Suzuki Y - Search Results

1

Association of the hCLCA1 gene with childhood and adult asthma.

Kamada F, Suzuki Y, Shao C, Tamari M, Hasegawa K, Hirota T, Shimizu M, Takahashi N, Mao XQ, Doi S, Fujiwara H, Miyatake A, Fujita K, Chiba Y, Aoki Y, Kure S, Tamura G, Shirakawa T, Matsubara Y. Kamada F, et al. Among authors: suzuki y. Genes Immun. 2004 Nov;5(7):540-7. doi: 10.1038/sj.gene.6364124. Genes Immun. 2004. PMID: 15318163

2

Haplotype analysis suggests that the two predominant mutations in Japanese patients with holocarboxylase synthetase deficiency are founder mutations.

Yang X, Aoki Y, Li X, Sakamoto O, Hiratsuka M, Gibson KM, Kure S, Narisawa K, Matsubara Y, Suzuki Y. Yang X, et al. Among authors: suzuki y. J Hum Genet. 2000;45(6):358-62. doi: 10.1007/s100380070008. J Hum Genet. 2000. PMID: 11185745

3

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

4

A novel mutation in glial fibrillary acidic protein gene in a patient with Alexander disease.

Aoki Y, Haginoya K, Munakata M, Yokoyama H, Nishio T, Togashi N, Ito T, Suzuki Y, Kure S, Iinuma K, Brenner M, Matsubara Y. Aoki Y, et al. Among authors: suzuki y. Neurosci Lett. 2001 Oct 19;312(2):71-4. doi: 10.1016/s0304-3940(01)02139-5. Neurosci Lett. 2001. PMID: 11595337

5

Purification and properties of bovine liver holocarboxylase synthetase.

Chiba Y, Suzuki Y, Aoki Y, Ishida Y, Narisawa K. Chiba Y, et al. Among authors: suzuki y. Arch Biochem Biophys. 1994 Aug 15;313(1):8-14. doi: 10.1006/abbi.1994.1351. Arch Biochem Biophys. 1994. PMID: 8053691

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: suzuki y. 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

Glycogen storage disease type Ib: structural and mutational analysis of the microsomal glucose-6-phosphate transporter gene.

Hou DC, Kure S, Suzuki Y, Hasegawa Y, Hara Y, Inoue T, Kida Y, Matsubara Y, Narisawa K. Hou DC, et al. Among authors: suzuki y. Am J Med Genet. 1999 Sep 17;86(3):253-7. doi: 10.1002/(sici)1096-8628(19990917)86:3<253::aid-ajmg11>3.0.co;2-7. Am J Med Genet. 1999. PMID: 10482875

8

Heterogeneous mutations in the glucose-6-phosphatase gene in Japanese patients with glycogen storage disease type Ia.

Takahashi K, Akanuma J, Matsubara Y, Fujii K, Kure S, Suzuki Y, Wataya K, Sakamoto O, Aoki Y, Ogasawara M, Ohura T, Miyabayashi S, Narisawa K. Takahashi K, et al. Among authors: suzuki y. Am J Med Genet. 2000 May 15;92(2):90-4. Am J Med Genet. 2000. PMID: 10797430

9

Glycogen storage disease type Ib without neutropenia.

Kure S, Hou DC, Suzuki Y, Yamagishi A, Hiratsuka M, Fukuda T, Sugie H, Kondo N, Matsubara Y, Narisawa K. Kure S, et al. Among authors: suzuki y. J Pediatr. 2000 Aug;137(2):253-6. doi: 10.1067/mpd.2000.107472. J Pediatr. 2000. PMID: 10931421

10

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: suzuki 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

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