A genome-wide association study identifies genetic variants in the CDKN2BAS locus associated with endometriosis in Japanese - Wikidata - wikimedia - TriplyDB

A genome-wide association study identifies genetic variants in the CDKN2BAS locus associated with endometriosis in Japanese

A genome-wide association study identifies genetic variants in the CDKN2BAS locus associated with endometriosis in Japanese

http://www.wikidata.org/entity/Q28286993

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Genome-wide association meta-analysis identifies new endometriosis risk loci Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis Genetics of endometriosis Genetics of primary ovarian insufficiency: new developments and opportunities Defining future directions for endometriosis research: workshop report from the 2011 World Congress of Endometriosis In Montpellier, France Molecular aspects of development and regulation of endometriosis The genetic basis of female reproductive disorders: etiology and clinical testing Guidelines for the design, analysis and interpretation of 'omics' data: focus on human endometrium Genome-wide association study link novel loci to endometriosis Apolipoprotein E polymorphisms and spontaneous pregnancy loss in patients with endometriosis Genetic variants underlying risk of endometriosis: insights from meta-analysis of eight genome-wide association and replication datasets ANRIL: molecular mechanisms and implications in human health A genome-wide association study in the Japanese population confirms 9p21 and 14q23 as susceptibility loci for primary open angle glaucoma Influence of common genetic variation on lung cancer risk: meta-analysis of 14 900 cases and 29 485 controls Islet biology, the CDKN2A/B locus and type 2 diabetes risk.Expression of linear and novel circular forms of an INK4/ARF-associated non-coding RNA correlates with atherosclerosis risk.Genome-wide genetic analyses highlight mitogen-activated protein kinase (MAPK) signaling in the pathogenesis of endometriosis.Revealing phenotype-associated functional differences by genome-wide scan of ancient haplotype blocks.Genome-wide association analysis of pain severity in dysmenorrhea identifies association at chromosome 1p13.2, near the nerve growth factor locus.Meta-analysis identifies five novel loci associated with endometriosis highlighting key genes involved in hormone metabolism The dynamics of nuclear receptors and nuclear receptor coregulators in the pathogenesis of endometriosis.CYP19 gene variant confers susceptibility to endometriosis-associated infertility in Chinese women.Autotaxin-lysophosphatidic acid-LPA3 signaling at the embryo-epithelial boundary controls decidualization pathways Endometriosis is associated with rare copy number variants.A polymorphism in a let-7 microRNA binding site of KRAS in women with endometriosis.Common variants in the CYP2C19 gene are associated with susceptibility to endometriosis.Risk Factors for Endometriosis in a German Case-Control Study.Advances in the genetics of endometriosis Common variants on chromosome 9p21 are associated with normal tension glaucoma.Common chromosomal imbalances and stemness-related protein expression markers in endometriotic lesions from different anatomical sites: the potential role of stem cells.Association between endometriosis and the interleukin 1A (IL1A) locus.An analysis of the association between a polymorphism of KCNJ11 and diabetic retinopathy in a Chinese Han population.Somatic copy number alterations associated with Japanese or endometriosis in ovarian clear cell adenocarcinoma Contribution of SLC30A8 variants to the risk of type 2 diabetes in a multi-ethnic population: a case control study.Whole-exome sequencing of endometriosis identifies frequent alterations in genes involved in cell adhesion and chromatin-remodeling complexes.Coding regions of INHBA, SFRP4 and HOXA10 are not implicated in familial endometriosis linked to chromosome 7p13-15.Ovarian cancer: new developments in clear cell carcinoma and hopes for targeted therapy.Genetic variation in the sex hormone metabolic pathway and endometriosis risk: an evaluation of candidate genes.Allelic Imbalance in Regulation of ANRIL through Chromatin Interaction at 9p21 Endometriosis Risk Locus Activated glucocorticoid and eicosanoid pathways in endometriosis.

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A genome-wide association study identifies genetic variants in the CDKN2BAS locus associated with endometriosis in Japanese

http://www.wikidata.org/entity/Q28286993

description

2010 nî lūn-bûn

@nan

2010 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի օգոստոսին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

@zh-hant

2010年論文

@zh-hk

2010年論文

@zh-mo

2010年論文

@zh-tw

2010年论文

@wuu

name

A genome-wide association stud ...... with endometriosis in Japanese

@ast

A genome-wide association stud ...... with endometriosis in Japanese

@en

A genome-wide association stud ...... with endometriosis in Japanese

@nl

type

label

A genome-wide association stud ...... with endometriosis in Japanese

@ast

A genome-wide association stud ...... with endometriosis in Japanese

@en

A genome-wide association stud ...... with endometriosis in Japanese

@nl

prefLabel

A genome-wide association stud ...... with endometriosis in Japanese

@ast

A genome-wide association stud ...... with endometriosis in Japanese

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A genome-wide association stud ...... with endometriosis in Japanese

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P1433

Nature Genetics

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A genome-wide association stud ...... with endometriosis in Japanese

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P2093

Akira Hirasawa

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Atsushi Takahashi

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Hitoshi Zembutsu

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Koichi Hirata

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Michiaki Kubo

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Satoko Uno

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Tomoko Akahane

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Yusuke Nakamura

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P2860

Chromosome 9p21 SNPs Associated with Multiple Disease Phenotypes Correlate with ANRIL Expression

INK4/ARF transcript expression is associated with chromosome 9p21 variants linked to atherosclerosis

Sexually dimorphic development of the mammalian reproductive tract requires Wnt-7a

New common variants affecting susceptibility to basal cell carcinoma

Genome-wide association study of intracranial aneurysm identifies three new risk loci

Genomewide association analysis of coronary artery disease

PLINK: a tool set for whole-genome association and population-based linkage analyses

Haploview: analysis and visualization of LD and haplotype maps

Molecular cloning, expression pattern, and chromosomal localization of human CDKN2D/INK4d, an inhibitor of cyclin D-dependent kinases

Efficiency and power in genetic association studies

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707-10

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scholarly article

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2433345

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10.1038/NG.612

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8

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42

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Naoyuki Kamatani

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2010-08-01T00:00:00Z

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20601957

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genome-wide association study