Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Dmitry S Mikhaylenko"'
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:
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:
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:
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
Autor:
N. Yu. Safronova, G. D. Efremov, Andrey Kaprin, Dmitry S. Mikhaylenko, B. Ya. Alekseev, S. A. Sergienko
Publikováno v:
Experimental and Сlinical Urology. 12:42-51
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aac76a9e58863a123a7916c2bc264687
https://doi.org/10.29188/2222-8543-2020-12-1-42-51
https://doi.org/10.29188/2222-8543-2020-12-1-42-51
Autor:
Irina V. Bure, Ekaterina A. Alekseeva, Dmitry S. Mikhaylenko, Vladimir V Strelnikov, Marina V. Nemtsova, A.I. Kalinkin, Tatiana L Ushakova, Dmitry V. Zaletaev, Ekaterina B. Kuznetsova, Sergey I. Kutsev, Tatiana P. Kazubskaya, O. V. Babenko, Galina G. Chesnokova, Alexander S Tanas, Valentina M. Kozlova
Publikováno v:
Cancers, Vol 13, Iss 5068, p 5068 (2021)
Cancers
Volume 13
Issue 20
Cancers
Volume 13
Issue 20
Our aim was to identify RB1 alterations causing hereditary low penetrance retinoblastoma and to evaluate how the parental origin of an RB1 mutation affects its phenotypic expression. By NGS and MLPA, RB1 mutations were found in 191 from 332 unrelated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4c97c700def6768c140e782e667b2cc
https://www.mdpi.com/2072-6694/13/20/5068
https://www.mdpi.com/2072-6694/13/20/5068
Autor:
Vladimir V Strelnikov, Alexander S Tanas, Dmitry S. Mikhaylenko, T. V. Khorobrykh, Marina V. Nemtsova, Ekaterina B. Kuznetsova, Irina V. Bure, A.I. Kalinkin, Ekaterina A. Alekseeva, I. I. Bykov
Publikováno v:
Cancers, Vol 13, Iss 4586, p 4586 (2021)
Cancers
Volume 13
Issue 18
Cancers
Volume 13
Issue 18
Simple Summary Epigenetic mechanisms, such as DNA methylation/demethylation, covalent modifications of histone proteins, and chromatin remodeling, create specific patterns of gene expression. Epigenetic deregulations are associated with oncogenesis,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d63a34c0607daf1276718329507c2955
https://www.mdpi.com/2072-6694/13/18/4586
https://www.mdpi.com/2072-6694/13/18/4586