Unknown,Transcriptomics,Genomics,Proteomics

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Somatic CNV profile of congenital ectopic thyroids


ABSTRACT: To assess whether specific genes have relevant somatic genetic or epigenetic alterations in ectopic tissue, we used a combined analysis of transcriptome (confirmed by qRT-PCR on 68 genes), methylome, structural genome variations (copy number variants, CNVs) and miRNA profile of ectopic compared with orthotopic thyroids. DNA form three ectopic thyroid compared with matched leucocytes.

ORGANISM(S): Homo sapiens

SUBMITTER: Johnny Deladoëy 

PROVIDER: E-GEOD-17463 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

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Publications

Transcriptome, methylome and genomic variations analysis of ectopic thyroid glands.

Abu-Khudir Rasha R   Paquette Jean J   Lefort Anne A   Libert Frederick F   Chanoine Jean-Pierre JP   Vassart Gilbert G   Deladoëy Johnny J  

PloS one 20101015 10


<h4>Background</h4>Congenital hypothyroidism from thyroid dysgenesis (CHTD) is predominantly a sporadic disease characterized by defects in the differentiation, migration or growth of thyroid tissue. Of these defects, incomplete migration resulting in ectopic thyroid tissue is the most common (up to 80%). Germinal mutations in the thyroid-related transcription factors NKX2.1, FOXE1, PAX-8, and NKX2.5 have been identified in only 3% of patients with sporadic CHTD. Moreover, a survey of monozygoti  ...[more]

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