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Syntaxin 18 Defects in Human and Zebrafish Unravel Key Roles in Early Cartilage and Bone Development.
Guillemyn B, De Saffel H, Bek JW, Tapaneeyaphan P, De Clercq A, Jarayseh T, Debaenst S, Willaert A, De Rycke R, Byers PH, Rosseel T, Coucke P, Blaumeiser B, Syx D, Malfait F, Symoens S. Guillemyn B, et al. Among authors: symoens s. J Bone Miner Res. 2023 Nov;38(11):1718-1730. doi: 10.1002/jbmr.4914. Epub 2023 Sep 30. J Bone Miner Res. 2023. PMID: 37718532 Free article.
Defective Proteolytic Processing of Fibrillar Procollagens and Prodecorin Due to Biallelic BMP1 Mutations Results in a Severe, Progressive Form of Osteogenesis Imperfecta.
Syx D, Guillemyn B, Symoens S, Sousa AB, Medeira A, Whiteford M, Hermanns-Lê T, Coucke PJ, De Paepe A, Malfait F. Syx D, et al. Among authors: symoens s. J Bone Miner Res. 2015 Aug;30(8):1445-56. doi: 10.1002/jbmr.2473. Epub 2015 May 21. J Bone Miner Res. 2015. PMID: 25656619 Free article.
Loss of Type I Collagen Telopeptide Lysyl Hydroxylation Causes Musculoskeletal Abnormalities in a Zebrafish Model of Bruck Syndrome.
Gistelinck C, Witten PE, Huysseune A, Symoens S, Malfait F, Larionova D, Simoens P, Dierick M, Van Hoorebeke L, De Paepe A, Kwon RY, Weis M, Eyre DR, Willaert A, Coucke PJ. Gistelinck C, et al. Among authors: symoens s. J Bone Miner Res. 2016 Nov;31(11):1930-1942. doi: 10.1002/jbmr.2977. Epub 2016 Oct 24. J Bone Miner Res. 2016. PMID: 27541483 Free PMC article.
Zebrafish type I collagen mutants faithfully recapitulate human type I collagenopathies.
Gistelinck C, Kwon RY, Malfait F, Symoens S, Harris MP, Henke K, Hawkins MB, Fisher S, Sips P, Guillemyn B, Bek JW, Vermassen P, De Saffel H, Witten PE, Weis M, De Paepe A, Eyre DR, Willaert A, Coucke PJ. Gistelinck C, et al. Among authors: symoens s. Proc Natl Acad Sci U S A. 2018 Aug 21;115(34):E8037-E8046. doi: 10.1073/pnas.1722200115. Epub 2018 Aug 6. Proc Natl Acad Sci U S A. 2018. PMID: 30082390 Free PMC article.
Loss of TANGO1 Leads to Absence of Bone Mineralization.
Guillemyn B, Nampoothiri S, Syx D, Malfait F, Symoens S. Guillemyn B, et al. Among authors: symoens s. JBMR Plus. 2021 Jan 13;5(3):e10451. doi: 10.1002/jbm4.10451. eCollection 2021 Mar. JBMR Plus. 2021. PMID: 33778321 Free PMC article.
Mutations in FKBP10 cause recessive osteogenesis imperfecta and Bruck syndrome.
Kelley BP, Malfait F, Bonafe L, Baldridge D, Homan E, Symoens S, Willaert A, Elcioglu N, Van Maldergem L, Verellen-Dumoulin C, Gillerot Y, Napierala D, Krakow D, Beighton P, Superti-Furga A, De Paepe A, Lee B. Kelley BP, et al. Among authors: symoens s. J Bone Miner Res. 2011 Mar;26(3):666-72. doi: 10.1002/jbmr.250. J Bone Miner Res. 2011. PMID: 20839288 Free PMC article.
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