The effect of regulating MCU expression on experimental ischemic brain injury-Reference-Cited by-同舟云学术

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The effect of regulating MCU expression on experimental ischemic brain injury

Published:2023-04 Issue: Volume:362 Page:114329
ISSN:0014-4886
Container-title:Experimental Neurology
language:en
Short-container-title:Experimental Neurology

Author:

Qin Jin,Liu Lijuan,Liu Lin,Zhou Zhou,Zhou Yicong,Zhang Kun,Wang Binbin,Lu Honglin,Ran Jina,Ma Tianzhao,Zhang Yingzhen,Li Zhongzhong,Liu Xiaoyun

Funder

National Natural Science Foundation of China

Natural Science Foundation of Hebei Province

Publisher

Elsevier BV

Subject

Developmental Neuroscience,Neurology

Reference36 articles.

1. Ischemic stroke and mitochondria: mechanisms and targets;Andrabi;Protoplasma,2020

2. Mitochondrial fission and mitophagy are independent mechanisms regulating ischemia/reperfusion injury in primary neurons;Anzell;Cell Death Dis.,2021

3. Mitochondrial permeability transition: a molecular lesion with multiple drug targets;Briston;Trends Pharmacol. Sci.,2019

4. Comprehensive metabolomic characterization of coronary artery diseases;Fan;J. Am. Coll. Cardiol.,2016

5. Structure and mechanism of the mitochondrial Ca2+ uniporter holocomplex;Fan;Nature,2020

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1. MCU inhibition protects against intestinal ischemia‒reperfusion by inhibiting Drp1-dependent mitochondrial fission;Free Radical Biology and Medicine;2024-08

2. The expression profile of brain-derived exosomal miRNAs reveals the key molecules responsible for spontaneous motor function recovery in a rat model with permanent middle cerebral artery occlusion;Mammalian Genome;2024-07-12

3. Unravelling the complexity of the mitochondrial Ca2+ uniporter: regulation, tissue specificity, and physiological implications;Cell Calcium;2024-07

4. Rhodiola crenulata alleviates hypobaric hypoxia-induced brain injury by maintaining BBB integrity and balancing energy metabolism dysfunction;Phytomedicine;2024-06

5. Nuclear receptor subfamily 4 group A member 1 promotes myocardial ischemia/reperfusion injury through inducing mitochondrial fission factor-mediated mitochondrial fragmentation and inhibiting FUN14 domain containing 1-depedent mitophagy;International Journal of Biological Sciences;2024

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