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Home › Dataset Library › Transcription profiling of mouse NFI-C knock out embryonic fibroblasts

Dataset: Transcription profiling of mouse NFI-C knock out embryonic fibroblasts

The Nuclear Factor I C (NFI-C) transcription factor has been implicated in TGF-β signaling, extracellular matrix deposition and skin...

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The Nuclear Factor I C (NFI-C) transcription factor has been implicated in TGF-β signaling, extracellular matrix deposition and skin appendage pathologies. We performed a global gene expression analysis in NFI-C-/- and wild-type embryonic primary murine fibroblasts. This indicated that NFI-C acts mostly to repress gene expression in response to TGF-β1. Misregulated genes featured a prominent over-representation of regulators of connective tissue inflammation and repair. Experiment Overall Design: mRNAs were isolated from embryonic fibroblasts obtained from 3 wild-type and 3 NFI-C knock-out mice, and their levels were probed using microarrays. Prior to RNA extraction, fibroblast cultures were treated or not with TGF-β1 for 1 hour to examine the immediate response to the growth factor, or treated for 10 hours to assess the delayed response.

Species:
mouse

Samples:
18

Source:
E-GEOD-15871

PubMed:
19752192

Updated:
Dec.12, 2014

Registered:
Nov.11, 2014


Factors: (via ArrayExpress)
Sample
GSE15871GSM398437
GSE15871GSM398438
GSE15871GSM398439
GSE15871GSM398440
GSE15871GSM398441
GSE15871GSM398442
GSE15871GSM398443
GSE15871GSM398444
GSE15871GSM398445
GSE15871GSM398446
GSE15871GSM398447
GSE15871GSM398448
GSE15871GSM398449
GSE15871GSM398450
GSE15871GSM398451
GSE15871GSM398452
GSE15871GSM398453
GSE15871GSM398454

Tags

  • fibroblast
  • skin
  • skin appendage

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