Ontology highlight
ABSTRACT:
INSTRUMENT(S): Q Exactive HF
ORGANISM(S): Homo Sapiens (human)
TISSUE(S): Epithelial Cell, Cell Culture
DISEASE(S): Lung Cancer
SUBMITTER: Elena Ossipova
LAB HEAD: Meike J. Saul
PROVIDER: PXD016803 | Pride | 2020-03-02
REPOSITORIES: Pride
Action | DRS | |||
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Isabel_TMT_pool1.msf | Msf | |||
Isabel_TMT_pool2.msf | Msf | |||
Isabel_TMT_pool4.msf | Msf | |||
JLEOIB_20160324_P1_Fr01.raw | Raw | |||
JLEOIB_20160324_P1_Fr02.raw | Raw |
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Emmerich Anne C AC Wellstein Julia J Ossipova Elena E Baumann Isabell I Lengqvist Johan J Kultima Kim K Jakobsson Per-Johan PJ Steinhilber Dieter D Saul Meike J MJ
Frontiers in pharmacology 20200313
MicroRNAs (miRs) are one of the most important post-transcriptional repressors of gene expression. However, miR-574-5p has recently been shown to positively regulate the expression of microsomal prostaglandin E-synthase-1 (mPGES-1), a key enzyme in the prostaglandin E<sub>2</sub> (PGE<sub>2</sub>) biosynthesis, by acting as decoy to the RNA-binding protein CUG-RNA binding protein 1 (CUGBP1) in human lung cancer. miR-574-5p exhibits oncogenic properties and promotes lung tumor growth <i>in vivo</ ...[more]