Xuxia Zhang

Impaired osteoclast formation in bone marrow cultures of Fgf2 null mice in response to parathyroid hormone.

Non-tuberculous mycobacteria in China.

Comparison of gyrA gene mutations between laboratory-selected ofloxacin-resistant Mycobacterium tuberculosis strains and clinical isolates.

Discovery of aryl aminoquinazoline pyridones as potent, selective, and orally efficacious inhibitors of receptor tyrosine kinase c-Kit.

Discovery of a potent and selective c-Kit inhibitor for the treatment of inflammatory diseases.

Antagonists of CD117 (cKit) signaling inhibit mast cell accumulation in healing skin wounds.

Characterization of extensively drug-resistant Mycobacterium tuberculosis clinical isolates in China.

Identification of a novel IRGM promoter single nucleotide polymorphism associated with tuberculosis.

Evaluation of Spoligotyping and MIRU-VNTR for Mycobacterium bovis in Xinjiang, China.

Mycobacterial heparin-binding haemagglutinin adhesion-induced interferon & antibody for detection of tuberculosis.

Quinolinone-based agonists of S1P₁: use of a N-scan SAR strategy to optimize in vitro and in vivo activity.

Effect of composition of PDMAEMA-b-PAA block copolymers on their pH- and temperature-responsive behaviors.

Thermoresponsive diblock copolymer with tunable soluble-insoluble and soluble-insoluble-soluble transitions.

Decreased serum 5-oxoproline in TB patients is associated with pathological damage of the lung.

4-Methoxy-N-[2-(trifluoromethyl)biphenyl-4-ylcarbamoyl]nicotinamide: A Potent and Selective Agonist of S1P1.

Discovery of a Potent, S1P3-Sparing Benzothiazole Agonist of Sphingosine-1-Phosphate Receptor 1 (S1P1).

Discovery of AMG 369, a Thiazolo[5,4-b]pyridine Agonist of S1P1 and S1P5.

Optimization of a Potent, Orally Active S1P1 Agonist Containing a Quinolinone Core.

Ofloxacin resistance in Mycobacterium tuberculosis is associated with efflux pump activity independent of resistance pattern and genotype.

Factors impacting the mental health of the caregivers of children with asthma in china: effects of family socioeconomic status, symptoms control, proneness to shame, and family functioning.

Genotypic diversity analysis of Mycobacterium tuberculosis strains collected from Beijing in 2009, using spoligotyping and VNTR typing.

Association between interferon gamma receptor 1-56C/T gene polymorphism and tuberculosis susceptibility: a meta-analysis.

Multi-tunable self-assembled morphologies of stimuli-responsive diblock polyampholyte films on solid substrates.

Pharmaceutical Optimization of Peptide Toxins for Ion Channel Targets: Potent, Selective, and Long-Lived Antagonists of Kv1.3.

Discovery, Optimization, and in Vivo Evaluation of Benzimidazole Derivatives AM-8508 and AM-9635 as Potent and Selective PI3Kδ Inhibitors.

The profiles of gamma-H2AX along with ATM/DNA-PKcs activation in the lymphocytes and granulocytes of rat and human blood exposed to gamma rays.

Niclosamide sensitizes triple-negative breast cancer cells to ionizing radiation in association with the inhibition of Wnt/β-catenin signaling.

Discovery and in Vivo Evaluation of the Potent and Selective PI3Kδ Inhibitors 2-((1S)-1-((6-Amino-5-cyano-4-pyrimidinyl)amino)ethyl)-6-fluoro-N-methyl-3-(2-pyridinyl)-4-quinolinecarboxamide (AM-0687) and 2-((1S)-1-((6-Amino-5-cyano-4-pyrimidinyl)amino)ethyl)-5-fluoro-N-methyl-3-(2-pyridinyl)-4-quinolinecarboxamide (AM-1430).

Establishment of a γ-H2AX foci-based assay to determine biological dose of radon to red bone marrow in rats.

γ-H2AX/53BP1/pKAP-1 foci and their linear tracks induced by in vitro exposure to radon and its progeny in human peripheral blood lymphocytes.