نتایج جستجو برای: amyloid disaggregation

تعداد نتایج: 39890  

2016
Hye Yun Kim Hyunjin Vincent Kim Seonmi Jo C. Justin Lee Seon Young Choi Dong Jin Kim YoungSoo Kim

dependent cognitive deficits in APP/PS1 mice by disaggregation of amyloid-b oligomers and plaques Hye Yun Kim, Hyunjin Vincent Kim, Seonmi Jo, C. Justin Lee, Seon Young Choi, Dong Jin Kim & YoungSoo Kim Nature Communications 6:8997 doi: 10.1038/ncomms9997 (2015); Published 8 Dec 2015; Updated 15 Feb 2016 This Article contains errors in Figs 3 and 4. In Fig. 3h, the x axis should have been label...

2012
Nelson Ferreira Maria João Saraiva Maria Rosário Almeida

BACKGROUND Familial amyloidotic polyneuropathy (FAP) is a neurodegenerative disease caused by the extracellular deposition of mutant transthyretin (TTR), with special involvement of the peripheral nervous system (PNS). Currently, hepatic transplantation is considered the most efficient therapy to halt the progression of clinical symptoms in FAP since more than 95% of TTR is produced by the live...

Journal: :Journal of Alzheimer's Disease 2021

Alzheimer’s disease (AD) is the most common age-related neurodegenerative disorder, responsible for nearly two-thirds of all dementia cases. In this review, we report potential AD treatment strategies focusing on natural polyphenol molecules (green chemistry) and more specifically inhibition polyphenol-induced amyloid aggregation/disaggregation pathways: in bulk biosurfaces. We discuss how thes...

2015
Patrick Droste André Frenzel Miriam Steinwand Thibaut Pelat Philippe Thullier Michael Hust Hilal Lashuel Stefan Dübel

BACKGROUND Beside neurofibrillary tangles, amyloid plaques are the major histological hallmarks of Alzheimer's disease (AD) being composed of aggregated fibrils of β-amyloid (Aβ). During the underlying fibrillogenic pathway, starting from a surplus of soluble Aβ and leading to mature fibrils, multiple conformations of this peptide appear, including oligomers of various shapes and sizes. To furt...

Journal: :Genetics 2012
Michael Reidy Marika Miot Daniel C Masison

Saccharomyces cerevisiae Hsp104 and Escherichia coli ClpB are Hsp100 family AAA+ chaperones that provide stress tolerance by cooperating with Hsp70 and Hsp40 to solubilize aggregated protein. Hsp104 also remodels amyloid in vitro and promotes propagation of amyloid prions in yeast, but ClpB does neither, leading to a view that Hsp104 evolved these activities. Although biochemical analyses ident...

Journal: :Genetics 2006
Guo-Chiuan Hung Daniel C Masison

Hsp104 is a hexameric protein chaperone that resolubilizes stress-damaged proteins from aggregates. Hsp104 promotes [PSI(+)] prion propagation by breaking prion aggregates, which propagate as amyloid fibers, into more numerous prion "seeds." Inactivating Hsp104 cures cells of [PSI(+)] and other amyloid-like yeast prions. Overexpressing Hsp104 also eliminates [PSI(+)], presumably by completely r...

Journal: :Journal of neurochemistry 2007
M Garcia-Alloza L A Borrelli A Rozkalne B T Hyman B J Bacskai

Alzheimer's disease (AD) is characterized by senile plaques and neurodegeneration although the neurotoxic mechanisms have not been completely elucidated. It is clear that both oxidative stress and inflammation play an important role in the illness. The compound curcumin, with a broad spectrum of anti-oxidant, anti-inflammatory, and anti-fibrilogenic activities may represent a promising approach...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2007
Maria Becker Vered Lavie Beka Solomon

Neurogenesis is a subject of intense interest and extensive research, but it stands at the center of a bitter debate over ethical and practical problems. Neurodegenerative diseases, such as Alzheimer's disease (AD), accompanied by a shifting balance between neurogenesis and neurodegeneration, are suitable for stimulation of neurogenesis for the benefit of diseased patients. We have previously s...

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