نتایج جستجو برای: amyloid β

تعداد نتایج: 204360  

Journal: :Alzheimers & Dementia 2023

Background Among other emerging amyloid-targeting blood-based biomarkers, Multimer Detection System-Oligomeric Amyloid-β (MDS-OAβ) measures dynamic changes in concentration of oligomeric amyloid-β (OAβ), which is considered the main pathogenic culprit Alzheimer’s disease (AD), plasma after spiking with synthetic (Aβ). We aimed to investigate predictability MDS-OAβ on amyloid Positron Emission T...

2011
Ahmadul Kadir Amelia Marutle Daniel Gonzalez Michael Schöll Ove Almkvist Malahat Mousavi Tamanna Mustafiz Taher Darreh-Shori Inger Nennesmo Agneta Nordberg

The accumulation of β-amyloid in the brain is an early event in Alzheimer's disease. This study presents the first patient with Alzheimer's disease who underwent positron emission tomography imaging with the amyloid tracer, Pittsburgh Compound B to visualize fibrillar β-amyloid in the brain. Here we relate the clinical progression, amyloid and functional brain positron emission tomography imagi...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2012
James C Stroud Cong Liu Poh K Teng David Eisenberg

Although amyloid fibers are found in neurodegenerative diseases, evidence points to soluble oligomers of amyloid-forming proteins as the cytotoxic species. Here, we establish that our preparation of toxic amyloid-β(1-42) (Abeta42) fibrillar oligomers (TABFOs) shares with mature amyloid fibrils the cross-β structure, in which adjacent β-sheets adhere by interpenetration of protein side chains. W...

2017
Chris Mezias Ashish Raj

While the spread of some neurodegenerative disease-associated proteinopathies, such as tau and α-synuclein, is well studied and clearly implicates transsynaptic pathology transmission, research into the progressive spread of amyloid-β pathology has been less clear. In fact, prior analyses of transregional amyloid-β pathology spread have implicated both transsynaptic and other intracellular- as ...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2011
Franziska Langer Yvonne S Eisele Sarah K Fritschi Matthias Staufenbiel Lary C Walker Mathias Jucker

Cerebral β-amyloidosis and associated pathologies can be exogenously induced by the intracerebral injection of small amounts of pathogenic Aβ-containing brain extract into young β-amyloid precursor protein (APP) transgenic mice. The probable β-amyloid-inducing factor in the brain extract has been identified as a species of aggregated Aβ that is generated in its most effective conformation or co...

2017
N. Nespovitaya P. Mahou R. F. Laine G. S. Kaminski Schierle C. F. Kaminski

The aggregation promoter heparin is commonly used to study the aggregation kinetics and biophysical properties of protein amyloids. However, the underlying mechanism for amyloid promotion by heparin remains poorly understood. In the case of the neuropeptide β-endorphin that can reversibly adopt a functional amyloid form in nature, aggregation in the presence of heparin leads to a loss of functi...

2016
Yazan S. Batarseh Quoc-Viet Duong Youssef M. Mousa Sweilem B. Al Rihani Khaled Elfakhri Amal Kaddoumi

Amyloid-β (Aβ) pathology is known to promote chronic inflammatory responses in the brain. It was thought previously that Aβ is only associated with Alzheimer's disease and Down syndrome. However, studies have shown its involvement in many other neurological disorders. The role of astrocytes in handling the excess levels of Aβ has been highlighted in the literature. Astrocytes have a distinctive...

2013
Justin Read Cenk Suphioglu

The β-site amyloid precursor protein cleaving enzyme 1 (BACE1) is an important regulator for the production of amyloid plaques, a characteristic of the Alzheimer’s disease (AD) brain. The proteolytic cleavage of the amyloid precursor protein (APP), by BACE1, produces an insoluble amyloid-β (Aβ) fragment which has the ability to aggregate and migrate onto the dendrites and cell body of neuronal ...

2017
Ming-Chien Hsieh Chen Liang Anil K Mehta David G Lynn Martha A Grover

Defining pathways for amyloid assembly could impact therapeutic strategies for as many as 50 disease states. Here we show that amyloid assembly is subject to different forces regulating nucleation and propagation steps and provide evidence that the more global β-sheet/β-sheet facial complementarity is a critical determinant for amyloid nucleation and structural selection.

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