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PXD039214

PXD039214 is an original dataset announced via ProteomeXchange.

Dataset Summary
TitlePatient-derived podocyte spheroids reveals new insights into the etiopathogenesis of Alport Syndrome
DescriptionAlport syndrome (AS) is a rare disease characterized by defective glomerular basement membranes, caused by mutations in COL4A3, COL4A4 and COL4A5, which synthesize collagen type IV. Patients present with progressive proteinuria, hematuria and podocyte loss. There is currently no cure for AS, and this is mainly due to its complex and variable pathogenesis, as well as the lack of models that can faithfully mimic the human phenotype.
HostingRepositoryPRIDE
AnnounceDate2023-11-14
AnnouncementXMLSubmission_2023-11-14_09:00:21.434.xml
DigitalObjectIdentifier
ReviewLevelPeer-reviewed dataset
DatasetOriginOriginal dataset
RepositorySupportUnsupported dataset by repository
PrimarySubmitterSadr Shaheed
SpeciesList scientific name: Homo sapiens (Human); NCBI TaxID: 9606;
ModificationListmonohydroxylated residue
InstrumentOrbitrap Fusion
Dataset History
RevisionDatetimeStatusChangeLog Entry
02023-01-03 01:00:49ID requested
12023-02-21 05:11:17announced
22023-11-14 09:00:21announced2023-11-14: Updated project metadata.
Publication List
Dataset with its publication pending
Keyword List
submitter keyword: human disease model, proteomics,Alport syndrome, hiPSCs, stem cells, kidney, spheroids
Contact List
Dr Sadr ul Shaheed
contact affiliationNuffield department of Surgical Sciences, University of Oxford UK
contact emailsadr.shaheed@nds.ox.ac.uk
lab head
Sadr Shaheed
contact affiliationNuffield Department of Surgical Sciences, University of Oxford, Oxford, United Kingdom
contact emailsadr.shaheed@nds.ox.ac.uk
dataset submitter
Full Dataset Link List
Dataset FTP location
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PRIDE project URI
Repository Record List
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