“
“The aim of this study was to determine if laser zona thinning could improve the rates of pregnancy and
implantation for vitrified-warmed embryo transfer at the cleavage stage. A total of 400 vitrified-warmed embryo transfer cycles were randomly assigned LDN-193189 chemical structure to either the test group or the control group. The zona pellucida of vitrified-warmed embryos in the patients of the control group was untreated, whereas in the test group it was partially thinned by laser just before embryo transfer. In the test group, the clinical pregnancy and implantation rates were significantly lower as compared with that of the control group (28.5 versus 43.0, P = 0.002, and 11.2 versus 16.7, P = 0.004, respectively). Therefore the results of this learn more investigation show that laser zona thinning may have an unexpected adverse effect on the rates of clinical pregnancy and implantation of vitrified-warmed embryos at the cleavage stage. (C) 2009, Reproductive Healthcare
Ltd. Published by Elsevier Ltd. All rights reserved.”
“Aims: To analyze all evidence on the possible increase in morbidity and mortality determined by the use of inhibitors of gastric acid secretion (IGAS) drugs. Materials and Methods: We review all evidence exploring the adverse events associated with IGAS use in neonates. Results: Despite being prescribed in an off-label manner because of the perceived safety and potential benefit demonstrated for older populations, IGAS are being increasingly used in the neonatal period with much evidence derived from adults and children. Few data are available BAY 73-4506 price for neonates and indicate an association between IGAS use with infections and necrotizing enterocolitis (NEC), and with an increased mortality. Delayed gastric emptying,
increased gastric mucus viscosity, modification in microbiota, and impairment of neutrophils functions are possible mechanisms of adverse events associated with IGAS use. Conclusions: A careful prescription of IGAS is crucial in order to reduce iatrogenic damage in neonates.”
“DNA methylation involves biochemical modification of DNA by addition of methyl groups onto CpG dinucleotides, and this epigenetic mechanism regulates gene expression in disease and development. Mammalian DNA methyltransferases, DNMT (DNMT1, DNMT3A and DNMT3B), together with the accessory protein DNMT3L establish specific DNA methylation patterns in the genome during gametogenesis, embryogenesis and somatic tissue development. The present study addresses the structural and functional conservation of the DNMT in humans, mice and cattle and the patterns of mRNA abundance of the different enzymes during embryogenesis to improve understanding of epigenetic regulation in early development. The findings showed a high degree of structural and functional conservation among the human, mouse, and bovine DNMT.