The FOXE1 locus is a major genetic determinant for radiation-related thyroid carcinoma in Chernobyl.
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Thyroid transcription factors in development, differentiation and diseaseEfficient replication of over 180 genetic associations with self-reported medical dataDiscovery of common variants associated with low TSH levels and thyroid cancer riskFollow-up studies on genome damage in children after Chernobyl nuclear power plant accident.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 familyFOXE1 association with differentiated thyroid cancer and its progression.Investigation of DNA repair-related SNPs underlying susceptibility to papillary thyroid carcinoma reveals MGMT as a novel candidate gene in Belarusian children exposed to radiation.Genome-wide association and expression quantitative trait loci studies identify multiple susceptibility loci for thyroid cancerSignificant SNPs have limited prediction ability for thyroid cancer.The clinical features of papillary thyroid cancer in Hashimoto's thyroiditis patients from an area with a high prevalence of Hashimoto's disease.A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid functionCommon single nucleotide polymorphisms in genes related to immune function and risk of papillary thyroid cancer.Genetic predisposition to papillary thyroid carcinoma: involvement of FOXE1, TSHR, and a novel lincRNA gene, PTCSC2Association of the ATM gene polymorphisms with papillary thyroid cancer.An epistatic interaction between the PAX8 and STK17B genes in papillary thyroid cancer susceptibility.Thyroid-specific transcription factors and their roles in thyroid cancer.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 genetic variants related to genomic integrity and risk of papillary thyroid cancerVariants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studiesCommon 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.Common genetic variants in sex hormone pathway genes and papillary thyroid cancer risk.A single nucleotide polymorphism associated with isolated cleft lip and palate, thyroid cancer and hypothyroidism alters the activity of an oral epithelium and thyroid enhancer near FOXE1Replication and Meta-Analysis of Common Gene Mutations in TTF1 and TTF2 with Papillary Thyroid Cancer.Runs of homozygosity and inbreeding in thyroid cancer.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.Common genetic variants in metabolism and detoxification pathways and the risk of papillary thyroid cancerA gene expression signature distinguishes normal tissues of sporadic and radiation-induced papillary thyroid carcinomas.The HABP2 G534E variant is an unlikely cause of familial non-medullary thyroid cancer.A long non-coding RNA, PTCSC3, as a tumor suppressor and a target of miRNAs in thyroid cancer cells.Common genetic variants in pituitary-thyroid axis genes and the risk of differentiated thyroid cancer.Patterns of FOXE1 expression in papillary thyroid carcinoma by immunohistochemistry.Selected single-nucleotide polymorphisms in FOXE1, SERPINA5, FTO, EVPL, TICAM1 and SCARB1 are associated with papillary and follicular thyroid cancer risk: replication study in a German population.Clinical features of Hispanic thyroid cancer cases and the role of known genetic variants on disease riskrs965513 polymorphism as a common risk marker is associated with papillary thyroid cancerQuantitative assessment of common genetic variants on FOXE1 and differentiated thyroid cancer risk
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P2860
The FOXE1 locus is a major genetic determinant for radiation-related thyroid carcinoma in Chernobyl.
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年学术文章
@wuu
2010年学术文章
@zh
2010年学术文章
@zh-cn
2010年学术文章
@zh-hans
2010年学术文章
@zh-my
2010年学术文章
@zh-sg
2010年學術文章
@yue
2010年學術文章
@zh-hant
name
The FOXE1 locus is a major gen ...... hyroid carcinoma in Chernobyl.
@en
The FOXE1 locus is a major gen ...... hyroid carcinoma in Chernobyl.
@nl
type
label
The FOXE1 locus is a major gen ...... hyroid carcinoma in Chernobyl.
@en
The FOXE1 locus is a major gen ...... hyroid carcinoma in Chernobyl.
@nl
prefLabel
The FOXE1 locus is a major gen ...... hyroid carcinoma in Chernobyl.
@en
The FOXE1 locus is a major gen ...... hyroid carcinoma in Chernobyl.
@nl
P2093
P2860
P50
P356
P1476
The FOXE1 locus is a major gen ...... thyroid carcinoma in Chernobyl
@en
P2093
Chanavee Ratanajaraya
Fumihiko Matsuda
Hisako Takigawa-Imamura
Larisa I Danilova
Mark Lathrop
Maxim L Lushchik
Meiko Takahashi
Natallia M Akulevich
Noboru Takamura
Simon Heath
P2860
P304
P356
10.1093/HMG/DDQ123
P577
2010-03-29T00:00:00Z