Duchenne muscular dystrophy (DMD) is a neuromuscular disorder that results from mutations in the DMD gene. Gene therapies for DMD change genetic material in a person’s body to treat this condition.

Payments firm PayPal (PYPL) said it is expanding its peer-to-peer service by adding cryptocurrency transfers to its payment flow, the company announced on Monday. Mit der Anmeldung erhalten Sie ...

Nintendo closed out Nintendo Direct September 2025 with the announcement of Fire Emblem: Fortune's Weave. The debut trailer, below, shows off tactical combat, a bunch of cinematics, and teased the ...

Transgenic and adeno-associated virus approaches were used to overexpress DWORF in the heart. Mice underwent transverse aortic constriction (TAC) to model pressure overload–induced heart failure.

Tompkins Cortland Community College graduates in the Sustainable Farming and Food Systems Program now have a direct transfer path to Cornell’s College of Agriculture and Life Sciences. TC3 President ...

In a breakthrough study, scientists have transferred a courtship behavior from one species to another, triggering the recipient to perform this completely foreign act as if it was its own. While genes ...

The University of Miami is fighting back against the Wisconsin Badgers' lawsuit over Xavier Lucas leaving the school to join the Hurricanes. As expected, Miami filed a motion to dismiss the case, ...

EXCLUSIVE: A book about the rise and fall of Barneys is about to become a TV series. Shiny Penny Productions and Five All in the Fifth Entertainment are developing Gene Pressman’s forthcoming memoir ...

Four patients with infantile-onset Pompe’s disease received a single intravenous injection of an adeno-associated virus serotype 9 vector carrying codon-optimized complementary DNA encoding human acid ...

DAMASCUS, June 19 (Reuters) - Syria this week carried out its first international bank transfer via the SWIFT international payment system since the outbreak of the country’s 14-year civil war, ...

Adeno-associated virus (AAV)–mediated gene therapy has emerged as a promising treatment for hemophilia B. Data on safety and durability from 13 years of follow-up in a cohort of patients who had been ...

The illustration shows how high trafficking of blood stem cells in the circulation early post-natally allows lentiviral-vector mediated in vivo gene transfer. Credit: Ella Maru studio Researchers have ...