<HashMap><database>biostudies-other</database><scores/><additional><omics_type>Unknown</omics_type><volume>3(1)</volume><submitter>Milev MP</submitter><journal>Molecular &amp; Cellular Oncology</journal><pagination>e1057314</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4845208</full_dataset_link><abstract>Mitosis is a highly orchestrated process with morphologically defined stages and is subject to checkpoints that ensure the proper distribution of chromosomes. Centromere-associated protein E (CENP-E), a protein expressed during mitosis, is a potential target of cancer therapeutics. Our laboratory has recently implicated a protein called TRAMM (trafficking of membranes and mitosis) in the recruitment of CENP-E to kinetochores.</abstract><repository>biostudies-other</repository><data_source>Europe PMC</data_source><pubmed_authors>Milev MP</pubmed_authors><pubmed_authors>Sacher M</pubmed_authors></additional><is_claimable>false</is_claimable><name>TRAMM, a new player in CENP-E biology.</name><description>Mitosis is a highly orchestrated process with morphologically defined stages and is subject to checkpoints that ensure the proper distribution of chromosomes. Centromere-associated protein E (CENP-E), a protein expressed during mitosis, is a potential target of cancer therapeutics. Our laboratory has recently implicated a protein called TRAMM (trafficking of membranes and mitosis) in the recruitment of CENP-E to kinetochores.</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Jan</publication><modification>2019-08-04T08:29:54Z</modification><creation>2019-08-04T08:29:54Z</creation></dates><accession>S-EPMC4845208</accession><cross_references><DOI>10.1080/23723556.2015.1057314 </DOI></cross_references></HashMap>