Biologists say they will revolutionize medicine by using a gene-based editing technology that can transform a gene into a gene therapy.

The National Institutes of Health announced Friday that the National Science Foundation has awarded $10 million to the Broad Institute of the University of Pennsylvania and the Massachusetts Institute of Technology to develop a gene editing system.

The Broad Institute is a Massachusetts Institute Of Technology spinoff.

The MIT-Penn grant is the largest biomedical research grant in the institute’s history, according to the National Institutes Of Health.

The research team will work with other groups at the Broad and the University to develop the gene editing technology, which is being developed by scientists at the Institute of Medicine.

The gene editing process involves the gene being copied and modified to alter the protein sequence.

The new technology could dramatically improve gene therapies for rare diseases, such as the rare form of inherited blindness called retinitis pigmentosa, which affects some people of color, said Richard Wysocki, president and CEO of the Broad.

Gene editing is not currently available for humans.

It was only discovered about a decade ago.

The system would allow scientists to edit genes in living organisms, such like plants and animals, and thereby to alter their behavior.

It is an area of intense research in the biomedical world, with more than 300 research institutions worldwide using the technology, according the NIH.

Gene-edited organisms are produced by combining the DNA of two different organisms.

Gene modification technology has been used for decades to create viruses and bacteria that can infect humans, but scientists have yet to modify human cells.

The genes that control the activity of a cell’s gene expression, which control how that cell functions, can also be altered in animals.

But gene-edited organisms can be much more powerful.

The process could eventually allow the creation of powerful therapies to treat disease, said Andrew Wiebe, a professor of biology at Stanford University who has worked on gene editing and human genome engineering.

Scientists have been developing gene-modified organisms for decades.

In 2007, the NIH awarded a $3.5 million grant to the University at Buffalo to study how to create a gene that would change the gene coding for a gene called CRISPR-Cas9, the technology that allows scientists to insert and manipulate DNA in cells.

Gene technology was also used to produce the first human genome, which has since been sequenced, or copied, to make a complete copy of our genetic code.

But those efforts, combined with the advancement of technology such as CRISP-Cas, have made gene editing a reality in humans.

Scientists hope that gene editing will be used in treating diseases such as cancer, autoimmune diseases and other diseases that can occur in cells in the body, including the immune system, said Dr. Wiebbe.

Gene therapy is still in its infancy, but it is an exciting area of research.

“We have a new tool to be able to create very large-scale, targeted, targeted gene therapies that can be applied to the whole genome,” said Wiebel, who is a member of the National Academies Advisory Council on Gene Therapy.

Gene therapies can be used to treat a wide range of diseases, from cancer to a number of other conditions.

Gene medicine could become the first field to develop in humans a fully-functional version of a human immune system.

It could also transform medicine by allowing doctors to target disease-causing genes in their patients, Wieborn said.

The process of editing a gene in living cells has been tried in animals and is currently a science fiction project in the lab of scientists at Massachusetts General Hospital.

Scientists will have to work for years to develop gene-modification technology to treat many diseases, but the scientists will be able make changes to gene-containing genes to target the problem.

“It is a revolutionary step forward in gene therapy,” said James R. Lee, professor of genetics at Harvard Medical School and a member on the NIH’s BRAIN Initiative, the largest research effort to develop new technology for the brain.

The scientists said they hope to develop these new gene editing technologies by 2019.

Development Is Supported By

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