Therapeutic genes, often referred to as therapeutic or gene therapy, represent a cutting-edge field in medical research and treatment. These are specific genes employed for the purpose of treating or preventing diseases by targeting the root cause at the genetic level. Gene therapy aims to introduce, alter, or replace genetic material within a patient's cells to correct or compensate for a genetic anomaly. The therapeutic genes can be delivered using various vectors, such as viral vectors or non-viral methods, to reach the target cells. This innovative approach holds promise for addressing a wide array of genetic disorders, including inherited conditions, certain cancers, and other chronic diseases. As the field advances, researchers are continually exploring novel therapeutic gene delivery methods and refining techniques to enhance precision and efficacy. The exploration of therapeutic genes represents a pivotal step toward personalized medicine, offering tailored treatments based on an individual's unique genetic makeup. While challenges remain, the progress in therapeutic genes opens up new possibilities for transforming the landscape of medical interventions and providing innovative solutions for previously incurable conditions.
Title : Renewed novel biotech ideas, with bioreactor bioengineering economic impact
Murray Moo Young, University of Waterloo, Canada
Title : Improving health in over 40,000 patients: The impact of nanomedicine fighting antibiotic resistant infections
Thomas J Webster, Brown University, United States
Title : Osmotic lysis–driven Extracellular Vesicle (EV) engineering
Limongi Tania, University of Turin, Italy
Title : Evaluating cell compatibility and subcutaneous host response of silk fibroin–chitosan plug composites as potential resorbable implants
Luis Jesus Villarreal Gomez, Universidad Autonoma de Baja California, Mexico
Title : Comparative study of endo-?-1,4-mannanases from novel bacterial strains for the production of galactomanno-oligosaccharides
Shruti Saini, National Agri-food and Bio-manufacturing Institute, India
Title : Engineering Sf9 host cells with AcMNPV genes to control baculovirus infection dynamics and heterologous gene expression
Tamer Z Salem, Zewail City of Science and Technology, Egypt