12 results on '"Priola, Suzette A."'
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2. PrP Knockout Cells Expressing Transmembrane PrP Resist Prion Infection
3. A Specific Population of Abnormal Prion Protein Aggregates Is Preferentially Taken Up by Cells and Disaggregated in a Strain-Dependent Manner
4. Lack of Prion Infectivity in Fixed Heart Tissue from Patients with Creutzfeldt-Jakob Disease or Amyloid Heart Disease
5. Cells Expressing Anchorless Prion Protein Are Resistant to Scrapie Infection
6. How Animal Prions Cause Disease in Humans
7. Cyclic Tetrapyrrole Sulfonation, Metals, and Oligomerization in Antiprion Activity
8. Multiple Amino Acid Residues within the Rabbit Prion Protein Inhibit Formation of Its Abnormal Isoform
9. Deletion of β-Strand and α-Helix Secondary Structure in Normal Prion Protein Inhibits Formation of Its Protease-Resistant Isoform
10. Efficient Conversion of Normal Prion Protein (PrP) by Abnormal Hamster PrP Is Determined by Homology at Amino Acid Residue 155
11. A Specific Population of Abnormal Prion Protein Aggregates Is Preferentially Taken Up by Cells and Disaggregated in a Strain- Dependent Manner.
12. Species-Independent Inhibition of Abnormal Prion Protein (PrP) Formation by a Peptide Containing a Conserved PrP Sequence
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