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Analytica Chimica Acta|September 6, 2017
Simultaneous fluorescent detection of multiple metal ions based on the DNAzymes and graphene oxideWen Yun, Hong Wu, Xingyan Liu, et al.
The Journal of Urology|April 17, 2002
Decreased renal expression of the putative calcium oxalate inhibitor Tamm-Horsfall protein in the ethylene glycol rat model of calcium oxalate urolithiasisSusan Ruth Marengo, Daniel H-C Chen, Hue-Lee C Kaung, et al.
Ophthalmic Genetics|June 29, 2018
Clinical and genetic features of eight Chinese autosomal-dominant optic atrophy pedigrees with six novel OPA1 pathogenic variantsHuajin Li, Evan M Jones, Hui Li, et al.
Analytical Methods : Advancing Methods and Applications|May 16, 2023
Dual-amplification colorimetric detection of bisphenol A based on catalytic hairpin assembly and DNAzyme-caused fragment self-assembly hybridization chain reactionWen Yun, Yiyan Lin, Ruiqi Wang, et al.
Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy|December 21, 2020
A "turn-on" and proximity ligation assay dependent DNA tweezer for one-step amplified fluorescent detection of DNAWen Yun, Hanhong Zhu, Hong Wu, et al.
Experimental Eye Research|December 10, 2020
Clinical and genetic analysis of the ABCA4 gene associated retinal dystrophy in a large Chinese cohortZixi Sun, Lizhu Yang, Hui Li, et al.
Analytical Chemistry|April 20, 2026
Overcoming the Thermodynamic Diffusion Barrier in DNA Cascade Amplifiers via Spatially Confined Entropy Reduction: A Versatile Kinetic Engineering FrameworkZhenyu Wang, Youwei Chen, Zhiyi Wu, et al.
Investigative Ophthalmology & Visual Science|May 2, 2017
IFT81 as a Candidate Gene for Nonsyndromic Retinal DegenerationRachayata Dharmat, Wei Liu, Zhongqi Ge, et al.
Oncology Reports|July 20, 2016
A novel double carbonyl analog of curcumin induces the apoptosis of human lung cancer H460 cells via the activation of the endoplasmic reticulum stress signaling pathwayHui Ye, Xiaoyan Wei, Zhankun Wang, et al.
Investigative Ophthalmology & Visual Science|December 6, 2014
A homozygous missense mutation in NEUROD1 is associated with nonsyndromic autosomal recessive retinitis pigmentosaFeng Wang, Huajin Li, Mingchu Xu, et al.
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