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Mouse genomic screen reveals novel host regulator of metastasis.

Author(s): Celià-Terrassa, Toni; Kang, Yibin

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dc.contributor.authorCelià-Terrassa, Toni-
dc.contributor.authorKang, Yibin-
dc.date.accessioned2020-02-25T20:11:25Z-
dc.date.available2020-02-25T20:11:25Z-
dc.date.issued2017-02-16en_US
dc.identifier.citationCelià-Terrassa, Toni, Kang, Yibin. (2017). Mouse genomic screen reveals novel host regulator of metastasis.. Genome biology, 18 (1), 31 - ?. doi:10.1186/s13059-017-1170-xen_US
dc.identifier.issn1474-7596-
dc.identifier.urihttp://arks.princeton.edu/ark:/88435/pr10z0b-
dc.description.abstractTumor cells have to overcome challenges in the host tissue microenvironment to metastasize successfully to distant organs. In a recent Nature study, a genome-wide functional screen demonstrated that deficiency of the sphingosine-1-phoshate (S1P) transporter gene Spns2 in endothelium increased immune-mediated cell killing by T cells and natural killer (NK) cells, thereby suppressing metastatic colonization.en_US
dc.format.extent1 - 3en_US
dc.languageengen_US
dc.language.isoenen_US
dc.relation.ispartofGenome biologyen_US
dc.rightsFinal published version. Article is made available in OAR by the publisher's permission or policy.en_US
dc.titleMouse genomic screen reveals novel host regulator of metastasis.en_US
dc.typeJournal Articleen_US
dc.identifier.doidoi:10.1186/s13059-017-1170-x-
dc.identifier.eissn1474-760X-
pu.type.symplectichttp://www.symplectic.co.uk/publications/atom-terms/1.0/journal-articleen_US

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