Enhancing the chondroregenerative activities of mesenchymal stem cells via therapeutic gene transfer as reinforced sources of implantable cells in sites of cartilage injury is a promising tool to improve the natural processes of cartilage repair. In the present study, we show that overexpression of the Dickkopf-related protein 1 (DKK1) via clinically adapted recombinant adeno-associated viral (rAAV) vectors is capable of significantly stimulating proliferative, anabolic, and chondrodifferentiation events in primary human mesenchymal stem cells compared with control (reporter rAAV lacZ) transduction over an extended period of time in vitro (21 days). Strikingly, administration of the rAAV DKK1 candidate vector concomitantly restrained unwant...
Adult articular cartilage has a limited repair capacity. This leads to an increasing demand for opti...
Articular hyaline cartilage is an avascular, aneural and alymphatic tissue that has a very limited c...
Background: The delivery of therapeutic genes in sites of articular cartilage lesions using non-inva...
[Abstract] Application of chondroreparative gene vectors in cartilage defects is a powerful approach...
Application of chondroreparative gene vectors in cartilage defects is a powerful approach to directl...
Therapeutic gene transfer into articular cartilage is a potential means to stimulate reparative acti...
[Abstract] The application of chondrogenic gene sequences to human bone marrow-derived mesenchymal s...
Background: Articular cartilage has a limited potential for self-healing. Transplantation of genetic...
Gene therapy for osteoarthritis offers powerful, long-lasting tools that are well adapted to treat s...
Direct administration of therapeutic candidate gene sequences using the safe and effective recombina...
The repair of focal articular cartilage defects remains a problem. Combining gene therapy with tissu...
Cell-based regeneration of damaged or diseased articular cartilage still faces significant clinical ...
Scaffold-assisted gene therapy is a highly promising tool to treat articular cartilage lesions upon ...
The aim of this thesis project was to investigate the use of a recombinant adenoassociated virus (rA...
Ana Rey-Rico,1 Jagadeesh K Venkatesan,1 Gertrud Schmitt,1 Angel Concheiro,2 Henning Madry,1,3 Carmen...
Adult articular cartilage has a limited repair capacity. This leads to an increasing demand for opti...
Articular hyaline cartilage is an avascular, aneural and alymphatic tissue that has a very limited c...
Background: The delivery of therapeutic genes in sites of articular cartilage lesions using non-inva...
[Abstract] Application of chondroreparative gene vectors in cartilage defects is a powerful approach...
Application of chondroreparative gene vectors in cartilage defects is a powerful approach to directl...
Therapeutic gene transfer into articular cartilage is a potential means to stimulate reparative acti...
[Abstract] The application of chondrogenic gene sequences to human bone marrow-derived mesenchymal s...
Background: Articular cartilage has a limited potential for self-healing. Transplantation of genetic...
Gene therapy for osteoarthritis offers powerful, long-lasting tools that are well adapted to treat s...
Direct administration of therapeutic candidate gene sequences using the safe and effective recombina...
The repair of focal articular cartilage defects remains a problem. Combining gene therapy with tissu...
Cell-based regeneration of damaged or diseased articular cartilage still faces significant clinical ...
Scaffold-assisted gene therapy is a highly promising tool to treat articular cartilage lesions upon ...
The aim of this thesis project was to investigate the use of a recombinant adenoassociated virus (rA...
Ana Rey-Rico,1 Jagadeesh K Venkatesan,1 Gertrud Schmitt,1 Angel Concheiro,2 Henning Madry,1,3 Carmen...
Adult articular cartilage has a limited repair capacity. This leads to an increasing demand for opti...
Articular hyaline cartilage is an avascular, aneural and alymphatic tissue that has a very limited c...
Background: The delivery of therapeutic genes in sites of articular cartilage lesions using non-inva...