Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Olga A. Kondakova"'
Autor:
Dmitriy L. Granovskiy, Nelli S. Khudainazarova, Ekaterina A. Evtushenko, Ekaterina M. Ryabchevskaya, Olga A. Kondakova, Marina V. Arkhipenko, Marina V. Kovrizhko, Elena P. Kolpakova, Tatyana I. Tverdokhlebova, Nikolai A. Nikitin, Olga V. Karpova
Publikováno v:
Viruses, Vol 16, Iss 3, p 438 (2024)
Rotavirus infection is a leading cause of severe dehydrating gastroenteritis in children under 5 years of age. Although rotavirus-associated mortality has decreased considerably because of the introduction of the worldwide rotavirus vaccination, the
Externí odkaz:
https://doaj.org/article/726d9b38064a484a88af8c30cafcf465
New formulation of a recombinant anthrax vaccine stabilised with structurally modified plant viruses
Autor:
Dmitriy L. Granovskiy, Ekaterina M. Ryabchevskaya, Ekaterina A. Evtushenko, Olga A. Kondakova, Marina V. Arkhipenko, Tatiana B. Kravchenko, Irina V. Bakhteeva, Vitalii S. Timofeev, Nikolai A. Nikitin, Olga V. Karpova
Publikováno v:
Frontiers in Microbiology, Vol 13 (2022)
Anthrax is a disease caused by Bacillus anthracis. The most promising approach to the development of anthrax vaccine is use of the anthrax protective antigen (PA). At the same time, recombinant PA is a very unstable protein. Previously, the authors h
Externí odkaz:
https://doaj.org/article/c032d7ead96f40cca3b559631c88aff4
Autor:
Ekaterina M. Ryabchevskaya, Ekaterina A. Evtushenko, Dmitry L. Granovskiy, Peter A. Ivanov, Joseph G. Atabekov, Olga A. Kondakova, Nikolai A. Nikitin, Olga V. Karpova
Publikováno v:
Human Vaccines & Immunotherapeutics, Vol 17, Iss 2, Pp 560-565 (2021)
Anthrax is a zoonotic disease caused by the gram-positive spore-forming bacteria Bacillus anthracis. There is a need for safe, highly effective, long-term storage vaccine formulations for mass vaccination. However, the development of new subunit vacc
Externí odkaz:
https://doaj.org/article/ff134226c1d5462d8d222d5e8d3105d0
Autor:
Angelina O. Kovalenko, Ekaterina M. Ryabchevskaya, Ekaterina A. Evtushenko, Tatiana I. Manukhova, Olga A. Kondakova, Peter A. Ivanov, Marina V. Arkhipenko, Vladimir A. Gushchin, Nikolai A. Nikitin, Olga V. Karpova
Publikováno v:
Frontiers in Microbiology, Vol 13 (2022)
A recombinant vaccine candidate has been developed based on the major coronaviruses’ antigen (S protein) fragments and a novel adjuvant—spherical particles (SPs) formed during tobacco mosaic virus thermal remodeling. The receptor-binding domain a
Externí odkaz:
https://doaj.org/article/9e193bbd791f498e9a5a83183e379092
Autor:
Ekaterina M. Ryabchevskaya, Dmitriy L. Granovskiy, Ekaterina A. Evtushenko, Peter A. Ivanov, Olga A. Kondakova, Nikolai A. Nikitin, Olga V. Karpova
Publikováno v:
Pharmaceutics, Vol 14, Iss 4, p 806 (2022)
Anthrax is a disease caused by Bacillus anthracis that affects mammals, including humans. Recombinant B. anthracis protective antigen (rPA) is the most common basis for modern anthrax vaccine candidates. However, this protein is characterised by low
Externí odkaz:
https://doaj.org/article/f7fdbfeb8ab04f979e388f3ec9dc0171
Autor:
Anastasiya A. Kozina, Elena G. Okuneva, Natalia V. Baryshnikova, Olga B. Kondakova, Ekaterina A. Nikolaeva, Inessa D. Fedoniuk, Svetlana V. Mikhailova, Anna Y. Krasnenko, Ivan F. Stetsenko, Nikolay A. Plotnikov, Olesia I. Klimchuk, Yaroslav V. Popov, Ekaterina I. Surkova, Peter A. Shatalov, Alexander S. Rakitko, Valery V. Ilinsky
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 7, Pp n/a-n/a (2020)
Abstract Background Neuronal ceroid lipofuscinoses (NCLs) are a group of neurodegenerative disorders characterized by an accumulation of lipofuscin in the body's tissues. NCLs are associated with variable age of onset and progressive symptoms includi
Externí odkaz:
https://doaj.org/article/0554e990adb0470cb866ee945df34886
Autor:
Sofia G. Popovich, Lyudmila M. Kuzenkova, Olga B. Kondakova, Alexey I. Firumyants, Tatyana V. Podkletnova, Eugeniya V. Uvakina
Publikováno v:
L.O. Badalyan Neurological Journal. 3:122-126
Leukodystrophies are a group of hereditary progressive diseases of the central nervous system characterized by selective lesions in white matter with specific involvement of glial cells. There are hypomyelinating (absence of myelin deposition), demye
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cd5cde73be38c0116de56f3c6d190a9b
https://doi.org/10.46563/2686-8997-2022-3-3-122-126
https://doi.org/10.46563/2686-8997-2022-3-3-122-126
Autor:
Olga A, Kondakova, Ekaterina A, Evtushenko, Oleg A, Baranov, Nikolai A, Nikitin, Olga V, Karpova
Publikováno v:
Biochemistry (Moscow). 87:548-558
Structurally modified virus particles can be obtained from the rod-shaped or filamentous virions of plant viruses and bacteriophages by thermal or chemical treatment. They have recently attracted attention of the researchers as promising biogenic pla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::45d798852318174793c4ea677e9b36f3
https://doi.org/10.1134/s0006297922060062
https://doi.org/10.1134/s0006297922060062
Autor:
Tatyana V. Podkletnova, Olga B. Kondakova, Eugeniya V. Uvakina, Dariya A. Fisenko, Anastasiya A. Lyalina, Sophiya G. Popovich, Lyudmila M. Kuzenkova, Aleksey L. Kurenkov, Lale A. Pak, Bella I. Bursagova
Publikováno v:
L.O. Badalyan Neurological Journal. 2:227-232
Duchenne muscular dystrophy (DMD) is a hereditary progressive muscular dystrophy, mainly manifested in boys, is characterized by the onset at an early age, gradual symmetrical atrophy of the striated musculature of the limbs, trunk, as well as damage
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::da3ce42c6f1a493da185a3aeda0b652d
https://doi.org/10.46563/2686-8997-2021-2-4-227-232
https://doi.org/10.46563/2686-8997-2021-2-4-227-232
Autor:
Aleksey A. Pushkov, Alexey Kurenkov, Tatyana Podkletnova, Olga B. Kondakova, Lale A. Pak, Iulia I. Davydova, Dmitry I. Grebenkin, Kirill Savostyanov, L. M. Kuzenkova, Anastasiya A. Lyalina, Bella Bursagova
Publikováno v:
L.O. Badalyan Neurological Journal. 2:159-166
Duchenne muscular dystrophy (DMD) is a disease with an X-linked recessive type of inheritance, belonging to a group of disorders with primary muscle damage, caused by pathogenic variants in the DMD gene and associated with dysfunction of the dystroph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bda7687ad9b56a0b01196060a08d7223
https://doi.org/10.46563/2686-8997-2021-2-3-159-166
https://doi.org/10.46563/2686-8997-2021-2-3-159-166