Amyloidoses represent a group of pathological conditions characterized by amyloid fibrils
accumulating in the form of deposits in intra-or extracellular space, leading to tissue …

The amyloidoses are diseases associated with nonnative folding of proteins and
characterized by the presence of protein amyloid aggregates. The ability of quercetin …

Exogenous insulin, used as a therapeutic agent for diabetes, forms insoluble deposits
containing amyloid fibrillar structures near the administration site. We have analyzed the in …

Amyloidosis is primarily characterized by the deposition of misfolded protein aggregates.
Although the natural polyphenols have long been known as effective amyloid inhibitors, the …

Amyloid aggregates of proteins are one of the most abundant and important naturally
occurring self-associated assemblies. Formation of poly/peptide amyloid aggregates is also …

Green tea polyphenols (GTPs) are found to be potent inhibitors of amyloid fibril formation.
We report the effective inhibitory property of (−)-epicatechin gallate (ECG) during the alkali …

The formation of amyloid aggregates is the hallmark of systemic and neurodegenerative
diseases, also known as amyloidosis. Many proteins have been found to aggregate into …

In the present study, we have investigated the effects of protein concentration and stirring on
the in vitro assembly of Hen Egg White Lysozyme (HEWL), particularly with regard to the …

Amyloidosis is the process of fibril formation responsible for causing several diseases in the
human being that involve protein aggregation such as Alzheimer's, Parkinson's …

Systemic amyloidosis is a hereditary disorder that mostly arises as a result of specific point
mutations to the wild type gene of lysozyme, forming mutant lysozyme variants leading to …