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Two New Ways to Treat A Deadly Disease: Spinal Muscular Atrophy
I don’t think I’ll ever tire of covering new ways to treat genetic diseases that I’d always thought hopeless.
Date:
November 02, 2017
A Molecular Switch to Control Gene Expression
Our genome contains thousands of genes, each of which has to be turned on and off at precisely the right times, or serious dysfunction in our bodi
Date:
October 19, 2017
Pilot study of population-based newborn screening for spinal muscular atrophy in New York state
Jennifer N Kraszewski MPH, Denise M Kay PhD, Colleen F Stevens PhD, Carrie Koval MS, Biana Haser BS,
Date:
October 12, 2017
New CRISPR-Gold Tool Repairs Muscular Dystrophy in Mice
Scientists at the University of California, Berkeley, have created a new way to deliver the gene-editing tool CRISPR.
Date:
October 06, 2017
Maple syrup urine disease: mechanisms and management | TACG - Dove Medical Press
Maple syrup urine disease: mechanisms and management | TACG Dove Medical Press
Date:
September 06, 2017