M. Diry

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Connexin 33 Impairs Gap Junction Functionality by Accelerating Connexin 43 Gap Junction Plaque Endocytosis

J. Gilleron, C. Fiorini, D. Segretain, 2009, Traffic.

PXR-dependent induction of human CYP3A4 gene expression by organochlorine pesticides.

X. Coumoul, R. Barouki, M. Diry, 2002, Biochemical pharmacology.

Nedd9/Hef1/Cas-L mediates the effects of environmental pollutants on cell migration and plasticity

X. Coumoul, R. Barouki, J. Raingeaud, 2009, Oncogene.

Multiple genetic alterations in vitamin K epoxide reductase complex subunit 1 gene (VKORC1) can explain the high dose requirement during oral anticoagulation in humans

M. Loriot, L. Bodin, M. Horellou, 2008, Journal of thrombosis and haemostasis : JTH.

A suicide gene therapy combining the improvement of cyclophosphamide tumor cytotoxicity and the development of an anti-tumor immune response.

P. Beaune, E. Tartour, I. de Waziers, 2014, Current gene therapy.

MERRF family with 8344 mutation in tRNA (lys). Evidence of a mitochondrial vasculopathy in muscle biopsies

M. Malgat, J. Mazat, A. Vital, 1993, Neuromuscular Disorders.

Activation of the dioxin/aryl hydrocarbon receptor (AhR) modulates cell plasticity through a JNK-dependent mechanism

X. Coumoul, R. Barouki, K. Bock, 2006, Oncogene.

Intrafamilial heterogeneous clinical presentation of the mitochondrial 3243 MELAS mutation; molecular investigations among four generations

F. Viader, B. Lechevalier, F. Chapon, 1995, European journal of neurology.

A case of mitochondrial encephalomyopathy associated with a muscle coenzyme Q10 deficiency

P. Rustin, E. Boitier, G. Ponsot, 1998, Journal of the Neurological Sciences.

Isolation of heparin‐binding growth factors from dogfish (Mustela canis) brain and retina

Y. Courtois, M. Diry, O. Lagente, 1986, FEBS letters.

Biochemical and genetic studies of four patients with pyruvate dehydrogenase E1α deficiency

S. Seneca, G. Ponsot, W. Lissens, 1997, Human Genetics.

El Pyruvate Dehydrogenase Deficiency in a Child with Motor Neuropathy

G. Ponsot, W. Lissens, G. Bonne, 1993, Pediatric Research.

Xenobiotic-Metabolizing Enzymes and Transporters in the Normal Human Brain: Regional and Cellular Mapping as a Basis for Putative Roles in Cerebral Function

M. Loriot, P. Beaune, C. Duyckaerts, 2009, Drug Metabolism and Disposition.

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M. Loriot, P. Beaune, C. Duyckaerts, 2009 .

Differential regulation of cytochrome P450 1A1 and 1B1 by a combination of dioxin and pesticides in the breast tumor cell line MCF-7.

X. Coumoul, R. Barouki, C. Robillot, 2001, Cancer research.

A near homoplasmic T8993G mtDNA mutation in a patient with atypic Leigh syndrome not present in the mother's tissues

G. Ponsot, I. Desguerre, B. Héron, 1997, Journal of Inherited Metabolic Disease.

Biochemical and genetic studies of four patients with pyruvate dehydrogenase E1 alpha deficiency.

S. Seneca, L. de Meirleir, G. Ponsot, 1997, Human genetics.

Clinical, biochemical, and molecular analysis of a maternally inherited case of Leight syndrome (MILS) associated with the mtDNA T8993G point mutation

D. Rodriguez, G. Ponsot, I. Desguerre, 1995, Journal of Inherited Metabolic Disease.

Myo‐leukoencephalopathy in twins: Study of 3243‐myopathy, encephalopathy, lactic acidosis, and strokelike episodes mitochondrial DNA mutation

J. Lloreta, C. Marsac, M. Diry, 1994, Annals of neurology.

Improvement of Cyclophosphamide Activation by CYP2B6 Mutants: From in Silico to ex Vivo

Laurent Corcos, François André, Marcel Delaforge, 2008, Molecular Pharmacology.

Xenobiotic-Metabolizing Enzymes and Transporters in the Normal Human Brain: Regional and Cellular Mapping as a Basis for Putative Roles in Cerebral Function

M. Loriot, P. Beaune, C. Duyckaerts, 2009, Drug Metabolism and Disposition.

Differential regulation of cytochrome P450 1A1 and 1B1 by a combination of dioxin and pesticides in the breast tumor cell line MCF-7.

X. Coumoul, R. Barouki, C. Robillot, 2001, Cancer research.