Tie2Cre-mediated inactivation of plexinD1 results in congenital heart, vascular and skeletal defects
10.1016/j.ydbio.2008.09.031
Saved in:
Main Authors: | Zhang, Ying, Singh, Manvendra K, Degenhardt, Karl R, Lu, Min Min, Bennett, Jean, Yoshida, Yutaka, Epstein, Jonathan A |
---|---|
其他作者: | INSTITUTE OF DATA SCIENCE |
格式: | Article |
語言: | English |
出版: |
ACADEMIC PRESS INC ELSEVIER SCIENCE
2021
|
主題: | |
在線閱讀: | https://scholarbank.nus.edu.sg/handle/10635/201390 |
標簽: |
添加標簽
沒有標簽, 成為第一個標記此記錄!
|
相似書籍
-
GENETIC ANALYSIS AND FUNCTIONAL CHARACTERIZATIONS OF SEMAPHORIN 5A AND PLEXIN-B3 IN HUMAN GLIOMAS
由: FATHIMA RIFKHANA SHAH JAHAN
出版: (2015) -
Semaphorin3E-PlexinD1 signaling in coronary artery and lymphatic vessel development with clinical implications in myocardial recovery
由: Maruyama, Kazuaki, et al.
出版: (2021) -
Characterization of Sema5A/plexin-B3 signaling in the oligodendrocyte cell line OLN-93
由: YANG JIA
出版: (2011) -
Semaphorin 3E/PlexinD1 Signaling Is Required for Cardiac Ventricular Compaction.
由: SANDIREDDY REDDEMMA, et al.
出版: (2020) -
Characterization of signaling pathways and significance of the axon guidance molecule plexin-B3 in glioma progression
由: LI XINHUA
出版: (2010)