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Downstream STING pathways IRF3 and NF-κB differentially regulate CCL22 in response to cytosolic dsDNA.

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Title: Downstream STING pathways IRF3 and NF-κB differentially regulate CCL22 in response to cytosolic dsDNA.
Authors: Kim J; Department of Biomedical Sciences, Mercer University School of Medicine, Macon, GA, USA., Pena JV; Department of Biomedical Sciences, Mercer University School of Medicine, Macon, GA, USA., McQueen HP; Department of Biomedical Sciences, Mercer University School of Medicine, Macon, GA, USA., Kong L; Department of Biomedical Sciences, Mercer University School of Medicine, Macon, GA, USA., Michael D; Department of Biomedical Sciences, Mercer University School of Medicine, Macon, GA, USA., Lomashvili EM; Department of Biomedical Sciences, Mercer University School of Medicine, Macon, GA, USA., Cook PR; Department of Biomedical Sciences, Mercer University School of Medicine, Macon, GA, USA. cook_p@mercer.edu.
Source: Cancer gene therapy [Cancer Gene Ther] 2024 Jan; Vol. 31 (1), pp. 28-42. Date of Electronic Publication: 2023 Nov 21.
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 9432230 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-5500 (Electronic) Linking ISSN: 09291903 NLM ISO Abbreviation: Cancer Gene Ther Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Downstream STING pathways IRF3 and NF-κB differentially regulate CCL22 in response to cytosolic dsDNA.
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  Data: <searchLink fieldCode="AU" term="%22Kim+J%22">Kim J</searchLink>; Department of Biomedical Sciences, Mercer University School of Medicine, Macon, GA, USA.<br /><searchLink fieldCode="AU" term="%22Pena+JV%22">Pena JV</searchLink>; Department of Biomedical Sciences, Mercer University School of Medicine, Macon, GA, USA.<br /><searchLink fieldCode="AU" term="%22McQueen+HP%22">McQueen HP</searchLink>; Department of Biomedical Sciences, Mercer University School of Medicine, Macon, GA, USA.<br /><searchLink fieldCode="AU" term="%22Kong+L%22">Kong L</searchLink>; Department of Biomedical Sciences, Mercer University School of Medicine, Macon, GA, USA.<br /><searchLink fieldCode="AU" term="%22Michael+D%22">Michael D</searchLink>; Department of Biomedical Sciences, Mercer University School of Medicine, Macon, GA, USA.<br /><searchLink fieldCode="AU" term="%22Lomashvili+EM%22">Lomashvili EM</searchLink>; Department of Biomedical Sciences, Mercer University School of Medicine, Macon, GA, USA.<br /><searchLink fieldCode="AU" term="%22Cook+PR%22">Cook PR</searchLink>; Department of Biomedical Sciences, Mercer University School of Medicine, Macon, GA, USA. cook_p@mercer.edu.
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  Data: <searchLink fieldCode="JN" term="%229432230%22">Cancer gene therapy</searchLink> [Cancer Gene Ther] 2024 Jan; Vol. 31 (1), pp. 28-42. <i>Date of Electronic Publication: </i>2023 Nov 21.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Nature+Publishing+Group%22">Nature Publishing Group </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>9432230 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1476-5500 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2209291903%22">09291903 </searchLink><i>NLM ISO Abbreviation: </i>Cancer Gene Ther <i>Subsets: </i>MEDLINE
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        Value: 10.1038/s41417-023-00678-z
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