Abstract α-Synuclein (α-Syn) has been extensively studied for its structural and biophysical
properties owing to its pathophysiological role in Parkinson's disease (PD). Lewy bodies …

Many neurodegenerative diseases, such as Alzheimer's disease, Parkinson's disease, and
amyotrophic lateral sclerosis, are characterized by the progressive appearance of abnormal …

Year-round access to good quality forage is a physiological priority for ruminants and an
economic priority for farmers. Ensiling is a method for preserving moist crops based on …

Aberrant accumulation of misfolded proteins into amyloid deposits is a hallmark in many age-
related neurodegenerative diseases, including Alzheimer's disease (AD), Parkinson's …

Chronic wasting disease (CWD) is a transmissible spongiform encephalopathy (TSE) that
affects members of the cervidae family. The infectious agent is a misfolded isoform (PrPSC) …

Abnormal accumulation of aggregated α-synuclein (α-Syn) is seen in a variety of
neurodegenerative diseases, including Parkinson's disease (PD), multiple system atrophy …

Prion diseases are transmissible, progressive and invariably fatal neurodegenerative
conditions associated with misfolding and aggregation of a host-encoded cellular prion …

Abnormal prion proteins are responsible for several fatal neurodegenerative diseases in
humans and in animals, including Creutzfeldt–Jakob disease (CJD), Gerstmann–Sträussler …

Prion, or PrPSc, is the pathological isoform of the cellular prion protein (PrPC) and it is the
etiological agent of transmissible spongiform encephalopathies (TSE) affecting humans and …

Increasing evidence suggests that neurodegenerative disorders share a common
pathogenic feature: the presence of deposits of misfolded proteins with altered …