Mutational analysis of the FOXP3 gene and evidence for genetic heterogeneity in the immunodysregulation, polyendocrinopathy, enteropathy syndrome.
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IPEX as a result of mutations in FOXP3FOXP3: genetic and epigenetic implications for autoimmunityInsights into type 1 diabetes from the autoimmune polyendocrine syndromesA Systems Pharmacology Approach to Determine Active Compounds and Action Mechanisms of Xipayi KuiJie'an enema for Treatment of Ulcerative colitis.Autoimmune polyendocrine syndromes: clues to type 1 diabetes pathogenesis.From IPEX syndrome to FOXP3 mutation: a lesson on immune dysregulation.Defective regulatory and effector T cell functions in patients with FOXP3 mutations.Analysis of the cellular mechanism of antitumor responses and autoimmunity in patients treated with CTLA-4 blockade.Autoimmune enteropathy in children and adults.The stages of type 1A diabetes: 2005.Mutations in the Kir6.2 subunit of the KATP channel and permanent neonatal diabetes: new insights and new treatment.Regulatory T cells in immunologic self-tolerance and autoimmune disease.Immune dysregulation, polyendocrinopathy, enteropathy, x-linked syndrome: a paradigm of immunodeficiency with autoimmunityGenetic Susceptibility to Multiple Sclerosis: The Role of FOXP3 Gene Polymorphism.The dual role of the X-linked FoxP3 gene in human cancersSearching for the Achilles Heel of FOXP3Functional dynamics of Foxp3⁺ regulatory T cells in mice and humans.Extremely Early Onset IPEX Syndrome Caused by a Novel Small Exonic Deletion in FOXP3.Role of Foxp3 gene in maternal susceptibility to pre-eclampsia - a study from South India.Proteomics plus genomics approaches in primary immunodeficiency: the case of immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome.Quantitative and qualitative normal regulatory T cells are not capable of inducing suppression in SLE patients due to T-cell resistance.The synergic effects of CTLA-4/Foxp3-related genotypes and chromosomal aberrations on the risk of recurrent spontaneous abortion among a Chinese Han population.
P2860
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P2860
Mutational analysis of the FOXP3 gene and evidence for genetic heterogeneity in the immunodysregulation, polyendocrinopathy, enteropathy syndrome.
description
2003 nî lūn-bûn
@nan
2003 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Mutational analysis of the FOX ...... nopathy, enteropathy syndrome.
@ast
Mutational analysis of the FOX ...... nopathy, enteropathy syndrome.
@en
Mutational analysis of the FOX ...... nopathy, enteropathy syndrome.
@nl
type
label
Mutational analysis of the FOX ...... nopathy, enteropathy syndrome.
@ast
Mutational analysis of the FOX ...... nopathy, enteropathy syndrome.
@en
Mutational analysis of the FOX ...... nopathy, enteropathy syndrome.
@nl
prefLabel
Mutational analysis of the FOX ...... nopathy, enteropathy syndrome.
@ast
Mutational analysis of the FOX ...... nopathy, enteropathy syndrome.
@en
Mutational analysis of the FOX ...... nopathy, enteropathy syndrome.
@nl
P2093
P356
P1476
Mutational analysis of the FOX ...... nopathy, enteropathy syndrome.
@en
P2093
Alain Lachaux
Catherine J Owen
Claire E Jennings
Helen Imrie
Nicola A Bridges
Simon H S Pearce
Tim D Cheetham
P304
P356
10.1210/JC.2003-031080
P407
P577
2003-12-01T00:00:00Z