Deletion of the Tail Domain of the Kinesin-5 Cin8 Affects Its Directionality

Por Düselder, André, Fridman, Vladimir, Thiede, Christina, Wiesbaum, Alice, Goldstein, Alina, Klopfenstein, Dieter R., Zaitseva, Olga, Janson, Marcel E., Gheber, Larisa, Schmidt, Christoph F.
Publicado no J Biol Chem (2015)

High Entropy Oxide Phases with Perovskite Structure

Por Vinnik, Denis A., Trofimov, Evgeny A., Zhivulin, Vladimir E., Gudkova, Svetlana A., Zaitseva, Olga V., Zherebtsov, Dmitry A., Starikov, Andrey Yu., Sherstyuk, Darya P., Amirov, Abdulkarim A., Kalgin, Alexandr V., Trukhanov, Sergey V., Podgornov, Fedor V.
Publicado no Nanomaterials (Basel) (2020)

Extremely Polysubstituted Magnetic Material Based on Magnetoplumbite with a Hexagonal Structure: Synthesis, Structure, Properties, Prospects

Por Vinnik, Denis A., Zhivulin, Vladimir E., Trofimov, Evgeny A., Starikov, Andrey Y., Zherebtsov, Dmitry A., Zaitseva, Olga V., Gudkova, Svetlana A., Taskaev, Sergey V., Klygach, Denis S., Vakhitov, Maxim G., Sander, Elena E., Sherstyuk, Darya P., Trukhanov, Alexey V.
Publicado no Nanomaterials (Basel) (2019)

High frequency of BRCA1, but not CHEK2 or NBS1 (NBN), founder mutations in Russian ovarian cancer patients

Por Suspitsin Evgeny N, Sherina Nathalia, Ponomariova Daria N, Sokolenko Anna P, Iyevleva Aglaya G, Gorodnova Tatyana V, Zaitseva Olga A, Yatsuk Olga S, Togo Alexandr V, Tkachenko Nathalia N, Shiyanov Grigory A, Lobeiko Oksana S, Krylova Nadezhda, Matsko Dmitry E, Maximov Sergey, Urmancheyeva Adel F, Porhanova Nathalia V, Imyanitov Evgeny N
Publicado em 2009-02-01

Large family with both parents affected by distinct BRCA1 mutations: implications for genetic testing

Por Sokolenko, Anna P, Voskresenskiy, Dmitry A, Iyevleva, Aglaya G, Bit-Sava, Elena M, Gutkina, Nadezhda I, Anisimenko, Maxim S, Yu Sherina, Nathalia, Mitiushkina, Nathalia V, Ulibina, Yulia M, Yatsuk, Olga S, Zaitseva, Olga A, Suspitsin, Evgeny N, Togo, Alexandr V, Pospelov, Valery A, Kovalenko, Sergey P, Semiglazov, Vladimir F, Imyanitov, Evgeny N
Publicado em 2009

High frequency of BRCA1, but not CHEK2 or NBS1 (NBN), founder mutations in Russian ovarian cancer patients

Por Suspitsin, Evgeny N, Sherina, Nathalia Yu, Ponomariova, Daria N, Sokolenko, Anna P, Iyevleva, Aglaya G, Gorodnova, Tatyana V, Zaitseva, Olga A, Yatsuk, Olga S, Togo, Alexandr V, Tkachenko, Nathalia N, Shiyanov, Grigory A, Lobeiko, Oksana S, Krylova, Nadezhda Yu, Matsko, Dmitry E, Maximov, Sergey Ya, Urmancheyeva, Adel F, Porhanova, Nathalia V, Imyanitov, Evgeny N
Publicado em 2009