His Geometry study frequently involves adjacent topics like Curvature and Growth rate. Curvature and Geometry are two areas of study in which Dominique Chretien engages in interdisciplinary research. He integrates Cell biology with Biophysics in his study. He performs integrative study on Biophysics and Biochemistry in his works. His Biochemistry study frequently links to adjacent areas such as GTP'. His research on GTP' often connects related areas such as Guanosine triphosphate. He integrates Guanosine triphosphate with Hydrolysis in his study. In his research, Dominique Chretien undertakes multidisciplinary study on Hydrolysis and Enzyme. Dominique Chretien combines Enzyme and Cell biology in his research.
Respiratory chain and Mitochondrial respiratory chain are the focus of his Mitochondrion studies. His Biochemistry study frequently draws connections between adjacent fields such as Oxidative phosphorylation. He integrates many fields, such as Oxidative phosphorylation and Mitochondrion, in his works. He conducted interdisciplinary study in his works that combined Cell biology and Biophysics. In his works, he conducts interdisciplinary research on Biophysics and Biochemistry. He integrates many fields, such as Microtubule and Tubulin, in his works. Dominique Chretien integrates Tubulin with Microtubule in his study. In his articles, Dominique Chretien combines various disciplines, including Gene and Mitochondrial disease. He undertakes multidisciplinary studies into Mitochondrial disease and Mitochondrial DNA in his work.
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Biochemical and molecular investigations in respiratory chain deficiencies
P. Rustin;D. Chretien;T. Bourgeron;B. Gérard.
Clinica Chimica Acta (1994)
Aconitase and mitochondrial iron-sulphur protein deficiency in Friedreich ataxia.
Agnès Rötig;Pascale de Lonlay;Dominique Chretien;Françoise Foury.
Nature Genetics (1997)
Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency
Thomas Bourgeron;Pierre Rustin;Dominique Chretien;Mark Birch-Machin.
Nature Genetics (1995)
Mutation of RRM2B, encoding p53-controlled ribonucleotide reductase (p53R2), causes severe mitochondrial DNA depletion.
Alice Bourdon;Limor Minai;Valérie Serre;Valérie Serre;Jean-Philippe Jais.
Nature Genetics (2007)
Quinone-responsive multiple respiratory-chain dysfunction due to widespread coenzyme Q10 deficiency
Agnés Rötig;Eeva-Liisa Appelkvist;Vanna Geromel;Dominique Chretien.
The Lancet (2000)
CABC1 Gene Mutations Cause Ubiquinone Deficiency with Cerebellar Ataxia and Seizures
Julie Mollet;Agnès Delahodde;Valérie Serre;Dominique Chretien.
American Journal of Human Genetics (2008)
A mutant mitochondrial respiratory chain assembly protein causes complex III deficiency in patients with tubulopathy, encephalopathy and liver failure
Pascale De Lonlay;Isabelle Valnot;Antoni Barrientos;Marina Gorbatyuk.
Nature Genetics (2001)
Prenyldiphosphate synthase, subunit 1 (PDSS1) and OH-benzoate polyprenyltransferase (COQ2) mutations in ubiquinone deficiency and oxidative phosphorylation disorders
Julie Mollet;Irina Giurgea;Dimitri Schlemmer;Gustav Dallner.
Journal of Clinical Investigation (2007)
Large-Scale Deletion and Point Mutations of the Nuclear NDUFV1 and NDUFS1 Genes in Mitochondrial Complex I Deficiency
Paule Bénit;Dominique Chretien;Nohman Kadhom;Pascale de Lonlay-Debeney.
American Journal of Human Genetics (2001)
Nuclear Outsourcing of RNA Interference Components to Human Mitochondria
Simonetta Bandiera;Silvia Rüberg;Muriel Girard;Nicolas Cagnard.
PLOS ONE (2011)
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