Genome Editing Cures Muscular Dystrophy in Mice
Researchers from Duke University have used the CRISPR technology to cure Duchenne muscular dystrophy in a mouse. It is the first time that the gene editing...
Delivering genetic material as treatment – vectors, targeting, and emerging ways to control it.
16 articles
Researchers from Duke University have used the CRISPR technology to cure Duchenne muscular dystrophy in a mouse. It is the first time that the gene editing...
Elizabeth Parrish, CEO of biotech startup BioViva, declared in the website Reddit having undergone an anti-aging gene therapy in a secret location in Latin America, dodging...
New CRISPR discovered by original CRISPR/Cas9 discovery team promises simpler and more flexible gene editing with fewer legal tangles. Broad Institute Researchers at Massachusetts Institute...
AMSBIO has introduced an expanded range of Adeno-associated virus (AAV) cloning and packaging services. AAV is a small (20 nm), replication-defective, nonenveloped, non-pathogenic virus which infects...
Illumina announced formation of a customer focused company that seeks to provide affordable sequencing and analysis tools marketplace through third party providers at affordable costs....
A research team from University of California at Berkeley has developed a technique that makes gene editing much easier and cheaper. Rebecca Heald has directed...
Scientists from Harvard and University of California have designed an online tool to optimize CRISPR (clustered regularly interspaced short palindromic repeats)/Cas9 targeting. The researchers compared...
Researchers from Dankook University in Korea have found a new method of introducing transgenes with therapeutic purposes. The study, published in Nucleic Acid Therapeutics, describes how targeting the passenger strand...