Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Anastasia A, Zharikova"'
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:
Anna A. Valyaeva, Maria A. Tikhomirova, Daria M. Potashnikova, Alexandra N. Bogomazova, Galina P. Snigiryova, Aleksey A. Penin, Maria D. Logacheva, Eugene A. Arifulin, Anna A. Shmakova, Diego Germini, Anastasia I. Kachalova, Aleena A. Saidova, Anastasia A. Zharikova, Yana R. Musinova, Andrey A. Mironov, Yegor S. Vassetzky, Eugene V. Sheval
Publikováno v:
PeerJ, Vol 10, p e13986 (2022)
An increased frequency of B-cell lymphomas is observed in human immunodeficiency virus-1 (HIV-1)-infected patients, although HIV-1 does not infect B cells. Development of B-cell lymphomas may be potentially due to the action of the HIV-1 Tat protein,
Externí odkaz:
https://doaj.org/article/628949be0414488794c8155eeb09a019
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:
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:
Nucleic Acids Research. 50:W534-W540
Extensive amounts of data from next-generation sequencing and omics studies have led to the accumulation of information that provides insight into the evolutionary landscape of related proteins. Here, we present OrthoQuantum, a web server that allows
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6b3ea8c5021fc66410f1f3d63996417
https://doi.org/10.1093/nar/gkac385
https://doi.org/10.1093/nar/gkac385
Publikováno v:
Genes, Vol 13, Iss 14, p 14 (2022)
Genes
Genes
Parkinson’s disease (PD) is a widespread neuronal degenerative disorder with unexplored etiology. It is associated with various pathological events. In particular, the prefrontal cortex Brodmann area 9 (BA9) region is affected in PD. This frontal l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::004a1673f63a275b5c01b483b0ec5443
https://www.mdpi.com/2073-4425/13/1/14
https://www.mdpi.com/2073-4425/13/1/14
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5546a6dbbc436882c10a5191413271e5
Autor:
Anastasia Victorovna Blokhina, Alexandra Igorevna Ershova, Elena Vitalievna Zyatenkova, Alexey Nikolaevich Meshkov, Anna Vitalievna Kiseleva, Marina Vyacheslavovna Klimushina, Evgeniia Andreevna Sotnikova, Olga Petrovna Skirko, Anastasia Alexandrovna Zharikova, Yurii Valerievich Doludin, Maria Sergeevna Kharlap, Oxana Mikhailovna Drapkina
Publikováno v:
Personalized medicine. 19(2)
The results of molecular genetic testing may affect recommended treatment or therapeutic decisions and risk assessment, may help with identification of family members at risk. Here, we report a case of a young patient with a paradoxical combination o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1cd14c15f3ddfee1f0fc5ee4a7fc3de
https://pubmed.ncbi.nlm.nih.gov/35060774
https://pubmed.ncbi.nlm.nih.gov/35060774
Autor:
Vasily A. Popkov, Anastasia A. Zharikova, Evgenia A. Demchenko, Nadezda V. Andrianova, Dmitry B. Zorov, Egor Y. Plotnikov
Publikováno v:
International Journal of Molecular Sciences; Volume 23; Issue 1; Pages: 483
International Journal of Molecular Sciences, Vol 23, Iss 483, p 483 (2022)
International Journal of Molecular Sciences
International Journal of Molecular Sciences, Vol 23, Iss 483, p 483 (2022)
International Journal of Molecular Sciences
Uremic retention solutes are the compounds that accumulate in the blood when kidney excretory function is impaired. Some of these compounds are toxic at high concentrations and are usually known as “uremic toxins”. The cumulative detrimental effe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65580f185f51a808f7e0190c8b11d44d
Autor:
Andrey V. Marakhonov, Andreas Brodehl, Roman P. Myasnikov, Peter A. Sparber, Anna V. Kiseleva, Olga V. Kulikova, Alexey N. Meshkov, Anastasia A. Zharikova, Serguey N. Koretsky, Maria S. Kharlap, Caroline Stanasiuk, Elena A. Mershina, Valentin E. Sinitsyn, Alexey O. Shevchenko, Natalia P. Mozheyko, Oksana M. Drapkina, Sergey A. Boytsov, Hendrik Milting, Mikhail Yu. Skoblov
Publikováno v:
Human Mutation. 40
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1d1ea98f70c37af219c89d2cc8e27420
https://doi.org/10.1002/humu.23796
https://doi.org/10.1002/humu.23796