Ontology highlight
ABSTRACT:
INSTRUMENT(S): LTQ Orbitrap Velos
ORGANISM(S): Mus Musculus (mouse)
TISSUE(S): Pancreatic Islet Cancer Cell
SUBMITTER: Matthew Monroe
LAB HEAD: Weijun Qian
PROVIDER: PXD003182 | Pride | 2016-01-21
REPOSITORIES: Pride
Action | DRS | |||
---|---|---|---|---|
MPI_SB1_Global.mgf | Mgf | |||
MPI_SB1_Global.pride.mgf.gz | Mgf | |||
MPI_SB1_Global.raw | Raw | |||
MPI_SB1_Global_1.mgf | Mgf | |||
MPI_SB1_Global_1.pride.mgf.gz | Mgf |
Items per page: 1 - 5 of 20 |
Cell metabolism 20151215 1
Although compensatory islet hyperplasia in response to insulin resistance is a recognized feature in diabetes, the factor(s) that promote β cell proliferation have been elusive. We previously reported that the liver is a source for such factors in the liver insulin receptor knockout (LIRKO) mouse, an insulin resistance model that manifests islet hyperplasia. Using proteomics we show that serpinB1, a protease inhibitor, which is abundant in the hepatocyte secretome and sera derived from LIRKO mic ...[more]