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The Assembly Pathway of Mitochondrial Respiratory Chain Complex I

Cell metabolism, 2017-01, Vol.25 (1), p.128-139

2017

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Novel defect in phosphatidylinositol 4‐kinase type 2‐alpha (PI4K2A) at the membrane‐enzyme interface is associated with metabolic cutis laxa

Journal of inherited metabolic disease, 2020-11, Vol.43 (6), p.1382-1391

2020

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Unraveling the complexity of mitochondrial complex I assembly: A dynamic process

Biochimica et biophysica acta, 2016-07, Vol.1857 (7), p.980-990

2016

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Evolution and structural organization of the mitochondrial contact site (MICOS) complex and the mitochondrial intermembrane space bridging (MIB) complex

Biochimica et biophysica acta, 2016-01, Vol.1863 (1), p.91-101

2016

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Locking loop movement in the ubiquinone pocket of complex I disengages the proton pumps

Nature communications, 2018-10, Vol.9 (1), p.4500-10, Article 4500

2018

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A salvage pathway maintains highly functional respiratory complex I

Nature communications, 2020-04, Vol.11 (1), p.1643-1643, Article 1643

2020

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A homozygous missense mutation in ERAL1, encoding a mitochondrial rRNA chaperone, causes Perrault syndrome

Human molecular genetics, 2017-07, Vol.26 (13), p.2541-2550

2017

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MR-1S Interacts with PET100 and PET117 in Module-Based Assembly of Human Cytochrome c Oxidase

Cell reports (Cambridge), 2017-02, Vol.18 (7), p.1727-1738

2017

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Accessory NUMM (NDUFS6) subunit harbors a Zn-binding site and is essential for biogenesis of mitochondrial complex I

Proceedings of the National Academy of Sciences - PNAS, 2015-05, Vol.112 (18), p.5685-5690

2015

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Complexome Profiling-Exploring Mitochondrial Protein Complexes in Health and Disease

Frontiers in cell and developmental biology, 2022-01, Vol.9, p.796128-796128

2022

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Mitochondrial Unselective Channels throughout the eukaryotic domain

Mitochondrion, 2011-05, Vol.11 (3), p.382-390

2011

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Deactivation of mitochondrial complex I after hypoxia–ischemia in the immature brain

Journal of cerebral blood flow and metabolism, 2019-09, Vol.39 (9), p.1790-1802

2019

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COmplexome Profiling ALignment (COPAL) reveals remodeling of mitochondrial protein complexes in Barth syndrome

Bioinformatics (Oxford, England), 2019-09, Vol.35 (17), p.3083-3091

2019

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Identification and evolutionary analysis of tissue-specific isoforms of mitochondrial complex I subunit NDUFV3

Biochimica et biophysica acta. Bioenergetics, 2017-03, Vol.1858 (3), p.208-217

2017

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The m-AAA Protease Associated with Neurodegeneration Limits MCU Activity in Mitochondria

Molecular cell, 2016-10, Vol.64 (1), p.148-162

2016

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Multiplexed complexome profiling using tandem mass tags

Biochimica et biophysica acta. Bioenergetics, 2021-09, Vol.1862 (9), p.148448-148448, Article 148448

2021

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TMEM70 functions in the assembly of complexes I and V

Biochimica et biophysica acta. Bioenergetics, 2020-08, Vol.1861 (8), p.148202-148202, Article 148202

2020

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A homozygous missense mutation in ERAL1, encoding a mitochondrial rRNA chaperone, causes Perrault syndrome

Human molecular genetics, 2017-07, Vol.26 (13), p.2541-2550

2017

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Barth syndrome cells display widespread remodeling of mitochondrial complexes without affecting metabolic flux distribution

Biochimica et biophysica acta. Molecular basis of disease, 2018-11, Vol.1864 (11), p.3650-3658

2018

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CEDAR, an online resource for the reporting and exploration of complexome profiling data

Biochimica et biophysica acta. Bioenergetics, 2021-07, Vol.1862 (7), p.148411-148411, Article 148411

2021

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Complexome analysis of the nitrite-dependent methanotroph Methylomirabilis lanthanidiphila

Biochimica et biophysica acta. Bioenergetics, 2019-09, Vol.1860 (9), p.734-744

2019

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ZBTB11 dysfunction: spectrum of brain abnormalities, biochemical signature and cellular consequences

Brain (London, England : 1878), 2022-07, Vol.145 (7), p.2602-2616

2022

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Staphylococcus epidermidis: metabolic adaptation and biofilm formation in response to different oxygen concentrations

Pathogens and disease, 2016-02, Vol.74 (1), p.ftv111-ftv111

2016

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AIFM1 is a component of the mitochondrial disulfide relay that drives complex I assembly through efficient import of NDUFS5

The Assembly Pathway of Mitochondrial Respiratory Chain Complex I

Novel defect in phosphatidylinositol 4‐kinase type 2‐alpha (PI4K2A) at the membrane‐enzyme interface is associated with metabolic cutis laxa

Unraveling the complexity of mitochondrial complex I assembly: A dynamic process

Evolution and structural organization of the mitochondrial contact site (MICOS) complex and the mitochondrial intermembrane space bridging (MIB) complex

Locking loop movement in the ubiquinone pocket of complex I disengages the proton pumps

A salvage pathway maintains highly functional respiratory complex I

A homozygous missense mutation in ERAL1, encoding a mitochondrial rRNA chaperone, causes Perrault syndrome

MR-1S Interacts with PET100 and PET117 in Module-Based Assembly of Human Cytochrome c Oxidase

Accessory NUMM (NDUFS6) subunit harbors a Zn-binding site and is essential for biogenesis of mitochondrial complex I

Complexome Profiling-Exploring Mitochondrial Protein Complexes in Health and Disease

Mitochondrial Unselective Channels throughout the eukaryotic domain

Deactivation of mitochondrial complex I after hypoxia–ischemia in the immature brain

COmplexome Profiling ALignment (COPAL) reveals remodeling of mitochondrial protein complexes in Barth syndrome

Identification and evolutionary analysis of tissue-specific isoforms of mitochondrial complex I subunit NDUFV3

The m-AAA Protease Associated with Neurodegeneration Limits MCU Activity in Mitochondria

Multiplexed complexome profiling using tandem mass tags

TMEM70 functions in the assembly of complexes I and V

A homozygous missense mutation in ERAL1, encoding a mitochondrial rRNA chaperone, causes Perrault syndrome

Barth syndrome cells display widespread remodeling of mitochondrial complexes without affecting metabolic flux distribution

CEDAR, an online resource for the reporting and exploration of complexome profiling data

Complexome analysis of the nitrite-dependent methanotroph Methylomirabilis lanthanidiphila

Bi-allelic Mutations in the Mitochondrial Ribosomal Protein MRPS2 Cause Sensorineural Hearing Loss, Hypoglycemia, and Multiple OXPHOS Complex Deficiencies

ZBTB11 dysfunction: spectrum of brain abnormalities, biochemical signature and cellular consequences

Staphylococcus epidermidis: metabolic adaptation and biofilm formation in response to different oxygen concentrations

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