Pages that link to "Q34084209"
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The following pages link to Sensitive detection of pathological prion protein by cyclic amplification of protein misfolding (Q34084209):
Displaying 50 items.
- Scrapie Agent (Strain 263K) can transmit disease via the oral route after persistence in soil over years (Q21144451) (← links)
- Transmission of prions (Q24540228) (← links)
- Selective incorporation of polyanionic molecules into hamster prions (Q24596538) (← links)
- Prion hypothesis: the end of the controversy? (Q24599702) (← links)
- Darwinian evolution of prions in cell culture (Q24607587) (← links)
- Formation of native prions from minimal components in vitro (Q24676353) (← links)
- Evaluation of quinacrine treatment for prion diseases (Q24682427) (← links)
- Gut Feelings About α-Synuclein in Gastrointestinal Biopsies: Biomarker in the Making? (Q26769620) (← links)
- Insights into Mechanisms of Chronic Neurodegeneration (Q26771732) (← links)
- The diverse roles of mononuclear phagocytes in prion disease pathogenesis (Q26823101) (← links)
- Distinct origins of dura mater graft-associated Creutzfeldt-Jakob disease: past and future problems (Q26823411) (← links)
- Quantum dots and prion proteins: is this a new challenge for neurodegenerative diseases imaging? (Q27008857) (← links)
- Highly efficient protein misfolding cyclic amplification (Q27312316) (← links)
- Synthetic prions with novel strain-specified properties (Q27316313) (← links)
- De novo generation of infectious prions in vitro produces a new disease phenotype (Q27317045) (← links)
- Transgenic Rabbits Expressing Ovine PrP Are Susceptible to Scrapie (Q27318296) (← links)
- Intraperitoneal Infection of Wild-Type Mice with Synthetically Generated Mammalian Prion (Q27319284) (← links)
- Urine proteins identified by two-dimensional differential gel electrophoresis facilitate the differential diagnoses of scrapie (Q27319880) (← links)
- De novo generation of prion strains (Q28249136) (← links)
- The state of the prion (Q28288758) (← links)
- Protein folding activity of ribosomal RNA is a selective target of two unrelated antiprion drugs (Q28472742) (← links)
- Expression of mutant or cytosolic PrP in transgenic mice and cells is not associated with endoplasmic reticulum stress or proteasome dysfunction (Q28477995) (← links)
- Ultra-efficient PrP(Sc) amplification highlights potentialities and pitfalls of PMCA technology (Q28478072) (← links)
- Kosmotropic anions promote conversion of recombinant prion protein into a PrPSc-like misfolded form (Q28480574) (← links)
- Prion seeding activities of mouse scrapie strains with divergent PrPSc protease sensitivities and amyloid plaque content using RT-QuIC and eQuIC (Q28484853) (← links)
- Re-assessment of PrP(Sc) distribution in sporadic and variant CJD (Q28534501) (← links)
- Shaking alone induces de novo conversion of recombinant prion proteins to β-sheet rich oligomers and fibrils (Q28539309) (← links)
- Isolation of a Defective Prion Mutant from Natural Scrapie (Q28553700) (← links)
- A route for prion neuroinvasion. (Q30328574) (← links)
- Ultrasonication-dependent production and breakdown lead to minimum-sized amyloid fibrils. (Q30378508) (← links)
- The sour side of neurodegenerative disorders: the effects of protein glycation. (Q30386079) (← links)
- Effect of ultrasound on the function and structure of a membrane protein: The case study of photosynthetic Reaction Center from Rhodobacter sphaeroides. (Q30393071) (← links)
- Preclinical detection of variant CJD and BSE prions in blood (Q30436588) (← links)
- Proper calibration of ultrasonic power enabled the quantitative analysis of the ultrasonication-induced amyloid formation process (Q30459645) (← links)
- Inactivation of template-directed misfolding of infectious prion protein by ozone (Q30465032) (← links)
- Conformational stability of PrP amyloid fibrils controls their smallest possible fragment size (Q30491031) (← links)
- Getting a grip on prions: oligomers, amyloids, and pathological membrane interactions (Q30492360) (← links)
- Production of cattle lacking prion protein. (Q30492928) (← links)
- Tetracyclines affect prion infectivity (Q30531528) (← links)
- Anle138b: a novel oligomer modulator for disease-modifying therapy of neurodegenerative diseases such as prion and Parkinson's disease (Q30540027) (← links)
- Human prion protein sequence elements impede cross-species chronic wasting disease transmission. (Q30639674) (← links)
- Detection of prion protein using a capillary electrophoresis-based competitive immunoassay with laser-induced fluorescence detection and cyclodextrin-aided separation (Q30781710) (← links)
- Detection of prion seeding activity in the olfactory mucosa of patients with Fatal Familial Insomnia (Q30844542) (← links)
- Aptamers against prion proteins and prions. (Q30860694) (← links)
- Prion protein self-peptides modulate prion interactions and conversion (Q30924592) (← links)
- Rationale for diagnosing human prion disease. (Q30936688) (← links)
- Detection of sub-clinical CWD infection in conventional test-negative deer long after oral exposure to urine and feces from CWD+ deer (Q30946000) (← links)
- Isolation and characterization of a polymerized prion protein. (Q31050944) (← links)
- Prion-seeding activity in cerebrospinal fluid of deer with chronic wasting disease (Q31144537) (← links)
- Prion replication without host adaptation during interspecies transmissions. (Q31155113) (← links)