Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Dmitry Y. Trofimov"'
Autor:
Maria V. Kuznetsova, Narine M. Tonoyan, Elena V. Trubnikova, Dmitry V. Zelensky, Ksenia A. Svirepova, Leila V. Adamyan, Dmitry Y. Trofimov, Gennady T. Sukhikh
Publikováno v:
Diseases, Vol 11, Iss 4, p 156 (2023)
Uterine leiomyomas are the most common benign tumors in women of childbearing age. They may lead to problems of conception or complications during the gestational period. The methods of treatment include surgical (myomectomy and hysterectomy, emboliz
Externí odkaz:
https://doaj.org/article/ec6ba124b4084c70968c9ab53229639a
Autor:
Kirill R. Butov, Natalia A. Karetnikova, Dmitry Y. Pershin, Dmitry Y. Trofimov, Mikhail A. Panteleev
Publikováno v:
Current Issues in Molecular Biology, Vol 44, Iss 6, Pp 2710-2716 (2022)
Procoagulant activity in amniotic fluid (AF) is positively correlated with phosphatidylserine (PS) and tissue factor (TF)-expressing(+) extracellular vesicles (EVs). However, it is unknown if pathological fetal conditions may affect the composition,
Externí odkaz:
https://doaj.org/article/8fe04449b7cf496584c5cc186c63f03c
Autor:
Elena A. Pudova, George S. Krasnov, Anastasiya A. Kobelyatskaya, Maria V. Savvateeva, Maria S. Fedorova, Vladislav S. Pavlov, Kirill M. Nyushko, Andrey D. Kaprin, Boris Y. Alekseev, Dmitry Y. Trofimov, Gennady T. Sukhikh, Anastasiya V. Snezhkina, Anna V. Kudryavtseva
Publikováno v:
Frontiers in Genetics, Vol 11 (2021)
Prostate cancer (PC) is one of the most common cancers among men worldwide, and advanced PCs, such as locally advanced PC (LAPC) and castration-resistant PC (CRPC), present the greatest challenges in clinical management. Current indicators have limit
Externí odkaz:
https://doaj.org/article/36eca3fb79ac491ea97efade78208265
Autor:
Maria S. Fedorova, Anastasiya V. Snezhkina, Anastasiya V. Lipatova, Vladislav S. Pavlov, Anastasiya A. Kobelyatskaya, Zulfiya G. Guvatova, Elena A. Pudova, Maria V. Savvateeva, Irina A. Ishina, Tatiana B. Demidova, Nadezhda N. Volchenko, Dmitry Y. Trofimov, Gennady T. Sukhikh, George S. Krasnov, Anna V. Kudryavtseva
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
The NETO2 gene (neuropilin and tolloid-like 2) encodes a protein that acts as an accessory subunit of kainate receptors and is predominantly expressed in the brain. Upregulation of NETO2 has been observed in several tumors; however, its role in tumor
Externí odkaz:
https://doaj.org/article/b79f2c8e9c4e4da8aee7ca3391d15a78
Autor:
Maria V. Kuznetsova, Nelly S. Sogoyan, Andrew J. Donnikov, Dmitry Y. Trofimov, Leila V. Adamyan, Natalia D. Mishina, Jekaterina Shubina, Dmitry V. Zelensky, Gennady T. Sukhikh
Publikováno v:
Biomedicines, Vol 10, Iss 2, p 508 (2022)
In order to determine genetic loci associated with decreasing risk of uterine leiomyomata (UL), a genome-wide association study (GWAS) was performed. We analyzed a group of patients with a family history of UL and a control group consisting of patien
Externí odkaz:
https://doaj.org/article/6592f1a327dc4635b5a0b95f4c7710c8
Autor:
Jekaterina Shubina, Ilya Y. Barkov, Olga K. Stupko, Maria V. Kuznetsova, Andrey Y. Goltsov, Taisya O. Kochetkova, Dmitry Y. Trofimov, Gennady T. Sukhikh
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 10, Pp n/a-n/a (2020)
Abstract Background PWS is challenging to diagnose prenatally due to a lack of precise and well‐characterized fetal phenotypes and noninvasive markers. Here we present the case of prenatal diagnosis of Prader‐Willi syndrome, which was suspected w
Externí odkaz:
https://doaj.org/article/56a5d6807763434d9ebe6ac65825c5e6
Autor:
Anastasiya A. Kobelyatskaya, Elena A. Pudova, Anastasiya V. Snezhkina, Maria S. Fedorova, Vladislav S. Pavlov, Zulfiya G. Guvatova, Maria V. Savvateeva, Nataliya V. Melnikova, Alexey A. Dmitriev, Dmitry Y. Trofimov, Gennady T. Sukhikh, Kirill M. Nyushko, Boris Y. Alekseev, Sergey V. Razin, George S. Krasnov, Anna V. Kudryavtseva
Publikováno v:
Life, Vol 11, Iss 6, p 588 (2021)
Currently, seven molecular subtypes of prostate cancer (PCa) are known, the most common of which being the subtype characterized by the presence of the TMPRSS2–ERG fusion transcript. While there is a considerable amount of work devoted to the influ
Externí odkaz:
https://doaj.org/article/18b6424550a34b7c85479c71d805dea8