Ontology highlight
ABSTRACT:
INSTRUMENT(S): Orbitrap Fusion Lumos
ORGANISM(S): Homo Sapiens (human)
TISSUE(S): Hepatic Stellate Cell
SUBMITTER: Baoying Yuan
LAB HEAD: Zhaochong Zeng
PROVIDER: PXD011242 | Pride | 2018-12-04
REPOSITORIES: pride
Action | DRS | |||
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Lumos3_YBY.pep.xml | Pepxml | |||
Lumos3_YBY.prot.xml | Xml | |||
Lumos3_YBY_11_20171015.raw | Raw | |||
Lumos3_YBY_12_20171015.raw | Raw | |||
Lumos3_YBY_13_20171015.raw | Raw |
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Yuan Baoying B Chen Yuhan Y Wu Zhifeng Z Zhang Li L Zhuang Yuan Y Zhao Xiaomei X Niu Hao H Cheng Jason Chia-Hsien JC Zeng Zhaochong Z
Journal of proteome research 20181210 1
Hepatic stellate cells (HSCs) are the main target of radiation damage and primarily contribute to the development of radiation-induced liver fibrosis. However, the molecular events underlying the radiation-induced activation of HSCs are not fully elucidated. In the present study, human HSC line LX2 was treated with X-ray irradiation and/or TGF-β1, and profibrogenic molecules were evaluated. The iTRAQ LC-MS/MS technology was performed to identify global protein expression profiles in LX2 followin ...[more]