Publication
Building the right centriole for each cell type
dc.contributor.author | Loncarek, Jadranka | |
dc.contributor.author | Bettencourt-Dias, Mónica | |
dc.date.accessioned | 2018-02-07T11:55:42Z | |
dc.date.available | 2018-06-01T00:30:08Z | |
dc.date.issued | 2017-12-28 | |
dc.description | The 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.description | This deposit is composed by the main article, and it hasn't any supplementary materials associated. | pt_PT |
dc.description.abstract | The 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.sponsorship | Gulbenkian 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.version | info:eu-repo/semantics/publishedVersion | pt_PT |
dc.identifier.citation | Building the right centriole for each cell type Jadranka Loncarek, Mónica Bettencourt-Dias J Cell Biol Dec 2017, jcb.201704093; DOI: 10.1083/jcb.201704093 | pt_PT |
dc.identifier.doi | 10.1083/jcb.201704093 | pt_PT |
dc.identifier.uri | http://hdl.handle.net/10400.7/829 | |
dc.language.iso | eng | pt_PT |
dc.peerreviewed | yes | pt_PT |
dc.publisher | Rockefeller University Press | pt_PT |
dc.relation | CoG683528 | pt_PT |
dc.relation | "Length matters: Causes and consequences of centriole length deregulation in cancer" | |
dc.relation.publisherversion | http://jcb.rupress.org/content/early/2017/12/27/jcb.201704093 | pt_PT |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-sa/4.0/ | pt_PT |
dc.subject | Centrioles | pt_PT |
dc.subject | cell cycle | pt_PT |
dc.subject | Cilia | pt_PT |
dc.title | Building the right centriole for each cell type | pt_PT |
dc.type | review | |
dspace.entity.type | Publication | |
oaire.awardTitle | "Length matters: Causes and consequences of centriole length deregulation in cancer" | |
oaire.awardURI | info:eu-repo/grantAgreement/FCT/3599-PPCDT/PTDC%2FBIM-ONC%2F6858%2F2014/PT | |
oaire.citation.title | Journal of Cell Biology | pt_PT |
oaire.fundingStream | 3599-PPCDT | |
project.funder.identifier | http://doi.org/10.13039/501100001871 | |
project.funder.name | Fundação para a Ciência e a Tecnologia | |
rcaap.embargofct | The 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.rights | embargoedAccess | pt_PT |
rcaap.type | review | pt_PT |
relation.isProjectOfPublication | 8282ac35-73a1-4f8e-95da-dbed8651602e | |
relation.isProjectOfPublication.latestForDiscovery | 8282ac35-73a1-4f8e-95da-dbed8651602e |
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