Novel STAT3 mutation causing hyper-IgE syndrome: studies of the clinical course and immunopathology. (Q45876992)

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10 March 2020

title

Novel STAT3 mutation causing hyper-IgE syndrome: studies of the clinical course and immunopathology (English)

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10 March 2020

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4

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10 March 2020

Mikael Sundin

1

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10 March 2020

Bianca Tesi

2

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10 March 2020

Samuel C Chiang

6

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10 March 2020

author name string

Maria Sund Böhme

3

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10 March 2020

Katrin Pütsep

5

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10 March 2020

Sarah Thunberg

7

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10 March 2020

Jacek Winiarski

8

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10 March 2020

Ann-Charlotte Wikström

9

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publication date

14 March 2014

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Journal of Clinical Immunology

10 March 2020

published in

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volume

34

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10 March 2020

issue

4

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10 March 2020

page(s)

469-477

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https://scigraph.springernature.com/pub.10.1007/s10875-014-0011-x

10 March 2020

exact match

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cites work

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The hyperimmunoglobulin E syndrome--clinical manifestation diversity in primary immune deficiency

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The JAK-STAT signaling pathway: input and output integration

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Cytokine signaling modules in inflammatory responses

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The hyper-IgE syndrome

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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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Mutations in STAT3 and IL12RB1 impair the development of human IL-17-producing T cells

21 January 2018

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

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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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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Genetic linkage of hyper-IgE syndrome to chromosome 4.

21 January 2018

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Mutations in STAT3 and diagnostic guidelines for hyper-IgE syndrome

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

21 January 2018

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Defective cytotoxic lymphocyte degranulation in syntaxin-11 deficient familial hemophagocytic lymphohistiocytosis 4 (FHL4) patients

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HLH-2004: Diagnostic and therapeutic guidelines for hemophagocytic lymphohistiocytosis.

21 January 2018

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Development and evaluation of a flow-cytometric assay of specific cell-mediated immune response in activated whole blood for the detection of cell-mediated immunity against varicella-zoster virus

21 January 2018

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Deficiency of antibacterial peptides in patients with morbus Kostmann: an observation study.

21 January 2018

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Transitional B cells in humans: characterization and insight from B lymphocyte reconstitution after hematopoietic stem cell transplantation.

21 January 2018

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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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IL-5- and eosinophil-mediated inflammation: from discovery to therapy

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21 January 2018

IL-13 effector functions

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Regulation of immunoglobulin production in hyper-IgE (Job’s) syndrome

21 January 2018

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Low plasma levels of the protein pro-LL-37 as an early indication of severe disease in patients with chronic neutropenia

21 January 2018

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A new method for measuring lymphoproliferation at the single-cell level in whole blood cultures by flow cytometry

21 January 2018

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12 December 2020

STAT3 is required for IL-21-induced secretion of IgE from human naive B cells

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12 December 2020

Diagnostic approach to the hyper-IgE syndromes: Immunologic and clinical key findings to differentiate hyper-IgE syndromes from atopic dermatitis

1 reference

12 December 2020

Comparison of primary human cytotoxic T-cell and natural killer cell responses reveal similar molecular requirements for lytic granule exocytosis but differences in cytokine production

1 reference

12 December 2020

10.1007/S10875-014-0011-X

Identifiers

DOI

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Dimensions Publication ID

10 March 2020

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1 reference

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