Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

FOXP3 forkhead domain mutation and regulatory T cells in the IPEX syndrome.

The New England journal of medicine - 22 Oct 2009

d'Hennezel Eva, Ben-Shoshan Moshe, Ochs Hans D, Torgerson Troy R, Russell Laura J, Lejtenyi Christine, Noya Francisco J, Jabado Nada, Mazer Bruce, Piccirillo Ciriaco A

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Abnormalities, Multiple
Share to Autoimmune Diseases
Share to Fatal Outcome
Share to Forkhead Transcription Factors

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Infant, Premature

Share to Intestinal Diseases

Share to Polyendocrinopathies, Autoimmune

Share to T-Lymphocytes, Regulatory

Source

Identifiers

PMID: 19846862
DOI: 10.1056/NEJMc0907093

Genes

FOXP3

Provenance

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

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

FOXP3 forkhead domain mutation and regulatory T cells in the IPEX syndrome.PMID 19846862Read ↗

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

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

Beyond the Classical Triad: Atypical Presentations and Regulatory T Cell Phenotyping in a Cohort of IPEX Patients.Semantic proximity Read ↗

From IPEX syndrome to FOXP3 mutation: a lesson on immune dysregulation.Semantic proximity Read ↗

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 ↗

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

Clinical and molecular findings in IPEX syndrome.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 ↗

Foxp3: a genetic foundation for regulatory T cell differentiation and function.Semantic proximity Read ↗

Epigenetic and immunological indicators of IPEX disease in subjects with FOXP3 gene mutation.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.