Kubo S - Search Results

1

Immunohistochemical and subcellular localization of Parkin protein: absence of protein in autosomal recessive juvenile parkinsonism patients.

Shimura H, Hattori N, Kubo S, Yoshikawa M, Kitada T, Matsumine H, Asakawa S, Minoshima S, Yamamura Y, Shimizu N, Mizuno Y. Shimura H, et al. Among authors: kubo s. Ann Neurol. 1999 May;45(5):668-72. doi: 10.1002/1531-8249(199905)45:5<668::aid-ana19>3.0.co;2-z. Ann Neurol. 1999. PMID: 10319893

2

Familial Parkinson disease gene product, parkin, is a ubiquitin-protein ligase.

Shimura H, Hattori N, Kubo Si, Mizuno Y, Asakawa S, Minoshima S, Shimizu N, Iwai K, Chiba T, Tanaka K, Suzuki T. Shimura H, et al. Among authors: kubo si. Nat Genet. 2000 Jul;25(3):302-5. doi: 10.1038/77060. Nat Genet. 2000. PMID: 10888878

3

Molecular mechanisms of nigral neurodegeneration in Park2 and regulation of parkin protein by other proteins.

Hattori N, Machida Y, Sato S, Noda K, Iijima-Kitami M, Kubo S, Mizuno Y. Hattori N, et al. Among authors: kubo s. J Neural Transm Suppl. 2006;(70):205-8. doi: 10.1007/978-3-211-45295-0_31. J Neural Transm Suppl. 2006. PMID: 17017530 Review.

4

Autosomal recessive juvenile parkinsonism: a key to understanding nigral degeneration in sporadic Parkinson's disease.

Hattori N, Shimura H, Kubo S, Kitada T, Wang M, Asakawa S, Minashima S, Shimizu N, Suzuki T, Tanaka K, Mizuno Y. Hattori N, et al. Among authors: kubo s. Neuropathology. 2000 Sep;20 Suppl:S85-90. doi: 10.1046/j.1440-1789.2000.00312.x. Neuropathology. 2000. PMID: 11037196 Review.

5

Importance of familial Parkinson's disease and parkinsonism to the understanding of nigral degeneration in sporadic Parkinson's disease.

Hattori N, Shimura H, Kubo S, Wang M, Shimizu N, Tanaka K, Mizuno Y. Hattori N, et al. Among authors: kubo s. J Neural Transm Suppl. 2000;(60):101-16. doi: 10.1007/978-3-7091-6301-6_6. J Neural Transm Suppl. 2000. PMID: 11205133 Review.

6

[Autosomal recessive juvenile parkinsonism: its pathogenesis is involved in the ubiquitin-proteasome pathway].

Hattori N, Shimura H, Kubo S, Suzuki T, Tanaka K, Mizuno Y. Hattori N, et al. Among authors: kubo s. Rinsho Shinkeigaku. 2000 Dec;40(12):1293-6. Rinsho Shinkeigaku. 2000. PMID: 11464483 Review. Japanese.

7

Familial Parkinson's disease. Alpha-synuclein and parkin.

Mizuno Y, Hattori N, Kitada T, Matsumine H, Mori H, Shimura H, Kubo S, Kobayashi H, Asakawa S, Minoshima S, Shimizu N. Mizuno Y, et al. Among authors: kubo s. Adv Neurol. 2001;86:13-21. Adv Neurol. 2001. PMID: 11553970 Review.

8

Association between a polymorphism of ubiquitin carboxy-terminal hydrolase L1 (UCH-L1) gene and sporadic Parkinson's disease.

Zhang J, Hattori N, Leroy E, Morris HR, Kubo S, Kobayashi T, Wood NW, Polymeropoulos MH, Mizuno Y. Zhang J, et al. Among authors: kubo s. Parkinsonism Relat Disord. 2000 Oct 1;6(4):195-197. doi: 10.1016/s1353-8020(00)00015-8. Parkinsonism Relat Disord. 2000. PMID: 10900392

9

[A 57-year-old woman with progressive disturbance of gait and mental deterioration].

Kubo S, Hattori T, Takanashi M, Mori H, Mizutani Y, Suda K, Hattori N, Mizuno Y. Kubo S, et al. No To Shinkei. 2000 Nov;52(11):1035-44. No To Shinkei. 2000. PMID: 11217688 Japanese.

10

Unmet needs of patients with Parkinson's disease: interview survey of patients and caregivers.

Hatano T, Kubo SI, Shimo Y, Nishioka K, Hattori N. Hatano T, et al. Among authors: kubo si. J Int Med Res. 2009 May-Jun;37(3):717-26. doi: 10.1177/147323000903700315. J Int Med Res. 2009. PMID: 19589255 Free article.

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