People genetically susceptible to Huntington's disease often see their movement ... or CAG, on one strand of the DNA and cytosine-thymine-guanine, or CTG, on the complementary strand—begin ...

People genetically susceptible to Huntington's disease often see their movement ... or CAG, on one strand of the DNA and cytosine-thymine-guanine, or CTG, on the complementary strand-begin ...

four (Huntington's disease, various spinocerebellar ataxias, Friedreich's ataxia and myotonic dystrophy types 1 and 2) exhibit an unusual expansion of repeat sequences in DNA, and four (ataxia ...

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

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.

TREs occur when sections of a DNA strand are repeated two or more times ... identified a molecule that can contract TREs in ...

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

Colossal, a genetics startup, has birthed three pups that contain ancient DNA retrieved from the remains of the animal’s ...

Why not, then, create a lethal mutation and insert it into the DNA of a mosquito ... people who carry genes for disorders such as Huntington’s disease. More problematically, it could encourage ...

Researchers found that inhibiting GSK-3 led to less defects in the axonal transport process and less neuronal cell death, while inhibiting ERK1 led to more transport problems and more cell death.

The number of people who have the gene that causes Huntington's disease in Northern Scotland has been accurately counted for the first time in 35 years in new research from the University of ...