Research team finds that a nontoxic molecule closely related to resveratrol can overcome barriers to delivering gene therapy into stem cells
Added to gene therapy, compound enable faster and effective treatments
Gene Therapy
Nanocapsules deliver gene-editing payload
Structures are alternatives to viral vectors for gene therapy using the CRISPR-Cas9 system
Gene editing enables researchers to correct mutation in muscle stem cells
Duchenne muscular dystrophy (DMD) is a rare but devastating genetic disorder that causes muscle loss and physical impairments. Researchers have shown that CRISPR may provide the means for lifelong correction of the genetic mutation responsible for the disorder
Stem cell researchers reactivate ‘back-up genes’ in the lab
Researchers have unravelled parts of a mechanism that may one day help to treat Rett syndrome and other genetic disorders linked to the X chromosome.
3rd Euroscicon Conference on Cell and Gene Therapy
March 11-12, 2020
Prague , Czech Republic
Prague , Czech Republic
3rd World Congress on Genetics and Genetics Disorder
April 20-21, 2020
Dubai, UAE
Dubai, UAE
12th World Congress on Precision and Personalized Medicine
April 06-07, 2020
Bangkok, Thailand
Bangkok, Thailand
International Conference on Genetic Disorders and Gene Therapy
May 18-19, 2020
Osaka, Japan
Osaka, Japan
13th International Conference on Stem Cell and Regenerative Medicine
April 20-21, 2020
Kuala Lumpur, Malaysia
Kuala Lumpur, Malaysia