Collaborate Disseminate
Yale scientists have discovered a new potential treatment avenue to fight cancer. Using CRISPR gene-editing, the team eliminated extra chromosomes from cancer cells and found that they could no longer grow out of control.Continue ReadingCategory: Medic… Continue reading Cancer breakthrough uses CRISPR to target extra chromosomes
CRISPR-Cas9 has been the household name of genetic engineering tools over the past decade, but there might be other, better ways. MIT scientists have now demonstrated an alternative called Fanzor, which is naturally found in animals so could be a bette… Continue reading Potential CRISPR alternative gene-editing tool occurs naturally in animals
As a way of treating hemophilia, Japanese researchers have, for the first time, delivered gene therapy directly into the livers of baboons without using a viral carrier. The study’s results indicate that the method is safe and effective and may lead to… Continue reading Liver-targeted non-viral gene therapy gives hope to hemophiliacs
As a way of treating hemophilia, Japanese researchers have, for the first time, delivered gene therapy directly into the livers of baboons without using a viral carrier. The study’s results indicate that the method is safe and effective and may lead to… Continue reading Liver-targeted non-viral gene therapy gives hope to hemophiliacs
Getting your cat spayed is a normal part of pet ownership, but it can be expensive, invasive and not very practical on strays. Now scientists have developed and tested a new method that renders female cats permanently sterile with a single gene therapy… Continue reading Contraceptive gene therapy injections in cats replaces surgical spaying
Age-related hearing loss impacts one in three adults between the ages of 64 and 75 in the US, and around half of these numbers are down to genes.Continue ReadingCategory: Medical, ScienceTags: Hearing Impaired, Hearing, Genetics, Aging, Age-Related, ge… Continue reading Hope for age-related hearing loss with novel gene therapy
Scientists in Canada have developed a new technique that may one day help restore some sight to patients with inherited vision impairment. The regenerative therapy works by expressing genes that convert dormant cells into new light-sensing cells in the… Continue reading Gene therapy could help restore vision lost to degenerative disease
Researchers have developed a highly efficient new gene-editing method that uses virus-based protein fragments. The method could be used to level up existing cell and gene therapies used to treat cancer and other diseases.Continue ReadingCategory: Medic… Continue reading Special cell-penetrating peptides turn the PAGE for next-gen gene editing
The high eye pressure seen in glaucoma slowly leads to blindness. For some, the first-line treatment, eye drops, doesn’t work. Researchers have used gene therapy to develop a promising new way of treating the high eye pressure associated with glaucoma…. Continue reading New gene therapy lowers eye pressure to treat glaucoma
Developing effective treatments for genetic lung diseases such as cystic fibrosis has proven challenging. That might not be the case for much longer, with scientists developing a new type of nanoparticle that can carry gene-editing technology directly … Continue reading New nanoparticles deliver gene-editing tech directly into the lungs