Results 201 to 210 of about 78,455 (315)
A characteristic of many neurodegenerative disorders, such as Parkinson’s and Alzheimer’s, is amyloidogenic protein aggregation, for which there are currently no proven cures. Aging, mutation, and physiological stress can cause proteins to deviate from their natural folding patterns, potentially leading to the formation of hazardous protein aggregates.
Md. Tauqir Alam +4 more
wiley +1 more source
Challenges and Revisions in Diagnostic Criteria: Advancing Early Detection of Prion Diseases. [PDF]
Shimamura MI, Satoh K.
europepmc +1 more source
ABSTRACT White‐tailed deer (Odocoileus virginianus) are the most abundant and widespread cervid in North America. Genetic data are used as a tool to monitor populations and make management decisions for this game species. However, the development and use of genomic tools that can generate a set of markers suitable for longitudinal genomic data ...
David Navarro +24 more
wiley +1 more source
Characteristics of Different Types of Prion Diseases - China's Surveillance. [PDF]
Shi Q +8 more
europepmc +1 more source
ABSTRACT Objectives Endoscopic retrograde cholangiopancreatography (ERCP) is frequently indicated in patients who underwent Roux‐en‐Y gastric bypass (RYGB) surgery. Endoscopic ultrasound‐directed ERCP (EDGE) is a technique that is used to create a gastro‐gastrostomy by placing a lumen‐apposing metal stent (LAMS) between the gastric pouch and the ...
A. G. Overdevest +10 more
wiley +1 more source
Downregulation of STAT3 transcription factor reverses synaptotoxic phenotype of reactive astrocytes associated with prion diseases. [PDF]
Kushwaha R +3 more
europepmc +1 more source
Prospective 25-year surveillance of prion diseases in France, 1992 to 2016: a slow waning of epidemics and an increase in observed sporadic forms. [PDF]
Denouel A +10 more
europepmc +1 more source
Familial Creutzfeldt-Jakob Disease: Codon 200 Prion Disease in Libyan Jews
Zeev Meiner +2 more
openalex +1 more source

