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Page 1
Exome sequencing identifies a nonsense mutation in Fam46a associated with bone abnormalities in a new mouse model for skeletal dysplasia.
Diener S, Bayer S, Sabrautzki S, Wieland T, Mentrup B, Przemeck GK, Rathkolb B, Graf E, Hans W, Fuchs H, Horsch M, Schwarzmayr T, Wolf E, Klopocki E, Jakob F, Strom TM, Hrabě de Angelis M, Lorenz-Depiereux B. Diener S, et al. Among authors: mentrup b. Mamm Genome. 2016 Apr;27(3-4):111-21. doi: 10.1007/s00335-016-9619-x. Epub 2016 Jan 23. Mamm Genome. 2016. PMID: 26803617
Low-energy trauma-induced intercondylar femoral fracture.
Aeby M, Wyss T, Mentrup B, Kunstmann E, Jakob F, Aeberli D. Aeby M, et al. Among authors: mentrup b. Clin Cases Miner Bone Metab. 2016 May-Aug;13(2):151-153. doi: 10.11138/ccmbm/2016.13.2.151. Epub 2016 Oct 5. Clin Cases Miner Bone Metab. 2016. PMID: 27920814 Free PMC article.
Recombinant Enzyme Replacement Therapy in Hypophosphatasia.
Hofmann C, Jakob F, Seefried L, Mentrup B, Graser S, Plotkin H, Girschick HJ, Liese J. Hofmann C, et al. Among authors: mentrup b. Subcell Biochem. 2015;76:323-41. doi: 10.1007/978-94-017-7197-9_15. Subcell Biochem. 2015. PMID: 26219718 Review.
Novel molecular cues for dental defects in hypophosphatasia.
Melms H, Herrmann M, Förstner K, Bharti R, Schneider D, Mentrup B, Rudert M, Schlagenhauf U, Jakob F, Graser S. Melms H, et al. Among authors: mentrup b. Exp Cell Res. 2020 Jul 15;392(2):112026. doi: 10.1016/j.yexcr.2020.112026. Epub 2020 Apr 22. Exp Cell Res. 2020. PMID: 32333908 Free article.
29 results