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Joseph Samaha, Jim Dagher, Shayan Abdollah Zadegan

Huntington’s disease (HD) is a neurodegenerative disease inherited in an autosomal dominant manner. It is caused by an expansion of cytosine, adenine, guanine (CAG) repeats within the huntingtin (HTT) gene, which is located on chromosome 4. This pathological expansion of CAG repeats results in the production of a mutant huntingtin protein with an abnormally long polyglutamine […]

Targeting Sepiapterin Reductase to Treat Neuropathic Pain

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Published Online: Jul 24th 2015

Alban Latremoliere, Michael Costigan, and Clifford Woolf describe how they genetically manipulated the tetrahydrobiopterin synthesis pathway in mice to formally validate its role in neuropathic and inflammatory pain hypersensitivity and show that inhibition of this pathway by targeting sepiapterin reductase both reduces chronic pain without adverse effects and generates a treatment biomarker.

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