Prions induce toxic huntingtin oligomers

Neurodegenerative diseases like Alzheimer's, Parkinson's or Huntington's disease are characterized by the deposition of protein clumps, so-called protein aggregates, in the brains of patients. Even though disease-relevant ...

New insights into Huntington's disease

Huntington's chorea is a hereditary disease that leads to cognitive and motor impairments and death. Scientists at the University of Bremen have worked with international partners to elucidate the mechanism by which the mutated ...

Team develops first genetic switch for C. elegans

With their first ever RNA-based inducible system for switching on genes in the roundworm Caenorhabditis elegans (C. elegans), two researchers from the University of Konstanz have closed a significant gap in genetic switches. ...

The cryo-electron microscopy structure of huntingtin

Mutations on a single gene, the huntingtin gene, are the cause of Huntington's disease. They lead to an incorrect form of the correspondent protein. With the help of cryo-electron microscopy researchers from the Max Planck ...

Huntington proteins and their nasty 'social network'

Researchers at the Buck Institute have identified and categorized thousands of protein interactions involving huntingtin, the protein responsible for Huntington's disease (HD). To use an analogy of a human social network, ...

New drugs target delay of Huntington's symptoms

(Medical Xpress) -- McMaster researchers have discovered a new drug target that may be effective at preventing the onset of Huntington's disease, working much the same way heart medications slow the progression of heart disease ...