Articles with "g51d mutation" as a keyword



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Physicochemical characterization of the G51D mutation of α-synuclein that is responsible for its severe cytotoxicity

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Published in 2021 at "Neuroscience Letters"

DOI: 10.1016/j.neulet.2021.136077

Abstract: Fibril formation and aggregation of α-synuclein are important for the pathogenesis of neurodegenerative disorders including Parkinson's disease. In familial Parkinson's disease, the G51D mutation of α-synuclein causes severe symptoms and rapid progression. α-Synuclein, an intrinsically… read more here.

Keywords: g51d synuclein; g51d mutation; synuclein monomer; synuclein ... See more keywords
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The Pathological G51D Mutation in Alpha-Synuclein Oligomers Confers Distinct Structural Attributes and Cellular Toxicity

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Published in 2022 at "Molecules"

DOI: 10.3390/molecules27041293

Abstract: A wide variety of oligomeric structures are formed during the aggregation of proteins associated with neurodegenerative diseases. Such soluble oligomers are believed to be key toxic species in the related disorders; therefore, identification of the… read more here.

Keywords: mutation alpha; g51d mutation; pathological g51d; toxicity ... See more keywords