In vivo correction of COX deficiency by activation of the AMPK/PGC-1α axis.
about
AAV-mediated liver-specific MPV17 expression restores mtDNA levels and prevents diet-induced liver failureEmerging therapeutic roles for NAD(+) metabolism in mitochondrial and age-related disordersMitochondrial disorders in children: toward development of small-molecule treatment strategiesMitochondrial cytochrome c oxidase deficiencyDysregulated metabolism contributes to oncogenesisMitochondrial targets for pharmacological intervention in human diseaseMitochondrial biogenesis through activation of nuclear signaling proteinsPGC-1α, mitochondrial dysfunction, and Huntington's diseaseInternational Paediatric Mitochondrial Disease ScaleToward a therapy for mitochondrial diseaseBezafibrate administration improves behavioral deficits and tau pathology in P301S miceFunctional analysis of missense mutations of OAT, causing gyrate atrophy of choroid and retinaUpregulation of Mitochondrial Content in Cytochrome c Oxidase Deficient FibroblastsScreening for active small molecules in mitochondrial complex I deficient patient's fibroblasts, reveals AICAR as the most beneficial compoundPrimary respiratory chain disease causes tissue-specific dysregulation of the global transcriptome and nutrient-sensing signaling networkNitrite activates AMP kinase to stimulate mitochondrial biogenesis independent of soluble guanylate cyclaseMitochondria in the spotlight of aging and idiopathic pulmonary fibrosisMitochondria: in sickness and in healthGLTSCR2/PICT1 links mitochondrial stress and Myc signaling.Metabolite profiles reveal energy failure and impaired beta-oxidation in liver of mice with complex III deficiency due to a BCS1L mutation.β-Aminoisobutyric acid induces browning of white fat and hepatic β-oxidation and is inversely correlated with cardiometabolic risk factors.NAD(+)-dependent activation of Sirt1 corrects the phenotype in a mouse model of mitochondrial disease.A method to identify and validate mitochondrial modulators using mammalian cells and the worm C. elegans.The role of PGC-1 coactivators in aging skeletal muscle and heart.Therapies in inborn errors of oxidative metabolism.The optic nerve: a "mito-window" on mitochondrial neurodegenerationEffective treatment of mitochondrial myopathy by nicotinamide riboside, a vitamin B3Long-term bezafibrate treatment improves skin and spleen phenotypes of the mtDNA mutator mouse.Mitochondrial dysfunction and lipid accumulation in the human diaphragm during mechanical ventilation.Mitochondrial Diseases Part I: mouse models of OXPHOS deficiencies caused by defects in respiratory complex subunits or assembly factors.Opa1 overexpression ameliorates the phenotype of two mitochondrial disease mouse models.Pharmacologic activation of mitochondrial biogenesis exerts widespread beneficial effects in a transgenic mouse model of Huntington's diseaseTranscriptome analysis of complex I-deficient patients reveals distinct expression programs for subunits and assembly factors of the oxidative phosphorylation system.Mitochondrial Diseases Part III: Therapeutic interventions in mouse models of OXPHOS deficiencies.The Arabidopsis KINβγ Subunit of the SnRK1 Complex Regulates Pollen Hydration on the Stigma by Mediating the Level of Reactive Oxygen Species in Pollen.Mitochondria: the next (neurode)generationCopper and bezafibrate cooperate to rescue cytochrome c oxidase deficiency in cells of patients with SCO2 mutations.Exploring the therapeutic space around NAD+.AFG3L2 supports mitochondrial protein synthesis and Purkinje cell survival.Tissue-specific implications of mitochondrial alterations in aging.
P2860
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P2860
In vivo correction of COX deficiency by activation of the AMPK/PGC-1α axis.
description
2011 nî lūn-bûn
@nan
2011 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
In vivo correction of COX deficiency by activation of the AMPK/PGC-1α axis.
@ast
In vivo correction of COX deficiency by activation of the AMPK/PGC-1α axis.
@en
type
label
In vivo correction of COX deficiency by activation of the AMPK/PGC-1α axis.
@ast
In vivo correction of COX deficiency by activation of the AMPK/PGC-1α axis.
@en
prefLabel
In vivo correction of COX deficiency by activation of the AMPK/PGC-1α axis.
@ast
In vivo correction of COX deficiency by activation of the AMPK/PGC-1α axis.
@en
P2093
P2860
P50
P1433
P1476
In vivo correction of COX deficiency by activation of the AMPK/PGC-1α axis.
@en
P2093
Carlo Viscomi
Emanuela Bottani
Eric A Schon
Gabriele Civiletto
Raffaele Cerutti
P2860
P356
10.1016/J.CMET.2011.04.011
P577
2011-07-01T00:00:00Z