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The function and the role of the mitochondrial glycerol-3-phosphate dehydrogenase in mammalian tissues

Biochimica et biophysica acta, 2013-03, Vol.1827 (3), p.401-410

2013

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Myocardial iron content and mitochondrial function in human heart failure: a direct tissue analysis

European journal of heart failure, 2017-04, Vol.19 (4), p.522-530

2017

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Cytochrome c Oxidase Subunit 4 Isoform Exchange Results in Modulation of Oxygen Affinity

Cells (Basel, Switzerland), 2020-02, Vol.9 (2), p.443

2020

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Mitochondrial targets of metformin—Are they physiologically relevant?

BioFactors (Oxford), 2019-09, Vol.45 (5), p.703-711

2019

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YME1L controls the accumulation of respiratory chain subunits and is required for apoptotic resistance, cristae morphogenesis, and cell proliferation

Molecular biology of the cell, 2012-03, Vol.23 (6), p.1010-1023

2012

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ROS generation and multiple forms of mammalian mitochondrial glycerol-3-phosphate dehydrogenase

Biochimica et biophysica acta, 2014-01, Vol.1837 (1), p.98-111

2014

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Role of cytochrome c oxidase nuclear-encoded subunits in health and disease

Physiological research, 2020-11, Vol.69 (6), p.947-965

2020

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Wars2 is a determinant of angiogenesis

Nature communications, 2016-07, Vol.7 (1), p.12061-12061, Article 12061

2016

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Mitochondrial ATP synthasome: Expression and structural interaction of its components

Biochemical and biophysical research communications, 2015-08, Vol.464 (3), p.787-793

2015

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TMEM70 mutations cause isolated ATP synthase deficiency and neonatal mitochondrial encephalocardiomyopathy

Nature genetics, 2008-11, Vol.40 (11), p.1288-1290

2008

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Loss of COX4I1 Leads to Combined Respiratory Chain Deficiency and Impaired Mitochondrial Protein Synthesis

Cells (Basel, Switzerland), 2021-02, Vol.10 (2), p.369

2021

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ROS production in brown adipose tissue mitochondria: the question of UCP1-dependence

Biochimica et biophysica acta, 2014-12, Vol.1837 (12), p.2017-2030

2014

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Role of the mitochondrial ATP synthase central stalk subunits γ and δ in the activity and assembly of the mammalian enzyme

Biochimica et biophysica acta. Bioenergetics, 2018-05, Vol.1859 (5), p.374-381

2018

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Mitochondrial ATP synthase deficiency due to a mutation in the ATP5E gene for the F1 ε subunit

Human molecular genetics, 2010-09, Vol.19 (17), p.3430-3439

2010

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TMEM70 facilitates biogenesis of mammalian ATP synthase by promoting subunit c incorporation into the rotor structure of the enzyme

The FASEB journal, 2019-12, Vol.33 (12), p.14103-14117

2019

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Role of Mitochondrial Glycerol-3-Phosphate Dehydrogenase in Metabolic Adaptations of Prostate Cancer

Cells (Basel, Switzerland), 2020-07, Vol.9 (8), p.1764

2020

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Current progress in the therapeutic options for mitochondrial disorders

Physiological research, 2020-12, Vol.69 (6), p.967-994

2020

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Mitochondrial encephalocardio-myopathy with early neonatal onset due to TMEM70 mutation

Archives of disease in childhood, 2010-04, Vol.95 (4), p.296-301

2010

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Sex difference in the sensitivity of cardiac mitochondrial permeability transition pore to calcium load

Molecular and cellular biochemistry, 2016-01, Vol.412 (1-2), p.147-154

2016

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Tissue- and species-specific differences in cytochrome c oxidase assembly induced by SURF1 defects

Biochimica et biophysica acta, 2016-04, Vol.1862 (4), p.705-715

2016

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Mitochondrial translation is the primary determinant of secondary mitochondrial complex I deficiencies

iScience, 2024-08, Vol.27 (8), p.110560, Article 110560

2024

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Evaluation of basic mitochondrial functions using rat tissue homogenates

Mitochondrion, 2011-09, Vol.11 (5), p.722-728

2011

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High efficiency of ROS production by glycerophosphate dehydrogenase in mammalian mitochondria

Archives of biochemistry and biophysics, 2009, Vol.481 (1), p.30-36

2009

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The function and the role of the mitochondrial glycerol-3-phosphate dehydrogenase in mammalian tissues

Myocardial iron content and mitochondrial function in human heart failure: a direct tissue analysis

Cytochrome c Oxidase Subunit 4 Isoform Exchange Results in Modulation of Oxygen Affinity

Mitochondrial targets of metformin—Are they physiologically relevant?

Acadian variant of Fanconi syndrome is caused by mitochondrial respiratory chain complex I deficiency due to a non-coding mutation in complex I assembly factor NDUFAF6

YME1L controls the accumulation of respiratory chain subunits and is required for apoptotic resistance, cristae morphogenesis, and cell proliferation

ROS generation and multiple forms of mammalian mitochondrial glycerol-3-phosphate dehydrogenase

Role of cytochrome c oxidase nuclear-encoded subunits in health and disease

Wars2 is a determinant of angiogenesis

The clinical, biochemical and genetic features associated with RMND1-related mitochondrial disease

Mitochondrial ATP synthasome: Expression and structural interaction of its components

TMEM70 mutations cause isolated ATP synthase deficiency and neonatal mitochondrial encephalocardiomyopathy

Loss of COX4I1 Leads to Combined Respiratory Chain Deficiency and Impaired Mitochondrial Protein Synthesis

ROS production in brown adipose tissue mitochondria: the question of UCP1-dependence

Role of the mitochondrial ATP synthase central stalk subunits γ and δ in the activity and assembly of the mammalian enzyme

Mitochondrial ATP synthase deficiency due to a mutation in the ATP5E gene for the F1 ε subunit

TMEM70 facilitates biogenesis of mammalian ATP synthase by promoting subunit c incorporation into the rotor structure of the enzyme

Role of Mitochondrial Glycerol-3-Phosphate Dehydrogenase in Metabolic Adaptations of Prostate Cancer

Current progress in the therapeutic options for mitochondrial disorders

Mitochondrial encephalocardio-myopathy with early neonatal onset due to TMEM70 mutation

Sex difference in the sensitivity of cardiac mitochondrial permeability transition pore to calcium load

Tissue- and species-specific differences in cytochrome c oxidase assembly induced by SURF1 defects

Mitochondrial translation is the primary determinant of secondary mitochondrial complex I deficiencies

Evaluation of basic mitochondrial functions using rat tissue homogenates

High efficiency of ROS production by glycerophosphate dehydrogenase in mammalian mitochondria

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