Silva S

No ORCID on file · 3 papers in corpus
2024
Frontiers in medicine ·doi:10.3389/fmed.2024.1343547

IntroductionHereditary angioedema (HAE) due to C1 inhibitor (C1-INH) deficiency is an ultra-rare autosomal dominant inherited disease that affects 1 in 67,000 people in the world. The attacks are based on subcutaneous and submucosal edema t…

2013
PloS one ·doi:10.1371/journal.pone.0056376

Mice deficient for the fibulin-5 gene (Fbln5(-/-)) develop pelvic organ prolapse (POP) due to compromised elastic fibers and upregulation of matrix metalloprotease (MMP)-9. Here, we used casein zymography, inhibitor profiling, affinity pull…

2012
Human reproduction (Oxford, England) ·doi:10.1093/humrep/der436

BackgroundAlthough histological dating of endometrial biopsies provides little help for prediction or diagnosis of infertility, analysis of individual endometrial proteins, proteomic profiling and transcriptome analysis have suggested sever…