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Molecular Pathogenesis of Neuroendocrine Tumors: Implications for Current and Future Therapeutic Approaches

Clinical cancer research, 2013-06, Vol.19 (11), p.2842-2849

2013

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Parkin gene inactivation alters behaviour and dopamine neurotransmission in the mouse

Human molecular genetics, 2003-09, Vol.12 (18), p.2277-2291

2003

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AAV-mediated intramuscular delivery of myotubularin corrects the myotubular myopathy phenotype in targeted murine muscle and suggests a function in plasma membrane homeostasis

Human molecular genetics, 2008-07, Vol.17 (14), p.2132-2143

2008

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Association between Early-Onset Parkinson's Disease and Mutations in the Parkin Gene

The New England journal of medicine, 2000-05, Vol.342 (21), p.1560-1567

2000

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In-depth haplotype analysis of ABCA1 gene polymorphisms in relation to plasma ApoA1 levels and myocardial infarction

Arteriosclerosis, thrombosis, and vascular biology, 2004-04, Vol.24 (4), p.775

2004

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Characterizing Short Stature by Insulin-like Growth Factor Axis Status and Genetic Associations: Results From the Prospective, Cross-sectional, Epidemiogenetic EPIGROW Study

The journal of clinical endocrinology and metabolism, 2013-06, Vol.98 (6), p.E1122-E1130

2013

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The contribution of genomics in the medicine of tomorrow, clinical applications and issues

Therapie, 2019-02, Vol.74 (1), p.9-15

2019

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Precision medicine in oncology: Challenges, stakes and new paradigms

Bulletin du cancer, 2019-02, Vol.106 (2), p.97

2019

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Complete Genomic Sequence of the Human ABCA1 Gene: Analysis of the Human and Mouse ATP-Binding Cassette A Promoter

Proceedings of the National Academy of Sciences - PNAS, 2000-07, Vol.97 (14), p.7987-7992

2000

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Somatic gene transfer of human ApoA-I inhibits atherosclerosis progression in mouse models

Circulation (New York, N.Y.), 1999-01, Vol.99 (1), p.105-110

1999

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Human ATP-Binding Cassette Transporter 1 (ABC1): Genomic Organization and Identification of the Genetic Defect in the Original Tangier Disease Kindred

Proceedings of the National Academy of Sciences - PNAS, 1999-10, Vol.96 (22), p.12685-12690

1999

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Protection Against Atherogenesis in Mice Mediated by Human Apolipoprotein A-IV

Science (American Association for the Advancement of Science), 1996-08, Vol.273 (5277), p.966-968

1996

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Tracking Cancer Genetic Evolution using OncoTrack

Scientific reports, 2016-07, Vol.6 (1), p.29647-29647, Article 29647

2016

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Academic expertise in assisting private companies in the fields of environment and environmental toxicology: the role of individual expertise

Environmental science and pollution research international, 2021, Vol.28 (2), p.1283-1286

2021

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Inhibition of atherosclerosis development in cholesterol-fed human apolipoprotein A-I-transgenic rabbits

Circulation (New York, N.Y.), 1996-08, Vol.94 (4), p.713-717

1996

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Origin of the Mutations in the parkin Gene in Europe: Exon Rearrangements Are Independent Recurrent Events, whereas Point Mutations May Result from Founder Effects

American journal of human genetics, 2001-03, Vol.68 (3), p.617-626

2001

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Reduction of restenosis after angioplasty in an atheromatous rabbit model by suicide gene therapy

Circulation (New York, N.Y.), 1997-07, Vol.96 (2), p.408-411

1997

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Transgenic rabbits expressing human apolipoprotein A-I in the liver

Arteriosclerosis, thrombosis, and vascular biology, 1996-12, Vol.16 (12), p.1424

1996

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Introduction to gene therapy: a clinical aftermath

Methods in molecular biology (Clifton, N.J.), 2011-01, Vol.737, p.27

Denèfle, Patrice P

2011

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Characterization of the ABCA Transporter Subfamily: Identification of Prokaryotic and Eukaryotic Members, Phylogeny and Topology

Journal of molecular biology, 2003-01, Vol.325 (2), p.259-274

2003

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Structure and interfacial properties of chicken apolipoprotein A-IV

Journal of lipid research, 2000-09, Vol.41 (9), p.1410-1418

2000

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A Wide Variety of Mutations in the Parkin Gene Are Responsible for Autosomal Recessive Parkinsonism in Europe

Human molecular genetics, 1999-04, Vol.8 (4), p.567-574

1999

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Correction of hypertriglyceridemia and impaired fat tolerance in lipoprotein lipase-deficient mice by adenovirus-mediated expression of human lipoprotein lipase

Arteriosclerosis, thrombosis, and vascular biology, 1997-11, Vol.17 (11), p.2532

1997

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Potential gene therapy for lecithin-cholesterol acyltransferase (LCAT)-deficient and hypoalphalipoproteinemic patients with adenovirus-mediated transfer of human LCAT gene

Circulation (New York, N.Y.), 1996-11, Vol.94 (9), p.2177-2184

1996

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Recombinational Construction in Escherichia coli of Infectious Adenoviral Genomes

Proceedings of the National Academy of Sciences - PNAS, 1997-02, Vol.94 (4), p.1414-1419

1997

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Molecular Pathogenesis of Neuroendocrine Tumors: Implications for Current and Future Therapeutic Approaches

Parkin gene inactivation alters behaviour and dopamine neurotransmission in the mouse

AAV-mediated intramuscular delivery of myotubularin corrects the myotubular myopathy phenotype in targeted murine muscle and suggests a function in plasma membrane homeostasis

Association between Early-Onset Parkinson's Disease and Mutations in the Parkin Gene

In-depth haplotype analysis of ABCA1 gene polymorphisms in relation to plasma ApoA1 levels and myocardial infarction

Characterizing Short Stature by Insulin-like Growth Factor Axis Status and Genetic Associations: Results From the Prospective, Cross-sectional, Epidemiogenetic EPIGROW Study

The contribution of genomics in the medicine of tomorrow, clinical applications and issues

Precision medicine in oncology: Challenges, stakes and new paradigms

Complete Genomic Sequence of the Human ABCA1 Gene: Analysis of the Human and Mouse ATP-Binding Cassette A Promoter

Somatic gene transfer of human ApoA-I inhibits atherosclerosis progression in mouse models

Human ATP-Binding Cassette Transporter 1 (ABC1): Genomic Organization and Identification of the Genetic Defect in the Original Tangier Disease Kindred

Protection Against Atherogenesis in Mice Mediated by Human Apolipoprotein A-IV

Tracking Cancer Genetic Evolution using OncoTrack

Academic expertise in assisting private companies in the fields of environment and environmental toxicology: the role of individual expertise

Inhibition of atherosclerosis development in cholesterol-fed human apolipoprotein A-I-transgenic rabbits

Origin of the Mutations in the parkin Gene in Europe: Exon Rearrangements Are Independent Recurrent Events, whereas Point Mutations May Result from Founder Effects

Reduction of restenosis after angioplasty in an atheromatous rabbit model by suicide gene therapy

Transgenic rabbits expressing human apolipoprotein A-I in the liver

Introduction to gene therapy: a clinical aftermath

Characterization of the ABCA Transporter Subfamily: Identification of Prokaryotic and Eukaryotic Members, Phylogeny and Topology

Structure and interfacial properties of chicken apolipoprotein A-IV

A Wide Variety of Mutations in the Parkin Gene Are Responsible for Autosomal Recessive Parkinsonism in Europe

Correction of hypertriglyceridemia and impaired fat tolerance in lipoprotein lipase-deficient mice by adenovirus-mediated expression of human lipoprotein lipase

Potential gene therapy for lecithin-cholesterol acyltransferase (LCAT)-deficient and hypoalphalipoproteinemic patients with adenovirus-mediated transfer of human LCAT gene

Recombinational Construction in Escherichia coli of Infectious Adenoviral Genomes

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