A RUNX2/PEBP2αA/CBFA1 mutation displaying impaired transactivation and Smad interaction in cleidocranial dysplasia

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書目詳細資料
發表在:Proc Natl Acad Sci U S A
Main Authors: Zhang, Yu-Wen, Yasui, Natsuo, Ito, Kosei, Huang, Gang, Fujii, Makiko, Hanai, Jun-ichi, Nogami, Hiroshi, Ochi, Takahiro, Miyazono, Kohei, Ito, Yoshiaki
格式: Artigo
語言:Inglês
出版: National Academy of Sciences 2000
主題:
Biological Sciences
在線閱讀:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC27062/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/10962029/
https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.180309597
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