Iida A - Search Results

1

Identification of sequence polymorphisms in CALM2 and analysis of association with hip osteoarthritis in a Japanese population.

Mototani H, Iida A, Nakamura Y, Ikegawa S. Mototani H, et al. Among authors: iida a. J Bone Miner Metab. 2010 Sep;28(5):547-53. doi: 10.1007/s00774-010-0161-8. Epub 2010 Mar 3. J Bone Miner Metab. 2010. PMID: 20198394

2

Allelic losses on chromosome band 11q13 in aldosterone-producing adrenal tumors.

Iida A, Blake K, Tunny T, Klemm S, Stowasser M, Hayward N, Gordon R, Nakamura Y, Imai T. Iida A, et al. Genes Chromosomes Cancer. 1995 Jan;12(1):73-5. doi: 10.1002/gcc.2870120114. Genes Chromosomes Cancer. 1995. PMID: 7534116

3

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

4

[Genetic alterations in familial and sporadic breast cancers].

Emi M, Iida A, Kasumi F, Nakamura Y. Emi M, et al. Among authors: iida a. Gan To Kagaku Ryoho. 1996 Mar;23 Suppl 1:80-3. Gan To Kagaku Ryoho. 1996. PMID: 8702317 Review. Japanese. No abstract available.

5

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

6

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

7

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

8

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

9

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

10

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

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