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Amyloid, ISSN 1350-6129, 10/2016, Volume 23, Issue 4, pp. 209 - 213
The Nomenclature Committee of the International Society of Amyloidosis (ISA) met during the XVth Symposium of the Society, 3 July-7 July 2016, Uppsala, Sweden,... 
inclusion body | nomenclature | amyloidosis | Amyloid fibril | amyloid protein | MEDICINE, RESEARCH & EXPERIMENTAL | BIOCHEMISTRY & MOLECULAR BIOLOGY | TRANSTHYRETIN AMYLOIDOSIS | MEDICINE, GENERAL & INTERNAL | TRANSMISSION | SEMEN | DISEASE | SENILE SYSTEMIC AMYLOIDOSIS | Staining and Labeling - methods | Prealbumin - genetics | Guidelines as Topic | Apolipoprotein C-III - chemistry | Protein Precursors - chemistry | Humans | Apolipoprotein C-III - metabolism | tau Proteins - metabolism | Amyloidosis - diagnosis | Amyloidogenic Proteins - chemistry | Apolipoprotein C-III - genetics | Apolipoprotein C-II - genetics | tau Proteins - chemistry | Sequence Analysis, Protein | tau Proteins - genetics | Amyloidosis - genetics | Amyloidosis - classification | Prealbumin - chemistry | alpha-Synuclein - genetics | Apolipoprotein C-II - chemistry | Amyloidogenic Proteins - genetics | Biomarkers - metabolism | Gene Expression | Protein Precursors - genetics | Amyloidosis - pathology | Terminology as Topic | Protein Precursors - metabolism | alpha-Synuclein - chemistry | Amyloidogenic Proteins - metabolism | Prealbumin - metabolism | Apolipoprotein C-II - metabolism | Birefringence | Congo Red - chemistry | alpha-Synuclein - metabolism | Coloring Agents - chemistry | Index Medicus | Basic Medicine | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper | Cell and Molecular Biology | Cell- och molekylärbiologi
Journal Article
Annual Review of Genetics, ISSN 0066-4197, 11/2013, Volume 47, Issue 1, pp. 601 - 623
Prions are proteins that acquire alternative conformations that become self-propagating. Transformation of proteins into prions is generally accompanied by an... 
neurodegeneration | prion | Neurodegeneration | Prion | PROTEIN-TAU TAU | AMYOTROPHIC-LATERAL-SCLEROSIS | CHRONIC TRAUMATIC ENCEPHALOPATHY | CEREBRAL BETA-AMYLOIDOSIS | PATHOLOGICAL ALPHA-SYNUCLEIN | GENETICS & HEREDITY | FAMILIAL ALZHEIMERS-DISEASE | CREUTZFELDT-JAKOB-DISEASE | STRAUSSLER-SCHEINKER DISEASE | PARKINSONS-DISEASE | TRANSGENIC MICE | Fungal Proteins - chemistry | Synucleins - physiology | Amyloidogenic Proteins - classification | Prion Diseases - genetics | Prions - genetics | Transcription Factors - chemistry | Tauopathies - genetics | Neurodegenerative Diseases - etiology | Humans | Virulence | mRNA Cleavage and Polyadenylation Factors - chemistry | Amyloidogenic Proteins - physiology | Amyloidogenic Proteins - chemistry | Neurofibrillary Tangles | mRNA Cleavage and Polyadenylation Factors - classification | Tauopathies - etiology | Plaque, Amyloid | Inclusion Bodies | tau Proteins - genetics | tau Proteins - physiology | Saccharomyces cerevisiae Proteins - classification | Peptide Termination Factors - physiology | Models, Molecular | Neurodegenerative Diseases - genetics | Fungal Proteins - classification | Mammals | Transcription Factors - classification | Peptide Termination Factors - classification | Fungal Proteins - physiology | Animals | Prions - physiology | Prion Diseases - etiology | Age of Onset | Protein Conformation | Peptide Termination Factors - chemistry | Saccharomyces cerevisiae Proteins - physiology | Neurodegenerative Diseases - epidemiology | Saccharomyces cerevisiae Proteins - chemistry | Prions | Physiological aspects | Causes of | Nervous system | Degeneration | Genetic aspects | Health aspects | Proteins | Fungi | Pathogenesis | Neurological disorders | Index Medicus
Journal Article