Ontology highlight
ABSTRACT:
INSTRUMENT(S):
ORGANISM(S): Mus Musculus (mouse)
TISSUE(S): Skeletal Muscle Myoblast, Cell Culture
SUBMITTER:
Brian McDonagh
LAB HEAD: Brian McDonagh
PROVIDER: PXD059735 | Pride | 2026-04-27
REPOSITORIES: Pride
| Action | DRS | |||
|---|---|---|---|---|
| 120mins_OTIT_FusionMS_Ctrl_1.raw | Raw | |||
| 120mins_OTIT_FusionMS_Ctrl_2.raw | Raw | |||
| 120mins_OTIT_FusionMS_Ctrl_3.raw | Raw | |||
| 120mins_OTIT_FusionMS_Ctrl_4.raw | Raw | |||
| 120mins_OTIT_FusionMS_Inhib_TM_1.raw | Raw |
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Casas-Martinez Jose C JC Xia Qin Q Li Penglin P Borja-Gonzalez Maria M Miranda-Vizuete Antonio A McDermott Emma E Dockery Peter P Quinlan Leo R LR Goljanek-Whysall Katarzyna K Samali Afshin A McDonagh Brian B
Cell death and differentiation 20251101 4
The transfer of information and metabolites between the mitochondria and the endoplasmic reticulum (ER) is mediated by mitochondria-ER contact sites (MERCS), allowing adaptations in response to changes in cellular homeostasis. MERCS are dynamic structures essential for maintaining cell homeostasis through the modulation of calcium transfer, redox signalling, lipid transfer, autophagy and mitochondrial dynamics. Under stress conditions such as ER protein misfolding, the Unfolded Protein Response ...[more]