Zobrazeno 1 - 10
of 10
pro vyhledávání: '"T S, Usenko"'
Autor:
A. I. Bezrukova, K. S. Basharova, I. V. Miliukhina, A. A. Timofeeva, K. A. Senkevich, S. N. Pchelina, T. S. Usenko
Publikováno v:
Учёные записки Санкт-Петербургского государственного медицинского университета им. Акад. И.П. Павлова, Vol 29, Iss 1, Pp 37-45 (2022)
The objective of the study was to validate our previous results obtained during the transcriptome analysis of the primary culture of peripheral blood macrophages in patients with Parkinson's disease associated with mutations in the GBA gene (GBA-PD)
Externí odkaz:
https://doaj.org/article/f09de606945041a1912502103af8acf2
Autor:
T. S. Usenko, K. A. Senkevich, A. I. Bezrukova, G. V. Baydakova, K. S. Basharova, A. S. Zhuravlev, E. V. Gracheva, A. V. Kudrevatykh, I. V. Miliukhina, I. V. Krasakov, L. A. Khublarova, I. V. Fursova, D. V. Zakharov, A. A. Timofeeva, Y. A. Irishina, E. I. Palchikova, N. M. Zalutskaya, A. K. Emelyanov, E. Y. Zakharova, S. N. Pchelina
Publikováno v:
Molecular Neurobiology. 59:2277-2287
Autor:
S. N. Pchelina, T. S. Usenko, N. A. Bogankova, A. F. Yakimovskii, A. K. Emelyanov, T. V. Vavilova, A. L. Shvartsman
Publikováno v:
Медицинская иммунология, Vol 14, Iss 1-2, Pp 149-152 (2014)
Abstract. Progressive loss of dopaminergic neurons from substantia nigra is the major pathomorphologicasign in Parkinson’s disease (PD). Neuronal death is suggested to occur by programmed cell death (apoptosis) in PD patients, thus being involved i
Externí odkaz:
https://doaj.org/article/5554853da64c40bbacf5a76c91bd7f11
Autor:
T S, Usenko, K A, Senkevich, A I, Bezrukova, G V, Baydakova, K S, Basharova, A S, Zhuravlev, E V, Gracheva, A V, Kudrevatykh, I V, Miliukhina, I V, Krasakov, L A, Khublarova, I V, Fursova, D V, Zakharov, A A, Timofeeva, Y A, Irishina, E I, Palchikova, N M, Zalutskaya, A K, Emelyanov, E Y, Zakharova, S N, Pchelina
Publikováno v:
Molecular neurobiology. 59(4)
The synucleinopathies are a group of neurodegenerative diseases characterized by the oligomerization of alpha-synuclein protein in neurons or glial cells. Recent studies provide data that ceramide metabolism impairment may play a role in the pathogen
Autor:
G.N. Salogub, M. V. Gorchakova, T. S. Usenko, E Yu Zakharova, M. A. Nikolaev, Yu. P. Koval’chuk, S. N. Pchelina, K. A. Senkevich, A E Kopytova, O. Berkovich, G. V. Baidakova, A. K. Emel’yanov
Publikováno v:
Cell and Tissue Biology. 13:100-106
Decreased activity of glucocerebrosidase (GCase) as a result of mutations in the GBA gene causes Gaucher’s disease (GD), which belongs to the group of lysosomal storage disorders. The risk of Parkinson’s disease in homo- and heterozygous carriers
Autor:
T S, Usenko, V V, Miroshnikova, E A, Bazhenova, M A, Nikolaev, D L, Brovin, A E, Kopytova, A A, Panteleeva, J, He, I A, Semenova, N D, Razgildina, A E, Neimark, O A, Berkovich, O D, Belyaeva, E I, Baranova, S N, Pchelina
Publikováno v:
Tsitologiia. 59(1)
The adipose tissue is considered today as an endocrine organ in which tissue-specific regulation of gene expression plays a key role in the processes of development of obesity and comorbidities, such as diabetes and cardiovascular disease. The presen
Publikováno v:
Molecular Biology. 48:1-10
Parkinson’s disease (PD) is a common neurodegenerative disorder whose symptoms are consistent with death of dopaminergic neurons in the substantia nigra of the brain. The pathogenesis of PD involves several factors, such as α-synuclein aggregation
Autor:
N A Bogan'kova, A L Shvartsman, A F Iakimovskiĭ, T. V. Vavilova, S N Pchelina, A K Emel'ianov, T S Usenko
Publikováno v:
Cell and Tissue Biology. 6:171-175
Mutations in the Leucine Reach Repeat Kinase 2 (LRRK2) gene are the most frequent cause of familial Parkinson's disease (PD). Although the precise physiological and pathological role of LRRK2 is unclear, a direct link between mutant LRRK2 and apoptos
Publikováno v:
Europe PubMed Central
Parkinson's disease (PD) is a common neurodegenerative disorder. Disease symptoms correlate with the degeneration of dopaminergic neurons in substantia nigra pars compacta. A number of factors are supposed to take part in PD pathogenesis including al
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::cfd6c2167a87fd230bff210615d6d069
http://europepmc.org/abstract/med/25842821
http://europepmc.org/abstract/med/25842821
Autor:
T S, Usenko, A K, Emel'ianov, A F, Iakimovskiĭ, N A, Bogan'kova, T V, Vavilova, A L, Shvartsman, S N, Pchelina
Publikováno v:
Europe PubMed Central
Mutations in the Leucine Reach Repeat Kinase 2 (LRRK2) gene are the most frequent cause of familial Parkinson's disease (PD). Although the precise physiological and pathological role of LRRK2 is unclear, a direct link between mutant LRRK2 and apoptos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::3401441494a8d90a5358f52e82016987
http://europepmc.org/abstract/med/22567899
http://europepmc.org/abstract/med/22567899