Pages that link to "Q47574601"
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The following pages link to Different forms of the bovine PrP gene have five or six copies of a short, G-C-rich element within the protein-coding exon (Q47574601):
Displaying 50 items.
- Prions (Q24633319) (← links)
- Genetics of Prion Disease in Cattle (Q26783714) (← links)
- Probing the role of structural features of mouse PrP in yeast by expression as Sup35-PrP fusions (Q27022544) (← links)
- Impaired motor coordination in mice lacking prion protein (Q28292921) (← links)
- Isolation from cattle of a prion strain distinct from that causing bovine spongiform encephalopathy (Q28469063) (← links)
- Monoclonal antibodies specific for the native, disease-associated isoform of the prion protein (Q30783514) (← links)
- Prion protein self-peptides modulate prion interactions and conversion (Q30924592) (← links)
- cDNA cloning of a novel heterogeneous nuclear ribonucleoprotein gene homologue in Caenorhabditis elegans using hamster prion protein cDNA as a hybridization probe (Q30986475) (← links)
- Molecular cloning of a candidate chicken prion protein (Q33191659) (← links)
- On-column purification and refolding of recombinant bovine prion protein: using its octarepeat sequences as a natural affinity tag. (Q33196059) (← links)
- Mapping of possible prion protein self-interaction domains using peptide arrays (Q33281952) (← links)
- Structure of the recombinant full-length hamster prion protein PrP(29-231): the N terminus is highly flexible (Q33705415) (← links)
- Variant Creutzfeldt-Jakob disease. (Q33706965) (← links)
- Prions in skeletal muscle (Q34020521) (← links)
- Distinct molecular phenotypes in bovine prion diseases (Q34165722) (← links)
- Generation of antibodies against bovine recombinant prion protein in various strains of mice (Q34325859) (← links)
- The UK epidemic of BSE: slow virus or chronic pesticide-initiated modification of the prion protein? Part 1: Mechanisms for a chemically induced pathogenesis/transmissibility (Q34390752) (← links)
- The UK epidemic of BSE: slow virus or chronic pesticide-initiated modification of the prion protein? Part 2: An epidemiological perspective (Q34390756) (← links)
- Molecular biology of prion diseases (Q34534878) (← links)
- Transmissible familial Creutzfeldt-Jakob disease associated with five, seven, and eight extra octapeptide coding repeats in the PRNP gene (Q34569015) (← links)
- Bovine spongiform encephalopathy: is it an autoimmune disease due to bacteria showing molecular mimicry with brain antigens? (Q34640695) (← links)
- Multiplicative genetic effects in scrapie disease susceptibility. (Q34789989) (← links)
- Characterization of Syrian hamster adapted prions derived from L-type and C-type bovine spongiform encephalopathies (Q35194921) (← links)
- Preparation and characterization of antibodies against mouse prion protein (PrP) peptides. (Q35224210) (← links)
- Molecular discrimination of atypical bovine spongiform encephalopathy strains from a geographical region spanning a wide area in Europe (Q35913879) (← links)
- Molecular biology and genetics of neurodegenerative diseases caused by prions (Q36063397) (← links)
- Purification and properties of the cellular prion protein from Syrian hamster brain (Q36277401) (← links)
- Prion Type-Dependent Deposition of PRNP Allelic Products in Heterozygous Sheep (Q36434304) (← links)
- Molecular biology and pathology of scrapie and the prion diseases of humans (Q36477026) (← links)
- The Scrapie Fibril Protein and Its Cellular Isoform (Q36549334) (← links)
- A critical analysis of disease-associated DNA polymorphisms in the genes of cattle, goat, sheep, and pig. (Q36571037) (← links)
- Identification of a second bovine amyloidotic spongiform encephalopathy: molecular similarities with sporadic Creutzfeldt-Jakob disease (Q36853707) (← links)
- Creutzfeldt-Jakob disease and bovine spongiform encephalopathy: any connection? (Q36892999) (← links)
- Prion protein gene (PRNP) variants and evidence for strong purifying selection in functionally important regions of bovine exon 3. (Q37589594) (← links)
- A monomer-dimer equilibrium of a cellular prion protein (PrPC) not observed with recombinant PrP. (Q38308795) (← links)
- Use of canonical discriminant analysis to study signatures of selection in cattle (Q39493614) (← links)
- Detection of bovine spongiform encephalopathy-specific PrP(Sc) by treatment with heat and guanidine thiocyanate (Q39596556) (← links)
- Animal spongiform encephalopathies--an update. Part II. Bovine spongiform encephalopathy (BSE). (Q40601775) (← links)
- The "brave new world" of transmissible spongiform encephalopathy (infectious cerebral amyloidosis). (Q40654343) (← links)
- The bovine genome map. (Q40712856) (← links)
- General aspects of transmissible spongiform encephalopathies and hypotheses about the agents (Q40721777) (← links)
- Transgenetics of prion diseases. (Q40975176) (← links)
- PrP genetics in sheep and the implications for scrapie and BSE (Q41570657) (← links)
- Prion Diseases and the BSE Crisis (Q41607167) (← links)
- Genetics of prions (Q41689443) (← links)
- An antibody raised against a conserved sequence of the prion protein recognizes pathological isoforms in human and animal prion diseases, including Creutzfeldt-Jakob disease and bovine spongiform encephalopathy. (Q41851684) (← links)
- Competing intrachain interactions regulate the formation of beta-sheet fibrils in bovine PrP peptides. (Q41925530) (← links)
- Comparative analysis of the prion protein open reading frame nucleotide sequences in peacock and parakeet (Q42649262) (← links)
- Sequencing analysis of prion genes from red deer and camel (Q42666822) (← links)
- Homozygosity for prion protein alleles encoding glutamine-171 renders sheep susceptible to natural scrapie (Q42693681) (← links)