Deev R.; Isaev A. (2013)
    Dysferlinopathies is a group of autosomal-recessive inherited neuromuscular diseases, which are characterized by defect in mRNA expression or in functionioning of dysferlin protein, appearing in about 1/200 000 births. ...
  • Yakovlev I.; Deev R.; Solovyeva V.; Rizvanov A.; Isaev A. (2016)
    Nowadays, a whole range of genetherapeutic methods is being used to restore a lost protein function due to mutation, a big number of preclinical and clinical studies of potential drugs that may allow to implement an ...
  • Yakovlev I.; Deev R.; Rizvanov A.; Isaev A. (2017)
    © 2016, Springer Science+Business Media New York.Due to lack of effective therapies, muscular dystrophies became a focus for gene therapy. Multiple pre-clinical studies have shown successful restoration of dystrofin and ...
  • Umakhanova Z.; Bardakov S.; Mavlikeev M.; Chernova O.; Magomedova R.; Akhmedova P.; Yakovlev I.; Dalgatov G.; Fedotov V.; Isaev A.; Deev R. (2017)
    © 2017 Umakhanova, Bardakov, Mavlikeev, Chernova, Magomedova, Akhmedova, Yakovlev, Dalgatov, Fedotov, Isaev and Deev.To date, over 30 genes with mutations causing limb-girdle muscle dystrophy have been described. ...

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