Summary of project PR001600
This data is available at the NIH Common Fund's National Metabolomics Data Repository (NMDR) website, the Metabolomics Workbench, https://www.metabolomicsworkbench.org, where it has been assigned Project ID PR001600. The data can be accessed directly via it's Project DOI: 10.21228/M8W70C This work is supported by NIH grant, U2C- DK119886.
See: https://www.metabolomicsworkbench.org/about/howtocite.php
Project ID: | PR001600 |
Project DOI: | doi: 10.21228/M8W70C |
Project Title: | Human neutrophil metabolomics |
Project Type: | MS qualitative analysis |
Project Summary: | Severe COVID-19 is characterized by an increase in the number and changes in the function of innate immune cells including neutrophils. However, it is not known how the metabolome of immune cells changes in COVID-19 patients or how metabolic changes may contribute to immune dysfunction. To address these questions, we analyzed the metabolome of neutrophils from patients with severe or mild COVID-19, or healthy controls. We identified widespread dysregulation of neutrophil metabolism with disease progression including in amino acid, redox, and central carbon metabolism. |
Institute: | UT Southwestern Medical Center |
Department: | Children's Research Institute |
Last Name: | Li |
First Name: | Yafeng |
Address: | 5323 Harry Hines Blvd, Children's Research Institute, Dallas, TX, 75309, USA |
Email: | yafeng.li@utsouthwestern.edu |
Phone: | 4047696693 |
Summary of all studies in project PR001600
Study ID | Study Title | Species | Institute | Analysis(* : Contains Untargted data) | Release Date | Version | Samples | Download(* : Contains raw data) |
---|---|---|---|---|---|---|---|---|
ST002477 | Neutrophil metabolomics in COVID-19 | Homo sapiens | UT Southwestern Medical Center | MS | 2023-02-26 | 1 | 89 | Uploaded data (14.7G)* |