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dc.contributor.authorLu, Yubing
dc.contributor.authorAlmeida, Sandra
dc.contributor.authorGao, Fen-Biao
dc.date2022-08-11T08:10:01.000
dc.date.accessioned2022-08-23T16:52:16Z
dc.date.available2022-08-23T16:52:16Z
dc.date.issued2021-07-01
dc.date.submitted2022-01-02
dc.identifier.citation<p>Lu Y, Almeida S, Gao FB. TBK1 haploinsufficiency in ALS and FTD compromises membrane trafficking. Acta Neuropathol. 2021 Jul;142(1):217-221. doi: 10.1007/s00401-021-02331-1. Epub 2021 Jun 3. PMID: 34081168; PMCID: PMC8500533. <a href="https://doi.org/10.1007/s00401-021-02331-1">Link to article on publisher's site</a></p>
dc.identifier.issn0001-6322 (Linking)
dc.identifier.doi10.1007/s00401-021-02331-1
dc.identifier.pmid34081168
dc.identifier.urihttp://hdl.handle.net/20.500.14038/42018
dc.description.abstractTANK-binding kinase 1 (TBK1) haploinsufficiency causes both amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD). TBK1 is an IKK-related serine/threonine kinase and primarily known for its involvement in inflammation and autophagy. In particular, TBK1 phosphorylates several autophagy adaptor proteins, including SQSTM1/p62, optineurin, and NDP52. However, other phosphorylation substrates of TBK1 are largely unknown.
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=34081168&dopt=Abstract">Link to Article in PubMed</a></p>
dc.relation.urlhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8500533/
dc.subjectALS
dc.subjectFTD
dc.subjectMembrane trafficking
dc.subjectNeurons
dc.subjectTBK 1
dc.subjectiPSC
dc.subjectNeuroscience and Neurobiology
dc.titleTBK1 haploinsufficiency in ALS and FTD compromises membrane trafficking
dc.typeJournal Article
dc.source.journaltitleActa neuropathologica
dc.source.volume142
dc.source.issue1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/oapubs/4820
dc.identifier.contextkey27074131
html.description.abstract<p>TANK-binding kinase 1 (<em>TBK1</em>) haploinsufficiency causes both amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD). TBK1 is an IKK-related serine/threonine kinase and primarily known for its involvement in inflammation and autophagy. In particular, TBK1 phosphorylates several autophagy adaptor proteins, including SQSTM1/p62, optineurin, and NDP52. However, other phosphorylation substrates of TBK1 are largely unknown.</p>
dc.identifier.submissionpathoapubs/4820
dc.contributor.departmentDepartment of Neurology
dc.source.pages217-221


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