Ishikawa K - Search Results

1

Physical map and haplotype analysis of 16q-linked autosomal dominant cerebellar ataxia (ADCA) type III in Japan.

Li M, Ishikawa K, Toru S, Tomimitsu H, Takashima M, Goto J, Takiyama Y, Sasaki H, Imoto I, Inazawa J, Toda T, Kanazawa I, Mizusawa H. Li M, et al. Among authors: ishikawa k. J Hum Genet. 2003;48(3):111-8. doi: 10.1007/s100380300017. J Hum Genet. 2003. PMID: 12624721

2

Novel Cav2.1 splice variants isolated from Purkinje cells do not generate P-type Ca2+ current.

Tsunemi T, Saegusa H, Ishikawa K, Nagayama S, Murakoshi T, Mizusawa H, Tanabe T. Tsunemi T, et al. Among authors: ishikawa k. J Biol Chem. 2002 Mar 1;277(9):7214-21. doi: 10.1074/jbc.M108222200. Epub 2001 Dec 27. J Biol Chem. 2002. PMID: 11756409 Free article.

3

Proteolytic cleavage and cellular toxicity of the human alpha1A calcium channel in spinocerebellar ataxia type 6.

Kubodera T, Yokota T, Ohwada K, Ishikawa K, Miura H, Matsuoka T, Mizusawa H. Kubodera T, et al. Among authors: ishikawa k. Neurosci Lett. 2003 Apr 24;341(1):74-8. doi: 10.1016/s0304-3940(03)00156-3. Neurosci Lett. 2003. PMID: 12676347

4

Mutation of the EYA1 gene in patients with branchio-oto syndrome.

Yashima T, Noguchi Y, Ishikawa K, Mizusawa H, Kitamura K. Yashima T, et al. Among authors: ishikawa k. Acta Otolaryngol. 2003 Jan;123(2):279-82. doi: 10.1080/0036554021000028103. Acta Otolaryngol. 2003. PMID: 12701758

5

A clinical and genetic study in a large cohort of patients with spinocerebellar ataxia type 6.

Takahashi H, Ishikawa K, Tsutsumi T, Fujigasaki H, Kawata A, Okiyama R, Fujita T, Yoshizawa K, Yamaguchi S, Tomiyasu H, Yoshii F, Mitani K, Shimizu N, Yamazaki M, Miyamoto T, Orimo T, Shoji S, Kitamura K, Mizusawa H. Takahashi H, et al. Among authors: ishikawa k. J Hum Genet. 2004;49(5):256-64. doi: 10.1007/s10038-004-0142-7. J Hum Genet. 2004. PMID: 15362569

6

An autosomal dominant cerebellar ataxia linked to chromosome 16q22.1 is associated with a single-nucleotide substitution in the 5' untranslated region of the gene encoding a protein with spectrin repeat and Rho guanine-nucleotide exchange-factor domains.

Ishikawa K, Toru S, Tsunemi T, Li M, Kobayashi K, Yokota T, Amino T, Owada K, Fujigasaki H, Sakamoto M, Tomimitsu H, Takashima M, Kumagai J, Noguchi Y, Kawashima Y, Ohkoshi N, Ishida G, Gomyoda M, Yoshida M, Hashizume Y, Saito Y, Murayama S, Yamanouchi H, Mizutani T, Kondo I, Toda T, Mizusawa H. Ishikawa K, et al. Am J Hum Genet. 2005 Aug;77(2):280-96. doi: 10.1086/432518. Epub 2005 Jul 6. Am J Hum Genet. 2005. PMID: 16001362 Free PMC article.

7

New RNAi strategy for selective suppression of a mutant allele in polyglutamine disease.

Kubodera T, Yokota T, Ishikawa K, Mizusawa H. Kubodera T, et al. Among authors: ishikawa k. Oligonucleotides. 2005 Dec;15(4):298-302. doi: 10.1089/oli.2005.15.298. Oligonucleotides. 2005. PMID: 16396623

8

[A case of spinocerebellar ataxia type 6 with its initial symptom of episodic ataxia-like phenotype].

Shimazaki H, Nakao K, Ishikawa K, Takiyama Y, Nakano I. Shimazaki H, et al. Among authors: ishikawa k. No To Shinkei. 2006 Jan;58(1):63-7. No To Shinkei. 2006. PMID: 16482924 Japanese.

9

A -16C>T substitution in the 5' UTR of the puratrophin-1 gene is prevalent in autosomal dominant cerebellar ataxia in Nagano.

Ohata T, Yoshida K, Sakai H, Hamanoue H, Mizuguchi T, Shimizu Y, Okano T, Takada F, Ishikawa K, Mizusawa H, Yoshiura KI, Fukushima Y, Ikeda SI, Matsumoto N. Ohata T, et al. Among authors: ishikawa k. J Hum Genet. 2006;51(5):461-466. doi: 10.1007/s10038-006-0385-6. Epub 2006 Apr 14. J Hum Genet. 2006. PMID: 16614795

10

On autosomal dominant cerebellar ataxia (ADCA) other than polyglutamine diseases, with special reference to chromosome 16q22.1-linked ADCA.

Ishikawa K, Mizusawa H. Ishikawa K, et al. Neuropathology. 2006 Aug;26(4):352-60. doi: 10.1111/j.1440-1789.2006.00719.x. Neuropathology. 2006. PMID: 16961073 Review.

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