ロード中...

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...

詳細記述

保存先:
書誌詳細
主要な著者: Wee, Hee-Jun, Huang, Gang, Shigesada, Katsuya, Ito, Yoshiaki
フォーマット: Artigo
言語:Inglês
出版事項: 2002
主題:
オンライン・アクセス: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
タグ: タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!