Transplantation of skin fibroblasts expressing BMP-2 promotes bone repair more effectively than those expressing Runx2 (Q52105340)

22 April 2018

title

Transplantation of skin fibroblasts expressing BMP-2 promotes bone repair more effectively than those expressing Runx2 (English)

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author name string

K. Hirata

1

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T. Tsukazaki

2

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A. Kadowaki

3

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K. Furukawa

4

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Y. Shibata

5

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T. Moriishi

6

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Y. Okubo

7

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K. Bessho

8

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T. Komori

9

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A. Mizuno

10

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A. Yamaguchi

11

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language of work or name

English

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National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=12753866

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publication date

1 May 2003

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22 April 2018

full work available at URL

https://api.elsevier.com/content/article/PII:S8756328203000541?httpAccept=text/xml

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https://api.elsevier.com/content/article/PII:S8756328203000541?httpAccept=text/plain

3 January 2024

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3 January 2024

1 reference

22 April 2018

volume

32

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22 April 2018

issue

5

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22 April 2018

page(s)

502-512

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22 April 2018

In Vitro andIn Vivo induction of bone formation using a recombinant adenoviral vector carrying the human BMP-2 gene

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Ex vivo gene therapy with stromal cells transduced with a retroviral vector containing the BMP4 gene completely heals critical size calvarial defect in rats.

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Adenoviral BMP-2 gene transfer in mesenchymal stem cells: in vitro and in vivo bone formation on biodegradable polymer scaffolds

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Induction of bone formation using a recombinant adenoviral vector carrying the human BMP-2 gene in a rabbit spinal fusion model

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Engineered human mesenchymal stem cells: a novel platform for skeletal cell mediated gene therapy

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Clonal isolation of muscle-derived cells capable of enhancing muscle regeneration and bone healing

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Effect of bone morphogenetic protein-2-expressing muscle-derived cells on healing of critical-sized bone defects in mice.

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Enhancement of bone healing based on ex vivo gene therapy using human muscle-derived cells expressing bone morphogenetic protein 2.

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Gene therapy for bone formation: in vitro and in vivo osteogenic activity of an adenovirus expressing BMP7.

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Gene therapy-directed osteogenesis: BMP-7-transduced human fibroblasts form bone in vivo

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Suppression of arthritic bone destruction by adenovirus-mediated csk gene transfer to synoviocytes and osteoclasts

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Possible involvement of the vascular endothelial growth factor-Flt-1-focal adhesion kinase pathway in chemotaxis and the cell proliferation of osteoclast precursor cells in arthritic joints

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Reciprocal role of ERK and NF-kappaB pathways in survival and activation of osteoclasts

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Modulation of osteoclast function by adenovirus vector-induced epidermal growth factor receptor

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Bone morphogenetic protein-transduced human fibroblasts convert to osteoblasts and form bone in vivo

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Infection efficiency of type 5 adenoviral vectors in synovial tissue can be enhanced with a type 16 fiber.

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Synergistic enhancement of bone formation and healing by stem cell-expressed VEGF and bone morphogenetic protein-4.

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Targeted disruption of Cbfa1 results in a complete lack of bone formation owing to maturational arrest of osteoblasts

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Regulation of osteoblast differentiation mediated by bone morphogenetic proteins, hedgehogs, and Cbfa1.

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Recombinant human bone morphogenetic protein-2 stimulates osteoblastic maturation and inhibits myogenic differentiation in vitro

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Effects of BMP-2, BMP-4, and BMP-6 on osteoblastic differentiation of bone marrow-derived stromal cell lines, ST2 and MC3T3-G2/PA6.

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The non-osteogenic mouse pluripotent cell line, C3H10T1/2, is induced to differentiate into osteoblastic cells by recombinant human bone morphogenetic protein-2

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Bone morphogenetic protein-2 converts the differentiation pathway of C2C12 myoblasts into the osteoblast lineage

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Cbfa1, a candidate gene for cleidocranial dysplasia syndrome, is essential for osteoblast differentiation and bone development

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Osf2/Cbfa1: a transcriptional activator of osteoblast differentiation

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Expression of bone morphogenetic protein-2 via adenoviral vector in C2C12 myoblasts induces differentiation into the osteoblast lineage

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Core-binding factor beta interacts with Runx2 and is required for skeletal development

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The effects of transplantation of osteoblastic cells with bone morphogenetic protein (BMP)/carrier complex on bone repair

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Cell-type-dependent up-regulation of in vitro mineralization after overexpression of the osteoblast-specific transcription factor Runx2/Cbfal

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Identifiers

1 reference

22 April 2018

1 reference

22 April 2018