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.

TREs occur when sections of a DNA strand are repeated two or more ... identified a molecule that can contract TREs in Huntington's disease. While more research is needed to identify how this ...

TREs occur when sections of a DNA strand are repeated two or more ... identified a molecule that can contract TREs in Huntington's disease. While more research is needed to identify how this ...

TREs occur when sections of a DNA strand are repeated two or more times ... identified a molecule that can contract TREs in Huntington's disease. While more research is needed to identify how this ...

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 ...

TREs occur when sections of a DNA strand are repeated two or more times ... identified a molecule that can contract TREs in Huntington’s disease. While more research is needed to identify how this ...

A decade ago, University at Buffalo researchers shed some light on an enduring neuroscience mystery: How exactly does a mutated huntingtin protein (HTT) cause Huntington's disease? They found that ...

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.