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We performed global phosphorylation quantitative proteomics analysis of neuronal HT-22 cells in response to iron deficiency. Our data applied SILAC-based quantitative analysis with replicates and studied the phosphorylation dynamics under acute, chronic iron deficiency as well as acute hypoxia.
ORGANISM(S): Mus musculus (Mouse) 
2021-09-09 | PXD023294 | Pride
The overall goal of the project was to identify proline hydroxylation dependent Brd4 interactome through label-free quantitative proteomics analysis.
ORGANISM(S): Homo sapiens (Human) 
2019-07-03 | PXD012633 | Pride
The goal of the project was to quantify the dynamics of BRD4 proline hydroxylation in response to oxygen depletion and differential enzyme regulations.
ORGANISM(S): Homo sapiens (Human) 
2019-07-03 | PXD012674 | Pride
In this study, we applied SILAC-based quantitative proteomics analysis to identify hypoxia response proteome in prostate cancer cells.
ORGANISM(S): Homo sapiens (Human) 
2021-09-09 | PXD017607 | Pride
To identify novel regulator of EGLN1/PHD2, we performed label-free quantitative interactome analysis. Stable Hela cell lines expressing Flag-tagged PHD2 and control vector were generated. Immunoprecipitation and mass spectrometry analysis were performed to identify novel interactors of PHD2 followed...
ORGANISM(S): Homo sapiens (Human) 
2021-09-08 | PXD014757 | Pride
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