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World Journal of Clinical Cases|March 17, 2023
Clinical manifestations of adult hereditary spherocytosis with novel SPTB gene mutations and hyperjaundice: A case reportNi Jiang, Wu-Yong Mao, Bing-Xue Peng, et al.
Physical Review. E|December 23, 2022
Eigenfunction and eigenmode-spacing statistics in chaotic photonic crystal graphsShukai Ma, Thomas M Antonsen, Steven M Anlage
Physical Review. E|June 17, 2021
Generalization of Wigner time delay to subunitary scattering systemsLei Chen, Steven M Anlage, Yan V Fyodorov
Journal of Human Genetics|June 21, 2022
A novel homozygous missense mutation in the FASTKD2 gene leads to Lennox-Gastaut syndromeTenghui Wu, Leilei Mao, Chen Chen, et al.
Biochemical and Biophysical Research Communications|November 19, 2016
Potential suppression of the high glucose and insulin-induced retinal neovascularization by Sirtuin 3 in the human retinal endothelial cellsXin-Bang Mao, Zhi-Peng You, Chen Wu, et al.
Neuromolecular Medicine|April 10, 2024
Circular RNA-GRIN2B Suppresses Neuropathic Pain by Targeting the NF-κB/SLICK PathwayKun Wang, Zicong Shen, Xin Peng, et al.
American Journal of Physiology. Renal Physiology|November 7, 2024
Soluble (pro)renin receptor as a novel regulator of renal medullary Na+ reabsorptionTianxin Yang, Zhong-Xiuzi Gao, Zi-Hui Mao, et al.
World Journal of Gastroenterology|May 19, 2007
Bile duct injuries associated with laparoscopic and open cholecystectomy: sixteen-year experienceJin-Shu Wu, Chuang Peng, Xian-Hai Mao, et al.
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