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Unraveling the Structural Facets of Prp127-132 Polymorphic Variants Using Combined Molecular Dynamics/Markov Modeling
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LINCS: A linear constraint solver for molecular simulations
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Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects
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Charge‐Induced Secondary Structure Transformation of Amyloid‐Derived Dipeptide Assemblies from β‐Sheet to α‐Helix
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Molecular Structure of Amyloid Fibrils Formed by Residues 127 to 147 of the Human Prion Protein
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Prion protein expression and the M129V polymorphism of the PRNP gene in patients with colorectal cancer
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Fatal Familial Insomnia: A Rare Disease with Unique Clinico‐Neurophysiological Features
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Knowledge‐based protein secondary structure assignment
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Amyloid fibrils from the viewpoint of protein folding
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Mutations of the Prion Protein Gene
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Prion strains: shining new light on old concepts
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VMD: Visual molecular dynamics
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Huntington disease
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The role of amyloid oligomers in neurodegenerative pathologies
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Met/Val129 polymorphism of the full-length human prion protein dictates distinct pathways of amyloid formation
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Markov state models of biomolecular conformational dynamics
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Cryo-EM of amyloid fibrils and cellular aggregates
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Prion hypothesis: the end of the controversy?
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Prion protein gene analysis in new variant cases of Creutzfeldt-Jakob disease
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BSE: a decade on—part I
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Conformational Dynamics of Intrinsically Disordered Proteins Regulate Biomolecular Condensate Chemistry
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PyEMMA 2: A Software Package for Estimation, Validation, and Analysis of Markov Models
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Influence of Amino Acid Substitutions Related to Inherited Human Prion Diseases on the Thermodynamic Stability of the Cellular Prion Protein
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Variational Approach to Molecular Kinetics
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Dynamics of an Intrinsically Disordered Protein Reveal Metastable Conformations That Potentially Seed Aggregation
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Markov State Models: From an Art to a Science
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Structure and Dynamics of the TIP3P, SPC, and SPC/E Water Models at 298 K
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CHARMM36m: an improved force field for folded and intrinsically disordered proteins
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Cryo-EM structure of an amyloid fibril formed by full-length human prion protein
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Clarifying the influence of core amino acid hydrophobicity, secondary structure propensity, and molecular volume on amyloid-β 16–22 self-assembly
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Equilibrium thermodynamics and folding kinetics of a short, fast-folding, beta-hairpin
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The Role of Prion Peptide Structure and Aggregation in Toxicity and Membrane Binding
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Neurodegenerative Diseases and Prions
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Laboratory Diagnosis of Creutzfeldt–Jakob Disease
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Efficient multiple time step method for use with Ewald and particle mesh Ewald for large biomolecular systems
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Polymorphic transitions in single crystals: A new molecular dynamics method
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Markov models of molecular kinetics: Generation and validation
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Identification of slow molecular order parameters for Markov model construction
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Variational selection of features for molecular kinetics
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Exploring the aggregation free energy landscape of the amyloid-β protein (1–40)
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Prion protein β 2– α 2 loop conformational landscape
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The prion protein and lipid rafts (Review)
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Prion protein codon 129 polymorphism in mild cognitive impairment and dementia: the Rotterdam Study
inferredcites →https://doi.org/10.1093/hmg/6.10.1699openalex-extracted
Human prion diseases and bovine spongiform encephalopathy (BSE)
inferredcites →https://doi.org/10.1103/physrevlett.72.3634openalex-extracted
Separation of a mixture of independent signals using time delayed correlations
inferredcites →https://doi.org/10.1126/science.274.5295.2079openalex-extracted
Evidence for the Conformation of the Pathologic Isoform of the Prion Protein Enciphering and Propagating Prion Diversity
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Prion Diseases and Neurodegeneration
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Physiology of the Prion Protein
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A Kinetic Model of Trp-Cage Folding from Multiple Biased Molecular Dynamics Simulations
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Structural and Hydration Properties of the Partially Unfolded States of the Prion Protein
inferredcites →https://doi.org/10.2147/ndt.s165445openalex-extracted
Characterization of mutations in PRNP (prion) gene and their possible roles in neurodegenerative diseases
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The review on: “Creutzfeldt-Jakob disease”
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Gerstmann-Sträussler-Scheinker Disease: A Case Report
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From Seeds to Fibrils and Back: Fragmentation as an Overlooked Step in the Propagation of Prions and Prion-Like Proteins
inferredcites →https://doi.org/10.3390/biom10101362openalex-extracted
Clustering and Fibril Formation during GNNQQNY Aggregation: A Molecular Dynamics Study
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Advances in Molecular Dynamics Simulations and Enhanced Sampling Methods for the Study of Protein Systems
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Comprehensive Review on Alzheimer’s Disease: Causes and Treatment
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Kuru, the First Human Prion Disease
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