Standout Papers
- Conversion of truncated and elongated prion proteins into the scrapie isoform in cultured cells. (1993)
- Epitope mapping of the Syrian hamster prion protein utilizing chimeric and mutant genes in a vaccinia virus expression system (1991)
- Release of the cellular prion protein from cultured cells after loss of its glycoinositol phospholipid anchor (1993)
- Selective Neuronal Targeting in Prion Disease (1997)
- Intracellular accumulation of the cellular prion protein after mutagenesis of its Asnlinked glycosylation sites (1990)
Citation Impact
Citing Papers
Why highly expressed proteins evolve slowly
2005 StandoutNobel
Normal development and behaviour of mice lacking the neuronal cell-surface PrP protein
1992 StandoutNatureNobel
Molecular biology and genetics of prion diseases
1994 StandoutNobel
Transgenetic investigations of prion diseases of humans and animals
1993 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
Chemistry and biology of prions
1992
Structural studies of the scrapie prion protein using mass spectrometry and amino acid sequencing
1993
Aggregates of scrapie-associated prion protein induce the cell-free conversion of protease-sensitive prion protein to the protease-resistant state
1995
Cell-free formation of protease-resistant prion protein
1994 Nature
Characterisation of antisera raised against species-specific peptide sequences from scrapie-associated fibril protein and their application for post-mortem immunodiagnosis of spongiform encephalopathies
1994
Glycosylinositol Phospholipid Anchors of the Scrapie and Cellular Prion Proteins Contain Sialic Acid
1992 StandoutNobel
Apolipoprotein B: structure, biosynthesis and role in the lipoprotein assembly process
1987
Transgenetic studies implicate interactions between homologous PrP isoforms in scrapie prion replication
1990 StandoutNobel
Mimicking Somatic Hypermutation: Affinity Maturation of Antibodies Displayed on Bacteriophage Using a Bacterial Mutator Strain
1996 StandoutNobel
Degeneration of skeletal muscle, peripheral nerves, and the central nervous system in transgenic mice overexpressing wild-type prion proteins
1994 StandoutNobel
Brefeldin A Reversibly Inhibits the Assembly of ApoB Containing Lipoproteins in McA-RH7777 Cells
1995
Molecular properties of complexes formed between the prion protein and synthetic peptides
1997 StandoutNobel
Patch‐clamp Analysis of Synaptic Transmission to Cerebellar Purkinje Cells of Prion Protein Knockout Mice
1995
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
Molecular evolution of bacteriophages: evidence of selection against the recognition sites of host restriction enzymes.
1986
Heritable disorder resembling neuronal storage disease in mice expressing prion protein with deletion of an α-helix
1997
Amyloid fibrils in Gerstmann-Sträussler-Scheinker disease (Indiana and Swedish Kindreds) express only PrP peptides encoded by the mutant allele
1994
Purification and characterization of TnsC, a Tn7 transposition protein that binds ATP and DNA
1992
The abnormal isoform of the prion protein accumulates in late‐endosome‐like organelles in scrapie‐infected mouse brain
1995
A conformational transition at the N terminus of the prion protein features in formation of the scrapie isoform 1 1Edited by M. Yaniv
1997 StandoutNobel
Eight prion strains have PrPSc molecules with different conformations
1998 Nobel
Propagation of prions with artificial properties in transgenic mice expressing chimeric PrP genes
1993
Insoluble wild–type and protease–resistant mutant prion protein in brains of patients with inherited prion disease
1996 StandoutNobel
Prion Protein Biology
1998 Nobel
Prion propagation in mice expressing human and chimeric PrP transgenes implicates the interaction of cellular PrP with another protein
1995 StandoutNobel
Chimeric prion protein expression in cultured cells and transgenic mice
1992 StandoutNobel
Prion (PrPSc)-specific epitope defined by a monoclonal antibody
1997 StandoutNatureNobel
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
A novel form of tissue-specific RNA processing produces apolipoprotein-B48 in intestine
1987
Ablation of the prion protein (PrP) gene in mice prevents scrapie and facilitates production of anti-PrP antibodies.
1993 StandoutNobel
Regional mapping of prion proteins in brain.
1992 StandoutNobel
The magical number seven, plus or minus two: Some limits on our capacity for processing information.
1956 Standout
Codon usage in yeast: cluster analysis clearly differentiates highly and lowly expressed genes
1986
Evidence for protein X binding to a discontinuous epitope on the cellular prion protein during scrapie prion propagation
1997 StandoutNobel
Studies on the assembly of apolipoprotein B-100- and B-48-containing very low density lipoproteins in McA-RH7777 cells.
1994
Prion Diseases and Neurodegeneration
1994 StandoutNobel
Prion protein (PrP) with amino-proximal deletions restoring susceptibility of PrP knockout mice to scrapie.
1996
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
Prion protein (PrP) synthetic peptides induce cellular PrP to acquire properties of the scrapie isoform.
1995 StandoutNobel
Prions and prion proteins 1
1991 StandoutNobel
Molecular Matchmakers
1993 StandoutScienceNobel
Evidence for the Conformation of the Pathologic Isoform of the Prion Protein Enciphering and Propagating Prion Diversity
1996 StandoutScienceNobel
The theory of planned behavior
1991 Standout
A Transmembrane Form of the Prion Protein in Neurodegenerative Disease
1998 ScienceNobel
Apolipoprotein B-48 Is the Product of a Messenger RNA with an Organ-Specific In-Frame Stop Codon
1987 Science
Prion Diseases and the BSE Crisis
1997 StandoutScienceNobel
A hypothalamic neuronal cell line persistently infected with scrapie prions exhibits apoptosis
1997 StandoutNobel
Prions
1998 StandoutNobel
NMR solution structure of the human prion protein
2000 StandoutNobel
Biosynthesis of Apolipoprotein B48-containing Lipoproteins
1996 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
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
Interactions between wild-type and mutant prion proteins modulate neurodegeneration in transgenic mice.
1996
Evidence for synthesis of scrapie prion proteins in the endocytic pathway.
1992 StandoutNobel
Three scrapie prion isolates exhibit different accumulation patterns of the prion protein scrapie isoform.
1993
Transmission of Creutzfeldt-Jakob disease from humans to transgenic mice expressing chimeric human-mouse prion protein.
1994 StandoutNobel
The magical number seven, plus or minus two: Some limits on our capacity for processing information.
1994 Standout
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
Replication of distinct scrapie prion isolates is region specific in brains of transgenic mice and hamsters.
1992 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
How Big Is a Chunk?
1974 StandoutScienceNobel
The codon adaptation index-a measure of directional synonymous codon usage bias, and its potential applications
1987 Standout
Recombinant scrapie-like prion protein of 106 amino acids is soluble
1996 StandoutNobel
Spontaneous Neurodegeneration in Transgenic Mice with Mutant Prion Protein
1990 StandoutScienceNobel
Works of Mark Rogers being referenced
Transmission of Information About Sucrose and Saline Solutions Through the Sense of Taste
1955
Selective Neuronal Targeting in Prion Disease
1997 StandoutNobel
The Cellular Isoform of the Prion Protein, PRPC, Is Associated with Caveolae in Mouse Neuroblastoma (N2a) Cells
1995
Release of the cellular prion protein from cultured cells after loss of its glycoinositol phospholipid anchor
1993 StandoutNobel
Characterization of a prion protein (PrP) gene from rabbit; a species with apparent resistance to infection by prions
1997
Epitope mapping of the Syrian hamster prion protein utilizing chimeric and mutant genes in a vaccinia virus expression system
1991 StandoutNobel
Selection pressures on codon usage in the complete genome of bacteriophage T7
1985
Analysis of Tn7 transposition
1986
Apolipoprotein B synthesis by human liver and intestine in vitro.
1986
Acquisition of protease resistance by prion proteins in scrapie-infected cells does not require asparagine-linked glycosylation.
1990
Intracellular accumulation of the cellular prion protein after mutagenesis of its Asnlinked glycosylation sites
1990 StandoutNobel
Conversion of truncated and elongated prion proteins into the scrapie isoform in cultured cells.
1993 StandoutNobel