Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility - Wikidata - awgldk - TriplyDB

Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility

Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility

http://www.wikidata.org/entity/Q24630647

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Chromosome 9p21 SNPs Associated with Multiple Disease Phenotypes Correlate with ANRIL Expression Known glioma risk loci are associated with glioma with a family history of brain tumours--a case-control gene association study Risk factors for oligodendroglial tumors: a pooled international study Association between adult height, genetic susceptibility and risk of glioma Personal history of diabetes, genetic susceptibility to diabetes, and risk of brain glioma: a pooled analysis of observational studies Joint effects between five identified risk variants, allergy, and autoimmune conditions on glioma risk Genome-wide association study of glioma and meta-analysis Joint associations between genetic variants and reproductive factors in glioma risk among women Genetic epidemiology of glioblastoma multiforme: confirmatory and new findings from analyses of human leukocyte antigen alleles and motifs Further confirmation of germline glioma risk variant rs78378222 in TP53 and its implication in tumor tissues via integrative analysis of TCGA data A subset-based approach improves power and interpretation for the combined analysis of genetic association studies of heterogeneous traits TRF2 recruits RTEL1 to telomeres in S phase to promote t-loop unwinding Replication of lung cancer susceptibility loci at chromosomes 15q25, 5p15, and 6p21: a pooled analysis from the International Lung Cancer Consortium Recent advances in the molecular understanding of glioblastoma Long Non-coding RNA ANRIL and Polycomb in Human Cancers and Cardiovascular Disease Association between XRCC1 polymorphism 399 G->A and glioma among Caucasians: a systematic review and meta-analysis.The TERT rs2736100 polymorphism and cancer risk: a meta-analysis based on 25 case-control studies Inflammatory mechanisms linking periodontal diseases to cardiovascular diseases Molecular functions and cellular roles of the ChlR1 (DDX11) helicase defective in the rare cohesinopathy Warsaw breakage syndrome RTEL1 (regulator of telomere elongation helicase 1), a DNA helicase essential for genome stability Emerging critical roles of Fe-S clusters in DNA replication and repair.The MGMT promoter SNP rs16906252 is a risk factor for MGMT methylation in glioblastoma and is predictive of response to temozolomide Telomere maintenance and the etiology of adult glioma A RAD52 genetic variant located in a miRNA binding site is associated with glioma risk in Han Chinese Telomerase reverse transcriptase locus polymorphisms and cancer risk: a field synopsis and meta-analysis Genetic polymorphisms in the 9p21 region associated with risk of multiple cancers RTEL1 tagging SNPs and haplotypes were associated with glioma development The Glioma International Case-Control Study: A Report From the Genetic Epidemiology of Glioma International Consortium Inherited variation in immune genes and pathways and glioblastoma risk Association between RTEL1, PHLDB1, and TREH Polymorphisms and Glioblastoma Risk: A Case-Control Study Recurrent epimutations activate gene body promoters in primary glioblastoma Meta-analysis of genome-wide association studies identifies multiple lung cancer susceptibility loci in never-smoking Asian women Association between DNA repair gene polymorphisms and risk of glioma: a systematic review and meta-analysis High frequency of the X-chromosome inactivation in young female patients with high-grade glioma Reproductive factors and risk of primary brain tumors in women A genetic variant in the APE1/Ref-1 gene promoter -141T/G may modulate risk of glioblastoma in a Chinese Han population.The epidemiology of glioma in adults: a "state of the science" review Traumatic brain injury and subsequent glioblastoma development: Review of the literature and case reports Understanding inherited genetic risk of adult glioma - a review Genetics in glioma: lessons learned from genome-wide association studies

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P2860

Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility

http://www.wikidata.org/entity/Q24630647

description

2009 nî lūn-bûn

@nan

2009 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի օգոստոսին հրատարակված գիտական հոդված

@hy

2009年の論文

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2009年論文

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2009年論文

@zh-hant

2009年論文

@zh-hk

2009年論文

@zh-mo

2009年論文

@zh-tw

2009年论文

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name

Variants in the CDKN2B and RTE ...... gh-grade glioma susceptibility

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Variants in the CDKN2B and RTE ...... gh-grade glioma susceptibility

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Variants in the CDKN2B and RTE ...... gh-grade glioma susceptibility

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type

label

Variants in the CDKN2B and RTE ...... gh-grade glioma susceptibility

@ast

Variants in the CDKN2B and RTE ...... gh-grade glioma susceptibility

@en

Variants in the CDKN2B and RTE ...... gh-grade glioma susceptibility

@nl

prefLabel

Variants in the CDKN2B and RTE ...... gh-grade glioma susceptibility

@ast

Variants in the CDKN2B and RTE ...... gh-grade glioma susceptibility

@en

Variants in the CDKN2B and RTE ...... gh-grade glioma susceptibility

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Nature Genetics

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Variants in the CDKN2B and RTE ...... gh-grade glioma susceptibility

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Amanda L Rynearson

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Brian P O'Neill

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Caterina Giannini

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Chandralekha Halder

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Charles Quesenberry

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Daniel H LaChance

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Ivan Smirnov

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Jan C Buckner

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

Jeffrey S Chang

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

Joe Patoka

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

P2860

Population structure and eigenanalysis

Identification of a shared genetic susceptibility locus for coronary heart disease and periodontitis

Lung cancer susceptibility locus at 5p15.33

Comprehensive genomic characterization defines human glioblastoma genes and core pathways

Haploview: analysis and visualization of LD and haplotype maps

Principal components analysis corrects for stratification in genome-wide association studies

Regulation of murine telomere length by Rtel: an essential gene encoding a helicase-like protein

A genome-wide association study identifies an association of a common variant in TERT with susceptibility to idiopathic pulmonary fibrosis.

A susceptibility locus for lung cancer maps to nicotinic acetylcholine receptor subunit genes on 15q25

Score tests for association between traits and haplotypes when linkage phase is ambiguous

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905-8

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scholarly article

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2020276

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10.1038/NG.408

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P433

8

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41

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Alexander R. Pico

Karla V Ballman

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2009-08-01T00:00:00Z

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26648280

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1019657607

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19578366

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2923561

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