Takiyama Y - Search Results

1

Japanese families with autosomal dominant pure cerebellar ataxia map to chromosome 19p13.1-p13.2 and are strongly associated with mild CAG expansions in the spinocerebellar ataxia type 6 gene in chromosome 19p13.1.

Ishikawa K, Tanaka H, Saito M, Ohkoshi N, Fujita T, Yoshizawa K, Ikeuchi T, Watanabe M, Hayashi A, Takiyama Y, Nishizawa M, Nakano I, Matsubayashi K, Miwa M, Shoji S, Kanazawa I, Tsuji S, Mizusawa H. Ishikawa K, et al. Among authors: takiyama y. Am J Hum Genet. 1997 Aug;61(2):336-46. doi: 10.1086/514867. Am J Hum Genet. 1997. PMID: 9311738 Free PMC article.

2

A large Japanese family with Machado-Joseph disease: clinical and genetic studies.

Takiyama Y, Ikemoto S, Tanaka Y, Mizuno Y, Yoshida M, Yasuda N. Takiyama Y, et al. Acta Neurol Scand. 1989 Mar;79(3):214-22. doi: 10.1111/j.1600-0404.1989.tb03741.x. Acta Neurol Scand. 1989. PMID: 2718740

3

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: takiyama y. Biochem Biophys Res Commun. 1995 Jul 17;212(2):341-6. doi: 10.1006/bbrc.1995.1975. Biochem Biophys Res Commun. 1995. PMID: 7626046

4

[The characteristics and the gene locus of Machado Joseph disease].

Takiyama Y, Tsuji S. Takiyama Y, et al. No To Shinkei. 1995 Feb;47(2):117-29. No To Shinkei. 1995. PMID: 7669410 Review. Japanese. No abstract available.

5

The effects of hydrocortisone and RU486 (mifepristone) on iodide uptake in porcine thyroid cells in primary culture.

Takiyama Y, Tanaka H, Takiyama Y, Makino I. Takiyama Y, et al. Endocrinology. 1994 Nov;135(5):1972-9. doi: 10.1210/endo.135.5.7956919. Endocrinology. 1994. PMID: 7956919

6

A clinical and pathologic study of a large Japanese family with Machado-Joseph disease tightly linked to the DNA markers on chromosome 14q.

Takiyama Y, Oyanagi S, Kawashima S, Sakamoto H, Saito K, Yoshida M, Tsuji S, Mizuno Y, Nishizawa M. Takiyama Y, et al. Neurology. 1994 Jul;44(7):1302-8. doi: 10.1212/wnl.44.7.1302. Neurology. 1994. PMID: 8035935

7

[Cerebral sinus thrombosis in a young man with hereditary protein C deficiency].

Shimazaki H, Ogawa M, Takiyama Y, Nishizawa M, Yoshida M. Shimazaki H, et al. Among authors: takiyama y. Rinsho Shinkeigaku. 1993 Oct;33(10):1083-5. Rinsho Shinkeigaku. 1993. PMID: 8293611 Review. Japanese.

8

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. Nat Genet. 1993 Jul;4(3):300-4. doi: 10.1038/ng0793-300. Nat Genet. 1993. PMID: 8358439

9

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

10

Non-Mendelian transmission in dentatorubral-pallidoluysian atrophy and Machado-Joseph disease: the mutant allele is preferentially transmitted in male meiosis.

Ikeuchi T, Igarashi S, Takiyama Y, Onodera O, Oyake M, Takano H, Koide R, Tanaka H, Tsuji S. Ikeuchi T, et al. Among authors: takiyama y. Am J Hum Genet. 1996 Apr;58(4):730-3. Am J Hum Genet. 1996. PMID: 8644735 Free PMC article.

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