The misfolding and aggregation of specific proteins within nervous system occur in most age-
associated neurodegenerative diseases including Alzheimer's disease (AD). This kind of …

A common pathological hallmark among different neurodegenerative diseases is the
accumulation of aggregated proteins that might cause cellular dysfunction and, eventually …

Specific protein misfolding and aggregation are mechanisms underlying various
neurodegenerative diseases such as prion disease and Alzheimer's disease (AD). The …

Many non-infectious neurodegenerative diseases are associated with the accumulation of
fibrillar proteins. These diseases all exhibit features that are reminiscent of those of …

The prototype of transmissible neurodegenerative proteinopathies is prion diseases,
characterized by aggregation of abnormally folded conformers of the native prion protein. A …

Introduction The proteopathic basis of AD Protein interactions in PD Induction and spread of
protein aggregates in NDDs Conclusions The misfolding and progressive aggregation of …

The accumulation and spread of prion-like proteins is a key feature of neurodegenerative
diseases (NDs) such as Alzheimer's disease, Parkinson's disease, or Amyotrophic Lateral …

Prion-like propagation of abnormal intracytoplasmic proteins, which are the defining features
of major neurodegenerative disorders, such as Alzheimer's disease (AD), Parkinson's …

The misfolding and aggregation of specific proteins is a common hallmark of many
neurodegenerative disorders, including highly prevalent illnesses such as Alzheimer's and …

The misfolding and aggregation of proteins is the neuropathological hallmark for numerous
diseases including Alzheimer's disease, Parkinson's disease, and prion diseases. It is …