Citation Impact
Citing Papers
Molecular biology and genetics of prion diseases
1994 StandoutNobel
The N-terminal Domain of a Glycolipid-anchored Prion Protein Is Essential for Its Endocytosis via Clathrin-coated Pits
1995
Unaltered susceptibility to BSE in transgenic mice expressing human prion protein
1995 Nature
NMR structure of the mouse prion protein domain PrP(121–231)
1996 StandoutNatureNobel
Chemistry and biology of prions
1992
Detecting prion protein gene mutations by denaturing gradient gel electrophoresis
1994 StandoutNobel
Prions
2011
Familial Creutzfeldt-Jakob Disease: Codon 200 Prion Disease in Libyan Jews
1997 StandoutNobel
Neurodegenerative Diseases and Prions
2001 Nobel
Degeneration of skeletal muscle, peripheral nerves, and the central nervous system in transgenic mice overexpressing wild-type prion proteins
1994 StandoutNobel
Conformational properties of the prion octa‐repeat and hydrophobic sequences
1997
Prion Protein Isoforms, a Convergence of Biological and Structural Investigations
1995 StandoutNobel
Structural Clues to Prion Replication
1994 StandoutScienceNobel
Genetic and Infectious Prion Diseases
1993
Protein folding and misfolding
2003 StandoutNature
Selective Neuronal Targeting in Prion Disease
1997 StandoutNobel
Human prion diseases
1994 StandoutNobel
Complete Genomic Sequence and Analysis of the Prion Protein Gene Region from Three Mammalian Species
1998 Nobel
Mutant and Infectious Prion Proteins Display Common Biochemical Properties in Cultured Cells
1996
A new point mutation of the prion protein gene in Creutzfeldt‐Jakob disease
1993
Protein misfolding and prion diseases
1999
The Amyloid State of Proteins in Human Diseases
2012 Standout
Insoluble wild–type and protease–resistant mutant prion protein in brains of patients with inherited prion disease
1996 StandoutNobel
Transmissions to mice indicate that ‘new variant’ CJD is caused by the BSE agent
1997 StandoutNature
Prion propagation in mice expressing human and chimeric PrP transgenes implicates the interaction of cellular PrP with another protein
1995 StandoutNobel
Molecular Mechanisms of Amyloidosis
2003 Standout
Molecular biology and pathogenesis of prion diseases
1996
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
Prion-inducing domain 2–114 of yeast Sup35 protein transforms in vitro into amyloid-like filaments
1997 StandoutNobel
Prion protein NMR structure and familial human spongiform encephalopathies
1998 StandoutNobel
Chemical chaperones interfere with the formation of scrapie prion protein.
1996 StandoutNobel
Complete Penetrance of Creutzfeldt-Jakob Disease in Libyan Jews Carrying the E200K Mutation in the Prion Protein Gene
1995
Evidence for protein X binding to a discontinuous epitope on the cellular prion protein during scrapie prion propagation
1997 StandoutNobel
GENETICS OF PRIONS
1997 StandoutNobel
Proposed three-dimensional structure for the cellular prion protein.
1994 StandoutNobel
Copper Homeostasis and Neurodegenerative Disorders (Alzheimer's, Prion, and Parkinson's Diseases and Amyotrophic Lateral Sclerosis)
2006 Standout
Marked decrease of neuropeptide Y Y2 receptor binding sites in the hippocampus in murine prion disease
1997 StandoutNobel
Once-Weekly Semaglutide in Adults with Overweight or Obesity
2021 Standout
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
Prions
1998 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
Obesity aggravates COVID‐19: An updated systematic review and meta‐analysis
2020
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
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
Two mutant prion proteins expressed in cultured cells acquire biochemical properties reminiscent of the scrapie isoform.
1996
Coupled prediction of protein secondary and tertiary structure
2003 StandoutNobel
Etiology and pathogenesis of prion diseases.
1995 StandoutNobel
COOH-terminal sequence of the cellular prion protein directs subcellular trafficking and controls conversion into the scrapie isoform
1997 StandoutNobel
Prion diseases of humans and animals
1996 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
Copper binding to the prion protein: Structural implications of four identical cooperative binding sites
1999 Nobel
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
Metals in Neurobiology: Probing Their Chemistry and Biology with Molecular Imaging
2008 Standout
Works of Rajkumar Doshi being referenced
Demographics, comorbidities and outcomes in hospitalized Covid-19 patients in rural southwest Georgia
2020
INHERITED PRION DISEASE WITH 144 BASE PAIR GENE INSERTION: 1. GENEALOGICAL AND MOLECULAR STUDIES
1992