Kono S - Search Results

1

Direct Comparison of Manganese Detoxification/Efflux Proteins and Molecular Characterization of ZnT10 Protein as a Manganese Transporter.

Nishito Y, Tsuji N, Fujishiro H, Takeda TA, Yamazaki T, Teranishi F, Okazaki F, Matsunaga A, Tuschl K, Rao R, Kono S, Miyajima H, Narita H, Himeno S, Kambe T. Nishito Y, et al. Among authors: kono s. J Biol Chem. 2016 Jul 8;291(28):14773-87. doi: 10.1074/jbc.M116.728014. Epub 2016 May 10. J Biol Chem. 2016. PMID: 27226609 Free PMC article.

2

Molecular and pathological basis of aceruloplasminemia.

Kono S, Miyajima H. Kono S, et al. Biol Res. 2006;39(1):15-23. doi: 10.4067/s0716-97602006000100003. Biol Res. 2006. PMID: 16629161 Free article.

3

[Familial Wernicke's-like encephalopathy].

Miyajima H, Kono S. Miyajima H, et al. Among authors: kono s. Rinsho Shinkeigaku. 2010 Nov;50(11):855-7. doi: 10.5692/clinicalneurol.50.855. Rinsho Shinkeigaku. 2010. PMID: 21921471 Japanese.

4

Biochemical analysis of a missense mutation in aceruloplasminemia.

Hellman NE, Kono S, Miyajima H, Gitlin JD. Hellman NE, et al. Among authors: kono s. J Biol Chem. 2002 Jan 11;277(2):1375-80. doi: 10.1074/jbc.M109123200. Epub 2001 Oct 31. J Biol Chem. 2002. PMID: 11689569 Free article.

5

Biological effects of mutant ceruloplasmin on hepcidin-mediated internalization of ferroportin.

Kono S, Yoshida K, Tomosugi N, Terada T, Hamaya Y, Kanaoka S, Miyajima H. Kono S, et al. Biochim Biophys Acta. 2010 Nov;1802(11):968-75. doi: 10.1016/j.bbadis.2010.07.011. Epub 2010 Jul 22. Biochim Biophys Acta. 2010. PMID: 20655381 Free article.

6

Aceruloplasminemia, an inherited disorder of iron metabolism.

Miyajima H, Takahashi Y, Kono S. Miyajima H, et al. Among authors: kono s. Biometals. 2003 Mar;16(1):205-13. doi: 10.1023/a:1020775101654. Biometals. 2003. PMID: 12572680

7

Increased lipid peroxidation and mitochondrial dysfunction in aceruloplasminemia brains.

Miyajima H, Kono S, Takahashi Y, Sugimoto M. Miyajima H, et al. Among authors: kono s. Blood Cells Mol Dis. 2002 Nov-Dec;29(3):433-8. doi: 10.1006/bcmd.2002.0561. Blood Cells Mol Dis. 2002. PMID: 12547232

8

An altered GABA-A receptor function in spinocerebellar ataxia type 6 and familial hemiplegic migraine type 1 associated with the CACNA1A gene mutation.

Kono S, Terada T, Ouchi Y, Miyajima H. Kono S, et al. BBA Clin. 2014 Sep 28;2:56-61. doi: 10.1016/j.bbacli.2014.09.005. eCollection 2014 Dec. BBA Clin. 2014. PMID: 26675662 Free PMC article.

9

Cys-881 is essential for the trafficking and secretion of truncated mutant ceruloplasmin in aceruloplasminemia.

Kono S, Suzuki H, Oda T, Shirakawa K, Takahashi Y, Kitagawa M, Miyajima H. Kono S, et al. J Hepatol. 2007 Dec;47(6):844-50. doi: 10.1016/j.jhep.2007.05.013. Epub 2007 Jun 18. J Hepatol. 2007. PMID: 17637479

10

Brain and liver iron accumulation in aceruloplasminemia.

Fujita K, Osaki Y, Harada M, Kono S, Miyajima H, Izumi Y, Kaji R. Fujita K, et al. Among authors: kono s. Neurology. 2013 Dec 10;81(24):2145-6. doi: 10.1212/01.wnl.0000437304.30227.bd. Neurology. 2013. PMID: 24323439 No abstract available.

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