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2017, Cold Spring Harbor perspectives in medicine, ISBN 9781621820109, ix, 676 pages
"Infectious proteins called prions are responsible for the devastating transmissible spongioform encephalopathy Creutzfeldt-Jakob disease. Prions are misfolded... 
Prion diseases | Prions
Book
2005, Archives of Virology. Supplementum, ISBN 9781032112435, Volume 19., 213
Significant zoonotic diseases have appeared with increasing frequency in recent years. At a symposium held in Galveston, Texas, in March 2004,many outstanding... 
Pathogenesis | Viral infections | Emerging infectious diseases | Virus diseases | Interna medicine | Congresses | Biomedicine | Virology | Tropical Medicine | Viral diseases | Zoonoses
Book
2017, Neuromethods, ISBN 149397209X, Volume 129.
Web Resource
2017, Neuromethods, ISBN 149397209X, Volume 129.
Web Resource
2004, 5th ed., ISBN 6610275130, 914
The knowledge and practice of clinical virology continues to expand. This new fifth edition has thirty-six comprehensive chapters, each of which has been... 
Virus diseases | Medical virology
eBook
2005, ISBN 9780813535715, Volume 9780813537894, xii, 191
Book
1996, Methods in molecular medicine, ISBN 9780896033429, Volume 3, xv, 317
In Prion Diseases leading researchers and clinicians describe their state-of-the-art findings and hypotheses arising from a variety of different approaches to... 
Prion Diseases | Prion diseases | Pathogenic microorganisms | Cytology | Cell Biology | Life Sciences
Book
2012, Protein biochemistry, synthesis, structure and cellular functions., ISBN 9781621000273, ix, 200
Book
Science, ISSN 0036-8075, 6/2002, Volume 296, Issue 5575, pp. 1991 - 1995
A broad range of neurodegenerative disorders is characterized by neuronal damage that may be caused by toxic, aggregation-prone proteins. As genes are... 
Nervous system diseases | Reviews | Neurodegenerative diseases | Disease models | Huntington disease | Parkinson disease | Prion diseases | Amyotrophic lateral sclerosis | Nervous system heredodegenerative disorders | Alzheimers disease | Genetic mutation | Parkinson Disease - therapy | Neurons - pathology | Prion Diseases - genetics | Humans | Peptides - genetics | Tauopathies - pathology | Alzheimer Disease - pathology | Peptides - metabolism | Tauopathies - therapy | Neurons - metabolism | Parkinson Disease - metabolism | Inclusion Bodies - metabolism | Prion Diseases - therapy | Parkinson Disease - pathology | Neurodegenerative Diseases - pathology | Amyotrophic Lateral Sclerosis - therapy | Amyotrophic Lateral Sclerosis - genetics | Alzheimer Disease - therapy | Neurodegenerative Diseases - genetics | Neurodegenerative Diseases - therapy | Prion Diseases - pathology | Neurodegenerative Diseases - metabolism | Parkinson Disease - genetics | Protein Folding | Trinucleotide Repeat Expansion | Proteins - genetics | Amyotrophic Lateral Sclerosis - pathology | Tauopathies - metabolism | Animals | Proteins - metabolism | Alzheimer Disease - metabolism | Amyotrophic Lateral Sclerosis - metabolism | Mutation | Proteins - chemistry | Alzheimer Disease - genetics | Prion Diseases - metabolism | Parkinson's disease | Nervous system | Degeneration | Research | Alzheimer's disease | Proteins | Neurological disorders
Journal Article
1997, ISBN 9780198547891, 205 p., [2] p. of plates
Book
2001, Methods in molecular medicine, ISBN 0896039242, Volume 59, 279
It is now widely agreed that the prion protein plays a key role in the molecular pathogenesis of prion diseases-diseases that involve the misfolding of... 
Prion diseases | physiopathology | Research | Methodology | Prions | etiology | Communicable diseases | Pathology | Medicine & Public Health
Book
2005, ISBN 4431255397, 271
Prion diseases recently have attracted interest not only scientifically but also socially because of the bovine spongiform encephalopathy (BSE) epidemic and... 
Drugs | Food safety | Prions | Safety measures | Prion diseases | Congresses | Neurology | Infectious Diseases | Medicine & Public Health | Neuroradiology
Book
2003, Clinics in laboratory medicine, Volume 23, no. 1., xvi, [1]-255 p., [29] p. of plates
Book
1993, British medical bulletin, ISBN 9780443049286, Volume 49, no. 4., ii, p. [725]-1015.
Book
2012, 1st ed., ISBN 0124158951, xvii, 355
In the past few decades, there have been great advances in the phylogenetic classification of infectious diseases of man. Taxonomic Guide to Infectious... 
Communicable diseases | Classification | Other branches of medicine | Eukaryota - classification
Book
Nature Cell Biology, ISSN 1465-7392, 2009, Volume 11, Issue 2, pp. 219 - 225
Sequence-specific nucleated protein aggregation is closely linked to the pathogenesis of most neurodegenerative diseases and constitutes the molecular basis of... 
IN-VITRO | PROTEIN MISFOLDING DISEASES | PEPTIDES | FIBRILS | MECHANISM | TOXICITY | HUNTINGTIN | PROPAGATION | YEAST PRION | CELL BIOLOGY | Prion Diseases - physiopathology | Humans | Cell Communication - physiology | Cytoplasm - metabolism | Cytoplasm - pathology | Peptides - metabolism | Peptides - toxicity | Amyloid - biosynthesis | Disease Transmission, Infectious | Inclusion Bodies - metabolism | Huntington Disease - physiopathology | Cell Line | Neurodegenerative Diseases - pathology | Amyloidosis - pathology | Amyloidosis - physiopathology | Neurodegenerative Diseases - metabolism | Neurofibrils - pathology | Huntington Disease - metabolism | Endocytosis - physiology | Neurodegenerative Diseases - physiopathology | Proteasome Endopeptidase Complex - ultrastructure | Trinucleotide Repeat Expansion - genetics | Proteasome Endopeptidase Complex - metabolism | Amyloidosis - metabolism | Prion Diseases - metabolism | Neurofibrils - metabolism | Amyloid beta-protein | Physiological aspects | Nervous system | Genetic aspects | Degeneration | Research | Glutamine | Index Medicus | Huntington Disease | Neurodegenerative Diseases | Peptides | Neurofibrils | Cell Communication | Proteasome Endopeptidase Complex | Trinucleotide Repeat Expansion | Life Sciences | Prion Diseases | Endocytosis | Inclusion Bodies | Amyloid | Amyloidosis | Cytoplasm
Journal Article
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