Autoimmunity, hypogammaglobulinemia, lymphoproliferation, and mycobacterial disease in patients with activating mutations in STAT3. - Wikidata - wikimedia - TriplyDB

Autoimmunity, hypogammaglobulinemia, lymphoproliferation, and mycobacterial disease in patients with activating mutations in STAT3.

Autoimmunity, hypogammaglobulinemia, lymphoproliferation, and mycobacterial disease in patients with activating mutations in STAT3.

http://www.wikidata.org/entity/Q34445129

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Medical case reports in the age of genomic medicine Unbalanced Immune System: Immunodeficiencies and Autoimmunity Flow Cytometry, a Versatile Tool for Diagnosis and Monitoring of Primary Immunodeficiencies Diminution of signal transducer and activator of transcription 3 signaling inhibits vascular permeability and anaphylaxis Editorial: Current Challenges in Immune and Other Acquired Cytopenias of Childhood Immunological loss-of-function due to genetic gain-of-function in humans: autosomal dominance of the third kind The Ying and Yang of STAT3 in Human Disease A novel human STAT3 mutation presents with autoimmunity involving Th17 hyperactivation.Signal transducer and activator of transcription 3: a year in review.STAT5B deficiency: Impacts on human growth and immunity Enrichment of rare variants in population isolates: single AICDA mutation responsible for hyper-IgM syndrome type 2 in Finland Up, Down, and All Around: Diagnosis and Treatment of Novel STAT3 Variant.Immune deficiency vs. immune excess in inflammatory bowel diseases-STAT3 as a rheo-STAT of intestinal homeostasis.Genomics of Immune Diseases and New Therapies.From Genes to Mechanisms: The Expanding Spectrum of Monogenic Disorders Associated with Inflammatory Bowel Disease.STAT3 signaling in immunity.Role of STAT3 in Genesis and Progression of Human Malignant Gliomas.Lung Disease in Primary Antibody Deficiencies.Targeted strategies directed at the molecular defect: Toward precision medicine for select primary immunodeficiency disorders.Intracellular B Lymphocyte Signalling and the Regulation of Humoral Immunity and Autoimmunity.Cytokine-Mediated Regulation of Human Lymphocyte Development and Function: Insights from Primary Immunodeficiencies.Distinct mutations at the same positions of STAT3 cause either loss or gain of function.Genomics is rapidly advancing precision medicine for immunological disorders.The effects of signal transducer and activator of transcription three mutations on human platelets.Treatment of Infantile Inflammatory Bowel Disease and Autoimmunity by Allogeneic Stem Cell Transplantation in LPS-Responsive Beige-Like Anchor Deficiency.Unexpectedly High Prevalence of Common Variable Immunodeficiency in Finland.Somatic STAT3 mutations in the Felty syndrome: an implication for a common pathogenesis with large granular lymphocyte leukemia.Niclosamide Prevents Systemic Sclerosis in a Reactive Oxygen Species-Induced Mouse Model.Hyperhomocysteinemia, Suppressed Immunity, and Altered Oxidative Metabolism Caused by Pathogenic Microbes in Atherosclerosis and Dementia.Quantitative specificity of STAT1 and several variants.Learning from Job: A Rare Genetic Disease and Lessons of Biblical Proportions.Signal Transducer and Activator of Transcription 3 Control of Human T and B Cell Responses.STAT3 regulates cytotoxicity of human CD57+ CD4+ T cells in blood and lymphoid follicles.Somatic STAT5b gain-of-function mutations in early onset nonclonal eosinophilia, urticaria, dermatitis, and diarrhea.From clinical observations and molecular dissection to novel therapeutic strategies for primary immunodeficiency disorders.Rare autoimmune disorders with Mendelian inheritance.Bacille Calmette–Guerin Complications in Newly Described Primary Immunodeficiency Diseases: 2010–2017.A New Perspective: Mitochondrial Stat3 as a Regulator for Lymphocyte Function.Frequent mutations in CD8 T cells from patients with pure red cell aplasia Gain-of-function mutation causes human combined immune deficiency

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P2860

Autoimmunity, hypogammaglobulinemia, lymphoproliferation, and mycobacterial disease in patients with activating mutations in STAT3.

http://www.wikidata.org/entity/Q34445129

description

2014 nî lūn-bûn

@nan

2014 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի հոտեմբերին հրատարակված գիտական հոդված

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年论文

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name

Autoimmunity, hypogammaglobuli ...... activating mutations in STAT3.

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Autoimmunity, hypogammaglobuli ...... activating mutations in STAT3.

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Autoimmunity, hypogammaglobuli ...... activating mutations in STAT3.

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type

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Autoimmunity, hypogammaglobuli ...... activating mutations in STAT3.

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Autoimmunity, hypogammaglobuli ...... activating mutations in STAT3.

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Autoimmunity, hypogammaglobuli ...... activating mutations in STAT3.

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Autoimmunity, hypogammaglobuli ...... activating mutations in STAT3.

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Autoimmunity, hypogammaglobuli ...... activating mutations in STAT3.

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Autoimmunity, hypogammaglobuli ...... activating mutations in STAT3.

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Autoimmunity, hypogammaglobuli ...... activating mutations in STAT3

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Arjan J van Adrichem

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Emma M Haapaniemi

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Hanna L M Rajala

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Heikki Kuusanmäki

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Kaarina Heiskanen

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Luca Trotta

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Marja-Liisa Karjalainen-Lindsberg

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Meri Kaustio

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Panu E Kovanen

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Petri Kulmala

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P2860

Opposing regulation of the locus encoding IL-17 through direct, reciprocal actions of STAT3 and STAT5

Somatic STAT3 mutations in large granular lymphocytic leukemia

STAT3 mutations in the hyper-IgE syndrome

STAT3 regulates cytokine-mediated generation of inflammatory helper T cells

FAS-L, IL-10, and double-negative CD4- CD8- TCR alpha/beta+ T cells are reliable markers of autoimmune lymphoproliferative syndrome (ALPS) associated with FAS loss of function

Stat3 as an oncogene

The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3

Autoantibodies against IL-17A, IL-17F, and IL-22 in patients with chronic mucocutaneous candidiasis and autoimmune polyendocrine syndrome type I

Human ITCH E3 ubiquitin ligase deficiency causes syndromic multisystem autoimmune disease.

Immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) and IPEX-related disorders: an evolving web of heritable autoimmune diseases.

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639-648

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10.1182/BLOOD-2014-04-570101

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4

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125

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Yenan T Bryceson

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2014-10-27T00:00:00Z

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267738530

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25349174

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