| P50 | author | Ken'ichi Hagiwara | Q67572558 |
| | Motohiro Horiuchi | Q90989136 |
| P2093 | author name string | Yuko Sato | |
| | Tetsutaro Sata | |
| | Hideyuki Hara | |
| | Hiroaki Shibata | |
| | Fumiko Ono | |
| | Yoshio Yamakawa | |
| | Minoru Tobiume | |
| | Yuko Okemoto-Nakamura | |
| P2860 | cites work | Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4 | Q25938983 |
| | Atypical BSE (BASE) transmitted from asymptomatic aging cattle to a primate | Q28473442 |
| | Intraspecies transmission of L-type-like Bovine Spongiform Encephalopathy detected in Japan. | Q48392599 |
| | Characterization of scrapie agent isolated from sheep in Japan | Q48560388 |
| | Atypical L-type bovine spongiform encephalopathy (L-BSE) transmission to cynomolgus macaques, a non-human primate | Q48923866 |
| | Experimental transmission of bovine spongiform encephalopathy (BSE) to cynomolgus macaques, a non-human primate. | Q50265921 |
| | Two-rung Model of a Left-handed β-Helix for Prions Explains Species Barrier and Strain Variation in Transmissible Spongiform Encephalopathies | Q55120853 |
| | BSE transmission to macaques | Q59098670 |
| | Stress response in the central nervous system of a transgenic mouse model of bovine spongiform encephalopathy | Q62594041 |
| | Pathogenesis of reticulum cell sarcoma in mice | Q69845732 |
| | Temporary and permanent modifications to a single strain of mouse scrapie on transmission to rats and hamsters | Q70345462 |
| | Transmission of the BSE agent to mice in the absence of detectable abnormal prion protein | Q71970964 |
| | New insight into abnormal prion protein using monoclonal antibodies | Q73278088 |
| | Characterization of two distinct prion strains derived from bovine spongiform encephalopathy transmissions to inbred mice | Q80370898 |
| | Conversion of the BASE prion strain into the BSE strain: the origin of BSE? | Q33277907 |
| | Structural properties of prion protein protofibrils and fibrils: an experimental assessment of atomic models | Q33343542 |
| | Emergence of classical BSE strain properties during serial passages of H-BSE in wild-type mice. | Q33802746 |
| | Distinct molecular phenotypes in bovine prion diseases | Q34165722 |
| | Mutation and selection of prions | Q34220952 |
| | Molecular analysis of prion strain variation and the aetiology of 'new variant' CJD. | Q34403513 |
| | Molecular modeling of prion transmission to humans | Q34423397 |
| | Evaluation of the zoonotic potential of transmissible mink encephalopathy | Q34533468 |
| | A cellular gene encodes scrapie PrP 27-30 protein | Q34557641 |
| | Adaptation of the bovine spongiform encephalopathy agent to primates and comparison with Creutzfeldt-- Jakob disease: implications for human health | Q35057650 |
| | Characterization of Syrian hamster adapted prions derived from L-type and C-type bovine spongiform encephalopathies | Q35194921 |
| | Acquired prion disease: iatrogenic CJD, variant CJD, kuru | Q35549020 |
| | Acquired transmissibility of sheep-passaged L-type bovine spongiform encephalopathy prion to wild-type mice | Q35844725 |
| | Oral transmission of L-type bovine spongiform encephalopathy in primate model | Q35845923 |
| | Classical bovine spongiform encephalopathy by transmission of H-type prion in homologous prion protein context. | Q35877485 |
| | Molecular discrimination of atypical bovine spongiform encephalopathy strains from a geographical region spanning a wide area in Europe | Q35913879 |
| | Detection and partial discrimination of atypical and classical bovine spongiform encephalopathies in cattle and primates using real-time quaking-induced conversion assay | Q36288523 |
| | Evaluation of the human transmission risk of an atypical bovine spongiform encephalopathy prion strain | Q36498169 |
| | Identification of a second bovine amyloidotic spongiform encephalopathy: molecular similarities with sporadic Creutzfeldt-Jakob disease | Q36853707 |
| | Transmission of atypical bovine prions to mice transgenic for human prion protein | Q37080870 |
| | Natural and synthetic prion structure from X-ray fiber diffraction | Q37386047 |
| | 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 |
| | BSE prions propagate as either variant CJD-like or sporadic CJD-like prion strains in transgenic mice expressing human prion protein | Q39686522 |
| | L-BSE experimentally transmitted to sheep presents as a unique disease phenotype. | Q40483717 |
| | Sheep-passaged bovine spongiform encephalopathy agent exhibits altered pathobiological properties in bovine-PrP transgenic mice. | Q42957132 |
| | Disease characteristics of bovine spongiform encephalopathy following inoculation into mice via three different routes | Q42970133 |
| | ImmunoAT method: An initial assessment for the detection of abnormal isoforms of prion protein in formalin-fixed and paraffin-embedded tissues | Q43163520 |
| | Distinct prion proteins in short and long scrapie incubation period mice | Q43408194 |
| | Distribution of PrP(Sc) in cattle with bovine spongiform encephalopathy slaughtered at abattoirs in Japan | Q44065375 |
| | Accumulation of mono-glycosylated form-rich, plaque-forming PrPSc in the second atypical bovine spongiform encephalopathy case in Japan. | Q44369942 |
| | Presence of subclinical infection in gene-targeted human prion protein transgenic mice exposed to atypical bovine spongiform encephalopathy | Q44489979 |
| | Transmissions to mice indicate that 'new variant' CJD is caused by the BSE agent | Q44592404 |
| | Antigenic characterization of an abnormal isoform of prion protein using a new diverse panel of monoclonal antibodies | Q44788460 |
| | Bovine spongiform encephalopathy agent in a prion protein (PrP)ARR/ARR genotype sheep after peripheral challenge: complete immunohistochemical analysis of disease-associated PrP and transmission studies to ovine-transgenic mice | Q45041274 |
| | A change in the conformation of prions accompanies the emergence of a new prion strain. | Q45939477 |
| | Alteration of the biological and biochemical characteristics of bovine spongiform encephalopathy prions during interspecies transmission in transgenic mice models | Q46195045 |
| | A bovine prion acquires an epidemic bovine spongiform encephalopathy strain-like phenotype on interspecies transmission | Q48124117 |
| | Characterization of antibodies raised against bovine-PrP-peptides. | Q48157642 |
| | Unique properties of the classical bovine spongiform encephalopathy strain and its emergence from H-type bovine spongiform encephalopathy substantiated by VM transmission studies | Q48167842 |
| | The host range of chronic wasting disease is altered on passage in ferrets | Q48338103 |
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 5 | |
| P304 | page(s) | e0216807 | |
| P577 | publication date | 2019-05-16 | |
| P1433 | published in | PLOS One | Q564954 |
| P1476 | title | Tracking and clarifying differential traits of classical- and atypical L-type bovine spongiform encephalopathy prions after transmission from cattle to cynomolgus monkeys | |
| P478 | volume | 14 | |