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Frontiers in Endocrinology|July 9, 2020
Human Fibroblasts as a Model for the Study of Bone DisordersLauria Claeys, Nathalie Bravenboer, Elisabeth M W Eekhoff, et al.Human Genetics|June 25, 2021
Collagen transport and related pathways in Osteogenesis ImperfectaLauria Claeys, Silvia Storoni, Marelise Eekhoff, et al.Frontiers in Endocrinology|March 27, 2023
Exploration of the skeletal phenotype of the Col1a1 +/Mov13 mouse model for haploinsufficient osteogenesis imperfecta type 1Lauria Claeys, Lidiia Zhytnik, Lisanne E Wisse, et al.International Journal of Molecular Sciences|March 28, 2024
In Vitro Modelling of Osteogenesis Imperfecta with Patient-Derived Induced Mesenchymal Stem CellsLauria Claeys, Lidiia Zhytnik, Laura Ventura, et al.Scientific Reports|August 29, 2022
Osteogenic transdifferentiation of primary human fibroblasts to osteoblast-like cells with human platelet lysateFerdy K Cayami, Lauria Claeys, Ruben de Ruiter, et al.American Journal of Human Genetics|October 14, 2020
Interaction between KDELR2 and HSP47 as a Key Determinant in Osteogenesis Imperfecta Caused by Bi-allelic Variants in KDELR2Fleur S van Dijk, Oliver Semler, Julia Etich, et al.Pageof 1