Igarashi S - Search Results

1

Trinucleotide repeat length and rate of progression of Huntington's disease.

Illarioshkin SN, Igarashi S, Onodera O, Markova ED, Nikolskaya NN, Tanaka H, Chabrashwili TZ, Insarova NG, Endo K, Ivanova-Smolenskaya IA, et al. Illarioshkin SN, et al. Among authors: igarashi s. Ann Neurol. 1994 Oct;36(4):630-5. doi: 10.1002/ana.410360412. Ann Neurol. 1994. PMID: 7944295

2

Progressive atrophy of cerebellum and brainstem as a function of age and the size of the expanded CAG repeats in the MJD1 gene in Machado-Joseph disease.

Onodera O, Idezuka J, Igarashi S, Takiyama Y, Endo K, Takano H, Oyake M, Tanaka H, Inuzuka T, Hayashi T, Yuasa T, Ito J, Miyatake T, Tsuji S. Onodera O, et al. Among authors: igarashi s. Ann Neurol. 1998 Mar;43(3):288-96. doi: 10.1002/ana.410430305. Ann Neurol. 1998. PMID: 9506544

3

Strong correlation between the number of CAG repeats in androgen receptor genes and the clinical onset of features of spinal and bulbar muscular atrophy.

Igarashi S, Tanno Y, Onodera O, Yamazaki M, Sato S, Ishikawa A, Miyatani N, Nagashima M, Ishikawa Y, Sahashi K, et al. Igarashi S, et al. Neurology. 1992 Dec;42(12):2300-2. doi: 10.1212/wnl.42.12.2300. Neurology. 1992. PMID: 1461383

4

Dentatorubral-pallidoluysian atrophy: clinical features are closely related to unstable expansions of trinucleotide (CAG) repeat.

Ikeuchi T, Koide R, Tanaka H, Onodera O, Igarashi S, Takahashi H, Kondo R, Ishikawa A, Tomoda A, Miike T, et al. Ikeuchi T, et al. Among authors: igarashi s. Ann Neurol. 1995 Jun;37(6):769-75. doi: 10.1002/ana.410370610. Ann Neurol. 1995. PMID: 7778850

5

Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA).

Koide R, Ikeuchi T, Onodera O, Tanaka H, Igarashi S, Endo K, Takahashi H, Kondo R, Ishikawa A, Hayashi T, et al. Koide R, et al. Among authors: igarashi s. Nat Genet. 1994 Jan;6(1):9-13. doi: 10.1038/ng0194-9. Nat Genet. 1994. PMID: 8136840

6

Isolated bilateral masseter atrophy in X-linked recessive bulbospinal neuronopathy.

Suzuki T, Endo K, Igarashi S, Fukuda M, Tanaka M. Suzuki T, et al. Among authors: igarashi s. Neurology. 1997 Feb;48(2):539-40. doi: 10.1212/wnl.48.2.539. Neurology. 1997. PMID: 9040758 No abstract available.

7

Spinocerebellar ataxia type 6: CAG repeat expansion in alpha1A voltage-dependent calcium channel gene and clinical variations in Japanese population.

Ikeuchi T, Takano H, Koide R, Horikawa Y, Honma Y, Onishi Y, Igarashi S, Tanaka H, Nakao N, Sahashi K, Tsukagoshi H, Inoue K, Takahashi H, Tsuji S. Ikeuchi T, et al. Among authors: igarashi s. Ann Neurol. 1997 Dec;42(6):879-84. doi: 10.1002/ana.410420609. Ann Neurol. 1997. PMID: 9403480

8

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: igarashi s. Am J Hum Genet. 1995 Nov;57(5):1050-60. Am J Hum Genet. 1995. PMID: 7485154 Free PMC article.

9

Direct detection of expanded (CAG/CTG) repeats in the myotonin-protein kinase genes of myotonic dystrophy patients using a high-stringency hybridization method.

Sanpei K, Igarashi S, Eguchi I, Takiyama Y, Tanaka H, Tsuji S. Sanpei K, et al. Among authors: igarashi s. Biochem Biophys Res Commun. 1995 Jul 17;212(2):341-6. doi: 10.1006/bbrc.1995.1975. Biochem Biophys Res Commun. 1995. PMID: 7626046

10

Evidence for inter-generational instability in the CAG repeat in the MJD1 gene and for conserved haplotypes at flanking markers amongst Japanese and Caucasian subjects with Machado-Joseph disease.

Takiyama Y, Igarashi S, Rogaeva EA, Endo K, Rogaev EI, Tanaka H, Sherrington R, Sanpei K, Liang Y, Saito M, et al. Takiyama Y, et al. Among authors: igarashi s. Hum Mol Genet. 1995 Jul;4(7):1137-46. doi: 10.1093/hmg/4.7.1137. Hum Mol Genet. 1995. PMID: 8528200

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