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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, Komure O, Matsuura S, Kobatake K, Morimoto N, Abe K, Suzuki N, Aoki M, Kawata A, Hirai T, Kato T, Ogasawara K, Hirano A, Takumi T, Kusaka H, Hagiwara K, Kaji R, Kawakami H. Maruyama H, et al. Among authors: hirano a. Nature. 2010 May 13;465(7295):223-6. doi: 10.1038/nature08971. Epub 2010 Apr 28. Nature. 2010. PMID: 20428114
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, Ihara M, Konishi T, Ogasawara K, Hirano A, Kusaka H, Kaji R, Takahashi R, Kawakami H. Ito H, et al. Among authors: hirano a. Acta Neuropathol. 2011 Aug;122(2):223-9. doi: 10.1007/s00401-011-0842-y. Epub 2011 Jun 5. Acta Neuropathol. 2011. PMID: 21644038
Optineurin is co-localized with FUS in basophilic inclusions of ALS with FUS mutation and in basophilic inclusion body disease.
Ito H, Fujita K, Nakamura M, Wate R, Kaneko S, Sasaki S, Yamane K, Suzuki N, Aoki M, Shibata N, Togashi S, Kawata A, Mochizuki Y, Mizutani T, Maruyama H, Hirano A, Takahashi R, Kawakami H, Kusaka H. Ito H, et al. Among authors: hirano a. Acta Neuropathol. 2011 Apr;121(4):555-7. doi: 10.1007/s00401-011-0809-z. Epub 2011 Feb 17. Acta Neuropathol. 2011. PMID: 21327942 No abstract available.
New consensus research on neuropathological aspects of familial amyotrophic lateral sclerosis with superoxide dismutase 1 (SOD1) gene mutations: inclusions containing SOD1 in neurons and astrocytes.
Kato S, Takikawa M, Nakashima K, Hirano A, Cleveland DW, Kusaka H, Shibata N, Kato M, Nakano I, Ohama E. Kato S, et al. Among authors: hirano a. Amyotroph Lateral Scler Other Motor Neuron Disord. 2000 Jun;1(3):163-84. doi: 10.1080/14660820050515160. Amyotroph Lateral Scler Other Motor Neuron Disord. 2000. PMID: 11464950 Review.
HtrA2/Omi-immunoreactive intraneuronal inclusions in the anterior horn of patients with sporadic and Cu/Zn superoxide dismutase (SOD1) mutant amyotrophic lateral sclerosis.
Kawamoto Y, Ito H, Kobayashi Y, Suzuki Y, Akiguchi I, Fujimura H, Sakoda S, Kusaka H, Hirano A, Takahashi R. Kawamoto Y, et al. Among authors: hirano a. Neuropathol Appl Neurobiol. 2010 Jun;36(4):331-44. doi: 10.1111/j.1365-2990.2010.01075.x. Epub 2010 Feb 25. Neuropathol Appl Neurobiol. 2010. PMID: 20202124
Colocalization of 14-3-3 proteins with SOD1 in Lewy body-like hyaline inclusions in familial amyotrophic lateral sclerosis cases and the animal model.
Okamoto Y, Shirakashi Y, Ihara M, Urushitani M, Oono M, Kawamoto Y, Yamashita H, Shimohama S, Kato S, Hirano A, Tomimoto H, Ito H, Takahashi R. Okamoto Y, et al. Among authors: hirano a. PLoS One. 2011;6(5):e20427. doi: 10.1371/journal.pone.0020427. Epub 2011 May 31. PLoS One. 2011. PMID: 21655264 Free PMC article.
1,300 results