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International Journal of Molecular Sciences|January 7, 2021
Intracellular and Extracellular Markers of Lethality in Osteogenesis Imperfecta: A Quantitative Proteomic ApproachLuca Bini, Domitille Schvartz, Chiara Carnemolla, et al.
The International Journal of Lower Extremity Wounds|December 6, 2015
A Rare Cause of Lower Extremity Ulcers: Prolidase DeficiencyEsra Adışen, Funda Bapur Erduran, Fatih Süheyl Ezgü, et al.
Calcified Tissue International|August 5, 2018
Early Fracture Healing is Delayed in the Col1a2+/G610C Osteogenesis Imperfecta Murine ModelRoberta Besio, Silvia Maruelli, Severine Battaglia, et al.
Life Sciences|December 20, 2024
A novel chemical chaperone ameliorates osteoblast homeostasis and extracellular matrix in osteogenesis imperfectaNadia Garibaldi, Roberta Besio, Valentina Pirota, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|February 13, 2018
4-PBA ameliorates cellular homeostasis in fibroblasts from osteogenesis imperfecta patients by enhancing autophagy and stimulating protein secretionRoberta Besio, Giusy Iula, Nadia Garibaldi, et al.
European Biophysics Journal : EBJ|May 6, 2009
Identifying the structure of the active sites of human recombinant prolidaseRoberta Besio, Stefania Alleva, Antonella Forlino, et al.
Frontiers in Endocrinology|August 28, 2020
Zebrafish: A Resourceful Vertebrate Model to Investigate Skeletal DisordersFrancesca Tonelli, Jan Willem Bek, Roberta Besio, et al.
Matrix Biology Plus|February 5, 2021
Osteoblasts mineralization and collagen matrix are conserved upon specific Col1a2 silencingSilvia Maruelli, Roberta Besio, Julie Rousseau, et al.
AIMS Genetics|November 13, 2018
Expression characterization and functional implication of the collagen-modifying Leprecan proteins in mouse gonadal tissue and mature spermSarah M Zimmerman, Roberta Besio, Melissa E Heard-Lipsmeyer, et al.
JIMD Reports|February 23, 2013
Partial Rescue of Biochemical Parameters After Hematopoietic Stem Cell Transplantation in a Patient with Prolidase Deficiency Due to Two Novel PEPD MutationsDésirée Caselli, Rolando Cimaz, Roberta Besio, et al.
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