S. Barbaux

发表

Hypertelorism and hypospadias associated with a de novo apparently balanced translocation between 8q22.3-23 and 20p13.

M. Fellous, K. McElreavey, A. Tar, 1997, American journal of medical genetics.

Identification of a novel member of the pentrax in family in Xenopus laevis

P. Sharp, A. Whitehead, S. Barbaux, 1993, Proceedings of the Royal Society of London. Series B: Biological Sciences.

Loss of sequences 3' to the testis-determining gene, SRY, including the Y pseudoautosomal boundary associated with partial testicular determination.

E. Vilain, M. Fellous, K. McElreavey, 1996, Proceedings of the National Academy of Sciences of the United States of America.

Association Between P-Selectin Gene Polymorphisms and Soluble P-Selectin Levels and Their Relation to Coronary Artery Disease

S. Blankenberg, L. Tiret, F. Cambien, 2001, Arteriosclerosis, thrombosis, and vascular biology.

Deletion of the Spata3 Gene Induces Sperm Alterations and In Vitro Hypofertility in Mice

S. Dupuis, S. Barbaux, C. Viollet, 2021, International journal of molecular sciences.

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

S. Brouillet, P. de Mazancourt, M. Dieudonné, 2012, Cellular and Molecular Life Sciences.

Cullins in human intra-uterine growth restriction: expressional and epigenetic alterations.

U. Simeoni, Daniel Vaiman, F. Mondon, 2010, Placenta.

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

Jean-Louis Golmard, Nadia Tahri, Laurence Tiret, 2002, Human molecular genetics.

Polymorphisms in 33 inflammatory genes and risk of myocardial infarction—a system genetics approach

D. Tregouet, C. Perret, A. Evans, 2007, Journal of Molecular Medicine.

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

D. Tregouet, S. Blankenberg, L. Tiret, 2003, Annals of human genetics.

Gene polymorphisms of the renin-angiotensin system and early development of hypertension.

P. Rudan, F. Cambien, I. Rudan, 2006, American journal of hypertension.

Corrigendum to “The methionine synthase reductase (MTRR) A66G polymorphism is a novel genetic determinant of plasma homocysteine concentrations” [ATH 157 (2001) 451–456]

A. Evans, L. Kluijtmans, J. Yarnell, 2003 .

Polymorphisms of genes controlling homocysteine/folate metabolism and cognitive function

R. Plomin, A. Whitehead, S. Barbaux, 2000, Neuroreport.

Differential haplotypic expression of the interleukin-18 gene

F. Cambien, S. Blankenberg, L. Tiret, 2007, European Journal of Human Genetics.

Nitroso-redox balance and mitochondrial homeostasis are regulated by STOX1, a pre-eclampsia-associated gene.

M. Ricchetti, L. Châtre, A. Lombès, 2014, Antioxidants & redox signaling.

Transcriptomic analysis of human placenta in intrauterine growth restriction

V. Tsatsaris, G. Gascoin, Daniel Vaiman, 2015, Pediatric Research.

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

A. Gabory, I. Fajardy, S. Mayeur, 2012, Journal of Developmental Origins of Health and Disease.

Oocyte ERM and EWI Proteins Are Involved in Mouse Fertilization

S. Barbaux, S. Marques, C. Gourier, 2022, Frontiers in Cell and Developmental Biology.

Use of degenerate oligonucleotide primed PCR (DOP-PCR) for the genotyping of low-concentration DNA samples

F. Cambien, O. Poirier, S. Barbaux, 2001, Journal of molecular medicine.

Endothelial cell dysfunction and cardiac hypertrophy in the STOX1 model of preeclampsia

P. Laissue, S. Jacques, Daniel Vaiman, 2016, Scientific Reports.

sY116, a human Y-linked polymorphic STS

R. Veitia, M. Fellous, G. M. Saifi, 2000, Journal of Genetics.

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

M. Weiss, T. Imaizumi-Scherrer, D. Faust, 1996, Molecular and cellular biology.

Identification of a New QTL Region on Mouse Chromosome 1 Responsible for Male Hypofertility: Phenotype Characterization and Candidate Genes

V. Firlej, X. Montagutelli, Daniel Vaiman, 2020, International journal of molecular sciences.

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

H. Ostrer, M. Jobling, R. Veitia, 1997, Human Genetics.

Preeclampsia-Like Symptoms Induced in Mice by Fetoplacental Expression of STOX1 Are Reversed by Aspirin Treatment

U. Simeoni, V. Baudrie, F. Le Provost, 2013, Hypertension.

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

S. Ingles, J. Concordet, Daniel Vaiman, 2012, Human molecular genetics.

Partial Sperm beta1 Integrin Subunit Deletion Proves Its Involvement in Mouse Gamete Adhesion/Fusion

J. Wolf, S. Barbaux, C. Chalas, 2020, International journal of molecular sciences.

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

Marc Fellous, Ken McElreavey, M. Gubler, 1997, Nature Genetics.

Sex chromosome mosaicism in males carrying Y chromosome long arm deletions.

L. Quintana-Murci, I. Seifer, M. Fellous, 2000, Human reproduction.

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

T. Bourgeron, A. Agulnik, M. Kasahara, 1997, Genomics.

Y-chromosome deletions in idiopathic severe testiculopathies.

C. Foresta, A. Ferlin, S. Barbaux, 1997, The Journal of clinical endocrinology and metabolism.

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

C. Foresta, E. Moro, A. Ferlin, 1998, Human reproduction.

The human SRY protein is present in fetal and adult Sertoli cells and germ cells.

M. Fellous, K. McElreavey, S. Barbaux, 1999, International Journal of Developmental Biology.

True hermaphroditism: clinical aspects and molecular studies in 16 cases.

V. Dichtchekenian, D. Damiani, N. Setian, 1997, European journal of endocrinology.

Ullrich-Turner Syndrome: Relevance of Searching for Y Chromosome Fragments

V. Dichtchekenian, T. Manna, D. Damiani, 1999, Journal of pediatric endocrinology & metabolism : JPEM.

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

T. Bourgeron, L. Quintana-Murci, M. Fellous, 1999, The Journal of clinical endocrinology and metabolism.

miR-34a expression, epigenetic regulation, and function in human placental diseases

Daniel Vaiman, S. Barbaux, L. Doridot, 2014, Epigenetics.

Testicular development in an SRY-negative 46,XX individual harboring a distal Xp deletion

E. Vilain, M. Fellous, K. McElreavey, 1995, Human Genetics.

In Vitro Fertilization and Embryo Culture Strongly Impact the Placental Transcriptome in the Mouse Model

P. Jouannet, L. Journot, L. Dandolo, 2010, PloS one.

Adhesion molecules and atherosclerosis.

S. Blankenberg, L. Tiret, S. Barbaux, 2003, Atherosclerosis.

Heterogeneity of linkage disequilibrium in human genes has implications for association studies of common diseases.

D. Trégouët, C. Perret, L. Tiret, 2002, Human molecular genetics.

The Gpr1/Zdbf2 locus provides new paradigms for transient and dynamic genomic imprinting in mammals

D. Bourc’his, I. Okamoto, N. Zamudio, 2014, Genes & development.

The Intensity of IUGR-Induced Transcriptome Deregulations Is Inversely Correlated with the Onset of Organ Function in a Rat Model

E. Ghigo, U. Simeoni, V. Achard, 2011, PLoS ONE.

Research resource: genome-wide profiling of methylated promoters in endometriosis reveals a subtelomeric location of hypermethylation.

P. Santulli, B. Borghese, C. Chapron, 2010, Molecular endocrinology.

Sperm SPACA6 protein is required for mammalian Sperm-Egg Adhesion/Fusion

Daniel Vaiman, J. Wolf, S. Barbaux, 2020, Scientific Reports.

Fertilization, but Not Post-Implantation Development, Can Occur in the Absence of Sperm and Oocyte Beta1 Integrin in Mice

S. Barbaux, I. Lagoutte, A. Ziyyat, 2022, International journal of molecular sciences.

The human and mouse methylenetetrahydrofolate reductase (MTHFR) genes: genomic organization, mRNA structure and linkage to the CLCN6 gene.

L. Kluijtmans, A. Whitehead, S. Barbaux, 2000, Gene.

The genetic basis of murine and human sex determination: a review

M. Fellous, K. McElreavey, A. Ion, 1995, Heredity.

A genome-wide search for new imprinted genes in the human placenta identifies DSCAM as the first imprinted gene on chromosome 21

Amélie C Pinard, M. Dieudonné, V. Tsatsaris, 2018, European Journal of Human Genetics.

Maternal genetic effects, exerted by genes involved in homocysteine remethylation, influence the risk of spina bifida.

M. McDonnell, L. E. Mitchell, A. Whitehead, 2002, American journal of human genetics.

FOXD1 mutations are related to repeated implantation failure, intra-uterine growth restriction and preeclampsia

P. Laissue, Daniel Vaiman, S. Barbaux, 2019, Molecular Medicine.

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

A. Evans, L. Kluijtmans, J. Yarnell, 2001, Atherosclerosis.

A genome-wide approach reveals novel imprinted genes expressed in the human placenta

Amélie C Pinard, A. Barlier, U. Simeoni, 2012, Epigenetics.

Re-evaluation of the role of STOX1 transcription factor in placental development and preeclampsia.

Daniel Vaiman, F. Mondon, S. Barbaux, 2009, Journal of reproductive immunology.

STOX1 Overexpression in Choriocarcinoma Cells Mimics Transcriptional Alterations Observed in Preeclamptic Placentas

Daniel Vaiman, F. Mondon, S. Barbaux, 2008, PloS one.

Trophoblasts, invasion, and microRNA

Daniel Vaiman, S. Barbaux, L. Doridot, 2013, Front. Genet..

The Xenopus laevis homologue of the 64-kDa subunit of cleavage stimulation factor.

A. Whitehead, S. Barbaux, G. Sellar, 1996, Comparative biochemistry and physiology. Part B, Biochemistry & molecular biology.

ZP2 heterozygous mutation in an infertile woman

L. E. El Khattabi, S. Barbaux, A. Ziyyat, 2017, Human Genetics.

Combination of promoter hypomethylation and PDX1 overexpression leads to TBX15 decrease in vascular IUGR placentas

J. Tost, F. Busato, C. Dussour, 2011, Epigenetics.

Haplotypes of the Caspase-1 Gene, Plasma Caspase-1 Levels, and Cardiovascular Risk

R. Schnabel, F. Cambien, S. Blankenberg, 2006, Circulation Research.

The single nucleotide polymorphism story.

F. Cambien, S. Barbaux, 2003, Pharmacogenetics.

The adhesion mediated by the P‐selectin P–selectin glycoprotein ligand‐1 (PSGL‐1) couple is stronger for shorter PSGL‐1 variants

L. Tiret, F. Pincet, O. Poirier, 2010, Journal of leukocyte biology.

Preeclampsia-like symptoms induced in mice by feto-placental expression of STOX 1 are reversed by aspirin treatment . STOX 1 mice develop preeclampsia symptoms

U. Simeoni, V. Baudrie, G. Germain, 2013 .

FOXD1 mutations are related to repeated implantation failure, intra-uterine growth restriction and preeclampsia

P. Laissue, Daniel Vaiman, S. Barbaux, 2019, Molecular medicine.

Accurate and rapid "multiplex heteroduplexing" method for genotyping key enzymes involved in folate/homocysteine metabolism.

L. Kluijtmans, A. Whitehead, S. Barbaux, 2000, Clinical chemistry.

The human T locus and spina bifida risk

L. E. Mitchell, A. Whitehead, S. Barbaux, 2004, Human Genetics.

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

D. Tregouet, S. Blankenberg, D. Trégouët, 2008, Journal of Molecular Medicine.

Placental BDNF/TrkB signaling system is modulated by fetal growth disturbances in rat and human.

C Junien, A. Gabory, I. Fajardy, 2010, Placenta.

Genetic Analysis of the Interleukin-18 System Highlights the Role of the Interleukin-18 Gene in Cardiovascular Disease

R. Schnabel, D. Tregouet, S. Blankenberg, 2005, Circulation.

Proximal deletions of the long arm of the Y chromosome suggest a critical region associated with a specific subset of characteristic Turner stigmata.

E. Vilain, M. Fellous, K. McElreavey, 1995, Human molecular genetics.