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Article

Identification of a novel germline FOXE1 variant in patients with familial non-medullary thyroid carcinoma (FNMTC)

9 Nov 2014

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Share to BRCA gene mutations in cancer
Share to FOXO transcription factor regulation
Share to Thyroid Cancer Diagnosis and Treatment

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 25381600
DOI: 10.1007/s12020-014-0470-0

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Related research

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Research trail→

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Identification of a novel germline FOXE1 variant in patients with familial non-medullary thyroid carcinoma (FNMTC)PMID 25381600Read ↗

The FOXE1 locus is a major genetic determinant for familial nonmedullary thyroid carcinoma.Semantic proximity Read ↗

FOXE1 polymorphisms are associated with familial and sporadic nonmedullary thyroid cancer susceptibility.Semantic proximity Read ↗

Familial nonmedullary thyroid cancer: screening, clinical, molecular and genetic findings.Semantic proximity Read ↗

Genetics of Familial Non-Medullary Thyroid Carcinoma (FNMTC)Semantic proximity Read ↗

Somatic Mutations of FOXE1 in Papillary Thyroid Cancer.Semantic proximity Read ↗

Identification of susceptibility gene mutations associated with the pathogenesis of familial nonmedullary thyroid cancer.Semantic proximity Read ↗

Targeted DNA Sequencing Detects Mutations Related to Susceptibility among Familial Non-medullary Thyroid Cancer.Semantic proximity Read ↗

Familial Non-Medullary Thyroid Carcinoma: An UpdateSemantic proximity Read ↗

BROX haploinsufficiency in familial nonmedullary thyroid cancer.Semantic proximity Read ↗

Identification of Rare Noncoding Variants in Familial Nonmedullary Thyroid Carcinoma.Semantic proximity Read ↗

Familial non-medullary thyroid cancer: unraveling the genetic maze.Semantic proximity Read ↗

Co-Occurrence of Familial Non-Medullary Thyroid Cancer (FNMTC) and Hereditary Non-Polyposis Colorectal Cancer (HNPCC) Associated Tumors-A Cohort Study.Semantic proximity Read ↗

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