AAV8-mediated in vivo overexpression of miR-155 enhances the protective capacity of genetically attenuated malarial parasites. Read more about AAV8-mediated in vivo overexpression of miR-155 enhances the protective capacity of genetically attenuated malarial parasites.
Interventional magnetic resonance imaging-guided cell transplantation into the brain with radially branched deployment. Read more about Interventional magnetic resonance imaging-guided cell transplantation into the brain with radially branched deployment.
Exploiting human CD34+ stem cell-conditioned medium for tissue repair. Read more about Exploiting human CD34+ stem cell-conditioned medium for tissue repair.
In vivo selection of transplanted hepatocytes by pharmacological inhibition of fumarylacetoacetate hydrolase in wild-type mice. Read more about In vivo selection of transplanted hepatocytes by pharmacological inhibition of fumarylacetoacetate hydrolase in wild-type mice.
Chemoselection of allogeneic HSC after murine neonatal transplantation without myeloablation or post-transplant immunosuppression. Read more about Chemoselection of allogeneic HSC after murine neonatal transplantation without myeloablation or post-transplant immunosuppression.
Design and selection of Toca 511 for clinical use: modified retroviral replicating vector with improved stability and gene expression. Read more about Design and selection of Toca 511 for clinical use: modified retroviral replicating vector with improved stability and gene expression.
Comparison of human induced pluripotent and embryonic stem cells: fraternal or identical twins? Read more about Comparison of human induced pluripotent and embryonic stem cells: fraternal or identical twins?
Gene therapy and bone marrow transplantation for thalassemia: changing of the guard? Read more about Gene therapy and bone marrow transplantation for thalassemia: changing of the guard?
Adenovirus-retrovirus hybrid vectors achieve highly enhanced tumor transduction and antitumor efficacy in vivo. Read more about Adenovirus-retrovirus hybrid vectors achieve highly enhanced tumor transduction and antitumor efficacy in vivo.
Nanoparticles modified with tumor-targeting scFv deliver siRNA and miRNA for cancer therapy. Read more about Nanoparticles modified with tumor-targeting scFv deliver siRNA and miRNA for cancer therapy.
