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

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

Contraceptive gene therapy injections in cats replaces surgical spaying

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

Hope for age-related hearing loss with novel gene therapy

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

Gene therapy could help restore vision lost to degenerative disease

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

Special cell-penetrating peptides turn the PAGE for next-gen gene editing

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

New gene therapy lowers eye pressure to treat glaucoma

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

New nanoparticles deliver gene-editing tech directly into the lungs

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

Calcium-control gene offers new avenue for Alzheimer’s disease therapy

Researchers have found the gene Surf4 plays a role in neural degeneration

Nearly six million Americans currently live with Alzheimer’s disease (AD), with the figure set to climb to 13.8 million by 2050. And with promising trials failing close to the finish line, researchers are desperate for any breakthroughs that will lead to halting the devastating neurodegenerative disease.

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Continue reading Calcium-control gene offers new avenue for Alzheimer’s disease therapy

Vision restored in mice thanks to refined CRISPR system

It’s been about seven years since researchers used the CRISPER gene-editing system to reverse a blindness-inducing condition called retinitis pigmentosa in stem cells outside the body. Now, using a more refined version of CRISPR, a different research t… Continue reading Vision restored in mice thanks to refined CRISPR system