Lan Xie

academy of military medical sciences - china

H指数:27

被引数:2,525

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Knockdown of PARM1 Alleviates Aortic Valve Calcification via the PRKCH-MAPK Signaling Pathway

PARM1敲低通过PRKCH-MAPK信号通路缓解主动脉瓣钙化

jacc basic to translational science

IF0

2025-05-280

Engineered M2 macrophage-derived extracellular vesicles with platelet membrane fusion for targeted therapy of atherosclerosis

重组M2型巨噬细胞衍生胞外囊泡与血小板膜融合靶向治疗动脉粥样硬化

BIOACTIVE MATERIALS

IF20.3

2024-05-015

OAAI

Unraveling the Roles of Dissolved Mn(2+) and Its Impact on the Electrode-Electrolyte Interface under Realistic Conditions

解开溶解的Mn(2) 的作用及其在现实条件下对电极-电解质界面的影响

ACS SUSTAINABLE CHEMISTRY & ENGINEERING

IF7.3

2024-04-180

PRE

Tailoring the Position of Ester Group on N-Alkyl Chains of Benzotriazole-based Small Molecule Acceptors for High-Performance Organic Solar Cells

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

IF16.9

2024-02-0511

PRE

Enhancing aortic valve drug delivery with PAR2-targeting magnetic nano-cargoes for calcification alleviation

NATURE COMMUNICATIONS

IF15.7

2024-01-165

OAAI

Fourier-Coefficients-Based Multiscale Seismic Inversion for Elastic and Fracture Parameters in Frequency Domain

IEEE TRANSACTIONS ON GEOSCIENCE AND REMOTE SENSING

IF8.6

2024-01-011

PRE

Emerging roles of macrophages in heart failure and associated treatment approaches

therapeutic advances in musculoskeletal disease

IF2.8

2023-04-286

OAAI

Piezo1 (Piezo-Type Mechanosensitive Ion Channel Component 1)-Mediated Mechanosensation in Macrophages Impairs Perfusion Recovery After Hindlimb Ischemia in Mice

Piezo1 (压电型机械敏感离子通道成分1) 介导的巨噬细胞机械感应损害小鼠后肢缺血后的灌注恢复

ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY

IF7.4

2023-04-0119

Palladium (II), platinum (II) and silver (I) complexes with oxazolines: Their synthesis, characterization, DFT calculation, molecular docking and antitumour effects

JOURNAL OF INORGANIC BIOCHEMISTRY

IF3.2

2023-02-013

PRE

Cardiac Piezo1 Exacerbates Lethal Ventricular Arrhythmogenesis by Linking Mechanical Stress with Ca2+Handling After Myocardial Infarction

RESEARCH

IF10.7

2023-01-0111

OAAI

FAIM Enhances the Efficacy of Mesenchymal Stem Cell Transplantation by Inhibiting JNK-Induced c-FLIP Ubiquitination and Degradation

STEM CELLS INTERNATIONAL

IF3.3

2022-09-301

OAAI

Lead Optimization: Synthesis and Biological Evaluation of PBT-1 Derivatives as Novel Antitumor Agents

ACS MEDICINAL CHEMISTRY LETTERS

IF4

2021-11-174

Design and Synthesis of Quinolizidine Derivatives as Influenza Virus and HIV-1 Inhibitors

CURRENT MEDICINAL CHEMISTRY

IF3.5

2021-08-134

Heme Oxygenase-1 in Macrophages Impairs the Perfusion Recovery After Hindlimb Ischemia by Suppressing Autolysosome-Dependent Degradation of NLRP3

巨噬细胞中的血红素Oxygenase-1通过抑制NLRP3的自溶酶体依赖性降解来损害后肢缺血后的灌注恢复

ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY

IF7.4

2021-05-0512

Scaffold Hopping-Driven Optimization of 4-(Quinazolin-4-yl)-3,4-dihydroquinoxalin-2(1H)-ones as Novel Tubulin Inhibitors

支架跳跃驱动的4-(Quinazolin-4-yl)-3，4-二氢喹喔啉-2 (1h)-酮作为新型微管蛋白抑制剂的优化

ACS MEDICINAL CHEMISTRY LETTERS

IF4

2019-12-3012

OAAI

Combining New Non-Nucleoside Reverse Transcriptase Inhibitors (RTIs) with AZT Results in Strong Synergism against Multi-RTI-Resistant HIV-1 Strains

MOLECULES

IF4.6

2018-07-024

OAAI

In Vivo and Mechanistic Studies on Antitumor Lead 7-Methoxy-4-(2-methylquinazolin-4-yl)-3,4-dihydroquinoxalin-2(1H)-one and Its Modification as a Novel Class of Tubulin-Binding Tumor-Vascular Disrupting Agents

JOURNAL OF MEDICINAL CHEMISTRY

IF6.8

2017-06-2735

OAAI

Synthesis, biological evaluation, and physicochemical property assessment of 4-substituted 2-phenylaminoquinazolines as Mer tyrosine kinase inhibitors (vol 24, pg 3083, 2016)

BIOORGANIC & MEDICINAL CHEMISTRY

IF3

2017-05-010

OAAI

Synthesis, biological evaluation, and physicochemical property assessment of 4-substituted 2-phenylaminoquinazolines as Mer tyrosine kinase inhibitors

4-取代的2-苯基氨基喹唑啉作为Mer酪氨酸激酶抑制剂的合成，生物学评估和理化性质评估

BIOORGANIC & MEDICINAL CHEMISTRY

IF3

2016-07-019

OAAI

Novel HIV-1 Non-nucleoside Reverse Transcriptase Inhibitor Agents: Optimization of Diarylanilines with High Potency against Wild-Type and Rilpivirine-Resistant E138K Mutant Virus

JOURNAL OF MEDICINAL CHEMISTRY

IF6.8

2016-04-1234

OAAI

Lan Xie

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