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Träfflista för sökning "WFRF:(Ansari H) srt2:(2010-2014)"

Sökning: WFRF:(Ansari H) > (2010-2014)

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2.
  • Khalaf, H, et al. (författare)
  • The First Liver Transplant in Qatar
  • 2012
  • Ingår i: LIVER TRANSPLANTATION. - 1527-6465. ; 18, s. S279-S279
  • Konferensbidrag (övrigt vetenskapligt/konstnärligt)
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3.
  • van Asseldonk, Dirk P, et al. (författare)
  • Difficulties and possibilities with thiopurine therapy in inflammatory bowel disease-Proceedings of the first Thiopurine Task Force meeting
  • 2011
  • Ingår i: DIGESTIVE AND LIVER DISEASE. - : Elsevier Science B.V., Amsterdam. - 1590-8658. ; 43:4, s. 270-276
  • Tidskriftsartikel (refereegranskat)abstract
    • Background: Thiopurines, such as azathioprine and mercaptopurine, are of pivotal importance in the treatment of inflammatory bowel disease. Although these drugs have been used for several decades, still many questions remain unanswered. Aim: To provide an overview of clinically and scientifically challenging topics concerning thiopurine therapy in inflammatory bowel disease treatment. Methods: The first meeting of the Thiopurine Task Force Interest Group was held during the 2009 United European Gastroenterology Week in London (GASTRO2009). The topics of this meeting were of particular clinical and scientific interest. Additional literature was identified by performing a Pubmed search using the search terms inflammatory bowel disease, azathioprine, 6-mercaptopurine and thioguanine. Results: The following topics were discussed: therapeutic drug monitoring; the synergy of thiopurines with aminosalicylates and allopurinol; serious adverse events such as opportunistic infections, hepatotoxicity, carcinogenicity and pancreatitis; prolongation of thiopurines during clinical remission; indications for thiopurines in the postoperative setting; and the potential use of thioguanine. Specific interesting and clinically relevant topics for potential future research are provided. Conclusions: Thiopurines remain central to inflammatory bowel disease treatment, although future studies are required to substantiate a more personalised medicine approach to their use.
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4.
  • Al-Ani, Thair, et al. (författare)
  • Trace elements in water and sediments of the Tigris river, Baghdad City, Iraq
  • 2014
  • Ingår i: Journal of Environmental Hydrology. - 1058-3912 .- 1996-7918. ; 22
  • Tidskriftsartikel (refereegranskat)abstract
    • Industrial, agricultural and rural activities may result in pollution of watercourses with elevated trace metal concentrations and implications for water supply and ecosystem functioning. The concentration of the trace metals Fe, Mn, Zn, Co, Pb, Cu, and Cd in the water and clay fractions (<2μm) of the bank sediments of River Tigris in Baghdad city were determined. Dissolved trace metals concentrations were far below the upper permissible limits during 2012-2013. There was no consistent pattern between element concentrations and river discharge. Seasonal interrelations between water and sediments were most obvious for Fe that decreased in both environments with rising flows during autumn. Although independent of discharge, Mn in water and sediments often followed each other at all stations. Zinc, however, increased in the sediments and decreased in the water with discharge. The clay fractions were slightly to strongly enriched in trace metals with the gradient Co > Fe > Zn > Mn > Cu suggesting absorption of the metals on sediment substrate.
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5.
  • Godoy, Patricio, et al. (författare)
  • Recent advances in 2D and 3D in vitro systems using primary hepatocytes, alternative hepatocyte sources and non-parenchymal liver cells and their use in investigating mechanisms of hepatotoxicity, cell signaling and ADME
  • 2013
  • Ingår i: Archives of Toxicology. - : Springer Science and Business Media LLC. - 0340-5761 .- 1432-0738. ; 87:8, s. 1315-1530
  • Forskningsöversikt (refereegranskat)abstract
    • This review encompasses the most important advances in liver functions and hepatotoxicity and analyzes which mechanisms can be studied in vitro. In a complex architecture of nested, zonated lobules, the liver consists of approximately 80 % hepatocytes and 20 % non-parenchymal cells, the latter being involved in a secondary phase that may dramatically aggravate the initial damage. Hepatotoxicity, as well as hepatic metabolism, is controlled by a set of nuclear receptors (including PXR, CAR, HNF-4 alpha, FXR, LXR, SHP, VDR and PPAR) and signaling pathways. When isolating liver cells, some pathways are activated, e.g., the RAS/MEK/ERK pathway, whereas others are silenced (e.g. HNF-4 alpha), resulting in up- and downregulation of hundreds of genes. An understanding of these changes is crucial for a correct interpretation of in vitro data. The possibilities and limitations of the most useful liver in vitro systems are summarized, including three-dimensional culture techniques, co-cultures with non-parenchymal cells, hepatospheres, precision cut liver slices and the isolated perfused liver. Also discussed is how closely hepatoma, stem cell and iPS cell-derived hepatocyte-like-cells resemble real hepatocytes. Finally, a summary is given of the state of the art of liver in vitro and mathematical modeling systems that are currently used in the pharmaceutical industry with an emphasis on drug metabolism, prediction of clearance, drug interaction, transporter studies and hepatotoxicity. One key message is that despite our enthusiasm for in vitro systems, we must never lose sight of the in vivo situation. Although hepatocytes have been isolated for decades, the hunt for relevant alternative systems has only just begun.
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