Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Artem E. Komissarov"'
Autor:
Olga I. Bolshakova, Alina A. Borisenkova, Ilya M. Golomidov, Artem E. Komissarov, Alexandra D. Slobodina, Elena V. Ryabova, Irina S. Ryabokon, Evgenia M. Latypova, Elizaveta E. Slepneva, Svetlana V. Sarantseva
Publikováno v:
Cells, Vol 12, Iss 1, p 170 (2022)
Huntington’s disease (HD) is one of the human neurodegenerative diseases for which there is no effective treatment. Therefore, there is a strong demand for a novel neuroprotective agent that can alleviate its course. Fullerene derivatives are consi
Externí odkaz:
https://doaj.org/article/a0538d5a2d764febb664779f6a1c9273
Autor:
Darya A. Golovkina, Elena V. Zhurishkina, Olga N. Ayrapetyan, Artem E. Komissarov, Anastasiya S. Krylova, Elizaveta N. Vinogradova, Stepan V. Toshchakov, Filipp K. Ermilov, Artak M. Barsegyan, Anna A. Kulminskaya, Irina M. Lapina
Publikováno v:
Foods, Vol 12, Iss 1, p 47 (2022)
Kombucha tea was made by the fermentation of SCOBY culture of green tea broth with the addition of Fucus vesiculosus algae extract, Cetraria islandica lichen extract and their mixture. Kombucha was also made without the herbal supplements as a contro
Externí odkaz:
https://doaj.org/article/cd79cf93cca94f75aeafe1c50e406afe
Autor:
Pavel A. Melentev, Elena V. Ryabova, Nina V. Surina, Darya R. Zhmujdina, Artem E. Komissarov, Ekaterina A. Ivanova, Natalia P. Boltneva, Galina F. Makhaeva, Mariana I. Sliusarenko, Andriy S. Yatsenko, Iryna I. Mohylyak, Nataliya P. Matiytsiv, Halyna R. Shcherbata, Svetlana V. Sarantseva
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 15, p 8275 (2021)
Various neurodegenerative disorders are associated with human NTE/PNPLA6 dysfunction. Mechanisms of neuropathogenesis in these diseases are far from clearly elucidated. Hereditary spastic paraplegia belongs to a type of neurodegeneration associated w
Externí odkaz:
https://doaj.org/article/fe55db69c04c4a98b30e17e6ce666416
Autor:
Elena V. Ryabova, Pavel A. Melentev, Artem E. Komissarov, Nina V. Surina, Ekaterina A. Ivanova, Natalia Matiytsiv, Halyna R. Shcherbata, Svetlana V. Sarantseva
Publikováno v:
Cells, Vol 10, Iss 3, p 529 (2021)
Glia are crucial for the normal development and functioning of the nervous system in many animals. Insects are widely used for studies of glia genetics and physiology. Drosophila melanogaster surface glia (perineurial and subperineurial) form a blood
Externí odkaz:
https://doaj.org/article/367815fd467a42e5878e28143fd6c021
Autor:
Ilia M. Golomidov, Evgenia M. Latypova, Elena V. Ryabova, Olga I. Bolshakova, Artem E. Komissarov, Svetlana V. Sarantseva
Publikováno v:
Journal of Neurogenetics. 36:1-10
Parkinson’s disease (PD) is a neurodegenerative disease characterised by the formation of Lewy bodies and progressive loss of dopaminergic (DA) neurons in the substantia nigra. Lewy bodies mainly consist of α-synuclein, which plays a critical role
Autor:
Elena Shagimardanova, Leila H. Shigapova, Margarita V. Savina, Svetlana V. Sarantseva, Evgenija A. Kochenova, Alexandra D. Slobodina, Olga E. Agranovich, Artem E Komissarov, Svetlana I. Trofimova, Elena L. Gabbasova
Publikováno v:
Pediatric Traumatology, Orthopaedics and Reconstructive Surgery. 8:333-342
Congenital contractures are a heterogeneous group of various diseases with different etiology and pathogenesis. The article describes a family case of hereditary sensory-motor polyneuropathy caused by a mutation with 943GA (p Arg315Trp) in the TRPV4
Autor:
Nina V Surina, Pavel A. Melentev, Mariana I Sliusarenko, Artem E Komissarov, N. P. Boltneva, I. I. Mohylyak, Galina F. Makhaeva, Halyna R. Shcherbata, Andriy S. Yatsenko, Ekaterina A. Ivanova, Darya R Zhmujdina, N. P. Matiytsiv, Elena V Ryabova, S. V. Sarantseva
Publikováno v:
International Journal of Molecular Sciences
Volume 22
Issue 15
International Journal of Molecular Sciences, Vol 22, Iss 8275, p 8275 (2021)
Volume 22
Issue 15
International Journal of Molecular Sciences, Vol 22, Iss 8275, p 8275 (2021)
Various neurodegenerative disorders are associated with human NTE/PNPLA6 dysfunction. Mechanisms of neuropathogenesis in these diseases are far from clearly elucidated. Hereditary spastic paraplegia belongs to a type of neurodegeneration associated w
Autor:
Pavel A. Melentev, Artem E Komissarov, Darya R Zhmujdina, Svetlana V. Sarantseva, Elena V Ryabova
Publikováno v:
Neuroscience for Medicine and Psychology.