Kimura H - Search Results

1

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. Among authors: kimura h. Int J Legal Med. 1995;107(6):280-2. doi: 10.1007/BF01246873. Int J Legal Med. 1995. PMID: 7577689

2

Significance of each of three missense mutations, G484A, G667A, and G808A, present in an inactive allele of the human Lewis gene (FUT3) for alpha(1,3/1,4)fucosyltransferase inactivation.

Pang H, Koda Y, Soejima M, Kimura H. Pang H, et al. Among authors: kimura h. Glycoconj J. 1998 Oct;15(10):961-7. doi: 10.1023/a:1006981724233. Glycoconj J. 1998. PMID: 10211701

3

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. Among authors: kimura h. Blood. 1993 Nov 1;82(9):2915-9. Blood. 1993. PMID: 8219240 Free article.

4

A fatal case of hyperthermia due to tricyclic antidepressant intoxication.

Fujitani N, Koda Y, Okamura T, Hattori H, Kimura H. Fujitani N, et al. Among authors: kimura h. Leg Med (Tokyo). 2000 Oct;2(3):152-5. doi: 10.1016/s1344-6223(00)80015-2. Leg Med (Tokyo). 2000. PMID: 12935717

5

Contrasting patterns of polymorphisms at the ABO-secretor gene (FUT2) and plasma alpha(1,3)fucosyltransferase gene (FUT6) in human populations.

Koda Y, Tachida H, Pang H, Liu Y, Soejima M, Ghaderi AA, Takenaka O, Kimura H. Koda Y, et al. Among authors: kimura h. Genetics. 2001 Jun;158(2):747-56. doi: 10.1093/genetics/158.2.747. Genetics. 2001. PMID: 11404338 Free PMC article.

6

Polymorphism of the human ABO-Secretor locus (FUT2) in four populations in Asia: indication of distinct Asian subpopulations.

Pang H, Koda Y, Soejima M, Fujitani N, Ogaki T, Saito A, Kawasaki T, Kimura H. Pang H, et al. Among authors: kimura h. Ann Hum Genet. 2001 Sep;65(Pt 5):429-37. doi: 10.1017/S0003480001008788. Ann Hum Genet. 2001. PMID: 11806852

7

Identification of human phosphoglucomutase 3 (PGM3) as N-acetylglucosamine-phosphate mutase (AGM1).

Pang H, Koda Y, Soejima M, Kimura H. Pang H, et al. Among authors: kimura h. Ann Hum Genet. 2002 Mar;66(Pt 2):139-44. doi: 10.1017/S0003480002001033. Ann Hum Genet. 2002. PMID: 12174217

8

Pigment epithelium-derived factor Met72Thr polymorphism in patients with diabetic microangiopathy.

Yamagishi S, Amano S, Inagaki Y, Okamoto T, Koda Y, Soejima M, Kimura H. Yamagishi S, et al. Among authors: kimura h. Int J Clin Pharmacol Res. 2002;22(3-4):67-71. Int J Clin Pharmacol Res. 2002. PMID: 12837042

9

Myocardial "elektive disseminierte Parenchymnekrose" revisited.

Fujitani N, Koda Y, Onishi S, Kimura H. Fujitani N, et al. Among authors: kimura h. Leg Med (Tokyo). 1999 Sep;1(3):174-5. doi: 10.1016/s1344-6223(99)80032-7. Leg Med (Tokyo). 1999. PMID: 12935490

10

The polymorphisms of fucosyltransferases.

Koda Y, Soejima M, Kimura H. Koda Y, et al. Among authors: kimura h. Leg Med (Tokyo). 2001 Mar;3(1):2-14. doi: 10.1016/s1344-6223(01)00005-0. Leg Med (Tokyo). 2001. PMID: 12935727

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