Mitofusin 2 is required to maintain mitochondrial coenzyme Q levels. - Wikidata - wikimedia - TriplyDB

Mitofusin 2 is required to maintain mitochondrial coenzyme Q levels.

Mitofusin 2 is required to maintain mitochondrial coenzyme Q levels.

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Metabolic regulation of mitochondrial dynamics Intra-mitochondrial Methylation Deficiency Due to Mutations in SLC25A26 Imbalanced OPA1 processing and mitochondrial fragmentation cause heart failure in mice Cellular Allometry of Mitochondrial Functionality Establishes the Optimal Cell Size Applying a systems approach to thyroid physiology: Looking at the whole with a mitochondrial perspective instead of judging single TSH values or why we should know more about mitochondria to understand metabolism.Mitofusin 2 ablation increases endoplasmic reticulum-mitochondria coupling.Lack of aprataxin impairs mitochondrial functions via downregulation of the APE1/NRF1/NRF2 pathway.The abundance of the ARL2 GTPase and its GAP, ELMOD2, at mitochondria are modulated by the fusogenic activity of mitofusins and stressors.Supplementation of Coenzyme Q10 among Patients with Type 2 Diabetes Mellitus.Mitochondrial protein functions elucidated by multi-omic mass spectrometry profiling.Of yeast, mice and men: MAMs come in two flavors.Mitochondrial-Shaping Proteins in Cardiac Health and Disease - the Long and the Short of It!Mitochondrial fusion, fission, and mitochondrial toxicity.Age-related accumulation of phosphorylated mitofusin 2 protein in retinal ganglion cells correlates with glaucoma progression.Mitochondrial fission and fusion in secondary brain damage after CNS insults.The Role of Exercise and TFAM in Preventing Skeletal Muscle Atrophy.Mitochondrial Dynamics in Regulating the Unique Phenotypes of Cancer and Stem Cells.Selective mitochondrial depletion, apoptosis resistance, and increased mitophagy in human Charcot-Marie-Tooth 2A motor neurons.Leishmania donovani restricts mitochondrial dynamics to enhance miRNP stability and target RNA repression in host macrophages.Mitochondria-Associated Membranes As Networking Platforms and Regulators of Cancer Cell Fate.Obesity-induced oocyte mitochondrial defects are partially prevented and rescued by supplementation with co-enzyme Q10 in a mouse model Dynamin-related Protein 1 Inhibition Mitigates Bisphenol A-mediated Alterations in Mitochondrial Dynamics and Neural Stem Cell Proliferation and Differentiation.Signalling mechanisms underlying doxorubicin and Nox2 NADPH oxidase-induced cardiomyopathy: involvement of mitofusin-2.Implications of mitochondrial network organization in mitochondrial stress signalling in NARP cybrid and Rho0 cells.The Mitochondrial Basis of Aging and Age-Related Disorders.When centromeres fill in for telomeres.Transcriptomic and proteomic landscape of mitochondrial dysfunction reveals secondary coenzyme Q deficiency in mammals.The ARL2 GTPase regulates mitochondrial fusion from the intermembrane space.Regulation of mitochondrial bioenergetics by the non-canonical roles of mitochondrial dynamics proteins in the heart.Over Six Decades of Discovery and Characterization of the Architecture at Mitochondria-Associated Membranes (MAMs).Mitochondrial energetics in the kidney.Mitofusin 2: from functions to disease.Mitofusin 2 keeps the respiratory chain on Q.Perturbed Redox Signaling Exacerbates a Mitochondrial Myopathy A high-throughput screen of real-time ATP levels in individual cells reveals mechanisms of energy failure

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P2860

Mitofusin 2 is required to maintain mitochondrial coenzyme Q levels.

http://www.wikidata.org/entity/Q35094282

description

2015 nî lūn-bûn

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2015 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

2015 թվականի փետրվարին հրատարակված գիտական հոդված

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2015年の論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年论文

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name

Mitofusin 2 is required to maintain mitochondrial coenzyme Q levels.

@ast

Mitofusin 2 is required to maintain mitochondrial coenzyme Q levels.

@en

type

label

Mitofusin 2 is required to maintain mitochondrial coenzyme Q levels.

@ast

Mitofusin 2 is required to maintain mitochondrial coenzyme Q levels.

@en

prefLabel

Mitofusin 2 is required to maintain mitochondrial coenzyme Q levels.

@ast

Mitofusin 2 is required to maintain mitochondrial coenzyme Q levels.

@en

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Journal of Cell Biology

P1476

Mitofusin 2 is required to maintain mitochondrial coenzyme Q levels

@en

P2093

Christoph Dieterich

http://www.w3.org/2001/XMLSchema#string

Elisa Motori

http://www.w3.org/2001/XMLSchema#string

Gunter Rappl

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Kjell Hultenby

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Marie Lagouge

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Nils-Göran Larsson

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Susanne Brodesser

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Tobias Brandt

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Gene ontology: tool for the unification of biology

Dynamin-related protein Drp1 is required for mitochondrial division in mammalian cells

KEGG: kyoto encyclopedia of genes and genomes

Prenyldiphosphate synthase, subunit 1 (PDSS1) and OH-benzoate polyprenyltransferase (COQ2) mutations in ubiquinone deficiency and oxidative phosphorylation disorders

Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources

Computer visualization of three-dimensional image data using IMOD

A practical recipe for stable isotope labeling by amino acids in cell culture (SILAC)

The GTPase superfamily: a conserved switch for diverse cell functions

Membrane topology and mitochondrial targeting of mitofusins, ubiquitous mammalian homologs of the transmembrane GTPase Fzo

Mitofusins Mfn1 and Mfn2 coordinately regulate mitochondrial fusion and are essential for embryonic development

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429-442

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10.1083/JCB.201411100

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4

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208

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Ilian Atanassov

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2015-02-01T00:00:00Z

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25688136

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4332246

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