Published in Biochim Biophys Acta on July 25, 2006
A systematic survey identifies prions and illuminates sequence features of prionogenic proteins. Cell (2009) 6.20
Recombinant prion protein induces a new transmissible prion disease in wild-type animals. Acta Neuropathol (2010) 3.19
The same primary structure of the prion protein yields two distinct self-propagating states. J Biol Chem (2008) 1.64
Conformational switching within individual amyloid fibrils. J Biol Chem (2009) 1.31
Conformational stability of PrP amyloid fibrils controls their smallest possible fragment size. J Mol Biol (2008) 1.27
A new mechanism for transmissible prion diseases. J Neurosci (2012) 1.25
Role of the highly conserved middle region of prion protein (PrP) in PrP-lipid interaction. Biochemistry (2010) 1.11
Design of anti- and pro-aggregation variants to assess the effects of methionine oxidation in human prion protein. Proc Natl Acad Sci U S A (2009) 1.10
Prion dynamics and the quest for the genetic determinant in protein-only inheritance. Curr Opin Microbiol (2009) 1.08
Switching in amyloid structure within individual fibrils: implication for strain adaptation, species barrier and strain classification. FEBS Lett (2009) 1.00
Distinct subregions of Swi1 manifest striking differences in prion transmission and SWI/SNF function. Mol Cell Biol (2010) 0.92
Can infections cause Alzheimer's disease? Epidemiol Rev (2013) 0.83
Sialylation Controls Prion Fate in Vivo. J Biol Chem (2016) 0.78
Limited understanding of the functional diversity of N-linked glycans as a major gap of prion biology. Prion (2017) 0.75
Fibril specific, conformation dependent antibodies recognize a generic epitope common to amyloid fibrils and fibrillar oligomers that is absent in prefibrillar oligomers. Mol Neurodegener (2007) 4.15
In vitro conversion of full-length mammalian prion protein produces amyloid form with physical properties of PrP(Sc). J Mol Biol (2004) 2.59
Antiparallel beta-sheet: a signature structure of the oligomeric amyloid beta-peptide. Biochem J (2009) 2.07
Synthetic prions generated in vitro are similar to a newly identified subpopulation of PrPSc from sporadic Creutzfeldt-Jakob Disease. Protein Sci (2005) 1.62
Fibrillar oligomers nucleate the oligomerization of monomeric amyloid beta but do not seed fibril formation. J Biol Chem (2009) 1.53
Methylene blue inhibits amyloid Abeta oligomerization by promoting fibrillization. Biochemistry (2007) 1.44
Polymorphism and ultrastructural organization of prion protein amyloid fibrils: an insight from high resolution atomic force microscopy. J Mol Biol (2006) 1.44
Annealing prion protein amyloid fibrils at high temperature results in extension of a proteinase K-resistant core. J Biol Chem (2005) 1.44
Conformation dependent monoclonal antibodies distinguish different replicating strains or conformers of prefibrillar Aβ oligomers. Mol Neurodegener (2010) 1.34
Copper(II) inhibits in vitro conversion of prion protein into amyloid fibrils. Biochemistry (2005) 1.28
Site-specific conformational studies of prion protein (PrP) amyloid fibrils revealed two cooperative folding domains within amyloid structure. J Biol Chem (2007) 1.14
Accelerated neurodegeneration through chaperone-mediated oligomerization of tau. J Clin Invest (2013) 1.12
Chemoenzymatic synthesis of HIV-1 V3 glycopeptides carrying two N-glycans and effects of glycosylation on the peptide domain. J Org Chem (2005) 1.06
Dichotomous versus palm-type mechanisms of lateral assembly of amyloid fibrils. Protein Sci (2006) 1.04
Noncovalent DNA binding drives DNA alkylation by leinamycin: evidence that the Z,E-5-(thiazol-4-yl)-penta-2,4-dienone moiety of the natural product serves as an atypical DNA intercalator. J Am Chem Soc (2011) 0.94
Vaccination with a non-human random sequence amyloid oligomer mimic results in improved cognitive function and reduced plaque deposition and micro hemorrhage in Tg2576 mice. Mol Neurodegener (2012) 0.92
The presence of valine at residue 129 in human prion protein accelerates amyloid formation. FEBS Lett (2005) 0.91
Hemicentin assembly in the extracellular matrix is mediated by distinct structural modules. J Biol Chem (2006) 0.88
Targeting the chameleon: a focused look at α-synuclein and its roles in neurodegeneration. Mol Neurobiol (2012) 0.81
Agrochemicals, α-synuclein, and Parkinson's disease. Mol Neurobiol (2012) 0.80
The macrocycle of leinamycin imparts hydrolytic stability to the thiol-sensing 1,2-dithiolan-3-one 1-oxide unit of the natural product. Bioorg Med Chem Lett (2012) 0.79
Mechanistic and structural analysis of Drosophila melanogaster arylalkylamine N-acetyltransferases. Biochemistry (2014) 0.78
Mechanistic and Structural Analysis of a Drosophila melanogaster Enzyme, Arylalkylamine N-Acetyltransferase Like 7, an Enzyme That Catalyzes the Formation of N-Acetylarylalkylamides and N-Acetylhistamine. Biochemistry (2015) 0.77
Effects of Polymer Hydrophobicity on Protein Structure and Aggregation Kinetics in Crowded Milieu. Biochemistry (2015) 0.75
Disorder in Milk Proteins: α -Lactalbumin. Part A. Structural Properties and Conformational Behavior. Curr Protein Pept Sci (2016) 0.75
A putative role of the Sup35p C-terminal domain in the cytoskeleton organization during yeast mitosis. Mol Biosyst (2014) 0.75
α-Lactalbumin: Of Camels and Cows. Protein Pept Lett (2016) 0.75
High throughput characterization of structural differences between closely related proteins in solution. Biochim Biophys Acta (2012) 0.75
Disorder in Milk Proteins: α-Lactalbumin. Part B. A Multifunctional Whey Protein Acting as an Oligomeric Molten Globular "Oil Container" in the Anti-Tumorigenic Drugs, Liprotides. Curr Protein Pept Sci (2016) 0.75
Disorder in Milk Proteins: α-Lactalbumin. Part C. Peculiarities of Metal Binding. Curr Protein Pept Sci (2016) 0.75