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Articles

MIB1 mutations reduce Notch signaling activation and contribute to congenital heart disease

Binbin Li, Liwei Yu, Dong Liu, Xueyan Yang, Yufang Zheng, Yonghao Gui, Hongyan Wang
Journal: Clinical Science
Clin Sci (Lond) (2018) 132 (23): 2483–2491.
https://doi.org/10.1042/CS20180732
Published: 05 December 2018
View article titled, MIB1 mutations reduce Notch signaling activation and contribute to congenital heart disease
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Includes: Supplementary data
Articles

Genetic analysis of rare coding mutations of CELSR1–3 in congenital heart and neural tube defects in Chinese people

Xiaojin Qiao, Yahui Liu, Peiqiang Li, Zhongzhong Chen, Huili Li, Xueyan Yang, Richard H. Finnell, Zhangmin Yang, Ting Zhang, Bin Qiao, Yufang Zheng, Hongyan Wang
Journal: Clinical Science
Clin Sci (Lond) (2016) 130 (24): 2329–2340.
https://doi.org/10.1042/CS20160686
Published: 15 November 2016
View article titled, Genetic analysis of rare coding mutations of CELSR1–3 in congenital heart and neural tube defects in Chinese people
Open the PDF for Genetic analysis of rare coding mutations of CELSR1–3 in congenital heart and neural tube defects in Chinese people in another window
Includes: Supplementary data