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Seminars in Cell and Developmental Biology, ISSN 1084-9521, 2004, Volume 15, Issue 1, pp. 17 - 29
Human misfolding diseases result from the failure of proteins to reach their active state or from the accumulation of aberrantly folded proteins. The... 
Misfolding diseases | Amyloid | Polyglutamine diseases | Molecular chaperones | Ubiquitin–proteasome system | Ubiquitin-proteasome system | HEREDITARY SPASTIC PARAPLEGIA | misfolding diseases | HUMAN OBESITY SYNDROME | DEVELOPMENTAL BIOLOGY | ALPHA-SYNUCLEIN | CELL BIOLOGY | HEAT-SHOCK PROTEINS | ubiquitin-proteasome system | amyloid | AMYLOID-LIKE FIBRILS | IN-VIVO | BARDET-BIEDL-SYNDROME | MISSENSE MUTATION | molecular chaperones | polyglutamine diseases | HUNTINGTONS-DISEASE | PARKINSONS-DISEASE | Chaperonin 60 - physiology | HSP90 Heat-Shock Proteins - physiology | Humans | alpha-Crystallins - physiology | Amyloid - chemistry | Group II Chaperonins | Proteasome Endopeptidase Complex | alpha-Crystallins - genetics | Cysteine Endopeptidases - physiology | Disease - etiology | Heat-Shock Proteins - genetics | Eye Proteins - genetics | Proteins - physiology | Amyloid - physiology | Chaperonin 60 - genetics | Chaperonins - physiology | Endoplasmic Reticulum - physiology | Molecular Chaperones - genetics | Intracellular Signaling Peptides and Proteins | Ubiquitins - physiology | Molecular Chaperones - physiology | Protein Folding | Membrane Proteins | Models, Biological | Multienzyme Complexes - physiology | Cytosol - physiology | HSP70 Heat-Shock Proteins - physiology | Eye Proteins - physiology | Mutation | Proteins - chemistry | Heat-Shock Proteins - physiology
Journal Article
NeuroMolecular Medicine, ISSN 1535-1084, 3/2016, Volume 18, Issue 1, pp. 1 - 15
Journal Article
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
Journal Article