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EG-VEGF controls placental growth and survival in normal and pathological pregnancies: case of fetal growth restriction (FGR)

Cellular and molecular life sciences : CMLS, 2013-02, Vol.70 (3), p.511-525

2013

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Cullins in Human Intra-Uterine Growth Restriction: Expressional and Epigenetic Alterations

Placenta (Eastbourne), 2010-02, Vol.31 (2), p.151-157

2010

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Placental BDNF/TrkB Signaling System is Modulated by Fetal Growth Disturbances in Rat and Human

Placenta (Eastbourne), 2010-09, Vol.31 (9), p.785-791

2010

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Polymorphisms of the tumor necrosis factor-alpha (TNF) and the TNF-alpha converting enzyme (TACE/ADAM17) genes in relation to cardiovascular mortality: the AtheroGene study

Journal of molecular medicine (Berlin, Germany), 2008-10, Vol.86 (10), p.1153-1161

2008

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High frequency of well-defined Y-chromosome deletions in idiopathic Sertoli cell-only syndrome

Human reproduction (Oxford), 1998-02, Vol.13 (2), p.302-307

1998

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Adhesion molecules and atherosclerosis

Atherosclerosis, 2003-10, Vol.170 (2), p.191-203

2003

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Placental expression of the obesity-associated gene FTO is reduced by fetal growth restriction but not by macrosomia in rats and humans

Journal of developmental origins of health and disease, 2013-04, Vol.4 (2), p.134-138

2013

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Association between P-selectin gene polymorphisms and soluble P-selectin levels and their relation to coronary artery disease

Arteriosclerosis, thrombosis, and vascular biology, 2001-10, Vol.21 (10), p.1668

2001

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Genome-Wide Profiling of Methylation in Endometriosis Reveals New Molecular Markers for the Disease and Clues for Its Pathophysiology

Journal of minimally invasive gynecology, 2010-11, Vol.17 (6), p.S52-S53

2010

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STOX1 overexpression in mice induces severe preeclampsia-like symptoms prevented by aspirin at low doses

Journal of Reproductive Immunology, 2012-05, Vol.94 (1), p.6-7

2012

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HOX-A and HOX-C Genes Deregulation in Endometriosis and Potential Role for Antisense RNAs

Journal of minimally invasive gynecology, 2011, Vol.18 (6), p.S16-S16

2011

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A high frequency of Y chromosome deletions in males with nonidiopathic infertility

The journal of clinical endocrinology and metabolism, 1999-10, Vol.84 (10), p.3606-3612

1999

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Gene sequence, localization, and evolutionary conservation of DAZLA, a candidate male sterility gene

Genomics (San Diego, Calif.), 1997-04, Vol.41 (2), p.227-235

1997

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Genetic and epigenetic mechanisms collaborate to control SERPINA3 expression and its association with placental diseases

Human molecular genetics, 2012-05, Vol.21 (9), p.1968-1978

2012

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SELPLG Gene Polymorphisms in Relation to Plasma SELPLG Levels and Coronary Artery Disease

Annals of human genetics, 2003-11, Vol.67 (6), p.504-511

2003

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Mutations and sequence variants in the testis-determining region of the Y chromosome in individuals with a 46,XY female phenotype

Human genetics, 1997-05, Vol.99 (5), p.648-652

1997

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Genetic analysis of the interleukin-18 system highlights the role of the interleukin-18 gene in cardiovascular disease

Circulation (New York, N.Y.), 2005-08, Vol.112 (5), p.643-650

2005

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Loss of Sequences 3′ to the Testis-Determining Gene, SRY, Including the Y Pseudoautosomal Boundary Associated with Partial Testicular Determination

Proceedings of the National Academy of Sciences - PNAS, 1996-08, Vol.93 (16), p.8590-8594

1996

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The intensity of IUGR-induced transcriptome deregulations is inversely correlated with the onset of organ function in a rat model

PloS one, 2011-06, Vol.6 (6), p.e21222-e21222

2011

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Donor splice-site mutations in WT1 are responsible for Frasier syndrome

Nature genetics, 1997-12, Vol.17 (4), p.467-470

1997

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The methionine synthase reductase (MTRR) A66G polymorphism is a novel genetic determinant of plasma homocysteine concentrations

Atherosclerosis, 2001-08, Vol.157 (2), p.451-456

2001

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Specific haplotypes of the P-selectin gene are associated with myocardial infarction

Human molecular genetics, 2002-08, Vol.11 (17), p.2015-2023

2002

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Maternal Genetic Effects, Exerted by Genes Involved in Homocysteine Remethylation, Influence the Risk of Spina Bifida

American journal of human genetics, 2002-11, Vol.71 (5), p.1222-1226

2002

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The activity of the highly inducible mouse phenylalanine hydroxylase gene promoter is dependent upon a tissue-specific, hormone-inducible enhancer

Molecular and Cellular Biology, 1996-06, Vol.16 (6), p.3125-3137

1996

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EG-VEGF controls placental growth and survival in normal and pathological pregnancies: case of fetal growth restriction (FGR)

Cullins in Human Intra-Uterine Growth Restriction: Expressional and Epigenetic Alterations

Placental BDNF/TrkB Signaling System is Modulated by Fetal Growth Disturbances in Rat and Human

Polymorphisms of the tumor necrosis factor-alpha (TNF) and the TNF-alpha converting enzyme (TACE/ADAM17) genes in relation to cardiovascular mortality: the AtheroGene study

IFPA meeting 2014 workshop report: Animal models to study pregnancy pathologies; new approaches to study human placental exposure to xenobiotics; biomarkers of pregnancy pathologies; placental genetics and epigenetics; the placenta and stillbirth and fetal growth restriction

High frequency of well-defined Y-chromosome deletions in idiopathic Sertoli cell-only syndrome

Adhesion molecules and atherosclerosis

Placental expression of the obesity-associated gene FTO is reduced by fetal growth restriction but not by macrosomia in rats and humans

Association between P-selectin gene polymorphisms and soluble P-selectin levels and their relation to coronary artery disease

Genome-Wide Profiling of Methylation in Endometriosis Reveals New Molecular Markers for the Disease and Clues for Its Pathophysiology

STOX1 overexpression in mice induces severe preeclampsia-like symptoms prevented by aspirin at low doses

HOX-A and HOX-C Genes Deregulation in Endometriosis and Potential Role for Antisense RNAs

A high frequency of Y chromosome deletions in males with nonidiopathic infertility

Gene sequence, localization, and evolutionary conservation of DAZLA, a candidate male sterility gene

Genetic and epigenetic mechanisms collaborate to control SERPINA3 expression and its association with placental diseases

SELPLG Gene Polymorphisms in Relation to Plasma SELPLG Levels and Coronary Artery Disease

Mutations and sequence variants in the testis-determining region of the Y chromosome in individuals with a 46,XY female phenotype

Genetic analysis of the interleukin-18 system highlights the role of the interleukin-18 gene in cardiovascular disease

Loss of Sequences 3′ to the Testis-Determining Gene, SRY, Including the Y Pseudoautosomal Boundary Associated with Partial Testicular Determination

The intensity of IUGR-induced transcriptome deregulations is inversely correlated with the onset of organ function in a rat model

Donor splice-site mutations in WT1 are responsible for Frasier syndrome

The methionine synthase reductase (MTRR) A66G polymorphism is a novel genetic determinant of plasma homocysteine concentrations

Specific haplotypes of the P-selectin gene are associated with myocardial infarction

Maternal Genetic Effects, Exerted by Genes Involved in Homocysteine Remethylation, Influence the Risk of Spina Bifida

The activity of the highly inducible mouse phenylalanine hydroxylase gene promoter is dependent upon a tissue-specific, hormone-inducible enhancer

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