scholarly article | Q13442814 |
P2860 | cites work | Generating a prion with bacterially expressed recombinant prion protein | Q24626352 |
Prions | Q24633319 | ||
The physical relationship between infectivity and prion protein aggregates is strain-dependent | Q27315010 | ||
Prion disease susceptibility is affected by -structure folding propensity and local side-chain interactions in PrP | Q27665543 | ||
Evidence of presynaptic location and function of the prion protein | Q28145703 | ||
Ultra-efficient PrP(Sc) amplification highlights potentialities and pitfalls of PMCA technology | Q28478072 | ||
The highly conserved, N-terminal (RXXX)8 motif of mouse Shadoo mediates nuclear accumulation | Q28508804 | ||
Knockout of the prion protein (PrP)-like Sprn gene does not produce embryonic lethality in combination with PrP(C)-deficiency | Q28509844 | ||
De novo generation of a transmissible spongiform encephalopathy by mouse transgenesis | Q30485527 | ||
Getting a grip on prions: oligomers, amyloids, and pathological membrane interactions | Q30492360 | ||
Small-molecule activators of a proenzyme | Q33515227 | ||
Association thermodynamics and conformational stability of beta-sheet amyloid beta(17-42) oligomers: effects of E22Q (Dutch) mutation and charge neutralization | Q33598957 | ||
Molecular interactions between prions as seeds and recombinant prion proteins as substrates resemble the biological interspecies barrier in vitro | Q33769143 | ||
Rapid end-point quantitation of prion seeding activity with sensitivity comparable to bioassays | Q33769767 | ||
Three-dimensional molecular theory of solvation coupled with molecular dynamics in Amber | Q33819349 | ||
Dissociation of infectivity from seeding ability in prions with alternate docking mechanism | Q33967960 | ||
Self-assembling small molecules form nanofibrils that bind procaspase-3 to promote activation | Q34069805 | ||
Dominant-negative inhibition of prion replication in transgenic mice | Q34191612 | ||
Characterization of peptides obtained from digests of bovine brain which accelerate structural conversions of the recombinant bovine prion protein | Q34572778 | ||
A systematic mammalian genetic interaction map reveals pathways underlying ricin susceptibility | Q34581520 | ||
Prion replication alters the distribution of synaptophysin and caveolin 1 in neuronal lipid rafts | Q35103328 | ||
Comparative analysis of essential collective dynamics and NMR-derived flexibility profiles in evolutionarily diverse prion proteins | Q35578781 | ||
Change in the characteristics of ferritin induces iron imbalance in prion disease affected brains | Q35777814 | ||
Characterization of prion protein (PrP)-derived peptides that discriminate full-length PrPSc from PrPC. | Q35865508 | ||
Molecular architecture of human prion protein amyloid: a parallel, in-register beta-structure | Q36277140 | ||
Real time quaking-induced conversion analysis of cerebrospinal fluid in sporadic Creutzfeldt-Jakob disease | Q36281277 | ||
Mechanisms of prion protein assembly into amyloid | Q36497270 | ||
Exploiting position effects and the gypsy retrovirus insulator to engineer precisely expressed transgenes | Q36580731 | ||
Post-translational changes to PrP alter transmissible spongiform encephalopathy strain properties | Q36664699 | ||
Hydration effects on the HET-s prion and amyloid-beta fibrillous aggregates, studied with three-dimensional molecular theory of solvation | Q36957378 | ||
Rapid creation and quantitative monitoring of high coverage shRNA libraries | Q37440284 | ||
Prion-like mechanisms in neurodegenerative diseases | Q37661351 | ||
The propagation of prion-like protein inclusions in neurodegenerative diseases | Q37759499 | ||
The amyloid state of proteins in human diseases | Q37994283 | ||
Real-time quaking-induced conversion: a highly sensitive assay for prion detection | Q39439895 | ||
Accelerated accumulation of misfolded prion protein and spongiform degeneration in a Drosophila model of Gerstmann-Sträussler-Scheinker syndrome. | Q40265194 | ||
3D-RISM-Dock: A New Fragment-Based Drug Design Protocol | Q40276857 | ||
Amyloid fibrils of human prion protein are spun and woven from morphologically disordered aggregates | Q41929396 | ||
Characterization of the nucleation barriers for protein aggregation and amyloid formation | Q41950121 | ||
Multiple substitutions of methionine 129 in human prion protein reveal its importance in the amyloid fibrillation pathway | Q42252589 | ||
Spatiotemporal gene expression targeting with the TARGET and gene-switch systems in Drosophila | Q44768547 | ||
Exploring the essential collective dynamics of interacting proteins: application to prion protein dimers | Q45760615 | ||
Toward molecular dissection of PrPC-PrPSc interactions | Q46247921 | ||
Dynamics of essential collective motions in proteins: theory | Q47951149 | ||
The prion or the related Shadoo protein is required for early mouse embryogenesis. | Q48454584 | ||
Efficient treatment of solvation shells in 3D molecular theory of solvation. | Q50957533 | ||
Conformational modes in biomolecules: dynamics and approximate invariance. | Q51391602 | ||
Exploring the essential collective dynamics of interacting proteins: Application to prion protein dimers | Q57014315 | ||
Structural Domains and Main-Chain Flexibility in Prion Proteins† | Q57014374 | ||
Heparin Binding by Murine Recombinant Prion Protein Leads to Transient Aggregation and Formation of RNA-Resistant Species | Q57084698 | ||
Symmetry-based constant-time homonuclear dipolar recoupling in solid state NMR | Q57098982 | ||
Prion protein expression level alters regional copper, iron and zinc content in the mouse brain | Q57610257 | ||
Reversion of prion protein conformational changes by synthetic b-sheet breaker peptides | Q59691802 | ||
P433 | issue | sup1 | |
P304 | page(s) | 81-104 | |
P577 | publication date | 2013-04-01 | |
P1433 | published in | Prion | Q26842757 |
P1476 | title | Protein Structure and Biology: Poster Abstracts | |
P478 | volume | 7 |
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