Pages that link to "Q34201802"
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The following pages link to A prion protein epitope selective for the pathologically misfolded conformation (Q34201802):
Displaying 50 items.
- A camelid anti-PrP antibody abrogates PrP replication in prion-permissive neuroblastoma cell lines (Q21562652) (← links)
- Transmissible Spongiform Encephalopathies Affecting Humans (Q24549130) (← links)
- Insoluble cellular prion protein and its association with prion and Alzheimer diseases (Q27012706) (← links)
- Prion protein-specific antibodies that detect multiple TSE agents with high sensitivity (Q27316704) (← links)
- Insight into the PrPC-->PrPSc conversion from the structures of antibody-bound ovine prion scrapie-susceptibility variants (Q28270774) (← links)
- Parallel in-register intermolecular β-sheet architectures for prion-seeded prion protein (PrP) amyloids. (Q30364768) (← links)
- Monoclonal antibodies recognize distinct conformational epitopes formed by polyglutamine in a mutant huntingtin fragment (Q30490726) (← links)
- The structure of the infectious prion protein: experimental data and molecular models (Q30768165) (← links)
- Novel single chain antibodies to the prion protein identified by phage display (Q30826530) (← links)
- Aptamers against prion proteins and prions. (Q30860694) (← links)
- Prion protein self-peptides modulate prion interactions and conversion (Q30924592) (← links)
- The expanding universe of prion diseases (Q33239695) (← links)
- Directed evolution of an anti-prion protein scFv fragment to an affinity of 1 pM and its structural interpretation (Q33256919) (← links)
- Probing structural differences in prion protein isoforms by tyrosine nitration (Q33280623) (← links)
- Mapping of possible prion protein self-interaction domains using peptide arrays (Q33281952) (← links)
- Thioaptamer interactions with prion proteins: sequence-specific and non-specific binding sites (Q33283775) (← links)
- A novel real-time ultrasonic method for prion protein detection using plasminogen as a capture molecule (Q33292021) (← links)
- Anti-idiotypic antibodies: a new approach in prion research (Q33419724) (← links)
- Molecular dynamics simulations capture the misfolding of the bovine prion protein at acidic pH (Q33649818) (← links)
- Tracing conformational transition of abnormal prion proteins during interspecies transmission by using novel antibodies (Q33782462) (← links)
- Specific binding of the pathogenic prion isoform: development and characterization of a humanized single-chain variable antibody fragment (Q33809258) (← links)
- Immunodetection of disease-associated mutant PrP, which accelerates disease in GSS transgenic mice (Q33893587) (← links)
- PrP(Sc)-specific antibodies with the ability to immunodetect prion oligomers. (Q33916451) (← links)
- PrP(Sc)-specific antibodies do not induce prion disease or misfolding of PrP(C) in highly susceptible Tga20 mice (Q34051202) (← links)
- Misfolded mutant SOD1 directly inhibits VDAC1 conductance in a mouse model of inherited ALS (Q34139970) (← links)
- PrionHome: a database of prions and other sequences relevant to prion phenomena (Q34171372) (← links)
- Conformation-dependent high-affinity monoclonal antibodies to prion proteins (Q34211212) (← links)
- Detection of prion protein particles in blood plasma of scrapie infected sheep (Q34261862) (← links)
- Transmissible spongiform encephalopathies. (Q34289917) (← links)
- Generation of antibodies against bovine recombinant prion protein in various strains of mice (Q34325859) (← links)
- Nanopore analysis reveals differences in structural stability of ovine PrP(C) proteins corresponding to scrapie susceptible (VRQ) and resistance (ARR) genotypes (Q34362541) (← links)
- Prion protein-specific antibodies-development, modes of action and therapeutics application (Q34423386) (← links)
- Immunomodulation for prion and prion-related diseases (Q34565644) (← links)
- The N-terminal sequence of prion protein consists an epitope specific to the abnormal isoform of prion protein (PrP(Sc)) (Q34612763) (← links)
- Superparamagnetic nanoparticle capture of prions for amplification (Q34742787) (← links)
- Sequence-independent control of peptide conformation in liposomal vaccines for targeting protein misfolding diseases (Q34799960) (← links)
- Human prions and plasma lipoproteins (Q34983985) (← links)
- Biological effects and use of PrPSc- and PrP-specific antibodies generated by immunization with purified full-length native mouse prions (Q35076872) (← links)
- Specificity of lymphoreticular accumulation of prion protein for variant Creutzfeldt-Jakob disease. (Q35587468) (← links)
- Prion diseases: from molecular biology to intervention strategies (Q35602374) (← links)
- Mammalian prion biology: one century of evolving concepts (Q35639302) (← links)
- A Structural and Functional Comparison Between Infectious and Non-Infectious Autocatalytic Recombinant PrP Conformers (Q35678593) (← links)
- Localization of a conformational epitope common to non-native and fibrillar immunoglobulin light chains. (Q35699410) (← links)
- Identifying polyglutamine protein species in situ that best predict neurodegeneration (Q35729286) (← links)
- Technical aspects of the development and validation of tests for variant Creutzfeldt-Jakob disease in blood transfusion (Q35743772) (← links)
- Molecular diagnostic tools in Creutzfeldt-Jakob disease and other prion disorders (Q35770573) (← links)
- Screening assays for transmissible spongiform encephalopathies (TSEs). (Q35812894) (← links)
- Could immunomodulation be used to prevent prion diseases? (Q35875915) (← links)
- Diagnosing prion diseases: needs, challenges and hopes (Q35892062) (← links)
- Prion diseases--close to effective therapy? (Q35906120) (← links)