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Immunomodulatory effects of deacetylase inhibitors: therapeutic targeting of FOXP3(+) regulatory T cells

Classical zinc-dependent histone deacetylases (HDACs) catalyse the removal of acetyl groups from histone tails and also from many non-histone proteins, including the transcription factor FOXP3, a key regulator of the development and function of regulatory T cells. Many HDAC inhibitors are in cancer...

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Détails bibliographiques
Auteurs principaux: Wang, Liqing, de Zoeten, Edwin F., Greene, Mark I., Hancock, Wayne W.
Format: Artigo
Langue:Inglês
Publié: 2009
Sujets:
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC2884987/
https://ncbi.nlm.nih.gov/pubmed/19855427
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/nrd3031
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