Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Dmitry S, Mikhaylenko"'
Autor:
Dmitry S. Mikhaylenko, Vsevolod B. Matveev, Margarita G. Filippova, Kirill I. Anoshkin, Nikolay A. Kozlov, Alexander V. Khachaturyan, Alexandra V. Semyanikhina, Sergey D. Nifatov, Alexander S. Tanas, Marina V. Nemtsova, Dmitry V. Zaletayev
Publikováno v:
Case Reports in Oncology, Vol 14, Iss 2, Pp 963-971 (2021)
We report a case of Birt-Hogg-Dube syndrome (BHDS), a rare hereditary syndrome, the main visible sign of which is the development of multiple skin fibrofolliculomas. In our case, there was a manifestation of BHDS consisting in the absence of fibrofol
Externí odkaz:
https://doaj.org/article/0dd3042c5aff494eb7ffd0085285b07e
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:
Ilya S Dantsev, Evgeniy V Ivkin, Aleksey A Tryakin, Dmitriy N Godlevski, Oleg Yu Latyshev, Victoriya V Rudenko, Dmitry S Mikhaylenko, Vyacheslav B Chernykh, Elena A Volodko, Aleksey B Okulov, Oleg B Loran, Marina V Nemtsova
Publikováno v:
Asian Journal of Andrology, Vol 20, Iss 6, Pp 593-599 (2018)
Testicular microlithiasis (TM) is one of the symptoms of testicular dysgenesis syndrome (TDS). TM is particularly interesting as an informative marker of testicular germ cell tumors (TGCTs). KIT ligand gene (KITLG), BCL2 antagonist/killer 1 (BAK1), a
Externí odkaz:
https://doaj.org/article/ade6ebe4f433401ebb9239d0e27dcb71
Autor:
Elena A. Pudova, Elena N. Lukyanova, Kirill M. Nyushko, Dmitry S. Mikhaylenko, Andrew R. Zaretsky, Anastasiya V. Snezhkina, Maria V. Savvateeva, Anastasiya A. Kobelyatskaya, Nataliya V. Melnikova, Nadezhda N. Volchenko, Gennady D. Efremov, Kseniya M. Klimina, Anastasiya A. Belova, Marina V. Kiseleva, Andrey D. Kaprin, Boris Y. Alekseev, George S. Krasnov, Anna V. Kudryavtseva
Publikováno v:
Frontiers in Genetics, Vol 10 (2019)
Older age is one of the main risk factors for cancer development. The incidence of prostate cancer, as a multifactorial disease, also depends upon demographic factors, race, and genetic predisposition. Prostate cancer most frequently occurs in men ov
Externí odkaz:
https://doaj.org/article/681d84d579e044259747d8b4d86688bf
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 E. Andreeva, Yuri Y. Shchegolev, Alexander M. Scherbakov, Ekaterina I. Mikhaevich, Danila V. Sorokin, Margarita V. Gudkova, Irina V. Bure, Ekaterina B. Kuznetsova, Dmitry S. Mikhaylenko, Marina V. Nemtsova, Dmitry V. Bagrov, Mikhail A. Krasil’nikov
Publikováno v:
Molecules, Vol 26, Iss 9, p 2499 (2021)
Exosomes are the small vesicles that are secreted by different types of normal and tumour cells and can incorporate and transfer their cargo to the recipient cells. The main goal of the present work was to study the tumour exosomes’ ability to accu
Externí odkaz:
https://doaj.org/article/6801056394864b1d961b91d1819f667a
Autor:
Alexandra V. Semyanikhina, Vsevolod Matveev, K.I. Anoshkin, Alexander V. Khachaturyan, D. V. Zaletayev, Marina V. Nemtsova, Nikolay A. Kozlov, Dmitry S. Mikhaylenko, Sergey D. Nifatov, Alexander S Tanas, Margarita G. Filippova
Publikováno v:
Case Reports in Oncology
Case Reports in Oncology, Vol 14, Iss 2, Pp 963-971 (2021)
Case Reports in Oncology, Vol 14, Iss 2, Pp 963-971 (2021)
We report a case of Birt-Hogg-Dube syndrome (BHDS), a rare hereditary syndrome, the main visible sign of which is the development of multiple skin fibrofolliculomas. In our case, there was a manifestation of BHDS consisting in the absence of fibrofol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9891b6a4485c87479ef2680e78c2c78
http://europepmc.org/articles/PMC8490858
http://europepmc.org/articles/PMC8490858
Autor:
Dmitry M. Hushpulian, Dmitry S. Mikhaylenko, B Y Alekseev, V. A. Kirsanova, Anastasia P Koval, Sergey Nikulin, Vsevolod I Kiselev, Elizaveta K. Nezhurina, Andrey A. Poloznikov, Udo Schumacher, Suraja A Akhmedova, I. K. Sviridova, A. I. Osipyants, Larisa V Bolotina, N. S. Sergeeva, Dmitry Shcherbo, Andrey F. Asachenko, Maxim A. Topchiy, N. N. Volchenko, P. A. Karalkin
Publikováno v:
Biochimie. 179:217-227
Epigenetic alterations represent promising therapeutic targets in cancer treatment. Recently it was revealed that small molecules have the potential to act as microRNA silencers. Capacity to bind the discrete stem-looped structure of pre-miR-21 and p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1807710ffcc0e8b5aba495e70dac5982
https://doi.org/10.1016/j.biochi.2020.10.007
https://doi.org/10.1016/j.biochi.2020.10.007
Autor:
Dmitry S. Mikhaylenko, Andrey A. Zamyatnin, Marina V. Nemtsova, Ekaterina B. Kuznetsova, I. I. Bykov
Publikováno v:
Biochemistry (Moscow). 85:735-748
Main factors involved in carcinogenesis are associated with somatic mutations in oncogenes and tumor suppressor genes representing changes in the DNA nucleotide sequence. Epigenetic changes, such as aberrant DNA methylation, modifications of histone
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ec2a631b3ff5af280ba627091f7e072
https://doi.org/10.1134/s0006297920070020
https://doi.org/10.1134/s0006297920070020
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::caa329e2122597ebc507a79acb971ba0
https://doi.org/10.1155/2020/7363102
https://doi.org/10.1155/2020/7363102