Cell-mediated and direct gene therapy for bone regeneration. - Wikidata - wikimedia - TriplyDB

Cell-mediated and direct gene therapy for bone regeneration.

Cell-mediated and direct gene therapy for bone regeneration.

http://www.wikidata.org/entity/Q37983112

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Translating stem cell therapies: the role of companion animals in regenerative medicine Characterization of scaffold carriers for BMP9-transduced osteoblastic progenitor cells in bone regeneration.Bone morphogenetic protein 9 (BMP9) induces effective bone formation from reversibly immortalized multipotent adipose-derived (iMAD) mesenchymal stem cells.Development of nanomaterials for bone repair and regeneration.The strategy and method in modulating finger regeneration.Effects of BMP2 and VEGF165 on the osteogenic differentiation of rat bone marrow-derived mesenchymal stem cells.Analysis of the mechanism by which nerve growth factor promotes callus formation in mice with tibial fracture.

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Cell-mediated and direct gene therapy for bone regeneration.

http://www.wikidata.org/entity/Q37983112

description

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article scientifique

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Cell-mediated and direct gene therapy for bone regeneration.

@en

Cell-mediated and direct gene therapy for bone regeneration.

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type

label

Cell-mediated and direct gene therapy for bone regeneration.

@en

Cell-mediated and direct gene therapy for bone regeneration.

@nl

prefLabel

Cell-mediated and direct gene therapy for bone regeneration.

@en

Cell-mediated and direct gene therapy for bone regeneration.

@nl

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14712598.2012.661709

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Expert Opinion on Biological Therapy

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Cell-mediated and direct gene therapy for bone regeneration.

@en

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Akikazu Ishihara

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Alicia L Bertone

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Essential requirement of BMPs-2/4 for both osteoblast and osteoclast formation in murine bone marrow cultures from adult mice: antagonism by noggin

Induction of pluripotent stem cells from adult human fibroblasts by defined factors

BMP signaling components are expressed in human fracture callus

LMO2-associated clonal T cell proliferation in two patients after gene therapy for SCID-X1

Bone morphogenetic proteins

Systemically administered mesenchymal stromal cells transduced with insulin-like growth factor-I localize to a fracture site and potentiate healing.

The use of bone morphogenetic protein-6 gene therapy for percutaneous spinal fusion in rabbits.

Overexpressed LIM mineralization proteins do not require LIM domains to induce bone.

Implantation of canine umbilical cord blood-derived mesenchymal stem cells mixed with beta-tricalcium phosphate enhances osteogenesis in bone defect model dogs.

Adenovirus encoding human platelet-derived growth factor-B delivered to alveolar bone defects exhibits safety and biodistribution profiles favorable for clinical use.

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411-423

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scholarly article

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10.1517/14712598.2012.661709

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2012-02-13T00:00:00Z

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22324829

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