Huiqing Liu
Wenhua West Road 44
Jinan, 250012, China
Jinan, 250012, China
Last Updated: 09/26/2026
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Found 50 publications
The protein arginine methyltransferase PRMT1 ameliorates cerebral ischemia-reperfusion injury by suppressing RIPK1-mediated necroptosis and apoptosis.
Journal: Acta pharmaceutica Sinica. B
Published: January 23, 2025
OTUD5 Protects Dopaminergic Neurons by Promoting the Degradation of α-Synuclein in Parkinson's Disease Model.
Journal: Advanced science (Weinheim, Baden-Wurttemberg, Germany)
Published: June 17, 2024
Molecular basis of CX-5461-induced DNA damage response in primary vascular smooth muscle cells.
Journal: Heliyon
Published: February 10, 2024
Identification of a small-molecule Tim-3 inhibitor to potentiate T cell-mediated antitumor immunotherapy in preclinical mouse models.
Journal: Science translational medicine
Published: November 15, 2023
E3 ubiquitin ligase TRIM31 alleviates dopaminergic neurodegeneration by promoting proteasomal degradation of VDAC1 in Parkinson's Disease model.
Journal: Cell death and differentiation
Published: July 11, 2023
OTUD1 ameliorates cerebral ischemic injury through inhibiting inflammation by disrupting K63-linked deubiquitination of RIP2.
Journal: Journal of neuroinflammation
Published: June 19, 2023
Blended learning model via small private online course improves active learning and academic performance of embryology.
Journal: Clinical anatomy (New York, N.Y.)
Published: September 11, 2021
USP5 attenuates NLRP3 inflammasome activation by promoting autophagic degradation of NLRP3.
Journal: Autophagy
Published: September 06, 2021
USP18 positively regulates innate antiviral immunity by promoting K63-linked polyubiquitination of MAVS.
Journal: Nature communications
Published: June 15, 2020
β-arrestin 2 negatively regulates NOD2 signalling pathway through association with TRAF6 in microglia after cerebral ischaemia/reperfusion injury.
Journal: Journal of cellular and molecular medicine
Published: September 19, 2018
Design, synthesis, and biologic evaluation of novel galloyl derivatives as HIV-1 RNase H inhibitors.
Design, synthesis, and biologic evaluation of novel galloyl derivatives as HIV-1 RNase H inhibitors.
Journal: Chemical biology & drug design
Published: July 24, 2018
Last Updated: 09/26/2026