Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8476985 | Molecular and Cellular Endocrinology | 2015 | 9 Pages |
Abstract
- GR ChIP-Seq identified primary targets in GC-treated mouse primary keratinocytes.
- Binding motifs for GR and Klf4 were over represented in GR ChIP-seq peaks.
- GR and Klf4 target Tsc22d3 and Zfp36, regulators of inflammation.
- GR is required for Klf4, Tsc22d3 and Zfp36 induction in terminal differentiation.
- GR negatively regulates Trp63 isoforms in keratinocytes.
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Authors
Lisa M. Sevilla, VÃctor Latorre, Elena Carceller, Julia Boix, Daniel Vodák, Ian Geoffrey Mills, Paloma Pérez,