55 Stories, most recent news story added Fri Nov 27, 4:55 am ET
The standard treatment for venous leg ulcers, lower limb compression, takes up to six months to heal and is unsuccessful in 30 -70 percent of cases. The new treatment involved injecting venous leg ulcers with a non-replicating adenovirus that expresses platelet-derived growth factor-β (PDGF-β).
French scientists mixed gene therapy and bone marrow transplants in two boys to seemingly halt a brain disease that can kill by adolescence. The surprise ingredient: They disabled the HIV virus so it couldn't cause AIDS, and then used it to carry in the... Gene therapy - HIV - Disease - AIDS - Brain
AMSTERDAM, November 11 /PRNewswire-FirstCall/ -- Amsterdam Molecular Therapeutics (Euronext: AMT), a leader in the field of human gene therapy, announced today that it has successfully treated Duchenne muscular dystrophy (DMD) in an animal model with its proprietary gene therapy.
A strategy that combines gene therapy with blood stem cell therapy may be a useful tool for treating a fatal brain disease, French researchers have found.
( The StopALD Foundation ) First gene therapy success in boys with fatal brain disorder -- the Stop ALD Foundation, having spurred a successful European gene therapy trial, is now pressing to bring this therapy to the US. The foundation was started by families with children who have died or suffered from adrenoleukodystrophy, the disease highlighted in the movie Lorenzo's Oil. A report of the ...
By Gina Kolata THE NEW YORK TIMES Not long ago, gene therapy seemed troubled by insurmountable difficulties. After decades of hype and dashed hopes, many who once embraced the idea of correcting genetic disorders by giving people new genes all but gave up the idea.
A strategy that combines gene therapy with blood stem cell therapy may be a useful tool for treating a fatal brain disease, French researchers have found. These findings appear in the Nov. 6, 2009, issue of the journal Science, which is published by AAAS, the nonprofit science society.
A single injection in a patient's eye brings 'astounding' results. The findings may offer hope for those with macular degeneration and retinitis pigmentosa. Pennsylvania researchers using gene therapy have made significant improvements in vision in 12 patients with a rare inherited visual defect, a finding that suggests it may be possible to produce similar improvements in a much larger number ...
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( Montana State University ) Montana State University has a new grant to tap into the talent that viruses have for invading cells and seizing control.
Pioneering work may offer hope for patients with adrenoleukodystrophy
GINA KOLATA Three recent successes, though small, prompted hopes among scientists that a still-experimental idea for correcting genetic disorders might be back.
The ELA Association represents the largest funder for research on this fatal brain diseaseThe ELA association and Zinedine Zidane, its emblematic ambassador, are proud to announce a world premiere: the results regarding the gene therapy in adrenoleukodystrophy conducted in France have just been published in the prestigious journal Science.
WASHINGTON -- French scientists have mixed gene therapy and bone marrow transplants in two boys to seemingly halt a brain disease that can kill by adolescence. The surprise ingredient: They disabled the HIV virus so it couldn't cause AIDS, and then used it to carry in the healthy new gene. The experiment marks the first time researchers have tried that step in people -- and the first ...
( ELA Association ) The ELA Association and Zinedine Zidane, its emblematic ambassador, are proud to announce a world premiere: the results regarding the gene therapy in adrenoleukodystrophy conducted in France have just been published in the prestigious journal Science. Two children have been treated and their diseases have been halted. The children are doing well, which is unexpected for a ...
After years of complications and high-profile setbacks, a series of small but intriguing advances has suggested that gene therapy may hold real future potential for treatment
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