Single-nucleotide polymorphisms and copy number variations of the FCGR2A and FCGR3A genes in healthy Japanese subjects. - Wikidata - awgldk - TriplyDB

Single-nucleotide polymorphisms and copy number variations of the FCGR2A and FCGR3A genes in healthy Japanese subjects.

Single-nucleotide polymorphisms and copy number variations of the FCGR2A and FCGR3A genes in healthy Japanese subjects.

http://www.wikidata.org/entity/Q37567714

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Genes with mutation significance were highly associated with the clinical pattern of patients with breast cancer.FcγRIIa defunctioning polymorphism in paediatric patients with renal allograft.

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Single-nucleotide polymorphisms and copy number variations of the FCGR2A and FCGR3A genes in healthy Japanese subjects.

http://www.wikidata.org/entity/Q37567714

description

article científic

@ca

article scientifique

@fr

articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 06 December 2013

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Single-nucleotide polymorphism ...... in healthy Japanese subjects.

@en

Single-nucleotide polymorphism ...... in healthy Japanese subjects.

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type

label

Single-nucleotide polymorphism ...... in healthy Japanese subjects.

@en

Single-nucleotide polymorphism ...... in healthy Japanese subjects.

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prefLabel

Single-nucleotide polymorphism ...... in healthy Japanese subjects.

@en

Single-nucleotide polymorphism ...... in healthy Japanese subjects.

@nl

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Biomedical Reports

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Single-nucleotide polymorphism ...... s in healthy Japanese subjects

@en

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Hiroyuki Moriya

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

Katsuhiko Saito

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

Masahiko Takasaki

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

Masato Takahashi

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

Michiaki Yamakage

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

Nahoko Kurosawa

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

Naomi Hayashi

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

Shigekazu Sugino

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

Takeru Sawaguchi

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

P2860

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

Immunoglobulin G Fc receptor FcgammaRIIIa 158 V/F polymorphism correlates with rituximab-induced neutropenia after autologous transplantation in patients with non-Hodgkin's lymphoma.

Copy number, linkage disequilibrium and disease association in the FCGR locus.

Copy number variation in the human genome and its implication in autoimmunity.

Fc gammaRIIIa-158V/F polymorphism influences the binding of IgG by natural killer cell Fc gammaRIIIa, independently of the Fc gammaRIIIa-48L/R/H phenotype.

Copy number variation at the FCGR locus includes FCGR3A, FCGR2C and FCGR3B but not FCGR2A and FCGR2B.

Increased natural killer cell expression of CD16, augmented binding and ADCC activity to rituximab among individuals expressing the Fc{gamma}RIIIa-158 V/V and V/F polymorphism

Genetic diversity in human Fc receptor II for immunoglobulin G: Fc gamma receptor IIA ligand-binding polymorphism.

Genetic association analysis of copy-number variation (CNV) in human disease pathogenesis

Copy number variation of Fc gamma receptor genes and disease predisposition.

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265-269

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scholarly article

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10.3892/BR.2013.210

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2

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2

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2013-12-06T00:00:00Z

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260951568

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24649108

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single-nucleotide polymorphism

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3917743

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