Foldamers Reveal and Validate Novel Therapeutic Targets Associated with Toxic α-synuclein Self-Assembly
Selected by
Joanna Zell
Novel insights in the pathophysiology of α-synuclein dysregulation on D2 receptor activity contributing to the vulnerability of dopamine neurons
Selected by
Emma Wilson
Selectivity of Protein Interactions along the Aggregation Pathway of α-synuclein
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Utrecht Protein Folding and Assembly
CSPα reduces aggregates and rescues striatal dopamine release in αsynuclein transgenic mice
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Kristina Kuhbandner
In situ architecture of neuronal α-synuclein inclusions
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Tessa Sinnige
FUS gene is dual-coding with both proteins united in FUS-mediated toxicity
Selected by
Madhuja Samaddar
Skd3 (human CLPB) is a potent mitochondrial protein disaggregase that is inactivated by 3-methylglutaconic aciduria-linked mutations
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Tessa Sinnige
Selective K-ATP channel-dependent loss of pacemaking in vulnerable nigrostriatal dopamine neurons by α-synuclein aggregates
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Jessica Xie
HSP110 dependent HSP70 disaggregation machinery mediates prion-like propagation of amyloidogenic proteins in metazoa
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Tessa Sinnige
The properties of α-synuclein secondary nuclei are dominated by the solution conditions rather than the seed fibril strain
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Tessa Sinnige
Negative Regulation of Autophagy by UBA6-BIRC6–Mediated Ubiquitination of LC3
Selected by
Sandra Malmgren Hill
A non-canonical arm of UPRER mediates longevity through ER remodeling and lipophagy.
Selected by
Sandra Franco Iborra