Results 101 to 110 of about 95,914 (208)
Nanoscale profiling of evolving intermolecular interactions in ageing FUS condensates
Protein condensates can exist in different states with distinct material properties, corresponding to specific cellular functions. These material properties, however, remain difficult to characterise, in part due to the technical challenges associated ...
Alyssa Miller +6 more
doaj +1 more source
Protein Aggregates and Polyglutamine Tracts In Neurodegenerative Disease [PDF]
The incidence of neurodegenerative diseases such as Alzheimer\u27s Disease, Parkinson\u27s Disease, Huntington\u27s Disease and other Polyglutamine Diseases is projected to dramatically increase throughout the developed world, and yet the pathology of ...
Mack, John
core +1 more source
“Prion-like” seeding and propagation of oligomeric protein assemblies in neurodegenerative disorders
Intra- or extracellular aggregates of proteins are central pathogenic features in most neurodegenerative disorders. The accumulation of such proteins in diseased brains is believed to be the end-stage of a stepwise aggregation of misfolded monomers to ...
Silvia Zampar +12 more
doaj +1 more source
The N88S mutation in human seipin causes a dominant motor neuron disease marked by ER stress and inclusion body formation, lipid imbalance, and oxidative damage.
Vítor Moreira +3 more
doaj +1 more source
Mutations of Gly277 in <i>CPA1</i>-related chronic pancreatitis: clinical clues for misfolding aetiology. [PDF]
Zheng Y +4 more
europepmc +1 more source
Adjacent domains drive the emergence of misfolded intermediates in the folding pathway of the PDZ4 from MAGI1. [PDF]
Pennacchietti V +6 more
europepmc +1 more source
A widespread protein misfolding mechanism is differentially rescued in vitro by chaperones based on gene essentiality. [PDF]
Sitarik I +5 more
europepmc +1 more source
Destabilization of Helix III Initiates Early Serum Amyloid A Misfolding by Exposing Its Amyloidogenic Core. [PDF]
Nadwa H +4 more
europepmc +1 more source

