1-3 of 3
Hongyan Wang
Close
Save search
Follow your search
Access your saved searches in your account
Would you like to receive an alert when new items match your search?
Close Modal
Sort by
Articles

Rare mutations of ADAM17 from TOFs induce hypertrophy in human embryonic stem cell-derived cardiomyocytes via HB-EGF signaling

Yifang Xie, Anyun Ma, Boshi Wang, Rui Peng, Yingchun Jing, Deqian Wang, Richard H. Finnell, Bin Qiao, Yongming Wang, Hongyan Wang, Yufang Zheng
Journal: Clinical Science
Clin Sci (Lond) (2019) 133 (2): 225–238.
DOI: https://doi.org/10.1042/CS20180842
Published: 22 January 2019
View article titled, Rare mutations of ADAM17 from TOFs induce hypertrophy in human embryonic stem cell-derived cardiomyocytes via HB-EGF signaling
Open the PDF for Rare mutations of ADAM17 from TOFs induce hypertrophy in human embryonic stem cell-derived cardiomyocytes via HB-EGF signaling in another window
Includes: Supplementary data
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.
DOI: 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
Open the PDF for MIB1 mutations reduce Notch signaling activation and contribute to congenital heart disease in another window
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.
DOI: 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