An antibody-deficiency syndrome due to mutations in the CD19 gene - Wikidata - wikimedia - TriplyDB

An antibody-deficiency syndrome due to mutations in the CD19 gene

An antibody-deficiency syndrome due to mutations in the CD19 gene

http://www.wikidata.org/entity/Q28238166

about

Screening of functional and positional candidate genes in families with common variable immunodeficiency CD20 deficiency in humans results in impaired T cell-independent antibody responses CD19 chimeric antigen receptor (CD19 CAR)-redirected adoptive T-cell immunotherapy for the treatment of relapsed or refractory B-cell Non-Hodgkin's Lymphomas International Consensus Document (ICON): Common Variable Immunodeficiency Disorders Humoral immunodeficiency : awareness for better support Comparison of diagnostic criteria for common variable immunodeficiency disorder Antigen-based immunotherapy for the treatment of acute lymphoblastic leukemia: the emerging role of blinatumomab Targeting CD19 in B-cell lymphoma: emerging role of SAR3419 Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity Rac-mediated Stimulation of Phospholipase Cγ2 Amplifies B Cell Receptor-induced Calcium Signaling.Unbalanced Immune System: Immunodeficiencies and Autoimmunity Educational paper: primary antibody deficiencies Update in understanding common variable immunodeficiency disorders (CVIDs) and the management of patients with these conditions Germline mutations in NFKB2 implicate the noncanonical NF-κB pathway in the pathogenesis of common variable immunodeficiency Granulomatous disease in common variable immunodeficiency.Autoimmune cytopenias in common variable immunodeficiency.Common variable immunodeficiency: etiological and treatment issues.Unique DNA repair gene variations and potential associations with the primary antibody deficiency syndromes IgAD and CVID CD81 gene defect in humans disrupts CD19 complex formation and leads to antibody deficiency.A machine learning approach for genome-wide prediction of morbid and druggable human genes based on systems-level data.The many faces of common variable immunodeficiency.The clinical utility of molecular diagnostic testing for primary immune deficiency disorders: a case based review.How I treat common variable immune deficiency.Toll-like receptor 7 and 9 defects in common variable immunodeficiency.Autoimmunity in common variable immunodeficiency.Role of B cells in common variable immune deficiency.A custom 148 gene-based resequencing chip and the SNP explorer software: new tools to study antibody deficiency.Exhaustion of bacteria-specific CD4 T cells and microbial translocation in common variable immunodeficiency disorders.Morbidity and mortality in common variable immune deficiency over 4 decades Induction of interleukin-6 production by rituximab in human B cells.Infections in 252 patients with common variable immunodeficiency.Critical role of SHP2 (PTPN11) signaling in germinal center-derived lymphoma.Simultaneous downregulation of KLF5 and Fli1 is a key feature underlying systemic sclerosis.CD19 as a molecular target in CNS autoimmunity.Pathogenesis, diagnosis, and management of primary antibody deficiencies and infections.Interferon signature in the blood in inflammatory common variable immune deficiency Clinical and technical phosphoproteomic research.Novel sequencing-based strategies for high-throughput discovery of genetic mutations underlying inherited antibody deficiency disorders Proteomic analysis of sera from common variable immunodeficiency patients undergoing replacement intravenous immunoglobulin therapy.Cloning and Expression of CD19, a Human B-Cell Marker in NIH-3T3 Cell Line.

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An antibody-deficiency syndrome due to mutations in the CD19 gene

http://www.wikidata.org/entity/Q28238166

description

2006 nî lūn-bûn

@nan

2006 թուականի Մայիսին հրատարակուած գիտական յօդուած

@hyw

2006 թվականի մայիսին հրատարակված գիտական հոդված

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2006年の論文

@ja

2006年論文

@yue

2006年論文

@zh-hant

2006年論文

@zh-hk

2006年論文

@zh-mo

2006年論文

@zh-tw

2006年论文

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name

An antibody-deficiency syndrome due to mutations in the CD19 gene

@ast

An antibody-deficiency syndrome due to mutations in the CD19 gene

@en

An antibody-deficiency syndrome due to mutations in the CD19 gene

@nl

type

label

An antibody-deficiency syndrome due to mutations in the CD19 gene

@ast

An antibody-deficiency syndrome due to mutations in the CD19 gene

@en

An antibody-deficiency syndrome due to mutations in the CD19 gene

@nl

prefLabel

An antibody-deficiency syndrome due to mutations in the CD19 gene

@ast

An antibody-deficiency syndrome due to mutations in the CD19 gene

@en

An antibody-deficiency syndrome due to mutations in the CD19 gene

@nl

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P3181

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P1433

The New England Journal of Medicine

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An antibody-deficiency syndrome due to mutations in the CD19 gene

@en

P2093

Bodo Grimbacher

http://www.w3.org/2001/XMLSchema#string

Carel J M van Noesel

http://www.w3.org/2001/XMLSchema#string

Cristina Woellner

http://www.w3.org/2001/XMLSchema#string

Diana Castaño

http://www.w3.org/2001/XMLSchema#string

Ismail Reisli

http://www.w3.org/2001/XMLSchema#string

Jacques J M van Dongen

http://www.w3.org/2001/XMLSchema#string

José L Franco

http://www.w3.org/2001/XMLSchema#string

Maarten J D van Tol

http://www.w3.org/2001/XMLSchema#string

Mirjam van der Burg

http://www.w3.org/2001/XMLSchema#string

Pablo J Patiño

http://www.w3.org/2001/XMLSchema#string

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1901-12

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scholarly article

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3102868

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10.1056/NEJMOA051568

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18

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354

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Menno C van Zelm

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2006-05-04T00:00:00Z

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16672701

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P921

positive regulation of release of sequestered calcium ion into cytosol