Thyroid cancer susceptibility polymorphisms: confirmation of loci on chromosomes 9q22 and 14q13, validation of a recessive 8q24 locus and failure to replicate a locus on 5q24 - Wikidata - wikimedia - TriplyDB

Thyroid cancer susceptibility polymorphisms: confirmation of loci on chromosomes 9q22 and 14q13, validation of a recessive 8q24 locus and failure to replicate a locus on 5q24

Thyroid cancer susceptibility polymorphisms: confirmation of loci on chromosomes 9q22 and 14q13, validation of a recessive 8q24 locus and failure to replicate a locus on 5q24

http://www.wikidata.org/entity/Q28731755

about

Candidate locus analysis of the TERT-CLPTM1L cancer risk region on chromosome 5p15 identifies multiple independent variants associated with endometrial cancer risk Inherited variants in genes somatically mutated in thyroid cancer.Familial multinodular goiter syndrome with papillary thyroid carcinomas: mutational analysis of the associated genes in 5 cases from 1 Chinese family FOXE1 association with differentiated thyroid cancer and its progression.Genome-wide association and expression quantitative trait loci studies identify multiple susceptibility loci for thyroid cancer Significant SNPs have limited prediction ability for thyroid cancer.Polymorphisms on 8q24 are associated with lung cancer risk and survival in Han Chinese Association between the rs2910164 polymorphism in pre-Mir-146a sequence and thyroid carcinogenesis.Association of the miR-149 Rs2292832 polymorphism with papillary thyroid cancer risk and clinicopathologic characteristics in a Chinese population Genetic predisposition to papillary thyroid carcinoma: involvement of FOXE1, TSHR, and a novel lincRNA gene, PTCSC2 An epistatic interaction between the PAX8 and STK17B genes in papillary thyroid cancer susceptibility.Novel genetic variants in differentiated thyroid cancer and assessment of the cumulative risk.Common variants at the 9q22.33, 14q13.3 and ATM loci, and risk of differentiated thyroid cancer in the Cuban population.A functional insertion/deletion polymorphism in the promoter region of the NFKB1 gene increases the risk of papillary thyroid carcinoma.Common variants at 9q22.33, 14q13.3, and ATM loci, and risk of differentiated thyroid cancer in the French Polynesian population.Multiple functional variants in long-range enhancer elements contribute to the risk of SNP rs965513 in thyroid cancer.Replication and Meta-Analysis of Common Gene Mutations in TTF1 and TTF2 with Papillary Thyroid Cancer.Association of Pre-miR-146a rs2910164 Polymorphism with Papillary Thyroid Cancer Association between microRNA polymorphisms and papillary thyroid cancer susceptibility.The polymorphism rs944289 predisposes to papillary thyroid carcinoma through a large intergenic noncoding RNA gene of tumor suppressor type.The 8q24 rs6983267G variant is associated with increased thyroid cancer risk.PTCSC3 Is Involved in Papillary Thyroid Carcinoma Development by Modulating S100A4 Gene Expression.Long noncoding RNA CCAT2 as a novel biomaker of metastasis and prognosis in human cancer: a meta-analysis.The HABP2 G534E variant is an unlikely cause of familial non-medullary thyroid cancer.Patterns of FOXE1 expression in papillary thyroid carcinoma by immunohistochemistry.Clinical features of Hispanic thyroid cancer cases and the role of known genetic variants on disease risk Are pre-miR-146a and PTTG1 associated with papillary thyroid cancer?rs965513 polymorphism as a common risk marker is associated with papillary thyroid cancer Quantitative assessment of common genetic variants on FOXE1 and differentiated thyroid cancer risk Genetic variation at 8q24, family history of cancer, and upper gastrointestinal cancers in a Chinese population.MicroRNA-related sequence variations in human cancers.Genetic predisposition for nonmedullary thyroid cancer.Molecular genetics of thyroid cancer.Association of rs6983267 Polymorphism and Thyroid Cancer Susceptibility: A Systematic Review and Meta-Analysis.Thyroid cancer with concurrent breast tubular cancer: A case report and literature review.Fine-mapping of two differentiated thyroid carcinoma susceptibility loci at 9q22.33 and 14q13.3 detects novel candidate functional SNPs in Europeans from metropolitan France and Melanesians from New Caledonia.Papillary Thyroid Carcinoma: Association Between Germline DNA Variant Markers and Clinical Parameters.Association between 8q24 rs6983267 polymorphism and cancer susceptibility: a meta-analysis involving 170,737 subjects.Thyroid transcription factor FOXE1 interacts with ETS factor ELK1 to co-regulate TERT.Genetic polymorphisms of non-coding RNAs associated with increased head and neck cancer susceptibility: a systematic review and meta-analysis.

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Thyroid cancer susceptibility polymorphisms: confirmation of loci on chromosomes 9q22 and 14q13, validation of a recessive 8q24 locus and failure to replicate a locus on 5q24

http://www.wikidata.org/entity/Q28731755

description

2012 nî lūn-bûn

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2012 թուականի Մարտին հրատարակուած գիտական յօդուած

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Thyroid cancer susceptibility ...... e to replicate a locus on 5q24

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JMEDGENET-2011-100586

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Journal of Medical Genetics

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Thyroid cancer susceptibility ...... e to replicate a locus on 5q24

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Andrew Coatesworth

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Angela M Jones

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Caroline Bremmer

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Catherine Lemon

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Craig Martin

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Danielle Power

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Elena Macias

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Georgina Gerrard

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Hisham Mehanna

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Hosahalli Mohan

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P2860

A flexible and accurate genotype imputation method for the next generation of genome-wide association studies

The role of microRNA genes in papillary thyroid carcinoma

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

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

Haploview: analysis and visualization of LD and haplotype maps

Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer

A new multipoint method for genome-wide association studies by imputation of genotypes

Fine-mapping of colorectal cancer susceptibility loci at 8q23.3, 16q22.1 and 19q13.11: refinement of association signals and use of in silico analysis to suggest functional variation and unexpected candidate target genes.

Pathogenetic mechanisms in thyroid follicular-cell neoplasia.

Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations

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