Citation Impact
Citing Papers
Molecular Cloning of a Human Prion Protein cDNA
1986 StandoutNobel
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
Molecular biology and genetics of prion diseases
1994 StandoutNobel
Transgenetic investigations of prion diseases of humans and animals
1993 StandoutNobel
Genetic Aspects of Unconventional Virus Infections: The Basis of the Virino Hypothesis
2007
NMR structure of the mouse prion protein domain PrP(121–231)
1996 StandoutNatureNobel
Chemistry and biology of prions
1992
Different allelic effects of the codons 136 and 171 of the prion protein gene in sheep with natural scrapie
1995
Prions and Neurodegenerative Diseases
1987 StandoutNobel
Mutation of the Prion Protein in Libyan Jews with Creutzfeldt–Jakob Disease
1991 StandoutNobel
The new biology of spongiform encephalopathy: infectious amyloidoses with a genetic twist
1991 Nobel
Transgenetic studies implicate interactions between homologous PrP isoforms in scrapie prion replication
1990 StandoutNobel
BIOLOGY AND GENETICS OF PRION DISEASES
1994
Identification of five allelic variants of the sheep PrP gene and their association with natural scrapie
1995
A 'unified theory' of prion propagation
1991 Nature
Degeneration of skeletal muscle, peripheral nerves, and the central nervous system in transgenic mice overexpressing wild-type prion proteins
1994 StandoutNobel
Swaledale sheep affected by natural scrapie differ significantly in PrP genotype frequencies from healthy sheep and those selected for reduced incidence of scrapie
1993
Linkage of a prion protein missense variant to Gerstmann–Sträussler syndrome
1989 StandoutNatureNobel
Structural Clues to Prion Replication
1994 StandoutScienceNobel
Genetic and Infectious Prion Diseases
1993
Transgenic mice expressing hamster prion protein produce species-specific scrapie infectivity and amyloid plaques
1989 StandoutNobel
Immunologic and Molecular Biologic Studies of Prion Proteins in Bovine Spongiform Encephalopathy
1993 StandoutNobel
Phenotypic characteristics of familial Creutzfeldt‐Jakob disease assoicated with the codon 178AsnPRNP mutation
1992
PrP genotypes and experimental scrapie in orally inoculated Suffolk sheep in the United States.
1997
Restriction fragment length polymorphisms of the scrapie-associated fibril protein (PrP) gene and their association with susceptibility to natural scrapie in British sheep
1991
Transmissible spongiform encephalopathies (TSE) virus-induced amyloidoses of the central nervous system (CNS)
1991
PrP Genotype and Agent Effects in Scrapie: Change In Allelic Interaction With Different Isolates of Agent in Sheep, a Natural Host of Scrapie
1994
Different scrapie-associated fibril proteins (PrP) are encoded by lines of sheep selected for different alleles of the Sip gene
1991
Prion propagation in mice expressing human and chimeric PrP transgenes implicates the interaction of cellular PrP with another protein
1995 StandoutNobel
Transmission dynamics and epidemiology of BSE in British cattle
1996 Nature
Molecular biology and pathogenesis of prion diseases
1996
Scrapie prions aggregate to form amyloid-like birefringent rods
1983 StandoutNobel
Transmissible spongiform encephalopathies: The threat of BSE to man
1990
Two alleles of a neural protein gene linked to scrapie in sheep.
1990 Standout
Detection of the Scrapie Agent in Tissues of Normal Mice
1968 Nature
Experimental Transmission of Scrapie To Goats and Sheep By the Oral Route
1961
Familial Creutzfeldt-Jakob disease
1980 Nobel
Prion-inducing domain 2–114 of yeast Sup35 protein transforms in vitro into amyloid-like filaments
1997 StandoutNobel
Linkage of prion protein and scrapie incubation time genes
1986 StandoutNobel
Ablation of the prion protein (PrP) gene in mice prevents scrapie and facilitates production of anti-PrP antibodies.
1993 StandoutNobel
Scrapie : A modified membrane hypothesis
1968
Regional mapping of prion proteins in brain.
1992 StandoutNobel
CEREBRAL AMYLOIDOSIS IN SCRAPIE IN THE MOUSE: EFFECT OF AGENT STRAIN AND MOUSE GENOTYPE
1976
Evidence for protein X binding to a discontinuous epitope on the cellular prion protein during scrapie prion propagation
1997 StandoutNobel
Purification and structural studies of a major scrapie prion protein
1984 StandoutNobel
Scrapie: A transmissible and hereditary disease of sheep
1962
Resistance of the scrapie agent to formalin
1965
Scrapie in mice
1973
Post-mortem immunodiagnosis of scrapie and bovine spongiform encephalopathy
1989
Novel Proteinaceous Infectious Particles Cause Scrapie
1982 StandoutScienceNobel
Survival of Creutzfeldt-Jakob-Disease Virus in Formol-Fixed Brain Tissue
1976 StandoutNobel
Identification of a Protein That Purifies with the Scrapie Prion
1982 StandoutScienceNobel
Course of Experimental Scrapie Virus Infection in the Goat
1974
Virus-Like Sensitivity of the Scrapie Agent to Heat Inactivation
1984 Science
Evidence for the Conformation of the Pathologic Isoform of the Prion Protein Enciphering and Propagating Prion Diversity
1996 StandoutScienceNobel
Prion Diseases and the BSE Crisis
1997 StandoutScienceNobel
Scrapie: A Transmissible Hereditary Disease of Sheep
1960 Nature
EXPERIMENTAL TRANSMISSION OF SCRAPIE TO GOLDEN HAMSTERS
1963
Slow-Virus Infections of the Nervous System
1967 StandoutNobel
Prions
1998 StandoutNobel
Predicted alpha-helical regions of the prion protein when synthesized as peptides form amyloid.
1992 StandoutNobel
NMR solution structure of the human prion protein
2000 StandoutNobel
Scrapie: A Prototype Slow Infection
1972
Unusual Topogenic Sequence Directs Prion Protein Biogenesis
1990 StandoutScienceNobel
Solution structure of a 142-residue recombinant prion protein corresponding to the infectious fragment of the scrapie isoform
1997 StandoutNobel
Identification of a gene which controls the incubation period of some strains of scrapie agent in mice
1968
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
Virologic and Neurohistologic Findings in Dairy Goats Affected with Natural Scrapie
1980
Scrapie infectious agent is virus-like in size and susceptibility to inactivation
1984 Nature
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
Transmission of Creutzfeldt-Jakob disease from humans to transgenic mice expressing chimeric human-mouse prion protein.
1994 StandoutNobel
Transmission of Scrapie in Hamsters
1985 StandoutNobel
Does the Agent of Scrapie Replicate without Nucleic Acid ?
1967 Nature
Further Experimental Observations on Scrapie
1961
Scrapie and cellular PrP isoforms are encoded by the same chromosomal gene
1986 StandoutNobel
French autochthonous scrapied sheep without the 136Val PrP polymorphism
1993
Molecular Biology of Prion Diseases
1991 StandoutScienceNobel
Attempts to Demonstrate a Transmissible Agent in Kuru, Amyotrophic Lateral Sclerosis, and other Sub-Acute and Chronic Nervous System Degenerations of Man
1964 StandoutNatureNobel
Transmissible mink encephalopathy: pathogenesis and nature of the aetiological agent
1972
Natural Infection of Suffolk Sheep with Scrapie Virus
1982
Prion liposomes
1990 StandoutNobel
A comparison of some biological characteristics of the mouse-passaged scrapie agents, 22A and ME7
1969
Antibodies to a scrapie prion protein
1984 StandoutNatureNobel
Spontaneous Neurodegeneration in Transgenic Mice with Mutant Prion Protein
1990 StandoutScienceNobel
Experimental Subacute Spongiform Virus Encephalopathies in Primates and Other Laboratory Animals
1973 StandoutScienceNobel
Creutzfeldt-Jakob Disease: Hypothesis for High Incidence in Libyan Jews in Israel
1974 StandoutScienceNobel
Works of J.T. Stamp being referenced
Experimental scrapie : some recent work.
1960
Spread of scrapie by contact to goats and sheep
1968
Further Studies on Scrapie
1959
Scrapie in a Dorset Down ram. A confirmation of the histological diagnosis by means of intracerebral inoculation of mice with formol fixed brain tissue
1965
Scrapie disease of sheep.
1961
Experimental scrapie in Cheviot and Suffolk sheep
1969
An analysis of natural scrapie in suffolk sheep
1965
Maternal and lateral transmission of scrapie in sheep
1974
Some factors controlling the incidence of scrapie in Cheviot sheep injected with a Cheviot-passaged scrapie agent
1968
A note on the distribution of scrapie in sheep of different ages
1964