Latest Genetic genealogy Stories
More than 700 people from the Greater Philadelphia area are registered to take a small step to fund powerful progress for the Muscular Dystrophy Association. King
ELK GROVE VILLAGE, Ill., March 2, 2015 /PRNewswire/ -- Cure SMA recently announced a new $315,000 drug discovery grant to the California Institute of Biomedical Research (CALIBR).
CARLSBAD, Calif., March 2, 2015 /PRNewswire/ -- Isis Pharmaceuticals, Inc.
MDA research grantee Charles Gersbach announces potentially game-changing advance in gene modification for boys and young men with DMD. Chicago, IL (PRWEB) February
Product holds potential for replacing glucocorticoids in Duchenne muscular dystrophy and other chronic inflammatory states SILVER SPRING, Md. and CHICAGO, Feb.
Researchers at Nationwide Children's Hospital have developed a way to measure upper extremity movement in patients with muscular dystrophy using interactive video game technology. Their hope is to expand inclusion criteria for clinical trials to incorporate patients using wheelchairs.
Study could lead to mitochondrial DNA blood tests to foretell future risk.
ISIS-DMPK Rx Extends the Targeting of Antisense Drugs to Include Muscle Tissue CARLSBAD, Calif., Dec. 16, 2014 /PRNewswire/ -- Isis Pharmaceuticals, Inc.
A Newport Beach based charity committed to raising awareness about Duchenne muscular dystrophy and funding for research, has awarded University of California, Los Angeles Professor Rachelle Crosbie-Watson
Eighteenth Annual Muscle Team Set for Jan.