Mitochondrial fission and cristae disruption increase the response of cell models of Huntington's disease to apoptotic stimuli.
about
Structural insights into oligomerization and mitochondrial remodelling of dynamin 1-like proteinDefining the role of the Bcl-2 family proteins in Huntington's diseasePhysiological and pathological significance of dynamin-related protein 1 (drp1)-dependent mitochondrial fission in the nervous systemMitochondrial morphology-emerging role in bioenergeticsMetabolic disturbances in diseases with neurological involvementPGC-1α, mitochondrial dysfunction, and Huntington's diseaseImpaired mitochondrial dynamics and Nrf2 signaling contribute to compromised responses to oxidative stress in striatal cells expressing full-length mutant huntingtinHuntington's disease induced cardiac amyloidosis is reversed by modulating protein folding and oxidative stress pathways in the Drosophila heartShaping the role of mitochondria in the pathogenesis of Huntington's diseaseMitochondrial dysfunction in neurodegenerative diseasesInhibition of mitochondrial protein import by mutant huntingtinMitochondrial lipids in neurodegenerationBax activation initiates the assembly of a multimeric catalyst that facilitates Bax pore formation in mitochondrial outer membranesMitochondria: in sickness and in healthDuring autophagy mitochondria elongate, are spared from degradation and sustain cell viability.The HIV Protein gp120 Alters Mitochondrial Dynamics in Neurons.Crucial role of calbindin-D28k in the pathogenesis of Alzheimer's disease mouse model.Increased mitochondrial fission and neuronal dysfunction in Huntington's disease: implications for molecular inhibitors of excessive mitochondrial fissionAltered Ca(2+) signaling in skeletal muscle fibers of the R6/2 mouse, a model of Huntington's diseaseAbnormal mitochondrial dynamics, mitochondrial loss and mutant huntingtin oligomers in Huntington's disease: implications for selective neuronal damage.Molecular strategies for targeting antioxidants to mitochondria: therapeutic implications.Mitochondrial translocation and interaction of cofilin and Drp1 are required for erucin-induced mitochondrial fission and apoptosis.Neurodegenerative processes in Huntington's disease.Implications of mitochondrial dynamics on neurodegeneration and on hypothalamic dysfunction.Calcium Handling by Endoplasmic Reticulum and Mitochondria in a Cell Model of Huntington's Disease.Oxidative metabolism in YAC128 mouse model of Huntington's disease.Mitochondrial dynamics in cancer and neurodegenerative and neuroinflammatory diseases.Mitochondrial Ca(2+) and neurodegenerationMitochondria: the next (neurode)generationNovel Metabolic Abnormalities in the Tricarboxylic Acid Cycle in Peripheral Cells From Huntington's Disease PatientsPolyglutamine Tract Expansion Increases S-Nitrosylation of Huntingtin and Ataxin-1.PINK1-induced mitophagy promotes neuroprotection in Huntington's diseaseAltered Mitochondrial Dynamics and TBI Pathophysiology.Synaptic dysfunction, memory deficits and hippocampal atrophy due to ablation of mitochondrial fission in adult forebrain neuronsMitochondria-targeted molecules MitoQ and SS31 reduce mutant huntingtin-induced mitochondrial toxicity and synaptic damage in Huntington's disease.S-nitrosylation of dynamin-related protein 1 mediates mutant huntingtin-induced mitochondrial fragmentation and neuronal injury in Huntington's disease.Mitochondrial cristae shape determines respiratory chain supercomplexes assembly and respiratory efficiencyDynamin assembly strategies and adaptor proteins in mitochondrial fission.Enhanced mitochondrial biogenesis ameliorates disease phenotype in a full-length mouse model of Huntington's disease.Inhibition of mitochondrial fragmentation diminishes Huntington's disease-associated neurodegeneration.
P2860
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P2860
Mitochondrial fission and cristae disruption increase the response of cell models of Huntington's disease to apoptotic stimuli.
description
2010 nî lūn-bûn
@nan
2010 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Mitochondrial fission and cris ...... disease to apoptotic stimuli.
@ast
Mitochondrial fission and cris ...... disease to apoptotic stimuli.
@en
Mitochondrial fission and cris ...... disease to apoptotic stimuli.
@nl
type
label
Mitochondrial fission and cris ...... disease to apoptotic stimuli.
@ast
Mitochondrial fission and cris ...... disease to apoptotic stimuli.
@en
Mitochondrial fission and cris ...... disease to apoptotic stimuli.
@nl
prefLabel
Mitochondrial fission and cris ...... disease to apoptotic stimuli.
@ast
Mitochondrial fission and cris ...... disease to apoptotic stimuli.
@en
Mitochondrial fission and cris ...... disease to apoptotic stimuli.
@nl
P2093
P2860
P50
P356
P1476
Mitochondrial fission and cris ...... disease to apoptotic stimuli.
@en
P2093
Dmitri Lim
Gennady Ermak
Kelvin J A Davies
Roman Hudec
Veronica Costa
P2860
P304
P356
10.1002/EMMM.201000102
P577
2010-12-01T00:00:00Z