Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Anna V Kiseleva"'
Autor:
Mikhail G Divashuk, Thi Mai L Khuat, Pavel Yu Kroupin, Ilya V Kirov, Dmitry V Romanov, Anna V Kiseleva, Ludmila I Khrustaleva, Dmitry G Alexeev, Alexandr S Zelenin, Marina V Klimushina, Olga V Razumova, Gennady I Karlov
Publikováno v:
PLoS ONE, Vol 11, Iss 4, p e0154241 (2016)
Speciation and allopolyploidization in cereals may be accompanied by dramatic changes in abundance of centromeric repeated transposable elements. Here we demonstrate that the reverse transcriptase part of Ty3/gypsy centromeric retrotransposon (RT-CR)
Externí odkaz:
https://doaj.org/article/c59cb8cb33ec4888a4d50173cf2f789a
Autor:
Alexey N. Meshkov, Roman P. Myasnikov, Anna V. Kiseleva, Olga V. Kulikova, Evgeniia A. Sotnikova, Maria M. Kudryavtseva, Anastasia A. Zharikova, Sergey N. Koretskiy, Elena A. Mershina, Vasily E. Ramensky, Marija Zaicenoka, Yuri V. Vyatkin, Maria S. Kharlap, Tatiana G. Nikityuk, Valentin E. Sinitsyn, Mikhail G. Divashuk, Vladimir A. Kutsenko, Elena N. Basargina, Vladimir I. Barskiy, Nataliya A. Sdvigova, Olga P. Skirko, Irina A. Efimova, Maria S. Pokrovskaya, Oxana M. Drapkina
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 10 (2023)
BackgroundLeft ventricular noncompaction (LVNC) cardiomyopathy is a disorder that can be complicated by heart failure, arrhythmias, thromboembolism, and sudden cardiac death. The aim of this study is to clarify the genetic landscape of LVNC in a larg
Externí odkaz:
https://doaj.org/article/61d78b7b95c7462a967d6fde37b4102a
Autor:
Anastasia V. Blokhina, Alexandra I. Ershova, Alexey N. Meshkov, Anna V. Kiseleva, Marina V. Klimushina, Anastasia A. Zharikova, Evgeniia A. Sotnikova, Vasily E. Ramensky, Oxana M. Drapkina
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 9 (2022)
One of the most common autosomal dominant disorders is familial hypercholesterolemia (FH), causing premature atherosclerotic cardiovascular diseases and a high risk of death due to lifelong exposure to elevated low-density lipoprotein cholesterol (LD
Externí odkaz:
https://doaj.org/article/b2d0004e163a4fe693bff5c150365aa7
Autor:
Olga V. Kulikova, Roman P. Myasnikov, Elena A. Mershina, Polina S. Pilus, Sergei N. Koretskiy, Aleksei N. Meshkov, Anna V. Kiseleva, Mariia S. Kharlap, Valentin E. Sinitsyn, Nataliia A. Sdvigova, Leila A. Gandaeva, Vladimir I. Barskiy, Yuliia V. Derevnina, Olga P. Zharova, Elena N. Basargina, Sergey A. Boytsov, Oksana M. Drapkina
Publikováno v:
Терапевтический архив, Vol 93, Iss 4, Pp 381-388 (2021)
Aim. To analyze and demonstrate various phenotypes in patients with familial left ventricular noncompaction (LVNC). Materials and methods. In 2013 was created a multicenter registry of LVNC patients. On its basis 30 families with a familial LVNC w
Externí odkaz:
https://doaj.org/article/48bd70e002424e6fb802d25d3a8f2b88
Autor:
Alena S. Limonova, Alexandra I. Ershova, Alexey N. Meshkov, Anna V. Kiseleva, Mikhail G. Divashuk, Marina V. Kurkina, Oxana M. Drapkina
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 8 (2022)
We reported a case of sitosterolemia, which is a rare genetic disease, characterized by increased plant sterol absorption and great heterogeneity of clinical manifestations. Our patient was initially referred to the lipid clinic due to high cholester
Externí odkaz:
https://doaj.org/article/5c21cccf1e2b488898712ae83db851c8
Autor:
Vasily E. Ramensky, Alexandra I. Ershova, Marija Zaicenoka, Anna V. Kiseleva, Anastasia A. Zharikova, Yuri V. Vyatkin, Evgeniia A. Sotnikova, Irina A. Efimova, Mikhail G. Divashuk, Olga V. Kurilova, Olga P. Skirko, Galina A. Muromtseva, Olga A. Belova, Svetlana A. Rachkova, Maria S. Pokrovskaya, Svetlana A. Shalnova, Alexey N. Meshkov, Oxana M. Drapkina
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
We performed a targeted sequencing of 242 clinically important genes mostly associated with cardiovascular diseases in a representative population sample of 1,658 individuals from the Ivanovo region northeast of Moscow. Approximately 11% of 11,876 de
Externí odkaz:
https://doaj.org/article/aa7bf729e49a4e249249cfb790f6db90
Publikováno v:
Vestnik Chuvashskogo universiteta. :74-82
Purpose of the study. The relevance of the article is due to scientific interest in recent events of modern Russia, the process of formation of executive and representative authorities in Russian municipalities. At the same time, historical science i
Autor:
Alena S. Limonova, Alexandra I. Ershova, Alexey N. Meshkov, Anna V. Kiseleva, Mikhail G. Divashuk, Vladimir A. Kutsenko, Oxana M. Drapkina
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 7 (2021)
We present a case of a 40-year-old male with premature atherosclerosis, with evidence of both eruptive and tendinous xanthomas, which could imply an increase in both low-density lipoprotein (LDL) and triglyceride (TG) levels. However, his LDL was 2.0
Externí odkaz:
https://doaj.org/article/0b50748fd00040b899fec4263de85b6b
Publikováno v:
Historical Search. 3:44-55
The relevance of the article is to highlight previously unexplored process showing evolvement of local self-government bodies in modern Russia when a new system of public relations was created before the adoption of the country’s Constitution in 19
Autor:
Evgeniia A. Sotnikova, Anna V. Kiseleva, Vladimir A. Kutsenko, Anastasia A. Zharikova, Vasily E. Ramensky, Mikhail G. Divashuk, Yuri V. Vyatkin, Marina V. Klimushina, Alexandra I. Ershova, Karina Z. Revazyan, Olga P. Skirko, Marija Zaicenoka, Irina A. Efimova, Maria S. Pokrovskaya, Oksana V. Kopylova, Anush M. Glechan, Svetlana A. Shalnova, Alexey N. Meshkov, Oxana M. Drapkina
Publikováno v:
Journal of Personalized Medicine; Volume 12; Issue 7; Pages: 1132
Cystic fibrosis, phenylketonuria, alpha-1 antitrypsin deficiency, and sensorineural hearing loss are among the most common autosomal recessive diseases, which require carrier screening. The evaluation of population allele frequencies (AF) of pathogen