4 Einträge gefunden

1. The WNT1G177C mutation specifically affects skeletal integrity in a mouse model of osteogenesis imperfecta type XV

   1. Vollersen, Nele
   2. Zhao, Wenbo
   3. Rolvien, Tim
   4. Lange, Fabiola
   5. Schmidt, Felix Nikolai
   6. Sonntag, Stephan
   7. Shmerling, Doron

   2021 - Forschungsinformationssystem des UKE - frei zugänglich
2. Mice carrying a ubiquitous R235W mutation of Wnt1 display a bone-specific phenotype

   1. Yorgan, Timur
   2. Rolvien, Tim
   3. Stürznickel, Julian
   4. Vollersen, Nele
   5. Lange, Fabiola
   6. Zhao, Wenbo
   7. Baranowsky, Anke

   2020 - Forschungsinformationssystem des UKE
3. Analysis of the FLVR motif of SHIP1 and its importance for the protein stability of SH2 containing signaling proteins

   1. Ehm, Patrick A H
   2. Lange, Fabiola
   3. Hentschel, Carolin
   4. Jepsen, Anneke
   5. Glück, Madeleine
   6. Nelson, Nina
   7. Bettin, Bettina

   2019 - Forschungsinformationssystem des UKE
4. Analysis of the FLVR motif of SHIP1 and its importance for the protein stability of SH2 containing signaling proteins

   1. Ehm, Patrick A.H.
   2. Lange, Fabiola
   3. Hentschel, Carolin
   4. Jepsen, Anneke
   5. Glück, Madeleine
   6. Nelson, Nina
   7. Bettin, Bettina

   2019 - Forschungsinformationssystem der UHH