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Mice heterozygous for an osteogenesis imperfecta-linked MBTPS2 variant display a compromised subchondral osteocyte lacunocanalicular network associated with abnormal articular cartilage.
Danyukova T, Alimy AR, Velho RV, Yorgan TA, Di Lorenzo G, von Kroge S, Tidow H, Wiegert JS, Hermans-Borgmeyer I, Schinke T, Rolvien T, Pohl S. Danyukova T, et al. Among authors: von kroge s. Bone. 2023 Dec;177:116927. doi: 10.1016/j.bone.2023.116927. Epub 2023 Oct 4. Bone. 2023. PMID: 37797712
Piezo1 Inactivation in Chondrocytes Impairs Trabecular Bone Formation.
Hendrickx G, Fischer V, Liedert A, von Kroge S, Haffner-Luntzer M, Brylka L, Pawlus E, Schweizer M, Yorgan T, Baranowsky A, Rolvien T, Neven M, Schumacher U, Beech DJ, Amling M, Ignatius A, Schinke T. Hendrickx G, et al. Among authors: von kroge s. J Bone Miner Res. 2021 Feb;36(2):369-384. doi: 10.1002/jbmr.4198. Epub 2020 Nov 12. J Bone Miner Res. 2021. PMID: 33180356 Free article.
The WNT1G177C mutation specifically affects skeletal integrity in a mouse model of osteogenesis imperfecta type XV.
Vollersen N, Zhao W, Rolvien T, Lange F, Schmidt FN, Sonntag S, Shmerling D, von Kroge S, Stockhausen KE, Sharaf A, Schweizer M, Karsak M, Busse B, Bockamp E, Semler O, Amling M, Oheim R, Schinke T, Yorgan TA. Vollersen N, et al. Among authors: von kroge s. Bone Res. 2021 Nov 10;9(1):48. doi: 10.1038/s41413-021-00170-0. Bone Res. 2021. PMID: 34759273 Free PMC article.
Human Heterozygous ENPP1 Deficiency Is Associated With Early Onset Osteoporosis, a Phenotype Recapitulated in a Mouse Model of Enpp1 Deficiency.
Oheim R, Zimmerman K, Maulding ND, Stürznickel J, von Kroge S, Kavanagh D, Stabach PR, Kornak U, Tommasini SM, Horowitz MC, Amling M, Thompson D, Schinke T, Busse B, Carpenter TO, Braddock DT. Oheim R, et al. Among authors: von kroge s. J Bone Miner Res. 2020 Mar;35(3):528-539. doi: 10.1002/jbmr.3911. Epub 2019 Dec 5. J Bone Miner Res. 2020. PMID: 31805212 Free PMC article.
33 results