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Michael Schlame
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS (2013)
Barth syndrome: Cellular compensation of mitochondrial dysfunction and apoptosis inhibition due to changes in cardiolipin remodeling linked to tafazzin (TAZ) gene mutation
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Comparison of cardiolipins from Drosophila strains with mutations in putative remodeling enzymes
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CHEMISTRY AND PHYSICS OF LIPIDS (2012)
Myocardial Regulation of Lipidomic Flux by Cardiolipin Synthase SETTING THE BEAT FOR BIOENERGETIC EFFICIENCY
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JOURNAL OF BIOLOGICAL CHEMISTRY (2012)
The Cardiolipin Transacylase, Tafazzin, Associates with Two Distinct Respiratory Components Providing Insight into Barth Syndrome (vol 19, pg 5143, 2008)
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MOLECULAR BIOLOGY OF THE CELL (2012)
The physical state of lipid substrates provides transacylation specificity for tafazzin
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The complexity of cardiolipin in health and disease
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TRENDS IN BIOCHEMICAL SCIENCES (2012)
Cardiolipin Affects the Supramolecular Organization of ATP Synthase in Mitochondria
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Mitochondrial Phosphatase PTPMT1 Is Essential for Cardiolipin Biosynthesis
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Characterization of a Transgenic Short Hairpin RNA-Induced Murine Model of Tafazzin Deficiency
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A mitochondrial phosphatase required for cardiolipin biosynthesis: the PGP phosphatase Gep4
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OPA1 disease alleles causing dominant optic atrophy have defects in cardiolipin-stimulated GTP hydrolysis and membrane tubulation
Tadato Ban et al.
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ALCAT1 is a polyglycerophospholipid acyltransferase potently regulated by adenine nucleotide and thyroid status
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The enigmatic role of tafazzin in cardiolipin metabolism
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Mitochondrial Cardiolipin Involved in Outer-Membrane Protein Biogenesis: Implications for Barth Syndrome
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Identification of a Cardiolipin-specific Phospholipase Encoded by the Gene CLD1 (YGR110W) in Yeast
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Coassembly of Mgm1 isoforms requires cardiolipin and mediates mitochondrial inner membrane fusion
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Cardiolipin provides an essential activating platform for caspase-8 on mitochondria
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Loss of tafazzin in yeast leads to increased oxidative stress during respiratory growth
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Microfluidics-based electrospray ionization enhances the intrasource separation of lipid classes and extends identification of individual molecular species through multi-dimensional mass spectrometry: development of an automated high-throughput platform for shotgun lipidomics
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RAPID COMMUNICATIONS IN MASS SPECTROMETRY (2008)
The Cardiolipin Transacylase, Tafazzin, Associates with Two Distinct Respiratory Components Providing Insight into Barth Syndrome
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Genetic ablation of calcium-independent phospholipase A2γ leads to alterations in mitochondrial lipid metabolism and function resulting in a deficient mitochondrial bioenergetic phenotype
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Motor-free mitochondrial presequence translocase drives membrane integration of preproteins
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NATURE CELL BIOLOGY (2007)
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Yang Xu et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2006)
Barth syndrome, a human disorder of cardiolipin metabolism
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A Drosophila model of Barth syndrome
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PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2006)
Mitochondrial mislocalization and altered assembly of a cluster of Barth syndrome mutant tafazzins
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JOURNAL OF CELL BIOLOGY (2006)
Contribution of peroxidized cardiolipin to inactivation of bovine heart cytochrome c oxidase
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FREE RADICAL BIOLOGY AND MEDICINE (2006)
Identification and characterization of human cardiolipin synthase
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Cardiolipin is essential for organization of complexes III and IV into a supercomplex in intact yeast mitochondria
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JOURNAL OF BIOLOGICAL CHEMISTRY (2005)
Monolysocardiolipins accumulate in Barth syndrome but do not lead to enhanced apoptosis
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A novel cardiolipin-remodeling pathway revealed by a gene encoding an endoplasmic reticulum-associated acyl-CoA:lysocardiolipin acyltransferase (ALCAT1) in mouse
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ZM Gu et al.
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The human TAZ gene complements mitochondrial dysfunction in the Yeast taz1Δ mutant -: Implications for Barth syndrome
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Cardiolipin stabilizes respiratory chain supercomplexes
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JOURNAL OF BIOLOGICAL CHEMISTRY (2003)
Phospholipid abnormalities in children with Barth syndrome
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JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2003)
Choline head groups stabilize the matrix loop regions of the ATP/ADP carrier ScAAC2
V Panneels et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2003)
Gluing the respiratory chain together - Cardiolipin is required for supercomplex formation in the inner mitochondrial membrane
M Zhang et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2002)
Cardiolipin prevents rate-dependent uncoupling and provides osmotic stability in yeast mitochondria
V Koshkin et al.
BIOCHEMICAL JOURNAL (2002)
Deficiency of tetralinoleoyl-cardiolipin in Barth syndrome
M Schlame et al.
ANNALS OF NEUROLOGY (2002)
Absence of cardiolipin in the crd1 null mutant results in decreased mitochondrial membrane potential and reduced mitochondrial function
F Jiang et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2000)
The cytochrome bc1 and cytochrome c oxidase complexes associate to form a single supracomplex in yeast mitochondria
CM Cruciat et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2000)
Oxidative phosphorylation in cardiolipin-lacking yeast mitochondria
V Koshkin et al.
BIOCHEMICAL JOURNAL (2000)
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