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Maternal diets trigger sex-specific divergent trajectories of gene expression and epigenetic systems in mouse placenta

PloS one, 2012-11, Vol.7 (11), p.e47986-e47986

2012

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Association of modifiers and other genetic factors explain Marfan syndrome clinical variability

European journal of human genetics : EJHG, 2018-12, Vol.26 (12), p.1759-1772

2018

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MFAP5 Loss-of-Function Mutations Underscore the Involvement of Matrix Alteration in the Pathogenesis of Familial Thoracic Aortic Aneurysms and Dissections

American journal of human genetics, 2014-12, Vol.95 (6), p.736-743

2014

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The clinical presentation of Marfan syndrome is modulated by expression of wild-type FBN1 allele

Human molecular genetics, 2015-05, Vol.24 (10), p.2764-2770

2015

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C57BL/6J and A/J Mice Fed a High-Fat Diet Delineate Components of Metabolic Syndrome

Obesity (Silver Spring, Md.), 2007-08, Vol.15 (8), p.1996-2005

2007

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Sex- and diet-specific changes of imprinted gene expression and DNA methylation in mouse placenta under a high-fat diet

PloS one, 2010-12, Vol.5 (12), p.e14398-e14398

2010

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Core-Shell Polymer-Based Nanoparticles Deliver miR-155-5p to Endothelial Cells

Molecular therapy. Nucleic acids, 2019-09, Vol.17, p.210-222

2019

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Quantifying the Genetic Basis of Marfan Syndrome Clinical Variability

Genes, 2020-05, Vol.11 (5), p.574

2020

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Dietary alleviation of maternal obesity and diabetes: increased resistance to diet-induced obesity transcriptional and epigenetic signatures

PloS one, 2013, Vol.8 (6), p.e66816-e66816

2013

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Reference Expression Profile of Three FBN1 Transcript Isoforms and Their Association with Clinical Variability in Marfan Syndrome

Genes, 2019-02, Vol.10 (2), p.128

2019

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Nutri-epigenomics : lifelong remodelling of our epigenomes by nutritional and metabolic factors and beyond

Clinical chemistry and laboratory medicine, 2007-01, Vol.45 (3), p.321-327

2007

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Marfan Syndrome Variability: Investigation of the Roles of Sarcolipin and Calcium as Potential Transregulator of FBN1 Expression

Genes, 2018-08, Vol.9 (9), p.421

2018

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Resistance to high-fat diet in the female progeny of obese mice fed a control diet during the periconceptual, gestation, and lactation periods

American journal of physiology: endocrinology and metabolism, 2007-04, Vol.292 (4), p.E1095-E1100

2007

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Épigénomique nutritionnelle du syndrome métabolique

M.S. Médecine sciences, 2005-04, Vol.21 (4), p.396-404

2005

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Unbalanced Expression of 11p15 Imprinted Genes in Focal Forms of Congenital Hyperinsulinism : Association with a Reduction to Homozygosity of a Mutation in ABCC8 or KCNJ11

The American journal of pathology, 2001-06, Vol.158 (6), p.2177-2184

2001

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ABCC8 (SUR1) and KCNJ11 (KIR6.2) mutations in persistent hyperinsulinemic hypoglycemia of infancy and evaluation of different therapeutic measures

Journal of Pediatric Endocrinology and Metabolism, 2002-07, Vol.15 (7), p.993

2002

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Core-Shell Polymer-Based Nanoparticles Deliver miR-155-5p to Endothelial Cells

Molecular therapy. Nucleic acids, 2019-09, Vol.17, p.210-222

2019

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Identification of germline mutations in the RB1 gene by denaturant gradient gel electrophoresis and polymerase chain reaction direct sequencing

Human molecular genetics, 1993-07, Vol.2 (7), p.975-979

1993

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Unbalanced Expression of 11p15 Imprinted Genes in Focal Forms of Congenital Hyperinsulinism

The American journal of pathology, 2001-06, Vol.158 (6), p.2177-2184

2001

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The human placental protein 14 (PP14) gene is localized on chromosome 9q34

Human genetics, 1991-03, Vol.86 (5), p.515-518

1991

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RFLP identified by the anonymous DNA segment OLVIIDI on chromosome 6 [HGM9 no.D6S47]

Nucleic acids research, 1989-02, Vol.17 (4), p.1789-1789

1989

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Paternal mutation of the sulfonylurea receptor (SUR1) gene and maternal loss of 11p15 imprinted genes lead to persistent hyperinsulinism in focal adenomatous hyperplasia

The Journal of clinical investigation, 1998-10, Vol.102 (7), p.1286-1291

1998

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Maternal diets trigger sex-specific divergent trajectories of gene expression and epigenetic systems in mouse placenta

Association of modifiers and other genetic factors explain Marfan syndrome clinical variability

MFAP5 Loss-of-Function Mutations Underscore the Involvement of Matrix Alteration in the Pathogenesis of Familial Thoracic Aortic Aneurysms and Dissections

The clinical presentation of Marfan syndrome is modulated by expression of wild-type FBN1 allele

C57BL/6J and A/J Mice Fed a High-Fat Diet Delineate Components of Metabolic Syndrome

Sex- and diet-specific changes of imprinted gene expression and DNA methylation in mouse placenta under a high-fat diet

Core-Shell Polymer-Based Nanoparticles Deliver miR-155-5p to Endothelial Cells

Quantifying the Genetic Basis of Marfan Syndrome Clinical Variability

Dietary alleviation of maternal obesity and diabetes: increased resistance to diet-induced obesity transcriptional and epigenetic signatures

TGFB2 mutations cause familial thoracic aortic aneurysms and dissections associated with mild systemic features of Marfan syndrome

Pathogenic variants in THSD4, encoding the ADAMTS-like 6 protein, predispose to inherited thoracic aortic aneurysm

Reference Expression Profile of Three FBN1 Transcript Isoforms and Their Association with Clinical Variability in Marfan Syndrome

Nutri-epigenomics : lifelong remodelling of our epigenomes by nutritional and metabolic factors and beyond

Marfan Syndrome Variability: Investigation of the Roles of Sarcolipin and Calcium as Potential Transregulator of FBN1 Expression

Resistance to high-fat diet in the female progeny of obese mice fed a control diet during the periconceptual, gestation, and lactation periods

Épigénomique nutritionnelle du syndrome métabolique

Unbalanced Expression of 11p15 Imprinted Genes in Focal Forms of Congenital Hyperinsulinism : Association with a Reduction to Homozygosity of a Mutation in ABCC8 or KCNJ11

ABCC8 (SUR1) and KCNJ11 (KIR6.2) mutations in persistent hyperinsulinemic hypoglycemia of infancy and evaluation of different therapeutic measures

Core-Shell Polymer-Based Nanoparticles Deliver miR-155-5p to Endothelial Cells

Identification of germline mutations in the RB1 gene by denaturant gradient gel electrophoresis and polymerase chain reaction direct sequencing

Unbalanced Expression of 11p15 Imprinted Genes in Focal Forms of Congenital Hyperinsulinism

The human placental protein 14 (PP14) gene is localized on chromosome 9q34

TGFB2 loss of function mutations cause familial thoracic aortic aneurysms and acute aortic dissections associated with mild systemic features of the Marfan syndrome

RFLP identified by the anonymous DNA segment OLVIIDI on chromosome 6 [HGM9 no.D6S47]

Paternal mutation of the sulfonylurea receptor (SUR1) gene and maternal loss of 11p15 imprinted genes lead to persistent hyperinsulinism in focal adenomatous hyperplasia

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