Works matching AU A., Prokofyeva


Results: 55
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    Nonsense mutation p.Q548X in BLM, the gene mutated in Bloom's syndrome, is associated with breast cancer in Slavic populations.

    Published in:
    Breast Cancer Research & Treatment, 2013, v. 137, n. 2, p. 533, doi. 10.1007/s10549-012-2357-1
    By:
    • Prokofyeva, Darya;
    • Bogdanova, Natalia;
    • Dubrowinskaja, Natalia;
    • Bermisheva, Marina;
    • Takhirova, Zalina;
    • Antonenkova, Natalia;
    • Turmanov, Nurzhan;
    • Datsyuk, Ihor;
    • Gantsev, Shamil;
    • Christiansen, Hans;
    • Park-Simon, Tjoung-Won;
    • Hillemanns, Peter;
    • Khusnutdinova, Elza;
    • Dörk, Thilo
    Publication type:
    Article
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    A Splice Site Variant of CDK12 and Breast Cancer in Three Eurasian Populations.

    Published in:
    Frontiers in Oncology, 2019, p. N.PAG, doi. 10.3389/fonc.2019.00493
    By:
    • Bogdanova, Natalia V.;
    • Schürmann, Peter;
    • Valova, Yana;
    • Dubrowinskaja, Natalia;
    • Turmanov, Nurzhan;
    • Yugay, Tatyana;
    • Essimsiitova, Zura;
    • Mingazheva, Elvira;
    • Prokofyeva, Darya;
    • Bermisheva, Marina;
    • Khusnutdinova, Elza;
    • Dörk, Thilo
    Publication type:
    Article
    33

    Receptor tyrosine kinase inhibition leads to regression of acral melanoma by targeting the tumor microenvironment.

    Published in:
    Journal of Experimental & Clinical Cancer Research (17569966), 2024, v. 43, n. 1, p. 1, doi. 10.1186/s13046-024-03234-1
    By:
    • Smith, Eric A.;
    • Belote, Rachel L.;
    • Cruz, Nelly M.;
    • Moustafa, Tarek E.;
    • Becker, Carly A.;
    • Jiang, Amanda;
    • Alizada, Shukran;
    • Prokofyeva, Anastasia;
    • Chan, Tsz Yin;
    • Seasor, Tori A.;
    • Balatico, Michael;
    • Cortes-Sanchez, Emilio;
    • Lum, David H.;
    • Hyngstrom, John R.;
    • Zeng, Hanlin;
    • Deacon, Dekker C.;
    • Grossmann, Allie H.;
    • White, Richard M.;
    • Zangle, Thomas A.;
    • Judson-Torres, Robert L.
    Publication type:
    Article
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    Prevalence of the BLM nonsense mutation, p.Q548X, in ovarian cancer patients from Central and Eastern Europe.

    Published in:
    Familial Cancer, 2015, v. 14, n. 1, p. 145, doi. 10.1007/s10689-014-9748-x
    By:
    • Bogdanova, Natalia;
    • Togo, Alexandr;
    • Ratajska, Magdalena;
    • Kluźniak, Wojtek;
    • Takhirova, Zalina;
    • Tarp, Theresa;
    • Prokofyeva, Darya;
    • Bermisheva, Marina;
    • Yanus, Grigoriy;
    • Gorodnova, Tatiana;
    • Sokolenko, Anna;
    • Kuźniacka, Alina;
    • Podolak, Amira;
    • Stukan, Maciej;
    • Wokołorczyk, Dominika;
    • Gronwald, Jacek;
    • Vasilevska, Danuta;
    • Rudaitis, Vilius;
    • Runnebaum, Ingo;
    • Dürst, Matthias
    Publication type:
    Article
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    Exome sequencing study of Russian breast cancer patients suggests a predisposing role for USP39.

    Published in:
    Breast Cancer Research & Treatment, 2020, v. 179, n. 3, p. 731, doi. 10.1007/s10549-019-05492-6
    By:
    • Kuligina, Ekaterina S.;
    • Sokolenko, Anna P.;
    • Bizin, Ilya V.;
    • Romanko, Alexandr A.;
    • Zagorodnev, Kirill A.;
    • Anisimova, Maria O.;
    • Krylova, Daria D.;
    • Anisimova, Elena I.;
    • Mantseva, Maria A.;
    • Varma, Ashok K.;
    • Hasan, Syed K.;
    • Ni, Valeria I.;
    • Koloskov, Andrey V.;
    • Suspitsin, Evgeny N.;
    • Venina, Aigul R.;
    • Aleksakhina, Svetlana N.;
    • Sokolova, Tatiana N.;
    • Milanović, Ana Marija;
    • Schürmann, Peter;
    • Prokofyeva, Darya S.
    Publication type:
    Article
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