R
Rosa Maria Borzì
Researcher at I.O.R.
Publications - 71
Citations - 3757
Rosa Maria Borzì is an academic researcher from I.O.R.. The author has contributed to research in topics: Chondrocyte & Cellular differentiation. The author has an hindex of 28, co-authored 69 publications receiving 3164 citations. Previous affiliations of Rosa Maria Borzì include University of Bologna.
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NF-κB Signaling: Multiple Angles to Target OA
TL;DR: Growing evidence points to NF-kappaB signaling as not only playing a central role in the pro-inflammatory stress-related responses of chondrocytes to extra- and intra-cellular insults, but also in the control of their differentiation program.
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Roles of inflammatory and anabolic cytokines in cartilage metabolism: signals and multiple effectors converge upon MMP-13 regulation in osteoarthritis
Mary B. Goldring,Miguel Otero,Darren A. Plumb,Cecilia Dragomir,Marta Favero,Karim El Hachem,Ko Hashimoto,Helmtrud I. Roach,Eleonora Olivotto,Rosa Maria Borzì,Kenneth B. Marcu +10 more
TL;DR: A thorough understanding of the similarities and particularly the marked differences in mechanisms of cartilage remodeling during development, osteoarthritis, and aging may lead to more effective strategies for preventing cartilage damage and promoting repair.
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Biomaterials: Foreign Bodies or Tuners for the Immune Response?
TL;DR: Recent research breakthroughs have provided a broader insight on the correct choice of biomaterial physicochemical modifications to tune the reaction of the host immune system to implanted biomaterial and to favor integration and healing.
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Enhanced and coordinated in vivo expression of inflammatory cytokines and nitric oxide synthase by chondrocytes from patients with osteoarthritis
Cinzia Melchiorri,Riccardo Meliconi,L. Frizziero,Tania Silvestri,Lia Pulsatelli,Ilaria Mazzetti,Rosa Maria Borzì,Mariagrazia Uguccioni,Andrea Facchini +8 more
TL;DR: The enhanced and coordinated expression of IL-1beta, TNFalpha, and iNOS by chondrocytes strongly supports the hypothesis that chondROcytes are the major site of production of mediators of inflammation in human OA, thus playing a primary role in the pathogenesis of this disease.
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p16INK4a and its regulator miR-24 link senescence and chondrocyte terminal differentiation-associated matrix remodeling in osteoarthritis
Didier Philipot,Didier Philipot,David Guérit,David Guérit,Daniela Platano,Paul Chuchana,Paul Chuchana,Eleonora Olivotto,Francisco Espinoza,Francisco Espinoza,Anne Dorandeu,Yves-Marie Pers,Yves-Marie Pers,Jacques Piette,Rosa Maria Borzì,Christian Jorgensen,Christian Jorgensen,Danièle Noël,Danièle Noël,Jean-Marc Brondello,Jean-Marc Brondello +20 more
TL;DR: In this article, the role of the senescence marker p16INK4a and its regulation by microRNAs (miRs) during OA and terminal chondrogenesis was evaluated.