Gene therapy approaches to regenerating the musculoskeletal system
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[1] J. Hoyland,et al. Use of genetically modified muscle and fat grafts to repair defects in bone and cartilage. , 2009, European cells & materials.
[2] F. Michetti,et al. Ex vivo-transduced autologous skin fibroblasts expressing human Lim mineralization protein-3 efficiently form new bone in animal models , 2008, Gene Therapy.
[3] W. Zhou,et al. Angiogenic gene‐modified myoblasts promote vascularization during repair of skeletal muscle defects , 2015, Journal of tissue engineering and regenerative medicine.
[4] H. Drissi,et al. Suicide gene approach using a dual-expression lentiviral vector to enhance the safety of ex vivo gene therapy for bone repair , 2013, Gene Therapy.
[5] James D. Kang,et al. Potential applications of gene therapy to the treatment of intervertebral disc disorders. , 2000, Clinical orthopaedics and related research.
[6] P. Robbins,et al. Osteoarthritis gene therapy , 2004, Gene Therapy.
[7] F. Jakob,et al. BMP12 and BMP13 gene transfer induce ligamentogenic differentiation in mesenchymal progenitor and anterior cruciate ligament cells. , 2010, Cytotherapy.
[8] Freddie H. Fu,et al. Gene transfer to the tendon-bone insertion site , 2004, Knee Surgery, Sports Traumatology, Arthroscopy.
[9] F. Gao,et al. Lentivirus-mediated Wnt10b overexpression enhances fracture healing in a rat atrophic non-union model , 2014, Biotechnology Letters.
[10] C. Ha,et al. Initial phase I safety of retrovirally transduced human chondrocytes expressing transforming growth factor-beta-1 in degenerative arthritis patients , 2012, Cytotherapy.
[11] Synthetic scaffold coating with adeno-associated virus encoding BMP2 to promote endogenous bone repair , 2012, Cell and Tissue Research.
[12] K. Lau,et al. Lentiviral‐based BMP4 in vivo gene transfer strategy increases pull‐out tensile strength without an improvement in the osteointegration of the tendon graft in a rat model of biceps tenodesis , 2011, The journal of gene medicine.
[13] M. Göken,et al. Cell-based resurfacing of large cartilage defects: long-term evaluation of grafts from autologous transgene-activated periosteal cells in a porcine model of osteoarthritis. , 2008, Arthritis and rheumatism.
[14] Jo Wixon,et al. Gene therapy clinical trials worldwide to 2012 – an update , 2013, The journal of gene medicine.
[15] Wenzhong Li,et al. Non-viral gene delivery methods. , 2013, Current pharmaceutical biotechnology.
[16] Freddie H. Fu,et al. Enhancement of Tendon-Bone Integration of Anterior Cruciate Ligament Grafts with Bone Morphogenetic Protein-2 Gene Transfer: A Histological and Biomechanical Study , 2002, The Journal of bone and joint surgery. American volume.
[17] L. Begum,et al. Implantation of rAAV5-IGF-I transduced autologous chondrocytes improves cartilage repair in full-thickness defects in the equine model. , 2015, Molecular therapy : the journal of the American Society of Gene Therapy.
[18] R. Porter,et al. Ex vivo adenoviral transfer of bone morphogenetic protein 12 (BMP-12) cDNA improves Achilles tendon healing in a rat model , 2008, Gene Therapy.
[19] M. Bouxsein,et al. Direct percutaneous gene delivery to enhance healing of segmental bone defects. , 2006, The Journal of bone and joint surgery. American volume.
[20] 野崎 正浩. Improved muscle healing after contusion injury by the inhibitory effect of suramin on myostatin, a negative regulator of muscle growth , 2009 .
[21] Piyush Koria,et al. Delivery of Growth Factors for Tissue Regeneration and Wound Healing , 2012, BioDrugs.
[22] K. Xin,et al. Adeno-associated virus-2-mediated bFGF gene transfer to digital flexor tendons significantly increases healing strength. an in vivo study. , 2008, The Journal of bone and joint surgery. American volume.
[23] P. Robbins,et al. Dual transduction of insulin‐like growth factor‐I and interleukin‐l receptor antagonist protein controls cartilage degradation in an osteoarthritic culture model , 2005, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.
[24] J. Affeldt,et al. The feasibility study , 2019, The Information System Consultant’s Handbook.
[25] S. Goldstein,et al. Stimulation of new bone formation by direct transfer of osteogenic plasmid genes. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[26] C. Archer,et al. Enhanced Adenovirus Transduction of hMSCs Using 3D Hydrogel Cell Carriers , 2013, Molecular Biotechnology.
[27] F. O'Brien,et al. The development of non-viral gene-activated matrices for bone regeneration using polyethyleneimine (PEI) and collagen-based scaffolds. , 2012, Journal of controlled release : official journal of the Controlled Release Society.
[28] J. Li,et al. Adenoviral‐mediated transfer of human BMP‐6 gene accelerates healing in a rabbit ulnar osteotomy model , 2004, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.
[29] P. Robbins,et al. Direct adenovirus-mediated insulin-like growth factor I gene transfer enhances transplant chondrocyte function. , 2001, Human gene therapy.
[30] Freddie H. Fu,et al. The timing of administration of a clinically relevant dose of losartan influences the healing process after contusion induced muscle injury. , 2013, Journal of applied physiology.
[31] H. Madry,et al. Overexpression of human IGF-I via direct rAAV-mediated gene transfer improves the early repair of articular cartilage defects in vivo , 2014, Gene Therapy.
[32] J. Schertzer,et al. Comparative evaluation of IGF-I gene transfer and IGF-I protein administration for enhancing skeletal muscle regeneration after injury , 2006, Gene Therapy.
[33] Freddie H. Fu,et al. Transfer of lacZ marker gene to the meniscus. , 1999, The Journal of bone and joint surgery. American volume.
[34] S. Gambhir,et al. "Same day" ex-vivo regional gene therapy: a novel strategy to enhance bone repair. , 2011, Molecular therapy : the journal of the American Society of Gene Therapy.
[35] Dong Han,et al. Repair of bone defect by using vascular bundle implantation combined with Runx II gene-transfected adipose-derived stem cells and a biodegradable matrix , 2013, Cell and Tissue Research.
[36] R. Guldberg,et al. Biological effects of rAAV-caAlk2 coating on structural allograft healing. , 2005, Molecular therapy : the journal of the American Society of Gene Therapy.
[37] Xin Fu,et al. Adenovirus-mediated transfer of siRNA against Runx2/Cbfa1 inhibits the formation of heterotopic ossification in animal model. , 2006, Biochemical and biophysical research communications.
[38] Freddie H. Fu,et al. Cartilage repair in a rat model of osteoarthritis through intraarticular transplantation of muscle-derived stem cells expressing bone morphogenetic protein 4 and soluble Flt-1. , 2009, Arthritis and rheumatism.
[39] Christian Lattermann,et al. A gene therapy approach to accelerating bone healing Evaluation of gene expression in a New Zealand white rabbit model , 1999, Knee Surgery, Sports Traumatology, Arthroscopy.
[40] J. Lou,et al. Engineered allogeneic mesenchymal stem cells repair femoral segmental defect in rats , 2003, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.
[41] P. Robbins,et al. Genetically augmented tissue engineering of the musculoskeletal system. , 1999, Clinical orthopaedics and related research.
[42] F. Ambrosio,et al. Effect of VEGF on the regenerative capacity of muscle stem cells in dystrophic skeletal muscle. , 2009, Molecular therapy : the journal of the American Society of Gene Therapy.
[43] K. Swan,et al. Raoul Hoffmann and his external fixator. , 2007, The Journal of bone and joint surgery. American volume.
[44] P. Robbins,et al. Arthritis gene therapy and its tortuous path into the clinic. , 2013, Translational research : the journal of laboratory and clinical medicine.
[45] M. Bouxsein,et al. Healing of segmental bone defects by direct percutaneous gene delivery: effect of vector dose. , 2007, Human gene therapy.
[46] J. West,et al. Rapid healing of femoral defects in rats with low dose sustained BMP2 expression from PEGDA hydrogel microspheres , 2013, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.
[47] Adam Bagg,et al. Fatal systemic inflammatory response syndrome in a ornithine transcarbamylase deficient patient following adenoviral gene transfer. , 2003, Molecular genetics and metabolism.
[48] Antonios G Mikos,et al. Osteochondral tissue regeneration through polymeric delivery of DNA encoding for the SOX trio and RUNX2. , 2014, Acta biomaterialia.
[49] R. Warren,et al. Acceleration of cartilage repair by genetically modified chondrocytes over expressing bone morphogenetic protein‐7 , 2003, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.
[50] P. Leng,et al. Enhanced Meniscal Repair by Overexpression of hIGF-1 in a Full-thickness Model , 2009, Clinical orthopaedics and related research.
[51] P. Robbins,et al. Inhibition of cartilage destruction by double gene transfer of IL-1Ra and IL-10 involves the activin pathway , 2002, Gene Therapy.
[52] Xin Zhang,et al. Targeted delivery of non-viral vectors to cartilage in vivo using a chondrocyte-homing peptide identified by phage display. , 2011, Biomaterials.
[53] Johnny Huard,et al. Synergistic enhancement of bone formation and healing by stem cell-expressed VEGF and bone morphogenetic protein-4. , 2002, The Journal of clinical investigation.
[54] Toby King,et al. The burden of musculoskeletal diseases in the United States. , 2016, Seminars in arthritis and rheumatism.
[55] Matthew J. Silva,et al. BMP‐12 gene transfer augmentation of lacerated tendon repair , 2001, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.
[56] C. Evans. Gene therapy for the regeneration of bone. , 2011, Injury.
[57] P. Beredjiklian,et al. Effect of interleukin-10 overexpression on the properties of healing tendon in a murine patellar tendon model. , 2008, The Journal of hand surgery.
[58] P. Bourgine,et al. Engineering of a functional bone organ through endochondral ossification , 2013, Proceedings of the National Academy of Sciences.
[59] P. S. Rachakonda,et al. Application of inflammation-responsive promoter for an in vitro arthritis model. , 2008, Arthritis and rheumatism.
[60] T Ochi,et al. Early biological effect of in vivo gene transfer of platelet-derived growth factor (PDGF)-B into healing patellar ligament , 1998, Gene Therapy.
[61] A. Mikos,et al. Strategies for controlled delivery of biologics for cartilage repair. , 2015, Advanced drug delivery reviews.
[62] C. Pilapil,et al. Genetically enhanced engineering of meniscus tissue using ex vivo delivery of transforming growth factor-beta 1 complementary deoxyribonucleic acid. , 2007, Tissue engineering.
[63] A J Nixon,et al. Genetic modification of chondrocytes with insulin-like growth factor-1 enhances cartilage healing in an equine model. , 2007, The Journal of bone and joint surgery. British volume.
[64] H. Madry,et al. Direct rAAV SOX9 administration for durable articular cartilage repair with delayed terminal differentiation and hypertrophy in vivo , 2012, Journal of Molecular Medicine.
[65] Mark Vrahas,et al. Facilitated endogenous repair: making tissue engineering simple, practical, and economical. , 2007, Tissue engineering.
[66] Freddie H. Fu,et al. Use of an antifibrotic agent improves the effect of platelet-rich plasma on muscle healing after injury. , 2013, The Journal of bone and joint surgery. American volume.
[67] Cameron S. Osborne,et al. LMO2-Associated Clonal T Cell Proliferation in Two Patients after Gene Therapy for SCID-X1 , 2003, Science.
[68] F. Ambrosio,et al. Relationships between transforming growth factor-beta1, myostatin, and decorin: implications for skeletal muscle fibrosis. , 2007, The Journal of biological chemistry.
[69] M. Knopp,et al. Direct delayed human adenoviral BMP-2 or BMP-6 gene therapy for bone and cartilage regeneration in a pony osteochondral model. , 2011, Osteoarthritis and cartilage.
[70] Yubo Fan,et al. A histological and biomechanical study of bone stress and bone remodeling around immediately loaded implants , 2014, Science China Life Sciences.
[71] Lawrence V. Gulotta,et al. Bone Marrow–Derived Mesenchymal Stem Cells Transduced With Scleraxis Improve Rotator Cuff Healing in a Rat Model , 2011, The American journal of sports medicine.
[72] Freddie H. Fu,et al. Development of approaches to improve the healing following muscle contusion. , 1998, Cell transplantation.
[73] L. Jeng,et al. LARGE‐SCALE BICORTICAL SKULL BONE REGENERATION USING EX VIVO REPLICATION‐DEFECTIVE ADENOVIRAL‐MEDIATED BONE MORPHOGENETIC PROTEIN—2 GENE—TRANSFERRED BONE MARROW STROMAL CELLS AND COMPOSITE BIOMATERIALS , 2009, Neurosurgery.
[74] V. Rosen,et al. Ectopic induction of tendon and ligament in rats by growth and differentiation factors 5, 6, and 7, members of the TGF-beta gene family. , 1997, The Journal of clinical investigation.
[75] K. Lau,et al. Retroviral‐based gene therapy with cyclooxygenase‐2 promotes the union of bony callus tissues and accelerates fracture healing in the rat , 2008, The journal of gene medicine.
[76] M. Ferretti,et al. Adeno-associated viral gene transfer of transforming growth factor-β1 to human mesenchymal stem cells improves cartilage repair , 2007, Gene Therapy.
[77] E Schneider,et al. Effect of BMP-2 gene transfer on bone healing in sheep , 2006, Gene Therapy.
[78] Tarun Garg,et al. Scaffold: a novel carrier for cell and drug delivery. , 2012, Critical reviews in therapeutic drug carrier systems.
[79] Lian Zhu,et al. Enhanced healing of goat femur‐defect using BMP7 gene‐modified BMSCs and load‐bearing tissue‐engineered bone , 2009, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.
[80] M. Alini,et al. Barriers and strategies for the clinical translation of advanced orthopaedic tissue engineering protocols. , 2014, European cells & materials.
[81] E Schneider,et al. Direct adenoviral transfer of bone morphogenetic protein-2 cDNA enhances fracture healing in osteoporotic sheep. , 2006, Human gene therapy.
[82] C. Evans. Advances in regenerative orthopedics. , 2013, Mayo Clinic proceedings.
[83] D. Docheva,et al. Conversion of human bone marrow-derived mesenchymal stem cells into tendon progenitor cells by ectopic expression of scleraxis. , 2012, Stem cells and development.
[84] T Minas,et al. A primer in cartilage repair. , 2012, The Journal of bone and joint surgery. British volume.
[85] James D Kang,et al. Gene therapy for intervertebral disk degeneration. , 2011, The Orthopedic clinics of North America.
[86] Jonathan M. Brunger,et al. Tissue-engineered cartilage with inducible and tunable immunomodulatory properties. , 2014, Biomaterials.
[87] Yan Jin,et al. The promotion of bone regeneration through positive regulation of angiogenic-osteogenic coupling using microRNA-26a. , 2013, Biomaterials.
[88] Lin Lin,et al. Effects of transforming growth factor-β1 and vascular endothelial growth factor 165 gene transfer on Achilles tendon healing , 2009 .
[89] Hiromu Ito,et al. Remodeling of cortical bone allografts mediated by adherent rAAV-RANKL and VEGF gene therapy , 2005, Nature Medicine.
[90] D. Zurakowski,et al. Improved tissue repair in articular cartilage defects in vivo by rAAV-mediated overexpression of human fibroblast growth factor 2. , 2005, Molecular therapy : the journal of the American Society of Gene Therapy.
[91] Johnny Huard,et al. The Use of an Antifibrosis Agent to Improve Muscle Recovery after Laceration * , 2001, The American journal of sports medicine.
[92] Marjolein C H van der Meulen,et al. Mesenchymal stem cells and insulin‐like growth factor‐I gene‐enhanced mesenchymal stem cells improve structural aspects of healing in equine flexor digitorum superficialis tendons , 2009, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.
[93] M. Bouxsein,et al. Delayed administration of adenoviral BMP-2 vector improves the formation of bone in osseous defects , 2007, Gene Therapy.
[94] J. Lieberman,et al. Influence of short-term adenoviral vector and prolonged lentiviral vector mediated bone morphogenetic protein-2 expression on the quality of bone repair in a rat femoral defect model. , 2008, Bone.
[95] Martin Majewski,et al. Biologics for tendon repair , 2014, Advanced drug delivery reviews.
[96] C. Evans. Using genes to facilitate the endogenous repair and regeneration of orthopaedic tissues , 2014, International Orthopaedics.
[97] Jonathan M. Brunger,et al. Scaffold-mediated lentiviral transduction for functional tissue engineering of cartilage , 2014, Proceedings of the National Academy of Sciences.
[98] E. Chang,et al. SEIZURE CHARACTERISTICS AND CONTROL AFTER MICROSURGICAL RESECTION OF SUPRATENTORIAL CEREBRAL CAVERNOUS MALFORMATIONS , 2009, Neurosurgery.
[99] Lawrence V. Gulotta,et al. Adenoviral-Mediated Gene Transfer of Human Bone Morphogenetic Protein–13 Does Not Improve Rotator Cuff Healing in a Rat Model , 2011, The American journal of sports medicine.
[100] L. Zekas,et al. Dermal fibroblast‐mediated BMP2 therapy to accelerate bone healing in an equine osteotomy model , 2009, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.
[101] M. Kunz,et al. Direct bone morphogenetic protein 2 and Indian hedgehog gene transfer for articular cartilage repair using bone marrow coagulates. , 2015, Osteoarthritis and cartilage.
[102] A. Mikos,et al. Gene delivery strategies for cartilage tissue engineering. , 2006, Advanced drug delivery reviews.
[103] James M. Wilson,et al. Humoral Immune Response to AAV , 2013, Front. Immunol..
[104] D. Stewart,et al. Effect of cell‐based VEGF gene therapy on healing of a segmental bone defect , 2009, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.
[105] W. Hauswirth,et al. scAAV-Mediated Gene Transfer of Interleukin 1-Receptor Antagonist to Synovium and Articular Cartilage in Large Mammalian Joints , 2012, Gene Therapy.
[106] Yong Li,et al. Angiotensin II Receptor Blockade Administered after Injury Improves Muscle Regeneration and Decreases Fibrosis in Normal Skeletal Muscle , 2008, The American journal of sports medicine.
[107] Gil Navon,et al. Neotendon formation induced by manipulation of the Smad8 signalling pathway in mesenchymal stem cells. , 2006, The Journal of clinical investigation.
[108] P. Aspenberg,et al. Mechanical Load and BMP Signaling During Tendon Repair: A Role for Follistatin? , 2008, Clinical orthopaedics and related research.
[109] C. Herzog,et al. [Interleukin 1 and tumor necrosis factor]. , 1987, Zeitschrift fur Rheumatologie.
[110] Juan Li,et al. Decorin gene transfer promotes muscle cell differentiation and muscle regeneration. , 2007, Molecular therapy : the journal of the American Society of Gene Therapy.
[111] Johnny Huard,et al. BMP4-expressing muscle-derived stem cells differentiate into osteogenic lineage and improve bone healing in immunocompetent mice. , 2002, Molecular therapy : the journal of the American Society of Gene Therapy.
[112] S. Ghivizzani,et al. Orthopedic gene therapy—lost in translation? , 2012, Journal of cellular physiology.
[113] J. Huard,et al. Regenerative medicine for the musculoskeletal system based on muscle-derived stem cells. , 2008, The Journal of the American Academy of Orthopaedic Surgeons.
[114] E. Schwarz,et al. Self-complementary AAV2.5-BMP2-coated femoral allografts mediated superior bone healing versus live autografts in mice with equivalent biomechanics to unfractured femur. , 2011, Molecular therapy : the journal of the American Society of Gene Therapy.
[115] H. Madry,et al. Nonviral gene transfer to human meniscal cells. Part I: transfection analyses and cell transplantation to meniscus explants , 2014, International Orthopaedics.
[116] P. Robbins,et al. Getting arthritis gene therapy into the clinic , 2011, Nature Reviews Rheumatology.
[117] M. Spector,et al. Gene delivery to cartilage defects using coagulated bone marrow aspirate , 2004, Gene Therapy.
[118] C. Yu,et al. Non-virus-mediated transfer of siRNAs against Runx2 and Smad4 inhibit heterotopic ossification in rats , 2010, Gene Therapy.
[119] Freddie H. Fu,et al. Biological approaches to improve skeletal muscle healing after injury and disease. , 2012, Birth defects research. Part C, Embryo today : reviews.
[120] A. Montag,et al. BMP-14 gene therapy increases tendon tensile strength in a rat model of Achilles tendon injury. , 2007, The Journal of bone and joint surgery. American volume.
[121] Yong Li,et al. Gamma interferon as an antifibrosis agent in skeletal muscle , 2003, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.
[122] W. Dhert,et al. Non-viral gene therapy for bone tissue engineering , 2013, Biotechnology & genetic engineering reviews.
[123] J. Huard,et al. The Use of Relaxin Improves Healing in Injured Muscle , 2005, Annals of the New York Academy of Sciences.
[124] C. Evans,et al. Potential biologic therapies for the intervertebral disc. , 2006, The Journal of bone and joint surgery. American volume.
[125] J. Rasko,et al. Successful transduction of liver in hemophilia by AAV-Factor IX and limitations imposed by the host immune response , 2006, Nature Medicine.
[126] P. Robbins,et al. Ex vivo gene transfer to chondrocytes in full-thickness articular cartilage defects: a feasibility study. , 1997, Osteoarthritis and cartilage.
[127] R Krauspe,et al. Potential role of direct adenoviral gene transfer in enhancing fracture repair. , 2000, Clinical orthopaedics and related research.
[128] D. Zurakowski,et al. Transplanted articular chondrocytes co-overexpressing IGF-I and FGF-2 stimulate cartilage repair in vivo , 2011, Knee Surgery, Sports Traumatology, Arthroscopy.
[129] C. Hidaka,et al. Evaluation of direct in vivo gene transfer in an equine metacarpal IV ostectomy model using an adenoviral vector encoding the bone morphogenetic protein-2 and protein-7 gene. , 2012, Veterinary surgery : VS.
[130] C. Dani,et al. Enhancement of myogenic and muscle repair capacities of human adipose-derived stem cells with forced expression of MyoD. , 2009, Molecular therapy : the journal of the American Society of Gene Therapy.
[131] D. Matičić,et al. Articular cartilage repair by genetically modified bone marrow aspirate in sheep , 2011, Gene Therapy.
[132] Kjeld Søballe,et al. Freeze-dried tendon allografts as tissue-engineering scaffolds for Gdf5 gene delivery. , 2008, Molecular therapy : the journal of the American Society of Gene Therapy.
[133] D. Kohn,et al. rAAV-mediated overexpression of FGF-2 promotes cell proliferation, survival, and α-SMA expression in human meniscal lesions , 2009, Gene Therapy.