Narisawa K - Search Results

1

Structural and expression analyses of normal and mutant mRNA encoding glycine decarboxylase: three-base deletion in mRNA causes nonketotic hyperglycinemia.

Kure S, Narisawa K, Tada K. Kure S, et al. Among authors: narisawa k. Biochem Biophys Res Commun. 1991 Feb 14;174(3):1176-82. doi: 10.1016/0006-291x(91)91545-n. Biochem Biophys Res Commun. 1991. PMID: 1996985

2

Depletion of cerebral D-serine in non-ketotic hyperglycinemia: possible involvement of glycine cleavage system in control of endogenous D-serine.

Iwama H, Takahashi K, Kure S, Hayashi F, Narisawa K, Tada K, Mizoguchi M, Takashima S, Tomita U, Nishikawa T. Iwama H, et al. Among authors: narisawa k. Biochem Biophys Res Commun. 1997 Feb 24;231(3):793-6. doi: 10.1006/bbrc.1997.6184. Biochem Biophys Res Commun. 1997. PMID: 9070895

3

Nonketotic hyperglycinemia: biochemical, molecular, and neurological aspects.

Kure S, Tada K, Narisawa K. Kure S, et al. Among authors: narisawa k. Jpn J Hum Genet. 1997 Mar;42(1):13-22. doi: 10.1007/BF02766917. Jpn J Hum Genet. 1997. PMID: 9183995 Review.

4

A missense mutation (His42Arg) in the T-protein gene from a large Israeli-Arab kindred with nonketotic hyperglycinemia.

Kure S, Mandel H, Rolland MO, Sakata Y, Shinka T, Drugan A, Boneh A, Tada K, Matsubara Y, Narisawa K. Kure S, et al. Among authors: narisawa k. Hum Genet. 1998 Apr;102(4):430-4. doi: 10.1007/s004390050716. Hum Genet. 1998. PMID: 9600239

5

A one-base deletion (183delC) and a missense mutation (D276H) in the T-protein gene from a Japanese family with nonketotic hyperglycinemia.

Kure S, Shinka T, Sakata Y, Osamu N, Takayanagi M, Tada K, Matsubara Y, Narisawa K. Kure S, et al. Among authors: narisawa k. J Hum Genet. 1998;43(2):135-7. doi: 10.1007/s100380050055. J Hum Genet. 1998. PMID: 9621520

6

Molecular analysis of glycogen storage disease type Ib: identification of a prevalent mutation among Japanese patients and assignment of a putative glucose-6-phosphate translocase gene to chromosome 11.

Kure S, Suzuki Y, Matsubara Y, Sakamoto O, Shintaku H, Isshiki G, Hoshida C, Izumi I, Sakura N, Narisawa K. Kure S, et al. Among authors: narisawa k. Biochem Biophys Res Commun. 1998 Jul 20;248(2):426-31. doi: 10.1006/bbrc.1998.8985. Biochem Biophys Res Commun. 1998. PMID: 9675154

7

Human glycine decarboxylase gene (GLDC) and its highly conserved processed pseudogene (psiGLDC): their structure and expression, and the identification of a large deletion in a family with nonketotic hyperglycinemia.

Takayanagi M, Kure S, Sakata Y, Kurihara Y, Ohya Y, Kajita M, Tada K, Matsubara Y, Narisawa K. Takayanagi M, et al. Among authors: narisawa k. Hum Genet. 2000 Mar;106(3):298-305. doi: 10.1007/s004390051041. Hum Genet. 2000. PMID: 10798358

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: narisawa k. J Hum Genet. 2001;46(7):378-84. doi: 10.1007/s100380170057. J Hum Genet. 2001. PMID: 11450847

9

Glutamate triggers internucleosomal DNA cleavage in neuronal cells.

Kure S, Tominaga T, Yoshimoto T, Tada K, Narisawa K. Kure S, et al. Among authors: narisawa k. Biochem Biophys Res Commun. 1991 Aug 30;179(1):39-45. doi: 10.1016/0006-291x(91)91330-f. Biochem Biophys Res Commun. 1991. PMID: 1679329

10

Identification of a common mutation in patients with medium-chain acyl-CoA dehydrogenase deficiency.

Matsubara Y, Narisawa K, Miyabayashi S, Tada K, Coates PM, Bachmann C, Elsas LJ 2nd, Pollitt RJ, Rhead WJ, Roe CR. Matsubara Y, et al. Among authors: narisawa k. Biochem Biophys Res Commun. 1990 Aug 31;171(1):498-505. doi: 10.1016/0006-291x(90)91421-n. Biochem Biophys Res Commun. 1990. PMID: 2393404

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