Role of cardiolipin alterations in mitochondrial dysfunction and disease. - Wikidata - awgldk - TriplyDB

Role of cardiolipin alterations in mitochondrial dysfunction and disease.

Role of cardiolipin alterations in mitochondrial dysfunction and disease.

http://www.wikidata.org/entity/Q36561388

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Cancer as a metabolic disease Mitochondria-targeted disruptors and inhibitors of cytochrome c/cardiolipin peroxidase complexes: a new strategy in anti-apoptotic drug discovery LC/MS characterization of rotenone induced cardiolipin oxidation in human lymphocytes: implications for mitochondrial dysfunction associated with Parkinson's disease Characterization of cardiolipins and their oxidation products by LC-MS analysis Acyl coenzyme A thioesterase Them5/Acot15 is involved in cardiolipin remodeling and fatty liver development Making heads or tails of phospholipids in mitochondria Shotgun lipidomics reveals the temporally dependent, highly diversified cardiolipin profile in the mammalian brain: temporally coordinated postnatal diversification of cardiolipin molecular species with neuronal remodeling Identification of the human mitochondrial linoleoyl-coenzyme A monolysocardiolipin acyltransferase (MLCL AT-1)Cardiolipin and electron transport chain abnormalities in mouse brain tumor mitochondria: lipidomic evidence supporting the Warburg theory of cancer Alterations in myocardial cardiolipin content and composition occur at the very earliest stages of diabetes: a shotgun lipidomics study Fatty old hearts: role of cardiac lipotoxicity in age-related cardiomyopathy Barth Syndrome: From Mitochondrial Dysfunctions Associated with Aberrant Production of Reactive Oxygen Species to Pluripotent Stem Cell Studies Αlpha-Synuclein as a Mediator in the Interplay between Aging and Parkinson's Disease Altered Traffic of Cardiolipin during Apoptosis: Exposure on the Cell Surface as a Trigger for "Antiphospholipid Antibodies"Successful management of Barth syndrome: a systematic review highlighting the importance of a flexible and multidisciplinary approach Myoglobin and mitochondria: a relationship bound by oxygen and nitric oxide The dynamics of the mitochondrial organelle as a potential therapeutic target The role of peroxidation of mitochondrial membrane phospholipids in pancreatic β -cell failure Models of plasma membrane organization can be applied to mitochondrial membranes to target human health and disease with polyunsaturated fatty acids Cardiolipin and its different properties in mitophagy and apoptosis Structural and functional analysis of PTPMT1, a phosphatase required for cardiolipin synthesis Misregulation of a DDHD Domain-containing Lipase Causes Mitochondrial Dysfunction in Yeast Quality control systems in cardiac aging Expression, folding, and proton transport activity of human uncoupling protein-1 (UCP1) in lipid membranes: evidence for associated functional forms Cardiolipin remodeling by TAZ/tafazzin is selectively required for the initiation of mitophagy First-in-class cardiolipin-protective compound as a therapeutic agent to restore mitochondrial bioenergetics A lipidomic approach to the study of human CD4(+) T lymphocytes in multiple sclerosis Lipids in the assembly of membrane proteins and organization of protein supercomplexes: implications for lipid-linked disorders Calcium signaling and mitochondrial destabilization in the triggering of the NLRP3 inflammasome Disorders of phospholipid metabolism: an emerging class of mitochondrial disease due to defects in nuclear genes Resistance of young rat hepatic mitochondria to bile acid-induced permeability transition: potential role of alpha-tocopherol Dietary macronutrients modulate the fatty acyl composition of rat liver mitochondrial cardiolipins Mitochondrial dysfunction in cardiac aging Evaluation of the cardiolipin biosynthetic pathway and its interactions in the diabetic heart Mitochondrial dysfunction in diabetic cardiomyopathy Mitochondria as a source and target of lipid peroxidation products in healthy and diseased heart Sex-specific cardiac cardiolipin remodelling after doxorubicin treatment The complexity of cardiolipin in health and disease Biosynthesis of oxidized lipid mediators via lipoprotein-associated phospholipase A2 hydrolysis of extracellular cardiolipin induces endothelial toxicity Oxidative stress, cardiolipin and mitochondrial dysfunction in nonalcoholic fatty liver disease

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P2860

Role of cardiolipin alterations in mitochondrial dysfunction and disease.

http://www.wikidata.org/entity/Q36561388

description

2006 nî lūn-bûn

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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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2006年論文

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2006年論文

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2006年论文

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2006年论文

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2006年论文

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Role of cardiolipin alterations in mitochondrial dysfunction and disease.

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Role of cardiolipin alterations in mitochondrial dysfunction and disease.

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Role of cardiolipin alterations in mitochondrial dysfunction and disease.

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Role of cardiolipin alterations in mitochondrial dysfunction and disease.

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AJPCELL.00243.2006

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American Journal of Physiology - Cell Physiology

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Role of cardiolipin alterations in mitochondrial dysfunction and disease.

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Adam J Chicco

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Genevieve C Sparagna

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P2860

Defective remodeling of cardiolipin and phosphatidylglycerol in Barth syndrome

The human TAZ gene complements mitochondrial dysfunction in the yeast taz1Delta mutant. Implications for Barth syndrome

Relationship between lipid saturation and lipid-protein interaction in liver mitochondria modified by catalytic hydrogenation with reference to cardiolipin molecular species

Lysocardiolipin formation and reacylation in isolated rat liver mitochondria

Mitochondrial lipid abnormality and electron transport chain impairment in mice lacking alpha-synuclein

Shotgun lipidomics of cardiolipin molecular species in lipid extracts of biological samples

Expression of monolysocardiolipin acyltransferase activity is regulated in concert with the level of cardiolipin and cardiolipin biosynthesis in the mammalian heart

Selective remodeling of cardiolipin fatty acids in the aged rat heart

Specific roles of protein-phospholipid interactions in the yeast cytochrome bc1 complex structure.

Taz1, an outer mitochondrial membrane protein, affects stability and assembly of inner membrane protein complexes: implications for Barth Syndrome

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10.1152/AJPCELL.00243.2006

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