Prion diseases of humans and animals: their causes and molecular basis.

By J. Collinge. Annual Review of Neuroscience, 2001

1,339 citations recorded by the source corpus.

Subfields: Molecular Biology, Neurology, Nutrition and Dietetics

View Paper: https://www.semanticscholar.org/paper/650f8f4c880880d357e5dd82236ba611065e21cc

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

In Molecular Biology

1. Vladimir N Uversky
2. A. Fink
3. C. Hetz
4. Claudio Soto
5. A. Keith Dunker
6. Christopher J. Oldfield
7. Peter Tompa
8. Lukasz Kurgan

In Neurology

1. Vladimir N Uversky
2. C. Hetz
3. Claudio Soto
4. A. Fink
5. Christopher M. Dobson

In Nutrition and Dietetics

1. Claudio Soto
2. Vladimir N Uversky
3. A. Fink

Citations in the corpus

• Conformational constraints for amyloid fibrillation: the importance of being unfolded. (2004, background): “Although unstructured in the isolated molecule, the N-terminal region contains tight binding sites for Cu + ions and therefore may acquire structure following copper binding [108–110].”
• In vitro generation of infectious scrapie prions. (2005, background): “The group is comprised of CreutzfeldtJakob disease (CJD), kuru, Gerstmann-Sträussler Sheinker syndrome (GSS), and fatal familial insomnia (FFI) in humans and scrapie, bovine spongiform encephalopathy (BSE), and chronic wasting disease (CWD) in animals (Collinge, 2001).”