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Genomic Analysis and Comparison of Pakistani Camels (Camelus dromedarius) by Prion Gene
(Universidade Federal do Rio Grande do Sul, 2017)
Aplicación de la inmunohistoquímica en óbex de caprinos para la detección de proteínas priónicas
(Universidad de Chile, 2017)
El Scrapie es una enfermedad neurodegenerativa y fatal que afecta a pequeños rumiantes
como ovinos, caprinos y muflones. El causante de esta enfermedad es una partícula
proteinácea infecciosa llamada prión, que se origina ...
Use of immunohistochemestry to search prion protein in third eyelid of sheep in Chile Uso de la inmunohistoquímica para la búsqueda de proteínas priónicas en tercer párpado de ovinos en Chile
(Universidad Austral de Chile, 2014)
An immunohistochemstry (IHC) method to detect scrapie in sheep third eyelid lymphoid tissue was applied in post mortem animals. This method would allow to carry out the diagnosis in Chile, including the preclinical phase ...
Unveiling the mysteries of hereditary prion diseases in Brazil
(Academia Brasileira de Neurologia, 2017)
Abnormal calcium homeostasis and proteinfolding stress at the ER: A common factor in familial and infectious prion disorders
(2011)
Prion-related disorders (PrDs) are caused by the accumulation of a misfolded and protease-resistant form of the cellular prion, leading to neuronal dysfunction and massive neuronal loss. In humans, PrDs have distinct ...
The Endoplasmic Reticulum Chaperone GRP78/BiP Modulates Prion Propagation in vitro and in vivo
(Nature Publishing Group, 2017)
© The Author(s) 2017. Prion diseases are fatal neurodegenerative disorders affecting several mammalian species, characterized by the accumulation of the misfolded form of the prion protein, which is followed by the induction ...
De novo generation of infectious prions in vitro produces a new disease phenotype
(2009)
Prions are the proteinaceous infectious agents responsible for Transmissible Spongiform Encephalopathies. Compelling evidence supports the hypothesis that prions are composed exclusively of a misfolded version of the prion ...