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LRRK2 P755L variant in sporadic Parkinson's disease.
Tomiyama H, Mizuta I, Li Y, Funayama M, Yoshino H, Li L, Murata M, Yamamoto M, Kubo SI, Mizuno Y, Toda T, Hattori N. Tomiyama H, et al. Among authors: kubo si. J Hum Genet. 2008;53(11-12):1012-1015. doi: 10.1007/s10038-008-0336-5. Epub 2008 Oct 16. J Hum Genet. 2008. PMID: 18923807
Parkin is associated with cellular vesicles.
Kubo SI, Kitami T, Noda S, Shimura H, Uchiyama Y, Asakawa S, Minoshima S, Shimizu N, Mizuno Y, Hattori N. Kubo SI, et al. J Neurochem. 2001 Jul;78(1):42-54. doi: 10.1046/j.1471-4159.2001.00364.x. J Neurochem. 2001. PMID: 11432972 Free article.
Recessive Parkinson's disease.
Kubo S, Hattori N, Mizuno Y. Kubo S, et al. Mov Disord. 2006 Jul;21(7):885-93. doi: 10.1002/mds.20841. Mov Disord. 2006. PMID: 16615060 Review.
Clinicogenetic study of mutations in LRRK2 exon 41 in Parkinson's disease patients from 18 countries.
Tomiyama H, Li Y, Funayama M, Hasegawa K, Yoshino H, Kubo S, Sato K, Hattori T, Lu CS, Inzelberg R, Djaldetti R, Melamed E, Amouri R, Gouider-Khouja N, Hentati F, Hatano Y, Wang M, Imamichi Y, Mizoguchi K, Miyajima H, Obata F, Toda T, Farrer MJ, Mizuno Y, Hattori N. Tomiyama H, et al. Mov Disord. 2006 Aug;21(8):1102-8. doi: 10.1002/mds.20886. Mov Disord. 2006. PMID: 16622854
Leucine-rich repeat kinase 2 associates with lipid rafts.
Hatano T, Kubo S, Imai S, Maeda M, Ishikawa K, Mizuno Y, Hattori N. Hatano T, et al. Hum Mol Genet. 2007 Mar 15;16(6):678-90. doi: 10.1093/hmg/ddm013. Epub 2007 Mar 6. Hum Mol Genet. 2007. PMID: 17341485
88 results