Novel mutations of FOXP3 in two Japanese patients with immune dysregulation, polyendocrinopathy, enteropathy, X linked syndrome (IPEX)
about
Clinical and molecular features of the immunodysregulation, polyendocrinopathy, enteropathy, X linked (IPEX) syndromeFOXP3(+) Treg Cells and Gender Bias in Autoimmune DiseasesFOXP3: genetic and epigenetic implications for autoimmunityStructure of a Domain-Swapped FOXP3 Dimer on DNA and Its Function in Regulatory T CellsRegulation of IL-2 gene expression by Siva and FOXP3 in human T cells.Stable hematopoietic cell engraftment after low-intensity nonmyeloablative conditioning in patients with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndromeFrom IPEX syndrome to FOXP3 mutation: a lesson on immune dysregulation.Requirements for growth and IL-10 expression of highly purified human T regulatory cellsExome sequencing identifies a novel FOXP3 mutation in a 2-generation family with inflammatory bowel disease.T regulatory cells: aid or hindrance in the clearance of disease?FOXP3 acts as a rheostat of the immune response.Mutations in the Kir6.2 subunit of the KATP channel and permanent neonatal diabetes: new insights and new treatment.Immune dysregulation, polyendocrinopathy, enteropathy, x-linked syndrome: a paradigm of immunodeficiency with autoimmunityClinical heterogeneity in patients with FOXP3 mutations presenting with permanent neonatal diabetesMoving to tolerance: clinical application of T regulatory cellsOn the interactions between mesenchymal stem cells and regulatory T cells for immunomodulation in transplantation.The role of regulatory T cells in neurodegenerative diseases.Promoting transplantation tolerance; adoptive regulatory T cell therapy.T-cell tolerance in cancer.Renal involvement in the immunodysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) disorder.Altered balance between self-reactive T helper (Th)17 cells and Th10 cells and between full-length forkhead box protein 3 (FoxP3) and FoxP3 splice variants in Hashimoto's thyroiditis.Paradoxically increased FOXP3+ T cells in IBD do not preferentially express the isoform of FOXP3 lacking exon 2.Role of Foxp3 gene in maternal susceptibility to pre-eclampsia - a study from South India.Foxp3 promoter polymorphism (rs3761548) in breast cancer progression: a study from India.A novel mutation and unusual clinical features in a patient with immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome.A potential screening tool for IPEX syndrome.Clinical and molecular characteristics of immunodysregulation, polyendocrinopathy, enteropathy, X-linked syndrome in China.Alternative Splicing of FOXP3-Virtue and Vice.Clinical, Immunological, and Molecular Heterogeneity of 173 Patients With the Phenotype of Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked (IPEX) Syndrome
P2860
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P2860
Novel mutations of FOXP3 in two Japanese patients with immune dysregulation, polyendocrinopathy, enteropathy, X linked syndrome (IPEX)
description
2001 nî lūn-bûn
@nan
2001 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
Novel mutations of FOXP3 in tw ...... athy, X linked syndrome (IPEX)
@ast
Novel mutations of FOXP3 in tw ...... athy, X linked syndrome (IPEX)
@en
Novel mutations of FOXP3 in tw ...... athy, X linked syndrome (IPEX)
@nl
type
label
Novel mutations of FOXP3 in tw ...... athy, X linked syndrome (IPEX)
@ast
Novel mutations of FOXP3 in tw ...... athy, X linked syndrome (IPEX)
@en
Novel mutations of FOXP3 in tw ...... athy, X linked syndrome (IPEX)
@nl
prefLabel
Novel mutations of FOXP3 in tw ...... athy, X linked syndrome (IPEX)
@ast
Novel mutations of FOXP3 in tw ...... athy, X linked syndrome (IPEX)
@en
Novel mutations of FOXP3 in tw ...... athy, X linked syndrome (IPEX)
@nl
P2093
P356
P1476
Novel mutations of FOXP3 in tw ...... athy, X linked syndrome (IPEX)
@en
P2093
I Kobayashi
K Kobayashi
N Ishikawa
N Kawamura
P356
10.1136/JMG.38.12.874
P407
P577
2001-12-01T00:00:00Z