23 results on '"Priola, Suzette A."'
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2. The Size and Stability of Infectious Prion Aggregates Fluctuate Dynamically during Cellular Uptake and Disaggregation
3. Relative Abundance of apoE and Aβ1–42 Associated with Abnormal Prion Protein Differs between Creutzfeldt-Jakob Disease Subtypes.
4. Relative Abundance of apoE and Aβ1–42 Associated with Abnormal Prion Protein Differs between Creutzfeldt-Jakob Disease Subtypes
5. Molecular Aspects of Disease Pathogenesis in the Transmissible Spongiform Encephalopathies.
6. Proteomics Analysis of Amyloid and Nonamyloid Prion Disease Phenotypes Reveals Both Common and Divergent Mechanisms of Neuropathogenesis
7. Methods for Studying Prion Protein (PrP) Metabolism and the Formation of Protease-Resistant PrP in Cell Culture and Cell-Free Systems.
8. Amyloid Formation via Supramolecular Peptide Assemblies.
9. The role of the prion protein membrane anchor in prion infection
10. Cyclic Tetrapyrrole Sulfonation, Metals, and Oligomerization in Antiprion Activity
11. DNA Aptamers That Bind to PrPCand Not PrpScShow Sequence and Structure Specificity
12. Molecular Basis of Scrapie Strain Glycoform Variation*
13. Antiaggregating Antibody Raised Against Human PrP 106-126 Recognizes Pathological and Normal Isoforms of the Whole Prion Protein
14. Deletion of ß-Strand and a-Helix Secondary Structure in Normal Prion Protein Inhibits Formation of Its Protease-Resistant Isoform
15. N-terminal Truncation of Prion Protein Affects Both Formation and Conformation of Abnormal Protease-resistant Prion Protein Generatedin Vitro*
16. Efficient Conversion of Normal Prion Protein (PrP) by Abnormal Hamster PrP Is Determined by Homology at Amino Acid Residue 155
17. Species-Independent Inhibition of Abnormal Prion Protein (PrP) Formation by a Peptide Containing a Conserved PrP Sequence
18. Neuron-specific expression of a hamster prion protein minigene in transgenic mice induces susceptibility to hamster scrapie agent
19. A 60-kDa Prion Protein (PrP) with Properties of Both the Normal and Scrapie-associated Forms of PrP (∗)
20. Disinfection and Sterilization of Prion-Contaminated Medical Instruments
21. Identification of possible animal origins of prion disease in human beings.
22. Similar protein signatures for BSE and vCJD
23. Therapeutic Potential of Prion Protein Peptides in the Transmissible Spongiform Encephalopathies
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