Alveolar bone formation at dental implant dehiscence defects following guided bone regeneration and xenogeneic freeze-dried demineralized bone matrix

1998 ◽  
Vol 9 (6) ◽  
pp. 419-428 ◽  
Author(s):  
Kyoo-sung Cho ◽  
Seong-ho Choi ◽  
Kyung-ho Han ◽  
Jung-kiu Chai ◽  
Ulf M. E. Wikesjö ◽  
...  
1998 ◽  
Vol 69 (1) ◽  
pp. 26-33 ◽  
Author(s):  
Chong-Kwan Kim ◽  
Kyoo-Sung Cho ◽  
Seong-Ho Choi ◽  
Annamarie Prewett ◽  
Ulf M.E. Wikesjö

1998 ◽  
Vol 25 (10) ◽  
pp. 801-806 ◽  
Author(s):  
Nicholas Caplanis ◽  
Michael B. Lee ◽  
Grenith J. Zimmerman ◽  
Knut A. Selvig ◽  
Ulf M.E. Wikesjo

2002 ◽  
Vol 52 (5) ◽  
pp. 933-937 ◽  
Author(s):  
Roberto Giardino ◽  
Nicolo N. Aldini ◽  
Milena Fini ◽  
Gianluca Giavaresi ◽  
Paola Torricelli

MRS Bulletin ◽  
1996 ◽  
Vol 21 (11) ◽  
pp. 36-39 ◽  
Author(s):  
Ugo Ripamonti ◽  
Nicolaas Duneas

Recent advances in materials science and biotechnology have given birth to the new and exciting field of tissue engineering, in which the two normally disparate fields are merging into a profitable matrimony. In particular the use of biomaterials capable of initiating new bone formation via a process called osteoinduction is leading to quantum leaps for the tissue engineering of bone.The classic work of Marshall R. Urist and A. Hari Reddi opened the field of osteoinductive biomaterials. Urist discovered that, upon implantation of devitalized, demineralized bone matrix in the muscle of experimental animals, new bone formation occurs within two weeks, a phenomenon he described as bone formation by induction. The tissue response elicited by implantation of demineralized bone matrix in muscle or under the skin includes activation and migration of undifferentiated mesenchymal cells by chemotaxis, anchoragedependent cell attachment to the matrix, mitosis and proliferation of mesenchymal cells, differentiation of cartilage, mineralization of the cartilage, vascular invasion of the cartilage, differentiation of osteoblasts and deposition of bone matrix, and finally mineralization of bone and differentiation of marrow in the newly developed ossicle.The osteoinductive ability of the extracellular matrix of bone is abolished by the dissociative extraction of the demineralized matrix, but is recovered when the extracted component, itself inactive, is reconstituted with the inactive residue—mainly insoluble collagenous bone matrix. This important experiment showed that the osteoinductive signal resides in the solubilized component but needs to be reconstituted with an appropriate carrier to restore the osteoinductive activity. In this case, the carrier is the insoluble collagenous bone matrix—mainly crosslinked type I collagen.


2007 ◽  
Vol 89 (1) ◽  
pp. 139-147 ◽  
Author(s):  
Don M. Ranly ◽  
Barbara D. Boyan ◽  
Zvi Schwartz ◽  
Christoph H. Lohmann ◽  
Domenico Andreacchio

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