U Ullmann

Summary

Affiliation: Vrije Universiteit Brussel
Country: Belgium

Publications

  1. ncbi request reprint Epithelial-mesenchymal transition process in human embryonic stem cells cultured in feeder-free conditions
    U Ullmann
    Research Centre Reproduction and Genetics, University Hospital and Medical School of the Vrije Universiteit Brussel, VUB, Free University of Brussels, Brussels, Belgium
    Mol Hum Reprod 13:21-32. 2007
  2. doi request reprint GSK-3-specific inhibitor-supplemented hESC medium prevents the epithelial-mesenchymal transition process and the up-regulation of matrix metalloproteinases in hESCs cultured in feeder-free conditions
    U Ullmann
    Department of Embryology and Genetics, Universitair Ziekenhuis Brussel, Vrije Universiteit Brussel VUB, Laarbeeklaan 101, 1090 Brussels, Belgium
    Mol Hum Reprod 14:169-79. 2008
  3. pmc Increased serum resistance in Klebsiella pneumoniae strains producing extended-spectrum beta-lactamases
    H Sahly
    Department of Medical Microbiology and Virology, University of Kiel, Brunswiker Str 4, 24105 Kiel, Germany
    Antimicrob Agents Chemother 48:3477-82. 2004
  4. ncbi request reprint Derivation of human embryonic stem cell lines from embryos obtained after IVF and after PGD for monogenic disorders
    I Mateizel
    Research Centre for Reproduction and Genetics, University Hospital and Medical School of the Vrije Universiteit Brussel Dutch speaking Brussels Free University Laarbeeklaan 101, 1090 Brussels, Belgium
    Hum Reprod 21:503-11. 2006

Collaborators

  • Christine Gilles
  • Greet Cauffman
  • I Mateizel
  • H Sahly
  • H Van de Velde
  • I Liebaers
  • K Sermon
  • E Degreef
  • N De Temmerman
  • A Van Steirteghem
  • M De Rycke
  • P Devroey
  • D Sandvang
  • J M Tomas
  • V J Benedi
  • R Podschun
  • D S Hansen
  • D Sirot
  • H Aucken
  • V Fussing
  • C Forestier
  • I Ofek

Detail Information

Publications4

  1. ncbi request reprint Epithelial-mesenchymal transition process in human embryonic stem cells cultured in feeder-free conditions
    U Ullmann
    Research Centre Reproduction and Genetics, University Hospital and Medical School of the Vrije Universiteit Brussel, VUB, Free University of Brussels, Brussels, Belgium
    Mol Hum Reprod 13:21-32. 2007
    ..Taken together, our data suggest that culturing hESCs in feeder-free conditions enhances an early differentiation process identified as an EMT...
  2. doi request reprint GSK-3-specific inhibitor-supplemented hESC medium prevents the epithelial-mesenchymal transition process and the up-regulation of matrix metalloproteinases in hESCs cultured in feeder-free conditions
    U Ullmann
    Department of Embryology and Genetics, Universitair Ziekenhuis Brussel, Vrije Universiteit Brussel VUB, Laarbeeklaan 101, 1090 Brussels, Belgium
    Mol Hum Reprod 14:169-79. 2008
    ..This study showed that BIO, a GSK-3-specific inhibitor, prevents the EMT process which is associated with the feeder-free hESC culture. Nevertheless, BIO was not sufficient to expand hESCs in a long-term culture system...
  3. pmc Increased serum resistance in Klebsiella pneumoniae strains producing extended-spectrum beta-lactamases
    H Sahly
    Department of Medical Microbiology and Virology, University of Kiel, Brunswiker Str 4, 24105 Kiel, Germany
    Antimicrob Agents Chemother 48:3477-82. 2004
    ..The present findings suggest that ESBL-producing strains have a greater pathogenic potential than non-ESBL-producing strains, but the linkage between O serotypes, serum resistance, and ESBL production remains unclear at this stage...
  4. ncbi request reprint Derivation of human embryonic stem cell lines from embryos obtained after IVF and after PGD for monogenic disorders
    I Mateizel
    Research Centre for Reproduction and Genetics, University Hospital and Medical School of the Vrije Universiteit Brussel Dutch speaking Brussels Free University Laarbeeklaan 101, 1090 Brussels, Belgium
    Hum Reprod 21:503-11. 2006
    ..hES cell lines derived from blastocysts diagnosed as carrying a genetic disorder after PGD represent in vitro disease models...