Genetic Models Reveal cis and trans Immune-Regulatory Activities for lincRNA-Cox2.

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Title: Genetic Models Reveal cis and trans Immune-Regulatory Activities for lincRNA-Cox2.
Authors: Elling R; Program in Innate Immunity, Department of Medicine, University of Massachusetts Medical School, Worcester, MA, USA; Center for Pediatrics, Department of General Pediatrics, University of Freiburg, Freiburg, Germany., Robinson EK; Department of Molecular, Cell and Developmental Biology, University of California, Santa Cruz, Santa Cruz, CA, USA., Shapleigh B; Department of Molecular, Cell and Developmental Biology, University of California, Santa Cruz, Santa Cruz, CA, USA., Liapis SC; Harvard Stem Cell and Regenerative Biology Department, Harvard University, Cambridge, MA 02138, USA., Covarrubias S; Department of Molecular, Cell and Developmental Biology, University of California, Santa Cruz, Santa Cruz, CA, USA., Katzman S; Center for Biomolecular Science and Engineering, University of California, Santa Cruz, Santa Cruz, CA, USA., Groff AF; Harvard Stem Cell and Regenerative Biology Department, Harvard University, Cambridge, MA 02138, USA., Jiang Z; Program in Innate Immunity, Department of Medicine, University of Massachusetts Medical School, Worcester, MA, USA., Agarwal S; Program in Innate Immunity, Department of Medicine, University of Massachusetts Medical School, Worcester, MA, USA., Motwani M; Program in Innate Immunity, Department of Medicine, University of Massachusetts Medical School, Worcester, MA, USA., Chan J; Program in Innate Immunity, Department of Medicine, University of Massachusetts Medical School, Worcester, MA, USA., Sharma S; Program in Innate Immunity, Department of Medicine, University of Massachusetts Medical School, Worcester, MA, USA., Hennessy EJ; Department of Systems Pharmacology and Translational Therapeutics, Perelman School of Medicine, University of Pennsylvania, 3400 Civic Center Boulevard, Smilow, Philadelphia, PA 19104, USA., FitzGerald GA; Department of Systems Pharmacology and Translational Therapeutics, Perelman School of Medicine, University of Pennsylvania, 3400 Civic Center Boulevard, Smilow, Philadelphia, PA 19104, USA., McManus MT; Department of Microbiology and Immunology, University of California, San Francisco, San Francisco, CA, USA; UCSF Diabetes Center, University of California, San Francisco, San Francisco, CA, USA., Rinn JL; Harvard Stem Cell and Regenerative Biology Department, Harvard University, Cambridge, MA 02138, USA; Department of Biochemistry, BioFrontiers, University of Colorado Boulder, Boulder, CO 80301, USA., Fitzgerald KA; Program in Innate Immunity, Department of Medicine, University of Massachusetts Medical School, Worcester, MA, USA., Carpenter S; Department of Molecular, Cell and Developmental Biology, University of California, Santa Cruz, Santa Cruz, CA, USA. Electronic address: sucarpen@ucsc.edu.
Source: Cell reports [Cell Rep] 2018 Nov 06; Vol. 25 (6), pp. 1511-1524.e6.
Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Cell Press Country of Publication: United States NLM ID: 101573691 Publication Model: Print Cited Medium: Internet ISSN: 2211-1247 (Electronic) NLM ISO Abbreviation: Cell Rep Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:2211-1247
DOI:10.1016/j.celrep.2018.10.027