Ikeuchi T - Search Results

1

SORL1 is genetically associated with late-onset Alzheimer's disease in Japanese, Koreans and Caucasians.

Miyashita A, Koike A, Jun G, Wang LS, Takahashi S, Matsubara E, Kawarabayashi T, Shoji M, Tomita N, Arai H, Asada T, Harigaya Y, Ikeda M, Amari M, Hanyu H, Higuchi S, Ikeuchi T, Nishizawa M, Suga M, Kawase Y, Akatsu H, Kosaka K, Yamamoto T, Imagawa M, Hamaguchi T, Yamada M, Morihara T, Takeda M, Takao T, Nakata K, Fujisawa Y, Sasaki K, Watanabe K, Nakashima K, Urakami K, Ooya T, Takahashi M, Yuzuriha T, Serikawa K, Yoshimoto S, Nakagawa R, Kim JW, Ki CS, Won HH, Na DL, Seo SW, Mook-Jung I; Alzheimer Disease Genetics Consortium; St George-Hyslop P, Mayeux R, Haines JL, Pericak-Vance MA, Yoshida M, Nishida N, Tokunaga K, Yamamoto K, Tsuji S, Kanazawa I, Ihara Y, Schellenberg GD, Farrer LA, Kuwano R. Miyashita A, et al. Among authors: ikeuchi t. PLoS One. 2013;8(4):e58618. doi: 10.1371/journal.pone.0058618. Epub 2013 Apr 2. PLoS One. 2013. PMID: 23565137 Free PMC article.

2

Induction of distamycin A-inducible rare fragile sites and increased sister chromatid exchanges at the fragile site.

Tsuji H, Hitomi A, Takahashi E, Murata M, Ikeuchi T, Yamamoto K, Tsuji S, Hori T. Tsuji H, et al. Among authors: ikeuchi t. Hum Genet. 1991 Jul;87(3):254-60. doi: 10.1007/BF00200900. Hum Genet. 1991. PMID: 1864598

3

Refined determination of breakpoints of the translocation t(1;7) associated with signs of HMC syndrome.

Ikeuchi T, Motohashi N, Yamamoto K, Kuroda T. Ikeuchi T, et al. Jinrui Idengaku Zasshi. 1991 Jun;36(2):155-8. doi: 10.1007/BF01876578. Jinrui Idengaku Zasshi. 1991. PMID: 1920914

4

Ring chromosome 21 transmitted from mother to daughter: its stability in a lymphoblastoid cell line.

Ikeuchi T, Yamamoto K, Qiao F, Hayakawa K, Migita T, Nishikawa Y. Ikeuchi T, et al. Ann Genet. 1990;33(1):32-5. Ann Genet. 1990. PMID: 2369070

5

Molecular cloning of a full-length cDNA for dentatorubral-pallidoluysian atrophy and regional expressions of the expanded alleles in the CNS.

Onodera O, Oyake M, Takano H, Ikeuchi T, Igarashi S, Tsuji S. Onodera O, et al. Among authors: ikeuchi t. Am J Hum Genet. 1995 Nov;57(5):1050-60. Am J Hum Genet. 1995. PMID: 7485154 Free PMC article.

6

Dentatorubral-pallidoluysian atrophy (DRPLA). Molecular basis for wide clinical features of DRPLA.

Ikeuchi T, Koide R, Onodera O, Tanaka H, Oyake M, Takano H, Tsuji S. Ikeuchi T, et al. Clin Neurosci. 1995;3(1):23-7. Clin Neurosci. 1995. PMID: 7614090

7

[Genetic diagnosis of hereditary spinocerebellar degeneration].

Ikeuchi T, Tsuji S. Ikeuchi T, et al. Nihon Naika Gakkai Zasshi. 1994 Nov 10;83(11):2000-6. Nihon Naika Gakkai Zasshi. 1994. PMID: 7852812 Review. Japanese. No abstract available.

8

Dentatorubral-pallidoluysian atrophy and Haw River syndrome.

Burke JR, Ikeuchi T, Koide R, Tsuji S, Yamada M, Pericak-Vance MA, Vance JM. Burke JR, et al. Among authors: ikeuchi t. Lancet. 1994 Dec 17;344(8938):1711-2. doi: 10.1016/s0140-6736(94)90497-9. Lancet. 1994. PMID: 7996992 No abstract available.

9

[Familial myopathy associated with tubular aggregates--report of two siblings].

Ikeuchi T, Anezaki T, Ishiguro H, Tanaka M, Tanaka K, Tsuji S. Ikeuchi T, et al. Rinsho Shinkeigaku. 1995 Sep;35(9):1016-20. Rinsho Shinkeigaku. 1995. PMID: 8565338 Japanese.

10

Somatic mosaicism of expanded CAG repeats in brains of patients with dentatorubral-pallidoluysian atrophy: cellular population-dependent dynamics of mitotic instability.

Takano H, Onodera O, Takahashi H, Igarashi S, Yamada M, Oyake M, Ikeuchi T, Koide R, Tanaka H, Iwabuchi K, Tsuji S. Takano H, et al. Among authors: ikeuchi t. Am J Hum Genet. 1996 Jun;58(6):1212-22. Am J Hum Genet. 1996. PMID: 8651298 Free PMC article.

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