PMC:2626671 / 15058-15589 JSONTXT

Annnotations TAB JSON ListView MergeView

    bionlp-st-ge-2016-spacy-parsed

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role for Runx3 in effector CTL differentiation. (A) Western analysis of Runx3, Eomes, T-bet, and perforin expression in Runx3+/+ versus Runx3−/− CD8+ SP T cells differentiated for 6 d. β-Actin was used as a loading control. (B) Northern blot analysis of Prf1 mRNA expression in Runx3+/+ versus Runx3−/− CD8+ T cells differentiated for 6 d. β–Actin was used as a loading control. (C) Expression of granzyme B, IFN-γ, TNF, and IL-2 by resting or restimulated (6 h) Runx3+/+ versus Runx3−/− CD8+ SP T cells differentiated for 6 d."}

    GO-BP

    {"project":"GO-BP","denotations":[{"id":"T20181","span":{"begin":159,"end":179},"obj":"http://purl.obolibrary.org/obo/GO_0030154"},{"id":"T20182","span":{"begin":314,"end":334},"obj":"http://purl.obolibrary.org/obo/GO_0030154"},{"id":"T20183","span":{"begin":502,"end":522},"obj":"http://purl.obolibrary.org/obo/GO_0030154"}],"text":"Key role for Runx3 in effector CTL differentiation. (A) Western analysis of Runx3, Eomes, T-bet, and perforin expression in Runx3+/+ versus Runx3−/− CD8+ SP T cells differentiated for 6 d. β-Actin was used as a loading control. (B) Northern blot analysis of Prf1 mRNA expression in Runx3+/+ versus Runx3−/− CD8+ T cells differentiated for 6 d. β–Actin was used as a loading control. (C) Expression of granzyme B, IFN-γ, TNF, and IL-2 by resting or restimulated (6 h) Runx3+/+ versus Runx3−/− CD8+ SP T cells differentiated for 6 d."}

    GO-MF

    {"project":"GO-MF","denotations":[{"id":"T20465","span":{"begin":429,"end":433},"obj":"http://purl.obolibrary.org/obo/GO_0005134"}],"text":"Key role for Runx3 in effector CTL differentiation. (A) Western analysis of Runx3, Eomes, T-bet, and perforin expression in Runx3+/+ versus Runx3−/− CD8+ SP T cells differentiated for 6 d. β-Actin was used as a loading control. (B) Northern blot analysis of Prf1 mRNA expression in Runx3+/+ versus Runx3−/− CD8+ T cells differentiated for 6 d. β–Actin was used as a loading control. (C) Expression of granzyme B, IFN-γ, TNF, and IL-2 by resting or restimulated (6 h) Runx3+/+ versus Runx3−/− CD8+ SP T cells differentiated for 6 d."}

    GO-CC

    {"project":"GO-CC","denotations":[{"id":"T20467","span":{"begin":159,"end":164},"obj":"http://purl.obolibrary.org/obo/GO_0005623"},{"id":"T20468","span":{"begin":314,"end":319},"obj":"http://purl.obolibrary.org/obo/GO_0005623"},{"id":"T20469","span":{"begin":502,"end":507},"obj":"http://purl.obolibrary.org/obo/GO_0005623"}],"text":"Key role for Runx3 in effector CTL differentiation. (A) Western analysis of Runx3, Eomes, T-bet, and perforin expression in Runx3+/+ versus Runx3−/− CD8+ SP T cells differentiated for 6 d. β-Actin was used as a loading control. (B) Northern blot analysis of Prf1 mRNA expression in Runx3+/+ versus Runx3−/− CD8+ T cells differentiated for 6 d. β–Actin was used as a loading control. (C) Expression of granzyme B, IFN-γ, TNF, and IL-2 by resting or restimulated (6 h) Runx3+/+ versus Runx3−/− CD8+ SP T cells differentiated for 6 d."}

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    bionlp-st-ge-2016-reference

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