OPA1 mutation and late-onset cardiomyopathy: mitochondrial dysfunction and mtDNA instability - Wikidata - wikimedia - TriplyDB

OPA1 mutation and late-onset cardiomyopathy: mitochondrial dysfunction and mtDNA instability

OPA1 mutation and late-onset cardiomyopathy: mitochondrial dysfunction and mtDNA instability

http://www.wikidata.org/entity/Q36522684

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SIRT3 deacetylates and activates OPA1 to regulate mitochondrial dynamics during stress The Role of Mitochondrial Functional Proteins in ROS Production in Ischemic Heart Diseases An experimental approach to study the function of mitochondria in cardiomyopathy Mitochondrial dynamism and heart disease: changing shape and shaping change Mitoconfusion: noncanonical functioning of dynamism factors in static mitochondria of the heart Heart failure and mitochondrial dysfunction: the role of mitochondrial fission/fusion abnormalities and new therapeutic strategies Complex I deficiency due to selective loss of Ndufs4 in the mouse heart results in severe hypertrophic cardiomyopathy A neurodegenerative perspective on mitochondrial optic neuropathies Mitochondrial Quality Control in Cardiac Diseases Mitochondrial fusion and fission proteins as novel therapeutic targets for treating cardiovascular disease New therapeutics to modulate mitochondrial dynamics and mitophagy in cardiac diseases Imbalanced OPA1 processing and mitochondrial fragmentation cause heart failure in mice Molecular mechanisms of mitochondrial autophagy/mitophagy in the heart Mitochondrial quality control in the myocardium: cooperation between protein degradation and mitophagy Soulamarin isolated from Calophyllum brasiliense (Clusiaceae) induces plasma membrane permeabilization of Trypanosoma cruzi and mytochondrial dysfunction Disrupting KATP channels diminishes the estrogen-mediated protection in female mutant mice during ischemia-reperfusion.Mitochondrial proteome remodeling in ischemic heart failure Dissociation of mitochondrial from sarcoplasmic reticular stress in Drosophila cardiomyopathy induced by molecularly distinct mitochondrial fusion defects.Mitochondrial morphological features are associated with fission and fusion events Induced transcription and stability of CELF2 mRNA drives widespread alternative splicing during T-cell signaling Mitochondrial Diseases Part II: Mouse models of OXPHOS deficiencies caused by defects in regulatory factors and other components required for mitochondrial function.Increase in Cardiac Ischemia-Reperfusion Injuries in Opa1+/- Mouse Model.Fatal infantile mitochondrial encephalomyopathy, hypertrophic cardiomyopathy and optic atrophy associated with a homozygous OPA1 mutation.Cardiac myocyte exosomes: stability, HSP60, and proteomics Mitochondrial dynamics in the adult cardiomyocytes: which roles for a highly specialized cell?Lipoprotein(a) Interactions With Low-Density Lipoprotein Cholesterol and Other Cardiovascular Risk Factors in Premature Acute Coronary Syndrome (ACS).Mitochondrial fusion and fission proteins: novel therapeutic targets for combating cardiovascular disease.Mitochondrial-Shaping Proteins in Cardiac Health and Disease - the Long and the Short of It!Mitochondrial fusion proteins and human diseases.Cell death in the myocardium: my heart won't go on.Mitochondrial dynamics in the heart as a novel therapeutic target for cardioprotection.Mitochondrial dynamic changes in health and genetic diseases.Disturbed mitochondrial dynamics and neurodegenerative disorders.Mitochondrial dynamics, mitophagy and cardiovascular disease.Mitochondrial Dynamics and Heart Failure.Mitochondrial dynamics and cell death in heart failure.Mitochondrial redox status as a target for cardiovascular disease.The OPA1 Gene Mutations Are Frequent in Han Chinese Patients with Suspected Optic Neuropathy.Assessing the effects of mitofusin 2 deficiency in the adult heart using 3D electron tomography.Adult-onset obesity is triggered by impaired mitochondrial gene expression.

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P2860

OPA1 mutation and late-onset cardiomyopathy: mitochondrial dysfunction and mtDNA instability

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OPA1 mutation and late-onset c ...... function and mtDNA instability

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OPA1 mutation and late-onset c ...... function and mtDNA instability

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OPA1 mutation and late-onset c ...... function and mtDNA instability

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OPA1 mutation and late-onset c ...... function and mtDNA instability

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OPA1 mutation and late-onset c ...... function and mtDNA instability

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JAHA.112.003012

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Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease

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OPA1 mutation and late-onset c ...... function and mtDNA instability

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Alexey A Tomilov

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Alice Tran

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Anne A Knowlton

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Gino Cortopassi

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Le Chen

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Nipavan Chiamvimonvat

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Tingting Liu

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Vanessa Davies

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Xiyuan Lu

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P2860

OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28

OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes

Mitochondrial fusion in human cells is efficient, requires the inner membrane potential, and is mediated by mitofusins.

Roles of the mammalian mitochondrial fission and fusion mediators Fis1, Drp1, and Opa1 in apoptosis

Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy

A mutation in the mitochondrial fission gene Dnm1l leads to cardiomyopathy

Mitofusin-2 determines mitochondrial network architecture and mitochondrial metabolism. A novel regulatory mechanism altered in obesity

Mitochondrial dynamics--fusion, fission, movement, and mitophagy--in neurodegenerative diseases

Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A

Disruption of fusion results in mitochondrial heterogeneity and dysfunction

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5

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1

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Marcela Votruba

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2012-10-25T00:00:00Z

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23316298

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3541627

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