Project description:These are raw and mzXML data from mice tissue obtained from the Raffatellu lab. This excludes the fecal data collected from the time series.
Project description:These are raw and mzXML files from the PD17-PD36 mice obtained from Raffatellu lab. Mice were given antibiotics and gavaged with glycocholic acid, taurocholic acid, phenylalanacholic acid, leucocholic acid and tyrosocholic acid.
Project description:These are raw and mzXML files from the PD17-PD36 mice obtained from Raffatellu lab. Mice were given antibiotics and gavaged with glycocholic acid, taurocholic acid, phenylalanacholic acid, leucocholic acid and tyrosocholic acid.
Project description:This is a experment want to fish out the proteins in the mice brain can interact with sodium chanel protein Nav1.7, immuno precipatation and lab free mass spectrmetry were used to identify Nav1.7 Interation parter proteins.
Project description:Time series of urine samples collected from male and female mice after exposure to 6PPD and 6PPDQ. Analyzed with LC-DDA-MS/MS. Rerun of tissue samples from pregnant mice exposed to 6PPD and 6PPDQ.
Project description:With this study we wanted to evaluate the impact of murine norovirus infection of germfree mice and to compare it to germfree mice which have received fecal transplants of conventional mice.
Project description:To investigate the roles of deoxycholic acid in the regulation of cell function and gene expression of colonic tissue, we treated colitis mice with deoxycholic acid. Then, we performed gene expression profiling analysis using data obtained from RNA-seq of colonic tissue of colitis mice treated with or without deoxycholic acid.
Project description:To investigate the roles of 4-HDHA in the regulation of cell function and gene expression of colonic tissue, we treated colitis mice with 4-HDHA intravenously. Then, we performed gene expression profiling analysis using data obtained from RNA-seq of colonic tissue of colitis mice treated with or without 4-HDHA.
Project description:To investigate whether electroacupuncture (EA) promotes adipose tissue browning by regulating the expression of angiogenesis genes through EA, we sequenced the adipose tissue of mice fed high fat diet with and without electroacupuncture, as well as those fed normally. We then performed gene expression profiling analysis using data obtained from RNA-seq of 9 mice in three groups.