Iida A - Search Results

1

An aspartic acid repeat polymorphism in asporin inhibits chondrogenesis and increases susceptibility to osteoarthritis.

Kizawa H, Kou I, Iida A, Sudo A, Miyamoto Y, Fukuda A, Mabuchi A, Kotani A, Kawakami A, Yamamoto S, Uchida A, Nakamura K, Notoya K, Nakamura Y, Ikegawa S. Kizawa H, et al. Among authors: iida a. Nat Genet. 2005 Feb;37(2):138-44. doi: 10.1038/ng1496. Epub 2005 Jan 9. Nat Genet. 2005. PMID: 15640800

2

Isolation and characterization of a novel gene encoding nuclear protein at a locus (D11S636) tightly linked to multiple endocrine neoplasia type 1 (MEN1).

Toda T, Iida A, Miwa T, Nakamura Y, Imai T. Toda T, et al. Among authors: iida a. Hum Mol Genet. 1994 Mar;3(3):465-70. doi: 10.1093/hmg/3.3.465. Hum Mol Genet. 1994. PMID: 7912130

3

Catalog of 320 single nucleotide polymorphisms (SNPs) in 20 quinone oxidoreductase and sulfotransferase genes.

Iida A, Sekine A, Saito S, Kitamura Y, Kitamoto T, Osawa S, Mishima C, Nakamura Y. Iida A, et al. J Hum Genet. 2001;46(4):225-40. doi: 10.1007/s100380170093. J Hum Genet. 2001. PMID: 11322664

4

Identification of single-nucleotide polymorphisms (SNPs) of human N-acetyltransferase genes NAT1, NAT2, AANAT, ARD1 and L1CAM in the Japanese population.

Sekine A, Saito S, Iida A, Mitsunobu Y, Higuchi S, Harigae S, Nakamura Y. Sekine A, et al. Among authors: iida a. J Hum Genet. 2001;46(6):314-9. doi: 10.1007/s100380170065. J Hum Genet. 2001. PMID: 11393533

5

Seventy genetic variations in human microsomal and soluble epoxide hydrolase genes (EPHX1 and EPHX2) in the Japanese population.

Saito S, Iida A, Sekine A, Eguchi C, Miura Y, Nakamura Y. Saito S, et al. Among authors: iida a. J Hum Genet. 2001;46(6):325-9. doi: 10.1007/s100380170067. J Hum Genet. 2001. PMID: 11393535

6

Catalog of 434 single-nucleotide polymorphisms (SNPs) in genes of the alcohol dehydrogenase, glutathione S-transferase, and nicotinamide adenine dinucleotide, reduced (NADH) ubiquinone oxidoreductase families.

Iida A, Saito S, Sekine A, Kitamoto T, Kitamura Y, Mishima C, Osawa S, Kondo K, Harigae S, Nakamura Y. Iida A, et al. J Hum Genet. 2001;46(7):385-407. doi: 10.1007/s100380170058. J Hum Genet. 2001. PMID: 11450848

7

High-density single-nucleotide polymorphism (SNP) map of the 150-kb region corresponding to the human ATP-binding cassette transporter A1 (ABCA1) gene.

Iida A, Saito S, Sekine A, Kitamura Y, Kondo K, Mishima C, Osawa S, Harigae S, Nakamura Y. Iida A, et al. J Hum Genet. 2001;46(9):522-8. doi: 10.1007/s100380170034. J Hum Genet. 2001. PMID: 11558901

8

Identification of 197 genetic variations in six human methyltranferase genes in the Japanese population.

Saito S, Iida A, Sekine A, Miura Y, Sakamoto T, Ogawa C, Kawauchi S, Higuchi S, Nakamura Y. Saito S, et al. Among authors: iida a. J Hum Genet. 2001;46(9):529-37. doi: 10.1007/s100380170035. J Hum Genet. 2001. PMID: 11558902

9

Catalog of 46 single-nucleotide polymorphisms (SNPs) in the microsomal glutathione S-transferase 1 (MGST1) gene.

Iida A, Saito S, Sekine A, Harigae S, Osawa S, Mishima C, Kondo K, Kitamura Y, Nakamura Y. Iida A, et al. J Hum Genet. 2001;46(10):590-4. doi: 10.1007/s100380170026. J Hum Genet. 2001. PMID: 11587073

10

High-density single-nucleotide polymorphism (SNP) map in the 96-kb region containing the entire human DiGeorge syndrome critical region 2 (DGCR2) gene at 22q11.2.

Iida A, Ohnishi Y, Ozaki K, Ariji Y, Nakamura Y, Tanaka T. Iida A, et al. J Hum Genet. 2001;46(10):604-8. doi: 10.1007/s100380170029. J Hum Genet. 2001. PMID: 11589220

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