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International Journal of Molecular Medicine|June 28, 2012
Mutation screening of TRPM1, GRM6, NYX and CACNA1F genes in patients with congenital stationary night blindnessQin Wang, Yang Gao, Shiqiang Li, et al.
Analytica Chimica Acta|April 18, 2024
Confined DNA tetrahedral molecular sieve for size-selective electrochemiluminescence sensingShiqiang Li, Mingyu Leng, Zongbing Li, et al.
Nanotechnology|July 6, 2011
Sol-gel assisted ZnO nanorod array template to synthesize TiO(2) nanotube arraysJijun Qiu, Weidong Yu, Xiangdong Gao, et al.
Cancer Gene Therapy|October 27, 2018
Increased invasive phenotype of CSF-1R expression in glioma cells via the ERK1/2 signaling pathwayLibo Sun, Huaxin Liang, Weidong Yu, et al.
Polymers|November 27, 2024
High-Strength and Conductive Electrospun Nanofiber YarnsQingqing Shao, Bo Xing, Zhaoqun Du, et al.
International Journal of General Medicine|October 29, 2020
Artery of Percheron as a Rare Feeder of Hemorrhagic Thalamic Arteriovenous Malformation: A Case Report and Literature ReviewMengchao Zhang, Zheng Feng, Weidong Yu, et al.
Sensors (Basel, Switzerland)|May 14, 2025
A General Numerical Error Compensation Method for NLFM Signal in SAR System Based on Non-Start-Stop ModelGui Wang, Heng Zhang, Bo Li, et al.
International Journal of Molecular Medicine|August 2, 2011
KIF21A novel deletion and recurrent mutation in patients with congenital fibrosis of the extraocular muscles-1Panfeng Wang, Shiqiang Li, Xueshan Xiao, et al.
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