GSM1406031[Accession] - GEO DataSets - NCBI

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Items: 3

Select item 2000460301.

Selective demethylation and altered gene expression are associated with ICF Syndrome in human induced pluripotent stem cells and mesenchymal stem cells

(Submitter supplied) Immunodeficiency, Centromeric Instability, and Facial Anomalies Type I (ICF1) Syndrome is a rare genetic disease caused by mutations in DNMT3B, a de novo DNA methyltransferase. However, the molecular basis of how DNMT3B-deficiency leads to ICF1 pathogenesis is unclear. Induced pluripotent stem cell (iPSC) technology facilitates the study of early human developmental diseases via facile in vitro paradigms. more...

Organism:: Homo sapiens

Type:: Expression profiling by high throughput sequencing; Methylation profiling by high throughput sequencing

Platform:: GPL11154
7 Samples

Download data: BED, TXT

Series

Accession:: GSE46030

ID:: 200046030

PubMed Full text in PMC Similar studies Analyze with GEO2R SRA Run Selector

Select item 1000111542.

Illumina HiSeq 2000 (Homo sapiens)

Organism:: Homo sapiens

10407 Series
180383 Samples

Platform

Accession:: GPL11154

ID:: 100011154

Select item 3014060313.

IMR90 iPS (RNA-Seq)

Organism:: Homo sapiens

Source name:: induced pluripotent stem cell

Platform:: GPL11154
Series:: GSE46030

Sample

Accession:: GSM1406031

ID:: 301406031

SRA Run Selector

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GSM1406031[Accession] (3)
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