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Plos Genetics|March 29, 2016
TGFβ and BMP Dependent Cell Fate Changes Due to Loss of Filamin B Produces Disc Degeneration and Progressive Vertebral FusionsJennifer Zieba, Kimberly Nicole Forlenza, Jagteshwar Singh Khatra, et al.Scientific Reports|September 27, 2016
Destabilization of the IFT-B cilia core complex due to mutations in IFT81 causes a Spectrum of Short-Rib Polydactyly SyndromeIvan Duran, S Paige Taylor, Wenjuan Zhang, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|August 1, 2024
Loss of the long form of Plod2 phenocopies contractures of Bruck syndrome-osteogenesis imperfectaAlexander Kot, Cora Chun, Jorge H Martin, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|February 9, 2017
A Chaperone Complex Formed by HSP47, FKBP65, and BiP Modulates Telopeptide Lysyl Hydroxylation of Type I ProcollagenIvan Duran, Jorge H Martin, Mary Ann Weis, et al.Frontiers in Cell and Developmental Biology|February 2, 2023
Skeletal diseases caused by mutations in PTH1R show aberrant differentiation of skeletal progenitors due to dysregulation of DEPTORFabiana Csukasi, Michaela Bosakova, Tomas Barta, et al.European Journal of Nuclear Medicine and Molecular Imaging|July 21, 2019
Personalised radioembolization improves outcomes in refractory intra-hepatic cholangiocarcinoma: a multicenter studyHugo Levillain, Ivan Duran Derijckere, Lieveke Ameye, et al.Science Translational Medicine|September 21, 2018
The PTH/PTHrP-SIK3 pathway affects skeletogenesis through altered mTOR signalingFabiana Csukasi, Ivan Duran, Maya Barad, et al.Cilia|April 13, 2017
Mutations in IFT-A satellite core component genes IFT43 and IFT121 produce short rib polydactyly syndrome with distinctive campomeliaIvan Duran, S Paige Taylor, Wenjuan Zhang, et al.Journal of Surgical Oncology|November 14, 2019
The metabolic clinical risk score as a new prognostic model for surgical decision-making in patients with colorectal liver metastasesIvan Duran Derijckere, Hugo Levillain, Ali Bohlok, et al.Human Molecular Genetics|January 24, 2018
Regulation of ciliary function by fibroblast growth factor signaling identifies FGFR3-related disorders achondroplasia and thanatophoric dysplasia as ciliopathiesMichaela Kunova Bosakova, Miroslav Varecha, Marek Hampl, et al.Pageof 5