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2014, ISBN 9780300191141, xix, 320 pages
In 1997, Stanley B. Prusiner received a Nobel Prize, the world's most prestigious award for achievement in physiology or medicine. That he was the sole... 
History | Physicians | Prions | Biological Sciences | Autobiography | Prusiner, Stanley B., 1942 | History, 21st Century | History, 20th Century | history | Health Sciences | 1942 | Prusiner, Stanley | Biography
Book
2017, ISBN 1621820939, vii, 456 pages
"Prions are infectious proteins responsible for diseases such as Creutzfeldt-Jakob disease and "mad cow" disease. They are misfolded versions of normal... 
Life Sciences | Neuroscience | Biochimie | Prions (Virologie) | Prions | Prion diseases | Biochemistry | Maladies à prions
Book
2017, Cold Spring Harbor perspectives in medicine., ISBN 1621822834, ix, 676 pages
"Infectious proteins called prions are responsible for the devastating transmissible spongioform encephalopathy Creutzfeldt-Jakob disease. Prions are misfolded... 
Prion diseases | Neurosciences | Molecular biology | Prions
Book
2017, Cold Spring Harbor perspectives in biology, ISBN 9781621822844, vii, 456 pages
Book
1996, Current topics in microbiology and immunology, ISBN 9783540593430, Volume 207., 163
Book
2004, 2nd ed., Cold Spring Harbor monograph series, ISBN 9780879696931, xiii, 1050
Book
1999, Cold Spring Harbor monograph series, ISBN 0879695471, Volume monograph 38., xiii, 794
Book
1992, Ellis Horwood series in neuroscience, ISBN 9780137203277, xxvi, 583
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 | Pathogenic microorganisms | Cytology | Cell Biology | Life Sciences
Book
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
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 11/1998, Volume 95, Issue 23, pp. 13363 - 13383
Journal Article