نتایج جستجو برای: abcb11

تعداد نتایج: 428  

2017
Elana Judith Fertig

Genomic aberrations and gene expression-defined subtypes in the large METABRIC patient cohort have been used to stratify and predict survival. The present study used normalized gene expression signatures of paclitaxel drug response to predict outcome for different survival times in METABRIC patients receiving hormone (HT) and, in some cases, chemotherapy (CT) agents. This machine learning metho...

2014
J L Woodhead K Yang K L R Brouwer S Q Siler S H Stahl J L Ambroso D Baker P B Watkins B A Howell

Bile salt export pump (BSEP) inhibition has been proposed to be an important mechanism for drug-induced liver injury (DILI). Modeling can prioritize knowledge gaps concerning bile acid (BA) homeostasis and thus help guide experimentation. A submodel of BA homeostasis in rats and humans was constructed within DILIsym, a mechanistic model of DILI. In vivo experiments in rats with glibenclamide we...

2011
Jan Stindt Philipp Ellinger Claudia Stross Verena Keitel Dieter Häussinger Sander H. J. Smits Ralf Kubitz Lutz Schmitt

Homologous recombination in Saccharomyces cerevisiae is a well-studied process. Here, we describe a yeast-recombination-based approach to construct and mutate plasmids containing the cDNA of the human bile salt export pump (BSEP) that has been shown to be unstable in E. coli. Using this approach, we constructed the necessary plasmids for a heterologous overexpression of BSEP in the yeast Pichia...

Journal: :Human molecular genetics 2004
Luis Alvarez Paloma Jara Elena Sánchez-Sabaté Loreto Hierro Javier Larrauri María C Díaz Carmen Camarena Angela De la Vega Esteban Frauca Eduardo López-Collazo Pablo Lapunzina

Farnesoid X receptor (FXR) is a transcription factor that controls bile acid homeostasis. The phenotype of Fxr null mice is characterized by hypercholanaemia, impaired secretion of bile acids and failure to thrive. Human disorders with these characteristics include FIC1 disease (caused by mutations in ATP8B1, which encodes a putative aminophospholipid translocase, FIC1, whose function in bile h...

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