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Autophagy|November 4, 2010
Small heat shock proteins, protein degradation and protein aggregation diseasesMichel J Vos, Marianne P Zijlstra, Serena Carra, et al.
Elife|September 6, 2021
HspB8 prevents aberrant phase transitions of FUS by chaperoning its folded RNA-binding domainEdgar E Boczek, Julius Fürsch, Marie Laura Niedermeier, et al.
Frontiers in Neurology|January 23, 2023
Case report: p.Glu134del SOD1 mutation in two apparently unrelated ALS patients with mirrored phenotypeGiulia Gianferrari, Ilaria Martinelli, Cecilia Simonini, et al.
Cell Stress & Chaperones|May 31, 2025
Pathogenic mechanism of the K141E mutation in HSPB8: Insights from smFRET and simulationsDaniele Montepietra, Sveinn Bjarnason, Kristinn R Óskarsson, et al.
The Biochemical Journal|October 23, 2009
Identification of the key structural motifs involved in HspB8/HspB6-Bag3 interactionMargit Fuchs, Dominic J Poirier, Samuel J Seguin, et al.
Journal of Neurochemistry|April 23, 2013
Harnessing the power of yeast to unravel the molecular basis of neurodegenerationSandra Tenreiro, Matthias C Munder, Simon Alberti, et al.
Cell|April 7, 2009
A systematic survey identifies prions and illuminates sequence features of prionogenic proteinsSimon Alberti, Randal Halfmann, Oliver King, et al.
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