Ontology highlight
ABSTRACT:
INSTRUMENT(S): LTQ Orbitrap
ORGANISM(S): Mus Musculus (mouse)
TISSUE(S): Primary Cell, Early Embryonic Cell
SUBMITTER: Katherine Fantauzzo
LAB HEAD: Philippe Soriano
PROVIDER: PXD000779 | Pride | 2019-06-04
REPOSITORIES: Pride
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05142012KF3Aminus1.RAW | Raw | |||
05142012KF3Aminus2.RAW | Raw | |||
05142012KF3Aminus3.RAW | Raw | |||
05142012KF3Aminus4.RAW | Raw | |||
05142012KF3Aminus5.RAW | Raw |
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Fantauzzo Katherine A KA Soriano Philippe P
Genes & development 20140501 9
Previous studies have identified phosphatidylinositol 3-kinase (PI3K) as the main downstream effector of PDGFRα signaling during murine skeletal development. Autophosphorylation mutant knock-in embryos in which PDGFRα is unable to bind PI3K (Pdgfra(PI3K/PI3K)) exhibit skeletal defects affecting the palatal shelves, shoulder girdle, vertebrae, and sternum. To identify proteins phosphorylated by Akt downstream from PI3K-mediated PDGFRα signaling, we immunoprecipitated Akt phosphorylation substrate ...[more]