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JOURNAL OF LIPID RESEARCH, ISSN 0022-2275, 08/2008, Volume 49, Issue 8, pp. 1607 - 1620
In this article, the formation of prokaryotic and eukaryotic cardiolipin is reviewed in light of its biological function. I begin with a detailed account of... 
RESPIRATORY-CHAIN | POLYMORPHIC PHASE-BEHAVIOR | BIOCHEMISTRY & MOLECULAR BIOLOGY | ESCHERICHIA-COLI | BARTH-SYNDROME | phospholipids | CARRIER PROTEIN | RAT-LIVER MITOCHONDRIA | PHOSPHOLIPID SCRAMBLASE-3 | mitochondrial biogenesis | tafazzin | TETRALINOLEOYL-CARDIOLIPIN | BACILLUS-SUBTILIS | molecular species | CYTOCHROME-C RELEASE | Thematic Review
Journal Article
Biophysical Journal, ISSN 0006-3495, 08/2019, Volume 117, Issue 3, pp. 429 - 444
Cardiolipin is an anionic lipid found in the mitochondrial membranes of eukaryotes ranging from unicellular microorganisms to metazoans. This unique lipid... 
RAT-LIVER | TETRALINOLEOYL-CARDIOLIPIN | BILAYER THICKNESS | OUTER-MEMBRANE | PROTEIN INTERACTIONS | BIOPHYSICS | ELASTIC PROPERTIES | BARTH-SYNDROME | LIPID-COMPOSITION | INNER MEMBRANES | SOFTWARE NEWS | Molecular dynamics | Lipids | Models | Cardiolipin | Surface active agents | Analysis
Journal Article
International Journal of Cardiology, ISSN 0167-5273, 07/2019, Volume 287, pp. 96 - 105
Journal Article
IUBMB Life, ISSN 1521-6543, 07/2019, Volume 71, Issue 7, pp. 791 - 801
ABSTRACT Barth syndrome (BTHS) is a rare multisystemic genetic disorder caused by mutations in the TAZ gene. TAZ encodes a mitochondrial enzyme that remodels... 
cardiolipin | Barth syndrome | mitochondria | MUTANT | PROTEIN | BIOCHEMISTRY & MOLECULAR BIOLOGY | CARDIOMYOPATHY | YEAST MODEL | MITOPHAGY | DEFICIENCY | CELL BIOLOGY | TETRALINOLEOYL-CARDIOLIPIN | CARDIOSKELETAL MYOPATHY | PLURIPOTENT STEM-CELL | RESPIRATORY SUPERCOMPLEXES | Physiological aspects | Membrane lipids | Cardiolipin | Analysis
Journal Article
Journal of Lipid Research, ISSN 0022-2275, 05/2013, Volume 54, Issue 5, pp. 1312 - 1325
Journal Article
Journal Article
Chemistry and Physics of Lipids, ISSN 0009-3084, 04/2014, Volume 179, pp. 75 - 81
Journal Article
Journal Article
Autophagy, ISSN 1554-8627, 04/2015, Volume 11, Issue 4, pp. 643 - 652
Tafazzin (TAZ) is a phospholipid transacylase that catalyzes the remodeling of cardiolipin, a mitochondrial phospholipid required for oxidative... 
TLCL, tetralinoleoyl-cardiolipin | mitochondrial dysfunction | MLCL, monolysocardiolipin | BafA1, bafilomycin A | BTHS, Barth syndrome | Barth syndrome | mitophagosome | CCCP, carbonyl cyanide m-chlorophenylhydrazone | PARK2, parkin RBR E3 ubiquitin protein ligase | MAP1LC3B/LC3B, microtubule-associated protein 1 light chain 3 beta | TAZ, tafazzin | LTG, LysoTracker Green | autophagy | FCCP, carbonyl cyanide p-triflouromethoxyphenylhydrazone | PINK1, PTEN-induced putative kinase 1 | CL, cardiolipin | AdGFP-LC3, recombinant adenovirus expressing GFP tagged MAP1LC3B | AdTAZ, recombinant adenovirus expressing Myc-tagged TAZ | cardiolipin | tafazzin | 1 | mitophagy | MEF, mouse embryonic fibroblast | MTR, MitoTracker Red | SOD2, superoxide dismutase 2 mitochondrial | Dox, doxycycline | Tafazzin | Mitochondrial dysfunction | Mitophagosome | Cardiolipin | Mitophagy | Autophagy | RESPIRATORY-CHAIN | OXIDATIVE STRESS | FUSION | STABILITY | CARDIOMYOPATHY | BARTH-SYNDROME | CARDIAC-MUSCLE | MITOCHONDRIAL-MEMBRANE | CELL BIOLOGY | SKELETAL-MUSCLE | DISEASE | Cardiomyopathy, Dilated - genetics | Cardiomyopathy, Dilated - pathology | Humans | Transcription Factors - deficiency | Autophagy - physiology | Cardiolipins - metabolism | Transcription Factors - genetics | Mutation - genetics | Cardiomyopathy, Dilated - metabolism | Mitochondrial Degradation - physiology | Transcription Factors - metabolism | Animals | Mitochondria - genetics | Mice | Autophagy - genetics
Journal Article
Journal Article
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