Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Maria S. Pokrovskaya"'
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:
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
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
Autor:
A. V. Kiseleva, Petr Slominsky, Olga V. Kurilova, Alexey N Meshkov, Irina A. Efimova, Eleonora Khlebus, Svetlana A. Shalnova, A. I. Ershova, Olga P Skirko, M. V. Klimushina, Mikhail G. Divashuk, Oxana Drapkina, Anastasia Zharikova, Evgeniia Sotnikova, Maria S. Pokrovskaya
Publikováno v:
Pharmacogenomics and Personalized Medicine. 13:679-686
Purpose Cystic fibrosis (CF) is one of the most common monogenic diseases with an autosomal recessive inheritance. Carrier screening leads to a reduction in the number of children born with CF disease. The aim of this study was to develop the custom
Autor:
Maria S. Pokrovskaya, Oxana Drapkina, Victoria A. Metelskaya, Irina A. Efimova, Oksana Victorovna Sivakova, Aleksey Nikolaevich Meshkov, Svetlana A. Shalnova
Publikováno v:
Personalized Medicine. 16:501-509
The National Medical Research Center for Preventive Medicine of Russia (NMRCPM) conducts epidemiological and clinical research for the development of personalized medicine. This is why NMRCPM has faced the problem of how to standardize preanalytical
Autor:
Vladimir Barskiy, Valentin Sinitsyn, Mikhail G. Divashuk, Evgeniia Sotnikova, Alexey N Meshkov, O. V. Kulikova, Greta Marie Pohl, Hendrik Milting, Sergey Koretskiy, Elena Mershina, A. V. Kiseleva, Maria S. Pokrovskaya, M. V. Klimushina, Sergey Boytsov, Andreas Brodehl, M. S. Kharlap, R. P. Myasnikov, Anastasia Zharikova, Oxana Drapkina, E. N. Basargina, L. A. Gandaeva
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 6775, p 6775 (2021)
International Journal of Molecular Sciences
International Journal of Molecular Sciences
Left ventricular non-compaction cardiomyopathy (LVNC) is a rare heart disease, with or without left ventricular dysfunction, which is characterized by a two-layer structure of the myocardium and an increased number of trabeculae. The study of familia
Autor:
Ekaterina A. Snigir, Olga V. Kurilova, Olga P Skirko, A. V. Kiseleva, Malyshev Pp, A.D. Blokhina, Alexey N Meshkov, Rozhkova Ta, Vasily E. Ramensky, Alexsandra Akinshina, Daria A. Kashtanova, Anna Bukaeva, V V Kukharchuk, Valeriya Mikova, Mikhail G. Divashuk, Maria S. Pokrovskaya, Alena Limonova, A. I. Ershova, Zukhra Khasanova, Oxana Drapkina, Anna Petukhova, Evgeniia Sotnikova, Sergey Boytsov, Evgenia Zotova, Sergey I Mitrofanov, Valentin V. Makarov, Anastasia Zharikova, Sergey Yudin
Publikováno v:
Genes
Volume 12
Issue 1
Genes, Vol 12, Iss 66, p 66 (2021)
Volume 12
Issue 1
Genes, Vol 12, Iss 66, p 66 (2021)
Familial hypercholesterolemia (FH) is a common autosomal codominant disorder, characterized by elevated low-density lipoprotein cholesterol levels causing premature atherosclerotic cardiovascular disease. About 2900 variants of LDLR, APOB, and PCSK9
Autor:
Stanislav Poyarkov, Maria S. Pokrovskaya, Aalexey Novoselov, Tamara Mania, Marina Aksenova, Zlata Fedec, Anna Makovezkaya, Angelika V. Zagainova, Valentin V. Makarov, Andrey Kirilov, Lyudmila Khripach, Oxana Drapkina, Sergey Yudin, Anastasia Kaburova, Boris Zaitchik
Background Chronic heart failure (CHF) affects approximately 26 million people worldwide. Nearly half of CHF patients develop heart failure with preserved ejection fraction (HFpEF), which is associated with myocardial hypertrophy and fibrosis. Althou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b2da95e0809d6adc0471519153c63f30
https://doi.org/10.21203/rs.3.rs-94727/v1
https://doi.org/10.21203/rs.3.rs-94727/v1
Autor:
Maria S. Pokrovskaya, Evgeniia Sotnikova, A. I. Ershova, A. V. Kiseleva, Eleonora Khlebus, Svetlana A. Shalnova, Irina A. Efimova, Petr Slominsky, Olga V. Kurilova, Oxana Drapkina, M. V. Klimushina, Anastasia Zharikova, Olga P Skirko, Alexey N Meshkov, Mikhail G. Divashuk
Publikováno v:
Journal of Personalized Medicine, Vol 10, Iss 140, p 140 (2020)
Journal of Personalized Medicine
Volume 10
Issue 3
Journal of Personalized Medicine
Volume 10
Issue 3
Genetic screening is an advanced tool for reducing recessive disease burden. Nowadays, it is still unclear as to the number of genes or their variants that are necessary for effective screening. This paper describes the development of a carrier scree
Autor:
Anna R. Shuvalova, Andrey M. Sarana, Dmitrii V. Gladyshev, Sergey G. Scherbak, Oksana Victorovna Sivakova, Evgenii V. Vasiliev, Andrey S. Glotov, Oleg S. Glotov, Yury A. Barbitoff, Oxana Drapkina, Dmitrii E. Polev, Alexander V. Predeus, Maria S. Pokrovskaya, Yulia A. Nasykhova, Elena A. Serebryakova, Aleksey Nikolaevich Meshkov, Stanislav P. Urazov
Publikováno v:
Genes
GENES
Volume 9
Issue 8
Genes, Vol 9, Iss 8, p 415 (2018)
GENES
Volume 9
Issue 8
Genes, Vol 9, Iss 8, p 415 (2018)
Type 2 diabetes (T2D) and obesity are common chronic disorders with multifactorial etiology. In our study, we performed an exome sequencing analysis of 110 patients of Russian ethnicity together with a multi-perspective approach based on biologically