PXD028848 is an
original dataset announced via ProteomeXchange.
Dataset Summary
Title | i.e.Human Veinou malformation.iTraq/TMT |
Description | Proteomics and high connotation functional gene screening (HCS) were used to screen key functional genes that play important roles in the pathogenesis of venous malformation. |
HostingRepository | PRIDE |
AnnounceDate | 2022-02-16 |
AnnouncementXML | Submission_2022-02-16_15:49:31.583.xml |
DigitalObjectIdentifier | |
ReviewLevel | Peer-reviewed dataset |
DatasetOrigin | Original dataset |
RepositorySupport | Unsupported dataset by repository |
PrimarySubmitter | Song Wang |
SpeciesList | scientific name: Homo sapiens (Human); NCBI TaxID: 9606; |
ModificationList | TMT6plex-126 reporter+balance reagent acylated residue |
Instrument | LCQ Classic |
Dataset History
Revision | Datetime | Status | ChangeLog Entry |
0 | 2021-09-29 13:48:14 | ID requested | |
⏵ 1 | 2022-02-16 15:49:32 | announced | |
Publication List
Wang S, Zhou Z, Li J, Wang Y, Li H, Lv R, Xu G, Zhang J, Bi J, Huo R, Identification of ACTA2 as a Key Contributor to Venous Malformation. Front Cell Dev Biol, 9():755409(2021) [pubmed] |
Keyword List
submitter keyword: i.e.Human, Vein,iTraq/TMT |
Contact List
i.e.Jianhai Bi |
contact affiliation | shandong provical hospital |
contact email | bijianhai@126.com |
lab head | |
Song Wang |
contact affiliation | shandong provincial hospital |
contact email | risingws@hotmail.com |
dataset submitter | |
Full Dataset Link List
Dataset FTP location
NOTE: Most web browsers have now discontinued native support for FTP access within the browser window. But you can usually install another FTP app (we recommend FileZilla) and configure your browser to launch the external application when you click on this FTP link. Or otherwise, launch an app that supports FTP (like FileZilla) and use this address: ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2022/02/PXD028848 |
PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD028848
- Label: PRIDE project
- Name: i.e.Human Veinou malformation.iTraq/TMT