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Dysfunction of the cholesterol biosynthetic pathway in Huntington's disease.
Valenza M, Rigamonti D, Goffredo D, Zuccato C, Fenu S, Jamot L, Strand A, Tarditi A, Woodman B, Racchi M, Mariotti C, Di Donato S, Corsini A, Bates G, Pruss R, Olson JM, Sipione S, Tartari M, Cattaneo E. Valenza M, et al. Among authors: cattaneo e. J Neurosci. 2005 Oct 26;25(43):9932-9. doi: 10.1523/JNEUROSCI.3355-05.2005. J Neurosci. 2005. PMID: 16251441 Free PMC article.
Biological abnormalities of peripheral A(2A) receptors in a large representation of polyglutamine disorders and Huntington's disease stages.
Varani K, Bachoud-Lévi AC, Mariotti C, Tarditi A, Abbracchio MP, Gasperi V, Borea PA, Dolbeau G, Gellera C, Solari A, Rosser A, Naji J, Handley O, Maccarrone M, Peschanski M, DiDonato S, Cattaneo E. Varani K, et al. Among authors: cattaneo e. Neurobiol Dis. 2007 Jul;27(1):36-43. doi: 10.1016/j.nbd.2007.03.011. Epub 2007 Apr 5. Neurobiol Dis. 2007. PMID: 17512749
Severe deficiency of the fatty acid amide hydrolase (FAAH) activity segregates with the Huntington's disease mutation in peripheral lymphocytes.
Battista N, Bari M, Tarditi A, Mariotti C, Bachoud-Lévi AC, Zuccato C, Finazzi-Agrò A, Genitrini S, Peschanski M, Di Donato S, Cattaneo E, Maccarrone M. Battista N, et al. Among authors: cattaneo e. Neurobiol Dis. 2007 Jul;27(1):108-16. doi: 10.1016/j.nbd.2007.04.012. Epub 2007 May 6. Neurobiol Dis. 2007. PMID: 17553686
374 results