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ACS Omega|March 30, 2022
Integration of Phosphotungstic Acid into Zeolitic Imidazole Framework-67 for Efficient Methylene Blue AdsorptionShang Wei, Jiayi Wu, Peng Chen, et al.
Cell Death & Disease|July 20, 2023
circSLC4A7 accelerates stemness and progression of gastric cancer by interacting with HSP90 to activate NOTCH1 signaling pathwayYang Hui, Yuan Wenguang, Shang Wei, et al.
International Journal of Environmental Research and Public Health|July 11, 2020
Health Literacy of Osteoporosis Risks among Caregivers Serving in Disability Care FacilitiesLan-Ping Lin, Wei-Ju Lai, Shang-Wei Hsu, et al.
Kidney Research and Clinical Practice|April 10, 2023
An update on renal fibrosis: from mechanisms to therapeutic strategies with a focus on extracellular vesiclesCui Wang, Shang-Wei Li, Xin Zhong, et al.
BMC Nephrology|November 26, 2021
Identification of miRNA-mRNA network and immune-related gene signatures in IgA nephropathy by integrated bioinformatics analysisShi-Yao Wei, Shuang Guo, Bei Feng, et al.
International Journal of Biological Macromolecules|August 25, 2009
Effects of glutathione on amyloid fibrillation of hen egg-white lysozymeSteven S-S Wang, Shang-Wei Chou, Kuan-Nan Liu, et al.
Scientific Reports|February 9, 2022
Glucosamine-6-phosphate N-acetyltransferase gene silencing by parental RNA interference in rice leaf folder, Cnaphalocrocis medinalis (Lepidoptera: Pyralidae)Muhammad Shakeel, Juan Du, Shang-Wei Li, et al.
Annals of Noninvasive Electrocardiology : the Official Journal of the International Society for Holter and Noninvasive Electrocardiology, Inc|September 19, 2019
Value of ST-segment change in lead aVR in diagnosing left main disease in Non-ST-elevation acute coronary syndrome-A meta-analysisGien-Kuo Lee, Yen-Ping Hsieh, Shang-Wei Hsu, et al.
Molecular and Cellular Endocrinology|May 9, 2009
Analysis of differential expression and characterization of PIN in the gonads during sex reversal in the red-spotted grouperShang-Wei Li, Zhang-Fu Long, Juan Du, et al.
Molecular Genetics & Genomic Medicine|September 15, 2020
The single nucleotide variant at c.662A>G in human RRM2B is a loss-of-function mutationYen-Tzu Tseng, Shang-Wei Li, Wei-Chun HuangFu, et al.
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