Summary of project PR000725
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 PR000725. The data can be accessed directly via it's Project DOI: 10.21228/M8ZM3X This work is supported by NIH grant, U2C- DK119886.
See: https://www.metabolomicsworkbench.org/about/howtocite.php
Project ID: | PR000725 |
Project DOI: | doi: 10.21228/M8ZM3X |
Project Title: | Targeted metabolomics of SETD2 isogenic cell lines |
Project Summary: | SETD2, the histone methyltransferase responsible for the trimethylation of H3K36, is inactivated in approximately 10-32% of clear renal cell carcinoma (ccRCC) cases. To reveal the impact of SETD2 loss on metabolic alterations in ccRCC. In this study, SETD2 null isogenic 38E/38F clones derived from 786-O cells were generated by zinc finger nucleases, and the cellular metabolic changes were analyzed by GC-MS-based targeted metabolomics. |
Institute: | Arizona State University |
Department: | College of Health Solutions |
Last Name: | Liu |
First Name: | Jingping |
Address: | 13208 E. Shea Blvd, Scottsdale, AZ |
Email: | jliu381@asu.edu |
Phone: | 4802078529 |
Summary of all studies in project PR000725
Study ID | Study Title | Species | Institute | Analysis(* : Contains Untargted data) | Release Date | Version | Samples | Download(* : Contains raw data) |
---|---|---|---|---|---|---|---|---|
ST001086 | Targeted GC-MS of SETD2 isogenic cell lines | Homo sapiens | Arizona State University | MS | 2018-12-11 | 1 | 9 | Uploaded data (3.5M) |