Citation Impact
Citing Papers
Why highly expressed proteins evolve slowly
2005 StandoutNobel
Induced-fit tightens pleuromutilins binding to ribosomes and remote interactions enable their selectivity
2007 StandoutNobel
Identification of novel filament-forming proteins in Saccharomyces cerevisiae and Drosophila melanogaster
2010
Regulation of Heterochromatic Silencing and Histone H3 Lysine-9 Methylation by RNAi
2002 StandoutScience
A Genomewide Search for Ribozymes Reveals an HDV-Like Sequence in the Human CPEB3 Gene
2006 StandoutScienceNobel
Architecture of Ure2p Prion Filaments
2003
Ribonuclease A suggests how proteins self‐chaperone against amyloid fiber formation
2011
Conformational constraints for amyloid fibrillation: the importance of being unfolded
2004
Solution Structure of the E. coli 70S Ribosome at 11.5 Å Resolution
2000 StandoutNobel
Inherent toxicity of aggregates implies a common mechanism for protein misfolding diseases
2002 StandoutNature
RAP1 protein interacts with yeast telomeres in vivo: Overproduction alters telomere structure and decreases chromosome stability
1990
Cleavage of poly(ADP-ribose) polymerase by a proteinase with properties like ICE
1994 StandoutNature
Uncoupling of Initiation Factor eIF5B/IF2 GTPase and Translational Activities by Mutations that Lower Ribosome Affinity
2002
Prions of Yeast as Heritable Amyloidoses
2000
The Cryo-EM Structure of a Translation Initiation Complex from Escherichia coli
2005 StandoutNobel
Atomic structures of amyloid cross-β spines reveal varied steric zippers
2007 StandoutNature
Genetic instabilities in human cancers
1998 StandoutNature
A Critical Role for Amino-Terminal Glutamine/Asparagine Repeats in the Formation and Propagation of a Yeast Prion
1998
Filaments of the Ure2p prion protein have a cross-β core structure
2005
Quality control of mRNA 3′-end processing is linked to the nuclear exosome
2001 StandoutNatureNobel
Identification of stop codon readthrough genes in Saccharomyces cerevisiae
2003
Structure of the cross-β spine of amyloid-like fibrils
2005 StandoutNature
Metazoan Hsp70 machines use Hsp110 to power protein disaggregation
2012
Cap-dependent and cap-independent translation in eukaryotic systems
2004
Runaway telomere elongation caused by telomerase RNA gene mutations
1995 StandoutNatureNobel
Functional genomic analysis of C. elegans chromosome I by systematic RNA interference
2000 StandoutNature
The physical basis of how prion conformations determine strain phenotypes
2006 Nature
Molecular chaperones in protein folding and proteostasis
2011 StandoutNature
Multiple Gln/Asn-Rich Prion Domains Confer Susceptibility to Induction of the Yeast [PSI] Prion
2001
Molecular biology of transmissible spongiform encephalopathies
1996
Control of telomere growth by interactions of RAP1 with the most distal telomeric repeats
1996 StandoutNatureNobel
Cdk1-Dependent Phosphorylation of Cdc13 Coordinates Telomere Elongation during Cell-Cycle Progression
2009 StandoutNobel
Phase transitions in the assembly of multivalent signalling proteins
2012 StandoutNature
Subcellular localization of the yeast proteome
2002
The native-like conformation of Ure2p in fibrils assembled under physiologically relevant conditions switches to an amyloid-like conformation upon heat-treatment of the fibrils
2003
CENP-C, an autoantigen in scleroderma, is a component of the human inner kinetochore plate
1992
Switching and Signaling at the Telomere
2001 StandoutNobel
A synthetic homing endonuclease-based gene drive system in the human malaria mosquito
2011 StandoutNatureNobel
A Neuronal Isoform of the Aplysia CPEB Has Prion-Like Properties
2003 Nobel
Complilation and characteristics of dedicated transcription factors in Saccharomyces cerevisiae
1995
The yeast prion Ure2p retains its native alpha-helical conformation upon assembly into protein fibrils in vitro
2002
Global analysis of protein localization in budding yeast
2003 StandoutNature
The Exosome: A Conserved Eukaryotic RNA Processing Complex Containing Multiple 3′→5′ Exoribonucleases
1997
Rrp6p, the Yeast Homologue of the Human PM-Scl 100-kDa Autoantigen, Is Essential for Efficient 5.8 S rRNA 3′ End Formation
1998
The Mammalian Disaggregase Machinery: Hsp110 Synergizes with Hsp70 and Hsp40 to Catalyze Protein Disaggregation and Reactivation in a Cell-Free System
2011
Comparative assessment of large-scale data sets of protein–protein interactions
2002 StandoutNature
Molecular Basis of a Yeast Prion Species Barrier
2000
Possible cross-regulation of phosphate and sulfate metabolism in Saccharomyces cerevisiae.
1992
Deadly Conformations—Protein Misfolding in Prion Disease
1997
Translation termination efficiency can be regulated in Saccharomyces cerevisiae by environmental stress through a prion-mediated mechanism
1999
Proof and evolutionary analysis of ancient genome duplication in the yeast Saccharomyces cerevisiae
2004 Nature
NMR structures of three single-residue variants of the human prion protein
2000 StandoutNobel
Outcrossed sex allows a selfish gene to invade yeast populations
2001
Protein Misfolding, Functional Amyloid, and Human Disease
2006 Standout
Prion-inducing domain 2–114 of yeast Sup35 protein transforms in vitro into amyloid-like filaments
1997 StandoutNobel
A model for Ure2p prion filaments and other amyloids: The parallel superpleated β-structure
2004
Prion protein NMR structure and familial human spongiform encephalopathies
1998 StandoutNobel
Identification of Functionally Important Amino Acids of Ribosomal Protein L3 by Saturation Mutagenesis
2005
Mutation of the mouse klotho gene leads to a syndrome resembling ageing.
1997 Standout
A Nuclear 3′-5′ Exonuclease Involved in mRNA Degradation Interacts with Poly(A) Polymerase and the hnRNA Protein Npl3p
2000
Discrimination between related DNA sites by a single amino acid residue of Myc-related basic-helix-loop-helix proteins.
1992
Hypoxia-inducible factor 1 is a basic-helix-loop-helix-PAS heterodimer regulated by cellular O2 tension.
1995 StandoutNobel
GENETICS OF PRIONS
1997 StandoutNobel
An essential yeast protein, CBF5p, binds in vitro to centromeres and microtubules.
1993
Life with 6000 Genes
1996 StandoutScience
The genome-wide expression response to telomerase deletion in Saccharomyces cerevisiae
2002 StandoutNobel
Cell Cycle Control and Cancer
1994 StandoutScienceNobel
Identification of a Human Mitotic Checkpoint Gene: hsMAD2
1996 Science
Structure-Based Design of Functional Amyloid Materials
2014 StandoutNobel
Identification of a nonprocessive telomerase activity from mouse cells.
1993 StandoutNobel
The histone fold: evolutionary questions.
1995 StandoutNobel
The protein product of the het-s heterokaryon incompatibility gene of the fungus Podospora anserina behaves as a prion analog
1997
Emerging Principles of Conformation-Based Prion Inheritance
2003
Yeast prions [URE3] and [PSI + ] are diseases
2005
Marked decrease of neuropeptide Y Y2 receptor binding sites in the hippocampus in murine prion disease
1997 StandoutNobel
A General Mechanism for Network-Dosage Compensation in Gene Circuits
2010 StandoutScienceNobel
Ribosomal Protein L3 Mutants Alter Translational Fidelity and Promote Rapid Loss of the Yeast Killer Virus
1999
Spermidine in health and disease
2018 StandoutScience
Creating a Protein-Based Element of Inheritance
2000 Science
Prion Diseases and the BSE Crisis
1997 StandoutScienceNobel
Fission Yeast Homologs of Human CENP-B Have Redundant Functions Affecting Cell Growth and Chromosome Segregation
2000
NMR solution structure of the human prion protein
2000 StandoutNobel
Hydroxylation of the eukaryotic ribosomal decoding center affects translational accuracy
2014 StandoutNobel
Propagation of the yeast prion-like [psi+] determinant is mediated by oligomerization of the SUP35-encoded polypeptide chain release factor.
1996
A mutation in CSE4, an essential gene encoding a novel chromatin-associated protein in yeast, causes chromosome nondisjunction and cell cycle arrest at mitosis.
1995
Centromere DNA mutations induce a mitotic delay in Saccharomyces cerevisiae.
1992
Casting Metal Nanowires Within Discrete Self-Assembled Peptide Nanotubes
2003 StandoutScience
Structure of the recombinant full-length hamster prion protein PrP(29–231): The N terminus is highly flexible
1997 StandoutNobel
β-Helix is a likely core structure of yeast prion Sup35 amyloid fibers
2004
Structural Characterization of the Fibrillar Form of the Yeast Saccharomyces cerevisiae Prion Ure2p
2004
An essential yeast gene encoding a TTAGGG repeat-binding protein.
1993
Stress Granule Assembly Is Mediated by Prion-like Aggregation of TIA-1
2004
Structure and function of telomeres
1991 StandoutNatureNobel
Unique double-ring structure of the peroxisomal Pex1/Pex6 ATPase complex revealed by cryo-electron microscopy
2015 StandoutNobel
Head-to-tail interactions of the coiled-coil domains regulate ClpB activity and cooperation with Hsp70 in protein disaggregation
2014
Prion protein NMR structure and species barrier for prion diseases
1997 StandoutNobel
Support for the Prion Hypothesis for Inheritance of a Phenotypic Trait in Yeast
1996 Science
Liquid phase condensation in cell physiology and disease
2017 StandoutScience
Coordinated assembly of human translation initiation complexes by the hepatitis C virus internal ribosome entry site RNA
2004 StandoutNobel
Autophagy protects against de novo formation of the [PSI+] prion in yeast
2015
Identification of fission yeast nuclear markers using random polypeptide fusions with green fluorescent protein
1996 StandoutNobel
A new prion controls fungal cell fusion incompatibility
1997
Works of Daniel C. Masison being referenced
Deletion of the Hsp70 chaperone gene SSB causes hypersensitivity to guanidine toxicity and curing of the [ PSI + ] prion by increasing guanidine uptake in yeast
2003
Evidence for Two Prions in Yeast: [URE3] and [PSI]
1996
Prion-impairing mutations in Hsp70 chaperone Ssa1: Effects on ATPase and chaperone activities
2008
[PSI] and [URE3] as yeast prions
1995
Guanidine Hydrochloride Inhibits Hsp104 Activity In Vivo: A Possible Explanation for Its Effect in Curing Yeast Prions
2001
The Ski7 Antiviral Protein Is an EF1-α Homolog That Blocks Expression of Non-Poly(A) mRNA in Saccharomyces cerevisiae
1999
Decoying the Cap2 mRNA Degradation System by a Double-Stranded RNA Virus and Poly(A)2 mRNA Surveillance by a Yeast Antiviral System
1995
N-Terminal Domain of Yeast Hsp104 Chaperone Is Dispensable for Thermotolerance and Prion Propagation but Necessary for Curing Prions by Hsp104 Overexpression
2006
Species-specific collaboration of heat shock proteins (Hsp) 70 and 100 in thermotolerance and protein disaggregation
2011
A Role for Cytosolic Hsp70 in Yeast [PSI+] Prion Propagation and [PSI+] as a Cellular Stress
2000
Saccharomyces cerevisiae Hsp70 Mutations Affect [PSI+] Prion Propagation and Cell Growth Differently and Implicate Hsp40 and Tetratricopeptide Repeat Cochaperones in Impairment of [PSI+]
2003
[URE3] and [PSI] as prions ofSaccharomyces cerevisiae: genetic evidence and biochemical properties
1996
Antagonistic Interactions between Yeast [PSI+] and [URE3] Prions and Curing of [URE3] by Hsp70 Protein Chaperone Ssa1p but Not by Ssa2p
2002
Isolation of the Gene Encoding the Saccharomyces cerevisiae Centromere-Binding Protein CP1
1990
Isolation of the gene encoding the Saccharomyces cerevisiae centromere-binding protein CP1.
1990
The prion model for [URE3] of yeast: Spontaneous generation and requirements for propagation
1997
1996
Prion-Inducing Domain of Yeast Ure2p and Protease Resistance of Ure2p in Prion-Containing Cells
1995 Science