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TranscriptomicsScreening for chromosomal aberrations by array CGH in 74 patients with congenital hypothyroidism
Congenital Hypothyroidism occurs in 1:3500 live births and is therefore the most common congenital endocrine disorder. A spectrum of defective thyroid morphology, termed thyroid dysgenesis, represents 80% of permanent CH cases. Although several candidate genes have been implicated in thyroid develop...
ORGANISM(S): Homo sapiens 
2010-05-31 | E-GEOD-18152 | biostudies-arrayexpress
TranscriptomicsCongenital hypothryrodism and male rat liver: control vs congenital hypothryoidism
Transcriptional profiling of rat liver comparing male rats with congenital hypothyrodism (CH) vs intact at adulhood. Here we studied how CH influences liver gene expression program in adulthood. Thyroid hormones are required for normal growth and development in mammals. Congenital-neonatal hypothyro...
ORGANISM(S): Rattus norvegicus 
2012-03-10 | E-GEOD-32705 | biostudies-arrayexpress
GenomicsCongenital hypothyroidism in cats
Identification causal variant congenital hypothyroidism in cats
ORGANISM(S): Felis Catus 
2022-11-16 | PRJEB44876 | EVA
GenomicsThyroidal transcriptomic profiles of pathoadaptive responses to congenital hypothyroidism in XB130 knockout mic
Thyroidal transcriptomic profiles of pathoadaptive responses to congenital hypothyroidism in XB130 knockout mic
PRJNA808616 | ENA
Genomics
Congenital hypothyroidism in cats
PRJEB44876 | ENA
GenomicsEpigenome wide Association and Stochastic Epigenetic Mutation analysis on 23 twin pairs heterogeneously affected by Congenital Hypothyroidism (CH).
Epigenome wide Association and Stochastic Epigenetic Mutation analysis on 23 twin pairs heterogeneously affected by Congenital Hypothyroidism (CH).
PRJNA675352 | ENA
TranscriptomicsThyroidal transcriptomic profiles of pathoadaptive responses to congenital hypothyroidism in XB130 knockout mic
Congenital hypothyroidism is a genetic condition in which the thyroid gland fails to produce sufficient thyroid hormone (TH), resulting in metabolic dysfunction and growth retardation. Xb130-/- mice exhibit perturbations of thyrocyte cytoskeleton and polarity, develop postnatal transient growth reta...
ORGANISM(S): Mus musculus 
2024-10-12 | GSE197052 | GEO
GenomicsCHEG
genetic of congenital hypothyroidism with europic gland
PRJEB42666 | ENA
ProteomicsDiagnosis of congenital hypothyroidism using MALDI-TOF
Early diagnosis of Congenital Hypothyroidism (CH) is critical to prevent irreversible neurodevelopmental damage. However, current TSH-based newborn screening using Dried Blood Spots (DBS) is limited by factors that lead to false-positive and false-negative results, necessitating the development of a...
ORGANISM(S): Cellular Organisms 
PXD069100 | JPOST Repository
GenomicsScreening of mutations in congenital and isolated central hypothyroidism
Candidate gene sequencing of patients with congenital or isolated familial hypothyroidism.
ORGANISM(S): Homo Sapiens 
2021-05-21 | PRJEB45041 | EVA
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