Rchr
J-GLOBAL ID：200901009737373792
Update date: Feb. 04, 2025
Soejima Mikiko
ソエジマ ミキコ | Soejima Mikiko
Homepage URL (1)：
http://www.med.kurume-u.ac.jp/med/foren/
Research field (2)：
Forensic medicine
, Medical biochemistry
Research keywords (3)：
遺伝子多型
, Legal medicine
, Human genetics
Research theme for competitive and other funds (8)：
- 皮膚色の多様性に関わる遺伝子多型の同定
- 輸血副作用原因遺伝子の事前診断法の確立
- 血清蛋白質遺伝子の多型解析
- 糖転移酵素遺伝子の多型解析と分子進化
- Identification of polymorhisms for determination of variation of slin color.
- Establishments of diagnosis of causal mutations of anaphylactic reactions to transfusions.
- Analysis of polymorphisms of genes of serum proteins.
- Analysis of polymorphisms and molecular evolution of galactosyltransferase genes.
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Papers (30)：
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Mikiko Soejima, Yoshiro Koda. Rapid detection of phenotypes Bombay se del and nonsecretor rs200157007 SNP (302C > T) by real-time PCR-based methods. Scientific Reports. 2021. 11. 1
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Mikiko Soejima, Yoshiro Koda. Survey and characterization of nonfunctional alleles of FUT2 in a database. Scientific Reports. 2021. 11. 1
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Mikiko Soejima, Yoshiro Koda. Detection of the weak-secretor rs1047781 (385A>T) single nucleotide polymorphism using an unlabeled probe high-resolution melting-based method. Electrophoresis. 2021. 42. 12-13. 1362-1365
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Mikiko Soejima, Yoshiro Koda. Estimation of secretor status of ABO antigens by high-resolution melting analysis of rs601338 (428G > A). Clinica Chimica Acta. 2021. 517. 86-91
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Mikiko Soejima, Yoshiro Koda. High-resolution melting analysis for detection of fusion allele of FUT2. Electrophoresis. 2021. 42. 3. 315-318
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MISC (102)：
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Kwesi Teye, Yasushi Suga, Sanae Numata, Mikiko Soejima, Norito Ishii, Rafal P. Krol, Chika Ohata, Mitsuhiro Matsuda, Masaru Honma, Akemi Ishida-Yamamoto, et al. A founder deletion of corneodesmosin gene is prevalent in Japanese patients with peeling skin disease: Identification of 2 new cases. JOURNAL OF DERMATOLOGICAL SCIENCE. 2016. 82. 2. 134-137
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Hiromitsu Araki, Xiaoliang Pang, Nobukazu Komatsu, Mikiko Soejima, Nawoe Miyata, Mari Takaki, Shigeru Muta, Tetsuro Sasada, Masanori Noguchi, Yoshiro Koda, et al. Haptoglobin promoter polymorphism rs5472 as a prognostic biomarker for peptide vaccine efficacy in castration-resistant prostate cancer patients. Cancer Immunology, Immunotherapy. 2015. 64. 1565-1573
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副島 美貴子, 神田 芳郎, 阿草 哲郎, 岩田 久人, 田辺 信介, 藤原 純子, 竹下 治男, 國頭 恭, Vi Thi Mai Lan, Tu Binh Minh, et al. ベトナム人のハプトグロビン(HP)多型解析とHP欠失アリルHPdelの地理的分布. DNA多型. 2015. 23. 1. 108-111
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Takeshita H, Fujihara J, Ueki M, Iida R, Koda Y, Soejima M, Yuasa I, Kato H, Nakajima T, Kominato Y, et al. Nonsynonymous single-nucleotide polymorphisms of the human apoptosis-related endonuclease--DNA fragmentation factor beta polypeptide, endonuclease G, and Flap endonuclease-1--genes show a low degree of genetic heterogeneity. DNA Cell Biol. 2012. 31. 36-42
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SOEJIMA Mikiko, KODA Yoshiro. Identification of novel Alu-mediated deletion by TaqMan-based real-time PCR method. 2011. 19. 148-150
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Education (2)：
- - 1991 Kyushu University School of Sciences Department of Biology
- - 1991 Kyushu University Faculty of Science
Professional career (1)：
Association Membership(s) (3)：
日本DNA多型学会
, 日本分子生物学会
, 日本法医学会
