Copy number of FCGR3B, which is associated with systemic lupus erythematosus, correlates with protein expression and immune complex uptake. - Wikidata - awgldk - TriplyDB

Copy number of FCGR3B, which is associated with systemic lupus erythematosus, correlates with protein expression and immune complex uptake.

Copy number of FCGR3B, which is associated with systemic lupus erythematosus, correlates with protein expression and immune complex uptake.

http://www.wikidata.org/entity/Q36742257

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Genetics of immunological and inflammatory components in age-related macular degeneration Targeting the Fc receptor in autoimmune disease Fcγ Receptors in Solid Organ Transplantation Complex and multi-allelic copy number variation in human disease Genomic copy number variants: evidence for association with antibody response to anthrax vaccine adsorbed Wegener's granulomatosis: a model of auto-antibodies in mucosal autoimmunity The contribution of genetic variation and infection to the pathogenesis of ANCA-associated systemic vasculitis Genetic mechanism of human neutrophil antigen 2 deficiency and expression variations Genome-wide analysis of copy number variation in type 1 diabetes FcγRIIB and autoimmunity.Contrasting genetic association of IL2RA with SLE and ANCA-associated vasculitis Association of FCGR3A and FCGR3B copy number variations with systemic lupus erythematosus and rheumatoid arthritis in Taiwanese patients.GPI-anchor and GPI-anchored protein expression in PMM2-CDG patients.IgE-based immunotherapy of cancer: challenges and chances.Mechanisms of copy number variation and hybrid gene formation in the KIR immune gene complex.Copy number variation of FCGR genes in etiopathogenesis of sarcoidosis Contribution of Human FcγRs to Disease with Evidence from Human Polymorphisms and Transgenic Animal Studies Fcgamma receptors: structure, function and role as genetic risk factors in SLE Deficiency of activating Fcγ-receptors reduces hepatic clearance and deposition of IC and increases CIC levels in mercury-induced autoimmunity.Genetic factors predisposing to systemic lupus erythematosus and lupus nephritis.Copy number, linkage disequilibrium and disease association in the FCGR locus.Copy number variation in the human genome and its implication in autoimmunity.Copy number variation in human health, disease, and evolution.Novel expression signatures identified by transcriptional analysis of separated leucocyte subsets in systemic lupus erythematosus and vasculitis.Genomic pathology of SLE-associated copy-number variation at the FCGR2C/FCGR3B/FCGR2B locus.FcγR gene copy number in Kawasaki disease and intravenous immunoglobulin treatment response.Human FcR polymorphism and disease.Impairment of the antibody-dependent phagocytic function of PMNs through regulation of the FcγRs expression after porcine reproductive and respiratory syndrome virus infection.Olfactory copy number association with age at onset of Alzheimer disease The quest for genetic risk factors for Crohn's disease in the post-GWAS era Diagnosis and management of primary autoimmune neutropenia in children: insights for clinicians.Copy number variation of Fc gamma receptor genes in HIV-infected and HIV-tuberculosis co-infected individuals in sub-Saharan Africa Association of TLR7 and TSHR copy number variation with Graves' disease and Graves' ophthalmopathy in Chinese population in Taiwan Genetic susceptibility to systemic lupus erythematosus in the genomic era Induced expression of FcγRIIIa (CD16a) on CD4+ T cells triggers generation of IFN-γhigh subset.Inferring mechanisms of copy number change from haplotype structures at the human DEFA1A3 locus.A comparison of assays for accurate copy number measurement of the low-affinity Fc gamma receptor genes FCGR3A and FCGR3B.Protein abundance may regulate sensitivity to external cues in polarized cells Correlation of DEFA1 gene copy number variation with intestinal involvement in Behcet's disease.Fc-Gamma Receptor 3B Copy Number Variation Is Not a Risk Factor for Behçet's Disease.

P2860

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P2860

Copy number of FCGR3B, which is associated with systemic lupus erythematosus, correlates with protein expression and immune complex uptake.

http://www.wikidata.org/entity/Q36742257

description

2008 nî lūn-bûn

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2008年の論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年论文

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2008年论文

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2008年论文

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name

Copy number of FCGR3B, which i ...... ion and immune complex uptake.

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Copy number of FCGR3B, which i ...... ion and immune complex uptake.

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type

label

Copy number of FCGR3B, which i ...... ion and immune complex uptake.

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Copy number of FCGR3B, which i ...... ion and immune complex uptake.

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prefLabel

Copy number of FCGR3B, which i ...... ion and immune complex uptake.

@ast

Copy number of FCGR3B, which i ...... ion and immune complex uptake.

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P1433

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P2860

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P932

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P1433

Journal of Experimental Medicine

P1476

Copy number of FCGR3B, which i ...... ion and immune complex uptake.

@en

P2093

Alison M Condliffe

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Ann W Morgan

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Dwomoa Adu

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Elaine C Jolly

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James I Robinson

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Kenneth G C Smith

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Lisa C Willcocks

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Menna R Clatworthy

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

Paul A Lyons

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

Richard Watts

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

P2860

Global variation in copy number in the human genome

Alternative membrane forms of Fc gamma RIII(CD16) on human natural killer cells and neutrophils. Cell type-specific expression of two genes that differ in single nucleotide substitutions

Characterization of Potocki-Lupski syndrome (dup(17)(p11.2p11.2)) and delineation of a dosage-sensitive critical interval that can convey an autism phenotype

Risk for rheumatic disease in relation to ethnicity and admixture.

Fcgamma receptors: old friends and new family members

The influence of CCL3L1 gene-containing segmental duplications on HIV-1/AIDS susceptibility

Copy-number variation and association studies of human disease

Fc gamma RIII mediates neutrophil recruitment to immune complexes. a mechanism for neutrophil accumulation in immune-mediated inflammation

Relative impact of nucleotide and copy number variation on gene expression phenotypes

Genetic deficiency of CD16, the low-affinity receptor for immunoglobulin G, has no impact on the functional capacity of polymorphonuclear neutrophils.

P304

1573-1582

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P31

scholarly article

P356

10.1084/JEM.20072413

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P407

P433

7

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P478

205

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P50

Vincent Plagnol

Edwin R Chilvers

P577

2008-06-16T00:00:00Z

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P5875

5296186

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P698

18559452

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P932

2442635

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