Linking Fragile X Syndrome Proteins and RNA Editing Mistakes at Nerve-Muscle Junction

PHILADELPHIA - The most common form of heritable cognitive impairment is Fragile X Syndrome, caused by mutation or malfunction of the FMR1 gene. Loss of FMR1 function is also the most common genetic cause of autism. Understanding how this gene works is vital to finding new treatments to help Fragile X patients and others.

Karen Kreeger

Penn Study Explains Paradox of Insulin Resistance Genetics

PHILADELPHIA - Obesity and insulin resistance are almost inevitably associated with increases in lipid accumulation in the liver, a serious disease that can deteriorate to hepatitis and liver failure.  A real paradox in understanding insulin resistance is figuring out why insulin-resistant livers make more fat.  Insulin resistance occurs when the body does a poor j

Karen Kreeger

Penn Receives $12.5 Million From NIH to Speed Discovery to Patient Care

PHILADELPHIA —Three labs from the University of Pennsylvania have received $12.5 million from the National Institutes of Health (NIH) as part of its $143.8 million national grant program to challenge the scientific status quo with innovative ideas that have the potential to speed the translation of medical research into improved health for the American public.

Karen Kreeger

Penn Scientists Tracing an Elusive Killer Parasite in Peru

PHILADELPHIA —Despite what Hollywood would have you believe, not all epidemics involve people suffering from zombie-like symptoms--some can only be uncovered through door-to-door epidemiology and advanced mathematics.

Karen Kreeger

Enzymes Possible Targets for New Anti-Malaria Drugs, According to Penn-led Study

PHILADELPHIA —Researchers at the Perelman School of Medicine at the University of Pennsylvania, Monash University, and Virginia Tech have used a set of novel inhibitors to analyze how the malaria parasite, Plasmodium falciparum, uses enzymes to chew up human hemoglobin from host red blood cells as a food source.

Karen Kreeger