Citation Impact
Citing Papers
Distinct prion proteins in short and long scrapie incubation period mice
1987 StandoutNobel
Transgenetic investigations of prion diseases of humans and animals
1993 StandoutNobel
Scrapie in mice deficient in apolipoprotein E or glial fibrillary acidic protein
1996 StandoutNobel
Purification and properties of the cellular prion protein from Syrian hamster brain
1992 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
Chemistry and biology of prions
1992
Structural studies of the scrapie prion protein using mass spectrometry and amino acid sequencing
1993
Decreased receptor-mediated calcium response in prion-infected cells correlates with decreased membrane fluidity and IP sub 3 release
1996
Expression of Polyubiquitin and Heat‐Shock Protein 70 Genes Increases in the Later Stages of Disease Progression in Scrapie‐Infected Mouse Brain
1994
Glycosylinositol Phospholipid Anchors of the Scrapie and Cellular Prion Proteins Contain Sialic Acid
1992 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
Genetic Control of Prion Incubation Period in Mice
2007 Nobel
Recombinant full‐length murine prion protein, mPrP(23–231): purification and spectroscopic characterization
1997 StandoutNobel
The Neurochemistry of Prion Diseases
1993
Properties of the Scrapie Prion Protein: Quantitative Analysis of Protease Resistance
1994
Structural Clues to Prion Replication
1994 StandoutScienceNobel
Genetic and Infectious Prion Diseases
1993
Exon mutations uncouple 5′ splice site selection from U1 snRNA pairing
1990 StandoutNobel
Transgenic mice expressing hamster prion protein produce species-specific scrapie infectivity and amyloid plaques
1989 StandoutNobel
Sulfated glycosaminoglycans in amyloid plaques of prion diseases
1989 StandoutNobel
Immunologic and Molecular Biologic Studies of Prion Proteins in Bovine Spongiform Encephalopathy
1993 StandoutNobel
Selective Neuronal Targeting in Prion Disease
1997 StandoutNobel
NMR characterization of the full‐length recombinant murine prion protein, mPrP(23–231)
1997 StandoutNobel
Human prion proteins expressed in Escherichia coli and purified by high‐affinity column refolding
1997 StandoutNobel
The abnormal isoform of the prion protein accumulates in late‐endosome‐like organelles in scrapie‐infected mouse brain
1995
Hierarchy for 5′ splice site preference determined in vivo
1990
Prion propagation in mice expressing human and chimeric PrP transgenes implicates the interaction of cellular PrP with another protein
1995 StandoutNobel
Prion (PrPSc)-specific epitope defined by a monoclonal antibody
1997 StandoutNatureNobel
Scrapie prions aggregate to form amyloid-like birefringent rods
1983 StandoutNobel
Transmissible spongiform encephalopathies: The threat of BSE to man
1990
Measurement of the scrapie agent using an incubation time interval assay
1982 StandoutNobel
Prion-inducing domain 2–114 of yeast Sup35 protein transforms in vitro into amyloid-like filaments
1997 StandoutNobel
Properties of scrapie prion protein liposomes.
1988 StandoutNobel
Linkage of prion protein and scrapie incubation time genes
1986 StandoutNobel
Analyses of frequency of infection, specific infectivity, and prion protein biosynthesis in scrapie-infected neuroblastoma cell clones
1988
A prion protein cycles between the cell surface and an endocytic compartment in cultured neuroblastoma cells
1993
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
Chemical chaperones interfere with the formation of scrapie prion protein.
1996 StandoutNobel
Scrapie prions selectively modify the stress response in neuroblastoma cells.
1995
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
The sequential development of abnormal prion protein accumulation in mice with Creutzfeldt-Jakob disease.
1992
Conversion of alpha-helices into beta-sheets features in the formation of the scrapie prion proteins.
1993 Standout
Prion Diseases and Neurodegeneration
1994 StandoutNobel
Cholesterol depletion and modification of COOH-terminal targeting sequence of the prion protein inhibit formation of the scrapie isoform [published erratum appears in J Cell Biol 1995 Jul;130(2):501]
1995
Normal and scrapie-associated forms of prion protein differ in their sensitivities to phospholipase and proteases in intact neuroblastoma cells
1990
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
Prion Diseases and the BSE Crisis
1997 StandoutScienceNobel
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
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
Attempts to convert the cellular prion protein into the scrapie isoform in cell-free systems
1992 StandoutNobel
Synthesis and trafficking of prion proteins in cultured cells.
1992 StandoutNobel
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
High Prion and PrPSc Levels but Delayed Onset of Disease in Scrapie-Inoculated Mice Heterozygous for a Disrupted PrP Gene
1994
Separation and properties of cellular and scrapie prion proteins.
1986 StandoutNobel
Evidence for synthesis of scrapie prion proteins in the endocytic pathway.
1992 StandoutNobel
Neuropathological changes in scrapie and Alzheimer's disease are associated with increased expression of apolipoprotein E and cathepsin D in astrocytes
1991
Splice Variants of the α Subunit of the G Protein G s Activate Both Adenylyl Cyclase and Calcium Channels
1989 StandoutScienceNobel
Distinct PrP properties suggest the molecular basis of strain variation in transmissible mink encephalopathy
1994
A cellular gene encodes scrapie PrP 27-30 protein
1985 StandoutNobel
Experimental Scrapie in the Mouse: Electrophoretic and Sedimentation Properties of the Partially Purified Agent
1980 StandoutNobel
Scrapie prion rod formation in vitro requires both detergent extraction and limited proteolysis
1991 StandoutNobel
Protease sensitivity and nuclease resistance of the scrapie agent propagated in vitro in neuroblastoma cells
1991
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
Characterization of Detergent-insoluble Complexes Containing the Cellular Prion Protein and Its Scrapie Isoform
1997
Precise targeting of the pathology of the sialoglycoprotein, PrP, and vacuolar degeneration in mouse scrapie
1989
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
Molecular basis for two forms of the G protein that stimulates adenylate cyclase.
1986 StandoutNobel
Prion protein NMR structure and species barrier for prion diseases
1997 StandoutNobel
Works of Prusiner Sb being referenced
Electrospray mass spectrometry of the glycosylinositol phospholipid of the scrapie prion protein
1991
Molecular biology and pathogenesis of prion diseases
1996
Cloning and characterization of the myelin basic protein gene from mouse: one gene can encode both 14 kd and 18.5 kd MBPs by alternate use of exons
1985
Ultrastructural localization of scrapie prion proteins in cytoplasmic vesicles of infected cultured cells.
1991
Evidence for hydrophobic domains on the surface of the scrapie agent.
1978
Slow viruses: molecular properties of the agents causing scrapie in mice and hamsters.
1980
Structure determination of glycoinositol phospholipid anchors by permethylation and tandem mass spectrometry
1990
Immuno-gold localization of prion filaments in scrapie-infected hamster brains.
1987
Prions causing nervous system degeneration.
1987