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Ginkgo leaves are always resources for flavonoids pharmaceutical industry. However, the effect of the elevation and tree age changes on flavonoid biosynthesis have not been detailly explored in Ginkgo leaves. In addition, whether these environmental pressures have similar effects on the biosynthesis...
2020-12-14 | MTBLS962 | MetaboLights
iTRAQ-based quantitative proteomic technology was used to study the proteomic responses to food intake of C. nasus.
ORGANISM(S): Coilia Nasus 
2021-12-15 | PXD030433 |

Bee pollen is consumed for its nutritional and pharmacological benefits, but it also contains hazardous allergens which has not been identified. Here, we identified 2 potential allergens, glutaredoxin and oleosin-B2, in Brassica napus (B. napus) bee pollen using mass spectrometr...

2022-03-23 | MTBLS3950 | MetaboLights
To identify potential proteins interacting with Per2 in oral squamous carcinoma cells, we performed SDS-PAGE followed by LC-MS/MS analysis of FLAG-Per2 immunoprecipitated proteins in cell extracts from SCC25 cells transfected with the FLAG-Per2 plasmid.
ORGANISM(S): Homo Sapiens 
2025-03-19 | PXD062046 |
The present NGST, TMT and Q-TOF MS platform should provide unprecedented resources to address such questions as to how hypoxic condition affects gene, miRNA, protein, and metabolite expression and changes the molecular pathways, and whether miRNAs participate in this process. For this purpose, we ch...
ORGANISM(S): Tachysurus Vachellii 
2020-07-18 | PXD020425 |
Investigation into the structure of the human m6A writer complex.
ORGANISM(S): Homo Sapiens 
2022-08-18 | PXD036144 |
Background: Plants attenuate their responses to a variety of bacterial and fungal pathogens, leading to higher incidences of pathogen infection at night. However, little is known about the molecular mechanism responsible for the light-induced defence response; transcriptome data would likely facilit...
ORGANISM(S): Solanum lycopersicum 
Osteogenesis imperfecta (OI) is a serious genetic bone disorder characterized by congenital low bone mass, deformity and frequent fractures. Type XV OI is a moderate to severe form of skeletal dysplasia caused by WNT1 mutations. In this cohort study from southern China, we summarized the clinical ph...
ORGANISM(S): Homo sapiens (Human) 
2024-10-17 | PXD050841 | Pride
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