12 results for author:"Komure O." in Literature citations
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| Clinicopathologic study on an ALS family with a heterozygous E478G optineurin mutation. Ito H., Nakamura M., Komure O., Ayaki T., Wate R., Maruyama H., Nakamura Y., Fujita K., Kaneko S., Okamoto Y. et al. Acta Neuropathol. 122:223-229(2011) · Mapped (3) |
| Mutations of optineurin in amyotrophic lateral sclerosis. Maruyama H., Morino H., Ito H., Izumi Y., Kato H., Watanabe Y., Kinoshita Y., Kamada M., Nodera H., Suzuki H. et al. |
| Expression of Kruppel-like factor 5 gene in human brain and association of the gene with the susceptibility to schizophrenia. Yanagi M., Hashimoto T., Kitamura N., Fukutake M., Komure O., Nishiguchi N., Kawamata T., Maeda K., Shirakawa O. Schizophr. Res. 100:291-301(2008) · Mapped (6) |
| Phenotypic heterogeneity within a new family with the MAPT P301S mutation. Yasuda M., Nakamura Y., Kawamata T., Kaneyuki H., Maeda K., Komure O. |
| The effect of tau genotype on clinical features in FTDP-17. Baba Y., Tsuboi Y., Baker M.C., Uitti R.J., Hutton M.L., Dickson D.W., Farrer M., Putzke J.D., Woodruff B.K., Ghetti B. et al. Parkinsonism Relat. Disord. 11:205-208(2005) · Mapped (6) |
| SCA8 repeat expansion: large CTA/CTG repeat alleles are more common in ataxic patients, including those with SCA6. Izumi Y., Maruyama H., Oda M., Morino H., Okada T., Ito H., Sasaki I., Tanaka H., Komure O., Udaka F. et al. Am. J. Hum. Genet. 72:704-709(2003) · Mapped (8) |
| Clinical and genetic studies of families with the tau N279K mutation (FTDP-17). Tsuboi Y., Baker M., Hutton M.L., Uitti R.J., Rascol O., Delisle M.-B., Soulages X., Murrell J.R., Ghetti B., Yasuda M. et al. Neurology 59:1791-1793(2002) · UniProtKB (1) |
| Contribution of the interleukin-1beta gene polymorphism in multiple system atrophy. Nishimura M., Kawakami H., Komure O., Maruyama H., Morino H., Izumi Y., Nakamura S., Kaji R., Kuno S. Mov. Disord. 17:808-811(2002) · Mapped (4) |
| A mutation in the microtubule-associated protein tau in pallido-nigro-luysian degeneration. Yasuda M., Kawamata T., Komure O., Kuno S., D'Souza I., Poorkaj P., Kawai J., Tanimukai S., Yamamoto Y., Hasegawa H. et al. Neurology 53:864-868(1999) · UniProtKB (1) |
| A novel missense mutant inactivates GTP cyclohydrolase I in dopa-responsive dystonia. Hirano M., Komure O., Ueno S. Neurosci. Lett. 260:181-184(1999) · UniProtKB (1) |
| Transgenic mice harboring a full-length human mutant DRPLA gene exhibit age-dependent intergenerational and somatic instabilities of CAG repeats comparable with those in DRPLA patients. Sato T., Oyake M., Nakamura K., Nakao K., Fukusima Y., Onodera O., Igarashi S., Takano H., Kikugawa K., Ishida Y. et al. Hum. Mol. Genet. 8:99-106(1999) · Mapped (2) |
| A unique origin and multistep process for the generation of expanded DRPLA triplet repeats. Yanagisawa H., Fujii K., Nagafuchi S., Nakahori Y., Nakagome Y., Akane A., Nakamura M., Sano A., Komure O., Kondo I. et al. Hum. Mol. Genet. 5:373-379(1996) · UniProtKB (1) |