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Accumulation of ubiquitin conjugates in a polyglutamine disease model occurs without global ubiquitin/proteasome system impairment.
Maynard CJ, Böttcher C, Ortega Z, Smith R, Florea BI, Díaz-Hernández M, Brundin P, Overkleeft HS, Li JY, Lucas JJ, Dantuma NP. Maynard CJ, et al. Among authors: brundin p. Proc Natl Acad Sci U S A. 2009 Aug 18;106(33):13986-91. doi: 10.1073/pnas.0906463106. Epub 2009 Jul 30. Proc Natl Acad Sci U S A. 2009. PMID: 19666572 Free PMC article.
Huntington's disease: a synaptopathy?
Li JY, Plomann M, Brundin P. Li JY, et al. Among authors: brundin p. Trends Mol Med. 2003 Oct;9(10):414-20. doi: 10.1016/j.molmed.2003.08.006. Trends Mol Med. 2003. PMID: 14557053 Review.
Orexin loss in Huntington's disease.
Petersén A, Gil J, Maat-Schieman ML, Björkqvist M, Tanila H, Araújo IM, Smith R, Popovic N, Wierup N, Norlén P, Li JY, Roos RA, Sundler F, Mulder H, Brundin P. Petersén A, et al. Among authors: brundin p. Hum Mol Genet. 2005 Jan 1;14(1):39-47. doi: 10.1093/hmg/ddi004. Epub 2004 Nov 3. Hum Mol Genet. 2005. PMID: 15525658
Cholinergic neuronal defect without cell loss in Huntington's disease.
Smith R, Chung H, Rundquist S, Maat-Schieman ML, Colgan L, Englund E, Liu YJ, Roos RA, Faull RL, Brundin P, Li JY. Smith R, et al. Among authors: brundin p. Hum Mol Genet. 2006 Nov 1;15(21):3119-31. doi: 10.1093/hmg/ddl252. Epub 2006 Sep 20. Hum Mol Genet. 2006. PMID: 16987871
Late onset vascular dysfunction in the R6/1 model of Huntington's disease.
Rahman A, Ekman M, Shakirova Y, Andersson KE, Mörgelin M, Erjefält JS, Brundin P, Li JY, Swärd K. Rahman A, et al. Among authors: brundin p. Eur J Pharmacol. 2013 Jan 5;698(1-3):345-53. doi: 10.1016/j.ejphar.2012.10.026. Epub 2012 Oct 29. Eur J Pharmacol. 2013. PMID: 23117088
440 results