Ex vivo-expanded but not in vitro-induced human regulatory T cells are candidates for cell therapy in autoimmune diseases thanks to stable demethylation of the FOXP3 regulatory T cell-specific demethylated region

10.4049/jimmunol.1401145

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Main Authors:	Rossetti M., Spreafico R., Saidin S., Chua C., Moshref M., Leong J.Y., Tan York Kiat, Albani Salvatore
Other Authors:	DUKE-NUS GRADUATE MEDICAL SCHOOL S'PORE
Format:	Article
Published:	American Association of Immunologists 2016
Online Access:	http://scholarbank.nus.edu.sg/handle/10635/127464
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Institution:	National University of Singapore

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spelling	sg-nus-scholar.10635-1274642023-10-30T07:44:09Z Ex vivo-expanded but not in vitro-induced human regulatory T cells are candidates for cell therapy in autoimmune diseases thanks to stable demethylation of the FOXP3 regulatory T cell-specific demethylated region Rossetti M. Spreafico R. Saidin S. Chua C. Moshref M. Leong J.Y. Tan York Kiat Albani Salvatore DUKE-NUS GRADUATE MEDICAL SCHOOL S'PORE 10.4049/jimmunol.1401145 Journal of Immunology 194 1 113-124 2016-09-09T00:55:11Z 2016-09-09T00:55:11Z 2015 Article Rossetti M., Spreafico R., Saidin S., Chua C., Moshref M., Leong J.Y., Tan York Kiat, Albani Salvatore (2015). Ex vivo-expanded but not in vitro-induced human regulatory T cells are candidates for cell therapy in autoimmune diseases thanks to stable demethylation of the FOXP3 regulatory T cell-specific demethylated region. Journal of Immunology 194 (1) : 113-124. ScholarBank@NUS Repository. https://doi.org/10.4049/jimmunol.1401145 221767 http://scholarbank.nus.edu.sg/handle/10635/127464 000346700500014 American Association of Immunologists
institution	National University of Singapore
building	NUS Library
continent	Asia
country	Singapore Singapore
content_provider	NUS Library
collection	ScholarBank@NUS
description	10.4049/jimmunol.1401145
author2	DUKE-NUS GRADUATE MEDICAL SCHOOL S'PORE
author_facet	DUKE-NUS GRADUATE MEDICAL SCHOOL S'PORE Rossetti M. Spreafico R. Saidin S. Chua C. Moshref M. Leong J.Y. Tan York Kiat Albani Salvatore
format	Article
author	Rossetti M. Spreafico R. Saidin S. Chua C. Moshref M. Leong J.Y. Tan York Kiat Albani Salvatore
spellingShingle	Rossetti M. Spreafico R. Saidin S. Chua C. Moshref M. Leong J.Y. Tan York Kiat Albani Salvatore Ex vivo-expanded but not in vitro-induced human regulatory T cells are candidates for cell therapy in autoimmune diseases thanks to stable demethylation of the FOXP3 regulatory T cell-specific demethylated region
author_sort	Rossetti M.
title	Ex vivo-expanded but not in vitro-induced human regulatory T cells are candidates for cell therapy in autoimmune diseases thanks to stable demethylation of the FOXP3 regulatory T cell-specific demethylated region
title_short	Ex vivo-expanded but not in vitro-induced human regulatory T cells are candidates for cell therapy in autoimmune diseases thanks to stable demethylation of the FOXP3 regulatory T cell-specific demethylated region
title_full	Ex vivo-expanded but not in vitro-induced human regulatory T cells are candidates for cell therapy in autoimmune diseases thanks to stable demethylation of the FOXP3 regulatory T cell-specific demethylated region
title_fullStr	Ex vivo-expanded but not in vitro-induced human regulatory T cells are candidates for cell therapy in autoimmune diseases thanks to stable demethylation of the FOXP3 regulatory T cell-specific demethylated region
title_full_unstemmed	Ex vivo-expanded but not in vitro-induced human regulatory T cells are candidates for cell therapy in autoimmune diseases thanks to stable demethylation of the FOXP3 regulatory T cell-specific demethylated region
title_sort	ex vivo-expanded but not in vitro-induced human regulatory t cells are candidates for cell therapy in autoimmune diseases thanks to stable demethylation of the foxp3 regulatory t cell-specific demethylated region
publisher	American Association of Immunologists
publishDate	2016
url	http://scholarbank.nus.edu.sg/handle/10635/127464
_version_	1781790377119842304

Ex vivo-expanded but not in vitro-induced human regulatory T cells are candidates for cell therapy in autoimmune diseases thanks to stable demethylation of the FOXP3 regulatory T cell-specific demethylated region

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