Citation Impact
Citing Papers
Structural studies of the scrapie prion protein by electron crystallography
2002 Nobel
Protein characterization of Saccharomyces cerevisiae RNA polymerase II after in vivo cross-linking
2007 StandoutNobel
Synthetic Mammalian Prions
2004 ScienceNobel
Protein Misfolding, Amyloid Formation, and Human Disease: A Summary of Progress Over the Last Decade
2017 Standout
Innate Antiviral Responses by Means of TLR7-Mediated Recognition of Single-Stranded RNA
2004 StandoutScience
Sleep Drives Metabolite Clearance from the Adult Brain
2013 StandoutScience
A 7-kDa Prion Protein (PrP) Fragment, an Integral Component of the PrP Region Required for Infectivity, Is the Major Amyloid Protein in Gerstmann-Sträussler-Scheinker Disease A117V
2001
Caspase-12 and endoplasmic reticulum stress mediate neurotoxicity of pathological prion protein
2003
The role of liquid–liquid phase separation in aggregation of the TDP-43 low-complexity domain
2019 Standout
The role of dynamic conformational ensembles in biomolecular recognition
2009 Standout
Prion-like behavior of MAVS in RIG-I signaling
2011 StandoutNobel
Mammalian Prion Biology
2004
An Integrated Mass Spectrometry-based Proteomic Approach
2005
Pathway Complexity of Prion Protein Assembly into Amyloid
2002 Nobel
Retrovirus infection strongly enhances scrapie infectivity release in cell culture
2006
Construction of Robust Bio‐nanotubes using the Controlled Self‐Assembly of Component Proteins of Bacteriophage T4
2010 StandoutNobel
Oxyl radicals, redox-sensitive signalling cascades and antioxidants
2007 Standout
Familial and sporadic fatal insomnia
2003
Affinity purification‐mass spectrometry
2003
Antibodies inhibit prion propagation and clear cell cultures of prion infectivity
2001 NatureNobel
Regional distribution of protease‐resistant prion protein in fatal familial insomnia
1995
Prions
2011
First experimental transmission of fatal familial insomnia
1995 NatureNobel
Engineering the prion protein using chemical synthesis
2001 Nobel
Exosomes: Current knowledge of their composition, biological functions, and diagnostic and therapeutic potentials
2012 Standout
Toxicity of novel C‐terminal prion protein fragments and peptides harbouring disease‐related C‐terminal mutations
2001
Dendrimer Effects on Peptide and Protein Fibrillation
2007
Protein Identification by Mass Spectrometry
2003
Packaging of prions into exosomes is associated with a novel pathway of PrP processing
2007
Mammalian prion proteins
2000
Rapid cell-surface prion protein conversion revealed using a novel cell system
2011
Studies on peptide fragments of prion proteins
2001
TREM2 Lipid Sensing Sustains the Microglial Response in an Alzheimer’s Disease Model
2015 Standout
Structure of the cross-β spine of amyloid-like fibrils
2005 StandoutNature
Copper binding to octarepeat peptides of the prion protein monitored by mass spectrometry
2000
Heme Oxygenase-1/Carbon Monoxide: From Basic Science to Therapeutic Applications
2006 Standout
Rapid online buffer exchange for screening of proteins, protein complexes and cell lysates by native mass spectrometry
2020 StandoutNobel
Channels formed with a mutant prion protein PrP(82-146) homologous to a 7-kDa fragment in diseased brain of GSS patients
2003
Protein aggregation and neurodegenerative disease
2004 Standout
Pannexin‐1 mediates large pore formation and interleukin‐1β release by the ATP‐gated P2X7 receptor
2006 Standout
Evidence that the 127–164 Region of Prion Proteins Has Two Equi-Energetic Conformations with β or α Features
2001
Exosomes – vesicular carriers for intercellular communication
2009 Standout
Biological inorganic and bioinorganic chemistry of neurodegeneration based on prion and Alzheimer diseases
2004
The N-terminal Region of the Prion Protein Ectodomain Contains a Lipid Raft Targeting Determinant
2003
Selective Neuronal Targeting in Prion Disease
1997 StandoutNobel
The Octapeptide Repeats in Mammalian Prion Protein Constitute a pH-dependent Folding and Aggregation Site
2003
Review: Contribution of transgenic models to understanding human prion disease
2010
Structural biology of NCAM homophilic binding and activation of FGFR
2005
Fatal Familial Insomnia and Familial Creutzfeldt‐Jakob Disease: Clinical, Pathological and Molecular Features
1995
Protein misfolding and prion diseases
1999
The Amyloid State of Proteins in Human Diseases
2012 Standout
Prion recognition elements govern nucleation, strain specificity and species barriers
2007 Nature
Evidence for the Formation of Symmetric and Asymmetric DLPC-DAPC Lipid Bilayer Domains
2013 Standout
Membrane-Anchored Aβ Accelerates Amyloid Formation and Exacerbates Amyloid-Associated Toxicity in Mice
2013
Cell death and endoplasmic reticulum stress: disease relevance and therapeutic opportunities
2008 Standout
The Extracellular Architecture of Adherens Junctions Revealed by Crystal Structures of Type I Cadherins
2011 StandoutNobel
Classification, Functions, and Clinical Relevance of Extracellular Vesicles
2012 Standout
Prions: Protein Aggregation and Infectious Diseases
2009
Prevalence of lymphoreticular prion protein accumulation in UK tissue samples
2004
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
The toxic Aβ oligomer and Alzheimer's disease: an emperor in need of clothes
2012 Standout
Specificities of secretion and uptake of exosomes and other extracellular vesicles for cell-to-cell communication
2018 Standout
Structural Biology of Prions
2000
Extracellular vesicles: biology and emerging therapeutic opportunities
2013 Standout
Molecular Mechanisms of Amyloidosis
2003 Standout
Prions on the move
2011
Extracellular vesicles: Exosomes, microvesicles, and friends
2013 Standout
Protein Misfolding, Functional Amyloid, and Human Disease
2006 Standout
Characterization of Protein Cross-Links via Mass Spectrometry and an Open-Modification Search Strategy
2008
Potent inhibition of scrapie prion replication in cultured cells by bis-acridines
2003 Nobel
Chronic Wasting Disease of Deer and Elk: A Review with Recommendations for Management
2002 Standout
Normal Modes of Prion Proteins: From Native to Infectious Particle
2011 StandoutNobel
Branched Polyamines Cure Prion-Infected Neuroblastoma Cells
2001 Nobel
GENETICS OF PRIONS
1997 StandoutNobel
Review: Prion‐like mechanisms of transactive response DNA binding protein of 43 kDa (TDP ‐43) in amyotrophic lateral sclerosis (ALS )
2014
Transmissible Spongiform Encephalopathies in Humans
1999
Disruption of prion rods generates 10-nm spherical particles having high alpha-helical content and lacking scrapie infectivity
1996 StandoutNobel
Copper Homeostasis and Neurodegenerative Disorders (Alzheimer's, Prion, and Parkinson's Diseases and Amyotrophic Lateral Sclerosis)
2006 Standout
Emerging Principles of Conformation-Based Prion Inheritance
2003
Transfusion-related mortality: the ongoing risks of allogeneic blood transfusion and the available strategies for their prevention
2009 Standout
Biology and Genetics of Prions Causing Neurodegeneration
2013 Nobel
Ecological Impacts of Deer Overabundance
2004 Standout
A structural model for Alzheimer's β-amyloid fibrils based on experimental constraints from solid state NMR
2002 Standout
Prion infection impairs the cellular response to oxidative stress
2000
Evidence for the Conformation of the Pathologic Isoform of the Prion Protein Enciphering and Propagating Prion Diversity
1996 StandoutScienceNobel
Dangerous Liaisons between a Microbe and the Prion Protein
2003
Isotope Signatures Allow Identification of Chemically Cross-Linked Peptides by Mass Spectrometry: A Novel Method to Determine Interresidue Distances in Protein Structures through Cross-Linking
2010 StandoutNobel
The Glycosylphosphatidylinositol Anchor: A Complex Membrane-Anchoring Structure for Proteins
2008 StandoutNobel
Evidence for assembly of prions with left-handed β-helices into trimers
2004 Nobel
Coupled prediction of protein secondary and tertiary structure
2003 StandoutNobel
Prion protein recruits its neuronal receptor NCAM to lipid rafts to activate p59fyn and to enhance neurite outgrowth
2005
Dendrimers Designed for Functions: From Physical, Photophysical, and Supramolecular Properties to Applications in Sensing, Catalysis, Molecular Electronics, Photonics, and Nanomedicine
2010 Standout
Internal Disequilibria and Phenotypic Diversification during Replication of Hepatitis C Virus in a Noncoevolving Cellular Environment
2017 StandoutNobel
Interactions of the Transmembrane Polymeric Rings of the Salmonella enterica Serovar Typhimurium Type III Secretion System
2010 StandoutNobel
Free Radicals in the Physiological Control of Cell Function
2002 Standout
Inherited prion diseases.
1994 StandoutNobel
Metals in Neurobiology: Probing Their Chemistry and Biology with Molecular Imaging
2008 Standout
Mass Spectrometry and Protein Analysis
2006 StandoutScience
Works of Patrick J. Bosque being referenced
Prions in skeletal muscle
2002 Nobel
Human Prion Disease and Relative Risk Associated with Chronic Wasting Disease
2006
Prion Protein of 106 Residues Creates an Artificial Transmission Barrier for Prion Replication in Transgenic Mice
1999 Nobel
Binding of neural cell adhesion molecules (N-CAMs) to the cellular prion protein
2001 Nobel
Cultured Cell Sublines Highly Susceptible to Prion Infection
2000 Nobel
Transmission of Elk and Deer Prions to Transgenic Mice
2006 Nobel
Inherited prion disease caused by the V210I mutation
2001 Nobel
A PrP gene codon 178 base substitution and a 24‐bp interstitial deletion in familial Creutzfeldt‐Jakob disease
1992