176 results on '"Barbaux, Sandrine"'
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2. Sperm SPACA6 protein is required for mammalian Sperm-Egg Adhesion/Fusion
3. FOXD1 mutations are related to repeated implantation failure, intra-uterine growth restriction and preeclampsia
4. Fertilization, but Not Post-Implantation Development, Can Occur in the Absence of Sperm and Oocyte Beta1 Integrin in Mice
5. ZP2 heterozygous mutation in an infertile woman
6. Re-evaluation of the role of STOX1 transcription factor in placental development and preeclampsia
7. Identification of a Novel Member of the Pentraxin Family in Xenopus laevis
8. Deletion of the Spata3 Gene Induces Sperm Alterations and In Vitro Hypofertility in Mice
9. Polymorphisms in 33 inflammatory genes and risk of myocardial infarction—a system genetics approach
10. Review for "Novel mutations in ZP1 : expanding the mutational spectrum associated with empty follicle syndrome in infertile women"
11. The human T locus and spina bifida risk
12. Identification of a New QTL Region on Mouse Chromosome 1 Responsible for Male Hypofertility: Phenotype Characterization and Candidate Genes
13. Partial Sperm beta1 Integrin Subunit Deletion Proves Its Involvement in Mouse Gamete Adhesion/Fusion
14. Use of degenerate oligonucleotide primed PCR (DOP-PCR) for the genotyping of low-concentration DNA samples
15. sY116, a human Y-linked polymorphic STS
16. Maternal genetic effects, exerted by genes involved in homocysteine remethylation, influence the risk of spina bifida. (Report)
17. Genetic and epigenetic mechanisms collaborate to control SERPINA3 expression and its association with placental diseases
18. Research Resource: Genome-Wide Profiling of Methylated Promoters in Endometriosis Reveals a Subtelomeric Location of Hypermethylation
19. Additional file 1: of FOXD1 mutations are related to repeated implantation failure, intra-uterine growth restriction and preeclampsia
20. Additional file 2: of FOXD1 mutations are related to repeated implantation failure, intra-uterine growth restriction and preeclampsia
21. Testicular development in an SRY-negative 46,XX individual harboring a distal Xp deletion
22. Specific haplotypes of the P-selectin gene are associated with myocardial infarction
23. Heterogeneity of linkage disequilibrium in human genes has implications for association studies of common diseases
24. The methionine synthase reductase (MTRR) A66G polymorphism is a novel genetic determinant of plasma homocysteine concentrations
25. A genome-wide search for new imprinted genes in the human placenta identifies DSCAM as the first imprinted gene on chromosome 21
26. Endothelial cell dysfunction and cardiac hypertrophy in the STOX1 model of preeclampsia
27. DSCAM, un nouveau gène soumis à empreinte parentale
28. A genome-wide search for new imprinted genes in the human placenta identifies DSCAMas the first imprinted gene on chromosome 21
29. Transcriptomic analysis of human placenta in intrauterine growth restriction
30. Nitroso-Redox Balance and Mitochondrial Homeostasis Are Regulated bySTOX1, a Pre-Eclampsia-Associated Gene
31. The Gpr1/Zdbf2 locus provides new paradigms for transient and dynamic genomic imprinting in mammals
32. sY116, a human Y-linked polymorphic STS
33. miR-34a expression, epigenetic regulation, and function in human placental diseases
34. Preeclampsia-Like Symptoms Induced in Mice by Fetoplacental Expression of STOX1 Are Reversed by Aspirin Treatment
35. Trophoblasts, invasion, and microRNA
36. A genome-wide approach reveals novel imprinted genes expressed in the human placenta
37. The Intensity of IUGR-Induced Transcriptome Deregulations Is Inversely Correlated with the Onset of Organ Function in a Rat Model
38. Combination of promoter hypomethylation and PDX1 overexpression leads toTBX15decrease in vascular IUGR placentas
39. In Vitro Fertilization and Embryo Culture Strongly Impact the Placental Transcriptome in the Mouse Model
40. The adhesion mediated by the P-selectin P–selectin glycoprotein ligand-1 (PSGL-1) couple is stronger for shorter PSGL-1 variants
41. Altérations de l’expression des gènes dans les Retards de Croissance Intra-Utérin
42. STOX1 Overexpression in Choriocarcinoma Cells Mimics Transcriptional Alterations Observed in Preeclamptic Placentas
43. Differential haplotypic expression of the interleukin-18 gene
44. Haplotypes of the Caspase-1 Gene, Plasma Caspase-1 Levels, and Cardiovascular Risk
45. Genetic Analysis of the Interleukin-18 System Highlights the Role of the Interleukin-18 Gene in Cardiovascular Disease
46. Adhesion molecules and atherosclerosis
47. The single nucleotide polymorphism story
48. Corrigendum to “The methionine synthase reductase (MTRR) A66G polymorphism is a novel genetic determinant of plasma homocysteine concentrations” [ATH 157 (2001) 451–456]
49. Association Between P-Selectin Gene Polymorphisms and Soluble P-Selectin Levels and Their Relation to Coronary Artery Disease
50. Sex chromosome mosaicism in males carrying Y chromosome long arm deletions
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