Cargando…

Chronic wasting disease: Emerging prions and their potential risk

Detalles Bibliográficos
Autores principales:	Hannaoui, Samia, Schatzl, Hermann M., Gilch, Sabine
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Public Library of Science 2017
Materias:	Pearls
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5667731/ https://www.ncbi.nlm.nih.gov/pubmed/29095921 http://dx.doi.org/10.1371/journal.ppat.1006619

Ejemplares similares

Cervid Prion Protein Polymorphisms: Role in Chronic Wasting Disease Pathogenesis
por: Arifin, Maria Immaculata, et al.
Publicado: (2021)

Cellulose ether treatment in vivo generates chronic wasting disease prions with reduced protease resistance and delayed disease progression
por: Hannaoui, Samia, et al.
Publicado: (2019)

Transmission of cervid prions to humanized mice demonstrates the zoonotic potential of CWD
por: Hannaoui, Samia, et al.
Publicado: (2022)

Gene-edited murine cell lines for propagation of chronic wasting disease prions
por: Walia, Rupali, et al.
Publicado: (2019)

Early detection of chronic wasting disease prions in urine of pre-symptomatic deer by real-time quaking-induced conversion assay
por: John, Theodore R., et al.
Publicado: (2013)

Early and Non-Invasive Detection of Chronic Wasting Disease Prions in Elk Feces by Real-Time Quaking Induced Conversion
por: Cheng, Yo Ching, et al.
Publicado: (2016)

Loss of small GTPase Rab7 activation in prion infection negatively affects a feedback loop regulating neuronal cholesterol metabolism
por: Cherry, Pearl, et al.
Publicado: (2023)

Cholesterol Balance in Prion Diseases and Alzheimer’s Disease
por: Hannaoui, Samia, et al.
Publicado: (2014)

The Elusive Role of the Prion Protein and the Mechanism of Toxicity in Prion Disease
por: Chiesa, Roberto
Publicado: (2015)

Prion propagation and cellular dysfunction in prion disease: Disconnecting the dots
por: Foliaki, Simote T., et al.
Publicado: (2023)

Peculiarities of Prion Diseases
por: Jackson, Walker S., et al.
Publicado: (2014)

Silent Prions and Covert Prion Transmission
por: Mathiason, Candace K.
Publicado: (2015)

Five Questions on Prion Diseases
por: Aguzzi, Adriano, et al.
Publicado: (2012)

Behavior of Prions in the Environment: Implications for Prion Biology
por: Bartelt-Hunt, Shannon L., et al.
Publicado: (2013)

The Importance of Prions
por: Telling, Glenn C.
Publicado: (2013)

Yeast Prions: Proteins Templating Conformation and an Anti-prion System
por: Wickner, Reed B., et al.
Publicado: (2015)

The Role of Iron in Prion Disease and Other Neurodegenerative Diseases
por: Singh, Neena
Publicado: (2014)

Mutation and Selection of Prions
por: Weissmann, Charles
Publicado: (2012)

Prion strains in mammals: Different conformations leading to disease
por: Morales, Rodrigo
Publicado: (2017)

Cerebral organoids as a new model for prion disease
por: Groveman, Bradley R., et al.
Publicado: (2021)

Combining autophagy stimulators and cellulose ethers for therapy against prion disease
por: Abdulrahman, Basant A., et al.
Publicado: (2019)

Elucidating the function of the prion protein
por: Legname, Giuseppe
Publicado: (2017)

Environmental Regulation of Prions in Yeast
por: Li, Liming, et al.
Publicado: (2012)

Prions—Not Your Immunologist’s Pathogen
por: Zabel, Mark D., et al.
Publicado: (2015)

Redox mechanisms and their pathological role in prion diseases: The road to ruin
por: Spiers, Jereme G., et al.
Publicado: (2023)

Gene-Edited Cell Models to Study Chronic Wasting Disease
por: Thapa, Simrika, et al.
Publicado: (2022)

The prion-like phenomenon in Alzheimer’s disease: Evidence of pathology transmission in humans
por: Gomez-Gutierrez, Ruben, et al.
Publicado: (2020)

The Role of Cofactors in Prion Propagation and Infectivity
por: Ma, Jiyan
Publicado: (2012)

Pathogenic prion structures at high resolution
por: Caughey, Byron, et al.
Publicado: (2022)

Propagation of PrP(Sc) in mice reveals impact of aggregate composition on prion disease pathogenesis
por: Chang, Sheng Chun, et al.
Publicado: (2023)

The Evolution of Transmissible Prions: The Role of Deformed Templating
por: Makarava, Natallia, et al.
Publicado: (2013)

Prion Strains and Amyloid Polymorphism Influence Phenotypic Variation
por: Stein, Kevin C., et al.
Publicado: (2014)

Chaperone functional specificity promotes yeast prion diversity
por: Killian, Andrea N., et al.
Publicado: (2018)

Understanding the link between the actin cytoskeleton and prion biology
por: Dorweiler, Jane E., et al.
Publicado: (2023)

Pernicious Pathogens or Expedient Elements of Inheritance: The Significance of Yeast Prions
por: Byers, James S., et al.
Publicado: (2014)

Prion infection impairs lysosomal degradation capacity by interfering with rab7 membrane attachment in neuronal cells
por: Shim, Su Yeon, et al.
Publicado: (2016)

The [Het-s] Prion, an Amyloid Fold as a Cell Death Activation Trigger
por: Saupe, Sven J., et al.
Publicado: (2012)

Prions are the greatest protein misfolding problem, and yeast has several solutions
por: Wickner, Reed B., et al.
Publicado: (2023)

Destabilizing polymorphism in cervid prion protein hydrophobic core determines prion conformation and conversion efficiency
por: Hannaoui, Samia, et al.
Publicado: (2017)

Oral administration of repurposed drug targeting Cyp46A1 increases survival times of prion infected mice
por: Ali, Tahir, et al.
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_tvpggk11ek54afet53q6f78jrc