المؤلفون: Lukic A; MRC Prion Unit and Department of Neurodegenerative Disease, UCL Institute of Neurology, London, UK., Uphill J; MRC Prion Unit and Department of Neurodegenerative Disease, UCL Institute of Neurology, London, UK., Brown CA; MRC Prion Unit and Department of Neurodegenerative Disease, UCL Institute of Neurology, London, UK., Beck J; MRC Prion Unit and Department of Neurodegenerative Disease, UCL Institute of Neurology, London, UK., Poulter M; MRC Prion Unit and Department of Neurodegenerative Disease, UCL Institute of Neurology, London, UK., Campbell T; MRC Prion Unit and Department of Neurodegenerative Disease, UCL Institute of Neurology, London, UK., Adamson G; MRC Prion Unit and Department of Neurodegenerative Disease, UCL Institute of Neurology, London, UK., Hummerich H; MRC Prion Unit and Department of Neurodegenerative Disease, UCL Institute of Neurology, London, UK., Whitfield J; MRC Prion Unit and Department of Neurodegenerative Disease, UCL Institute of Neurology, London, UK., Ponto C; Department of Neurology, Georg-August University Göttingen, Göttingen, Germany; German Center for Neurodegenrative Diseases (DZNE), Gottingen, Germany., Zerr I; Department of Neurology, Georg-August University Göttingen, Göttingen, Germany; German Center for Neurodegenrative Diseases (DZNE), Gottingen, Germany., Lloyd SE; MRC Prion Unit and Department of Neurodegenerative Disease, UCL Institute of Neurology, London, UK., Collinge J; MRC Prion Unit and Department of Neurodegenerative Disease, UCL Institute of Neurology, London, UK., Mead S; MRC Prion Unit and Department of Neurodegenerative Disease, UCL Institute of Neurology, London, UK. Electronic address: s.mead@prion.ucl.ac.uk.

المصدر: Neurobiology of aging [Neurobiol Aging] 2015 May; Vol. 36 (5), pp. 2004.e1-8. Date of Electronic Publication: 2015 Jan 22.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Elsevier Country of Publication: United States NLM ID: 8100437 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1558-1497 (Electronic) Linking ISSN: 01974580 NLM ISO Abbreviation: Neurobiol Aging Subsets: MEDLINE

مواضيع طبية MeSH: DNA Copy Number Variations/*genetics , Prion Diseases/*genetics , Prions/*genetics, 3' Untranslated Regions/genetics ; Aged ; Cells, Cultured ; Creutzfeldt-Jakob Syndrome/genetics ; Female ; Genetic Predisposition to Disease/genetics ; Genome-Wide Association Study ; Humans ; Kuru/genetics ; Loss of Heterozygosity/genetics ; Male ; Prion Proteins ; Risk ; Ubiquitin-Protein Ligases/genetics

المؤلفون: Mead S; MRC Prion Unit and Department of Neurodegenerative Disease, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK., Uphill J, Beck J, Poulter M, Campbell T, Lowe J, Adamson G, Hummerich H, Klopp N, Rückert IM, Wichmann HE, Azazi D, Plagnol V, Pako WH, Whitfield J, Alpers MP, Whittaker J, Balding DJ, Zerr I, Kretzschmar H, Collinge J

المصدر: Human molecular genetics [Hum Mol Genet] 2012 Apr 15; Vol. 21 (8), pp. 1897-906. Date of Electronic Publication: 2011 Dec 30.

نوع المنشور: Journal Article; Meta-Analysis; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1460-2083 (Electronic) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: MEDLINE

مواضيع طبية MeSH: Genetic Predisposition to Disease* , Genome-Wide Association Study* , Polymorphism, Single Nucleotide*, Prion Diseases/*genetics , Prions/*genetics, Case-Control Studies ; Creutzfeldt-Jakob Syndrome/genetics ; Disease Resistance ; Encephalopathy, Bovine Spongiform/genetics ; Female ; Humans ; Kuru/genetics ; Neoplasm Proteins/genetics ; Prion Proteins ; Risk Factors ; ras GTPase-Activating Proteins/genetics

SCR Disease Name: Acquired CJD

المؤلفون: Kaski DN; National Prion Clinic, National Hospital for Neurology and Neurosurgery, Queen Square, London, WC1N 3BG, UK., Pennington C, Beck J, Poulter M, Uphill J, Bishop MT, Linehan JM, O'Malley C, Wadsworth JD, Joiner S, Knight RS, Ironside JW, Brandner S, Collinge J, Mead S

المصدر: Brain : a journal of neurology [Brain] 2011 Jun; Vol. 134 (Pt 6), pp. 1829-38.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Oxford University Press Country of Publication: England NLM ID: 0372537 Publication Model: Print Cited Medium: Internet ISSN: 1460-2156 (Electronic) Linking ISSN: 00068950 NLM ISO Abbreviation: Brain Subsets: MEDLINE

مواضيع طبية MeSH: Family Health* , Genetic Predisposition to Disease* , Mutagenesis, Insertional*, Oligopeptides/*genetics , Prion Diseases/*genetics , Prions/*genetics, Aged ; Aged, 80 and over ; Cerebral Cortex/metabolism ; Cerebral Cortex/pathology ; Chi-Square Distribution ; Cognition Disorders/etiology ; Cognition Disorders/genetics ; Electroencephalography ; Female ; Genetic Testing ; Haplotypes ; Humans ; Male ; Middle Aged ; Prion Diseases/complications ; Prion Diseases/diagnostic imaging ; Prions/metabolism ; Tomography, X-Ray Computed/methods

المؤلفون: Mead S; Medical Research Council Prion Unit, Department of Neurodegenerative Disease, University College London Institute of Neurology, United Kingdom., Whitfield J, Poulter M, Shah P, Uphill J, Campbell T, Al-Dujaily H, Hummerich H, Beck J, Mein CA, Verzilli C, Whittaker J, Alpers MP, Collinge J

المصدر: The New England journal of medicine [N Engl J Med] 2009 Nov 19; Vol. 361 (21), pp. 2056-65.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Massachusetts Medical Society Country of Publication: United States NLM ID: 0255562 Publication Model: Print Cited Medium: Internet ISSN: 1533-4406 (Electronic) Linking ISSN: 00284793 NLM ISO Abbreviation: N Engl J Med Subsets: MEDLINE

مواضيع طبية MeSH: Genetic Predisposition to Disease* , Polymorphism, Genetic*, Kuru/*genetics , Prions/*genetics, Adolescent ; Adult ; Aged ; Cannibalism ; Disease Outbreaks ; Female ; Gene Frequency ; Genetic Fitness ; Genotype ; Haplotypes ; Humans ; Kuru/epidemiology ; Male ; Middle Aged ; Papua New Guinea/epidemiology ; Prion Proteins ; Young Adult

المؤلفون: Mead S; Department of Neurodegenerative Disease, MRC Prion Unit, UCL Institute of Neurology, National Hospital for Neurology and Neurosurgery, Queen Square, London, UK., Whitfield J, Poulter M, Shah P, Uphill J, Beck J, Campbell T, Al-Dujaily H, Hummerich H, Alpers MP, Collinge J

المصدر: Philosophical transactions of the Royal Society of London. Series B, Biological sciences [Philos Trans R Soc Lond B Biol Sci] 2008 Nov 27; Vol. 363 (1510), pp. 3741-6.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Royal Society Country of Publication: England NLM ID: 7503623 Publication Model: Print Cited Medium: Internet ISSN: 1471-2970 (Electronic) Linking ISSN: 09628436 NLM ISO Abbreviation: Philos Trans R Soc Lond B Biol Sci Subsets: MEDLINE

مواضيع طبية MeSH: Genetic Variation*, Ethnicity/*genetics , Genetic Predisposition to Disease/*genetics , Kuru/*epidemiology , Kuru/*genetics , Prions/*genetics, Female ; Gene Frequency ; Haplotypes/genetics ; Heterozygote ; Humans ; Male ; Papua New Guinea/epidemiology ; Prion Proteins ; Selection, Genetic

المؤلفون: Webb TE; Department of Neurodegenerative Disease and MRC Prion Unit, UCL Institute of Neurology, National Hospital for Neurology and Neurosurgery, Queen Square, London, UK., Poulter M, Beck J, Uphill J, Adamson G, Campbell T, Linehan J, Powell C, Brandner S, Pal S, Siddique D, Wadsworth JD, Joiner S, Alner K, Petersen C, Hampson S, Rhymes C, Treacy C, Storey E, Geschwind MD, Nemeth AH, Wroe S, Collinge J, Mead S

المصدر: Brain : a journal of neurology [Brain] 2008 Oct; Vol. 131 (Pt 10), pp. 2632-46. Date of Electronic Publication: 2008 Aug 30.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Oxford University Press Country of Publication: England NLM ID: 0372537 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1460-2156 (Electronic) Linking ISSN: 00068950 NLM ISO Abbreviation: Brain Subsets: MEDLINE

مواضيع طبية MeSH: Point Mutation*, Gerstmann-Straussler-Scheinker Disease/*genetics , Prions/*genetics, Adult ; Age of Onset ; Aged ; Brain/pathology ; Electrocardiography ; Electromyography ; England ; Europe ; Female ; Genealogy and Heraldry ; Genetic Testing ; Gerstmann-Straussler-Scheinker Disease/diagnosis ; Haplotypes ; Heterozygote ; Humans ; Magnetic Resonance Imaging ; Male ; Middle Aged ; Pedigree ; Phenotype ; Tomography, X-Ray Computed

المؤلفون: Thompson, A G B, Uphill, J, Lowe, J, Porter, M-C, Lukic, A, Carswell, C, Rudge, P, MacKay, A, Collinge, J, Mead, S

المصدر: Translational Psychiatry

مصطلحات موضوعية: Ankyrins, Bipolar Disorder, Hallucinations, Prions, Nerve Tissue Proteins, Polymorphism, Single Nucleotide, Creutzfeldt-Jakob Syndrome, Delusions, Prion Proteins, Prion Diseases, Cohort Studies, Humans, Depressive Disorder, Major, Depression, Mood Disorders, RNA-Binding Proteins, United Kingdom, Phosphotransferases (Alcohol Group Acceptor), Psychotic Disorders, Case-Control Studies, Argonaute Proteins, Schizophrenia, Original Article, Chromosomes, Human, Pair 6, Carrier Proteins, Genome-Wide Association Study

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::6dd0d378af97ff54a9712a8c7d420610
http://europepmc.org/articles/PMC4462605