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Mitochondrial dynamics and disease, OPA1

Mitochondrial dynamics and disease, OPA1

http://www.wikidata.org/entity/Q28243097

about

Formation of cristae and crista junctions in mitochondria depends on antagonism between Fcj1 and Su e/g.OPA1-related auditory neuropathy: site of lesion and outcome of cochlear implantation.Mitochondrial function in vascular endothelial cell in diabetes Loss of functional OPA1 unbalances redox state: implications in dominant optic atrophy pathogenesis Improved locus-specific database for OPA1 mutations allows inclusion of advanced clinical data.Complex patterns of mitochondrial dynamics in human pancreatic cells revealed by fluorescent confocal imaging.OPA1-related dominant optic atrophy is not strongly influenced by mitochondrial DNA background.Azidothymidine-triphosphate impairs mitochondrial dynamics by disrupting the quality control system.The cytosolic domain of Fis1 binds and reversibly clusters lipid vesicles.Mitochondrial optic neuropathies - disease mechanisms and therapeutic strategies.Association of OPA1 polymorphisms with NTG and HTG: a meta-analysis.Molecular machinery of mitochondrial fusion and fission.Direct binding of the dynamin-like GTPase, Dnm1, to mitochondrial dynamics protein Fis1 is negatively regulated by the Fis1 N-terminal arm Apoptosis-inducing factor: structure, function, and redox regulation.Underexpression of mitochondrial-DNA encoded ATP synthesis-related genes and DNA repair genes in systemic lupus erythematosus.Implications of mitochondrial dynamics on neurodegeneration and on hypothalamic dysfunction.Optic atrophy plus phenotype due to mutations in the OPA1 gene: two more Italian families.Genetic and Clinical Analyses of DOA and LHON in 304 Chinese Patients with Suspected Childhood-Onset Hereditary Optic Neuropathy.Assessment of the retinal posterior pole in dominant optic atrophy by spectral-domain optical coherence tomography and microperimetry Chemical inhibition of the mitochondrial division dynamin reveals its role in Bax/Bak-dependent mitochondrial outer membrane permeabilization Dendritic mitochondria reach stable positions during circuit development.Mitochondrial dynamics in the adult cardiomyocytes: which roles for a highly specialized cell?Inherited mitochondrial optic neuropathies.Mitochondrial fusion and division: Regulation and role in cell viability Insulin stimulates mitochondrial fusion and function in cardiomyocytes via the Akt-mTOR-NFκB-Opa-1 signaling pathway Lipid signaling on the mitochondrial surface.Quality control of mitochondrial proteostasis.Visualizing mitochondrial lipids and fusion events in Mammalian cells.Emerging role of protein-protein transnitrosylation in cell signaling pathways.Genetic and phenotypic variability of optic neuropathies.Dysfunctional Mitochondrial Dynamics in the Pathophysiology of Neurodegenerative Diseases.Mitochondrial dysfunctions in neurodegenerative diseases: relevance to Alzheimer's disease.Mitochondrial Dynamics and Heart Failure.[Pt(O,O'-acac)(γ-acac)(DMS)] versus cisplatin: apoptotic effects in B50 neuroblastoma cells.Mitochondrial remodeling: Rearranging, recycling, and reprogramming.S-nitrosylation of Cdk5: potential implications in amyloid-β-related neurotoxicity in Alzheimer disease.Mitochondrial Membrane Dynamics and Inherited Optic Neuropathies.Increased steroidogenesis promotes early-onset and severe vision loss in females with OPA1 dominant optic atrophy.Simultaneous impairment of mitochondrial fission and fusion reduces mitophagy and shortens replicative lifespan.Regulation of PGC-1alpha and PGC-1alpha-responsive genes with forskolin-induced Schwann cell differentiation.

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Mitochondrial dynamics and disease, OPA1

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2006 nî lūn-bûn

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2006 թուականին հրատարակուած գիտական յօդուած

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2006 թվականին հրատարակված գիտական հոդված

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2006年の論文

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2006年論文

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2006年論文

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2006年論文

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Aurélien Olichon

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Christian Hamel

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