Matsubara Y - Search Results

1

Direct correlation between ischemic injury and extracellular glycine concentration in mice with genetically altered activities of the glycine cleavage multienzyme system.

Oda M, Kure S, Sugawara T, Yamaguchi S, Kojima K, Shinka T, Sato K, Narisawa A, Aoki Y, Matsubara Y, Omae T, Mizoi K, Kinouchi H. Oda M, et al. Among authors: matsubara y. Stroke. 2007 Jul;38(7):2157-64. doi: 10.1161/STROKEAHA.106.477026. Epub 2007 May 17. Stroke. 2007. PMID: 17510459

2

Model mice for mild-form glycine encephalopathy: behavioral and biochemical characterizations and efficacy of antagonists for the glycine binding site of N-methyl D-aspartate receptor.

Kojima-ishii K, Kure S, Ichinohe A, Shinka T, Narisawa A, Komatsuzaki S, Kanno J, Kamada F, Aoki Y, Yokoyama H, Oda M, Sugawara T, Mizoi K, Nakahara D, Matsubara Y. Kojima-ishii K, et al. Among authors: matsubara y. Pediatr Res. 2008 Sep;64(3):228-33. doi: 10.1203/PDR.0b013e3181799562. Pediatr Res. 2008. PMID: 18414141

3

Structure and expression of the glycine cleavage system in rat central nervous system.

Sakata Y, Owada Y, Sato K, Kojima K, Hisanaga K, Shinka T, Suzuki Y, Aoki Y, Satoh J, Kondo H, Matsubara Y, Kure S. Sakata Y, et al. Among authors: matsubara y. Brain Res Mol Brain Res. 2001 Oct 19;94(1-2):119-30. doi: 10.1016/s0169-328x(01)00225-x. Brain Res Mol Brain Res. 2001. PMID: 11597772

4

Heterozygous GLDC and GCSH gene mutations in transient neonatal hyperglycinemia.

Kure S, Kojima K, Ichinohe A, Maeda T, Kalmanchey R, Fekete G, Berg SZ, Filiano J, Aoki Y, Suzuki Y, Izumi T, Matsubara Y. Kure S, et al. Among authors: matsubara y. Ann Neurol. 2002 Nov;52(5):643-6. doi: 10.1002/ana.10367. Ann Neurol. 2002. PMID: 12402263

5

Glycine cleavage system in neurogenic regions.

Ichinohe A, Kure S, Mikawa S, Ueki T, Kojima K, Fujiwara K, Iinuma K, Matsubara Y, Sato K. Ichinohe A, et al. Among authors: matsubara y. Eur J Neurosci. 2004 May;19(9):2365-70. doi: 10.1111/j.0953-816X.2004.03345.x. Eur J Neurosci. 2004. PMID: 15128390 Free article.

6

Mild variant of nonketotic hyperglycinemia with typical neonatal presentations: mutational and in vitro expression analyses in two patients.

Kure S, Ichinohe A, Kojima K, Sato K, Kizaki Z, Inoue F, Yamanaka C, Matsubara Y. Kure S, et al. Among authors: matsubara y. J Pediatr. 2004 Jun;144(6):827-9. doi: 10.1016/j.jpeds.2004.02.044. J Pediatr. 2004. PMID: 15192636

7

Mutations in genes encoding the glycine cleavage system predispose to neural tube defects in mice and humans.

Narisawa A, Komatsuzaki S, Kikuchi A, Niihori T, Aoki Y, Fujiwara K, Tanemura M, Hata A, Suzuki Y, Relton CL, Grinham J, Leung KY, Partridge D, Robinson A, Stone V, Gustavsson P, Stanier P, Copp AJ, Greene ND, Tominaga T, Matsubara Y, Kure S. Narisawa A, et al. Among authors: matsubara y. Hum Mol Genet. 2012 Apr 1;21(7):1496-503. doi: 10.1093/hmg/ddr585. Epub 2011 Dec 13. Hum Mol Genet. 2012. PMID: 22171071 Free PMC article.

8

Chromosomal localization, structure, single-nucleotide polymorphisms, and expression of the human H-protein gene of the glycine cleavage system (GCSH), a candidate gene for nonketotic hyperglycinemia.

Kure S, Kojima K, Kudo T, Kanno K, Aoki Y, Suzuki Y, Shinka T, Sakata Y, Narisawa K, Matsubara Y. Kure S, et al. Among authors: matsubara y. J Hum Genet. 2001;46(7):378-84. doi: 10.1007/s100380170057. J Hum Genet. 2001. PMID: 11450847

9

Assignment of Gldc encoding glycine decarboxylase to mouse chromosome 19C by in situ hybridization and a CA repeat polymorphism in the Gldc gene.

Shinka T, Kure S, Sakata Y, Takayanagi M, Matsubara Y, Narisawa K. Shinka T, et al. Among authors: matsubara y. Cytogenet Cell Genet. 1998;83(3-4):260-1. doi: 10.1159/000015200. Cytogenet Cell Genet. 1998. PMID: 10072599 No abstract available.

10

Transgenic expression of a dominant-negative connexin26 causes degeneration of the organ of Corti and non-syndromic deafness.

Kudo T, Kure S, Ikeda K, Xia AP, Katori Y, Suzuki M, Kojima K, Ichinohe A, Suzuki Y, Aoki Y, Kobayashi T, Matsubara Y. Kudo T, et al. Among authors: matsubara y. Hum Mol Genet. 2003 May 1;12(9):995-1004. doi: 10.1093/hmg/ddg116. Hum Mol Genet. 2003. PMID: 12700168

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