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Review
. 1998 Feb 3;95(3):930-2.
doi: 10.1073/pnas.95.3.930.

The environmental dependency of protein folding best explains prion and amyloid diseases

Affiliations
Review

The environmental dependency of protein folding best explains prion and amyloid diseases

J W Kelly. Proc Natl Acad Sci U S A. .
No abstract available

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Figures

Figure 1
Figure 1
Possible pathways for the formation of PrPsc in the sporadic case and in the seeded infectious case, based on the presence of an intermediate that is critical for prion formation.
Figure 2
Figure 2
Prion formation can be inhibited either by ligand binding to PrPc, which shifts the equilibrium toward Prpc under cellular conditions that normally would form the prionogenic intermediate (Upper; also see ref. 35), or by using peptidomimetics that bind to the prionogenic intermediate or other intermediates that precede prion formation (not shown).

Comment on

References

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