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American Journal of Physiology. Renal Physiology|February 15, 2018
Novel compound heterozygous CLCNKB gene mutations (c.1755A>G/c.848_850delTCT) cause classic Bartter syndromeChunli Wang, Ying Chen, Bixia Zheng, et al.
Journal of Molecular Endocrinology|July 19, 2011
Different effects of corticotropin-releasing factor and urocortin 2 on apoptosis of prostate cancer cells in vitroLai Jin, Qichun Zhang, Rui Guo, et al.
Chemico-Biological Interactions|August 1, 2024
Endothelial TRPV4 channel mediates the vasodilation induced by Tanshinone IIAPei Wang, Yuanyuan Gu, Jingping Lu, et al.
Clinical Epidemiology|August 31, 2023
Association Between Autoimmune Diseases and Sarcopenia: A Two-Sample Mendelian Randomization StudyQing Su, Chen Jin, Yi Yang, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|August 23, 2018
Long Non-Coding RNA MEG3 Functions as a Competing Endogenous RNA to Regulate HOXA11 Expression by Sponging miR-181a in Multiple MyelomaXuxing Shen, Hua Bai, Huayuan Zhu, et al.
Pflugers Archiv : European Journal of Physiology|January 15, 2021
A novel mutation in KCNH2 yields loss-of-function of hERG potassium channel in long QT syndrome 2Kai Gu, Duoduo Qian, Huiyuan Qin, et al.
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