Výsledky vyhledávání - "transmissible mink encephalopathy"

Akademický článek

Bovine adapted transmissible mink encephalopathy is similar to L-BSE after passage through sheep with the VRQ/VRQ genotype but not VRQ/ARQ

Autor: Eric Cassmann, Sarah Jo Moore, Robyn Kokemuller, Anne Balkema-Buschmann, Martin Groschup, Eric Nicholson, Justin Greenlee

Publikováno v: BMC Veterinary Research, Vol 16, Iss 1, Pp 1-14 (2020)

Abstract Background Transmissible mink encephalopathy (TME) is a fatal neurologic disease of farmed mink. Evidence indicates that TME and L-BSE are similar and may be linked in some outbreaks of TME. We previously transmitted bovine adapted TME (bTME

Externí odkaz: https://doaj.org/article/a6f770fae08e4bd9a12fdc7ec11a03fd

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Akademický článek

Sheep Are Susceptible to the Bovine Adapted Transmissible Mink Encephalopathy Agent by Intracranial Inoculation and Have Evidence of Infectivity in Lymphoid Tissues

Autor: Eric D. Cassmann, S. Jo Moore, Jodi D. Smith, Justin J. Greenlee

Publikováno v: Frontiers in Veterinary Science, Vol 6 (2019)

Transmissible mink encephalopathy (TME) is a food borne prion disease. Epidemiological and experimental evidence suggests similarities between the agents of TME and L-BSE. This experiment demonstrates the susceptibility of four different genotypes of

Externí odkaz: https://doaj.org/article/585f783ba86a4acba17aa59a2b5c41e4

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Incomplete glycosylation during prion infection unmasks a prion protein epitope that facilitates prion detection and strain discrimination

Autor: Jason C. Bartz, Sehun Kim, Jifeng Bian, Jenna Crowell, Hae Eun Kang, Sarah J. Kane, Glenn C. Telling, Vanessa Selwyn

Publikováno v: J Biol Chem

The causative factors underlying conformational conversion of cellular prion protein (PrP(C)) into its infectious counterpart (PrP(Sc)) during prion infection remain undetermined, in part because of a lack of monoclonal antibodies (mAbs) that can dis

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd6a8843c9f51f67c6ee6a3d6925df10
https://doi.org/10.1074/jbc.ra120.012796

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PRION 2019 emerging concepts

Autor: Anastasiia Stepanchuk, Andrew Castle, Helen Yao, Aleksandra Sergeeva, Frederic Lantier, Luca Varani, Charlotte Thomas

Publikováno v: Prion

Introduction: Transmissible mink encephalopathy (TME) is a fatal neurologic prion disease of farmed mink. Epidemiologic and experimental evidence following a Wisconsin outbreak in 1985 has linked TME to low-type bovine spongiform encephalopathy (BSE-

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::16bf6d564d3caf233423966ba9edc090
https://doi.org/10.1080/19336896.2019.1615197

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Akademický článek

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Bovine adapted transmissible mink encephalopathy is similar to L-BSE after passage through sheep with the VRQ/VRQ genotype but not VRQ/ARQ

Autor: Robyn Kokemuller, Martin H. Groschup, Eric M. Nicholson, Sarah Jo Moore, Justin J. Greenlee, Anne Balkema-Buschmann, Eric D. Cassmann

Publikováno v: BMC Veterinary Research
BMC Veterinary Research, Vol 16, Iss 1, Pp 1-14 (2020)

Background Transmissible mink encephalopathy (TME) is a fatal neurologic disease of farmed mink. Evidence indicates that TME and L-BSE are similar and may be linked in some outbreaks of TME. We previously transmitted bovine adapted TME (bTME) to shee

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc1ace1b9b8b8de1e230ecb0285b2300
http://europepmc.org/articles/PMC7545885

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Introduction to Current Progress in Advanced Research on Prions

Autor: Akikazu Sakudo, Takashi Onodera

Publikováno v: Current Issues in Molecular Biology
Volume 36
Issue 1
Pages 63-66

Prion diseases or transmissible spongiform encephalopathies (TSEs) are fatal neurological diseases that include Creutzfeldt-Jakob disease (CJD) in humans, scrapie in sheep and goats, bovine spongiform encephalopathy (BSE) in cattle, camel spongiform

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34fb794c224c767506b4b0916d3203ea
https://pubmed.ncbi.nlm.nih.gov/31559970

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How will prion disease evolve?

Autor: HuiXia Zhang, Li Chaoyang, Run Shi

Publikováno v: Chinese Science Bulletin. 62:16-24

Transmissible Spongiform Encephalopathy (TSE) or prion disease is caused by the infectious agent prion or scrapie prion protein (PrPSC). In animals, prion disease includes scrapie in sheep and goat; mink spongiform encephalopathy in mink; chronic was

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::a1b717128f17301789716d85101069b5
https://doi.org/10.1360/n972016-00913

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Pathogenic mechanisms of prion protein, amyloid-β and α-synuclein misfolding: the prion concept and neurotoxicity of protein oligomers

Autor: Andrew F. Hill, David Finkelstein, Victoria A. Lawson, Cathryn L Ugalde

Publikováno v: Journal of Neurochemistry. 139:162-180

Proteinopathies represent a group of diseases characterized by the unregulated misfolding and aggregation of proteins. Accumulation of misfolded protein in the central nervous system (CNS) is associated with neurodegenerative diseases, such as the tr

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::185012c98a7cd8bef7af0715b3a8bcad
https://doi.org/10.1111/jnc.13772

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