001     9742
005     20200402205832.0
024 7 _ |2 pmid
|a pmid:20017612
024 7 _ |2 DOI
|a 10.1089/rej.2009.0932
024 7 _ |2 WOS
|a WOS:000277602200020
037 _ _ |a PreJuSER-9742
041 _ _ |a eng
082 _ _ |a 610
084 _ _ |2 WoS
|a Geriatrics & Gerontology
100 1 _ |a Lüers, L.
|b 0
|u FZJ
|0 P:(DE-Juel1)VDB89563
245 _ _ |a Amyloid formation: Age-related mechanism in Creutzfeldt-Jakob disease?
260 _ _ |a Larchmont, NY
|b Liebert
|c 2010
300 _ _ |a
336 7 _ |a Journal Article
|0 PUB:(DE-HGF)16
|2 PUB:(DE-HGF)
336 7 _ |a Output Types/Journal article
|2 DataCite
336 7 _ |a Journal Article
|0 0
|2 EndNote
336 7 _ |a ARTICLE
|2 BibTeX
336 7 _ |a JOURNAL_ARTICLE
|2 ORCID
336 7 _ |a article
|2 DRIVER
440 _ 0 |a Rejuvenation Research
|x 1549-1684
|0 18202
|y 2
|v 13
500 _ _ |a Record converted from VDB: 12.11.2012
520 _ _ |a Protein aggregation occurs in many age-related neurodegenerative diseases, where it can lead to deposits of naturally occurring proteins in the brain. In case of Creutzfeldt-Jakob disease (CJD), these deposits consist of prion protein (PrP). CJD has three etiologies: spontaneous, genetic, or caused by infection. A polymorphism within the PrP gene is associated with susceptibility of infection. The main event in prion diseases is the conversion of PrP from its naturally occurring isoform to its disease-associated isoform. Here, we present the adaption of a previously reported in vitro conversion system based on hamster recombinant PrP to analyze amyloid fibril formation of human recombinant PrP. We further compare the aggregation characteristics of the human PrP according to the polymorphism variants M129 and V129.
536 _ _ |a Funktion und Dysfunktion des Nervensystems
|c P33
|2 G:(DE-HGF)
|0 G:(DE-Juel1)FUEK409
|x 0
536 _ _ |a BioSoft: Makromolekulare Systeme und biologische Informationsverarbeitung
|c P45
|0 G:(DE-Juel1)FUEK505
|x 1
588 _ _ |a Dataset connected to Web of Science, Pubmed
650 _ 2 |2 MeSH
|a Aging: metabolism
650 _ 2 |2 MeSH
|a Aging: physiology
650 _ 2 |2 MeSH
|a Amyloid: metabolism
650 _ 2 |2 MeSH
|a Circular Dichroism
650 _ 2 |2 MeSH
|a Congo Red: pharmacology
650 _ 2 |2 MeSH
|a Creutzfeldt-Jakob Syndrome: etiology
650 _ 2 |2 MeSH
|a Creutzfeldt-Jakob Syndrome: metabolism
650 _ 2 |2 MeSH
|a Creutzfeldt-Jakob Syndrome: pathology
650 _ 2 |2 MeSH
|a Humans
650 _ 2 |2 MeSH
|a Microscopy, Electron, Transmission
650 _ 2 |2 MeSH
|a Models, Biological
650 _ 2 |2 MeSH
|a PrPSc Proteins: chemistry
650 _ 2 |2 MeSH
|a PrPSc Proteins: metabolism
650 _ 2 |2 MeSH
|a Recombinant Proteins: analysis
650 _ 2 |2 MeSH
|a Recombinant Proteins: chemistry
650 _ 2 |2 MeSH
|a Recombinant Proteins: metabolism
650 _ 2 |2 MeSH
|a Staining and Labeling
650 _ 2 |2 MeSH
|a Thiazoles: pharmacology
650 _ 7 |0 0
|2 NLM Chemicals
|a Amyloid
650 _ 7 |0 0
|2 NLM Chemicals
|a PrPSc Proteins
650 _ 7 |0 0
|2 NLM Chemicals
|a Recombinant Proteins
650 _ 7 |0 0
|2 NLM Chemicals
|a Thiazoles
650 _ 7 |0 2390-54-7
|2 NLM Chemicals
|a thioflavin T
650 _ 7 |0 573-58-0
|2 NLM Chemicals
|a Congo Red
650 _ 7 |a J
|2 WoSType
700 1 _ |a Panza, G.
|b 1
|0 P:(DE-HGF)0
700 1 _ |a Henke, F.
|b 2
|u FZJ
|0 P:(DE-Juel1)VDB65871
700 1 _ |a Aygenim, T.
|b 3
|0 P:(DE-HGF)0
700 1 _ |a Weiß, J.
|b 4
|0 P:(DE-HGF)0
700 1 _ |a Willbold, D.
|b 5
|u FZJ
|0 P:(DE-Juel1)132029
700 1 _ |a Birkmann, E.
|b 6
|u FZJ
|0 P:(DE-Juel1)VDB65870
773 _ _ |a 10.1089/rej.2009.0932
|g Vol. 13
|q 13
|0 PERI:(DE-600)2155984-3
|t Rejuvenation research
|v 13
|y 2010
|x 1549-1684
856 7 _ |u http://dx.doi.org/10.1089/rej.2009.0932
909 C O |o oai:juser.fz-juelich.de:9742
|p VDB
913 1 _ |k P33
|v Funktion und Dysfunktion des Nervensystems
|l Funktion und Dysfunktion des Nervensystems
|b Gesundheit
|0 G:(DE-Juel1)FUEK409
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913 1 _ |k P45
|v BioSoft: Makromolekulare Systeme und biologische Informationsverarbeitung
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|b Schlüsseltechnologien
|0 G:(DE-Juel1)FUEK505
|x 1
913 2 _ |a DE-HGF
|b Key Technologies
|l BioSoft Fundamentals for future Technologies in the fields of Soft Matter and Life Sciences
|1 G:(DE-HGF)POF3-550
|0 G:(DE-HGF)POF3-553
|2 G:(DE-HGF)POF3-500
|v Physical Basis of Diseases
|x 0
914 1 _ |y 2010
915 _ _ |0 StatID:(DE-HGF)0010
|a JCR/ISI refereed
920 1 _ |d 31.12.2010
|g ISB
|k ISB-3
|l Strukturbiochemie
|0 I:(DE-Juel1)VDB942
|x 0
920 1 _ |0 I:(DE-82)080012_20140620
|k JARA-HPC
|l Jülich Aachen Research Alliance - High-Performance Computing
|g JARA
|x 1
970 _ _ |a VDB:(DE-Juel1)119732
980 _ _ |a VDB
980 _ _ |a ConvertedRecord
980 _ _ |a journal
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980 _ _ |a I:(DE-82)080012_20140620
980 _ _ |a UNRESTRICTED
981 _ _ |a I:(DE-Juel1)IBI-7-20200312
981 _ _ |a I:(DE-Juel1)ICS-6-20110106
981 _ _ |a I:(DE-Juel1)VDB1346


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