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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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Bibliografiske detaljer
Main Authors: Wee, Hee-Jun, Huang, Gang, Shigesada, Katsuya, Ito, Yoshiaki
Format: Artigo
Sprog:Inglês
Udgivet: 2002
Fag:
Online adgang: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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