Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Anastasia A, Ershova"'
Autor:
Aram A. Musaelyan, Ekaterina M. Anokhina, Alina I. Turdubaeva, Natalia V. Mitiushkina, Anastasia N. Ershova, Anna D. Shestakova, Aigul R. Venina, Evgeny N. Imyanitov, Sergey V. Orlov
Publikováno v:
Exploration of Targeted Anti-tumor Therapy, Vol 5, Iss 3, Pp 780-788 (2024)
Systemic chemotherapy is the main treatment option for patients with advanced intrahepatic cholangiocarcinoma (iCCA), however, its efficacy is limited. Herein, we report a young patient with NRAS-mutated chemoresistant metastatic iCCA, who received s
Externí odkaz:
https://doaj.org/article/15c6b988128b481890e948ca980a13a8
Autor:
Sema Öztürk Yıldırım, Mehmet Akkurt, Anastasia A. Ershova, Mikhail S. Grigoriev, Bruno G.M. Rocha, Ajaya Bhattarai
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications, Vol 79, Iss 4, Pp 292-296 (2023)
The title compound, C20H21F3N2O4, features a main twelve-membered difuryl ring with which the furan rings make dihedral angles of 76.14 (5) and 33.81 (5)°. The dihedral angle between the furan rings is 42.55 (7)°. The six-membered nitrogen heterocy
Externí odkaz:
https://doaj.org/article/7ab3717e0a934ea8bd1a6cf9e6a02fd6
Autor:
Aleksandr S. Martianov, Natalia V. Mitiushkina, Anastasia N. Ershova, Darya E. Martynenko, Mikhail G. Bubnov, Priscilla Amankwah, Grigory A. Yanus, Svetlana N. Aleksakhina, Vladislav I. Tiurin, Aigul R. Venina, Aleksandra A. Anuskina, Yuliy A. Gorgul, Anna D. Shestakova, Mikhail A. Maidin, Alexey M. Belyaev, Liliya S. Baboshkina, Aglaya G. Iyevleva, Evgeny N. Imyanitov
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 5, p 4868 (2023)
This study aimed to analyze clinical and regional factors influencing the distribution of actionable genetic alterations in a large consecutive series of colorectal carcinomas (CRCs). KRAS, NRAS and BRAF mutations, HER2 amplification and overexpressi
Externí odkaz:
https://doaj.org/article/a169542c441740c8ad3333e7f0a1b1f3
Autor:
Sema Öztürk Yıldırım, Mehmet Akkurt, Anastasia A. Ershova, Mikhail S. Grigoriev, Bruno G.M. Rocha, Ajaya Bhattarai
Publikováno v:
Acta Crystallographica Section E Crystallographic Communications. 79:292-296
The title compound, C20H21F3N2O4, features a main twelve-membered difuryl ring with which the furan rings make dihedral angles of 76.14 (5) and 33.81 (5)°. The dihedral angle between the furan rings is 42.55 (7)°. The six-membered nitrogen heterocy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e58dba0fa48d4dedf7ae7de8cd4c19aa
https://doi.org/10.1107/s2056989023001986
https://doi.org/10.1107/s2056989023001986
Autor:
Anastasia S. Ershova, Elena M. Suleymanova, Anastasia A. Grishchenko, Lyudmila V. Vinogradova, Ilya V. Sysoev
Publikováno v:
2022 6th Scientific School Dynamics of Complex Networks and their Applications (DCNA).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d3313a7bf3e944bb6dbc5d9fed8b91ca
https://doi.org/10.1109/dcna56428.2022.9923081
https://doi.org/10.1109/dcna56428.2022.9923081
Autor:
Alexander A. Titov, Maria D. Matveeva, Tatiana N. Borisova, Grigorii S. Astakhov, Leonid G. Voskressensky, Alexey V. Varlamov, Rinat R. Shigaev, Anastasia A. Ershova
Publikováno v:
Molecular Diversity. 25:2441-2446
A convenient protocol for the synthesis of 5,6-dihydropyrrolo[2,1-a]isoquinolines with various electron-withdrawing substituents at C-2 atom is described. This approach is based on the two-component domino reaction of 1-aroyl-3,4-dihydroisoquinolines
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::383cdce727a45826dc7400424daf7fde
https://doi.org/10.1007/s11030-020-10146-7
https://doi.org/10.1007/s11030-020-10146-7
Autor:
V. N. Maksimova, Anastasia I. Ershova, Mikhail Yu. Ievlev, Mikhail Yu. Belikov, Oleg V. Ershov
Publikováno v:
ChemistrySelect. 5:7243-7248
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a3ad90b1c01caf73d94ff922c2830b77
https://doi.org/10.1002/slct.202001710
https://doi.org/10.1002/slct.202001710
Autor:
Grigorii S, Astakhov, Rinat R, Shigaev, Tatiana N, Borisova, Anastasia A, Ershova, Alexander A, Titov, Alexey V, Varlamov, Leonid G, Voskressensky, Maria D, Matveeva
Publikováno v:
Molecular diversity. 25(4)
A convenient protocol for the synthesis of 5,6-dihydropyrrolo[2,1-a]isoquinolines with various electron-withdrawing substituents at C-2 atom is described. This approach is based on the two-component domino reaction of 1-aroyl-3,4-dihydroisoquinolines
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e3c604a99f262ab4b5eb49d255d931de
https://pubmed.ncbi.nlm.nih.gov/33040250
https://pubmed.ncbi.nlm.nih.gov/33040250
Autor:
Irina N. Trapeznikova, Vasily N. Petrov, Maksat K. Ovezov, Leo B. Matyushkin, Olga P. Chikalova-Luzina, Andrey N. Aleshin, Anastasia M. Ershova, Igor Shcherbakov
Publikováno v:
Synthetic Metals. 260:116291
The optical and electrical properties of films and field-effect transistors (FETs) based on pure MEH-PPV, neat CsPbBr3 nanocrystals (NCs), and MEH-PPV:CsPbBr3 NCs composites with different contents of CsPbBr3 NCs are investigated. The films were char
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::be29371408e9852075155b6dd6a33f1c
https://doi.org/10.1016/j.synthmet.2020.116291
https://doi.org/10.1016/j.synthmet.2020.116291
Autor:
Anna D. Zinoveva, Tatiana N. Borisova, Alexander A. Titov, Leonid G. Voskressensky, Van Tuyen Nguyen, Alexey V. Varlamov, Anastasia A. Ershova, Tuan Anh Le
Publikováno v:
Tetrahedron Letters. 60:151264
An effective strategy for the synthesis of benzo[h]pyrrolo[2,1-a]isoquinoline derivatives has been developed. The process can be described as a one-pot domino reaction that consists of an initial Michael addition, intramolecular cyclization, and subs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4f43d79b68c4040e48e21c0093b972f9
https://doi.org/10.1016/j.tetlet.2019.151264
https://doi.org/10.1016/j.tetlet.2019.151264