PHD3 regulates glucose metabolism by suppressing stress-induced signalling and optimising gluconeogenesis and insulin signalling in hepatocytes. [electronic resource]
Producer: 20191030Description: 14290 p. digitalISSN:- 2045-2322
- Animals
- Cyclic AMP -- metabolism
- Cyclic AMP-Dependent Protein Kinases -- metabolism
- Enzyme Activation
- Gene Expression Regulation
- Glucagon -- metabolism
- Gluconeogenesis
- Glucose -- metabolism
- Hepatocytes -- metabolism
- Humans
- Inflammation -- genetics
- Insulin -- metabolism
- Interleukin-6 -- metabolism
- JNK Mitogen-Activated Protein Kinases -- metabolism
- Male
- Mice, Inbred C57BL
- Models, Biological
- NF-kappa B -- metabolism
- Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha -- metabolism
- Procollagen-Proline Dioxygenase -- genetics
- Prolyl Hydroxylases -- metabolism
- Repressor Proteins -- metabolism
- STAT3 Transcription Factor -- metabolism
- STAT6 Transcription Factor -- metabolism
- Signal Transduction
- Stress, Physiological
- Trans-Activators -- metabolism
- Unfolded Protein Response
- p300-CBP Transcription Factors -- metabolism
No physical items for this record
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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