Hasil Pencarian - Fabiola Lange

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  1. 1
    Mice carrying a ubiquitous R235W mutation of Wnt1 display a bone-specific phenotype

    Mice carrying a ubiquitous R235W mutation of Wnt1 display a bone-specific phenotype oleh Timur Alexander Yorgan, Tim Rolvien, Julian Stürznickel, Nele Vollersen, Fabiola Lange, Anke Baranowsky, Irm Hermans-Borgmeyer, Jean-Pierre David, Ralf Oheim, Michael Amling, Thorsten Schinke

    Diterbitkan 2020-10-01
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  2. 2
    The WNT1 G177C mutation specifically affects skeletal integrity in a mouse model of osteogenesis imperfecta type XV

    The WNT1 G177C mutation specifically affects skeletal integrity in a mouse model of osteogenesis imperfecta type XV oleh Nele Vollersen, Wenbo Zhao, Tim Rolvien, Fabiola Lange, Felix Nikolai Schmidt, Stephan Sonntag, Doron Shmerling, Simon von Kroge, Kilian Elia Stockhausen, Ahmed Sharaf, Michaela Schweizer, Meliha Karsak, Björn Busse, Ernesto Bockamp, Oliver Semler, Michael Amling, Ralf Oheim, Thorsten Schinke, Timur Alexander Yorgan

    Diterbitkan 2021-11-01
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