Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Irina Alexeeva"'
Autor:
Irina Alexeeva
Publikováno v:
Translation Studies: Theory and Practice, Vol 1, Iss 1 (1) (2021)
Today the criteria for evaluating translations of literary texts combine vast practical experience, insights of the translation theory and the demands set by the contemporary society for the translation of literature. The article describes the stages
Externí odkaz:
https://doaj.org/article/adf7341700fa4773950d59036d23f9da
Publikováno v:
Emerging Infectious Diseases, Vol 14, Iss 9, Pp 1406-1412 (2008)
The route of transmission of most naturally acquired transmissible spongiform encephalopathy (TSE) infections remains speculative. To investigate urine as a potential source of TSE exposure, we used a sensitive method for detection and quantitation o
Externí odkaz:
https://doaj.org/article/b14177f37ef643f390c85e5754458b92
Autor:
Natallia Makarava, Gabor G Kovacs, Regina Savtchenko, Irina Alexeeva, Herbert Budka, Robert G Rohwer, Ilia V Baskakov
Publikováno v:
PLoS Pathogens, Vol 7, Iss 12, p e1002419 (2011)
The transmissible agent of prion disease consists of a prion protein in its abnormal, β-sheet rich state (PrP(Sc)), which is capable of replicating itself according to the template-assisted mechanism. This mechanism postulates that the folding patte
Externí odkaz:
https://doaj.org/article/2680c7a0ba544af6b6a9468c9d03a2b3
Autor:
Nuria Gonzalez-Montalban, Natallia Makarava, Valeriy G Ostapchenko, Regina Savtchenk, Irina Alexeeva, Robert G Rohwer, Ilia V Baskakov
Publikováno v:
PLoS Pathogens, Vol 7, Iss 2, p e1001277 (2011)
Protein misfolding cyclic amplification (PMCA) provides faithful replication of mammalian prions in vitro and has numerous applications in prion research. However, the low efficiency of conversion of PrP(C) into PrP(Sc) in PMCA limits the applicabili
Externí odkaz:
https://doaj.org/article/de877afacd3b40daa9de71b2cc82b102
Autor:
Irina Alexeeva, Vladimir G. Budanov, Dmitry Efremenko, Vladimir Lepsky, Yakov Svirskiy, Vadim Rozin, Larisa Kiyashchenko, Irina Chernikova, Vyacheslav Semenovich Stepin, Irina A. Gerasimova, Marina Burgete, Vladimir I. Arshinov
Publikováno v:
Philosophy of Science and Technology. 22:5-29
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::70f03988dd7cc6885663180df2c29f55
https://doi.org/10.21146/2413-9084-2017-22-1-5-29
https://doi.org/10.21146/2413-9084-2017-22-1-5-29
Publikováno v:
The American Journal of Pathology. 186:1006-1014
Previous studies established that transmissible prion diseases could be induced by in vitro -produced recombinant prion protein (PrP) fibrils with structures that are fundamentally different from that of authentic PrP scrapie isoform (PrP Sc ). To ex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4391daaa488031f59bce139f60ed561a
https://doi.org/10.1016/j.ajpath.2015.11.013
https://doi.org/10.1016/j.ajpath.2015.11.013
Autor:
Olga V. Bocharova, Herbert Budka, Irina Alexeeva, Gabor G. Kovacs, Regina Savtchenko, Robert G. Rohwer, Ilia V. Baskakov, Natallia Makarava
Publikováno v:
Acta Neuropathologica
Prion disease is a neurodegenerative malady, which is believed to be transmitted via a prion protein in its abnormal conformation (PrPSc). Previous studies have failed to demonstrate that prion disease could be induced in wild-type animals using reco
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3ae75999079aed11309814a9bb919e31
https://doi.org/10.1007/s00401-009-0633-x
https://doi.org/10.1007/s00401-009-0633-x
Autor:
Regina Savtchenk, Ilia V. Baskakov, Irina Alexeeva, Robert G. Rohwer, Natallia Makarava, Valeriy G. Ostapchenko
Publikováno v:
Prion Biology: Research and Advances
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::22ab95249f3e9958efc98190e0106000
https://doi.org/10.1201/b14793-4
https://doi.org/10.1201/b14793-4
Autor:
Regina Savtchenko, Herbert Budka, Irina Alexeeva, Natallia Makarava, Robert G. Rohwer, Gabor G. Kovacs, Ilia V. Baskakov
Transmission of prions to a new host is frequently accompanied by strain adaptation, a phenomenon that involves reduction of the incubation period, a change in neuropathological features and, sometimes, tissue tropism. Here we show that a strain of s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32c1c3d982b421f1d4da8e04fc89845e
https://www.zora.uzh.ch/id/eprint/68640/
https://www.zora.uzh.ch/id/eprint/68640/
Autor:
Robert G. Rohwer, Irina Alexeeva, Gabor G. Kovacs, Natallia Makarava, Ilia V. Baskakov, Regina Savtchenko, Herbert Budka
Publikováno v:
PLoS Pathogens
PLoS Pathogens, Vol 7, Iss 12, p e1002419 (2011)
PLoS Pathogens, Vol 7, Iss 12, p e1002419 (2011)
The transmissible agent of prion disease consists of a prion protein in its abnormal, β-sheet rich state (PrPSc), which is capable of replicating itself according to the template-assisted mechanism. This mechanism postulates that the folding pattern
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::270fbef0053b9ef4ba57af54e179cd0f
https://pubmed.ncbi.nlm.nih.gov/22144901
https://pubmed.ncbi.nlm.nih.gov/22144901