PXD011283 is an
original dataset announced via ProteomeXchange.
Dataset Summary
| Title | Comparative proteomic analysis of microvescicoles and exosomes isolated from urine of medullary sponge kidney disease (MSK) versus Autosomal dominant polycystic kidney disease (ADPKD) patients. |
| Description | Microvescicles (MV) and exosomes (EX) seem to be involved in the pathogenetic machinery of the autosomal dominant polycystic kidney disease (ADPKD), but, at the moment, no studies have assessed their role in medullary sponge kidney disease (MSK), a sporadic kidney malformation featuring cysts, nephrocalcinosis and recurrent renal stones. To discover their role in this disease we employed a proteomic-based research strategy. |
| HostingRepository | PRIDE |
| AnnounceDate | 2019-11-25 |
| AnnouncementXML | Submission_2019-11-25_01:40:59.xml |
| DigitalObjectIdentifier | |
| ReviewLevel | Peer-reviewed dataset |
| DatasetOrigin | Original dataset |
| RepositorySupport | Unsupported dataset by repository |
| PrimarySubmitter | Andrea Petretto |
| SpeciesList | scientific name: Homo sapiens (Human); NCBI TaxID: 9606; |
| ModificationList | iodoacetamide derivatized residue |
| Instrument | Orbitrap Fusion ETD |
Dataset History
| Revision | Datetime | Status | ChangeLog Entry |
| 0 | 2018-10-04 08:05:07 | ID requested | |
| ⏵ 1 | 2019-11-25 01:41:00 | announced | |
Publication List
| Dataset with its publication pending |
Keyword List
| submitter keyword: Huma, LC-MS/MS, MSK, ADPKD |
Contact List
| Andrea Petretto |
| contact affiliation | Istituto Gaslini |
| contact email | andrapetretto@gaslini.org |
| lab head | |
| Andrea Petretto |
| contact affiliation | Gaslini Children's Hospital |
| contact email | a.petretto@gmail.com |
| dataset submitter | |
Full Dataset Link List
Dataset FTP location
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| PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD011283
- Label: PRIDE project
- Name: Comparative proteomic analysis of microvescicoles and exosomes isolated from urine of medullary sponge kidney disease (MSK) versus Autosomal dominant polycystic kidney disease (ADPKD) patients.