Showing results (241-250 of 298) with videos related to
Sort By:
Pageof 30
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery|August 4, 2011
[Cochlear implantation with pericanal electrode insertion technique]Tingting Cui, Hong Jiang, Xiaowei Chen, et al.Journal of Ethnopharmacology|April 4, 2020
Anti-tumor effects and mechanisms of Astragalus membranaceus (AM) and its specific immunopotentiation: Status and prospectShanshan Li, Yi Sun, Jin Huang, et al.International Endodontic Journal|January 19, 2024
Circ-ZNF236 mediates stem cells from apical papilla differentiation by regulating LGR4-induced autophagyYa Xiao, Luyao Chen, Yunlong Xu, et al.Ophthalmic Research|November 21, 2023
The Impact of Parental Myopia and High Myopia on the Hyperopia Reserve of Preschool ChildrenJianing Pu, Yuxin Fang, Zhen Zhou, et al.Cell Death Discovery|January 20, 2022
DDX39B contributes to the proliferation of colorectal cancer through direct binding to CDK6/CCND1Haonan Zhang, Chengcheng He, Xuxue Guo, et al.BMC Ophthalmology|January 31, 2025
The prevalence and 6-year incidence of myopic tessellation in a Chinese rural adult population: the Handan Eye StudyCaixia Lin, Jian Wu, Kai Cao, et al.Experimental & Molecular Medicine|June 2, 2024
METTL3-mediated pre-miR-665/DLX3 m6A methylation facilitates the committed differentiation of stem cells from apical papillaTingjie Gu, Rong Guo, Yuxin Fang, et al.Ophthalmic Research|October 19, 2022
Hospital-Based Study of Risk Factors Associated with Development of Myopic Macular Neovascularization in Highly Myopic EyesRan Du, Shiqi Xie, Hongshuang Lu, et al.Journal of Human Genetics|December 15, 2010
Novel missense mutations in MYO7A underlying postlingual high- or low-frequency non-syndromic hearing impairment in two large families from ChinaYi Sun, Jing Chen, Hanjun Sun, et al.American Journal of Medical Genetics. Part A|September 10, 2005
Cosegregation of the G7444A mutation in the mitochondrial COI/tRNA(Ser(UCN)) genes with the 12S rRNA A1555G mutation in a Chinese family with aminoglycoside-induced and nonsyndromic hearing lossHuijun Yuan, Yaping Qian, Yanjun Xu, et al.Pageof 30