Zobrazeno 1 - 10
of 27
pro vyhledávání: '"A S Vetchinova"'
Publikováno v:
Анналы клинической и экспериментальной неврологии, Vol 17, Iss 4, Pp 58-63 (2023)
Introduction. Induced pluripotent stem cells (iPSCs) culturing allows modelling of neurodegenerative diseases in vitro and discovering its early biomarkers. Our objective was to evaluate the activity of genes involved in mitochondrial dynamics and
Externí odkaz:
https://doaj.org/article/107c1acb3d8d4fa09786d296a23f321a
Autor:
Anna S. Vetchinova, Marina R. Kapkaeva, Mikhail V. Ivanov, Kristina A. Kutukova, Natalia M. Mudzhiri, Lydia E. Frumkina, Anatoly V. Brydun, Vladimir S. Sukhorukov, Sergey N. Illarioshkin
Publikováno v:
Current Issues in Molecular Biology, Vol 45, Iss 10, Pp 8395-8411 (2023)
Parkinson’s disease (PD) is the second most common neurodegenerative disease. Some cases of PD may be caused by genetic factors, among which mutations in the LRRK2 and SNCA genes play an important role. To develop effective neuroprotective strategi
Externí odkaz:
https://doaj.org/article/92addc3dbffb49a99bb77514da92d9d0
Autor:
Yu. A. Shpilyukova, E. Yu. Fedotova, T. V. Pogoda, N. Yu. Abramycheva, A. S. Vetchinova, M. N. Zakharova, S. N. Illarioshkin
Publikováno v:
Нервно-мышечные болезни, Vol 8, Iss 2, Pp 33-41 (2018)
Externí odkaz:
https://doaj.org/article/fcec782708154077a2d6f1746820167a
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 17, p 9608 (2021)
Neurogenesis is a key mechanism of brain development and plasticity, which is impaired in chronic neurodegeneration, including Parkinson’s disease. The accumulation of aberrant α-synuclein is one of the features of PD. Being secreted, this protein
Externí odkaz:
https://doaj.org/article/e086492be2fe4c4abbddd090c388b69f
Publikováno v:
Анналы клинической и экспериментальной неврологии, Vol 9, Iss 4, Pp 59-64 (2017)
A number of fundamental breakthroughs in cellular and molecularbiology provided the basis for several modern sophisticatedapproaches to modeling of human neurological (primarily neurodegenerative)diseases. In particular, targeted genome editingby art
Externí odkaz:
https://doaj.org/article/090becf8972f4d6699a49bc04b485b9d
Autor:
N. Yu. Abramycheva, E. V. Lysogorskaya, Yu. S. Shpilyukova, A. S. Vetchinova, M. N. Zakharova, S. N. Illarioshkin
Publikováno v:
Нервно-мышечные болезни, Vol 6, Iss 4, Pp 21-27 (2017)
Externí odkaz:
https://doaj.org/article/bea568ff397243559b6cb15536752cc3
Publikováno v:
Neurochemical Journal. 15:359-366
Autor:
A. S. Vetchinova, N. Yu. Abramycheva, E. P. Nuzhnyi, S. A. Klyushnikov, M. N. Andreev, Sergei N. Illarioshkin, E. Yu. Fedotova
Publikováno v:
Russian neurological journal. 25:28-36
Introduction . Ataxia with impaired DNA repair is a group of inherited diseases with a wide range of neurological and extraneural manifestations. There are some difficulties in the differential diagnosis of this group of ataxias due to significant
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 9608, p 9608 (2021)
International Journal of Molecular Sciences
International Journal of Molecular Sciences
Neurogenesis is a key mechanism of brain development and plasticity, which is impaired in chronic neurodegeneration, including Parkinson’s disease. The accumulation of aberrant α-synuclein is one of the features of PD. Being secreted, this protein
Autor:
V. V. Simonova, Sergey N. Illarioshkin, Leonid G. Khaspekov, A S Vetchinova, E. V. Novosadova
Publikováno v:
Biochemistry (Moscow). 83:1040-1045
The prevalent form of familial parkinsonism is caused by mutations in the LRRK2 gene encoding for the mitochondrial protein kinase. In the review, we discuss possible causes of appearance of tetraploid cells in neuronal precursors obtained from induc