Results 191 to 200 of about 14,159 (251)
Redox environment modulates in vitro aggregation of Ataxin‐3, the protein implicated in spinocerebellar ataxia type 3. Reducing conditions stabilize native monomers and prevent aggregation, whereas oxidative conditions promote the formation of non‐native conformers and disulfide‐linked oligomers within the Josephin domain (JD).
Martyna Podlasiak +10 more
wiley +1 more source
ABSTRACT Aim Neurodegenerative diseases and disordered eating have become rapidly expanding areas of research. However, research addressing the relationship between the two is lacking. Methods A scoping review guided by the Joanna Briggs Institute methodological framework was completed to synthesise the evidence related to disordered eating behaviours ...
Emily Buttifant +2 more
wiley +1 more source
State of the art in biosafety at the European National Reference Laboratories for Transmissible Spongiform Encephalopathies. [PDF]
Begovoeva M +5 more
europepmc +1 more source
TDP‐43 pathology is a hallmark of amyotrophic lateral sclerosis (ALS) and frontotemporal dementia. Peptidyl‐prolyl cis–trans isomerase A (PPIA), a foldase and chaperone protein, modulates TDP‐43 function in an acetylation‐dependent manner. Here, we show that inhibition of lysine deacetylation with vorinostat (SAHA) increases PPIA acetylation and ...
Serena Scozzari +10 more
wiley +1 more source
Understanding the Phenotypic Heterogeneity Within the Sporadic Creutzfeldt–Jakob Disease MV1 Subtype
We present the clinical, pathological and prion biophysical features of three atypical cases of the MV1 subtype of sporadic Creutzfeldt–Jakob disease (sCJD). We propose that these heterozygous cases exist on a spectrum ranging from MM1‐like to VV1‐like phenotypes and recommend that subtyping be performed at pH 6.9 to avoid missing atypical or mixed ...
Satish K. Nemani +6 more
wiley +1 more source
Infecting human brain organoids with FFI or sCJD preserves prion traits regardless of host genotype. [PDF]
Groveman BR +6 more
europepmc +1 more source
Contrasting roles of autophagy in cellular prion infection. [PDF]
Abdulrahman B +9 more
europepmc +1 more source
The impact of formic acid treatment on brain tissues for prion inactivation. [PDF]
Shaaban D +7 more
europepmc +1 more source
Yeast Prions: Discovery, Nature, Cellular Manipulation and Implication. [PDF]
Son M.
europepmc +1 more source
Mutant knock-in mice display enhanced susceptibility to pure prion protein fibrils. [PDF]
Walsh DJ +4 more
europepmc +1 more source

