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Building the right centriole for each cell type

dc.contributor.authorLoncarek, Jadranka
dc.contributor.authorBettencourt-Dias, Mónica
dc.date.accessioned2018-02-07T11:55:42Z
dc.date.available2018-06-01T00:30:08Z
dc.date.issued2017-12-28
dc.descriptionThe deposited article version is the publisher version, which is in a "Epub Ahead of Print” state at the moment of the deposit.pt_PT
dc.descriptionThis deposit is composed by the main article, and it hasn't any supplementary materials associated.pt_PT
dc.description.abstractThe centriole is a multifunctional structure that organizes centrosomes and cilia and is important for cell signaling, cell cycle progression, polarity, and motility. Defects in centriole number and structure are associated with human diseases including cancer and ciliopathies. Discovery of the centriole dates back to the 19th century. However, recent advances in genetic and biochemical tools, development of high-resolution microscopy, and identification of centriole components have accelerated our understanding of its assembly, function, evolution, and its role in human disease. The centriole is an evolutionarily conserved structure built from highly conserved proteins and is present in all branches of the eukaryotic tree of life. However, centriole number, size, and organization varies among different organisms and even cell types within a single organism, reflecting its cell type-specialized functions. In this review, we provide an overview of our current understanding of centriole biogenesis and how variations around the same theme generate alternatives for centriole formation and function.pt_PT
dc.description.sponsorshipGulbenkian Foundation; European Research Council Consolidator Grant: (CoG683528); Fundaçao para a Ciencia e Tecnologia grant: (PTDC/BIM-ONC/6858/2014); National Institutes of Health; National Cancer Institute; Center for Cancer Research.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationBuilding the right centriole for each cell type Jadranka Loncarek, Mónica Bettencourt-Dias J Cell Biol Dec 2017, jcb.201704093; DOI: 10.1083/jcb.201704093pt_PT
dc.identifier.doi10.1083/jcb.201704093pt_PT
dc.identifier.urihttp://hdl.handle.net/10400.7/829
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherRockefeller University Presspt_PT
dc.relationCoG683528pt_PT
dc.relation"Length matters: Causes and consequences of centriole length deregulation in cancer"
dc.relation.publisherversionhttp://jcb.rupress.org/content/early/2017/12/27/jcb.201704093pt_PT
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/pt_PT
dc.subjectCentriolespt_PT
dc.subjectcell cyclept_PT
dc.subjectCiliapt_PT
dc.titleBuilding the right centriole for each cell typept_PT
dc.typereview
dspace.entity.typePublication
oaire.awardTitle"Length matters: Causes and consequences of centriole length deregulation in cancer"
oaire.awardURIinfo:eu-repo/grantAgreement/FCT/3599-PPCDT/PTDC%2FBIM-ONC%2F6858%2F2014/PT
oaire.citation.titleJournal of Cell Biologypt_PT
oaire.fundingStream3599-PPCDT
project.funder.identifierhttp://doi.org/10.13039/501100001871
project.funder.nameFundação para a Ciência e a Tecnologia
rcaap.embargofctThe deposited article has 6 months of embargo period in terms of access, because of the journal's policies and the publisher's copyright policy, which require a period of embargo between 6 months after the date of the publication, and since the article is in "Epub Ahead of Print" it has a extended date of embargo, as a preventive measure.pt_PT
rcaap.rightsembargoedAccesspt_PT
rcaap.typereviewpt_PT
relation.isProjectOfPublication8282ac35-73a1-4f8e-95da-dbed8651602e
relation.isProjectOfPublication.latestForDiscovery8282ac35-73a1-4f8e-95da-dbed8651602e

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