已发表成果:
WOK 论文 32 篇;中文核心 3 篇;专利发明 2 个;
Heat stress reduces brown adipose tissue activity by exacerbating mitochondrial damage in type 2 diabetic mice
Photocatalytic Polyamine Depletion for the Treatment of Psoriasis
N-Acylethanolamine acid amidase (NAAA) exacerbates psoriasis inflammation by enhancing dendritic cell (DCs) maturation
N-acylethanolamine acid amidase (NAAA) exacerbates psoriasis inflammation by enhancing dendritic cell (DCs) maturation (vol 185, 106491, 2022)
Phytochemical wedelolactone reverses obesity by prompting adipose browning through SIRT1/AMPK/ PPAR alpha pathway via targeting nicotinamide N-methyltransferase
Thermosensitive Poly(DHSe/PEG/PPG Urethane)-Based Hydrogel Extended Remdesivir Application in Ophthalmic Medication
NAAA inhibitor F96 attenuates BBB disruption and secondary injury after traumatic brain injury (TBI)
Ankfn1-mutant vestibular defects require loss of both ancestral and derived paralogs for penetrance in zebrafish
Spotlight on Isl1: A Key Player in Cardiovascular Development and Diseases
Inhibition of ceramide de novo synthesis ameliorates meibomian gland dysfunction induced by SCD1 deficiency
Zebrafish Models in Therapeutic Research of Cardiac Conduction Disease
NF-kappa B pathway play a role in SCD1 deficiency-induced ceramide de novo synthesis
Palmitoylethanolamide (PEA) reduces postoperative adhesions after experimental strabismus surgery in rabbits by suppressing canonical and non-canonical TGF beta signaling through PPAR alpha
Natural Potent NAAA Inhibitor Atractylodin Counteracts LPS-Induced Microglial Activation
N-Palmitoylethanolamine Maintains Local Lipid Homeostasis to Relieve Sleep Deprivation-Induced Dry Eye Syndrome
Immunomodulatory effect of oleoylethanolamide in dendritic cells via TRPV1/AMPK activation
Verruculosins A-B, New Oligophenalenone Dimers from the Soft Coral-Derived Fungus Talaromyces verruculosus
N-Acylethanolamine acid amidase (NAAA) inhibitor F215 as a novel therapeutic agent for osteoarthritis
Synthesis, biological evaluation, and structure activity relationship (SAR) study of pyrrolidine amide derivatives as N-acylethanolamine acid amidase (NAAA) inhibitors
Oleoylethanolamide alleviates macrophage formation via AMPK/PPAR alpha/STAT3 pathway
Inflammation-restricted anti-inflammatory activities of a N-acylethanolamine acid amidase (NAAA) inhibitor F215
N-oleoylethanolamide suppresses intimal hyperplasia after balloon injury in rats through AMPK/PPAR alpha pathway
Identification of highly potent N-acylethanolamine acid amidase (NAAA) inhibitors: Optimization of the terminal phenyl moiety of oxazolidone derivatives
Wedelolactone, a plant coumarin, prevents vascular smooth muscle cell proliferation and injury-induced neointimal hyperplasia through Akt and AMPK signaling
Design, synthesis, and biological evaluation of oxazolidone derivatives as highly potent N-acylethanolamine acid amidase (NAAA) inhibitors
Design and synthesis of uracil urea derivatives as potent and selective fatty acid amide hydrolase inhibitors
Discovery of Uracil Derivatives as Potent Inhibitors of Fatty Acid Amide Hydrolase
Stearoyl-CoA desaturase-1 mediated cell apoptosis in colorectal cancer by promoting ceramide synthesis
Oleoylethanolamide, an endogenous PPAR-alpha ligand, attenuates liver fibrosis targeting hepatic stellate cells
Atheroprotective Effect of Oleoylethanolamide (OEA) Targeting Oxidized LDL
Alteration of endocannabinoid system in human gliomas
Inhibition of tumor-induced edema by antisense VEGF is mediated by suppressive vesiculo-vacuolar organelles (VVO) formation
盾壳霉次生代谢活性成分研究进展
中国新药杂志,1003-3734,2018-9-30.独活挥发油对N-脂肪酰基乙醇胺水解酶的抑制作用及抗炎作用研究
中国中药杂志,1001-5302,2011.油酰乙醇胺对氧化性低密度脂蛋白诱发的动脉粥样硬化反应的作用
厦门大学学报(自然科学版),0438-0479,2011.