Pages that link to "Q40417166"

The following pages link to The AGAAAAGA palindrome in PrP is required to generate a productive PrPSc-PrPC complex that leads to prion propagation (Q40417166):

Displaying 45 items.

• The prion protein unstructured N‐terminal region is a broad‐spectrum molecular sensor with diverse and contrasting potential functions (Q27022256) (← links)
• Probing the role of structural features of mouse PrP in yeast by expression as Sup35-PrP fusions (Q27022544) (← links)
• Neurotoxicity of prion peptides mimicking the central domain of the cellular prion protein (Q28535083) (← links)
• Characterization of the genomic region containing the Shadow of Prion Protein (SPRN) gene in sheep (Q33286202) (← links)
• Molecular dynamics simulations capture the misfolding of the bovine prion protein at acidic pH (Q33649818) (← links)
• Live cell fluorescence resonance energy transfer predicts an altered molecular association of heterologous PrPSc with PrPC. (Q33726542) (← links)
• PrP conformational transitions alter species preference of a PrP-specific antibody. (Q33810140) (← links)
• Conservation of a glycine-rich region in the prion protein is required for uptake of prion infectivity (Q33924421) (← links)
• Copper binding extrinsic to the octarepeat region in the prion protein (Q33999707) (← links)
• Assessing proteinase K resistance of fish prion proteins in a scrapie-infected mouse neuroblastoma cell line (Q34580839) (← links)
• An N-terminal polybasic domain and cell surface localization are required for mutant prion protein toxicity (Q34800606) (← links)
• Unravelling the biodiversity of nanoscale signatures of spider silk fibres. (Q35068881) (← links)
• Structural polymorphism in amyloids: new insights from studies with Y145Stop prion protein fibrils. (Q35604887) (← links)
• A naturally occurring C-terminal fragment of the prion protein (PrP) delays disease and acts as a dominant-negative inhibitor of PrPSc formation. (Q35626193) (← links)
• Ion channels induced by the prion protein: mediators of neurotoxicity. (Q35918928) (← links)
• Cellular prion protein regulates its own α-cleavage through ADAM8 in skeletal muscle (Q35956641) (← links)
• Role of prion protein aggregation in neurotoxicity (Q36197275) (← links)
• Dodecylphosphocholine Micelles Induce Amyloid Formation of the PrP(110-136) Peptide via an α-Helical Metastable Conformation (Q36216213) (← links)
• X-Ray fiber and powder diffraction of PrP prion peptides. (Q36693073) (← links)
• Structural transitions in full-length human prion protein detected by xenon as probe and spin labeling of the N-terminal domain (Q37035847) (← links)
• The region approximately between amino acids 81 and 137 of proteinase K-resistant PrPSc is critical for the infectivity of the Chandler prion strain (Q37145304) (← links)
• The consequences of pathogenic mutations to the human prion protein (Q37285520) (← links)
• A New Transgenic Mouse Model of Gerstmann-Straussler-Scheinker Syndrome Caused by the A117V Mutation of PRNP. (Q37359955) (← links)
• Pathogenic mutations within the hydrophobic domain of the prion protein lead to the formation of protease-sensitive prion species with increased lethality (Q37644076) (← links)
• Mapping superoxide dismutase 1 domains of non-native interaction: roles of intra- and intermolecular disulfide bonding in aggregation (Q37707829) (← links)
• Proteolytic processing of the prion protein in health and disease. (Q38079239) (← links)
• The structure of human prions: from biology to structural models-considerations and pitfalls (Q38261710) (← links)
• Caprine PrP variants harboring Asp-146, His-154 and Gln-211 alleles display reduced convertibility upon interaction with pathogenic murine prion protein in scrapie infected cells (Q38734782) (← links)
• The hydrophobic core region governs mutant prion protein aggregation and intracellular retention (Q39680946) (← links)
• Cytosolic prion protein toxicity is independent of cellular prion protein expression and prion propagation (Q40191573) (← links)
• A conservative mutant of a proteolytic fragment produced during fibril formation enhances fibrillogenesis (Q41636026) (← links)
• PRNP and SPRN genes polymorphism in atypical bovine spongiform encephalopathy cases diagnosed in Polish cattle (Q42654796) (← links)
• Design of metastable β-sheet oligomers from natively unstructured peptide (Q42785452) (← links)
• Characterization of PRNP and SPRN coding regions from atypical scrapie cases diagnosed in Poland. (Q43893106) (← links)
• Do prion protein gene polymorphisms induce apoptosis in non-mammals? (Q46584144) (← links)
• Effects of the A117V mutation on the folding and aggregation of palindromic sequences (PrP113-120) in prion: insights from replica exchange molecular dynamics simulations (Q46801576) (← links)
• Different misfolding mechanisms converge on common conformational changes: human prion protein pathogenic mutants Y218N and E196K. (Q47572636) (← links)
• In vitro self-propagation of recombinant PrPSc-like conformation generated in the yeast cytoplasm (Q48475372) (← links)
• Optimal molecular structures of prion AGAAAAGA amyloid fibrils formatted by simulated annealing. (Q51612921) (← links)
• Impaired transmissibility of atypical prions from genetic CJD (Q58797388) (← links)
• Polymorphisms of SPRN (shadow of prion protein homology) in three breeds of sheep in China (Q83517206) (← links)
• Structural evidence for the critical role of the prion protein hydrophobic region in forming an infectious prion (Q91800637) (← links)
• Cryo-EM structure of a human prion fibril with a hydrophobic, protease-resistant core (Q91875083) (← links)
• Mutations in Prion Protein Gene: Pathogenic Mechanisms in C-Terminal vs. N-Terminal Domain, a Review (Q92150816) (← links)
• Polymorphisms of shadow of prion protein gene (SPRN) in Korean native cattle (Hanwoo) and Holstein cattle (Q99564884) (← links)