Demethylation analysis of the FOXP3 locus shows quantitative defects of regulatory T cells in IPEX-like syndrome-Reference-Cited by-同舟云学术

Demethylation analysis of the FOXP3 locus shows quantitative defects of regulatory T cells in IPEX-like syndrome

Published:2012-02 Issue:1 Volume:38 Page:49-58
ISSN:0896-8411
Container-title:Journal of Autoimmunity
language:en
Short-container-title:Journal of Autoimmunity

Author:

Barzaghi F.,Passerini L.,Gambineri E.,Ciullini Mannurita S.,Cornu T.,Kang E.S.,Choe Y.H.,Cancrini C.,Corrente S.,Ciccocioppo R.,Cecconi M.,Zuin G.,Discepolo V.,Sartirana C.,Schmidtko J.,Ikinciogullari A.,Ambrosi A.,Roncarolo M.G.,Olek S.,Bacchetta R.

Funder

Italian Telethon foundation

Seventh framework programme (FP7) of the European Community for research, technological development and demonstration activities

Italian Ministry of Health

Publisher

Elsevier BV

Subject

Immunology,Immunology and Allergy

Reference37 articles.

1. Breakdown of T cell tolerance and autoimmunity in primary immunodeficiency–lessons learned from monogenic disorders in mice and men;Westerberg;Curr Opin Immunol,2008

2. Regulatory T cell lineage specification by the forkhead transcription factor foxp3;Fontenot;Immunity,2005

3. Clinical and molecular features of the immunodysregulation, polyendocrinopathy, enteropathy, X linked (IPEX) syndrome;Wildin;J Med Genet,2002