Pages that link to "Q73024760"
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The following pages link to Quantitative trait loci affecting prion incubation time in mice (Q73024760):
Displaying 50 items.
- Doppel-induced cerebellar degeneration in transgenic mice (Q24555049) (← links)
- Selective incorporation of polyanionic molecules into hamster prions (Q24596538) (← links)
- A clinical study of kuru patients with long incubation periods at the end of the epidemic in Papua New Guinea (Q24642582) (← links)
- Kuru prions and sporadic Creutzfeldt-Jakob disease prions have equivalent transmission properties in transgenic and wild-type mice (Q24651920) (← links)
- A systems approach to prion disease (Q24656032) (← links)
- Formation of native prions from minimal components in vitro (Q24676353) (← links)
- Genetics of Prion Disease in Cattle (Q26783714) (← links)
- The state of the prion (Q28288758) (← links)
- Correlation analysis for the incubation period of prion disease (Q28729089) (← links)
- Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP (Q28943533) (← links)
- Binding of neural cell adhesion molecules (N-CAMs) to the cellular prion protein (Q30778772) (← links)
- HECTD2 is associated with susceptibility to mouse and human prion disease (Q33408776) (← links)
- HECTD2, a candidate susceptibility gene for Alzheimer's disease on 10q. (Q33503386) (← links)
- The intriguing prion disorders (Q33581653) (← links)
- Genes contributing to prion pathogenesis (Q33687685) (← links)
- The retinoic acid receptor beta (Rarb) region of Mmu14 is associated with prion disease incubation time in mouse (Q33769410) (← links)
- Evidence for varied aetiologies regulating the transmission of prion disease: implications for understanding the heritable basis of prion incubation times (Q33769832) (← links)
- The first report of RPSA polymorphisms, also called 37/67 kDa LRP/LR gene, in sporadic Creutzfeldt-Jakob disease (CJD). (Q33992073) (← links)
- Kuru in the 21st century--an acquired human prion disease with very long incubation periods (Q33997105) (← links)
- Sex effects in mouse prion disease incubation time (Q34103332) (← links)
- Molecular pathology of human prion disease (Q34462913) (← links)
- Review: contribution of transgenic models to understanding human prion disease. (Q34474868) (← links)
- Sod1 deficiency reduces incubation time in mouse models of prion disease (Q34563121) (← links)
- Detection of new quantitative trait Loci for susceptibility to transmissible spongiform encephalopathies in mice (Q34619306) (← links)
- The role of the NADPH oxidase NOX2 in prion pathogenesis (Q34682177) (← links)
- Influence of the prion protein gene, Prnp, on scrapie susceptibility in sheep (Q34685443) (← links)
- Mammalian prion proteins: enigma, variation and vaccination (Q34691392) (← links)
- Mouse models of prion disease transmission (Q34970614) (← links)
- Transgenesis applied to transmissible spongiform encephalopathies (Q35037396) (← links)
- Genome wide association studies and prion disease (Q35578768) (← links)
- Identification of multiple quantitative trait loci linked to prion disease incubation period in mice (Q35939147) (← links)
- Rational targeting for prion therapeutics. (Q35990277) (← links)
- Host Determinants of Prion Strain Diversity Independent of Prion Protein Genotype (Q36086340) (← links)
- In vitro amplification of scrapie and chronic wasting disease PrP(res) using baculovirus-expressed recombinant PrP as substrate (Q36147244) (← links)
- Genetic and environmental factors modify bovine spongiform encephalopathy incubation period in mice (Q36308139) (← links)
- Association mapping of genetic risk factors for chronic wasting disease in wild deer (Q36651717) (← links)
- Identification of new quantitative trait Loci (other than the PRNP gene) modulating the scrapie incubation period in sheep (Q36665974) (← links)
- Investigation of mcp1 as a quantitative trait gene for prion disease incubation time in mouse (Q36873781) (← links)
- Review. The origin of the prion agent of kuru: molecular and biological strain typing. (Q36968647) (← links)
- Association of a null allele of SPRN with variant Creutzfeldt-Jakob disease (Q36990542) (← links)
- Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study (Q37097991) (← links)
- Structural and functional analysis of the HSP90AA1 gene: distribution of polymorphisms among sheep with different responses to scrapie. (Q37151949) (← links)
- Assessing the susceptibility of transgenic mice overexpressing deer prion protein to bovine spongiform encephalopathy (Q37547316) (← links)
- Cross currents in protein misfolding disorders: interactions and therapy (Q37585420) (← links)
- Genetics of prion diseases (Q38091816) (← links)
- In vitro screen of prion disease susceptibility genes using the scrapie cell assay (Q38994453) (← links)
- Neurodegenerative Disease Transmission and Transgenesis in Mice. (Q39134078) (← links)
- A Copine family member, Cpne8, is a candidate quantitative trait gene for prion disease incubation time in mouse (Q40013569) (← links)
- The 37 kDa/67 kDa laminin receptor is required for PrP(Sc) propagation in scrapie-infected neuronal cells (Q40666067) (← links)
- Shadoo (Sprn) and prion disease incubation time in mice (Q42026968) (← links)