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PXD038911-1

PXD038911 is an original dataset announced via ProteomeXchange.

Dataset Summary
TitleMouse model for hypertrophic cardiomyopathy
DescriptionHypertrophic cardiomyopathy (HCM) caused by autosomal-dominant mutations in genes that code for the structural proteins of the sarcomere, is the most common inherited heart disease. HCM is associated with progressive myocardial hypertrophy and fibrosis, ventricular dysfunction, and arrhythmias. Disease onset during childhood and adolescence carries the risk of morbidity and sudden cardiac death. Hypoxia and the main regulator of the cellular hypoxic response hypoxia-inducible transcription factor-1a (HIF1A) have been associated with HCM, however their exact roles are not elucidated yet.
HostingRepositoryPRIDE
AnnounceDate2025-01-20
AnnouncementXMLSubmission_2025-01-20_07:59:23.422.xml
DigitalObjectIdentifier
ReviewLevelPeer-reviewed dataset
DatasetOriginOriginal dataset
RepositorySupportUnsupported dataset by repository
PrimarySubmitterJan Bernd Stöckl
SpeciesList scientific name: Mus musculus (Mouse); NCBI TaxID: 10090;
ModificationListiodoacetamide derivatized residue
InstrumentQ Exactive HF-X
Dataset History
RevisionDatetimeStatusChangeLog Entry
02022-12-19 03:14:22ID requested
12025-01-20 07:59:23announced
Publication List
10.1038/S41598-025-85187-9;
Keyword List
submitter keyword: mouse, proteomics, heart, hypertrophic cardiomyopathy, DDA
Contact List
Thomas Fröhlich
contact affiliationLudwig-Maximilians-Universität München Genzentrum Laboratory for Functional Genome Analysis Feodor-Lynen-Str. 25 D-81377 München
contact emailfrohlich@genzentrum.lmu.de
lab head
Jan Bernd Stöckl
contact affiliationGenzentrum der LMU München
contact emailstoeckl@genzentrum.lmu.de
dataset submitter
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Dataset FTP location
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PRIDE project URI
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