C Kordes

Summary

Country: Germany

Publications

  1. ncbi An in vitro vitellogenin bioassay for oestrogenic substances in the medaka (Oryzias latipes)
    C Kordes
    Institut fur Zoologie, Technische Universitat Dresden, Mommsenstrasse 13, 01062, Dresden, Germany
    Aquat Toxicol 58:151-64. 2002
  2. ncbi CD133+ hepatic stellate cells are progenitor cells
    Claus Kordes
    Clinic of Gastroenterology, Hepatology and Infectiology, Heinrich Heine University, Moorenstrasse 5, 40225 Dusseldorf, Germany
    Biochem Biophys Res Commun 352:410-7. 2007
  3. ncbi Induction of vitellogenin in vivo and in vitro in the model teleost medaka (Oryzias latipes): comparison of gene expression and protein levels
    Stefan Scholz
    Institute of Zoology, University of Dresden, D 01062, Germany
    Mar Environ Res 57:235-44. 2004
  4. ncbi Canonical Wnt signaling maintains the quiescent stage of hepatic stellate cells
    Claus Kordes
    Clinic of Gastroenterology, Hepatology and Infectiology, Heinrich Heine University, Moorenstrasse 5, 40225 Dusseldorf, Germany
    Biochem Biophys Res Commun 367:116-23. 2008
  5. ncbi Effects of angiotensin II on rat pancreatic stellate cells
    Roland Reinehr
    Clinic for Gastroenterology, Hepatology, and Infectiology, Heinrich-Heine-University, , Germany
    Pancreas 28:129-37. 2004
  6. ncbi Differential and synergistic effects of platelet-derived growth factor-BB and transforming growth factor-beta1 on activated pancreatic stellate cells
    Claus Kordes
    Clinic of Gastroenterology, Hepatology, and Infectiology, Heinrich-Heine-University, , Germany
    Pancreas 31:156-67. 2005

Collaborators

Detail Information

Publications6

  1. ncbi An in vitro vitellogenin bioassay for oestrogenic substances in the medaka (Oryzias latipes)
    C Kordes
    Institut fur Zoologie, Technische Universitat Dresden, Mommsenstrasse 13, 01062, Dresden, Germany
    Aquat Toxicol 58:151-64. 2002
    ..The hepatocyte cultures of male medaka in combination with the sandwich ELISA were shown to be a suitable tool to detect and quantify oestrogenic activity of chemicals...
  2. ncbi CD133+ hepatic stellate cells are progenitor cells
    Claus Kordes
    Clinic of Gastroenterology, Hepatology and Infectiology, Heinrich Heine University, Moorenstrasse 5, 40225 Dusseldorf, Germany
    Biochem Biophys Res Commun 352:410-7. 2007
    ..Their potential to differentiate into endothelial or hepatocyte lineages suggests important functions of CD133+ HSC during liver regeneration...
  3. ncbi Induction of vitellogenin in vivo and in vitro in the model teleost medaka (Oryzias latipes): comparison of gene expression and protein levels
    Stefan Scholz
    Institute of Zoology, University of Dresden, D 01062, Germany
    Mar Environ Res 57:235-44. 2004
    ..For long term studies with the need to detect weak estrogenic chemicals and a precise quantification, immuno-chemical detection may be favoured...
  4. ncbi Canonical Wnt signaling maintains the quiescent stage of hepatic stellate cells
    Claus Kordes
    Clinic of Gastroenterology, Hepatology and Infectiology, Heinrich Heine University, Moorenstrasse 5, 40225 Dusseldorf, Germany
    Biochem Biophys Res Commun 367:116-23. 2008
    ..The findings demonstrate that beta-catenin-dependent Wnt signaling maintains the quiescent state of HSC and, similar to stem and progenitor cells, influences their developmental fate...
  5. ncbi Effects of angiotensin II on rat pancreatic stellate cells
    Roland Reinehr
    Clinic for Gastroenterology, Hepatology, and Infectiology, Heinrich-Heine-University, , Germany
    Pancreas 28:129-37. 2004
    ..The data suggest that PSCs are targets of ATII action with potential pathophysiological relevance...
  6. ncbi Differential and synergistic effects of platelet-derived growth factor-BB and transforming growth factor-beta1 on activated pancreatic stellate cells
    Claus Kordes
    Clinic of Gastroenterology, Hepatology, and Infectiology, Heinrich-Heine-University, , Germany
    Pancreas 31:156-67. 2005
    ..Moreover, PDGF-BB facilitates degradation of extracellular matrix proteins by enhancement of MMP synthesis, but MMP activity was probably limited because of elevated tissue inhibitor of metalloproteinase 1 expression...