The effects of membrane lipid raft disruption on glucocorticoid, progesterone, and antagonist Mifepristone-induced rapid responses in human T cells
碩士 === 國立陽明大學 === 生理學研究所 === 101 === Background: In our previous study, hydrocortisone (HC), dexamethasone (DEX), and progesterone (P4) trigger T cell rapid-responses on inhibition of Na+/H+ exchanger 1 (NHE1) activity, the increases of intracellular acidification and C-terminal resides phosphorylat...
Main Authors: | Pin-Yi Lin, 林品儀 |
---|---|
Other Authors: | Eileen Jea Chien |
Format: | Others |
Language: | zh-TW |
Published: |
2013
|
Online Access: | http://ndltd.ncl.edu.tw/handle/50135006040944505974 |
Similar Items
-
Mifepristone increases the cytotoxicity of uterine natural killer cells by acting as a glucocorticoid antagonist via ERK activation.
by: Yuezhou Chen, et al.
Published: (2012-01-01) -
Mifepristone (RU486) inhibits dietary lipid digestion by antagonizing the role of glucocorticoid receptor on lipase transcription
by: Peng Ma, et al.
Published: (2021-06-01) -
Primary Generalized Glucocorticoid Hypersensitivity Treated with Mifepristone: A Case Report
by: Liu Y, et al.
Published: (2020-10-01) -
X-ray crystal structure of the ancestral 3-ketosteroid receptor-progesterone-mifepristone complex shows mifepristone bound at the coactivator binding interface.
by: Jennifer K Colucci, et al.
Published: (2013-01-01) -
Glucocorticoid Receptor Antagonist Mifepristone Does Not Alter Innate Anxiety-Like Behavior in Genetically-Selected Marchigian Sardinian (msP) Rats
by: Valentina Vozella, et al.
Published: (2021-03-01)