Amyloid: Toward terminology clarification Report from the Nomenclature Committee of the International Society of Amyloidosis
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Summary
The modern nomenclature of amyloidosis now includes 25 human and 8 animal fibril proteins, which have the characteristics ofAmyloid, including affinity for Congo red with resulting green birefringence.
- Type
- review
- Published
- 2005-03-01
- Cited by
- 347
- References
- 12
- OpenAlex
- https://openalex.org/W1969055742
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:12511613
Keywords
Amyloidosis, Amyloid (mycology), Nomenclature, Amyloid fibril, Terminology
References
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- Diseases of protein conformation: what do in vitro experiments tell us about in vivo diseases?
- Calcifying epithelial odontogenic (Pindborg) tumor-associated amyloid consists of a novel human protein.
- Ueber eine im Gehirn und Rückenmark des Menschen aufgefundene Substanz mit der chemischen Reaction der Cellulose
- Two different types of amyloid deposits—apolipoprotein A-IV and transthyretin—in a patient with systemic amyloidosis
- Classification of amyloid fibril proteins and their precursors: An ongoing discussion
- HIGH-RESOLUTION ELECTRON MICROSCOPIC ANALYSIS OF THE AMYLOID FIBRIL
- A Novel Localized Amyloidosis Associated with Lactoferrin in the Cornea
- General Introduction and a Brief History of Amyloidosis
- Amyloid Fibril Protein Nomenclature - 2002
- The 1990 Guidelines for Nomenclature and Classification of Amyloid and Amyloidosis
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- Cellular stress and protein misfolding during aging.
- Paired helical filaments contain small amounts of cholesterol, phosphatidylcholine and sphingolipids
- A primer of amyloid nomenclature
- Real-Time Monitoring of Apoptosis by Caspase-3-Like Protease Induced FRET Reduction Triggered by Amyloid Aggregation
- Short polyglutamine peptide forms a high-affinity binding site for thioflavin-T at the N-terminus.
- Amyloids here, amyloids there…What’s wrong with them?
- Methodological aspects and usefulness of Quantitative Sensory Testing in early small fiber polyneuropathy : a clinical study in Swedish hereditary transthyretin amyloidosis patients
- NMR studies on interactions between the amyloid β peptide and selected molecules
- Experimental inhibition of peptide fibrillogenesis by synthetic peptides, carbohydrates and drugs.
- Protein complexes : assembly, structure and function
- Protein Misfolding and Cellular Stress in Disease and Aging
- Protein Aggregation and Fibrillogenesis in Cerebral and Systemic Amyloid Disease
- Medin Amyloid in Human Arteries and its Association with Arterial Diseases
- The Alzheimer Aβ Peptide : Identification of Properties Distinctive for Toxic Prefibrillar Species
- Thermodynamic and structural analysis of protein aggregation and amyloid formation
- Evaluation of polyphenols as possible therapeutics for amyloidoses: Comparative analysis of Kaempferol and Catechin.
- Exceptional Cause of Massive Lymph Node Enlargement: Primary Localized Amyloidosis
- Structure, function, and amyloidogenesis of fungal prions: filament polymorphism and prion variants.
- Heparan sulfate proteoglycans in amyloidosis.
- Klinische Pathologie der renalen Amyloidosen
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