: Morbidity, lesion pattern, management and short-term outcomes of civilian vascular trauma are rarely evaluated. Therefore, analysis of in hospital results in patients with non-iatrogenic vascular trauma in a tertiary referral hospital was performed. : Retrospective evaluation of patients with vascular trauma from 2007-2017 was done.
View Article and Find Full Text PDFBackground: There are considerable geographical differences in the occurrence of extended-spectrum beta-lactamase(ESBL)-producing bacteria, both in the community and in the hospital setting. Our aim was to assess risk factors for blood stream, urinary tract, and vascular catheter-associated infections with ESBL-producing Escherichia coli and Klebsiella pneumoniae at a tertiary care hospital in a low-prevalence country.
Methods: We performed a case-control study comparing 58 patients with infections due to ESBL-producing E.
Nuclear hormone receptors play important roles in many physiological events. Small molecules, ie, ligands, can regulate these physiological effects by binding to the receptors forming a ligand-receptor complex, which in turn triggers a cascade of transcriptional events. Over the years, non-steroidal ligands for steroid receptors have been developed and have found extensive clinical use in cancer treatment, fertility regulation and hormone replacement therapy.
View Article and Find Full Text PDFThe screening of diverse libraries of small molecules created by combinatorial synthetic methods is a recent development which has the potential to accelerate the identification of lead compounds in drug discovery. We have developed a direct and rapid method to identify lead compounds in libraries involving affinity selection and mass spectrometry. In our strategy, the receptor or target molecule of interest is used to isolate the active components from the library physically, followed by direct structural identification of the active compounds bound to the target molecule by mass spectrometry.
View Article and Find Full Text PDFPeptoids, oligomers of N-substituted glycines, are described as a motif for the generation of chemically diverse libraries of novel molecules. Ramachandran-type plots were calculated and indicate a greater diversity of conformational states available for peptoids than for peptides. The monomers incorporate t-butyl-based side-chain and 9-fluorenylmethoxy-carbonyl alpha-amine protection.
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