Pages that link to "Q37040427"

The following pages link to Scrapie strain variation and its implications (Q37040427):

Displaying 44 items.

• Genetic and environmental factors affecting the de novo appearance of the [PSI+] prion in Saccharomyces cerevisiae (Q24533260) (← links)
• Darwinian evolution of prions in cell culture (Q24607587) (← links)
• Intraperitoneal Infection of Wild-Type Mice with Synthetically Generated Mammalian Prion (Q27319284) (← links)
• Biological and biochemical characterization of mice expressing prion protein devoid of the octapeptide repeat region after infection with prions (Q28482433) (← links)
• Prions in Saccharomyces and Podospora spp.: protein-based inheritance. (Q30323934) (← links)
• Post-translational modifications in PrP expand the conformational diversity of prions in vivo (Q30399619) (← links)
• Gene expression alterations in brains of mice infected with three strains of scrapie (Q33243428) (← links)
• Biochemical characterization of prion strains in bank voles (Q33456970) (← links)
• Distinct type of transmission barrier revealed by study of multiple prion determinants of Rnq1. (Q33527001) (← links)
• Mutation-dependent polymorphism of Cu,Zn-superoxide dismutase aggregates in the familial form of amyotrophic lateral sclerosis (Q33559556) (← links)
• Transmission of scrapie and sheep-passaged bovine spongiform encephalopathy prions to transgenic mice expressing elk prion protein (Q33580805) (← links)
• A new method for the characterization of strain-specific conformational stability of protease-sensitive and protease-resistant PrPSc (Q33697859) (← links)
• Successful transmission of three mouse-adapted scrapie strains to murine neuroblastoma cell lines overexpressing wild-type mouse prion protein (Q33794942) (← links)
• Progress toward an ultimate proof of the prion hypothesis (Q34033631) (← links)
• Effects of polymorphisms in ovine and caprine prion protein alleles on cell-free conversion (Q34632935) (← links)
• Suicidal [PSI+] is a lethal yeast prion (Q34750018) (← links)
• Prion infection of mouse brain reveals multiple new upregulated genes involved in neuroinflammation or signal transduction (Q35115616) (← links)
• Prion disease induced alterations in gene expression in spleen and brain prior to clinical symptoms. (Q35205306) (← links)
• Prions on the move (Q35512142) (← links)
• Striatal pathology underlies prion infection-mediated hyperactivity in mice (Q35714160) (← links)
• Local unfolding of Cu, Zn superoxide dismutase monomer determines the morphology of fibrillar aggregates (Q35873804) (← links)
• Late treatment with polyene antibiotics can prolong the survival time of scrapie-infected animals (Q36549164) (← links)
• Mouse prion protein polymorphism Phe-108/Val-189 affects the kinetics of fibril formation and the response to seeding: evidence for a two-step nucleation polymerization mechanism (Q36620764) (← links)
• Amphotericin B delays both scrapie agent replication and PrP-res accumulation early in infection (Q36637324) (← links)
• Role of Prion Replication in the Strain-dependent Brain Regional Distribution of Prions (Q37066538) (← links)
• Comparative profiling of highly enriched 22L and Chandler mouse scrapie prion protein preparations (Q37091434) (← links)
• Co-existence of distinct prion types enables conformational evolution of human PrPSc by competitive selection (Q37226238) (← links)
• Chronic wasting disease: fingerprinting the culprit in risk assessments (Q37997567) (← links)
• Implications of prion adaptation and evolution paradigm for human neurodegenerative diseases. (Q38176721) (← links)
• Neurodegenerative Disease Transmission and Transgenesis in Mice. (Q39134078) (← links)
• Adaptation and selection of prion protein strain conformations following interspecies transmission of transmissible mink encephalopathy (Q39591398) (← links)
• Strains of [PSI(+)] are distinguished by their efficiencies of prion-mediated conformational conversion (Q39646125) (← links)
• Stability of murine scrapie strain 87V after passage in sheep and comparison with the CH1641 ovine strain (Q40269642) (← links)
• Genesis and variability of [PSI] prion factors in Saccharomyces cerevisiae. (Q41815189) (← links)
• Species barrier in prion diseases: a kinetic interpretation based on the conformational adaptation of the prion protein (Q41960955) (← links)
• Molecular and transmission characteristics of primary-passaged ovine scrapie isolates in conventional and ovine PrP transgenic mice (Q41965529) (← links)
• The interpretation of disease phenotypes to identify TSE strains in mice: characterisation of BSE using PrPSc distribution patterns in the brain (Q42065914) (← links)
• Evidence for distinct chronic wasting disease (CWD) strains in experimental CWD in ferrets (Q42165503) (← links)
• Recombinant PrP and Its Contribution to Research on Transmissible Spongiform Encephalopathies. (Q47294251) (← links)
• Biological and biochemical characterization of M2B cells: Classical BSE prion is conserved in transgenic mice overexpressing bovine prion protein gene (Q47446061) (← links)
• Early appearance but lagged accumulation of detergent-insoluble prion protein in the brains of mice inoculated with a mouse-adapted Creutzfeldt-Jakob disease agent. (Q54028007) (← links)
• Use of different RT-QuIC substrates for detecting CWD prions in the brain of Norwegian cervids (Q91825802) (← links)
• All the Same? The Secret Life of Prion Strains within Their Target Cells (Q93005212) (← links)
• Scientific opinion on chronic wasting disease (II) (Q97070651) (← links)