Prion diseases are a family of rare progressive neurodegenerative disorders that affect both humans and animals. They are associated with the formation of aggregates of the prion protein, PrP. How ...
Particle size characterization in nanosuspensions often focuses on ‘majority’ features of the size distribution. Yet, for various suspensions in (bio)pharmaceuticals or fine chemicals, small fractions ...
EGFP-SOD1 G93A formed large aggregates in the cytoplasm of live NSC34 cells. The arrows indicate an intracellular aggregate. SOD1: Cu/Zn superoxide dismutase 1; G93A: glycine 93 changed to alanine.
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