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Article

Reduced FOXP3 expression causes IPEX syndrome onset: An implication from an IPEX patient and his disease-free twin brother.

Clinical immunology (Orlando, Fla.) - 1 Oct 2010

Wang Jingxue, Li Xiaowen, Jia Zhengcai, Tian Yi, Yu Jialin, Bao Lei, Wu Yuzhang, Ni Bing

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 20709600
DOI: 10.1016/j.clim.2010.07.006

Genes

FOXP3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

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Research trail→

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Reduced FOXP3 expression causes IPEX syndrome onset: An implication from an IPEX patient and his disease-free twin brother.PMID 20709600Read ↗

IPEX as a result of mutations in FOXP3.Semantic proximity Read ↗

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IPEX is a unique X-linked syndrome characterized by immune dysfunction, polyendocrinopathy, enteropathy, and a variety of autoimmune phenomena.Semantic proximity Read ↗

IPEX and the role of Foxp3 in the development and function of human Tregs.Semantic proximity Read ↗

Molecular feature and therapeutic perspectives of immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome.Semantic proximity Read ↗

Immune dysregulation, polyendocrinopathy, enteropathy, and X-linked inheritance (IPEX), a syndrome of systemic autoimmunity caused by mutations of FOXP3, a critical regulator of T-cell homeostasis.Semantic proximity Read ↗

IPEX due to an exon 7 skipping FOXP3 mutation with autoimmune diabetes mellitus cured by selective TReg cell engraftment.Semantic proximity Read ↗

FOXP3 deficiency, from the mechanisms of the disease to curative strategies.Semantic proximity Read ↗

Underlying IPEX Syndrome in a Patient With Idiopathic Juvenile Arthritis and VitiligoSemantic proximity Read ↗

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