Home > Publications Database > Propagation and spread of pathogenic protein assemblies in neurodegenerative diseases. > print

001     140231
005     20240321220753.0
024 7 _ |a 10.1038/s41593-018-0238-6
|2 doi
024 7 _ |a pmid:30258241
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024 7 _ |a pmc:PMC6375686
|2 pmc
024 7 _ |a 1097-6256
|2 ISSN
024 7 _ |a 1471-003X
|2 ISSN
024 7 _ |a 1471-0048
|2 ISSN
024 7 _ |a 1546-1726
|2 ISSN
024 7 _ |a altmetric:48915691
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037 _ _ |a DZNE-2020-06553
041 _ _ |a English
082 _ _ |a 570
100 1 _ |a Jucker, Mathias
|0 P:(DE-2719)2000010
|b 0
|e First author
245 _ _ |a Propagation and spread of pathogenic protein assemblies in neurodegenerative diseases.
260 _ _ |a London
|c 2018
|b Nature Publ. Group58142
264 _ 1 |3 online
|2 Crossref
|b Springer Science and Business Media LLC
|c 2018-09-26
264 _ 1 |3 print
|2 Crossref
|b Springer Science and Business Media LLC
|c 2018-10-01
336 7 _ |a article
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336 7 _ |a Output Types/Journal article
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336 7 _ |a Journal Article
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|s 1593424888_12124
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|x Review Article
336 7 _ |a ARTICLE
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336 7 _ |a JOURNAL_ARTICLE
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336 7 _ |a Journal Article
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520 _ _ |a Many neurodegenerative diseases, such as Alzheimer's disease, Parkinson's disease, and amyotrophic lateral sclerosis, are characterized by the progressive appearance of abnormal proteinaceous assemblies in the nervous system. Studies in experimental systems indicate that the assemblies originate from the prion-like seeded aggregation of specific misfolded proteins that proliferate and amass to form the intracellular and/or extracellular lesions typical of each disorder. The host in which the proteopathic seeds arise provides the biochemical and physiological environment that either supports or restricts their emergence, proliferation, self-assembly, and spread. Multiple mechanisms influence the spatiotemporal spread of seeds and the nature of the resulting lesions, one of which is the cellular uptake, release, and transport of seeds along neural pathways and networks. The characteristics of cells and regions in the affected network govern their vulnerability and thereby influence the neuropathological and clinical attributes of the disease. The propagation of pathogenic protein assemblies within the nervous system is thus determined by the interaction of the proteopathic agent and the host milieu.
536 _ _ |a 342 - Disease Mechanisms and Model Systems (POF3-342)
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542 _ _ |i 2018-09-26
|2 Crossref
|u http://www.springer.com/tdm
588 _ _ |a Dataset connected to CrossRef, PubMed,
650 _ 7 |a Prions
|2 NLM Chemicals
650 _ 2 |a Animals
|2 MeSH
650 _ 2 |a Cell Communication
|2 MeSH
650 _ 2 |a Humans
|2 MeSH
650 _ 2 |a Neurodegenerative Diseases: metabolism
|2 MeSH
650 _ 2 |a Neurodegenerative Diseases: pathology
|2 MeSH
650 _ 2 |a Prions: metabolism
|2 MeSH
650 _ 2 |a Prions: pathogenicity
|2 MeSH
700 1 _ |a Walker, Lary C
|0 P:(DE-2719)9000947
|b 1
|e Last author
773 1 8 |a 10.1038/s41593-018-0238-6
|b : Springer Science and Business Media LLC, 2018-09-26
|n 10
|p 1341-1349
|3 journal-article
|2 Crossref
|t Nature Neuroscience
|v 21
|y 2018
|x 1097-6256
773 _ _ |a 10.1038/s41593-018-0238-6
|g Vol. 21, no. 10, p. 1341 - 1349
|0 PERI:(DE-600)2028902-9
|n 10
|q 21:10<1341 - 1349
|p 1341-1349
|t Nature reviews / Neuroscience
|v 21
|y 2018
|x 1097-6256
856 7 _ |2 Pubmed Central
|u http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6375686
909 C O |p VDB
|o oai:pub.dzne.de:140231
910 1 _ |a Deutsches Zentrum für Neurodegenerative Erkrankungen
|0 I:(DE-588)1065079516
|k DZNE
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|6 P:(DE-2719)2000010
910 1 _ |a Deutsches Zentrum für Neurodegenerative Erkrankungen
|0 I:(DE-588)1065079516
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|6 P:(DE-2719)9000947
913 1 _ |a DE-HGF
|b Forschungsbereich Gesundheit
|l Erkrankungen des Nervensystems
|1 G:(DE-HGF)POF3-340
|0 G:(DE-HGF)POF3-342
|2 G:(DE-HGF)POF3-300
|v Disease Mechanisms and Model Systems
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914 1 _ |y 2018
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|2 Crossref
|o 10.1074/jbc.M115.652693
999 C 5 |a 10.1523/JNEUROSCI.3542-15.2016
|9 -- missing cx lookup --
|2 Crossref
|o 10.1523/JNEUROSCI.3542-15.2016
999 C 5 |a 10.1074/jbc.M114.589309
|9 -- missing cx lookup --
|2 Crossref
|o 10.1074/jbc.M114.589309
999 C 5 |a 10.1523/JNEUROSCI.2642-12.2013
|9 -- missing cx lookup --
|2 Crossref
|o 10.1523/JNEUROSCI.2642-12.2013
999 C 5 |a 10.1073/pnas.1206555109
|9 -- missing cx lookup --
|2 Crossref
|o 10.1073/pnas.1206555109
999 C 5 |a 10.1074/jbc.R113.511329
|9 -- missing cx lookup --
|2 Crossref
|o 10.1074/jbc.R113.511329
999 C 5 |a 10.1523/JNEUROSCI.0258-16.2016
|9 -- missing cx lookup --
|2 Crossref
|o 10.1523/JNEUROSCI.0258-16.2016
999 C 5 |a 10.1146/annurev-biochem-060614-033955
|9 -- missing cx lookup --
|2 Crossref
|o 10.1146/annurev-biochem-060614-033955
999 C 5 |a 10.1523/JNEUROSCI.1787-16.2017
|9 -- missing cx lookup --
|2 Crossref
|o 10.1523/JNEUROSCI.1787-16.2017
999 C 5 |a 10.1136/jnnp-2015-311321
|9 -- missing cx lookup --
|2 Crossref
|o 10.1136/jnnp-2015-311321
999 C 5 |a 10.1007/s00401-018-1829-8
|9 -- missing cx lookup --
|2 Crossref
|o 10.1007/s00401-018-1829-8
999 C 5 |a 10.3389/fneur.2017.00653
|9 -- missing cx lookup --
|2 Crossref
|o 10.3389/fneur.2017.00653
999 C 5 |a 10.1074/jbc.M115.681791
|9 -- missing cx lookup --
|2 Crossref
|o 10.1074/jbc.M115.681791
999 C 5 |a 10.1126/sciadv.1600947
|9 -- missing cx lookup --
|2 Crossref
|o 10.1126/sciadv.1600947
999 C 5 |a 10.1186/2051-5960-2-8
|9 -- missing cx lookup --
|2 Crossref
|o 10.1186/2051-5960-2-8
999 C 5 |a 10.1126/science.aah3374
|9 -- missing cx lookup --
|2 Crossref
|o 10.1126/science.aah3374
999 C 5 |a 10.1038/ncb3372
|9 -- missing cx lookup --
|2 Crossref
|o 10.1038/ncb3372
999 C 5 |a 10.1016/j.celrep.2018.04.056
|9 -- missing cx lookup --
|2 Crossref
|o 10.1016/j.celrep.2018.04.056
999 C 5 |a 10.15252/embr.201744067
|9 -- missing cx lookup --
|2 Crossref
|o 10.15252/embr.201744067
999 C 5 |a 10.1038/nn.2801
|9 -- missing cx lookup --
|2 Crossref
|o 10.1038/nn.2801
999 C 5 |a 10.1084/jem.20131685
|9 -- missing cx lookup --
|2 Crossref
|o 10.1084/jem.20131685
999 C 5 |a 10.1186/s13024-018-0241-0
|9 -- missing cx lookup --
|2 Crossref
|o 10.1186/s13024-018-0241-0
999 C 5 |a 10.1523/JNEUROSCI.19-19-08552.1999
|9 -- missing cx lookup --
|2 Crossref
|o 10.1523/JNEUROSCI.19-19-08552.1999
999 C 5 |a 10.1038/nn.4132
|9 -- missing cx lookup --
|2 Crossref
|o 10.1038/nn.4132
999 C 5 |a 10.1016/j.cell.2017.05.018
|9 -- missing cx lookup --
|2 Crossref
|o 10.1016/j.cell.2017.05.018
999 C 5 |a 10.1038/nature25158
|9 -- missing cx lookup --
|2 Crossref
|o 10.1038/nature25158
999 C 5 |a 10.3389/fnins.2018.00267
|9 -- missing cx lookup --
|2 Crossref
|o 10.3389/fnins.2018.00267
999 C 5 |a 10.1007/s00401-018-1855-6
|9 -- missing cx lookup --
|2 Crossref
|o 10.1007/s00401-018-1855-6
999 C 5 |a 10.1038/nature14377
|9 -- missing cx lookup --
|2 Crossref
|o 10.1038/nature14377
999 C 5 |a 10.1002/ana.24174
|9 -- missing cx lookup --
|2 Crossref
|o 10.1002/ana.24174
999 C 5 |a 10.1007/s00401-016-1582-9
|9 -- missing cx lookup --
|2 Crossref
|o 10.1007/s00401-016-1582-9

LibraryCollectionCLSMajorCLSMinorLanguageAuthor
Marc 21