Dysregulation of mitochondrial calcium signaling and superoxide flashes cause mitochondrial genomic DNA damage in Huntington disease.
about
PGC-1α, mitochondrial dysfunction, and Huntington's diseaseMitochondrial Biology and Neurological DiseasesGenome-wide loss of 5-hmC is a novel epigenetic feature of Huntington's diseaseRole and mechanism of Twist1 in modulating the chemosensitivity of FaDu cells.Altered Ca(2+) signaling in skeletal muscle fibers of the R6/2 mouse, a model of Huntington's diseaseThe role of mitochondrial DNA mutation on neurodegenerative diseases.Ca(2+) handling in isolated brain mitochondria and cultured neurons derived from the YAC128 mouse model of Huntington's diseaseA3 adenosine receptor agonist prevents the development of paclitaxel-induced neuropathic pain by modulating spinal glial-restricted redox-dependent signaling pathways.The Mitochondrial Permeability Transition Pore: Channel Formation by F-ATP Synthase, Integration in Signal Transduction, and Role in Pathophysiology.Endophilin B2 promotes inner mitochondrial membrane degradation by forming heterodimers with Endophilin B1 during mitophagy.Imaging ROS signaling in cells and animals.Mitochondrial Flash: Integrative Reactive Oxygen Species and pH Signals in Cell and Organelle Biology.Mitochondrial permeability transition pore induces mitochondria injury in Huntington disease.The Function of the Mitochondrial Calcium Uniporter in Neurodegenerative Disorders.The mitochondrial permeability transition pore: a mystery solved?Pharmacological protein targets in polyglutamine diseases: mutant polypeptides and their interactors.Static magnetic fields modulate X-ray-induced DNA damage in human glioblastoma primary cells.Imaging mitochondrial reactive oxygen species with fluorescent probes: current applications and challenges.Mutant Huntingtin and Elusive Defects in Oxidative Metabolism and Mitochondrial Calcium Handling.Destination Brain: the Past, Present, and Future of Therapeutic Gene Delivery.Mitochondrial Flashes: Elemental Signaling Events in Eukaryotic Cells.Mitochondrial flashes: new insights into mitochondrial ROS signalling and beyond.Adult neural progenitor cells from Huntington's disease mouse brain exhibit increased proliferation and migration due to enhanced calcium and ROS signals.Multiparametric optical analysis of mitochondrial redox signals during neuronal physiology and pathology in vivo.Protein Glutathionylation in the Pathogenesis of Neurodegenerative Diseases.RNA Aptamers Rescue Mitochondrial Dysfunction in a Yeast Model of Huntington’s Disease.A Mitochondria-Associated Oxidative Stress Perspective on Huntington's Disease
P2860
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P2860
Dysregulation of mitochondrial calcium signaling and superoxide flashes cause mitochondrial genomic DNA damage in Huntington disease.
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
2012年论文
@zh
2012年论文
@zh-cn
name
Dysregulation of mitochondrial ...... damage in Huntington disease.
@ast
Dysregulation of mitochondrial ...... damage in Huntington disease.
@en
type
label
Dysregulation of mitochondrial ...... damage in Huntington disease.
@ast
Dysregulation of mitochondrial ...... damage in Huntington disease.
@en
prefLabel
Dysregulation of mitochondrial ...... damage in Huntington disease.
@ast
Dysregulation of mitochondrial ...... damage in Huntington disease.
@en
P2093
P2860
P356
P1476
Dysregulation of mitochondrial ...... damage in Huntington disease.
@en
P2093
Caixia Guo
He-Ping Cheng
Jiu-Qiang Wang
Qiao-Chu Wang
Qinmiao Sun
Tie-Shan Tang
Xianhua Wang
P2860
P304
P356
10.1074/JBC.M112.407726
P407
P577
2012-12-17T00:00:00Z