Development of an ELISA assay for the quantification of soluble huntingtin in human blood cells

BACKGROUND: Huntington’s disease (HD) is a monogenic disorder caused by an aberrant expansion of CAG repeats in the huntingtin gene (HTT). Pathogenesis is associated with expression of the mutant (mHTT) protein in the CNS, with its levels most likely related to disease progression and symptom severi...

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Библиографические подробности
Опубликовано в: :BMC Biochem
Главные авторы: Massai, Luisa, Petricca, Lara, Magnoni, Letizia, Rovetini, Luca, Haider, Salman, Andre, Ralph, Tabrizi, Sarah J, Süssmuth, Sigurd D, Landwehrmeyer, Bernhard G, Caricasole, Andrea, Pollio, Giuseppe, Bernocco, Simonetta
Формат: Artigo
Язык:Inglês
Опубликовано: BioMed Central 2013
Предметы:
Methodology Article
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC4221641/
https://ncbi.nlm.nih.gov/pubmed/24274906
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2091-14-34
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