Related references
Note: Only part of the references are listed.Requirements for Mutant and Wild-Type Prion Protein Misfolding In Vitro
Geoffrey P. Noble et al.
BIOCHEMISTRY (2015)
Structural Studies of Truncated Forms of the Prion Protein PrP
William Wan et al.
BIOPHYSICAL JOURNAL (2015)
Charge Neutralization of the Central Lysine Cluster in Prion Protein (PrP) Promotes PrPSc-like Folding of Recombinant PrP Amyloids
Bradley R. Groveman et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2015)
Parallel In-register Intermolecular β-Sheet Architectures for Prion-seeded Prion Protein (PrP) Amyloids
Bradley R. Groveman et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2014)
Polyproline-II Helix in Proteins: Structure and Function
Alexei A. Adzhubei et al.
JOURNAL OF MOLECULAR BIOLOGY (2013)
Cofactor Molecules Induce Structural Transformation during Infectious Prion Formation
Michael B. Miller et al.
STRUCTURE (2013)
Proline Isomer-Specific Antibodies Reveal the Early Pathogenic Tau Conformation in Alzheimer's Disease
Kazuhiro Nakamura et al.
CELL (2012)
Isolation of phosphatidylethanolamine as a solitary cofactor for prion formation in the absence of nucleic acids
Nathan R. Deleault et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2012)
Toward the Molecular Basis of Inherited Prion Diseases: NMR Structure of the Human Prion Protein with V210I Mutation
Ivana Biljan et al.
JOURNAL OF MOLECULAR BIOLOGY (2011)
Conformational Conversion during Amyloid Formation at Atomic Resolution
Timo Eichner et al.
MOLECULAR CELL (2011)
Structural organization of brain-derived mammalian prions examined by hydrogen-deuterium exchange
Vytautas Smirnovas et al.
NATURE STRUCTURAL & MOLECULAR BIOLOGY (2011)
Role of the Highly Conserved Middle Region of Prion Protein (PrP) in PrP-Lipid Interaction
Fei Wang et al.
BIOCHEMISTRY (2010)
Prediction of Xaa-Pro peptide bond conformation from sequence and chemical shifts
Yang Shen et al.
JOURNAL OF BIOMOLECULAR NMR (2010)
NMR Structure of the Human Prion Protein with the Pathological Q212P Mutation Reveals Unique Structural Features
Gregor Ilc et al.
PLOS ONE (2010)
Generating a Prion with Bacterially Expressed Recombinant Prion Protein
Fei Wang et al.
SCIENCE (2010)
Rapid End-Point Quantitation of Prion Seeding Activity with Sensitivity Comparable to Bioassays
Jason M. Wilham et al.
PLOS PATHOGENS (2010)
Distinct Structures of Scrapie Prion Protein (PrPSc)-seeded Versus Spontaneous Recombinant Prion Protein Fibrils Revealed by Hydrogen/Deuterium Exchange
Vytautas Smirnovas et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2009)
A Generic Mechanism of β2-Microglobulin Amyloid Assembly at Neutral pH Involving a Specific Proline Switch
Timo Eichner et al.
JOURNAL OF MOLECULAR BIOLOGY (2009)
Identifying Key Components of the PrPC-PrPSc Replicative Interface
Gil C. Abalos et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2008)
A novel PRNP-P105S mutation associated with atypical prion disease and a rare PrPSc conformation
E. Tunnell et al.
NEUROLOGY (2008)
Molecular architecture of human prion protein amyloid:: A parallel, in-register β-structure
Nathan J. Cobb et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2007)
Formation of native prions from minimal components in vitro
Nathan R. Deleault et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2007)
β-Sheet core of human prion protein amyloid fibrils as determined by hydrogen/deuterium exchange
Xiaojun Lu et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2007)
Proline and glycine control protein self-organization into elastomeric or amyloid fibrils
Sarah Rauscher et al.
STRUCTURE (2006)
Childhood onset in familial prion disease with a novel mutation in the PRNP gene
Ekaterina Rogaeva et al.
ARCHIVES OF NEUROLOGY (2006)
Role of N-terminal familial mutations in prion protein fibrillization and prion amyloid propagation in vitro
EM Jones et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2006)
The prolyl isomerase Pin1 regulates amyloid precursor protein processing and amyloid-β production
L Pastorino et al.
NATURE (2006)
Protein production by auto-induction in high-density shaking cultures
FW Studier
PROTEIN EXPRESSION AND PURIFICATION (2005)
MUSCLE: multiple sequence alignment with high accuracy and high throughput
RC Edgar
NUCLEIC ACIDS RESEARCH (2004)
A simple, fast, and accurate algorithm to estimate large phylogenies by maximum likelihood
S Guindon et al.
SYSTEMATIC BIOLOGY (2003)
Structural changes in a hydrophobic domain of the prion protein induced by hydration and by Ala → Val and Pro → Leu substitutions
H Inouye et al.
JOURNAL OF MOLECULAR BIOLOGY (2000)
A synthetic peptide initiates Gerstmann-Straussler-Scheinker (GSS) disease in transgenic mice
K Kaneko et al.
JOURNAL OF MOLECULAR BIOLOGY (2000)
NMR solution structure of the human prion protein
R Zahn et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2000)
Share Paper
