5 Einträge gefunden

1. Skeletal deterioration in COL2A1-related spondyloepiphyseal dysplasia occurs prior to osteoarthritis

   1. Rolvien, Tim
   2. Yorgan, Timur Alexander
   3. Kornak, Uwe
   4. Hermans-Borgmeyer, Irm
   5. Mundlos, Stefan
   6. Schmidt, Tobias
   7. Niemeier, Andreas

   2020 - Forschungsinformationssystem des UKE
2. Whole-Exome Sequencing Identifies Novel Compound Heterozygous ZNF469 Mutations in Two Siblings with Mild Brittle Cornea Syndrome

   1. Rolvien, Tim
   2. Kornak, Uwe
   3. Linke, Stephan J
   4. Amling, Michael
   5. Oheim, Ralf

   2020 - Forschungsinformationssystem des UKE
3. Human Heterozygous ENPP1 Deficiency Is Associated With Early Onset Osteoporosis, a Phenotype Recapitulated in a Mouse Model of Enpp1 Deficiency

   1. Oheim, Ralf
   2. Zimmerman, Kristin
   3. Maulding, Nathan D
   4. Stürznickel, Julian
   5. von Kroge, Simon
   6. Kavanagh, Dillon
   7. Stabach, Paul R

   2020 - Forschungsinformationssystem des UKE
4. Mice lacking plastin-3 display a specific defect of cortical bone acquisition

   1. Yorgan, Timur
   2. Sari, Hatice
   3. Rolvien, Tim
   4. Windhorst, Sabine
   5. Failla, Antonio Virgilio
   6. Kornak, Uwe
   7. Oheim, Ralf

   2020 - Forschungsinformationssystem des UKE
5. Gnathodiaphyseal dysplasia is not recapitulated in a respective mouse model carrying a mutation of the Ano5 gene

   1. Rolvien, Tim
   2. Avci, Osman
   3. von Kroge, Simon
   4. Koehne, Till
   5. Selbert, Stefan
   6. Sonntag, Stephan
   7. Shmerling, Doron

   2020 - Forschungsinformationssystem des UKE