Jiaxin Yu

发表

ADP-Induced Conformational Transition of Human Adenylate Kinase 1 Is Triggered by Suppressing Internal Motion of α3α4 and α7α8 Fragments on the ps-ns Timescale

D. Lin, Chenyun Guo, Zhihua Wu, 2022, Biomolecules.

Per-6-substituted β-cyclodextrin libraries inhibit formation of β-amyloid-peptide (Aβ)-derived, soluble oligomers

Lei Chang, W. Klein, D. Venton, 2002, Journal of Molecular Neuroscience.

The Axl receptor tyrosine kinase is an adverse prognostic factor and a therapeutic target in esophageal adenocarcinoma

E. Montgomery, G. Riggins, J. Eshleman, 2010, Cancer biology & therapy.

Cocaine detoxification by combinatorially substituted β-Cyclodextrin libraries

Yongzhong Zhao, D. Venton, M. Holterman, 2002 .

ERα determines the chemo-resistant function of mutant p53 involving the switch between lincRNA-p21 and DDB2 expressions

Wei-Chung Cheng, Wei‐Chien Huang, Ya-Ling Wei, 2021, Molecular therapy. Nucleic acids.

R428, a selective small molecule inhibitor of Axl kinase, blocks tumor spread and prolongs survival in models of metastatic breast cancer.

Y. Hitoshi, D. Payan, Weiqun Li, 2010, Cancer research.

R 428 , a Selective Small Molecule Inhibitor of Axl Kinase , Blocks Tumor Spread and Prolongs Survival in Models of Metastatic Breast Cancer

Y. Hitoshi, D. Payan, Weiqun Li, 2010 .

Vaccination with soluble Aβ oligomers generates toxicity‐neutralizing antibodies

T. Morgan, C. Finch, Lei Chang, 2001, Journal of neurochemistry.

Utility of Circulating Tumor Cells for Detection of Early-Stage Luminal A Breast Cancer.

Qiang Sun, Yitong Wang, Jianyi Li, 2020, The American journal of the medical sciences.

DNA methylation‐mediated inhibition of MGARP is involved in impaired progeny testosterone synthesis in mice exposed to DBP in utero

Yan Yu, Jing Zhang, Minhui Liu, 2023, Environmental Toxicology.

Discovery of dual Axl/VEGF-R2 inhibitors as potential anti-angiogenic and anti-metastatic drugs for cancer chemotherapy.

Weiqun Li, D. Goff, Raj K. Singh, 2017, Bioorganic & medicinal chemistry letters.

Per-6-substituted beta-cyclodextrin libraries inhibit formation of beta-amyloid-peptide (A beta)-derived, soluble oligomers.

Lei Chang, W. Klein, D. Venton, 2002, Journal of molecular neuroscience : MN.

Selective Small Molecule Inhibitor of Axl Kinase , Blocks Tumor Spread and Prolongs Survival in Models of Metastatic Breast Cancer

Y. Hitoshi, D. Payan, Weiqun Li, 2010 .

Reduction-Hypersensitive Podophyllotoxin Prodrug Self-Assembled Nanoparticles for Cancer Treatment

C. Luo, Yuequan Wang, Shenwu Zhang, 2023, Pharmaceutics.