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Journal of Cellular Physiology|February 9, 2021
DOCK4 stimulates MUC2 production through its effect on goblet cell differentiationTingfeng Qin, Jie Yang, Dayin Huang, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|December 19, 2018
Hepatic mTOR-AKT2-Insig2 signaling pathway contributes to the improvement of hepatic steatosis after Roux-en-Y Gastric Bypass in miceQinling Pan, Tingfeng Qin, Yuan Gao, et al.
Ebiomedicine|June 4, 2018
Takeda G Protein-Coupled Receptor 5-Mechanistic Target of Rapamycin Complex 1 Signaling Contributes to the Increment of Glucagon-Like Peptide-1 Production after Roux-en-Y Gastric BypassHening Zhai, Zhi Li, Miao Peng, et al.
American Journal of Medical Genetics. Part A|September 13, 2022
Broadening the genotypic and phenotypic spectrum of MAF in three Chinese Han congenital cataracts familiesQiwei Wang, Tingfeng Qin, Haowen Tan, et al.
Genes|December 23, 2022
Whole-Exome Sequencing and Copy Number Analysis in a Patient with Warburg Micro SyndromeQiwei Wang, Tingfeng Qin, Xun Wang, et al.
Acta Pharmaceutica Sinica. B|June 13, 2020
Interleukin-27 decreases ghrelin production through signal transducer and activator of transcription 3-mechanistic target of rapamycin signalingHeng Zhang, Qingjie Li, Yuxin Teng, et al.
Ophthalmology Science|June 19, 2026
Anisometropia at Age 7 After Bilateral Secondary Intraocular Lens Implantation at 2 to Younger than 6 Years for Pediatric Aphakia: The CCPMOH ReportKun Hu, Wan Chen, Tingfeng Qin, et al.
JAMA Ophthalmology|May 15, 2025
Visual Acuity and Complications at Age 7 Years Following Bilateral Secondary Intraocular Lens Implantation at 2 to Younger Than 6 Years for Pediatric AphakiaKun Hu, Yu Zhang, Wan Chen, et al.
Genes|August 26, 2022
Unusual Presentation in WAGR Syndrome: Expanding the Phenotypic and Genotypic Spectrum of the DiseasesQiwei Wang, Xulin Zhang, Tingfeng Qin, et al.
BMC Medical Genomics|October 12, 2023
Novel compound heterozygous variants of the SEC23A gene in a Chinese family with cranio-lenticulo-sutural dysplasia based on data from a large cohort of congenital cataract patientsQiwei Wang, Xiaoshan Lin, Kunbei Lai, et al.
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