Citation Impact
Citing Papers
APP717, APP693, and PRIP gene mutations are rare in Alzheimer disease.
1991
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
Spontaneous Neurodegeneration in Transgenic Mice with Prion Protein Codon 101 Proline → Leucine Substitutiona
1991 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
Cognitive reserve, presynaptic proteins and dementia in the elderly
2012
Mutation of the Prion Protein in Libyan Jews with Creutzfeldt–Jakob Disease
1991 StandoutNobel
Glycosylinositol Phospholipid Anchors of the Scrapie and Cellular Prion Proteins Contain Sialic Acid
1992 StandoutNobel
Frontotemporal Dementia and Parkinsonism Linked to Chromosome 17: A New Group of Tauopathies
1998
BIOLOGY AND GENETICS OF PRION DISEASES
1994
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
Fatal Familial Insomnia, a Prion Disease with a Mutation at Codon 178 of the Prion Protein Gene
1992
Gerstmann‐Sträussler‐Scheinker Disease and the Indiana Kindred
1995
Spontaneous generation of infectious nucleating amyloids in the transmissible and nontransmissible cerebral amyloidoses
1994 Nobel
Structural Clues to Prion Replication
1994 StandoutScienceNobel
Genetic and Infectious Prion Diseases
1993
Mutations and polymorphisms in the prion protein gene
1993
A Familial Alzheimer's Disease Locus on Chromosome 1
1995 Science
Mutant prion proteins in Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles
1992 StandoutNobel
Identification of a novel family of presenilin homologues
2002
Amyloid fibrils in Gerstmann-Sträussler-Scheinker disease (Indiana and Swedish Kindreds) express only PrP peptides encoded by the mutant allele
1994
Human prion diseases
1994 StandoutNobel
Inherited Prion Diseases and Transmission to Rodents
1995
The PtdIns(3,4)P2 phosphatase INPP4A is a suppressor of excitotoxic neuronal death
2010 StandoutNatureNobel
Longitudinal Assessment of Neurocognitive Function after Coronary-Artery Bypass Surgery
2001 Standout
Cdk5 Regulates the Phosphorylation of Tyrosine 1472 NR2B and the Surface Expression of NMDA Receptors
2008
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
Tau is a candidate gene for chromosome 17 frontotemporal dementia
1998
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
Structure and polymorphism of the mouse prion protein gene.
1994 StandoutNobel
Mutation and polymorphism of the prion protein gene in Libyan Jews with Creutzfeldt-Jakob disease (CJD).
1993 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
The Amyloid Hypothesis of Alzheimer's Disease: Progress and Problems on the Road to Therapeutics
2002 StandoutScience
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
Prion Diseases and Neurodegeneration
1994 StandoutNobel
Transmissible familial Creutzfeldt-Jakob disease associated with five, seven, and eight extra octapeptide coding repeats in the PRNP gene.
1991 Nobel
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
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
Candidate Gene for the Chromosome 1 Familial Alzheimer's Disease Locus
1995 StandoutScience
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
Solution structure of a 142-residue recombinant prion protein corresponding to the infectious fragment of the scrapie isoform
1997 StandoutNobel
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
NMR structure of the bovine prion protein
2000 StandoutNobel
Transmission of Creutzfeldt-Jakob disease from humans to transgenic mice expressing chimeric human-mouse prion protein.
1994 StandoutNobel
The Caenorhabditis elegans IMPAS gene, imp-2, is essential for development and is functionally distinct from related presenilins
2004 StandoutNobel
Molecular Biology of Prion Diseases
1991 StandoutScienceNobel
A single hamster PrP amino acid blocks conversion to protease-resistant PrP in scrapie-infected mouse neuroblastoma cells
1995
COOH-terminal sequence of the cellular prion protein directs subcellular trafficking and controls conversion into the scrapie isoform
1997 StandoutNobel
Inherited prion diseases.
1994 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
Conversion of truncated and elongated prion proteins into the scrapie isoform in cultured cells.
1993 StandoutNobel
Deconstructing complexin function in activating and clamping Ca 2+ -triggered exocytosis by comparing knockout and knockdown phenotypes
2013 StandoutNobel
Prion protein preamyloid and amyloid deposits in Gerstmann-Sträussler-Scheinker disease, Indiana kindred.
1992 StandoutNobel
Spontaneous Neurodegeneration in Transgenic Mice with Mutant Prion Protein
1990 StandoutScienceNobel
Works of Gerald D. Schellenberg being referenced
A prion protein variant in a family with the telencephalic form of Gerstmann‐Straussler‐Scheinker syndrome
1991
Pathological correlates of dementia in a longitudinal, population‐based sample of aging
2007
Chromosome 17 and hereditary dementia
1997
Midlife cardiovascular risk factors, ApoE, and cognitive decline in elderly male twins
1998
Chromosome 14 and late-onset familial Alzheimer disease (FAD).
1993