Medical research

Gene therapy treatment extends lives of mice with fatal disease

A team of University of Missouri researchers has found that introducing a missing gene into the central nervous system could help extend the lives of patients with Spinal Muscular Atrophy (SMA) – the leading genetic ...

Medical research

Research suggests new cause to blame for spinal muscular atrophy

Over 15 years ago, researchers linked a defect in a gene called survival motor neuron -- or SMN -- with the fatal disease spinal muscular atrophy. Because SMN had a role in assembling the intracellular machinery that processes ...

Diseases, Conditions, Syndromes

Fasudil bypasses genetic cause of spinal birth defect

Scientists from the Ottawa Hospital Research Institute (OHRI) and the University of Ottawa (uOttawa) have discovered that a drug called fasudil can extend the average lifespan of mice with Spinal muscular atrophy (SMA) from ...

page 17 from 20