Area of research
Spectroscopy · Molecular Biology
Research interest
Research focused on Mass spectrometry and Proteomics, with related work in Type 2 diabetes, GPX4, Standardization. Notable publications include 'Multi-laboratory assessment of reproducibility, qualitative and quantitative performance of SWATH-mass spectrometry', 'Gut microbiome-related effects of berberine and probiotics on type 2 diabetes (the PREMOTE study)', and 'Rapid evolution of protein diversity by de novo origination in Oryza'.
Early prediction of preeclampsia from clinical, multi-omics and laboratory data using random forest model
AKAP1/PKA-mediated GRP75 phosphorylation at mitochondria-associated endoplasmic reticulum membranes protects cancer cells against ferroptosis
Multi-omics reveals immune response and metabolic profiles during high-altitude mountaineering
ER-associated degradation ligase HRD1 links ER stress to DNA damage repair by modulating the activity of DNA-PKcs
Noninvasive cervicovaginal proteomic biomarkers for spontaneous preterm birth
Establishing Integrated Models for Predicting Preeclampsia Using Clinical, Metabolic and Laboratory Data
SMURF2 predisposes cancer cell toward ferroptosis in GPX4-independent manners by promoting GSTP1 degradation
Long noncoding RNA HITT coordinates with RGS2 to inhibit PD-L1 translation in T cell immunity
iASPP suppresses Gp78-mediated TMCO1 degradation to maintain Ca <sup>2+</sup> homeostasis and control tumor growth and drug resistance
Multi-platform omics analysis reveals molecular signature for COVID-19 pathogenesis, prognosis and drug target discovery
Gut microbiome-related effects of berberine and probiotics on type 2 diabetes (the PREMOTE study)
Standardization and harmonization of distributed multi-center proteotype analysis supporting precision medicine studies
Rapid evolution of protein diversity by de novo origination in Oryza
Multi-laboratory assessment of reproducibility, qualitative and quantitative performance of SWATH-mass spectrometry
Systematic Analyses of the Transcriptome, Translatome, and Proteome Provide a Global View and Potential Strategy for the C-HPP