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Bioelectrochemistry (Amsterdam, Netherlands)|September 14, 2023
Dumbbell hybridization chain reaction coupled with positively charged Au@luminol nanoparticles for enhanced electrochemiluminescent sensing of exosomal miRNA-21Yun Zhang, Shiqiang Li, Chenxu Peng, 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.
Biochemical and Biophysical Research Communications|May 14, 2011
Identification of CYP4V2 mutation in 21 families and overview of mutation spectrum in Bietti crystalline corneoretinal dystrophyXueshan Xiao, Guiying Mai, Shiqiang Li, et al.
Analytica Chimica Acta|April 19, 2021
Zettomole electrochemical HIV DNA detection using 2D DNA-Au nanowire structure, hemin/G-quadruplex and polymerase chain reaction multi-signal synergistic amplificationZongbing Li, Huanwen Xu, Shiqiang Li, et al.
Molecular Vision|January 8, 2020
Spectrum, frequency, and genotype-phenotype of mutations in <i>SPATA7</i>Xueshan Xiao, Wenmin Sun, Shiqiang Li, et al.
Experimental Eye Research|October 19, 2019
Pathogenicity discrimination and genetic test reference for CRX variants based on genotype-phenotype analysisZhen Yi, Xueshan Xiao, Shiqiang Li, et al.
Molecular Vision|July 24, 2014
Mutation survey of candidate genes in 40 Chinese patients with congenital ectopia lentisJie Li, Xiaoyun Jia, Shiqiang Li, et al.
International Journal of Biological Macromolecules|March 9, 2026
ALP1 polysaccharide promotes porcine intestinal epithelial proliferation through a CDK4-Cyclin E-dependent G1/S transitionQiyuan Luo, Shiqiang Li, Chenglong Zhang, et al.
Molecular Vision|September 11, 2020
Genotypes and phenotypes of genes associated with achromatopsia: A reference for clinical genetic testingWenmin Sun, Shiqiang Li, Xueshan Xiao, et al.
Ophthalmic & Physiological Optics : the Journal of the British College of Ophthalmic Opticians (Optometrists)|March 21, 2020
A novel deep intronic COL2A1 mutation in a family with early-onset high myopia/ocular-only Stickler syndromeWenmin Sun, Xueshan Xiao, Shiqiang Li, et al.
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