308 results on '"Supattapone, Surachai"'
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2. Anti-prion drugs do not improve survival in novel knock-in models of inherited prion disease
3. Prion Seeds Distribute throughout the Eyes of Sporadic Creutzfeldt-Jakob Disease Patients
4. Correction: Emergence of Prions Selectively Resistant to Combination Drug Therapy
5. A Structural and Functional Comparison Between Infectious and Non-Infectious Autocatalytic Recombinant PrP Conformers.
6. Anti-prion drugs do not improve survival in knock-in models of inherited prion disease
7. Convergent generation of atypical prions in knock-in mouse models of genetic prion disease
8. Phospholipid cofactor solubilization inhibits formation of native prions
9. Cofactor Molecules Induce Structural Transformation during Infectious Prion Formation
10. Cofactor molecules: Essential partners for infectious prions
11. Structural Studies of the Scrapie Prion Protein by Electron Crystallography
12. Elimination of Prions by Branched Polyamines and Implications for Therapeutics
13. Conformational diversity in purified prions produced in vitro
14. SEC24A identified as an essential mediator of thapsigargin-induced cell death in a genome-wide CRISPR/Cas9 screen
15. The effects of endothelin on rat astrocytes
16. A single protective polymorphism in the prion protein blocks cross‐species prion replication in cultured cells
17. Expanding the prion disease repertoire
18. Cofactor Involvement in Prion Propagation
19. A single protective polymorphism in the prion protein blocks cross‐species prion replication in cultured cells.
20. Comparative Analysis of Mutant Huntingtin Binding Partners in Yeast Species
21. Cofactor molecules maintain infectious conformation and restrict strain properties in purified prions
22. Isolation of phosphatidylethanolamine as a solitary cofactor for prion formation in the absence of nucleic acids
23. What Makes a Prion Infectious?
24. Formation of Native Prions from Minimal Components in vitro
25. Alternating anti-prion regimens reduce combination drug resistance but do not further extend survival in scrapie-infected mice
26. Cyclic AMP-Dependent Phosphorylation of a Brain Inositol Trisphosphate Receptor Decreases Its Release of Calcium
27. Inositolphospholipid-Linked Glutamate Receptors Mediate Cerebellar Parallel-Fiber--Purkinje-Cell Synaptic Transmission
28. The Inositol 1,4,5,-Trisphosphate Receptor in Cerebellar Purkinje Cells: Quantitative Immunogold Labeling Reveals Concentration in an ER Subcompartment
29. SEC24A facilitates colocalization and Ca2+ flux between the endoplasmic reticulum and mitochondria
30. Cofactor Involvement in Prion Propagation
31. Prion protein conversion in vitro
32. RNA molecules stimulate prion protein conversion
33. On the horizon: a blood test for prions
34. Transmissible spongiform encephalopathies
35. Amplification of Purified Prions In Vitro
36. Identification of a homology-independent linchpin domain controlling mouse and bank vole prion protein conversion
37. A Genome-Wide CRISPR/Cas9 Screen Reveals that Riboflavin Regulates Hydrogen Peroxide Entry into HAP1 Cells
38. Emergence of prions selectively resistant to combination drug therapy
39. Cofactor and glycosylation preferences for in vitro prion conversion are predominantly determined by strain conformation
40. Disinfection of Prions
41. Which criteria best support the diagnosis of VV1 sporadic Creutzfeldt-Jakob disease?
42. Copper (II) ions potently inhibit purified PrPres amplification
43. Post-transcriptional suppression of pathogenic prion protein expression in Drosophila neurons
44. Full restoration of specific infectivity and strain properties from pure mammalian prion protein
45. Rescue of Transgenic Alzheimer’s Pathophysiology by Polymeric Cellular Prion Protein Antagonists
46. Species-dependent differences in cofactor utilization for formation of the protease-resistant prion protein in vitro
47. The stoichiometry of host Pr[P.sup.C] glycoforms modulates the efficiency of Pr[P.sup.Sc] formation in vitro
48. In vitro prion protein conversion in detergent-solubilized membranes
49. CAG Expansions Are Genetically Stable and Form Nontoxic Aggregates in Cells Lacking Endogenous Polyglutamine Proteins
50. Interallelic Transcriptional Enhancement as an in Vivo Measure of Transvection in Drosophila melanogaster
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