A5008707538- Microbial metabolism and enzyme function
- Biofuel production and bioconversion
- Aquaculture disease management and microbiota
- Invertebrate Immune Response Mechanisms
- Microbial Metabolic Engineering and Bioproduction
- Research in Cotton Cultivation
- Genomics and Phylogenetic Studies
- Mosquito-borne diseases and control
- RNA modifications and cancer
- Listeria monocytogenes in Food Safety
- MicroRNA in disease regulation
- Mathematical and Theoretical Epidemiology and Ecology Models
- Genomics, phytochemicals, and oxidative stress
- Biochemical Acid Research Studies
- Fungal and yeast genetics research
- Circular RNAs in diseases
- Enzyme Catalysis and Immobilization
- Biosensors and Analytical Detection
- Light effects on plants
- Spaceflight effects on biology
- Metalloenzymes and iron-sulfur proteins
- Plant pathogens and resistance mechanisms
- Plant Stress Responses and Tolerance
- Salmonella and Campylobacter epidemiology
- Porphyrin Metabolism and Disorders
Hubei Normal University
2023
Nanjing Agricultural University
2022
Jiangnan University
2015-2020
Nanjing Normal University
2017-2020
Wuxi People's Hospital
2019
Xian Yang Central Hospital
2019
In the present study, function of microRNA (miR)-214 on diabetic nephropathy (DN) and diabetes proximal tubular cells was investigated. Reverse transcription-quantitative polymerase chain reaction used measure expression miR-214 in rats with DN ELISA performed to oxidative stress ROS levels. Results indicated that peripheral blood significantly decreased DN. The vitro model upregulation reactive oxygen species (ROS) levels, but increased uncoupling protein 2 (UCP2), phosphorylated (p)-Akt...
Escherichia coli O157:H7, Staphylococcus aureus, and Salmonella are major foodborne pathogens that widespread in nature responsible for several outbreaks of food safety accidents. Thus, a rapid practical technique (PMA-mPCR) was developed the simultaneous detection viable E. S. pure culture matrix. To eliminate false positive results, propidium monoazide (PMA) applied to selectively suppress DNA amplification dead cells. The results showed optimum concentration PMA is 5.0 µg/mL. limit this...