Endo K - Search Results

1

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: endo k. Nat Genet. 1994 Jan;6(1):9-13. doi: 10.1038/ng0194-9. Nat Genet. 1994. PMID: 8136840

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: endo k. Ann Neurol. 1998 Mar;43(3):288-96. doi: 10.1002/ana.410430305. Ann Neurol. 1998. PMID: 9506544

3

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: endo k. Ann Neurol. 1994 Oct;36(4):630-5. doi: 10.1002/ana.410360412. Ann Neurol. 1994. PMID: 7944295

4

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: endo k. Hum Mol Genet. 1995 Jul;4(7):1137-46. doi: 10.1093/hmg/4.7.1137. Hum Mol Genet. 1995. PMID: 8528200

5

Hereditary progressive dystonia with marked diurnal fluctuation caused by mutations in the GTP cyclohydrolase I gene.

Ichinose H, Ohye T, Takahashi E, Seki N, Hori T, Segawa M, Nomura Y, Endo K, Tanaka H, Tsuji S, et al. Ichinose H, et al. Among authors: endo k. Nat Genet. 1994 Nov;8(3):236-42. doi: 10.1038/ng1194-236. Nat Genet. 1994. PMID: 7874165

6

The gene for Machado-Joseph disease maps to human chromosome 14q.

Takiyama Y, Nishizawa M, Tanaka H, Kawashima S, Sakamoto H, Karube Y, Shimazaki H, Soutome M, Endo K, Ohta S, et al. Takiyama Y, et al. Among authors: endo k. Nat Genet. 1993 Jul;4(3):300-4. doi: 10.1038/ng0793-300. Nat Genet. 1993. PMID: 8358439

7

Intergenerational instability of the CAG repeat of the gene for Machado-Joseph disease (MJD1) is affected by the genotype of the normal chromosome: implications for the molecular mechanisms of the instability of the CAG repeat.

Igarashi S, Takiyama Y, Cancel G, Rogaeva EA, Sasaki H, Wakisaka A, Zhou YX, Takano H, Endo K, Sanpei K, Oyake M, Tanaka H, Stevanin G, Abbas N, Dürr A, Rogaev EI, Sherrington R, Tsuda T, Ikeda M, Cassa E, Nishizawa M, Benomar A, Julien J, Weissenbach J, Wang GX, Agid Y, St George-Hyslop PH, Brice A, Tsuji S. Igarashi S, et al. Among authors: endo k. Hum Mol Genet. 1996 Jul;5(7):923-32. doi: 10.1093/hmg/5.7.923. Hum Mol Genet. 1996. PMID: 8817326

8

Strong linkage disequilibrium and haplotype analysis in Japanese pedigrees with Machado-Joseph disease.

Endo K, Sasaki H, Wakisaka A, Tanaka H, Saito M, Igarashi S, Takiyama Y, Sanpei K, Iwabuchi K, Suzuki Y, Onari K, Suzuki T, Weissenbach J, Weber JL, Nomura Y, Segawa M, Nishizawa M, Tsuji S. Endo K, et al. Am J Med Genet. 1996 Sep 20;67(5):437-44. doi: 10.1002/(SICI)1096-8628(19960920)67:5<437::AID-AJMG1>3.0.CO;2-H. Am J Med Genet. 1996. PMID: 8886159

9

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: endo k. Neurology. 1997 Feb;48(2):539-40. doi: 10.1212/wnl.48.2.539. Neurology. 1997. PMID: 9040758 No abstract available.

10

The gene for hereditary progressive dystonia with marked diurnal fluctuation maps to chromosome 14q.

Tanaka H, Endo K, Tsuji S, Nygaard TG, Weeks DE, Nomura Y, Segawa M. Tanaka H, et al. Among authors: endo k. Ann Neurol. 1995 Mar;37(3):405-8. doi: 10.1002/ana.410370319. Ann Neurol. 1995. PMID: 7695242

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