Evidence for physical association of mitochondrial fatty acid oxidation and oxidative phosphorylation complexes - Wikidata - wikimedia - TriplyDB

Evidence for physical association of mitochondrial fatty acid oxidation and oxidative phosphorylation complexes

Evidence for physical association of mitochondrial fatty acid oxidation and oxidative phosphorylation complexes

http://www.wikidata.org/entity/Q24604387

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Human METTL20 methylates lysine residues adjacent to the recognition loop of the electron transfer flavoprotein in mitochondria Identification and characterization of new long chain acyl-CoA dehydrogenases Combined defects in oxidative phosphorylation and fatty acid β-oxidation in mitochondrial disease Mitochondrial disease in childhood: nuclear encoded Observations regarding retinopathy in mitochondrial trifunctional protein deficiencies Mitochondrial structure, function and dynamics are temporally controlled by c-Myc Follistatin-like protein 1 enhances NLRP3 inflammasome-mediated IL-1β secretion from monocytes and macrophages Diacylglycerol acyltransferase-1 inhibition enhances intestinal fatty acid oxidation and reduces energy intake in rats Defects in mitochondrial and peroxisomal β-oxidation influence virulence in the maize pathogen Ustilago maydis.Anoxic androgen degradation by the denitrifying bacterium Sterolibacterium denitrificans via the 2,3-seco pathway Coenzyme q and the respiratory chain: coenzyme q pool and mitochondrial supercomplexes Mitochondrial and cellular mechanisms for managing lipid excess.Acute high-altitude hypoxic brain injury: Identification of ten differential proteins.Complex changes in the liver mitochondrial proteome of short chain acyl-CoA dehydrogenase deficient mice.Short-chain 3-hydroxyacyl-coenzyme A dehydrogenase associates with a protein super-complex integrating multiple metabolic pathways Mitochondrial malic enzyme 3 is important for insulin secretion in pancreatic β-cells SIRT3 and SIRT5 regulate the enzyme activity and cardiolipin binding of very long-chain acyl-CoA dehydrogenase.Cardiac metabolic pathways affected in the mouse model of barth syndrome.Nickel inhibits mitochondrial fatty acid oxidation.Defective Expression of the Mitochondrial-tRNA Modifying Enzyme GTPBP3 Triggers AMPK-Mediated Adaptive Responses Involving Complex I Assembly Factors, Uncoupling Protein 2, and the Mitochondrial Pyruvate Carrier.Characterization of Chorioretinopathy Associated with Mitochondrial Trifunctional Protein Disorders: Long-Term Follow-up of 21 Cases.The promiscuous enzyme medium-chain 3-keto-acyl-CoA thiolase triggers a vicious cycle in fatty-acid beta-oxidation.The elusive magic pill: finding effective therapies for mitochondrial disorders Molecular and cellular pathology of very-long-chain acyl-CoA dehydrogenase deficiency New protein-protein interactions of mitochondrial connexin 43 in mouse heart PPARs and Mitochondrial Metabolism: From NAFLD to HCC.New developments on the functions of coenzyme Q in mitochondria.Mitochondrial proteomics--a tool for the study of metabolic disorders.ECHS1 mutations cause combined respiratory chain deficiency resulting in Leigh syndrome.What is the proper precursor-to-product labeling relationship for calculating the fractional synthetic rate of muscle triglyceride?Complex I assembly function and fatty acid oxidation enzyme activity of ACAD9 both contribute to disease severity in ACAD9 deficiency.Application of an Image Cytometry Protocol for Cellular and Mitochondrial Phenotyping on Fibroblasts from Patients with Inherited Disorders.Fasting induces prominent proteomic changes in liver in very long chain Acyl-CoA dehydrogenase deficient mice.Lower mitochondrial DNA and altered mitochondrial fuel metabolism in hiv-exposed uninfected infants in cameroon.Elaidate, an 18-carbon trans-monoenoic fatty acid, inhibits β-oxidation in human peripheral blood macrophages.Lysine desuccinylase SIRT5 binds to cardiolipin and regulates the electron transport chain.Inflexibility of AMPK-mediated metabolic reprogramming in mitochondrial disease.Loss of the Mitochondrial Fatty Acid β-Oxidation Protein Medium-Chain Acyl-Coenzyme A Dehydrogenase Disrupts Oxidative Phosphorylation Protein Complex Stability and Function.Advances in the Understanding and Treatment of Mitochondrial Fatty Acid Oxidation Disorders.Mitochondrial Trifunctional Protein Deficiency: Severe Cardiomyopathy and Cardiac Transplantation.

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Evidence for physical association of mitochondrial fatty acid oxidation and oxidative phosphorylation complexes

http://www.wikidata.org/entity/Q24604387

description

2010 nî lūn-bûn

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2010 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի սեպտեմբերին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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name

Evidence for physical associat ...... tive phosphorylation complexes

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Evidence for physical associat ...... tive phosphorylation complexes

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Evidence for physical associat ...... tive phosphorylation complexes

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type

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Evidence for physical associat ...... tive phosphorylation complexes

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Evidence for physical associat ...... tive phosphorylation complexes

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Evidence for physical associat ...... tive phosphorylation complexes

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Evidence for physical associat ...... tive phosphorylation complexes

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Evidence for physical associat ...... tive phosphorylation complexes

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Evidence for physical associat ...... tive phosphorylation complexes

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JBC.M110.139493

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Journal of Biological Chemistry

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Evidence for physical associat ...... tive phosphorylation complexes

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Al-Walid Mohsen

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

Eric S Goetzman

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

Jerry Vockley

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

Stephanie J Mihalik

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Yudong Wang

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P2860

Supercomplexes in the respiratory chains of yeast and mammalian mitochondria

Structural basis for substrate fatty acyl chain specificity: crystal structure of human very-long-chain acyl-CoA dehydrogenase

Monomethyl branched-chain fatty acids play an essential role in Caenorhabditis elegans development

Lysine acetylation targets protein complexes and co-regulates major cellular functions

Yeast mitochondrial F1F0-ATP synthase exists as a dimer: identification of three dimer-specific subunits.

The protonmotive Q cycle. Energy transduction by coupling of proton translocation to electron transfer by the cytochrome bc1 complex

Short-chain acyl-coenzyme A dehydrogenase deficiency

Molecular cloning of cDNA encoding rat very long-chain acyl-CoA synthetase

Analysis of molecular masses and oligomeric states of protein complexes by blue native electrophoresis and isolation of membrane protein complexes by two-dimensional native electrophoresis

A role for the mitochondrial deacetylase Sirt3 in regulating energy homeostasis

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29834-41

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10.1074/JBC.M110.139493

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39

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285

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2010-09-24T00:00:00Z

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20663895

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phosphorylation

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2943265

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