(Q46972270)

27 December 2017

title

Clinical features, STAT3 gene mutations and Th17 cell analysis in nine children with hyper-IgE syndrome in mainland China (English)

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27 December 2017

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L-Y Zhang

1

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27 December 2017

W Tian

2

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27 December 2017

L Shu

3

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27 December 2017

L-P Jiang

4

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27 December 2017

Y-Z Zhan

5

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27 December 2017

W Liu

6

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27 December 2017

X-D Zhao

7

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27 December 2017

Y-X Cui

8

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27 December 2017

X-M Tang

9

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27 December 2017

M Wang

10

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27 December 2017

D-Q Wu

11

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27 December 2017

X-Q Yang

12

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27 December 2017

publication date

1 September 2013

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27 December 2017

Scandinavian Journal of Immunology

published in

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27 December 2017

volume

78

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27 December 2017

issue

3

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27 December 2017

page(s)

258-265

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27 December 2017

Hyper-IgE syndrome with recurrent infections--an autosomal dominant multisystem disorder

cites work

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Genetic linkage of hyper-IgE syndrome to chromosome 4.

21 January 2018

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Impaired T(H)17 cell differentiation in subjects with autosomal dominant hyper-IgE syndrome

21 January 2018

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Clinical, immunological and genetic features in Taiwanese patients with the phenotype of hyper-immunoglobulin E recurrent infection syndromes (HIES).

21 January 2018

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Hyper-IgE syndrome with STAT3 mutation: a case report in Mainland China

21 January 2018

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Cutaneous manifestations of hyper-IgE syndrome in infants and children

21 January 2018

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Hyperimmunoglobulin-E syndrome with recurrent infection: a review of current opinion and treatment

21 January 2018

1 reference

Novel signal transducer and activator of transcription 3 (STAT3) mutations, reduced T(H)17 cell numbers, and variably defective STAT3 phosphorylation in hyper-IgE syndrome

21 January 2018

1 reference

Mutations in STAT3 and diagnostic guidelines for hyper-IgE syndrome

21 January 2018

1 reference

Autosomal dominant STAT3 deficiency and hyper-IgE syndrome: molecular, cellular, and clinical features from a French national survey

21 January 2018

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Paucity of genotype-phenotype correlations in STAT3 mutation positive Hyper IgE Syndrome (HIES).

21 January 2018

1 reference

Combined immunodeficiency associated with DOCK8 mutations

21 January 2018

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Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome

21 January 2018

1 reference

Stat3: a STAT family member activated by tyrosine phosphorylation in response to epidermal growth factor and interleukin-6

21 January 2018

1 reference

Dominant-negative mutations in the DNA-binding domain of STAT3 cause hyper-IgE syndrome

21 January 2018

1 reference

GP130-STAT3 regulates epithelial cell migration and is required for repair of the bronchiolar epithelium

21 January 2018

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Molecular explanation for the contradiction between systemic Th17 defect and localized bacterial infection in hyper-IgE syndrome

21 January 2018

1 reference

Plasma metalloproteinase levels are dysregulated in signal transducer and activator of transcription 3 mutated hyper-IgE syndrome

21 January 2018

1 reference

A critical role for STAT3 transcription factor signaling in the development and maintenance of human T cell memory

21 January 2018

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B cell-intrinsic signaling through IL-21 receptor and STAT3 is required for establishing long-lived antibody responses in humans

21 January 2018

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Reduced memory B cells in patients with hyper IgE syndrome.

21 January 2018

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Heterozygous signal transducer and activator of transcription 3 mutations in hyper-IgE syndrome result in altered B-cell maturation

21 January 2018

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Immature B cells preferentially switch to IgE with increased direct Sμ to Sε recombination.

21 January 2018

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Interleukin 17-producing CD4+ effector T cells develop via a lineage distinct from the T helper type 1 and 2 lineages

21 January 2018

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The biological functions of T helper 17 cell effector cytokines in inflammation

21 January 2018

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Interleukins 1beta and 6 but not transforming growth factor-beta are essential for the differentiation of interleukin 17-producing human T helper cells

21 January 2018

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Surface phenotype and antigenic specificity of human interleukin 17-producing T helper memory cells

21 January 2018

1 reference

Deficiency of Th17 cells in hyper IgE syndrome due to mutations in STAT3

21 January 2018

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Chronic mucocutaneous candidiasis in humans with inborn errors of interleukin-17 immunity

21 January 2018

1 reference

Hyperimmunoglobulin E syndromes in pediatrics.

21 January 2018

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STAT3 mutations in the hyper-IgE syndrome

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1111/SJI.12063

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27 December 2017

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27 December 2017