Pages that link to "Q33937323"
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The following pages link to Amyloid fibrils from muscle myoglobin (Q33937323):
Displaying 50 items.
- Deficiency of disulfide bonds facilitating fibrillogenesis of endostatin (Q24293595) (← links)
- The 8 and 5 kDa fragments of plasma gelsolin form amyloid fibrils by a nucleated polymerization mechanism, while the 68 kDa fragment is not amyloidogenic (Q24316253) (← links)
- The structural basis of protein folding and its links with human disease (Q24524125) (← links)
- The 3D profile method for identifying fibril-forming segments of proteins (Q24545011) (← links)
- Sequence determinants of protein aggregation: tools to increase protein solubility (Q24795353) (← links)
- Regulation of protein homeostasis in neurodegenerative diseases: the role of coding and non-coding genes (Q26799208) (← links)
- Misfolding and amyloid aggregation of apomyoglobin (Q26830356) (← links)
- Deciphering the structure, growth and assembly of amyloid-like fibrils using high-speed atomic force microscopy (Q27318382) (← links)
- High-resolution molecular structure of a peptide in an amyloid fibril determined by magic angle spinning NMR spectroscopy (Q27642920) (← links)
- An α Helix to β Barrel Domain Switch Transforms the Transcription Factor RfaH into a Translation Factor (Q27670840) (← links)
- Different 3D domain-swapped oligomeric cyanovirin-N structures suggest trapped folding intermediates (Q27677513) (← links)
- Structural and oxygen binding properties of dimeric horse myoglobin (Q27681956) (← links)
- Folding proteins in fatal ways (Q28235206) (← links)
- Neuroserpin binds Abeta and is a neuroprotective component of amyloid plaques in Alzheimer disease (Q28252760) (← links)
- Induction of AApoAII amyloidosis by various heterogeneous amyloid fibrils (Q28254598) (← links)
- Aggresome formation and neurodegenerative diseases: therapeutic implications (Q28265926) (← links)
- Ectoine and hydroxyectoine inhibit aggregation and neurotoxicity of Alzheimer's beta-amyloid (Q28267119) (← links)
- Low levels of asparagine deamidation can have a dramatic effect on aggregation of amyloidogenic peptides: implications for the study of amyloid formation (Q28345108) (← links)
- Structural properties of trimers and tetramers of ribonuclease A (Q28359786) (← links)
- Solution conditions can promote formation of either amyloid protofilaments or mature fibrils from the HypF N-terminal domain (Q28364514) (← links)
- Protein-nanoparticle interactions (Q28651998) (← links)
- Functional capabilities of the earliest peptides and the emergence of life (Q28658952) (← links)
- Inherent toxicity of aggregates implies a common mechanism for protein misfolding diseases (Q29616535) (← links)
- Aggregation properties of a short peptide that mediates amyloid fibril formation in model proteins unrelated to disease. (Q30010250) (← links)
- The structure of a folding intermediate provides insight into differences in immunoglobulin amyloidogenicity (Q30157531) (← links)
- Short amino acid stretches can mediate amyloid formation in globular proteins: the Src homology 3 (SH3) case (Q30164098) (← links)
- Amyloid-like fibril formation in an all beta-barrel protein. Partially structured intermediate state(s) is a precursor for fibril formation. (Q30164898) (← links)
- beta-Fibrillogenesis from Rigid-Rod beta-Barrels: Hierarchical Preorganization Beyond Microns We thank J. Buffle and J. Dubochet for their fruitful discussions and the Swiss NSF (21-57059.99 (S.M.), 2000-050629.97 (K.J.W.), and the National Research (Q30165128) (← links)
- Structural polymorphism of Alzheimer Abeta and other amyloid fibrils (Q30319061) (← links)
- Differential effects of glycation on protein aggregation and amyloid formation. (Q30374807) (← links)
- Pathogenic or not? And if so, then how? Studying the effects of missense mutations using bioinformatics methods. (Q30375382) (← links)
- Specific chaperones and regulatory domains in control of amyloid formation. (Q30378979) (← links)
- Dynamics-stability relationships in apo- and holomyoglobin: a combined neutron scattering and molecular dynamics simulations study (Q30413166) (← links)
- High-resolution optical tweezers for single-molecule manipulation (Q30449157) (← links)
- Molecular Level Insights into Thermally Induced α-Chymotrypsinogen A Amyloid Aggregation Mechanism and Semiflexible Protofibril Morphology (Q30452231) (← links)
- Hexafluoroisopropanol induces amyloid fibrils of islet amyloid polypeptide by enhancing both hydrophobic and electrostatic interactions (Q30502077) (← links)
- A kinetic study of beta-lactoglobulin amyloid fibril formation promoted by urea (Q30849505) (← links)
- Hydrogen/deuterium exchange and aggregation of a polyvaline and a polyleucine alpha-helix investigated by matrix-assisted laser desorption ionization mass spectrometry (Q30862528) (← links)
- Monitoring disappearance of monomers and generation of resistance to proteolysis during the formation of the activation domain of human procarboxypeptidase A2 (ADA2h) amyloid fibrils by matrix-assisted laser-desorption ionization-time-of-flight-MS. (Q30937046) (← links)
- Reversible aggregation plays a crucial role on the folding landscape of p53 core domain (Q30951237) (← links)
- The assembly of individual chaplin peptides from Streptomyces coelicolor into functional amyloid fibrils (Q31007737) (← links)
- Structural characterization of apomyoglobin self-associated species in aqueous buffer and urea solution (Q31010275) (← links)
- Fluorescence correlation spectroscopy shows that monomeric polyglutamine molecules form collapsed structures in aqueous solutions (Q31072074) (← links)
- Mutations that reduce aggregation of the Alzheimer's Abeta42 peptide: an unbiased search for the sequence determinants of Abeta amyloidogenesis (Q31085628) (← links)
- Amyloid protofilaments from the calcium-binding protein equine lysozyme: formation of ring and linear structures depends on pH and metal ion concentration (Q31148826) (← links)
- Intermediacy of poly(L-proline) II and beta-strand conformations in poly(L-lysine) beta-sheet formation probed by temperature-jump/UV resonance Raman spectroscopy (Q33230663) (← links)
- Prediction of amyloidogenic and disordered regions in protein chains (Q33267899) (← links)
- Systematic analysis of aggregates from 38 kinds of non disease-related proteins: identifying the intrinsic propensity of polypeptides to form amyloid fibrils (Q33283933) (← links)
- Directed selection of a conformational antibody domain that prevents mature amyloid fibril formation by stabilizing Abeta protofibrils (Q33307478) (← links)
- Structural elements regulating amyloidogenesis: a cholinesterase model system (Q33324410) (← links)