Copy number variation of the activating FCGR2C gene predisposes to idiopathic thrombocytopenic purpura. - Wikidata - wikimedia - TriplyDB

Copy number variation of the activating FCGR2C gene predisposes to idiopathic thrombocytopenic purpura.

Copy number variation of the activating FCGR2C gene predisposes to idiopathic thrombocytopenic purpura.

http://www.wikidata.org/entity/Q33376582

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NK Cell-Mediated Antibody-Dependent Cellular Cytotoxicity in Cancer Immunotherapy Cross-presentation of IgG-containing immune complexes Contemporary management of primary immune thrombocytopenia in adults Molecular diagnosis of chronic granulomatous disease Targeting the Fc receptor in autoimmune disease Elusive copy number variation in the mouse genome Phase II open-label study to assess efficacy and safety of lenalidomide in combination with cetuximab in KRAS-mutant metastatic colorectal cancer Genome-wide association study identifies FCGR2A as a susceptibility locus for Kawasaki disease.CD16 and CD32 Gene Polymorphisms May Contribute to Risk of Idiopathic Thrombocytopenic Purpura.Genetic studies in pediatric ITP: outlook, feasibility, and requirements.CNR2 functional variant (Q63R) influences childhood immune thrombocytopenic purpura.FCGR2C genotyping by pyrosequencing reveals linkage disequilibrium with FCGR3A V158F and FCGR2A H131R polymorphisms in a Caucasian population.Low expression of FCGRIIB in macrophages of immune thrombocytopenia-affected individuals.A prominent lack of IgG1-Fc fucosylation of platelet alloantibodies in pregnancy Is dosing of therapeutic immunoglobulins optimal? A review of a three-decade long debate in europe A Study of Human Killer Cell Immunoglobulin-Like Receptor and Multidrug Resistance Gene Polymorphisms in Children With Immune Thrombocytopenia.The Elements Steering Pathogenesis in IgG-Mediated Alloimmune Diseases.Fcγ receptor expression on splenic macrophages in adult immune thrombocytopenia.Copy number variation of FCGR genes in etiopathogenesis of sarcoidosis Copy number variants in genetic susceptibility and severity of systemic lupus erythematosus 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 Mechanisms of Autoantibody-Induced Pathology.Genome-wide copy number variation (CNV) in patients with autoimmune Addison's disease.Copy number, linkage disequilibrium and disease association in the FCGR locus.Copy number variation in the human genome and its implication in autoimmunity.FcγR gene copy number in Kawasaki disease and intravenous immunoglobulin treatment response.IgG subclasses and allotypes: from structure to effector functions.Human FcR polymorphism and disease.Extensive variation in gene copy number at the killer immunoglobulin-like receptor locus in humans Prophylactic anti-D preparations display variable decreases in Fc-fucosylation of anti-D.Evaluation of High-Throughput Genomic Assays for the Fc Gamma Receptor Locus.Evolutionary history of copy-number-variable locus for the low-affinity Fcγ receptor: mutation rate, autoimmune disease, and the legacy of helminth infection.Low copy number of the FCGR3B gene and rheumatoid arthritis: a case-control study and meta-analysis.Distribution of FcγR gene polymorphisms among two sympatric populations in Mali: differing allele frequencies, associations with malariometric indices and implications for genetic susceptibility to malaria The role of Fc receptors in HIV prevention and therapy.Integrative analysis reveals an outcome-associated and targetable pattern of p53 and cell cycle deregulation in diffuse large B cell lymphoma.Comparison of Multiple Methods for Determination of FCGR3A/B Genomic Copy Numbers in HapMap Asian Populations with Two Public Databases.Functional and clinical consequences of Fc receptor polymorphic and copy number variants.Single-nucleotide polymorphisms and copy number variations of the FCGR2A and FCGR3A genes in healthy Japanese subjects.

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P2860

Copy number variation of the activating FCGR2C gene predisposes to idiopathic thrombocytopenic purpura.

http://www.wikidata.org/entity/Q33376582

description

2007 nî lūn-bûn

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2007 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

2007 թվականի սեպտեմբերին հրատարակված գիտական հոդված

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2007年の論文

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2007年学术文章

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2007年学术文章

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2007年学术文章

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2007年学术文章

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2007年学术文章

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2007年學術文章

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Copy number variation of the a ...... thic thrombocytopenic purpura.

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Copy number variation of the a ...... thic thrombocytopenic purpura.

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Copy number variation of the a ...... thic thrombocytopenic purpura.

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Copy number variation of the a ...... thic thrombocytopenic purpura.

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Dirk Roos

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Edwin van Mirre

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Harry R Koene

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Judy Geissler

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Marjolein Peters

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Marrie Bruin

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1029-1038

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Taco W Kuijpers

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