Proteomics

Dataset Information

0

The Proteomics landscape of human aorta and mice aorta


ABSTRACT: NOTCH1 mutation and deficiency is etiologically associated to aortopathy combined with bicuspid aortic valve malformation; currently no medication is available for its treatment. Therefore, in this study, our focus turns to seeking the key downstream target genes and pharmacotherapeutic possibilities for NOTCH1 deficient aortopathy.

INSTRUMENT(S): timsTOF

ORGANISM(S): Homo Sapiens (human)

TISSUE(S): Blood Vessel

SUBMITTER: Zhang Weijia  

LAB HEAD: Weijia Zhang

PROVIDER: PXD044019 | Pride | 2024-12-10

REPOSITORIES: Pride

Dataset's files

Source:
Action DRS
human-aorta_1.zip Other
human-aorta_10.zip Other
human-aorta_11.zip Other
human-aorta_12.zip Other
human-aorta_13.zip Other
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