Pages that link to "Q44568749"
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The following pages link to Sporadic Creutzfeldt-Jakob disease: co-occurrence of different types of PrP(Sc) in the same brain (Q44568749):
Displaying 50 items.
- Continuous quinacrine treatment results in the formation of drug-resistant prions (Q21090510) (← links)
- Analysis of prion strains by PrPSc profiling in sporadic Creutzfeldt-Jakob disease (Q24812893) (← links)
- Beyond PrP9res) type 1/type 2 dichotomy in Creutzfeldt-Jakob disease (Q28472532) (← links)
- Atypical BSE (BASE) transmitted from asymptomatic aging cattle to a primate (Q28473442) (← links)
- Post-translational modifications in PrP expand the conformational diversity of prions in vivo (Q30399619) (← links)
- Human prion diseases in the Netherlands (1998-2009): clinical, genetic and molecular aspects (Q30467870) (← links)
- Rationale for diagnosing human prion disease. (Q30936688) (← links)
- Regulating factors of PrP glycosylation in Creutzfeldt-Jakob disease--implications for the dissemination and the diagnosis of human prion strains (Q33355954) (← links)
- Experimental verification of a traceback phenomenon in prion infection (Q33725612) (← links)
- Molecular analysis of the abnormal prion protein during coinfection of mice by bovine spongiform encephalopathy and a scrapie agent (Q33834569) (← links)
- Protease-sensitive conformers in broad spectrum of distinct PrPSc structures in sporadic Creutzfeldt-Jakob disease are indicator of progression rate (Q34023019) (← links)
- Agent strain variation in human prion disease: insights from a molecular and pathological review of the National Institutes of Health series of experimentally transmitted disease (Q34163179) (← links)
- Prion strain interactions are highly selective (Q34185289) (← links)
- Molecular pathology of human prion disease (Q34462913) (← links)
- Review: contribution of transgenic models to understanding human prion disease. (Q34474868) (← links)
- Heterogeneity of the Abnormal Prion Protein (PrPSc) of the Chandler Scrapie Strain (Q34533548) (← links)
- Pathological diagnosis of variant Creutzfeldt-Jakob disease (Q34685462) (← links)
- Molecular biology and pathology of prion strains in sporadic human prion diseases. (Q34802620) (← links)
- Dementia, the fate of brain? Neuropathological point of view (Q34939816) (← links)
- Detection of type 1 prion protein in variant Creutzfeldt-Jakob disease (Q35070708) (← links)
- Peripheral tissue involvement in sporadic, iatrogenic, and variant Creutzfeldt-Jakob disease: an immunohistochemical, quantitative, and biochemical study (Q35083260) (← links)
- Different prion disease phenotypes result from inoculation of cattle with two temporally separated sources of sheep scrapie from Great Britain (Q35131038) (← links)
- Tracking protein aggregate interactions (Q35194896) (← links)
- White-tailed deer are susceptible to the agent of sheep scrapie by intracerebral inoculation (Q35420475) (← links)
- Diversity in prion protein oligomerization pathways results from domain expansion as revealed by hydrogen/deuterium exchange and disulfide linkage (Q35778086) (← links)
- Squirrel monkeys (Saimiri sciureus) infected with the agent of bovine spongiform encephalopathy develop tau pathology (Q35784863) (← links)
- Prion subcellular fractionation reveals infectivity spectrum, with a high titre-low PrPres level disparity. (Q35968334) (← links)
- Molecular pathogenesis of sporadic prion diseases in man. (Q36005158) (← links)
- Prion protein glycosylation. (Q36109133) (← links)
- Overlap between neurodegenerative disorders (Q36117422) (← links)
- Phenotypic variability in human prion diseases. (Q36310865) (← links)
- Emergence of two prion subtypes in ovine PrP transgenic mice infected with human MM2-cortical Creutzfeldt-Jakob disease prions (Q36550420) (← links)
- Bovine spongiform encephalopathy in Japan: history and recent studies on oxidative stress in prion diseases (Q36573251) (← links)
- The prion strain phenomenon: molecular basis and unprecedented features (Q36718712) (← links)
- Insights into prion strains and neurotoxicity (Q36856446) (← links)
- Consensus classification of human prion disease histotypes allows reliable identification of molecular subtypes: an inter-rater study among surveillance centres in Europe and USA (Q37050261) (← links)
- Prions: Beyond a Single Protein (Q37162363) (← links)
- Co-existence of scrapie prion protein types 1 and 2 in sporadic Creutzfeldt-Jakob disease: its effect on the phenotype and prion-type characteristics (Q37397268) (← links)
- Incidence and spectrum of sporadic Creutzfeldt-Jakob disease variants with mixed phenotype and co-occurrence of PrPSc types: an updated classification (Q37411403) (← links)
- Absence of Evidence for a Causal Link between Bovine Spongiform Encephalopathy Strain Variant L-BSE and Known Forms of Sporadic Creutzfeldt-Jakob Disease in Human PrP Transgenic Mice (Q37415429) (← links)
- Isolation of two distinct prion strains from a scrapie-affected sheep (Q37418072) (← links)
- Prion protein misfolding, strains, and neurotoxicity: an update from studies on Mammalian prions (Q37448617) (← links)
- Molecular pathology of human prion diseases (Q37462236) (← links)
- Novel strain properties distinguishing sporadic prion diseases sharing prion protein genotype and prion type (Q37587596) (← links)
- Phenotypic variability of sporadic human prion disease and its molecular basis: past, present, and future (Q37812313) (← links)
- Biochemical and strain properties of CJD prions: complexity versus simplicity (Q37905853) (← links)
- The contribution of different prion protein types and host polymorphisms to clinicopathological variations in Creutzfeldt-Jakob disease (Q37989099) (← links)
- Review: Creutzfeldt-Jakob disease: prion protein type, disease phenotype and agent strain. (Q37990996) (← links)
- Sporadic human prion diseases: molecular insights and diagnosis (Q38019773) (← links)
- A closer look at prion strains: characterization and important implications. (Q38077404) (← links)