Genomic pathology of SLE-associated copy-number variation at the FCGR2C/FCGR3B/FCGR2B locus. - Wikidata - awgldk - TriplyDB

Genomic pathology of SLE-associated copy-number variation at the FCGR2C/FCGR3B/FCGR2B locus.

Genomic pathology of SLE-associated copy-number variation at the FCGR2C/FCGR3B/FCGR2B locus.

http://www.wikidata.org/entity/Q34319137

about

Complex and multi-allelic copy number variation in human disease Solving the genetic puzzle of systemic lupus erythematosus.Association of FCGR3A and FCGR3B copy number variations with systemic lupus erythematosus and rheumatoid arthritis in Taiwanese patients.IgE-based immunotherapy of cancer: challenges and chances.Fcγ receptor IIIa single-nucleotide polymorphisms and haplotypes affect human IgG binding and are associated with lupus nephritis in African Americans Copy number variation of Fc gamma receptor genes in HIV-infected and HIV-tuberculosis co-infected individuals in sub-Saharan Africa 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.Association analysis of copy numbers of FC-gamma receptor genes for rheumatoid arthritis and other immune-mediated phenotypes.The complement receptor 3 (CD11b/CD18) agonist Leukadherin-1 suppresses human innate inflammatory signalling.Allelic-dependent expression of an activating Fc receptor on B cells enhances humoral immune responses.Understanding the Genomic Structure of Copy-Number Variation of the Low-Affinity Fcγ Receptor Region Allows Confirmation of the Association of FCGR3B Deletion with Rheumatoid Arthritis.Gene-function studies in systemic lupus erythematosus.Human gene copy number variation and infectious disease.Fcγ receptors: genetic variation, function, and disease.Fc-gamma receptor polymorphisms differentially influence susceptibility to systemic lupus erythematosus and lupus nephritis.Signaling by Antibodies: Recent Progress.SRBreak: A Read-Depth and Split-Read Framework to Identify Breakpoints of Different Events Inside Simple Copy-Number Variable Regions.Variability at the FCGR locus: characterization in Black South Africans and evidence for ethnic variation in and out of Africa.Low α-defensin gene copy number increases the risk for IgA nephropathy and renal dysfunction.Nonallelic homologous recombination of the FCGR2/3 locus results in copy number variation and novel chimeric FCGR2 genes with aberrant functional expression.Impact of allele copy number of polymorphisms in FCGR3A and FCGR3B genes on susceptibility to ulcerative colitis.FCGR3A and FCGR3B copy number variations are risk factors for sarcoidosis.Fcγ Receptor Function and the Design of Vaccination Strategies.FCGR Polymorphisms Influence Response to IL2 in Metastatic Renal Cell Carcinoma.Diversification of IgG effector functions.

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Genomic pathology of SLE-associated copy-number variation at the FCGR2C/FCGR3B/FCGR2B locus.

http://www.wikidata.org/entity/Q34319137

description

2012 nî lūn-bûn

@nan

2012 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2012 թվականի դեկտեմբերին հրատարակված գիտական հոդված

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2012年の論文

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2012年学术文章

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2012年学术文章

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2012年学术文章

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2012年学术文章

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2012年学术文章

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2012年學術文章

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Genomic pathology of SLE-assoc ...... he FCGR2C/FCGR3B/FCGR2B locus.

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Genomic pathology of SLE-assoc ...... he FCGR2C/FCGR3B/FCGR2B locus.

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Genomic pathology of SLE-assoc ...... he FCGR2C/FCGR3B/FCGR2B locus.

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Genomic pathology of SLE-assoc ...... he FCGR2C/FCGR3B/FCGR2B locus.

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Genomic pathology of SLE-assoc ...... he FCGR2C/FCGR3B/FCGR2B locus.

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prefLabel

Genomic pathology of SLE-assoc ...... he FCGR2C/FCGR3B/FCGR2B locus.

@ast

Genomic pathology of SLE-assoc ...... he FCGR2C/FCGR3B/FCGR2B locus.

@en

Genomic pathology of SLE-assoc ...... he FCGR2C/FCGR3B/FCGR2B locus.

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J.AJHG.2012.11.013

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American Journal of Human Genetics

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Genomic pathology of SLE-assoc ...... he FCGR2C/FCGR3B/FCGR2B locus.

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Abigail S Witherden

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Amy L Roberts

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Catherine Schaffner

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Chack-Yung Yu

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Evan E Eichler

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H Terence Cook

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Helmut Schaschl

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Karyn Meltz Steinberg

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Laurence Game

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Matthew E Hurles

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P2860

Mapping and sequencing of structural variation from eight human genomes

Fast and accurate short read alignment with Burrows-Wheeler transform

Monoclonal antibodies capable of discriminating the human inhibitory Fcgamma-receptor IIB (CD32B) from the activating Fcgamma-receptor IIA (CD32A): biochemical, biological and functional characterization

BLAT--the BLAST-like alignment tool

CNV-seq, a new method to detect copy number variation using high-throughput sequencing

Fast and accurate long-read alignment with Burrows-Wheeler transform

Genomic organization of classical human low-affinity Fcgamma receptor genes.

Parallel tagged sequencing on the 454 platform.

Human neutrophil Fcgamma receptors initiate and play specialized nonredundant roles in antibody-mediated inflammatory diseases

Genetic dissection of the effects of stimulatory and inhibitory IgG Fc receptors on murine lupus.

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28-40

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23261299

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