Zobrazeno 1 - 10
of 73
pro vyhledávání: '"Dmitry V, Zaletaev"'
Autor:
Alexey I. Kalinkin, Vladimir O. Sigin, Ekaterina B. Kuznetsova, Ekaterina O. Ignatova, Ilya I. Vinogradov, Maxim I. Vinogradov, Igor Y. Vinogradov, Dmitry V. Zaletaev, Marina V. Nemtsova, Sergey I. Kutsev, Alexander S. Tanas, Vladimir V. Strelnikov
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 24, p 17343 (2023)
Triple-negative breast cancer (TNBC) is the most aggressive molecular subtype, with a poor survival rate compared to others subtypes. For a long time, chemotherapy was the only systemic treatment for TNBC, and the identification of actionable molecul
Externí odkaz:
https://doaj.org/article/e17a39ef166046e4a8d47b650602e284
Autor:
Vladimir V. Strelnikov, Ekaterina B. Kuznetsova, Alexander S. Tanas, Viktoria V. Rudenko, Alexey I. Kalinkin, Elena V. Poddubskaya, Tatiana V. Kekeeva, Galina G. Chesnokova, Ivan D. Trotsenko, Sergey S. Larin, Sergey I. Kutsev, Dmitry V. Zaletaev, Marina V. Nemtsova, Olga A. Simonova
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-14 (2021)
Abstract Cell transmembrane receptors and extracellular matrix components play a pivotal role in regulating cell activity and providing for the concerted integration of cells in the tissue structures. We have assessed DNA methylation in the promoter
Externí odkaz:
https://doaj.org/article/9674b2bcc0154773b10c7499d5ce84fc
Autor:
Dmitry S. Mikhaylenko, Alexey V. Klimov, Vsevolod B. Matveev, Svetlana I. Samoylova, Vladimir V. Strelnikov, Dmitry V. Zaletaev, Ludmila N. Lubchenko, Boris Y. Alekseev, Marina V. Nemtsova
Publikováno v:
Frontiers in Oncology, Vol 9 (2020)
Hereditary papillary renal carcinoma (HPRC) is a rare autosomal dominant disease characterized by the development of multiple papillary type I renal cell carcinomas. This hereditary kidney cancer form is caused by activating mutations in MET. Descrip
Externí odkaz:
https://doaj.org/article/2377b74b1e024c23b906cfc4a1da5af4
Autor:
Marina V. Nemtsova, Dmitry V. Zaletaev, Irina V. Bure, Dmitry S. Mikhaylenko, Ekaterina B. Kuznetsova, Ekaterina A. Alekseeva, Marina I. Beloukhova, Andrei A. Deviatkin, Alexander N. Lukashev, Andrey A. Zamyatnin
Publikováno v:
Frontiers in Genetics, Vol 10 (2019)
Rheumatoid arthritis (RA) is a systemic autoimmune disease that affects about 1% of the world’s population. The etiology of RA remains unknown. It is considered to occur in the presence of genetic and environmental factors. An increasing body of ev
Externí odkaz:
https://doaj.org/article/a19fdd7a8147439e90df1f89fd65e0d6
Autor:
Olga A. Simonova, Ekaterina B. Kuznetsova, Alexander S. Tanas, Viktoria V. Rudenko, Elena V. Poddubskaya, Tatiana V. Kekeeva, Ivan D. Trotsenko, Sergey S. Larin, Sergei I. Kutsev, Dmitry V. Zaletaev, Marina V. Nemtsova, Vladimir V. Strelnikov
Publikováno v:
Biomedicines, Vol 8, Iss 5, p 116 (2020)
Matrix metalloproteinases (MMPs) and their tissue inhibitors (TIMPs) substantially contribute to the regulation of intercellular interactions and thereby play a role in maintaining the tissue structure and function. We examined methylation of a subse
Externí odkaz:
https://doaj.org/article/3a12362de9774f44892d4de6c4804808
Publikováno v:
Russian Journal of Skin and Venereal Diseases. 24:35-44
BACKGROUND: Mycosis fungoides (MF) is the most common disease among the cutaneous T-cell lymphomas (8590%). The accuracy of the diagnosis of MF, which is confirmed only by clinical, histological and immunohistochemical signs, is 5075%. AIMS: To inves
Publikováno v:
International Journal of Molecular Sciences, Vol 20, Iss 12, p 2870 (2019)
The epithelial−mesenchymal transition (EMT) is thought to be at the root of invasive and metastatic cancer cell spreading. E-cadherin is an important player in this process, which forms the structures that establish and maintain cell−cell interac
Externí odkaz:
https://doaj.org/article/9fdbb02ced0d4f768c055aafd9e22fdc
Autor:
Vladimir O. Sigin, Alexey I. Kalinkin, Alexandra F. Nikolaeva, Ekaterina O. Ignatova, Ekaterina B. Kuznetsova, Galina G. Chesnokova, Nikolai V. Litviakov, Matvey M. Tsyganov, Marina K. Ibragimova, Ilya I. Vinogradov, Maxim I. Vinogradov, Igor Y. Vinogradov, Dmitry V. Zaletaev, Marina V. Nemtsova, Sergey I. Kutsev, Alexander S. Tanas, Vladimir V. Strelnikov
Publikováno v:
Cancers; Volume 15; Issue 5; Pages: 1630
Despite advances in the diagnosis and treatment of breast cancer (BC), the main cause of deaths is resistance to existing therapies. An approach to improve the effectiveness of therapy in patients with aggressive BC subtypes is neoadjuvant chemothera
Publikováno v:
Journal of Oncology
Journal of Oncology, Vol 2020 (2020)
Journal of Oncology, Vol 2020 (2020)
Next generation sequencing (NGS) is widely used for diagnosing hereditary cancer syndromes. Often, exome sequencing and extended gene panel approaches are the only means that can be used to detect a pathogenic germline mutation in the case of multipl
Autor:
Igor Y. Vinogradov, Maksim I. Vinogradov, Matvey M. Tsyganov, Dmitry V. Zaletaev, Olga A Simonova, Alexander S Tanas, Ekaterina B. Kuznetsova, Vladimir O. Sigin, Ilya I. Vinogradov, Sergey I. Kutsev, Ilya V. Volodin, A.I. Kalinkin, Galina G. Chesnokova, Elena M. Slonimskaya, Nikolai V. Litviakov, Vladimir V Strelnikov, M.K. Ibragimova
Publikováno v:
Scientific Reports, Vol 10, Iss 1, Pp 1-9 (2020)
Scientific Reports
Scientific Reports
Despite the advantages of neoadjuvant chemotherapy (NACT), associated toxicity is a serious complication that renders monitoring of the patients’ response to NACT highly important. Thus, prediction of tumor response to treatment is imperative to av