Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Ivan N. Vlasov"'
Autor:
Elena V. Filatova, Natalia S. Krylova, Ivan N. Vlasov, Maria S. Maslova, Natalia G. Poteshkina, Petr A. Slominsky, Maria I. Shadrina
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 11, Pp n/a-n/a (2021)
Abstract Background Hypertrophic cardiomyopathy (HCM), described as the presence of hypertrophy of left ventricular, is the most prevalent heritable cardiovascular disease with predominantly an autosomal dominant type of inheritance. However, pathoge
Externí odkaz:
https://doaj.org/article/2e3c0cb32a2d42dabacb2b2e3626ff14
Autor:
Ekaterina I. Semenova, Ivan N. Vlasov, Suzanna A. Partevian, Anna V. Rosinskaya, Ivan N. Rybolovlev, Petr A. Slominsky, Maria I. Shadrina, Anelya Kh. Alieva
Publikováno v:
Cells, Vol 11, Iss 16, p 2599 (2022)
Parkinson’s disease (PD) is one of the most common neurodegenerative diseases. Investigating individuals with the most identical genetic background is optimal for minimizing the genetic contribution to gene expression. These individuals include mon
Externí odkaz:
https://doaj.org/article/6bbde47c4a0b41de95b91dc26dc7d5fd
Autor:
Ivan N. Vlasov, Anelya Kh. Alieva, Ekaterina V. Novosadova, Elena L. Arsenyeva, Anna V. Rosinskaya, Suzanna A. Partevian, Igor A. Grivennikov, Maria I. Shadrina
Publikováno v:
Cells, Vol 10, Iss 12, p 3478 (2021)
Parkinson’s Disease (PD) is a widespread severe neurodegenerative disease that is characterized by pronounced deficiency of the dopaminergic system and disruption of the function of other neuromodulator systems. Although heritable genetic factors c
Externí odkaz:
https://doaj.org/article/33881fe906cc4ba3b97805b6b0673fc6
Autor:
Marina V. Shulskaya, Anelya Kh. Alieva, Ivan N. Vlasov, Vladimir V. Zyrin, Ekaterina Yu. Fedotova, Natalia Yu. Abramycheva, Tatiana S. Usenko, Andrei F. Yakimovsky, Anton K. Emelyanov, Sofya N. Pchelina, Sergei N. Illarioshkin, Petr A. Slominsky, Maria I. Shadrina
Publikováno v:
Frontiers in Aging Neuroscience, Vol 10 (2018)
Background: Parkinson’s disease (PD) is a complex disease with its monogenic forms accounting for less than 10% of all cases. Whole-exome sequencing (WES) technology has been used successfully to find mutations in large families. However, because o
Externí odkaz:
https://doaj.org/article/060d9b909e7946ffb39f93050ede2a8d
Autor:
Anna V Rosinskaya, M.M. Rudenok, E. L. Arsenyeva, Anelya Kh. Alieva, Ivan N Vlasov, Petr Slominsky, E. V. Novosadova, Igor A. Grivennikov, Maria Shadrina
Publikováno v:
Journal of Molecular Neuroscience
Parkinson’s disease (PD) is one of the most common neurodegenerative diseases. In most cases, the development of the disease is sporadic and is not associated with any currently known mutations associated with PD. It is believed that changes associ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::28a3ceb6bed2bc61fa0efd988de383b9
https://doi.org/10.1007/s12031-019-01452-3
https://doi.org/10.1007/s12031-019-01452-3
Autor:
N G Poteshkina, Maria S. Maslova, Maria Shadrina, Elena V. Filatova, Ivan N Vlasov, Petr Slominsky, N S Krylova
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 11, Pp n/a-n/a (2021)
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine
Background Hypertrophic cardiomyopathy (HCM), described as the presence of hypertrophy of left ventricular, is the most prevalent heritable cardiovascular disease with predominantly an autosomal dominant type of inheritance. However, pathogenic allel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::deda2030929d0793d576cb47effa5e63
https://doi.org/10.1002/mgg3.1808
https://doi.org/10.1002/mgg3.1808