Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Marija Zaicenoka"'
Autor:
Anna Bukaeva, Roman Myasnikov, Olga Kulikova, Alexey Meshkov, Anna Kiseleva, Anna Petukhova, Evgenia Zotova, Peter Sparber, Alexandra Ershova, Evgeniia Sotnikova, Maria Kudryavtseva, Anastasia Zharikova, Sergey Koretskiy, Elena Mershina, Vasily Ramensky, Marija Zaicenoka, Yuri Vyatkin, Alisa Muraveva, Alexandra Abisheva, Tatiana Nikityuk, Valentin Sinitsyn, Mikhail Divashuk, Elena Dadali, Maria Pokrovskaya, Oxana Drapkina
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 14, p 7556 (2024)
A genetic diagnosis of primary cardiomyopathies can be a long-unmet need in patients with complex phenotypes. We investigated a three-generation family with cardiomyopathy and various extracardiac abnormalities that had long sought a precise diagnosi
Externí odkaz:
https://doaj.org/article/e5f8369f251a415b864ae0aeb61178b7
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:
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, Vol 12, Iss 7, p 1132 (2022)
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
Externí odkaz:
https://doaj.org/article/82e60cde053b406d994a09b529f74430