Citation Impact
Citing Papers
Normal development and behaviour of mice lacking the neuronal cell-surface PrP protein
1992 StandoutNatureNobel
Familial myoclonic dementia masquerading as Creutzfeldt‐Jakob disease
1986
Distinct prion proteins in short and long scrapie incubation period mice
1987 StandoutNobel
Molecular biology and genetics of prion diseases
1994 StandoutNobel
NMR structure of the mouse prion protein domain PrP(121–231)
1996 StandoutNatureNobel
Chapter 37: PrPSc causes nerve cell death and stimulates astrocyte proliferation: a paradox
1992
Structural studies of the scrapie prion protein using mass spectrometry and amino acid sequencing
1993
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
The 14-3-3 Brain Protein in Cerebrospinal Fluid as a Marker for Transmissible Spongiform Encephalopathies
1996
BIOLOGY AND GENETICS OF PRION DISEASES
1994
Potent Inhibition of Scrapie‐Associated PrP Accumulation by Congo Red
1992
Degeneration of skeletal muscle, peripheral nerves, and the central nervous system in transgenic mice overexpressing wild-type prion proteins
1994 StandoutNobel
Successful transmission of Creutzfeldt-Jakob disease from human to mouse verified by prion protein accumulation in mouse brains
1992
Linkage of a prion protein missense variant to Gerstmann–Sträussler syndrome
1989 StandoutNatureNobel
Scrapie-associated tubulofilamentous particles in human Creutzfeldt-Jakob disease
1992
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
Real and imagined clinicopathological limits of "prion dementia"
1993 Nobel
Human prion diseases
1994 StandoutNobel
Transmissible and non-transmissible amyloidoses: autocatalytic post-translational conversion of host precursor proteins to β-pleated sheet configurations
1988 Nobel
Creutzfeldt-Jakob disease from contaminated growth hormone extracts in France
1996
Human spongiform encephalopathy: The national institutes of health series of 300 cases of experimentally transmitted disease
1994 Nobel
Prion propagation in mice expressing human and chimeric PrP transgenes implicates the interaction of cellular PrP with another protein
1995 StandoutNobel
Creutzfeldt‐Jakob disease cosegregates with the codon 178AsnPRNP mutation in families of European origin
1992 Nobel
Non-hydrophobic extracytoplasmic determinant of stop transfer in the prion protein
1990 StandoutNatureNobel
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
Gerstmann-Straussler-Scheinker disease in an Alsatian family: clinical and genetic studies.
1992
Structure and polymorphism of the mouse prion protein gene.
1994 StandoutNobel
Prion-inducing domain 2–114 of yeast Sup35 protein transforms in vitro into amyloid-like filaments
1997 StandoutNobel
Prion isolate specified allotypic interactions between the cellular and scrapie prion proteins in congenic and transgenic mice.
1994 StandoutNobel
Ablation of the prion protein (PrP) gene in mice prevents scrapie and facilitates production of anti-PrP antibodies.
1993 StandoutNobel
Prion protein NMR structure and familial human spongiform encephalopathies
1998 StandoutNobel
Regional mapping of prion proteins in brain.
1992 StandoutNobel
Evidence for protein X binding to a discontinuous epitope on the cellular prion protein during scrapie prion propagation
1997 StandoutNobel
Proposed three-dimensional structure for the cellular prion protein.
1994 StandoutNobel
Immunoaffinity purification and neutralization of scrapie prion infectivity.
1988
Mice deficient for prion protein exhibit normal neuronal excitability and synaptic transmission in the hippocampus.
1996 StandoutNobel
Prion protein (PrP) synthetic peptides induce cellular PrP to acquire properties of the scrapie isoform.
1995 StandoutNobel
Molecular cloning and complete sequence of prion protein cDNA from mouse brain infected with the scrapie agent.
1986
Evidence for the Conformation of the Pathologic Isoform of the Prion Protein Enciphering and Propagating Prion Diversity
1996 StandoutScienceNobel
Prion-Protein Immunoreactivity in Human Transmissible Dementias
1986 StandoutNobel
Prion Diseases and the BSE Crisis
1997 StandoutScienceNobel
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
Astrocyte gene expression in Creutzfeldt-Jakob disease.
1987
Solution structure of a 142-residue recombinant prion protein corresponding to the infectious fragment of the scrapie isoform
1997 StandoutNobel
Abnormal isoform of prion proteins accumulates in the synaptic structures of the central nervous system in patients with Creutzfeldt-Jakob disease.
1992
Structure of the recombinant full-length hamster prion protein PrP(29–231): The N terminus is highly flexible
1997 StandoutNobel
Molecular cloning of a candidate chicken prion protein.
1992 StandoutNobel
Subcellular colocalization of the cellular and scrapie prion proteins in caveolae-like membranous domains
1996 StandoutNobel
Interactions between wild-type and mutant prion proteins modulate neurodegeneration in transgenic mice.
1996
NMR structure of the bovine prion protein
2000 StandoutNobel
Immunoblotting of Creutzfeldt‐Jakob disease prion proteins: Host species—specific epitopes
1987 StandoutNobel
Transmission of Creutzfeldt-Jakob disease from humans to transgenic mice expressing chimeric human-mouse prion protein.
1994 StandoutNobel
Antisera to scrapie-associated fibril protein and prion protein decorate scrapie-associated fibrils
1987
Conservation of infectivity in purified fibrillary extracts of scrapie-infected hamster brain after sequential enzymatic digestion or polyacrylamide gel electrophoresis.
1990 Nobel
Evidence that DNA is present in abnormal tubulofilamentous structures found in scrapie.
1988 Nobel
N-terminal truncation of the scrapie-associated form of PrP by lysosomal protease(s): implications regarding the site of conversion of PrP to the protease-resistant state
1991
Etiology and pathogenesis of prion diseases.
1995 StandoutNobel
Molecular Biology of Prion Diseases
1991 StandoutScienceNobel
The scrapie-associated form of PrP is made from a cell surface precursor that is both protease- and phospholipase-sensitive.
1991
COOH-terminal sequence of the cellular prion protein directs subcellular trafficking and controls conversion into the scrapie isoform
1997 StandoutNobel
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
Creutzfeldt‐Jakob disease: Clinical analysis of a consecutive series of 230 neuropathologically verified cases
1986 Nobel
Conversion of truncated and elongated prion proteins into the scrapie isoform in cultured cells.
1993 StandoutNobel
Nerve growth factor increases mRNA levels for the prion protein and the beta-amyloid protein precursor in developing hamster brain.
1988 StandoutNobel
Prion liposomes
1990 StandoutNobel
Serial transmission in rodents of neurodegeneration from transgenic mice expressing mutant prion protein.
1994
Prion protein preamyloid and amyloid deposits in Gerstmann-Sträussler-Scheinker disease, Indiana kindred.
1992 StandoutNobel
Purified prion proteins and scrapie infectivity copartition into liposomes.
1987 StandoutNobel
Mouse polyclonal and monoclonal antibody to scrapie-associated fibril proteins
1987
Spontaneous Neurodegeneration in Transgenic Mice with Mutant Prion Protein
1990 StandoutScienceNobel
Works of Kitty Pomeroy being referenced
Abnormal Tubulovesicular Particles in Brains of Hamsters with Scrapie
1987 Nobel
Diagnosis of Creutzfeldt-Jakob Disease by Western Blot Identification of Marker Protein in Human Brain Tissue
1986 Nobel