Zobrazeno 1 - 10
of 57
pro vyhledávání: '"Alexander S. Tanas"'
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-13 (2021)
Abstract The main types of thyroid neoplasms, follicular adenoma (FA), follicular thyroid carcinoma (FTC), classical and follicular variants of papillary carcinoma (clPTC and fvPTC), and anaplastic thyroid carcinoma (ATC), differ in prognosis, progre
Externí odkaz:
https://doaj.org/article/72b9d3fe521f46efad58e14192f452eb
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:
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:
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
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22ef7f03d73ecf4dc38b00694b2b83ab
https://doi.org/10.3390/cancers15051630
https://doi.org/10.3390/cancers15051630
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:
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c8128c9c63b7dcc79fd41a80a9b4f54
http://link.springer.com/article/10.1038/s41598-020-66197-1
http://link.springer.com/article/10.1038/s41598-020-66197-1
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
Autor:
Ekaterina A, Alekseeva, Olga V, Babenko, Valentina M, Kozlova, Tatiana L, Ushakova, Tatiana P, Kazubskaya, Marina V, Nemtsova, Galina G, Chesnokova, Dmitry S, Mikhaylenko, Irina V, Bure, Alexey I, Kalinkin, Ekaterina B, Kuznetsova, Alexander S, Tanas, Sergey I, Kutsev, Dmitry V, Zaletaev, Vladimir V, Strelnikov
Publikováno v:
Cancers
Simple Summary Some families with hereditary retinoblastoma exhibit mild phenotype with low penetrance and variable expressivity, including complete absence of clinical signs of the disease in some carriers of the germline RB1 mutation. The identific
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a67607cd9704d8aa22277248e4ec56d2
https://pubmed.ncbi.nlm.nih.gov/34680218
https://pubmed.ncbi.nlm.nih.gov/34680218