|
HIGH-CAPACITY LENTIVIRAL VECTORS
HIGH-CAPACITY LENTIVIRAL VECTORS
Researchers at Stanford have developed new lentiviral vectors that are able to deliver more genetic information than currently available vectors, aiding in the development of gene therapy.
Gene therapy is one of the most promising therapeutic avenues in translational medicine. This method involves the genetic engineering...
Published: 8/17/2023
|
Inventor(s): Michael Fischbach, Brian Caliando, Gabriel Filsinger
Keywords(s): Gene Therapy, Lentiviral Vector
Category(s): Technology Classifications > Biology
|
|
GENE THERAPY FOR IMMUNO-ONCOLOGY APPLICATIONS
GENE THERAPY FOR IMMUNO-ONCOLOGY APPLICATIONS
Researchers at the Chan Zuckerberg Biohub and UCSF have developed viral gene therapy delivery systems for therapeutic immuno-oncology applications.
Glioblastoma is the most common and deadliest primary malignant brain cancer with an overall median survival of 14.6 months. Therapies currently in use, and...
Published: 5/31/2023
|
Inventor(s): Nicole Paulk, Joseph DeRisi, David Raleigh
Keywords(s): Convection Enhanced Delivery, Gene Therapy, Glioblastoma, Immuno-Oncology, Interferon (IFN), Recombinant Adenoviral-Associated Virus (rAAV)
Category(s): Technology Classifications > Biology
|
|
INDUCIBLE VIRAL TRANSDUCTION SYSTEM FOR IN VIVO GENOME MODIFICATION
INDUCIBLE VIRAL TRANSDUCTION SYSTEM FOR IN VIVO GENOME MODIFICATION
Researchers at the Chan Zuckerberg Biohub have developed a cellular transduction method for target cell genome modification.
Gene therapy, or targeted genome modification, has great potential for biomedicine. There are several genome modification systems available for genome editing,...
Published: 3/17/2023
|
Inventor(s): Andrew May, Eleonore Tham, Lucy Maynard, Marco Mignardi, Nicole Paulk, Ryan Leenay
Keywords(s): Adenoviral Vectors, Gene Therapy, Genome Engineering
Category(s): Technology Classifications > Biology
|
