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dc.contributor.authorAmon, Angelika B.
dc.contributor.authorUnal, Elcin
dc.contributor.authorMiller, Matthew P.
dc.date.accessioned2018-06-06T18:28:04Z
dc.date.available2018-06-06T18:28:04Z
dc.date.issued2013-08
dc.identifier.issn0955-0674
dc.identifier.urihttp://hdl.handle.net/1721.1/116151
dc.description.abstractThe ultimate success of cell division relies on the accurate partitioning of the genetic material. Errors in this process occur in nearly all tumors and are the leading cause of miscarriages and congenital birth defects in humans. Two cell divisions, mitosis and meiosis, use common as well as unique mechanisms to ensure faithful chromosome segregation. In mitosis, alternating rounds of DNA replication and chromosome segregation preserve the chromosome complement of the progenitor cell. In contrast, during meiosis two consecutive rounds of nuclear division, meiosis I and meiosis II, follow a single round of DNA replication to reduce the chromosome complement by half. Meiosis likely evolved through changes to the mitotic cell division program. This review will focus on the recent findings describing the modifications that transform mitosis into meiosis.en_US
dc.publisherElsevier BVen_US
dc.relation.isversionofhttp://dx.doi.org/10.1016/J.CEB.2013.07.009en_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.titleMeiosis I: when chromosomes undergo extreme makeoveren_US
dc.typeArticleen_US
dc.identifier.citationMiller, Matthew P et al. “Meiosis I: When Chromosomes Undergo Extreme Makeover.” Current Opinion in Cell Biology 25, 6 (December 2013): 687–696 © 2013 Elsevieren_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.contributor.departmentKoch Institute for Integrative Cancer Research at MITen_US
dc.contributor.mitauthorMiller, Matthew Paul
dc.contributor.mitauthorAmon, Angelika B.
dc.contributor.mitauthorUnal, Elcin
dc.relation.journalCurrent Opinion in Cell 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.updated2018-06-05T17:52:47Z
dspace.orderedauthorsMiller, Matthew P; Amon, Angelika; Ünal, Elçinen_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0003-2012-7546
mit.licensePUBLISHER_CCen_US


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