Pages that link to "Q47593792"
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The following pages link to Linkage of the scrapie-associated fibril protein (PrP) gene and Sinc using congenic mice and restriction fragment length polymorphism analysis (Q47593792):
Displaying 50 items.
- Prions (Q24633319) (← links)
- Knockout of the prion protein (PrP)-like Sprn gene does not produce embryonic lethality in combination with PrP(C)-deficiency (Q28509844) (← links)
- Prion amyloid structure explains templating: how proteins can be genes (Q30392820) (← links)
- Copper(II)-induced conformational changes and protease resistance in recombinant and cellular PrP. Effect of protein age and deamidation (Q30881188) (← links)
- Two alleles of a neural protein gene linked to scrapie in sheep (Q33495492) (← links)
- The genetics of prions--a contradiction in terms? (Q33705857) (← links)
- Conservation of infectivity in purified fibrillary extracts of scrapie-infected hamster brain after sequential enzymatic digestion or polyacrylamide gel electrophoresis (Q33802052) (← links)
- Pathogenesis of prion diseases: a progress report (Q34202007) (← links)
- Spongiform encephalopathies: insights from transgenic models (Q34306690) (← links)
- Primary structure of prion protein may modify scrapie isolate properties (Q34307605) (← links)
- Species specificity in the cell-free conversion of prion protein to protease-resistant forms: a model for the scrapie species barrier (Q34393434) (← links)
- Molecular biology of prion diseases (Q34534878) (← links)
- Fibrils from brains of cows with new cattle disease contain scrapie-associated protein (Q34560735) (← links)
- Scrapie: Report of an outbreak and brief review (Q35193162) (← links)
- Natural and experimental prion diseases of humans and animals (Q35469443) (← links)
- Structure and polymorphism of the mouse prion protein gene (Q35573850) (← links)
- A single hamster PrP amino acid blocks conversion to protease-resistant PrP in scrapie-infected mouse neuroblastoma cells. (Q35852143) (← links)
- Molecular biology and genetics of neurodegenerative diseases caused by prions (Q36063397) (← links)
- Federal disease control--scrapie (Q36087866) (← links)
- Three scrapie prion isolates exhibit different accumulation patterns of the prion protein scrapie isoform (Q36413430) (← links)
- Molecular biology and pathology of scrapie and the prion diseases of humans (Q36477026) (← links)
- Molecular biology and transgenetics of prion diseases (Q36538997) (← links)
- Propagation of prion strains through specific conformers of the prion protein (Q36548578) (← links)
- Prion Protein Genes: Evolutionary and Functional Aspects (Q36549301) (← links)
- Genetics of Prion Diversity and Host Susceptibility (Q36549304) (← links)
- Novel Properties and Biology of Scrapie Prions (Q36549325) (← links)
- Heterologous PrP molecules interfere with accumulation of protease-resistant PrP in scrapie-infected murine neuroblastoma cells (Q36624152) (← links)
- Amphotericin B delays both scrapie agent replication and PrP-res accumulation early in infection (Q36637324) (← links)
- Sulfated polyanion inhibition of scrapie-associated PrP accumulation in cultured cells (Q36640586) (← links)
- Evidence for Biological and Structural Diversity Among Scrapie Strains (Q36719955) (← links)
- Three hamster species with different scrapie incubation times and neuropathological features encode distinct prion proteins (Q36721451) (← links)
- Evidence of mitochondrial involvement in scrapie infection (Q36791940) (← links)
- Genetics and polymorphism of the mouse prion gene complex: control of scrapie incubation time (Q36851207) (← links)
- Transmissible spongiform encephalopathies (TSE) virus-induced amyloidoses of the central nervous system (CNS) (Q36870423) (← links)
- Immunological analysis of host and agent effects on Creutzfeldt-Jakob disease and scrapie prion proteins (Q36872207) (← links)
- Natural Transmission and Genetic Control of Susceptibility of Sheep to Scrapie (Q37040430) (← links)
- A 'unified theory' of prion propagation (Q37257816) (← links)
- Enhancement of protein misfolding cyclic amplification by using concentrated cellular prion protein source (Q37375034) (← links)
- Prion liposomes (Q37581303) (← links)
- Novel structure and genetics of prions causing neurodegeneration in humans and animals (Q37610046) (← links)
- Expanding possibilities for intervention against small ruminant lentiviruses through genetic marker-assisted selective breeding. (Q38114795) (← links)
- Transmissible encephalopathies in animals. (Q38145149) (← links)
- Unraveling prion diseases through molecular genetics (Q38204819) (← links)
- Mutation of the prion protein in Libyan Jews with Creutzfeldt-Jakob disease (Q39080950) (← links)
- Search for a scrapie-specific nucleic acid: a progress report. (Q39604840) (← links)
- Prions, beta-sheets and transmissible dementias: is there still something missing? (Q40372882) (← links)
- Reflections on scrapie and related disorders, with consideration of the possibility of a viral aetiology (Q40420224) (← links)
- Animal spongiform encephalopathies--an update. Part 1. Scrapie and lesser known animal spongiform encephalopathies (Q40601771) (← links)
- The "brave new world" of transmissible spongiform encephalopathy (infectious cerebral amyloidosis). (Q40654343) (← links)
- General aspects of transmissible spongiform encephalopathies and hypotheses about the agents (Q40721777) (← links)