An integrated approach for measuring copy number variation at the FCGR3 (CD16) locus. - Wikidata - wikimedia - TriplyDB

An integrated approach for measuring copy number variation at the FCGR3 (CD16) locus.

An integrated approach for measuring copy number variation at the FCGR3 (CD16) locus.

http://www.wikidata.org/entity/Q43226483

about

The contribution of genetic variation and infection to the pathogenesis of ANCA-associated systemic vasculitis Simple and versatile molecular method of copy-number measurement using cloned competitors The CNVrd2 package: measurement of copy number at complex loci using high-throughput sequencing data.FCGR2C genotyping by pyrosequencing reveals linkage disequilibrium with FCGR3A V158F and FCGR2A H131R polymorphisms in a Caucasian population.Association of FCGR3A and FCGR3B copy number variations with systemic lupus erythematosus and rheumatoid arthritis in Taiwanese patients.Genotyping Single Nucleotide Polymorphisms and Copy Number Variability of the FCGRs Expressed on NK Cells.Determination of beta-defensin genomic copy number in different populations: a comparison of three methods.Copy number, linkage disequilibrium and disease association in the FCGR locus.Genomic pathology of SLE-associated copy-number variation at the FCGR2C/FCGR3B/FCGR2B locus.FCGR2B and FCRLB gene polymorphisms associated with IgA nephropathy.CNVrd, a read-depth algorithm for assigning copy-number at the FCGR locus: population-specific tagging of copy number variation at FCGR3B Accurate measurement of gene copy number for human alpha-defensin DEFA1A3.Copy number variation of Fc gamma receptor genes in HIV-infected and HIV-tuberculosis co-infected individuals in sub-Saharan Africa A comparison of assays for accurate copy number measurement of the low-affinity Fc gamma receptor genes FCGR3A and FCGR3B.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.Association analysis of copy numbers of FC-gamma receptor genes for rheumatoid arthritis and other immune-mediated phenotypes.Assessment of complement C4 gene copy number using the paralog ratio test.Association of variation in Fcgamma receptor 3B gene copy number with rheumatoid arthritis in Caucasian samples.FCGR3B copy number variation is associated with systemic lupus erythematosus risk in Afro-Caribbeans.Susceptibility for Lupus Nephritis by Low Copy Number of the FCGR3B Gene Is Linked to Increased Levels of Pathogenic Autoantibodies.Comparison of Multiple Methods for Determination of FCGR3A/B Genomic Copy Numbers in HapMap Asian Populations with Two Public Databases.HLA-DQA1 and PLA2R1 polymorphisms and risk of idiopathic membranous nephropathy.Single-nucleotide polymorphisms and copy number variations of the FCGR2A and FCGR3A genes in healthy Japanese subjects.Low-affinity Fcgamma receptors, autoimmunity and infection.β-Defensin Genomic Copy Number Does Not Influence the Age of Onset in Huntington's Disease.The clinical context of copy number variation in the human genome.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.Correlating multiallelic copy number polymorphisms with disease susceptibility.Human gene copy number variation and infectious disease.Fcγ receptors: genetic variation, function, and disease.Analysis of Copy Number Variation Using the Paralogue Ratio Test (PRT).A worldwide analysis of beta-defensin copy number variation suggests recent selection of a high-expressing DEFB103 gene copy in East Asia.Low α-defensin gene copy number increases the risk for IgA nephropathy and renal dysfunction.Accurate interrogation of FCGR3A rs396991 in European and Asian populations using a widely available TaqMan genotyping method.Association study of copy number variants in FCGR3A and FCGR3B gene with risk of ankylosing spondylitis in a Chinese population.Evidence for both copy number and allelic (NA1/NA2) risk at the FCGR3B locus in systemic lupus erythematosus.Automated design of paralogue ratio test assays for the accurate and rapid typing of copy number variation.Population genetics of immune-related multilocus copy number variation in Native Americans.Low copy number of FCGR3B is associated with lupus nephritis in a Chinese population.

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P2860

An integrated approach for measuring copy number variation at the FCGR3 (CD16) locus.

http://www.wikidata.org/entity/Q43226483

description

2009 nî lūn-bûn

@nan

2009年の論文

@ja

2009年学术文章

@wuu

2009年学术文章

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2009年学术文章

@zh-cn

2009年学术文章

@zh-hans

2009年学术文章

@zh-my

2009年学术文章

@zh-sg

2009年學術文章

@yue

2009年學術文章

@zh-hant

name

An integrated approach for measuring copy number variation at the FCGR3 (CD16) locus.

@en

An integrated approach for measuring copy number variation at the FCGR3

@nl

type

label

An integrated approach for measuring copy number variation at the FCGR3 (CD16) locus.

@en

An integrated approach for measuring copy number variation at the FCGR3

@nl

prefLabel

An integrated approach for measuring copy number variation at the FCGR3 (CD16) locus.

@en

An integrated approach for measuring copy number variation at the FCGR3

@nl

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An integrated approach for measuring copy number variation at the FCGR3 (CD16) locus.

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Edward J Hollox

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

Jan-Christoph Detering

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Tushna Dehnugara

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P2860

Fine-scale structural variation of the human genome

Extensive normal copy number variation of a beta-defensin antimicrobial-gene cluster.

Sequences of complementary DNAs that encode the NA1 and NA2 forms of Fc receptor III on human neutrophils

Global variation in copy number in the human genome

A haplotype map of 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

Beta-defensin genomic copy number is not a modifier locus for cystic fibrosis.

Detection of large-scale variation in the human genome

Segmental duplications and copy-number variation in the human genome.

Copy number polymorphism and expression level variation of the human alpha-defensin genes DEFA1 and DEFA3

P304

477-484

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scholarly article

P356

10.1002/HUMU.20911

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3

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30

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2009-03-01T00:00:00Z

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23786489

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19143032

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3600569

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