Bone morphogenetic proteins and tissue engineering: future directions.

G. M. Calori, D. Donati, C. Di Bella, L. Tagliabue

Research output: Contribution to journalArticle

44 Citations (Scopus)

Abstract

As long as bone repair and regeneration is considered as a complex clinical condition, the administration of more than one factor involved in fracture healing might be necessary. The effectiveness or not of bone morphogenetic proteins (BMPs) in association with other growth factors and with mesenchymal stem cells in bone regeneration for fracture healing and bone allograft integration is of great interest to the scientific community. In this study we point out possible future developments in BMPs, concerning research and clinical applications.

Original languageEnglish
JournalInjury
Volume40 Suppl 3
Publication statusPublished - Dec 2009

Fingerprint

Protein Engineering
Bone Morphogenetic Proteins
Bone Regeneration
Fracture Healing
Tissue Engineering
Bone Fractures
Mesenchymal Stromal Cells
Allografts
Intercellular Signaling Peptides and Proteins
Bone and Bones
Research
Direction compound

ASJC Scopus subject areas

  • Emergency Medicine
  • Orthopedics and Sports Medicine

Cite this

Calori, G. M., Donati, D., Di Bella, C., & Tagliabue, L. (2009). Bone morphogenetic proteins and tissue engineering: future directions. Injury, 40 Suppl 3.

Bone morphogenetic proteins and tissue engineering : future directions. / Calori, G. M.; Donati, D.; Di Bella, C.; Tagliabue, L.

In: Injury, Vol. 40 Suppl 3, 12.2009.

Research output: Contribution to journalArticle

Calori, GM, Donati, D, Di Bella, C & Tagliabue, L 2009, 'Bone morphogenetic proteins and tissue engineering: future directions.', Injury, vol. 40 Suppl 3.
Calori GM, Donati D, Di Bella C, Tagliabue L. Bone morphogenetic proteins and tissue engineering: future directions. Injury. 2009 Dec;40 Suppl 3.
Calori, G. M. ; Donati, D. ; Di Bella, C. ; Tagliabue, L. / Bone morphogenetic proteins and tissue engineering : future directions. In: Injury. 2009 ; Vol. 40 Suppl 3.
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