Contemporary All-inclusive Map Designed for FXR

8% after the DPT. Thus, maculopapular exanthema occurs in two-thirds of hypersensitivity reactions to BL; this is important, as these hypersensitivity reactions are more easily confused with viral reactions, as reported by others [10-12]. Moreover, we did not diagnose any serum sickness-like syndrome, and although one child had clinical symptoms compatible with this disorder, he developed maculopapular exanthema after the DPT. Summarizing, we analysed an important number of children with a history compatible with hypersensitivity reactions to beta-lactams and found that just 8% were finally confirmed FXR as allergic, most with non-immediate reactions. The drug provocation test was shown to be a necessary and safe tool for diagnosing these children. We thank Ian Johnstone for help with the English language version of the manuscript. None of the authors has any conflict of interest. None received money for this study. Research is part of their daily activities. All authors had full access to all the data (including statistical reports) and can take responsibility for the integrity of the data and the accuracy of the data analysis. The study was funded by the FIS-Thematic Networks and Co-operative Research Centres RIRAAF CB-5083 clinical trial (ISCIII RD012/0013), Spanish Health Ministry (PI12/02529) and Andalusia Innovation Ministry (CTS 06603). Fundaci��n Salud 2000. ""K-ras (KRAS) mutations are observed in around 40% of human colorectal adenomas and carcinomas. Previously, we developed and characterized a strain of transgenic mice with inducible intestinal epithelial expression of K-ras via a Cre/LoxP system. To evaluate the influence of mutant K-ras on carcinogen-induced colorectal tumourigenesis, we induced neoplastic alterations in the large intestines of wild-type and K-ras mice using the colon-selective carcinogen 1,2-dimethylhydrazine (DMH), which has Motolimod been widely used to induce colorectal tumours that are histopathologically similar to those observed in humans. K-ras expression significantly promoted DMH-induced colorectal tumourigenesis: the average lifespan of the mice decreased from 38.52 �� 1.97 weeks for 40 control mice to 32.42 �� 2.17 weeks for 26 K-ras mice (mean �� SEM, p