Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Yuri V. Vyatkin"'
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, Anna V. Kiseleva, Evgeniia A. Sotnikova, Anastasia A. Zharikova, Marija Zaicenoka, Yuri V. Vyatkin, Vasily E. Ramensky, Vladimir A. Kutsenko, Svetlana A. Shalnova, Alexey N. Meshkov, Oxana M. Drapkina
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 17, p 13159 (2023)
Familial dysbetalipoproteinemia (FD) is a highly atherogenic genetically based lipid disorder with an underestimated actual prevalence. In recent years, several biochemical algorithms have been developed to diagnose FD using available laboratory test
Externí odkaz:
https://doaj.org/article/1ff31eb3e3684a459155ae8a3c67abaf
Autor:
Elena V. Grigor'eva, Elena S. Drozdova, Diana A. Sorogina, Anastasia A. Malakhova, Sofia V. Pavlova, Yuri V. Vyatkin, Elena A. Khabarova, Jamil A. Rzaev, Sergey P. Medvedev, Suren M. Zakian
Publikováno v:
Stem Cell Research, Vol 59, Iss , Pp 102651- (2022)
Mutation in the glucocerebrosidase encoding gene (GBA) is one of the most frequent genetic cause of Parkinson's disease. ICGi034-A induced pluripotent stem cell (iPSC) line obtained by reprogramming peripheral blood mononuclear cells (PBMCs) of a pat
Externí odkaz:
https://doaj.org/article/6e4280cca5bb42a1b8c025ab96ee1e67
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:
Vladimir V. Sherstyuk, Sergey P. Medvedev, Evgeniy A. Elisaphenko, Evgeniya A. Vaskova, Maxim T. Ri, Yuri V. Vyatkin, Olga V. Saik, Dmitry N. Shtokalo, Evgeniy A. Pokushalov, Suren M. Zakian
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-12 (2017)
Abstract MicroRNAs (miRNAs) constitute a class of small noncoding RNAs that plays an important role in the post-transcriptional regulation of gene expression. Much evidence has demonstrated that miRNAs are involved in regulating the human and mouse p
Externí odkaz:
https://doaj.org/article/4290a1fa61c244d4b5bfea8034b6f997
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:
Elena V. Grigor'eva, Elena S. Drozdova, Diana A. Sorogina, Anastasia A. Malakhova, Sofia V. Pavlova, Yuri V. Vyatkin, Elena A. Khabarova, Jamil A. Rzaev, Sergey P. Medvedev, Suren M. Zakian
Publikováno v:
Stem Cell Research, Vol 59, Iss, Pp 102651-(2022)
Mutation in the glucocerebrosidase encoding gene (GBA) is one of the most frequent genetic cause of Parkinson's disease. ICGi034-A induced pluripotent stem cell (iPSC) line obtained by reprogramming peripheral blood mononuclear cells (PBMCs) of a pat