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Home › Dataset Library › Transcript level in F9 teratocarcinoma WT and RARalpha knockout in presence and absence of all-trans retinoic acid

Dataset: Transcript level in F9 teratocarcinoma WT and RARalpha knockout in presence and absence of all-trans retinoic acid

Retinoic acid receptors (RARs) α, β and γ are key regulators of embryonic development. Hematopoietic differentiation is regulated by...

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Retinoic acid receptors (RARs) α, β and γ are key regulators of embryonic development. Hematopoietic differentiation is regulated by RARα, and several types of leukemia show aberrant RARα activity. We demonstrate that RARα plays an important role in cellular memory and imprinting by regulating the CpG methylation status of specific promoter regions. We used microarrays to identify genes, which display differential expression in F9 RARalpha knockout (RARaKO) cells relative to F9 wt cells. F9 teratocarcinoma cells (WT and RARaKO) were treated for 8 hours with either vehicle (EtOH) or all-trans Retinoic Acid (atRA) in the presence of the protein synthesis inhibitor Cycloheximide

Species:
mouse

Samples:
12

Source:
E-GEOD-31280

Updated:
Dec.12, 2014

Registered:
Nov.11, 2014


Factors: (via ArrayExpress)
Sample GENOTYPE TREATMENT
GSM77529 RARaKO EtOH + cycloheximide
GSM775292 RARaKO atRA + cycloheximide
GSM775293 WT EtOH + cycloheximide
GSM775294 WT atRA + cycloheximide
GSM77529 RARaKO EtOH + cycloheximide
GSM775292 RARaKO atRA + cycloheximide
GSM775293 WT EtOH + cycloheximide
GSM775294 WT atRA + cycloheximide
GSM77529 RARaKO EtOH + cycloheximide
GSM775292 RARaKO atRA + cycloheximide
GSM775293 WT EtOH + cycloheximide
GSM775294 WT atRA + cycloheximide

Tags

  • leukemia
  • protein
  • teratocarcinoma

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