Koda Y - Search Results

1

Polymorphisms of sorbitol dehydrogenase (SDH) gene and susceptibility to diabetic retinopathy.

Amano S, Yamagishi S, Koda Y, Tsuneoka M, Soejima M, Okamoto T, Inagaki Y, Yamada K, Kimura H. Amano S, et al. Among authors: koda y. Med Hypotheses. 2003 Apr;60(4):550-1. doi: 10.1016/s0306-9877(03)00013-6. Med Hypotheses. 2003. PMID: 12615520

2

Detection of T to G mutation at position 59 in the Lewis gene by mismatch polymerase chain reaction.

Koda Y, Soejima M, Kimura H. Koda Y, et al. Int J Legal Med. 1995;107(6):280-2. doi: 10.1007/BF01246873. Int J Legal Med. 1995. PMID: 7577689

3

Detection of G to A missense mutation of Lewis-negative gene by PCR on genomic DNA.

Koda Y, Soejima M, Kimura H. Koda Y, et al. Vox Sang. 1994;67(3):327-8. doi: 10.1111/j.1423-0410.1994.tb01268.x. Vox Sang. 1994. PMID: 7863639 No abstract available.

4

Analysis of Lewis fucosyltransferase genes from the human gastric mucosa of Lewis-positive and -negative individuals.

Koda Y, Kimura H, Mekada E. Koda Y, et al. Blood. 1993 Nov 1;82(9):2915-9. Blood. 1993. PMID: 8219240 Free article.

5

Rubinstein-Taybi Syndrome with thymic hypoplasia.

Kimura H, Ito Y, Koda Y, Hase Y. Kimura H, et al. Among authors: koda y. Am J Med Genet. 1993 May 15;46(3):293-6. doi: 10.1002/ajmg.1320460311. Am J Med Genet. 1993. PMID: 8488874

6

Measurement of ABH blood group substances in human saliva by immunoassay using artificial antigens as standard substances.

Wang B, Wang Q, Koda Y, Akiyama K, Kimura H. Wang B, et al. Among authors: koda y. Nihon Hoigaku Zasshi. 1996 Apr;50(2):43-9. Nihon Hoigaku Zasshi. 1996. PMID: 8691648

7

Molecular basis for secretor type alpha(1,2)-fucosyltransferase gene deficiency in a Japanese population: a fusion gene generated by unequal crossover responsible for the enzyme deficiency.

Koda Y, Soejima M, Liu Y, Kimura H. Koda Y, et al. Am J Hum Genet. 1996 Aug;59(2):343-50. Am J Hum Genet. 1996. PMID: 8755920 Free PMC article.

8

PCR analysis of Lewis-negative gene mutations and the distribution of Lewis alleles in a Japanese population.

Liu Y, Koda Y, Soejima M, Uchida N, Kimura H. Liu Y, et al. Among authors: koda y. J Forensic Sci. 1996 Nov;41(6):1018-21. J Forensic Sci. 1996. PMID: 8914289

9

Two missense mutations of H type alpha(1,2)fucosyltransferase gene (FUT1) responsible for para-Bombay phenotype.

Wang B, Koda Y, Soejima M, Kimura H. Wang B, et al. Among authors: koda y. Vox Sang. 1997;72(1):31-5. doi: 10.1046/j.1423-0410.1997.00031.x. Vox Sang. 1997. PMID: 9031498 Clinical Trial.

10

Structure and expression of H-type GDP-L-fucose:beta-D-galactoside 2-alpha-L-fucosyltransferase gene (FUT1). Two transcription start sites and alternative splicing generate several forms of FUT1 mRNA.

Koda Y, Soejima M, Kimura H. Koda Y, et al. J Biol Chem. 1997 Mar 14;272(11):7501-5. doi: 10.1074/jbc.272.11.7501. J Biol Chem. 1997. PMID: 9054453 Free article.

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