نتایج جستجو برای: protein misfolding

تعداد نتایج: 1235138  

Journal: :Rinsho yakuri/Japanese Journal of Clinical Pharmacology and Therapeutics 2017

Journal: :Proceedings of the National Academy of Sciences 2004

Journal: :Journal of Glycomics & Lipidomics 2015

2017
Dimitra Athanasiou Monica Aguila Chikwado A. Opefi Kieron South James Bellingham Dalila Bevilacqua Peter M. Munro Naheed Kanuga Francesca E. Mackenzie Adam M. Dubis Anastasios Georgiadis Anna B. Graca Rachael A. Pearson Robin R. Ali Sanae Sakami Krzysztof Palczewski Michael Y. Sherman Philip J. Reeves Michael E. Cheetham

Protein misfolding caused by inherited mutations leads to loss of protein function and potentially toxic 'gain of function', such as the dominant P23H rhodopsin mutation that causes retinitis pigmentosa (RP). Here, we tested whether the AMPK activator metformin could affect the P23H rhodopsin synthesis and folding. In cell models, metformin treatment improved P23H rhodopsin folding and traffic....

Journal: :Biochemical and biophysical research communications 2014
Yanqin Liu John A Carver Lam H Ho Abigail K Elias Ian F Musgrave Tara L Pukala

Protein misfolding causes serious biological malfunction, resulting in diseases including Alzheimer's disease, Parkinson's disease and cataract. Molecules which inhibit protein misfolding are a promising avenue to explore as therapeutics for the treatment of these diseases. In the present study, thioflavin T fluorescence and transmission electron microscopy experiments demonstrated that hemin p...

Journal: :The Journal of chemical physics 2008
P F N Faísca R D M Travasso R C Ball E I Shakhnovich

We apply a simulational proxy of the phi-value analysis and perform extensive mutagenesis experiments to identify the nucleating residues in the folding "reactions" of two small lattice Go polymers with different native geometries. Our findings show that for the more complex native fold (i.e., the one that is rich in nonlocal, long-range bonds), mutation of the residues that form the folding nu...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2010
Rodrigo Morales Lisbell D Estrada Rodrigo Diaz-Espinoza Diego Morales-Scheihing Maria C Jara Joaquin Castilla Claudio Soto

The central event in protein misfolding disorders (PMDs) is the accumulation of a misfolded form of a naturally expressed protein. Despite the diversity of clinical symptoms associated with different PMDs, many similarities in their mechanism suggest that distinct pathologies may cross talk at the molecular level. The main goal of this study was to analyze the interaction of the protein misfold...

Journal: :Neurobiology of disease 2015
Leslie I Grad Sarah M Fernando Neil R Cashman

Prions, self-proliferating infectious agents consisting of misfolded protein, are most often associated with aggressive neurodegenerative diseases in animals and humans. Akin to the contiguous spread of a living pathogen, the prion paradigm provides a mechanism by which a mutant or wild-type misfolded protein can dominate pathogenesis through self-propagating protein misfolding, and subsequentl...

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