Hiratsuka M - Search Results

1

Determination of novel CYP2D6 haplotype using the targeted sequencing followed by the long-read sequencing and the functional characterization in the Japanese population.

Fukunaga K, Hishinuma E, Hiratsuka M, Kato K, Okusaka T, Saito T, Ikeda M, Yoshida T, Zembutsu H, Iwata N, Mushiroda T. Fukunaga K, et al. Among authors: hiratsuka m. J Hum Genet. 2021 Feb;66(2):139-149. doi: 10.1038/s10038-020-0815-x. Epub 2020 Aug 5. J Hum Genet. 2021. PMID: 32759992

2

Identification and characterization of mutations in patients with holocarboxylase synthetase deficiency.

Aoki Y, Li X, Sakamoto O, Hiratsuka M, Akaishi H, Xu L, Briones P, Suormala T, Baumgartner ER, Suzuki Y, Narisawa K. Aoki Y, et al. Among authors: hiratsuka m. Hum Genet. 1999 Feb;104(2):143-8. doi: 10.1007/s004390050927. Hum Genet. 1999. PMID: 10190325

3

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: hiratsuka m. J Hum Genet. 2000;45(6):358-62. doi: 10.1007/s100380070008. J Hum Genet. 2000. PMID: 11185745

4

Two novel single nucleotide polymorphisms (SNPs) of the CYP2D6 gene in Japanese individuals.

Ebisawa A, Hiratsuka M, Sakuyama K, Konno Y, Sasaki T, Mizugaki M. Ebisawa A, et al. Among authors: hiratsuka m. Drug Metab Pharmacokinet. 2005 Aug;20(4):294-9. doi: 10.2133/dmpk.20.294. Drug Metab Pharmacokinet. 2005. PMID: 16141609 Free article.

5

Functional characterization of 32 CYP2C9 allelic variants.

Niinuma Y, Saito T, Takahashi M, Tsukada C, Ito M, Hirasawa N, Hiratsuka M. Niinuma Y, et al. Among authors: hiratsuka m. Pharmacogenomics J. 2014 Apr;14(2):107-14. doi: 10.1038/tpj.2013.22. Epub 2013 Jun 11. Pharmacogenomics J. 2014. PMID: 23752738

6

Functional characterization of wild-type and 49 CYP2D6 allelic variants for N-desmethyltamoxifen 4-hydroxylation activity.

Muroi Y, Saito T, Takahashi M, Sakuyama K, Niinuma Y, Ito M, Tsukada C, Ohta K, Endo Y, Oda A, Hirasawa N, Hiratsuka M. Muroi Y, et al. Among authors: hiratsuka m. Drug Metab Pharmacokinet. 2014;29(5):360-6. doi: 10.2133/dmpk.dmpk-14-rg-014. Epub 2014 Mar 18. Drug Metab Pharmacokinet. 2014. PMID: 24647041 Free article.

7

Functional characterization of 21 CYP2C19 allelic variants for clopidogrel 2-oxidation.

Takahashi M, Saito T, Ito M, Tsukada C, Katono Y, Hosono H, Maekawa M, Shimada M, Mano N, Oda A, Hirasawa N, Hiratsuka M. Takahashi M, et al. Among authors: hiratsuka m. Pharmacogenomics J. 2015 Feb;15(1):26-32. doi: 10.1038/tpj.2014.30. Epub 2014 Jul 8. Pharmacogenomics J. 2015. PMID: 25001882

8

Genetic polymorphisms of dihydropyrimidinase in a Japanese patient with capecitabine-induced toxicity.

Hiratsuka M, Yamashita H, Akai F, Hosono H, Hishinuma E, Hirasawa N, Mori T. Hiratsuka M, et al. PLoS One. 2015 Apr 27;10(4):e0124818. doi: 10.1371/journal.pone.0124818. eCollection 2015. PLoS One. 2015. PMID: 25915935 Free PMC article.

9

Functional characterization of 21 allelic variants of dihydropyrimidinase.

Hishinuma E, Akai F, Narita Y, Maekawa M, Yamaguchi H, Mano N, Oda A, Hirasawa N, Hiratsuka M. Hishinuma E, et al. Among authors: hiratsuka m. Biochem Pharmacol. 2017 Nov 1;143:118-128. doi: 10.1016/j.bcp.2017.06.121. Epub 2017 Jun 19. Biochem Pharmacol. 2017. PMID: 28642038

10

Functional Characterization of 21 Allelic Variants of Dihydropyrimidine Dehydrogenase Identified in 1070 Japanese Individuals.

Hishinuma E, Narita Y, Saito S, Maekawa M, Akai F, Nakanishi Y, Yasuda J, Nagasaki M, Yamamoto M, Yamaguchi H, Mano N, Hirasawa N, Hiratsuka M. Hishinuma E, et al. Among authors: hiratsuka m. Drug Metab Dispos. 2018 Aug;46(8):1083-1090. doi: 10.1124/dmd.118.081737. Epub 2018 May 16. Drug Metab Dispos. 2018. PMID: 29769267

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