Currently we test and support the following browsers:
Please note that this is not intended to be an exhaustive list of browsers that support web standards, nor a test of browser compliance, nor a side-by-side comparison of various manufacturers’ browsers.
St. Jude Children’s Research Hospital scientists lead effort that reveals new details linking lipid build-up with catastrophic calcium imbalance in brain cells of patients with rare, inherited disorder.
The lack of a single protein usually thought of as a run-of-the-mill enzyme that helps to recycle molecules in cells causes an incurable and often fatal disease of children. Children with this disease, called sialidosis, suffer from enlarged spleens and often develop vision problems, loss of coordination and seizures, among other symptoms. The patients generally die within the first few years of life.
To find answers for children with "orphan diseases," one St. Jude researcher digs into the mysteries of the human cell.
Physicians might one day be able to treat a disease that destroys brain cells in children using genetically modified cells to transport a "drug" to the site of the dying neural cells (cells that transmit impulses).
Disruption of protein-folding in neuronal cells causes neurodegeneration and mental retardation.
Research conducted by St. Jude investigators led by Alessandra d'Azzo, PhD, may help uncover the genetic cause of certain muscle diseases that occur for unknown reasons in children.