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

Oncogene, 2006-09, Vol.25 (40), p.5570-5574

2006

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

Oncogene, 2009-10, Vol.28 (41), p.3642-3651

2009

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

Journal of thrombosis and haemostasis, 2008-08, Vol.6 (8), p.1436-1439

2008

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Xenobiotic-metabolizing enzymes and transporters in the normal human brain: regional and cellular mapping as a basis for putative roles in cerebral function

Drug metabolism and disposition, 2009-07, Vol.37 (7), p.1528-1538

2009

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

Biochemical pharmacology, 2002-11, Vol.64 (10), p.1513-1519

2002

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

Molecular pharmacology, 2008-04, Vol.73 (4), p.1122-1133

2008

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

Cancer research (Chicago, Ill.), 2001-05, Vol.61 (10), p.3942-3948

2001

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

Annals of neurology, 1994-03, Vol.35 (3), p.365-370

1994

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

Journal of the neurological sciences, 1998, Vol.156 (1), p.41-46

1998

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

Journal of inherited metabolic disease, 1997-03, Vol.20 (1), p.49-53

1997

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

Oncogene, 2009, Vol.28 (41), p.3642-3651

2009

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

European journal of neurology, 1995-12, Vol.2 (6), p.573-579

1995

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

FEBS letters, 1986-07, Vol.202 (2), p.207-210

1986

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

Neuromuscular disorders : NMD, 1993, Vol.3 (5), p.593-597

1993

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

Human genetics, 1997-06, Vol.99 (6), p.785-792

1997

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

Journal of inherited metabolic disease, 1995-11, Vol.18 (6), p.682-688

1995

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E1 pyruvate dehydrogenase deficiency in a child with motor neuropathy

Pediatric research, 1993-03, Vol.33 (3), p.284-288

1993

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

Journal of inherited metabolic disease, 1995, Vol.18 (6), p.682-688

1995

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Two-component spike nanoparticle vaccine protects macaques from SARS-CoV-2 infection

Cell, 2021-03, Vol.184 (5), p.1188-1200.e19

2021

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COVA1-18 neutralizing antibody protects against SARS-CoV-2 in three preclinical models

Nature communications, 2021-10, Vol.12 (1), p.6097-10, Article 6097

2021

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

Current gene therapy, 2014-01, Vol.14 (3), p.236-246

2014

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La bibliothèque et les papiers de Michel Vovelle sauvés et conservés à l’IHRF-IHMC et à la BIS

Annales historiques de la Révolution française, 2021, Vol.404 (2), p.157-164

2021

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Cold atom guidance by a holographically-generated Laguerre-Gaussian laser mode

The European physical journal. D, Atomic, molecular, and optical physics, 2010-03, Vol.57 (1), p.87-94

2010

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Caractérisation de la méthylation de l’ADN des corticosurrénalomes par digital-droplet-PCR

Annales d'endocrinologie, 2017-09, Vol.78 (4), p.267-267

2017

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Jean Y., Périgord M. Géographie rurale. La ruralité en France Paris, Armand Colin, Collection 128, 2009, 128 p

Annales de géographie, 2010-12, Vol.n°676 (6), p.712-712

Diry, Jean-Paul

2010

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

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

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

Xenobiotic-metabolizing enzymes and transporters in the normal human brain: regional and cellular mapping as a basis for putative roles in cerebral function

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

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

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

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

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

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

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

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

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

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

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

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

E1 pyruvate dehydrogenase deficiency in a child with motor neuropathy

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

Two-component spike nanoparticle vaccine protects macaques from SARS-CoV-2 infection

COVA1-18 neutralizing antibody protects against SARS-CoV-2 in three preclinical models

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

La bibliothèque et les papiers de Michel Vovelle sauvés et conservés à l’IHRF-IHMC et à la BIS

Cold atom guidance by a holographically-generated Laguerre-Gaussian laser mode

Caractérisation de la méthylation de l’ADN des corticosurrénalomes par digital-droplet-PCR

Jean Y., Périgord M. Géographie rurale. La ruralité en France Paris, Armand Colin, Collection 128, 2009, 128 p

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