Results 131 to 140 of about 5,185,837 (206)

Prion-like protein propagation in neurodegenerative diseases

Rinsho Shinkeigaku, 2012
Hasegawa, Masato, Nonaka, Takashi, Suzukake, Masami, Tsuji, Hiroshi, Tamaoka, Akira, Yoshida, Mari, Murayama, Shigeo, Arai, Tetsuaki, Akiyama, Haruhiko   +8 more
openaire   +3 more sources

Proteína prion celular (PrPc) altera a suscetibilidade ao etanol através da modulação do sistema dopaminérgico [PDF]

, 2013
Tese (doutorado) - Universidade Federal de Santa Catarina, Centro de Ciências Biológicas, Programa de Pós-Graduação em FarmacologiaO consumo de drogas com potencial aditivo, como o etanol, induz alterações sinápticas profundas na via mesocorticolímbica ...
Rial, Daniel
core  

Prion-like propagation and protein misfolding [PDF]

Prion, 2011
openaire   +1 more source

Prion Protein Scrapie and the Normal Cellular Prion Protein

, 2015
Prions are infectious proteins and over the past few decades, some prions have become renowned for their causative role in several neurodegenerative diseases in animals and humans.
Munn, Alan L, Atkinson, Caroline, Wiegmans, Adrian, Munn, Alan, Wei, Ming, Wei, Ming Q, Zhang, Kai, Atkinson, Caroline J   +7 more
core   +1 more source

Corrigendum: Prion-Like Propagation of Protein Misfolding and Aggregation in Amyotrophic Lateral Sclerosis. [PDF]

Front Mol Neurosci, 2019
McAlary L, Plotkin SS, Yerbury JJ, Cashman NR.   +3 more
europepmc   +1 more source

Genetic Modulators of Prion-Like Protein Propagation in Alzheimer's Disease

Journal of Student Research
Alzheimer's disease (AD) is a widespread neurodegenerative disorder with complex causes. Starting with a historical overview, this paper traces the foundational discoveries by Alois Alzheimer and subsequent research into the roles of Tau, beta-amyloid (Aß), and cellular prion protein (PrPc) in AD progression.
openaire   +1 more source

Small critical RNAs in the scrapie agent [PDF]

, 2009
Unconventional infectious agents cause transmissible spongiform encephalopathy (TSE) diseases including scrapie and bovine spongiform encephalopathy (BSE) in animals and Creutzfeldt-Jakob disease in humans. The protein only hypothesis claims that the TSE
Marie-Madeleine Ruchoux, Jean-Philippe Deslys, Nicolas Vignier, Pierre Lebon, Jean-Guy Fournier, Sophie Freire, Emmanuel Comoy, Steve Simoneau   +7 more
core  

Scalable assay to identify inhibitors of prion-like propagation of protein misfolding as potential therapeutics for neurodegeneration. [PDF]

Protein Sci
Narayan A, Neupane K, Woodside MT.
europepmc   +1 more source

Folding and fibril formation of prions [PDF]

Prions diseases are a group of fatal neurodegenerative disorders called the transmissible spongiform encephalopathies (TSEs), which include bovine spongiform encephalopathy in cattle, scrapie in sheep and Creutzfeldt-Jakob disease (CJD) in humans ...
Gierusz, Leszek A.
core  

Impairment of the Glial Phagolysosomal System Drives Prion-Like Propagation in a <i>Drosophila</i> Model of Huntington's Disease. [PDF]

J Neurosci
Davis GH, Zaya A, Pearce MMP.
europepmc   +1 more source