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In Vivo Cerebral Imaging of Mutant Huntingtin Aggregates Using (11)C-CHDI-180R PET in a Nonhuman Primate Model of Huntington Disease
Huntington disease (HD) is a neurodegenerative disorder caused by an expanded polyglutamine (CAG) trinucleotide expansion in the huntingtin (HTT) gene that encodes the mutant huntingtin protein (mHTT). Visualization and quantification of cerebral mHTT will provide a proxy for target engagement and a...
Autores principales: | Bertoglio, Daniele, Weiss, Alison R., Liguore, William, Martin, Lauren Drew, Hobbs, Theodore, Templon, John, Srinivasan, Sathya, Dominguez, Celia, Munoz-Sanjuan, Ignacio, Khetarpal, Vinod, Verhaeghe, Jeroen, Staelens, Steven, Link, Jeanne, Liu, Longbin, Bard, Jonathan A., McBride, Jodi L. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Society of Nuclear Medicine
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10586486/ https://www.ncbi.nlm.nih.gov/pubmed/37591545 http://dx.doi.org/10.2967/jnumed.123.265569 |
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