Sandrine Barbaux

ORCID: 0000-0002-8204-1855 · 4 papers in corpus
other 2019
FOXD1 mutations are related to repeated implantation failure, intra-uterine growth restriction and preeclampsia
Molecular medicine (Cambridge, Mass.) ·doi:10.1186/s10020-019-0104-3

BACKGROUND: Human reproductive disorders consist of frequently occurring dysfunctions including a broad range of phenotypes affecting fertility and women's health during pregnancy. Several female-related diseases have been associated with h…

2011
HOX-A and HOX-C Genes Deregulation in Endometriosis and Potential Role for Antisense RNAs
·doi:10.1016/j.jmig.2011.08.066
2010
Genome-Wide Profiling of Methylation in Endometriosis Reveals New Molecular Markers for the Disease and Clues for Its Pathophysiology
·doi:10.1016/j.jmig.2010.08.261
other 2010
Research resource: genome-wide profiling of methylated promoters in endometriosis reveals a subtelomeric location of hypermethylation
Molecular Endocrinology ·doi:10.1210/me.2010-0160

Several lines of evidence indicate that endometriosis could be partially due to selective epigenetic deregulations. Promoter hypermethylation of some key genes, such as progesterone receptor and aromatase, has been associated with the silen…