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[Here, we show that CXCR3(+) Treg are highly enriched in human ovarian carcinomas, particularly in solid tumor masses, where they represent the majority of Treg.Tumor-associated CXCR3(+.) Treg coexpress T-bet but do not secrete IFN-? ex vivo and suppress proliferation and IFN-? secretion of T effectors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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Gene-disease associations inferred from text-mining the literature.
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