Foxp3 expression in human cancer cells.

The expression of the regulatory T cell-specific forkhead box transcription factor FoxP3 is associated with poor prognosis in ovarian cancer.

Comprehensive analysis of FOXP3 mRNA expression in leukemia and transformed cell lines.

TGF-beta1 modulates Foxp3 expression and regulatory activity in distinct CD4+ T cell subsets.

Imbalance in distribution of functional autologous regulatory T cells in rheumatoid arthritis.

Foxp3 expression in pancreatic carcinoma cells as a novel mechanism of immune evasion in cancer.

Use of FoxP3 expression to identify regulatory T cells in healthy dogs and dogs with cancer.

[Changes of regulatory T cell number in hepatocellular carcinoma-bearing mice and its relationship with tumor growth]

Analysis of regulatory T cell associated forkhead box P3 expression in the lungs of patients with sarcoidosis.

Expression of Foxp3 in non-small cell lung cancer patients is significantly higher in tumor tissues than in normal tissues, especially in tumors smaller than 30 mm.

The regulatory T cell-associated transcription factor FoxP3 is expressed by tumor cells.

Infiltration of forkhead box P3-expressing cells in small intestinal mucosa in coeliac disease but not in type 1 diabetes.

Indian hedgehog signaling pathway: expression and regulation in pancreatic cancer.

Extracorporeal photochemotherapy is accompanied by increasing levels of circulating CD4+CD25+GITR+Foxp3+CD62L+ functional regulatory T-cells in patients with graft-versus-host disease.

FOXP3 regulates TLR10 expression in human T regulatory cells.

FoxP3(+)CD4(+)CD25(+) T cells with regulatory properties can be cultured from colonic mucosa of patients with Crohn's disease.

Expression and functional characterization of FOXP3+ CD4+ regulatory T cells in ulcerative colitis.

[Difference between FOXP3 gene expressions in donor grafts with or without acute graft-versus-host disease]

High prevalence of Foxp3 and IL17 in MMR-proficient colorectal carcinomas.

Characterization of CD4+ FOXP3+ T-cell clones established from chronic inflammatory lesions.