Health & Medicine

Gene Therapy’s Road to Redemption

Gene Therapy’s Road to Redemption

Pediatrics Nationwide magazine

Fifteen years ago, gene therapy suffered a highly visible fatality, leaving the field in shambles. Now, one team’s efforts at gene therapy for muscular dystrophy suggest the field may finally be on track to deliver on its initial promise.

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Anti-Alzheimer’s gene may have led to the rise of grandparents

Anti-Alzheimer’s gene may have led to the rise of grandparents

Science magazine

Evolutionarily speaking, we are born to make babies. Our bodies—and brains—don’t fall apart until we come to the end of our child-bearing years. So why are grandmothers, who don’t reproduce and who contribute little to food production, still around and still mentally sound?

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Researchers Identify Genetic Mutation Linked to Congenital Heart Disease

Researchers Identify Genetic Mutation Linked to Congenital Heart Disease

Nationwide Children’s Hospital

A mutation in a gene crucial to normal heart development could play a role in some types of congenital heart disease—the most common birth defect in the U.S. The finding could help narrow the search for genes that contribute to this defect, which affects as many as 40,000 newborns a year.

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A knowledge gap

A knowledge gap

Pediatrics Nationwide magazine

Many pediatricians don’t feel competent to treat patients with genetic disorders, according to a new study that raises questions about how to better prepare physicians for these cases.

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Baby steps

Baby steps

Pediatrics Nationwide magazine

Necrotizing enterocolitis affects about 2,000 to 4,000 infants each year, making it the most common gastrointestinal illness in neonatal intensive care units. A multicenter consortium studying the disease may be closer to understanding it.

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Boosting Immune Process with IFN-y Helps Clear Lethal Bacteria in Cystic Fibrosis

Boosting Immune Process with IFN-y Helps Clear Lethal Bacteria in Cystic Fibrosis

Nationwide Children’s Hospital

Boosting a key immune process called autophagy with interferon gamma (IFN-γ) could help clear a lethal bacterial infection in cystic fibrosis, a new study suggests. The work, led by a team in The Research Institute at Nationwide Children’s Hospital and published in PLoS One in May, offers new information about immune function in patients with the disease.

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