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PRIONES
(2019)
Perturbation of endoplasmic reticulum homeostasis facilitates prion replication
(2007)
Prion diseases are fatal and infectious neurodegenerative disorders characterized by the accumulation of an abnormally folded form of the prion protein ( PrP), termed PrPSc. Prion replication triggers endoplasmic reticulum ...
Herencia y memoria: ¿un nuevo rol para los priones?
(Universidad Autónoma de Bucaramanga UNAB, 2008-04-11)
ResumenLos priones causan las encefalopatÍas espongiformes en mamÍferos y humanos. Los agregados de proteÍnas presentes en estas entidades son similares a las de otras enfermedades neurodegenerativas como la enfermedad de ...
Protein misfolding, signaling abnormalities and altered fast axonal transport: Implications for Alzheimer and Prion diseases
(Frontiers Media S.A., 2019-07)
Histopathological studies revealed that progressive neuropathies including Alzheimer, and Prion diseases among others, include accumulations of misfolded proteins intracellularly, extracellularly, or both. Experimental ...
Low phenotypic penetrance and technological impact of yeast [GAR+] prion-like elements on winemaking
(Frontiers Research Foundation, 2018-12)
[GAR+] prion-like elements partially relieve carbon catabolite repression in Saccharomyces cerevisiae. They have been hypothesized to contribute to wine yeast survival and alcohol level reduction, as well as communication ...