A rare disorder called myotonic dystrophy type 1 (DM1) causes weakness and muscle loss that gets progressively worse... | ...

Scientists from The Hospital for Sick Children (SickKids) and University of Las Vegas Nevada (UNLV) have uncovered a genetic link between autism spectrum disorder (ASD) and a rare genetic condition ...

identified a molecule that can contract TREs in Huntington’s disease. While more research is needed to identify how this ...

Scientists found a genetic link between autism and DM1, where repeat DNA sequences disrupt brain gene splicing. This sheds light on ASD’s development and opens new paths for targeted treatments.

DM1 is an inherited condition which causes progressive ... Senior Scientist in the Genetics & Genome Biology program at SickKids, identified a molecule that can contract TREs in Huntington's ...

Researchers suggest discovery of genetic link between ASD and DM1 opens up potential new therapeutic avenues for ASD.

New research has uncovered a genetic connection between autism spectrum disorder (ASD) and myotonic dystrophy type 1 (DM1), a rare neuromuscular disease.

We also investigate the pathogenic mechanisms of myotonic dystrophy, type 1 (DM1), an autosomal dominant neuromuscular disorder affecting multiple tissues including muscle, heart and the central ...

The greatest amount of advancement and development in this field has been in the linker that links the toxin molecule to the antibody. T–DM1 uses an ImmunoGen linker that is non-cleavable in all ...

RNA is a key molecule that helps cells build proteins and function properly. The team found that when the DMPK gene ...