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Aging|October 12, 2023
A pan-cancer analysis of the role of HOXD1, HOXD3, and HOXD4 and validation in renal cell carcinomaLumin Wang, Xiaofei Wang, Haifeng Sun, et al.
Scientific Reports|October 28, 2024
Meloidogyne incognita genes involved in the repellent behavior in response to ascr#9Zhongchen Rao, Kang Dai, Richou Han, et al.
Yao Xue Xue Bao = Acta Pharmaceutica Sinica|June 24, 2009
[Establishment of pharmacological evaluation system for non-nucleoside reverse-transcriptase inhibitors resistant HIV-1]Ying-li Cao, Shao-xiong Li, Hong Chen, et al.
American Journal of Translational Research|May 10, 2016
VEGFR-3 blocking deteriorates inflammation with impaired lymphatic function and different changes in lymphatic vessels in acute and chronic colitisXiao-Lei Wang, Jing Zhao, Li Qin, et al.
Minerva Cardiology and Angiology|January 23, 2025
The effect of propolis supplementation on blood pressure: a systematic review and meta-analysis of controlled trialsHongyan Qu, Li Cao, Ziye Wen, et al.
BMC Complementary Medicine and Therapies|September 2, 2022
Effects of plant-based medicinal food on postoperative recurrence and lung metastasis of gastric cancer regulated by Wnt/β-catenin-EMT signaling pathway and VEGF-C/D-VEGFR-3 cascade in a mouse modelLin Tian, Xuxi Chen, Li Cao, et al.
IEEE Transactions on Neural Networks and Learning Systems|November 30, 2021
Learning Deep Blind Quality Assessment for Cartoon ImagesYuan Chen, Yang Zhao, Li Cao, et al.
Experimental and Molecular Pathology|September 3, 2019
Clinical features and molecular genetic analysis of thanatophoric dysplasia type I in a neonate with a de novo c.2419 T > C (p. Ter807Arg) (X807R) mutation in FGFR3Gaoli Jiang, Xuexin Chen, Dan Dai, et al.
International Journal of Clinical Pharmacy|November 8, 2022
Clinical effects of remimazolam alone or in combination with dexmedetomidine in patients receiving bronchoscopy and influences on postoperative cognitive function: a randomized-controlled trialShenqiang Gao, Tingting Wang, Li Cao, et al.
Annals of Clinical and Translational Neurology|January 9, 2023
PLP1 gene mutations cause spastic paraplegia type 2 in three familiesLi Yao, Zeyu Zhu, Chao Zhang, et al.
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