Citation Impact
Citing Papers
Normal development and behaviour of mice lacking the neuronal cell-surface PrP protein
1992 StandoutNatureNobel
Distinct prion proteins in short and long scrapie incubation period mice
1987 StandoutNobel
Prions and Neurodegenerative Diseases
1987 StandoutNobel
Transgenetic studies implicate interactions between homologous PrP isoforms in scrapie prion replication
1990 StandoutNobel
Degeneration of skeletal muscle, peripheral nerves, and the central nervous system in transgenic mice overexpressing wild-type prion proteins
1994 StandoutNobel
Transgenic mice expressing hamster prion protein produce species-specific scrapie infectivity and amyloid plaques
1989 StandoutNobel
PrP genotypes and experimental scrapie in orally inoculated Suffolk sheep in the United States.
1997
Transmissible spongiform encephalopathies (TSE) virus-induced amyloidoses of the central nervous system (CNS)
1991
Genome-Scale Identification of SARS-CoV-2 and Pan-coronavirus Host Factor Networks
2020 StandoutNobel
Scrapie prions aggregate to form amyloid-like birefringent rods
1983 StandoutNobel
NMR structures of three single-residue variants of the human prion protein
2000 StandoutNobel
Circumventing tolerance to generate autologous monoclonal antibodies to the prion protein.
1996 StandoutNobel
Identification of a prion protein epitope modulating transmission of bovine spongiform encephalopathy prions to transgenic mice
1997 StandoutNobel
Transmissible spongiform encephalopathies: The threat of BSE to man
1990
Structure and polymorphism of the mouse prion protein gene.
1994 StandoutNobel
Linkage of prion protein and scrapie incubation time genes
1986 StandoutNobel
Kuru with incubation periods exceeding two decades
1982 StandoutNobel
Prion protein NMR structure and familial human spongiform encephalopathies
1998 StandoutNobel
Regional mapping of prion proteins in brain.
1992 StandoutNobel
Oral Transmission of Kuru, Creutzfeldt-Jakob Disease, and Scrapie to Nonhuman Primates
1980
Unraveling prion diseases through molecular genetics
1989 StandoutNobel
Evidence for protein X binding to a discontinuous epitope on the cellular prion protein during scrapie prion propagation
1997 StandoutNobel
Precautions in Medical Care of, and in Handling Materials from, Patients with Transmissible Virus Dementia (Creutzfeldt-Jakob Disease)
1977 Nobel
Purification and structural studies of a major scrapie prion protein
1984 StandoutNobel
Biohazards of Investigations on the Transmissible Spongiform Encephalopathies
1980 StandoutNobel
Characterization of nucleic acids in membrane vesicles from scrapie-infected hamster brain
1985
Proposed three-dimensional structure for the cellular prion protein.
1994 StandoutNobel
Mice deficient for prion protein exhibit normal neuronal excitability and synaptic transmission in the hippocampus.
1996 StandoutNobel
Novel Proteinaceous Infectious Particles Cause Scrapie
1982 StandoutScienceNobel
Identification of a Protein That Purifies with the Scrapie Prion
1982 StandoutScienceNobel
Evidence for the Conformation of the Pathologic Isoform of the Prion Protein Enciphering and Propagating Prion Diversity
1996 StandoutScienceNobel
Creutzfeldt–Jakob Disease Prion Proteins in Human Brains
1985 StandoutNobel
Prion-Protein Immunoreactivity in Human Transmissible Dementias
1986 StandoutNobel
Prion Diseases and the BSE Crisis
1997 StandoutScienceNobel
Unconventional Viruses and the Origin and Disappearance of Kuru
1977 ScienceNobel
Prions
1998 StandoutNobel
Reversible Chemical Modification of the Scrapie Agent
1981 StandoutScienceNobel
NMR solution structure of the human prion protein
2000 StandoutNobel
Infection-Specific Particle from the Unconventional Slow Virus Diseases
1984 ScienceNobel
A protease-resistant protein is a structural component of the Scrapie prion
1983 StandoutNobel
Solution structure of a 142-residue recombinant prion protein corresponding to the infectious fragment of the scrapie isoform
1997 StandoutNobel
Thiocyanate and hydroxyl ions inactivate the scrapie agent.
1981 StandoutNobel
Transmissible and non-transmissible neurodegenerative disease: similarities in age of onset and genetics in relation to aetiology
1986
Structure of the recombinant full-length hamster prion protein PrP(29–231): The N terminus is highly flexible
1997 StandoutNobel
Subcellular colocalization of the cellular and scrapie prion proteins in caveolae-like membranous domains
1996 StandoutNobel
Separation and properties of cellular and scrapie prion proteins.
1986 StandoutNobel
Scrapie and Creutzfeldt-Jakob disease prion proteins share physical properties and antigenic determinants.
1985 StandoutNobel
Recombinant bovine respiratory syncytial virus with deletions of the G or SH genes: G and F proteins bind heparin
2001
Homozygosity for prion protein alleles encoding glutamine-171 renders sheep susceptible to natural scrapie.
1994 StandoutNobel
NMR structure of the bovine prion protein
2000 StandoutNobel
A cellular gene encodes scrapie PrP 27-30 protein
1985 StandoutNobel
A comparison of the biochemical changes induced in mouse brain by cuprizone toxicity and by scrapie infection
1974
Prions: Novel Infectious Pathogens
1984 StandoutNobel
Transmission of Scrapie in Hamsters
1985 StandoutNobel
Scrapie and cellular PrP isoforms are encoded by the same chromosomal gene
1986 StandoutNobel
Molecular Biology of Prion Diseases
1991 StandoutScienceNobel
Maternal and lateral transmission of scrapie in sheep
1974
Recombinant scrapie-like prion protein of 106 amino acids is soluble
1996 StandoutNobel
Prion protein NMR structure and species barrier for prion diseases
1997 StandoutNobel
Natural Infection of Suffolk Sheep with Scrapie Virus
1982
Some Speculations about Prions, Amyloid, and Alzheimer's Disease
1984 StandoutNobel
Nerve growth factor increases mRNA levels for the prion protein and the beta-amyloid protein precursor in developing hamster brain.
1988 StandoutNobel
Antibodies to a scrapie prion protein
1984 StandoutNatureNobel
Purified prion proteins and scrapie infectivity copartition into liposomes.
1987 StandoutNobel
Creutzfeldt-Jakob Disease: Hypothesis for High Incidence in Libyan Jews in Israel
1974 StandoutScienceNobel
Works of J. Jebbett being referenced
Monoclonal antibodies protect against respiratory syncytial virus infection in mice.
1984
Brain Cell Cultures from Mice Affected with Scrapie or Fed with Cuprizone
1971
Further Observations on the Production of Scrapie in Sheep by Oral Dosing with Foetal Membranes from Scrapie-Affected Sheep
1974
Spread of scrapie to sheep and goats by oral dosing with foetal membranes from scrapie-affected sheep
1972
Clinical and Histological Observations on Cuprizonc Toxicity and Scrapie in Mice
1971
Detection of the Scrapie Agent in Tissues of Normal Mice with Special Reference to the Possibility of Accidental Laboratory Contamination
1971
Unsuccessful Attempts to Produce Disease with Tissues from Mice Fed on a Diet Containing Cuprizone
1973