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dc.contributor.authorWong, Madeline Y
dc.contributor.authorShoulders, Matthew D
dc.date.accessioned2021-09-20T18:21:18Z
dc.date.available2021-09-20T18:21:18Z
dc.identifier.urihttps://hdl.handle.net/1721.1/132196
dc.description.abstract© 2019 Elsevier Ltd The collagenopathies are a diverse group of diseases caused primarily by mutations in collagen genes. The resulting disruptions in collagen biogenesis can impair development, cause cellular dysfunction, and severely impact connective tissues. Most existing treatment options only address patient symptoms. Yet, while the disease-causing genes and proteins themselves are difficult to target, increasing evidence suggests that resculpting the intracellular proteostasis network, meaning the machineries responsible for producing and ensuring the integrity of collagen, could provide substantial benefit. We present a proteostasis-focused perspective on the collagenopathies, emphasizing progress toward understanding how mechanisms of collagen proteostasis are disrupted in disease. In parallel, we highlight recent advances in small molecule approaches to tune endoplasmic reticulum proteostasis that may prove useful in these disorders.en_US
dc.language.isoen
dc.publisherElsevier BVen_US
dc.relation.isversionof10.1016/J.CBPA.2019.02.021en_US
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivs Licenseen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/en_US
dc.sourcePMCen_US
dc.titleTargeting defective proteostasis in the collagenopathiesen_US
dc.typeArticleen_US
dc.relation.journalCurrent Opinion in Chemical Biologyen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2020-09-23T12:35:29Z
dspace.orderedauthorsWong, MY; Shoulders, MDen_US
dspace.date.submission2020-09-23T12:35:31Z
mit.journal.volume50en_US
mit.licensePUBLISHER_CC
mit.metadata.statusAuthority Work and Publication Information Needed


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