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Clinical Chemistry and Laboratory Medicine|February 8, 2021
Detection and functional characterization of a novel <i>MEF2A</i> variation responsible for familial dilated cardiomyopathyQi Qiao, Cui-Mei Zhao, Chen-Xi Yang, et al.
Plant Communications|January 7, 2026
Evolutionary origin of neohesperidoside, a bitter metabolite, and its potential role in biotic defense and citrus disseminationGu Li, Huan Wen, Hanxin Zhou, et al.
IUBMB Life|May 5, 2018
Integrated microRNA and mRNA sequencing analysis of age-related changes to mouse thymic epithelial cellsHong-Ling Jia, Xiao-Qin Zeng, Feng Huang, et al.
ACS Applied Materials & Interfaces|December 22, 2022
Cinnamate-Functionalized Cellulose Nanocrystals as Interfacial Layers for Efficient and Stable Perovskite Solar CellsJiayan Liu, Nana Liu, Gu Li, et al.
Zhonghua Yu Fang Yi Xue Za Zhi [Chinese Journal of Preventive Medicine]|February 9, 2010
[Correlates of bronchial asthma in Uygur and Han adults in Turpan prefecture, Xinjiang]Jing Wang, Man-Gu-Li Wu-Shou-Er Qi, Xia Li, et al.
Zhongguo Zhong Xi Yi Jie He Za Zhi Zhongguo Zhongxiyi Jiehe Zazhi = Chinese Journal of Integrated Traditional and Western Medicine|April 25, 2014
[C825T polymorphism of G protein beta3 subunit gene and Uygur Hilit type of essential hypertension: a correlation study]Xiao-Xi Li, Yu-Nu-Si A-Yi-Gu-Li, Jing-Jing Huang, et al.
Stem Cell Research & Therapy|July 24, 2023
Dendritic cells mediated by small extracellular vesicles derived from MSCs attenuated the ILC2 activity via PGE2 in patients with allergic rhinitisXiao-Qing Liu, Ya-Qi Peng, Long-Xin Huang, et al.
International Heart Journal|September 6, 2019
A New ISL1 Loss-of-Function Mutation Predisposes to Congenital Double Outlet Right VentricleZhi Wang, Hao-Ming Song, Fei Wang, et al.
European Journal of Medical Genetics|September 16, 2018
HAND2 loss-of-function mutation causes familial dilated cardiomyopathyHua Liu, Ying-Jia Xu, Ruo-Gu Li, et al.
International Journal of Medical Sciences|August 29, 2013
PITX2c loss-of-function mutations responsible for congenital atrial septal defectsFang Yuan, Lan Zhao, Juan Wang, et al.
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