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Significance of Respirasomes for the Assembly/Stability of Human Respiratory Chain Complex I

The Journal of biological chemistry, 2004-08, Vol.279 (35), p.36349-36353

2004

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Functional F1-ATPase Essential in Maintaining Growth and Membrane Potential of Human Mitochondrial DNA-depleted ρ° Cells

The Journal of biological chemistry, 1998-09, Vol.273 (36), p.22983-22989

1998

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Leigh-like encephalopathy complicating Leber's hereditary optic neuropathy

Annals of neurology, 2002-09, Vol.52 (3), p.374-377

2002

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Sequence conservation from human to prokaryotes of Surf1, a protein involved in cytochrome c oxidase assembly, deficient in Leigh syndrome

FEBS letters, 1999-12, Vol.462 (3), p.416-420

1999

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New evidence of a mitochondrial genetic background paradox: impact of the J haplogroup on the A3243G mutation

BMC medical genetics, 2008-05, Vol.9 (1), p.41-41, Article 41

2008

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Mitochondria and reactive oxygen species in renal cancer

Biochimie, 2007-09, Vol.89 (9), p.1080-1088

2007

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Mitochondrial disorders in renal tumors

Mitochondrion, 2006-06, Vol.6 (3), p.105-117

2006

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Low mitochondrial respiratory chain content correlates with tumor aggressiveness in renal cell carcinoma

Carcinogenesis (New York), 2002-05, Vol.23 (5), p.759-768

2002

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Clonal expansion of mutated mitochondrial DNA is associated with tumor formation and complex I deficiency in the benign renal oncocytoma

Human molecular genetics, 2008-04, Vol.17 (7), p.986-995

2008

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HIF and reactive oxygen species regulate oxidative phosphorylation in cancer

Carcinogenesis (New York), 2008-08, Vol.29 (8), p.1528-1537

2008

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A new role for the von Hippel-Lindau tumor suppressor protein: stimulation of mitochondrial oxidative phosphorylation complex biogenesis

Carcinogenesis (New York), 2005-03, Vol.26 (3), p.531-539

2005

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Actuality of Warburg's views in our understanding of renal cancer metabolism

Journal of bioenergetics and biomembranes, 2007-06, Vol.39 (3), p.235-241

2007

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Mitochondrial complex I is deficient in renal oncocytomas

Carcinogenesis (New York), 2003-09, Vol.24 (9), p.1461-1466

2003

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Inhibition of cytochrome c oxidase subunit 4 precursor processing by the hypoxia mimic cobalt chloride

Biochemical and biophysical research communications, 2006-06, Vol.344 (4), p.1086-1093

2006

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Natural antisense transcripts of HIF-1α are conserved in rodents

Gene, 2004-09, Vol.339 (C), p.121-130

2004

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Mutations in the SURF1 gene associated with Leigh syndrome and cytochrome c oxidase deficiency

Human mutation, 2001-05, Vol.17 (5), p.374-381

2001

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Mitochondrial ATPase and high-energy phosphates in failing hearts

American journal of physiology. Heart and circulatory physiology, 2001-09, Vol.281 (3), p.H1319-H1326

2001

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Functional alteration of cytochrome c oxidase by SURF1 mutations in Leigh syndrome

Biochimica et biophysica acta, 2003-09, Vol.1639 (1), p.53-63

2003

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Physiological oxygenation status is required for fully differentiated phenotype in kidney cortex proximal tubules

American journal of physiology. Renal physiology, 2006-10, Vol.291 (4), p.F750-F760

2006

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Functional F1-ATPase Essential in Maintaining Growth and Membrane Potential of Human Mitochondrial DNA-depleted ÏÂ° Cells

The Journal of biological chemistry, 1998-09, Vol.273 (36), p.22983

1998

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ATPase-ATP-synthétase mitochondriale: Pathologies liées à ses déficiences

Annales de l'Institut Pasteur. Actualités, 2001 (9-10), p.87-100

GODINOT, Catherine

2001

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Missense mutations in SURF1 associated with deficient cytochrome c oxidase assembly in Leigh syndrome patients

Human genetics, 2000-02, Vol.106 (2), p.194-205

2000

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Functional characterization of novel mutations in the human cytochrome b gene

European journal of human genetics : EJHG, 2001-07, Vol.9 (7), p.510-518

2001

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Natural antisense transcripts of HIF-1alpha are conserved in rodents

Gene, 2004-09, Vol.339, p.121-130

2004

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Identification of a large-scale mitochondrial deoxyribonucleic acid deletion in endocrinopathies and deafness : Report of two unrelated cases with diabetes mellitus and adrenal insufficiency, respectively

The journal of clinical endocrinology and metabolism, 1997-09, Vol.82 (9), p.3063-3067

1997

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Significance of Respirasomes for the Assembly/Stability of Human Respiratory Chain Complex I

Functional F1-ATPase Essential in Maintaining Growth and Membrane Potential of Human Mitochondrial DNA-depleted ρ° Cells

Leigh-like encephalopathy complicating Leber's hereditary optic neuropathy

Sequence conservation from human to prokaryotes of Surf1, a protein involved in cytochrome c oxidase assembly, deficient in Leigh syndrome

New evidence of a mitochondrial genetic background paradox: impact of the J haplogroup on the A3243G mutation

Mitochondria and reactive oxygen species in renal cancer

Mitochondrial disorders in renal tumors

Low mitochondrial respiratory chain content correlates with tumor aggressiveness in renal cell carcinoma

Clonal expansion of mutated mitochondrial DNA is associated with tumor formation and complex I deficiency in the benign renal oncocytoma

HIF and reactive oxygen species regulate oxidative phosphorylation in cancer

A new role for the von Hippel-Lindau tumor suppressor protein: stimulation of mitochondrial oxidative phosphorylation complex biogenesis

Actuality of Warburg's views in our understanding of renal cancer metabolism

Mitochondrial complex I is deficient in renal oncocytomas

Inhibition of cytochrome c oxidase subunit 4 precursor processing by the hypoxia mimic cobalt chloride

Natural antisense transcripts of HIF-1α are conserved in rodents

Mutations in the SURF1 gene associated with Leigh syndrome and cytochrome c oxidase deficiency

Mitochondrial ATPase and high-energy phosphates in failing hearts

Functional alteration of cytochrome c oxidase by SURF1 mutations in Leigh syndrome

Physiological oxygenation status is required for fully differentiated phenotype in kidney cortex proximal tubules

Functional F1-ATPase Essential in Maintaining Growth and Membrane Potential of Human Mitochondrial DNA-depleted ÏÂ° Cells

ATPase-ATP-synthétase mitochondriale: Pathologies liées à ses déficiences

Missense mutations in SURF1 associated with deficient cytochrome c oxidase assembly in Leigh syndrome patients

Functional characterization of novel mutations in the human cytochrome b gene

Natural antisense transcripts of HIF-1alpha are conserved in rodents

Identification of a large-scale mitochondrial deoxyribonucleic acid deletion in endocrinopathies and deafness : Report of two unrelated cases with diabetes mellitus and adrenal insufficiency, respectively

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