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Published in 2021 at "Protein Science"
DOI: 10.1002/pro.4127
Abstract: Fusion transcription factors generated by genomic translocations are common drivers of several types of cancers including sarcomas and leukemias. Oncofusions of the FET (FUS, EWSR1, and TAF15) family proteins result from the fusion of the…
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Keywords:
protein;
chromatin;
prion like;
pld ... See more keywords
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Published in 2018 at "Journal of Neural Transmission"
DOI: 10.1007/s00702-018-1851-y
Abstract: The hallmark of age-related neurodegenerative diseases is the appearance of cellular protein deposits and spreading of this pathology throughout the central nervous system. Growing evidence has shown the involvement and critical role of proteins with…
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Keywords:
properties disease;
prion like;
disease relevant;
pathology ... See more keywords
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Published in 2017 at "Molecular Neurobiology"
DOI: 10.1007/s12035-017-0624-1
Abstract: The prion-like seeding of misfolded α-synuclein (αSyn) involved in the pathogenesis of Lewy body diseases (LBD) remains poorly understood at the molecular level. Using the real-time quaking-induced conversion (RT-QUIC) seeding assay, we investigated whether brain…
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Keywords:
prion like;
like seeding;
misfolded synuclein;
seeding misfolded ... See more keywords
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Published in 2019 at "Cell"
DOI: 10.1016/j.cell.2019.08.019
Abstract: Prion-like proteins can assume distinct conformational and physical states in the same cell. Sequence analysis suggests that prion-like proteins are prevalent in various species; however, it remains unclear what functional space they occupy in multicellular…
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Keywords:
like assembly;
amyloid like;
prion like;
prion ... See more keywords
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Published in 2018 at "Cell reports"
DOI: 10.1016/j.celrep.2017.12.009
Abstract: Recent evidence of prion-like propagation of α-synuclein (α-syn) into neighboring neurons set up a paradigm to elucidate the mechanism of progression of Parkinson's disease (PD) and to develop therapeutic strategies. Here, we show that FcγRIIB…
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Keywords:
prion like;
shp signaling;
signaling pathway;
riib shp ... See more keywords
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Published in 2020 at "Current Opinion in Neurobiology"
DOI: 10.1016/j.conb.2019.11.018
Abstract: A neuropathological hallmark of most neurodegenerative diseases is the appearance of characteristic inclusions composed of misfolded proteins in brains of patients. Increasing evidence shows that aggregation-prone proteins such as tau, α-synuclein and TDP-43 are accumulated…
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Keywords:
prion like;
prion;
protein aggregates;
properties assembled ... See more keywords
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Published in 2020 at "Current Opinion in Neurobiology"
DOI: 10.1016/j.conb.2019.11.022
Abstract: Emerging evidences linking pathological mechanisms of prions and tauopathies are accumulating. However, Tau assemblies do not yet fulfill all the criteria of prions. Here, we review recent data pointing similarities between prions and tauopathies and…
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Keywords:
tau assemblies;
properties tau;
prion like;
neurobiology ... See more keywords
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Published in 2020 at "Neuroscience Letters"
DOI: 10.1016/j.neulet.2020.135017
Abstract: Pathologic intracellular inclusions formed from polymers of misfolded α-synuclein (αsyn) protein define a group of neurodegenerative diseases termed synucleinopathies which includes Parkinson's disease (PD). Prion-like recruitment of endogenous cellular αsyn has been demonstrated to occur…
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Keywords:
prion like;
syn;
prion;
disease ... See more keywords
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Published in 2019 at "Biochemistry"
DOI: 10.1021/acs.biochem.9b00796
Abstract: The global transcription factor, p53, is a master regulator of gene expression in cells. Mutations in the TP53 gene promote unregulated cell growth through the inactivation of downstream effectors of the p53 pathway. In fact,…
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Keywords:
p53 amyloids;
prion like;
cancer;
p53 ... See more keywords
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Published in 2019 at "Laboratory Investigation"
DOI: 10.1038/s41374-019-0198-9
Abstract: Synucleinopathies are a group of neurodegenerative diseases characterized by the accumulation of insoluble, aggregated α-synuclein (αS) pathological inclusions. Multiple system atrophy (MSA) presents with extensive oligodendroglial αS pathology and additional more limited neuronal inclusions while…
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Keywords:
prion like;
system atrophy;
pathology;
msa ... See more keywords
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Published in 2021 at "Molecular Psychiatry"
DOI: 10.1038/s41380-021-01350-4
Abstract: If theories postulating that pathological proteins associated with neurodegenerative disorders behave similarly to prions were initially viewed with reluctance, it is now well-accepted that this occurs in several disease contexts. Notably, it has been reported…
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Keywords:
properties mutant;
huntingtin protein;
prion like;
prion ... See more keywords