Mizusawa H - Search Results

1

Spinocerebellar ataxia type 6 knockin mice develop a progressive neuronal dysfunction with age-dependent accumulation of mutant CaV2.1 channels.

Watase K, Barrett CF, Miyazaki T, Ishiguro T, Ishikawa K, Hu Y, Unno T, Sun Y, Kasai S, Watanabe M, Gomez CM, Mizusawa H, Tsien RW, Zoghbi HY. Watase K, et al. Among authors: mizusawa h. Proc Natl Acad Sci U S A. 2008 Aug 19;105(33):11987-92. doi: 10.1073/pnas.0804350105. Epub 2008 Aug 7. Proc Natl Acad Sci U S A. 2008. PMID: 18687887 Free PMC article.

2

[SCA6: From gene identification to recent progress on pathogenesis].

Watase K, Ishikawa K, Mizusawa H. Watase K, et al. Among authors: mizusawa h. Rinsho Shinkeigaku. 2010 Nov;50(11):858-60. doi: 10.5692/clinicalneurol.50.858. Rinsho Shinkeigaku. 2010. PMID: 21921472 Review. Japanese.

3

Development of Purkinje cell degeneration in a knockin mouse model reveals lysosomal involvement in the pathogenesis of SCA6.

Unno T, Wakamori M, Koike M, Uchiyama Y, Ishikawa K, Kubota H, Yoshida T, Sasakawa H, Peters C, Mizusawa H, Watase K. Unno T, et al. Among authors: mizusawa h. Proc Natl Acad Sci U S A. 2012 Oct 23;109(43):17693-8. doi: 10.1073/pnas.1212786109. Epub 2012 Oct 10. Proc Natl Acad Sci U S A. 2012. PMID: 23054835 Free PMC article.

4

[Clinical, neuropathological and genetic characteristics of spinocerebellar ataxia type 6 (SCA6)].

Ishikawa K, Mizusawa H. Ishikawa K, et al. Among authors: mizusawa h. Nihon Rinsho. 1999 Apr;57(4):880-5. Nihon Rinsho. 1999. PMID: 10222783 Review. Japanese.

5

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: mizusawa h. 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.

6

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: mizusawa h. Neurosci Lett. 2003 Apr 24;341(1):74-8. doi: 10.1016/s0304-3940(03)00156-3. Neurosci Lett. 2003. PMID: 12676347

7

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. Among authors: mizusawa h. Neuropathology. 2006 Aug;26(4):352-60. doi: 10.1111/j.1440-1789.2006.00719.x. Neuropathology. 2006. PMID: 16961073 Review.

8

Cell-type-specific alternative splicing in spinocerebellar ataxia type 6.

Tsunemi T, Ishikawa K, Jin H, Mizusawa H. Tsunemi T, et al. Among authors: mizusawa h. Neurosci Lett. 2008 Dec 5;447(1):78-81. doi: 10.1016/j.neulet.2008.09.065. Epub 2008 Sep 30. Neurosci Lett. 2008. PMID: 18835329

9

Analyses of copy number and mRNA expression level of the alpha-synuclein gene in multiple system atrophy.

Jin H, Ishikawa K, Tsunemi T, Ishiguro T, Amino T, Mizusawa H. Jin H, et al. Among authors: mizusawa h. J Med Dent Sci. 2008 Mar;55(1):145-53. J Med Dent Sci. 2008. PMID: 19845160

10

[Molecular genetic approach to spinocerebellar ataxias].

Ishikawa K, Ishiguro T, Takahashi M, Sato N, Amino T, Niimi Y, Mizusawa H. Ishikawa K, et al. Among authors: mizusawa h. Rinsho Shinkeigaku. 2009 Nov;49(11):907-9. doi: 10.5692/clinicalneurol.49.907. Rinsho Shinkeigaku. 2009. PMID: 20030245 Review. Japanese.

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