Search Results - "Scaranari, Monica"

  • Showing 1 - 5 results of 5
Refine Results
  1. 1

    Dual effect of platelet lysate on human articular cartilage: a maintenance of chondrogenic potential and a transient proinflammatory activity followed by an inflammation resolution by Pereira, Rui Cruz, Scaranari, Monica, Benelli, Roberto, Strada, Paolo, Reis, Rui L, Cancedda, Ranieri, Gentili, Chiara

    Published in Tissue engineering. Part A (01-06-2013)
    “…Platelet-rich plasma (PRP), a cocktail of platelet growth factors and bioactive proteins, has been proposed as a therapeutic agent to restore damaged articular…”
    Get more information
    Journal Article
  2. 2

    Beta‐tricalcium phosphate ceramic triggers fast and robust bone formation by human mesenchymal stem cells by Pereira, Rui C., Benelli, Roberto, Canciani, Barbara, Scaranari, Monica, Daculsi, Guy, Cancedda, Ranieri, Gentili, Chiara

    “…Due to their osteoconductive and inductive properties, a variety of calcium phosphate (CaP) scaffolds are commonly used in orthopaedics as graft material to…”
    Get full text
    Journal Article
  3. 3

    Recruitment of host’s progenitor cells to sites of human amniotic fluid stem cells implantation by Mirabella, Teodelinda, Poggi, Alessandro, Scaranari, Monica, Mogni, Massimo, Lituania, Mario, Baldo, Chiara, Cancedda, Ranieri, Gentili, Chiara

    Published in Biomaterials (01-06-2011)
    “…Abstract The amniotic fluid is a new source of multipotent stem cells with a therapeutic potential for human diseases. Cultured at low cell density, human…”
    Get full text
    Journal Article
  4. 4

    A refined physical and transcriptional map of the SPG9 locus on 10q23.3-q24.2 by Lo Nigro, C, Cusano, R, Scaranari, M, Cinti, R, Forabosco, P, Morra, V B, De Michele, G, Santoro, L, Davies, S, Hurst, J, Devoto, M, Ravazzolo, R, Seri, M

    Published in European journal of human genetics : EJHG (01-10-2000)
    “…Hereditary spastic paraplegia (HSP) is a genetically heterogeneous disorder characterised by progressive spasticity of the lower limbs. Beside 'pure' forms of…”
    Get full text
    Journal Article
  5. 5

    Prevalence and parental origin of de novo RET mutations in Hirschsprung's disease by Yin, L, Seri, M, Barone, V, Tocco, T, Scaranari, M, Romeo, G

    “…In contrast with the reported almost exclusive paternal origin of de novo mutations in MEN 2A, FMTC and MEN 2B, de novo mutations in Hirschsprung patients…”
    Get full text
    Journal Article