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Thematic Review Series: Glycerolipids. Cardiolipin synthesis for the assembly of bacterial and mitochondrial membranes

Journal of lipid research, 2008-08, Vol.49 (8), p.1607-1620

Schlame, Michael

2008

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The Function of Tafazzin, a Mitochondrial Phospholipid–Lysophospholipid Acyltransferase

Journal of molecular biology, 2020-08, Vol.432 (18), p.5043-5051

2020

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The role of cardiolipin in the structural organization of mitochondrial membranes

Biochimica et biophysica acta, 2009-10, Vol.1788 (10), p.2080-2083

2009

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Barth syndrome, a human disorder of cardiolipin metabolism

FEBS letters, 2006-10, Vol.580 (23), p.5450-5455

2006

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Metabolism and function of mitochondrial cardiolipin

Progress in lipid research, 2014-07, Vol.55, p.1-16

2014

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StaR-related lipid transfer-like domain-containing protein CLDP43 affects cardiolipin synthesis and mitochondrial function in Trypanosoma brucei

PloS one, 2022-04, Vol.17 (4), p.e0259752-e0259752

2022

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The Basis for Acyl Specificity in the Tafazzin Reaction

The Journal of biological chemistry, 2017-03, Vol.292 (13), p.5499-5506

2017

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Protein crowding in the inner mitochondrial membrane

Biochimica et biophysica acta. Bioenergetics, 2021-01, Vol.1862 (1), p.148305-148305, Article 148305

Schlame, Michael

2021

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The Enzymatic Function of Tafazzin

The Journal of biological chemistry, 2006-12, Vol.281 (51), p.39217-39224

2006

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Cardiolipin synthesis for the assembly of bacterial and mitochondrial membranes

Journal of lipid research, 2008-08, Vol.49 (8), p.1607-1620

Schlame, Michael

2008

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Cardiolipin remodeling and the function of tafazzin

Biochimica et biophysica acta, 2013-03, Vol.1831 (3), p.582-588

Schlame, Michael

2013

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Cardiolipin Affects the Supramolecular Organization of ATP Synthase in Mitochondria

Biophysical journal, 2011-05, Vol.100 (9), p.2184-2192

2011

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Loss of protein association causes cardiolipin degradation in Barth syndrome

Nature chemical biology, 2016-08, Vol.12 (8), p.641-647

2016

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Increased Reactive Oxygen Species-Mediated Ca2+/Calmodulin-Dependent Protein Kinase II Activation Contributes to Calcium Handling Abnormalities and Impaired Contraction in Barth Syndrome

Circulation (New York, N.Y.), 2021-05, Vol.143 (19), p.1894-1911

2021

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Mitochondrial cristae as insulated transformers of metabolic energy

The EMBO journal, 2019-11, Vol.38 (22), p.e103472-n/a

Schlame, Michael

2019

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LPGAT1 controls the stearate/palmitate ratio of phosphatidylethanolamine and phosphatidylcholine in sn-1 specific remodeling

The Journal of biological chemistry, 2022-03, Vol.298 (3), p.101685-101685, Article 101685

2022

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Extramitochondrial cardiolipin suggests a novel function of mitochondria in spermatogenesis

The Journal of cell biology, 2019-05, Vol.218 (5), p.1491-1502

2019

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Author Correction: Upregulation of the AMPK-FOXO1-PDK4 pathway is a primary mechanism of pyruvate dehydrogenase activity reduction in tafazzin-deficient cells

Scientific reports, 2024-06, Vol.14 (1), p.14633-1, Article 14633

2024

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Loss of tafazzin results in decreased myoblast differentiation in C2C12 cells: A myoblast model of Barth syndrome and cardiolipin deficiency

Biochimica et biophysica acta. Molecular and cell biology of lipids, 2018-08, Vol.1863 (8), p.857-865

2018

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Phospholipids can regulate complex I assembly independent of their role in maintaining mitochondrial membrane integrity

Cell reports (Cambridge), 2023-08, Vol.42 (8), p.112846-112846, Article 112846

2023

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The physical state of lipid substrates provides transacylation specificity for tafazzin

Nature chemical biology, 2012-10, Vol.8 (10), p.862-869

2012

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Upregulation of the AMPK-FOXO1-PDK4 pathway is a primary mechanism of pyruvate dehydrogenase activity reduction in tafazzin-deficient cells

Scientific reports, 2024-05, Vol.14 (1), p.11497-15, Article 11497

2024

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Formation of molecular species of mitochondrial cardiolipin. 1. A novel transacylation mechanism to shuttle fatty acids between sn-1 and sn-2 positions of multiple phospholipid species

Biochimica et biophysica acta, 2009-04, Vol.1791 (4), p.314-320

2009

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Role of Calcium-Independent Phospholipase A₂ in the Pathogenesis of Barth Syndrome

Proceedings of the National Academy of Sciences - PNAS, 2009-02, Vol.106 (7), p.2337-2341

2009

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The biosynthesis and functional role of cardiolipin

Progress in lipid research, 2000-05, Vol.39 (3), p.257-288

2000

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Thematic Review Series: Glycerolipids. Cardiolipin synthesis for the assembly of bacterial and mitochondrial membranes

The Function of Tafazzin, a Mitochondrial Phospholipid–Lysophospholipid Acyltransferase

The role of cardiolipin in the structural organization of mitochondrial membranes

Barth syndrome, a human disorder of cardiolipin metabolism

Metabolism and function of mitochondrial cardiolipin

StaR-related lipid transfer-like domain-containing protein CLDP43 affects cardiolipin synthesis and mitochondrial function in Trypanosoma brucei

The Basis for Acyl Specificity in the Tafazzin Reaction

Protein crowding in the inner mitochondrial membrane

The Enzymatic Function of Tafazzin

Cardiolipin synthesis for the assembly of bacterial and mitochondrial membranes

Cardiolipin remodeling and the function of tafazzin

Cardiolipin Affects the Supramolecular Organization of ATP Synthase in Mitochondria

Loss of protein association causes cardiolipin degradation in Barth syndrome

Increased Reactive Oxygen Species-Mediated Ca2+/Calmodulin-Dependent Protein Kinase II Activation Contributes to Calcium Handling Abnormalities and Impaired Contraction in Barth Syndrome

Mitochondrial cristae as insulated transformers of metabolic energy

LPGAT1 controls the stearate/palmitate ratio of phosphatidylethanolamine and phosphatidylcholine in sn-1 specific remodeling

Extramitochondrial cardiolipin suggests a novel function of mitochondria in spermatogenesis

Author Correction: Upregulation of the AMPK-FOXO1-PDK4 pathway is a primary mechanism of pyruvate dehydrogenase activity reduction in tafazzin-deficient cells

Loss of tafazzin results in decreased myoblast differentiation in C2C12 cells: A myoblast model of Barth syndrome and cardiolipin deficiency

Phospholipids can regulate complex I assembly independent of their role in maintaining mitochondrial membrane integrity

The physical state of lipid substrates provides transacylation specificity for tafazzin

Upregulation of the AMPK-FOXO1-PDK4 pathway is a primary mechanism of pyruvate dehydrogenase activity reduction in tafazzin-deficient cells

Formation of molecular species of mitochondrial cardiolipin. 1. A novel transacylation mechanism to shuttle fatty acids between sn-1 and sn-2 positions of multiple phospholipid species

Role of Calcium-Independent Phospholipase A₂ in the Pathogenesis of Barth Syndrome

The biosynthesis and functional role of cardiolipin

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