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dc.contributor.authorAndreadis, Athena
dc.date2022-08-11T08:07:57.000
dc.date.accessioned2022-08-23T15:37:17Z
dc.date.available2022-08-23T15:37:17Z
dc.date.issued2012-03-01
dc.date.submitted2012-03-28
dc.identifier.citationJ Cell Physiol. 2012 Mar;227(3):1220-5. doi: 10.1002/jcp.22842. <a href="http://dx.doi.org/10.1002/jcp.22842">Link to article on publisher's site</a>
dc.identifier.issn0021-9541 (Linking)
dc.identifier.doi10.1002/jcp.22842
dc.identifier.pmid21604267
dc.identifier.urihttp://hdl.handle.net/20.500.14038/25685
dc.description.abstractTau is a microtubule-associated protein that fulfills several functions critical for neuronal formation and health. Tau discharges its functions by producing multiple isoforms via regulated alternative splicing. These isoforms modulate tau function in normal brain by altering the domains of the protein, thereby influencing its localization, conformation, and post-translational modifications and hence its availability and affinity for microtubules and other ligands. Disturbances in tau expression result in disruption of the neuronal cytoskeleton and formation of tau structures (neurofibrillary tangles) found in brains of dementia sufferers. More specifically, aberrations in tau splicing regulation directly cause several neurodegenerative diseases, which lead to dementia. In this review, I present our cumulative knowledge of tau splicing regulation in connection with neurodegeneration and also briefly go over the still-extensive list of questions that are connected to tau (dys)function. J. Cell. Physiol. 227: 1220-1225, 2012. (c) 2011 Wiley Periodicals, Inc.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=21604267&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1002/jcp.22842
dc.subjectAlternative Splicing
dc.subjecttau Proteins
dc.subjectNeurodegenerative Diseases
dc.subjectCell Biology
dc.titleTau Splicing and the Intricacies of Dementia
dc.typeJournal Article
dc.source.journaltitleJournal of cellular physiology
dc.source.volume227
dc.source.issue3
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/andreadis/21
dc.identifier.contextkey2706198
html.description.abstract<p>Tau is a microtubule-associated protein that fulfills several functions critical for neuronal formation and health. Tau discharges its functions by producing multiple isoforms via regulated alternative splicing. These isoforms modulate tau function in normal brain by altering the domains of the protein, thereby influencing its localization, conformation, and post-translational modifications and hence its availability and affinity for microtubules and other ligands. Disturbances in tau expression result in disruption of the neuronal cytoskeleton and formation of tau structures (neurofibrillary tangles) found in brains of dementia sufferers. More specifically, aberrations in tau splicing regulation directly cause several neurodegenerative diseases, which lead to dementia. In this review, I present our cumulative knowledge of tau splicing regulation in connection with neurodegeneration and also briefly go over the still-extensive list of questions that are connected to tau (dys)function. J. Cell. Physiol. 227: 1220-1225, 2012. (c) 2011 Wiley Periodicals, Inc.</p>
dc.identifier.submissionpathandreadis/21
dc.contributor.departmentDepartment of Cell Biology
dc.source.pages1220-5


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