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Serine phosphorylation of RUNX2 with novel potential functions as negative regulatory mechanisms
The RUNX family represents a small group of heterodimeric transcription factors that master-regulate osteogenesis and hematopoiesis in mammals. Their genetic defects cause human diseases such as cleidocranial dysplasia (CCD) and acute myelogenous leukemia. However, the mechanism(s) regulating their...
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| Main Authors: | , , , |
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| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
2002
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1307622/ https://ncbi.nlm.nih.gov/pubmed/12231506 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/embo-reports/kvf193 |
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