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Soejima Mikiko
Department of Forensic Medicine
Associate Professor
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- Simultaneous Genotyping of Three SNVs, rs5471, rs5472, and rs2000999 Involved in Serum Haptoglobin Levels by Fluorescent Probe‐Based Melting Curve Analysis
Mikiko Soejima; Yoshiro Koda
ELECTROPHORESIS, 14 Oct. 2024 - Identification and Diagnosis of Complete Haptoglobin Gene Deletion, One of the Genes Responsible for Adverse Posttransfusion Reactions
Mikiko Soejima; Yoshiro Koda
Biomedicines, 03 Apr. 2024 - FUT1 variants responsible for Bombay or para-Bombay phenotypes in a database
Mikiko Soejima; Yoshiro Koda
Scientific Reports, 14 Oct. 2023 - Detection of c.375A>G, c.385A>T, c.571C>T, and sedel2 of FUT2 via Real-Time PCR in a Single Tube
Mikiko Soejima; Yoshiro Koda
Diagnostics, 10 Jun. 2023 - Estimation of Lewis Blood Group Status by Fluorescence Melting Curve Analysis in Simultaneous Genotyping of c.385>T and Fusion Gene in FUT2 and c.59>G and c.314C>T in FUT3
Mikiko Soejima; Yoshiro Koda
Diagnostics, 01 Mar. 2023 - Fluorescence Melting Curve Analysis for Concurrent Genotyping of Three Tag SNPs in FUT3
Mikiko Soejima; Yoshiro Koda
Diagnostics, 04 Dec. 2022 - Duplex dual‐labeled fluorescence probe‐based melting curve and endpoint genotyping assays for genotyping of rs2000999 and haptoglobin gene deletion
Mikiko Soejima; Yoshiro Koda
ELECTROPHORESIS, 11 Oct. 2022 - Detection of five common variants of ABO gene by a triplex probe-based fluorescence-melting-curve-analysis
Mikiko Soejima; Yoshiro Koda
Analytical Biochemistry, Jul. 2022 - Simultaneous genotyping of three major Se enzyme inactivating SNPs of FUT2 based on a triplex probe-based fluorescence melting-curve analysis
Mikiko Soejima; Yoshiro Koda
Clinica Chimica Acta, May 2022 - Real-time PCR-based detection of the Alu-mediated deletion of FUT2 (se)
Mikiko Soejima; Yoshiro Koda
Legal Medicine, Feb. 2022 - Rapid genotyping of 508G>A (rs3745635) and 1067T>A (rs3894326) of FUT3 by a duplex Eprobe‐mediated melting curve analysis
Mikiko Soejima; Yoshiro Koda
Vox Sanguinis, 12 Jan. 2022 - Rapid detection of phenotypes Bombay se del and nonsecretor rs200157007 SNP (302C>T) by real-time PCR-based methods
Mikiko Soejima; Yoshiro Koda
Scientific Reports, 01 Dec. 2021 - Survey and characterization of nonfunctional alleles of FUT2 in a database
Mikiko Soejima; Yoshiro Koda
Scientific Reports, 01 Dec. 2021 - Detection of the weak-secretor rs1047781 (385A>T) single nucleotide polymorphism using an unlabeled probe high-resolution melting-based method
Mikiko Soejima; Yoshiro Koda
Electrophoresis, 01 Jul. 2021 - Estimation of secretor status of ABO antigens by high-resolution melting analysis of rs601338 (428>A)
Mikiko Soejima; Yoshiro Koda
Clinica Chimica Acta, 01 Jun. 2021 - High-resolution melting analysis for detection of fusion allele of FUT2
Mikiko Soejima; Yoshiro Koda
Electrophoresis, 01 Feb. 2021 - Estimation of Lewis-negative alleles by high-resolution melting analysis of three tag SNPs of FUT3
Mikiko Soejima; Yoshiro Koda
Vox Sanguinis, 2021 - Haptoglobin polymorphisms in Latin American populations
Mikiko Soejima; Yoshiro Koda
Scientific Reports, 01 Dec. 2020 - FUT2 polymorphism in Latin American populations
Mikiko Soejima; Yoshiro Koda
Clinica Chimica Acta, 01 Jun. 2020 - Serum haptoglobin correlates positively with cholesterol and triglyceride concentrations in an obese Mongolian population.
Mikiko Soejima; Lkhagvasuren Munkhtulga; Kyoji Furukawa; Sadahiko Iwamoto; Yoshiro Koda
Clinica chimica acta; international journal of clinical chemistry, 07 Mar. 2020, [Reviewed] - Genetic variation of FUT2 in a Peruvian population: identification of a novel LTR-mediated deletion and characterization of 4 nonsynonymous single-nucleotide polymorphisms
Mikiko Soejima; Yoshiro Koda
Transfusion, 01 Jul. 2019 - The haptoglobin promoter polymorphism rs5471 is the most definitive genetic determinant of serum haptoglobin level in a Ghanaian population
Mikiko Soejima; Kwesi Teye; Yoshiro Koda
Clinica Chimica Acta, 01 Aug. 2018, [Reviewed] - HP genotyping of Vietnamese: global distribution of HPdel, complete deletion allele of the haptoglobin gene
Soejima, M; Agusa, T; Iwata, H; Fujihara, J; Kunito, T; Takeshita, H; Lan, V.T.M; Minh, T.B; Takahashi, S; Trang, P.T.K; Viet, P.H; Tanabe, S; Koda, Y
Legal Medicine, 2015, [Reviewed] - An autopsy case of subarachnoid hemorrhage due to ruptured cerebral aneurysm associated with polycystic kidney disease caused by a novel PKD1 mutation
Mikiko Soejima; Yasuo Sugita; Yoshiro Koda
FORENSIC SCIENCE INTERNATIONAL, Sep. 2014, [Reviewed] - Genetic factors associated with serum haptoglobin level in a Japanese population
Mikiko Soejima; Noriaki Sagata; Nobukazu Komatsu; Tetsuro Sasada; Atsushi Kawaguchi; Kyogo Itoh; Yoshiro Koda
CLINICA CHIMICA ACTA, Jun. 2014, [Reviewed] - Evaluation of point-of-care testing of C-reactive protein in forensic autopsy cases
Mikiko Soejima; Yoshiro Koda
FORENSIC SCIENCE INTERNATIONAL, Apr. 2014, [Reviewed] - Taq Man real-time polymerase chain reaction for detection of SEC1-FUT2 hybrid alleles: Identification of novel hybrid allele
Mikiko Soejima; Yoshiro Koda
CLINICA CHIMICA ACTA, Jan. 2013, [Reviewed] - Selective quantification of human DNA by real-time PCR of FOXP2
Mikiko Soejima; Kenichi Hiroshige; Joji Yoshimoto; Yoshiro Koda
FORENSIC SCIENCE INTERNATIONAL-GENETICS, Jul. 2012, [Reviewed] - Replication study of the association of SNPs in the LHX3-QSOX2 and IGF1 loci with adult height in the Japanese population; wide-ranging comparison of each SNP genotype distribution
Fujihara Junko; Takeshita Haruo; Kimura Kaori; Kataoka Kaori; Soejima Mikiko; Koda Yoshiro; Yuasa Isao; Iida Reiko; Ueki Misuzu; Nagao Masataka; Kominato Yoshihiko; Yasuda Toshihiro
Legal Medicine, 2012 - Genetic variation of FUT2 in a Vietnamese population: identification of two novel Se enzyme-inactivating mutations
Soejima, M; Fujimoto, R; Agusa, T; Iwata, H; Fujihara, J; Takeshita, H; Minh, T.B; Trang, P.T.K; Viet, P.H; Nakajima, T; Tanabe, S; Koda, Y
Transfusion, 2012, [Reviewed] - Polymorphic trial in oxidative damage of arsenic exposed Vietnamese
Fujihara Junko; Soejima Mikiko; Yasuda Toshihiro; Koda Yoshiro; Kunito Takashi; Iwata Hisato; Tanabe Shinsuke; Takeshita Haruo
TOXICOLOGY AND APPLIED PHARMACOLOGY, 15 Oct. 2011, [Reviewed] - Confirmation that SNPs in the high mobility group-A2 gene (HMGA2) are associated with adult height in the Japanese population; wide-ranging population survey of height-related SNPs in HMGA2
Haruo Takeshita; Junko Fujihara; Mikiko Soejima; Yoshiro Koda; Kaori Kimura-Kataoka; Rei-Ichiro Ono; Isao Yuasa; Reiko Iida; Misuzu Ueki; Masataka Nagao; Toshihiro Yasuda
ELECTROPHORESIS, Jul. 2011 - Rapid Detection of Haptoglobin Gene Deletion in Alkaline-Denatured Blood by Loop-Mediated Isothermal Amplification Reaction
Mikiko Soejima; Kouichi Egashira; Hiroyuki Kawano; Atsushi Kawaguchi; Kimitaka Sagawa; Yoshiro Koda
JOURNAL OF MOLECULAR DIAGNOSTICS, May 2011, [Reviewed] - TaqMan-based real-time polymerase chain reaction for detection of FUT2 copy number variations: identification of novel Alu-mediated deletion
Mikiko Soejima; Yoshiro Koda
TRANSFUSION, Apr. 2011, [Reviewed] - Functional and genetic survey of all known single-nucleotide polymorphisms within the human deoxyribonuclease I gene in wide-ranging ethnic groups.
Fujihara J; Ueki M; Yasuda T; Iida R; Soejima M; Koda Y; Kimura-Kataoka K; Kato H; Panduro A; Tongu M; Takeshita H
DNA and cell biology, Apr. 2011, [Reviewed] - First survey of the three gene polymorphisms (PON1 Q192R, eNOS E298D and eNOS C-786T) potentially associated with coronary artery spasm in African populations and comparison with worldwide data
Junko Fujihara; Toshihiro Yasuda; Yasuyuki Kawai; Norihiro Morikawa; Kenichiro Arakawa; Yoshiro Koda; Mikiko Soejima; Kaori Kimura-Kataoka; Haruo Takeshita
CELL BIOCHEMISTRY AND FUNCTION, Mar. 2011, [Reviewed] - Y染色体のハプログループを利用した民族推定法の開発
室 友紀; 今村 真二; 中村 博明; 藤原 純子; 木村 かおり; 竹下 治男; 飯田 礼子; 安田 年博; 湯浅 勲; 副島 美貴子; 神田 芳郎
DNA多型, 2011 - ヒ素代謝に関与するAS3MT M287T 多型はアジア人特異的低変異性を示す
藤原順子; 阿草哲郎; 副島美貴子; 中島たみ子; 岩田久人; 田辺信介; 竹下治男
DNA多型, 2009 - 心筋梗塞の新規な感受性遺伝子としてのDNase I遺伝子
藤原 純子; 竹下 治男; 高塚 尚和; 安田 年博; 植木 美鈴; 飯田 礼子; 河合 康幸; 中島 たみ子; 小湊 慶彦; 副島 美貴子; 神田 芳郎
DNA多型, 2008 - Pigment epithelium-derived factor Met72Thr polymorphism in patients with diabetic microangiopathy
S Yamagishi; S Amano; Y Inagaki; T Okamoto; Y Koda; M Soejima; H Kimura
INTERNATIONAL JOURNAL OF CLINICAL PHARMACOLOGY RESEARCH, 2002, [Reviewed] - PCR analysis of Lewis-negative gene mutations and the distribution of Lewis alleles in a Japanese population
YH Liu; Y Koda; M Soejima; N Uchida; H Kimura
JOURNAL OF FORENSIC SCIENCES, Nov. 1996, [Reviewed]
- A founder deletion of corneodesmosin gene is prevalent in Japanese patients with peeling skin disease: Identification of 2 new cases
Kwesi Teye; Yasushi Suga; Sanae Numata; Mikiko Soejima; Norito Ishii; Rafal P. Krol; Chika Ohata; Mitsuhiro Matsuda; Masaru Honma; Akemi Ishida-Yamamoto; Takahiro Hamada; Yoshiro Koda; Takashi Hashimoto
JOURNAL OF DERMATOLOGICAL SCIENCE, May 2016 - Haptoglobin promoter polymorphism rs5472 as a prognostic biomarker for peptide vaccine efficacy in castration-resistant prostate cancer patients
Hiromitsu Araki; Xiaoliang Pang; Nobukazu Komatsu; Mikiko Soejima; Nawoe Miyata; Mari Takaki; Shigeru Muta; Tetsuro Sasada; Masanori Noguchi; Yoshiro Koda; Kyogo Itoh; Satoru Kuhara; Kosuke Tashiro
Cancer Immunology, Immunotherapy, 01 Dec. 2015 - 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
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; Pham Thi Kim Trang; Pham Hung Viet; 高橋 真
DNA多型, Jul. 2015 - 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.
Takeshita H; Fujihara J; Ueki M; Iida R; Koda Y; Soejima M; Yuasa I; Kato H; Nakajima T; Kominato Y; Yasuda T
DNA Cell Biol, 2012 - Identification of novel Alu-mediated deletion by TaqMan-based real-time PCR method
SOEJIMA Mikiko; KODA Yoshiro
DNA多型 = DNA polymorphism, 30 May 2011 - Distribution of 42-bp variable tandem repeat polymorphism of the cold-induced autoinflammatory syndrome 1 (CIAS1) gene in eight human populations
Toshinori Omi; Yoshiro Koda; Mikiko Soejima; Lhagvasuren Munkhtulga; Sadahiko Iwamoto
LEGAL MEDICINE, Jan. 2011 - DNASE I exon内非同義置換SNP検索 酵素性状に及ぼす置換の影響
藤原 純子; 安田 年博; 植木 美鈴; 飯田 礼子; 木村 かおり; 高塚 尚和; 神田 芳郎; 副島 美貴子; 加藤 秀章
日本法医学雑誌, Dec. 2010 - Global analysis of single nucleotide polymorphisms in the exons of human deoxyribonuclease I-like 1 and 2 genes
Junko Fujihara; Toshihiro Yasuda; Reiko Iida; Kaori Kimura-Kataoka; Mikiko Soejima; Yoshiro Koda; Hideaki Kato; Arturo Panduro; Isao Yuasa; Haruo Takeshita
ELECTROPHORESIS, Oct. 2010 - A biochemical and genetic study on all non-synonymous single nucleotide polymorphisms of the gene encoding human deoxyribonuclease I potentially relevant to autoimmunity
Toshihiro Yasuda; Misuzu Ueki; Haruo Takeshita; Junko Fujihara; Kaori Kimura-Kataoka; Reiko Iida; Etsuko Tsubota; Mikiko Soejima; Yoshiro Koda; Hideaki Kato; Arturo Panduro
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, Jul. 2010 - Development and validation of a SYBR Green I-based real-time polymerase chain reaction method for detection of haptoglobin gene deletion in clinical materials
Mikiko Soejima; Yuji Tsuchiya; Kouichi Egashira; Hiroyuki Kawano; Kimitaka Sagawa; Yoshiro Koda
TRANSFUSION, Jun. 2010 - Two transferrin variants encountered in testing of congenital disorders of glycosylation
YUASA Isao; MATSUO Muneaki; SOEJIMA Mikiko; KODA Yoshiro
DNA多型 = DNA polymorphism, 30 May 2010 - Establishment of the method for determination of Copy Number Variation (CNV) of the FUT2 based on TaqMan real-time PCR method
SOEJIMA Mikiko; KODA Yoshiro
DNA多型 = DNA polymorphism, 30 May 2010 - Global analysis of genetic variation in human arsenic (+3 oxidation state) methyltransferase (AS3MT)
Junko Fujihara; Mikiko Soejima; Toshihiro Yasuda; Yoshiro Koda; Tetsuro Agusa; Takashi Kunito; Miki Tongu; Takaya Yamada; Haruo Takeshita
TOXICOLOGY AND APPLIED PHARMACOLOGY, Mar. 2010 - Ethnic variation in genotype frequencies of delta-aminolevulinic acid dehydratase (ALAD)
Junko Fujihara; Tetsuro Agusa; Toshihiro Yasuda; Mikiko Soejima; Hideaki Kato; Arturo Panduro; Yoshiro Koda; Kaori Kimura-Kataoka; Haruo Takeshita
TOXICOLOGY LETTERS, Dec. 2009 - GENOTYPING METHOD FOR COMMON POLYMORPHISMS OF HAPTOGLOBIN AND DISTRIBUTION OF HPDEL IN ASIA
Y. Koda; M. Soejima
VOX SANGUINIS, Nov. 2009 - Haptoglobin polymorphism in Mongolian population: Comparison of the two genotyping methods
Hitomi Nakamura; Mikiko Soejima; Lkhagvasuren Munkhtulga; Sadahiko Iwamoto; Yoshiro Koda
CLINICA CHIMICA ACTA, Oct. 2009 - Simple and Sensitive Method for Identification of Human DNA by Allele-Specific Polymerase Chain Reaction of FOXP2
Kenichi Hiroshige; Mikiko Soejima; Tomoki Nishioka; Shigeo Kamimura; Yoshiro Koda
JOURNAL OF FORENSIC SCIENCES, Jul. 2009 - Genetic variation of FUT3 in Ghanaians, Caucasians, and Mongolians
Mikiko Soejima; Lkhagvasuren Munkhtulga; Sadahiko Iwamoto; Yoshiro Koda
TRANSFUSION, May 2009 - Sequence Analysis of Human TRPV6 Suggests Positive Selection Outside Africa
Mikiko Soejima; Hidenori Tachida; Yoshiro Koda
BIOCHEMICAL GENETICS, Feb. 2009 - Gln222Arg (A2317G) polymorphism in the deoxyribonuclease I gene exhibits ethnic and functional differences
Haruo Takeshita; Mikiko Soejima; Yoshiro Koda; Toshihiro Yasuda; Hisakazu Takatsuka; Junko Fujihara
CLINICAL CHEMISTRY AND LABORATORY MEDICINE, Jan. 2009 - TaqMan-Based Real-Time PCR for Genotyping Common Polymorphisms of Haptoglobin (HP1 and HP2)
Mikiko Soejima; Yoshiro Koda
CLINICAL CHEMISTRY, Nov. 2008 - Rote of non-B DNA conformations in initiating the nonallelic homologous recombination-derived Se-fus allele and the interlocus gene conversion-derived See1-FUT2-Sec1 hybrid allele - Reply
Mikiko Soejima; Yoshiro Koda
TRANSFUSION, Jul. 2008 - Genetic variation of FUT2 in Ovambos, Turks, and Mongolians
Mikiko Soejima; Tamiko Nakajima; Junko Fujihara; Haruo Takeshita; Yoshiro Koda
Transfusion, Jul. 2008 - Asian specific low mutation frequencies of the M287T polymorphism in the human arsenic (+3 oxidation state) methyltransferase (AS3MT) gene
Junko Fujihara; Mikiko Soejima; Yoshiro Koda; Takashi Kunito; Haruo Takeshita
MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS, Jul. 2008 - Rapid real-time PCR detection of HPdel directly from diluted blood samples
Mikiko Soejima; Yoshiro Koda
CLINICAL CHEMISTRY, Jun. 2008 - Extremely high prevalence of DNASE1*1 allele in African populations
Haruo Takeshita; Junko Fujihara; Mikiko Soejima; Yoshiro Koda; Toshihiro Yasuda; Tamiko Nakajima
CELL BIOCHEMISTRY AND FUNCTION, Mar. 2008 - Sec1-FUT2-Sec1 hybrid allele generated by interlocus gene conversion
Mikiko Soejima; Junko Fujihara; Haruo Takeshita; Yoshiro Koda
TRANSFUSION, Mar. 2008 - Distinct single nucleotide polymorphism pattern at the FUT2 promoter among human populations
Mikiko Soejima; Yoshiro Koda
ANNALS OF HEMATOLOGY, Jan. 2008 - The distribution of haptoglobin-gene deletion (Hp(del)) is restricted to East Asians
Mikiko Soejima; Yoshiro Koda; Junko Fujihara; Haruo Takeshita
TRANSFUSION, Oct. 2007 - Genetic variation of FUT2 in a Ghanaian population: identification of four novel mutations and inference of balancing selection
Mikiko Soejima; Hao Pang; Yoshiro Koda
ANNALS OF HEMATOLOGY, Mar. 2007 - Possible role of a TRPV6 haplotype in selective adanvantage in non-African populations by its plausible increased calcium permeability
Yuka Sudo; Yasuhito Uezono; Kiyotaka Matsuo; Mikiko Soejima; Yoshiro Koda
JOURNAL OF PHARMACOLOGICAL SCIENCES, 2007 - Population differences of two coding SNPs in pigmentation-related genes SLC24A5 and SLC45A2
Mikiko Soejima; Yoshiro Koda
INTERNATIONAL JOURNAL OF LEGAL MEDICINE, Jan. 2007 - Expression of Mina53, a product of a Myc target gene in mouse testis
M Tsuneoka; Y Nishimune; K Ohta; K Teye; H Tanaka; M Soejima; H Iida; T Inokuchi; K Hiroshi; Y Koda
INTERNATIONAL JOURNAL OF ANDROLOGY, Apr. 2006 - Haptoglobin gene promoter polymorphism and haplotypes are unique in different populations
Kwesi Teye; Mikiko Soejima; Isaac K. E. Quaye; Hao Pang; Makoto Tsuneoka; Yoshiro Koda; Hiroshi Kimura
HUMAN BIOLOGY, Feb. 2006 - Evidence for recent positive selection at the human AIM1 locus in a European population
M Soejima; H Tachida; T Ishida; A Sano; Y Koda
MOLECULAR BIOLOGY AND EVOLUTION, Jan. 2006 - Denaturing high-performance liquid chromatography-based genotyping and genetic variation of FUT2 in Sri Lanka
M Soejima; Y Koda
TRANSFUSION, Dec. 2005 - Molecular mechanisms of Lewis antigen expression
Mikiko Soejima; Yoshiro Koda
Legal Medicine, Jul. 2005 - A novel Myc-target gene, mimitin, that is involved in cell proliferation of esophageal squamous cell carcinoma
M Tsuneoka; K Teye; N Arima; M Soejima; H Otera; K Ohashi; Y Koga; H Fujita; K Shirouzu; H Kimura; Y Koda
JOURNAL OF BIOLOGICAL CHEMISTRY, May 2005 - Nucleotide sequence analyses of human complement 6 (C6) gene suggest balancing selection
M Soejima; H Tachida; M Tsuneoka; O Takenaka; H Kimura; Y Koda
ANNALS OF HUMAN GENETICS, May 2005 - Two novel FUT3 alleles responsible for Lewis-null phenotypes in Sri Lanka
M Soejima; H Kimura; Y Koda
TRANSFUSION, Oct. 2004 - A novel tetrameric short tandem repeat located in the 3 ' flanking region of the human ABO-secretor gene (FUT2) and association between FUT2 and FUT2/01 loci
H Pang; M Soejima; Y Koda; H Kimura
HUMAN BIOLOGY, Oct. 2004 - A novel I247T missense mutation in the haptoglobin 2 beta-chain decreases the expression of the protein and is associated with ahaptoglobinemia
K Teye; IKE Quaye; Y Koda; M Soejima; H Pang; M Tsuneoka; AGB Amoah; A Adjei; H Kimura
HUMAN GENETICS, Apr. 2004 - Population differences in DNA sequence variation and linkage disequilibrium at the PON1 gene
Y Koda; H Tachida; M Soejima; O Takenaka; H Kimura
ANNALS OF HUMAN GENETICS, Mar. 2004 - DNA sequence variation of the human ABO-secretor locus (FUT2) in New Guinean populations: possible early human migration from Africa
Y Koda; T Ishida; H Tachida; BJ Wang; H Pang; M Soejima; A Soemantri; H Kimura
HUMAN GENETICS, Nov. 2003 - A-61C and C-101G Hp gene promoter polymorphisms are, respectively, associated with ahaptoglobinaemia and hypohaptoglobinaemia in Ghana
K Teye; IKE Quaye; Y Koda; M Soejima; M Tsuneoka; H Pang; Ekem, I; AGB Amoah; A Adjei; H Kimura
CLINICAL GENETICS, Nov. 2003 - Polymorphisms of sorbitol dehydrogenase (SDH) gene and susceptibility to diabetic retinopathy
S Amano; S Yamagishi; Y Koda; M Tsuneoka; M Soejima; T Okamoto; Y Inagaki; K Yamada; H Kimura
MEDICAL HYPOTHESES, Apr. 2003 - A novel Myc target gene, mina53, that is involved in cell proliferation
M Tsuneoka; Y Koda; M Soejima; K Teye; H Kimura
JOURNAL OF BIOLOGICAL CHEMISTRY, Sep. 2002 - Haptoglobin genotype and diabetic microangiopathies in Japanese diabetic patients
Y Koda; M Soejima; S Yamagishi; S Amano; T Okamoto; Y Inagaki; K Yamada; H Kimura
DIABETOLOGIA, Jul. 2002 - Heterozygosity for two novel null alleles of the KEL gene causes the Kell-null phenotype in a Japanese woman
Y Koda; M Soejima; M Tsuneoka; K Yasumoto; T Higashitani; K Sagawa; H Kimura
BRITISH JOURNAL OF HAEMATOLOGY, Apr. 2002 - Heterozygosity for two novel null alleles of the KEL gene causes the Kell-null phenotype in a Japanese woman
Y Koda; M Soejima; M Tsuneoka; K Yasumoto; T Higashitani; K Sagawa; H Kimura
BRITISH JOURNAL OF HAEMATOLOGY, Apr. 2002 - Identification of human phosphoglucomutase 3 (PGM(3)) as N-acetylglucosamine-phosphate mutase (AGM(1))
H Pang; Y Koda; M Soejima; H Kimura
ANNALS OF HUMAN GENETICS, Mar. 2002 - Polymorphisms of eight STR loci in Chinese and African (Xhosa) populations
BJ Wang; H Pang; Y Koda; M Soejima; H Kimura
FORENSIC SCIENCE INTERNATIONAL, Feb. 2002 - Polymorphisms of eight STR loci in Chinese and African (Xhosa) populations
BJ Wang; H Pang; Y Koda; M Soejima; H Kimura
FORENSIC SCIENCE INTERNATIONAL, Feb. 2002 - Three-base deletion and one-base insertion of the alpha(1,4)galactosyltransferase gene responsible for the p phenotype
Y Koda; M Soejima; H Sato; Y Maeda; H Kimura
TRANSFUSION, Jan. 2002 - A novel myc target gene, mina53, that is involved in cell proliferation.
J Biol Chem., 2002 - Three-base deletion and one-base insertion of the alpha(1,4)galactosyltransferase gene responsible for the p phenotype
Y Koda; M Soejima; H Sato; Y Maeda; H Kimura
TRANSFUSION, Jan. 2002 - Polymorphism of the human ABO-secretor locus (FUT2) in four populations in Asia: indication of distinct Asian subpopulations
H Pang; Y Koda; M Soejima; N Fujitani; T Ogaki; A Saito; T Kawasaki; H Kimura
ANNALS OF HUMAN GENETICS, Sep. 2001 - Polymorphism of the human ABO-secretor locus (FUT2) in four populations in Asia: indication of distinct Asian subpopulations
H Pang; Y Koda; M Soejima; N Fujitani; T Ogaki; A Saito; T Kawasaki; H Kimura
ANNALS OF HUMAN GENETICS, Sep. 2001 - Polymorphisms of human paraoxonase 1 (PON 1) gene promoter
KODA Yoshiro; SOEJIMA Mikiko; KIMURA Hiroshi
DNA多型 = DNA polymorphism, 30 Jun. 2001 - Contrasting patterns of polymorphisms at the ABO-secretor gene (FUT2) and plasma alpha(1,3)fucosyltransferase gene (FUT6) in human populations
Y Koda; H Tachida; H Pang; YH Liu; M Soejima; AA Ghaderi; O Takenaka; H Kimura
GENETICS, Jun. 2001 - Contrasting patterns of polymorphisms at the ABO-secretor gene (FUT2) and plasma alpha(1,3)fucosyltransferase gene (FUT6) in human populations
Y Koda; H Tachida; H Pang; YH Liu; M Soejima; AA Ghaderi; O Takenaka; H Kimura
GENETICS, Jun. 2001 - Caveolae in mesangial cells and caveolin expression in mesangial proliferative glomerulonephritis
O Tamai; N Oka; T Kikuchi; Y Koda; M Soejima; Y Wada; M Fujisawa; K Tamaki; H Kawachi; F Shimizu; H Kimura; T Imaizumi; S Okuda
KIDNEY INTERNATIONAL, Feb. 2001 - The polymorphisms of fucosyltransferases
Yoshiro Koda; Mikiko Soejima; Hiroshi Kimura
Legal Medicine, 2001 - Two Distinct Alu-Mediated Deletions of the Human ABO-Secretor (FUT2) Locus in Samoan and Bangladeshi Populations
Hao Pang; Noboru Fujitani; Mikiko Soejima; Yoshiro Koda; Mohammed Nasimul Islam; A. K. M. Shamsul Islam; Hiroshi Kimura
HUMAN MUTATION, Sep. 2000 - Two Distinct Alu-Mediated Deletions of the Human ABO-Secretor (FUT2) Locus in Samoan and Bangladeshi Populations
Hao Pang; Noboru Fujitani; Mikiko Soejima; Yoshiro Koda; Mohammed Nasimul Islam; A. K. M. Shamsul Islam; Hiroshi Kimura
HUMAN MUTATION, Sep. 2000 - Ancient origin of the null allele se(428) of the human ABO-Secretor locus (FUT2)
Y Koda; H Tachida; M Soejima; O Takenaka; H Kimura
JOURNAL OF MOLECULAR EVOLUTION, Mar. 2000 - Ancient origin of the null allele se(428) of the human ABO-Secretor locus (FUT2)
Y Koda; H Tachida; M Soejima; O Takenaka; H Kimura
JOURNAL OF MOLECULAR EVOLUTION, Mar. 2000 - Simple PCR detection of haptoglobin gene deletion in anhaptoglobinemic patients with antihaptoglobin antibody that causes anaphylactic transfusion reactions
Y Koda; Y Watanabe; M Soejima; E Shimada; M Nishimura; K Morishita; S Moriya; S Mitsunaga; K Tadokoro; H Kimura
BLOOD, Feb. 2000 - Simple PCR detection of haptoglobin gene deletion in anhaptoglobinemic patients with antihaptoglobin antibody that causes anaphylactic transfusion reactions
Y Koda; Y Watanabe; M Soejima; E Shimada; M Nishimura; K Morishita; S Moriya; S Mitsunaga; K Tadokoro; H Kimura
BLOOD, Feb. 2000 - An Alu-mediated large deletion of the FUT2 gene in individuals with the ABO-Bombay phenotype
Y Koda; M Soejima; PH Johnson; E Smart; H Kimura
HUMAN GENETICS, Jan. 2000 - An Alu-mediated large deletion of the FUT2 gene in individuals with the ABO-Bombay phenotype
Y Koda; M Soejima; PH Johnson; E Smart; H Kimura
HUMAN GENETICS, Jan. 2000 - Functional analysis of the 5 '-flanking region of FTA for expression of rat GDP-L-fucose :beta-D-galactoside 2-alpha-L-fucosyltransferase
M Soejima; Y Koda; BJ Wang; H Kimura
EUROPEAN JOURNAL OF BIOCHEMISTRY, Nov. 1999 - Functional analysis of the 5 '-flanking region of FTA for expression of rat GDP-L-fucose :beta-D-galactoside 2-alpha-L-fucosyltransferase
M Soejima; Y Koda; BJ Wang; H Kimura
EUROPEAN JOURNAL OF BIOCHEMISTRY, Nov. 1999 - Presence of H Type 3/4 chains of ABO histo-blood group system in serous cells of human submandibular gland and regulation of their expression by the secretor gene (FUT2)
YH Liu; N Fujitani; Y Koda; M Soejima; H Kimura
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, Jul. 1999 - Allelic diversity of the human plasma alpha(1,3)fucosyltransferase gene (FUT6)
H Pang; Y Koda; M Soejima; T Schlaphoff; ED Du Toit; H Kimura
ANNALS OF HUMAN GENETICS, Jul. 1999 - Presence of H Type 3/4 chains of ABO histo-blood group system in serous cells of human submandibular gland and regulation of their expression by the secretor gene (FUT2)
YH Liu; N Fujitani; Y Koda; M Soejima; H Kimura
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, Jul. 1999 - Allelic diversity of the human plasma α(1,3)fucosyltransferase gene (FUT6)
H. Pang; Y. Koda; M. Soejima; T. Schlaphoff; E. D. Du Toit; Hiroshi Kimura
Annals of Human Genetics, Jul. 1999 - Lewis (FUT3) genotypes in two different Chinese populations
YH Liu; Y Koda; M Soejima; H Pang; B Wang; H Kimura
JOURNAL OF FORENSIC SCIENCES, Jan. 1999 - The fusion gene at the ABO-secretor locus (FUT2): absence in Chinese populations
YH Liu; Y Koda; M Soejima; H Pang; BJ Wang; DS Kim; HB Oh; H Kimura
JOURNAL OF HUMAN GENETICS, 1999 - Lewis (FUT3) genotypes in two different Chinese populations
YH Liu; Y Koda; M Soejima; H Pang; B Wang; H Kimura
JOURNAL OF FORENSIC SCIENCES, Jan. 1999 - Lewis (FUT3) genotypes in two different Chinese populations
YH Liu; Y Koda; M Soejima; H Pang; B Wang; H Kimura
JOURNAL OF FORENSIC SCIENCES, Jan. 1999 - The fusion gene at the ABO-secretor locus (FUT2): absence in Chinese populations
YH Liu; Y Koda; M Soejima; H Pang; BJ Wang; DS Kim; HB Oh; H Kimura
JOURNAL OF HUMAN GENETICS, 1999 - 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
H Pang; Y Koda; M Soejima; H Kimura
GLYCOCONJUGATE JOURNAL, Oct. 1998 - 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
H Pang; Y Koda; M Soejima; H Kimura
GLYCOCONJUGATE JOURNAL, Oct. 1998 - Changing transcription start sites in H-type alpha(1,2)fucosyltransferase gene (FUT1) during differentiation of the human erythroid lineage
Y Koda; M Soejima; H Kimura
EUROPEAN JOURNAL OF BIOCHEMISTRY, Sep. 1998 - Extensive polymorphism of the FUT2 gene in an African (Xhosa) population of South Africa
YH Liu; Y Koda; M Soejima; H Pang; T Schlaphoff; ED du Toit; H Kimura
HUMAN GENETICS, Aug. 1998 - Extensive polymorphism of the FUT2 gene in an African (Xhosa) population of South Africa
YH Liu; Y Koda; M Soejima; H Pang; T Schlaphoff; ED du Toit; H Kimura
HUMAN GENETICS, Aug. 1998 - Five novel missense mutations of the Lewis gene (FUT3) in African (Xhosa) and Caucasian populations in South Africa
H Pang; YH Liu; Y Koda; M Soejima; JT Jia; T Schlaphoff; ED du Toit; H Kimura
HUMAN GENETICS, Jun. 1998 - Identification of a mutation (A1879G) of transferrin from cDNA prepared from peripheral blood cells
H Pang; Y Koda; M Soejima; H Kimura
ANNALS OF HUMAN GENETICS, May 1998 - Identification of a mutation (A1879G) of transferrin from cDNA prepared from peripheral blood cells
H Pang; Y Koda; M Soejima; H Kimura
ANNALS OF HUMAN GENETICS, May 1998 - The haptoglobin-gene deletion responsible for anhaptoglobinemia
Y Koda; M Soejima; N Yoshioka; H Kimura
AMERICAN JOURNAL OF HUMAN GENETICS, Feb. 1998 - Anhaptoglobinemia and hypohaptoglobinemia
Y. Koda; M. Soejima; H. Kimura
Ryōikibetsu shōkōgun shirīzu, 1998 - Missense mutation of FUT1 and deletion of FUT2 are responsible for Indian Bombay phenotype of ABO blood group system
Y Koda; M Soejima; PH Johnson; E Smart; H Kimura
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, Sep. 1997 - Structure and expression of the gene encoding secretor-type galactoside 2-alpha-L-fucosyltransferase (FUT2)
Y Koda; M Soejima; BJ Wang; H Kimura
EUROPEAN JOURNAL OF BIOCHEMISTRY, Jun. 1997 - 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
Y Koda; M Soejima; H Kimura
JOURNAL OF BIOLOGICAL CHEMISTRY, Mar. 1997 - Two missense mutations of H type alpha(1,2)fucosyltransferase gene (FUT1) responsible for para-bombay phenotype
BJ Wang; Y Koda; M Soejima; H Kimura
VOX SANGUINIS, 1997 - 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
Y Koda; M Soejima; YH Liu; H Kimura
AMERICAN JOURNAL OF HUMAN GENETICS, Aug. 1996 - Establishment and characterization of immortalized human coronary endothelial cells
R Nakano; N Murahashi; Y Sasaguri; A Tanimoto; M Soejima; N Arima; T Hamada
BIOCHEMISTRY AND MOLECULAR BIOLOGY INTERNATIONAL, Jul. 1995 - DETECTION OF G TO A MISSENSE MUTATION OF LEWIS-NEGATIVE GENE BY PCR ON GENOMIC DNA
Y KODA; M SOEJIMA; H KIMURA
VOX SANGUINIS, Oct. 1994 - Detection of T to G mutation at position 59 in the Lewis gene by mismatch polymerase chain reaction
International Journal of Legal Medicine
- 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.
