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Koda Yoshiro
Department of Forensic Medicine
Professor
Career
■ Career
- May 2003 - Present
Kurume University, School of Medicine, 教授 - Apr. 2000 - Apr. 2003
Kurume University, School of Medicine, 助教授 - Apr. 1997 - Mar. 2000
Kurume University, School of Medicine, 講師 - Jan. 1991 - Mar. 1997
Kurume University, School of Medicine, 助手 - Apr. 1989 - Dec. 1990
University of Occupational and Environmental Health, Japan, School of Medicine, 基礎研究医員
Research activity information
■ Award
■ Paper
■ Paper
- A 34-year-old man with tea-coloured urine.
Brianna Barsanti-Innes; Yoshiro Koda; Cyrus C Hsia; Benjamin Chin-Yee
CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne, 30 Nov. 2025, [Reviewed] - Duplex Probe-Based Fluorescence Melting Curve Analysis for Simultaneous Genotyping of rs1126728 and rs11208257 in the Phosphoglucomutase-1 Gene
Mikiko Soejima; Yoshiro Koda
Diagnostics, 16 Sep. 2025, [Reviewed]
Last, Corresponding - Measuring dissolved oxygen in Miso for forensic medicine and semisolid food analysis
Yoshiro Koda; Mikiko Soejima
Scientific Reports, 28 Aug. 2025, [Reviewed]
Lead, Corresponding - Alzheimer's Disease With Cardiac Transthyretin Amyloidosis: A Clinicopathological Study of Autopsy Cases
Yasuo Sugita; Takuya Furuta; Kenji Takahashi; Koichi Higaki; Yoshiro Koda; Shin‐ichiro Mori; Shoko Hongo; Hideomi Hamasaki; Akiyoshi Kakita; Mitsuharu Ueda; Keisuke Kitagawa
Neuropathology, Aug. 2025, [Reviewed] - Fluorescence melting curve analysis for genotyping of c.1396G > A (rs473267) of phosphoglucomutase-3 gene
Mikiko Soejima; Yoshiro Koda
Legal Medicine, Jul. 2025, [Reviewed]
Last, Corresponding - Simultaneous Genotyping of Three Nonsynonymous SNVs, rs1042602, rs1426654, and rs16891982 Involved in Skin Pigmentation by Fluorescent Probe‐Based Melting Curve Analysis
Mikiko Soejima; Yoshiro Koda
Human Mutation, Jan. 2025, [Reviewed]
Last, Corresponding - 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, Nov. 2024, [Reviewed]
Last, Corresponding - 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, [Reviewed]
Last, Corresponding - FUT1 variants responsible for Bombay or para-Bombay phenotypes in a database
Mikiko Soejima; Yoshiro Koda
Scientific Reports, 14 Oct. 2023, [Reviewed]
Last, Corresponding - 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, [Reviewed]
Last, Corresponding - Estimation of Lewis Blood Group Status by Fluorescence Melting Curve Analysis in Simultaneous Genotyping of c.385A>T and Fusion Gene in FUT2 and c.59T>G and c.314C>T in FUT3
Mikiko Soejima; Yoshiro Koda
Diagnostics, 01 Mar. 2023, [Reviewed]
Last, Corresponding - Fluorescence Melting Curve Analysis for Concurrent Genotyping of Three Tag SNPs in FUT3
Mikiko Soejima; Yoshiro Koda
Diagnostics, 04 Dec. 2022, [Reviewed]
Last, Corresponding - 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, Dec. 2022, [Reviewed]
Last, Corresponding - 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, [Reviewed]
Last, Corresponding - 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, May 2022, [Reviewed]
Last, Corresponding - Simultaneous genotyping of three major Se enzyme inactivating SNPs of FUT2 based on a triplex probe-based fluorescence melting-curve analysis.
Yoshiro Koda
Clinica chimica acta; international journal of clinical chemistry, 07 Mar. 2022, [Reviewed]
Last, Corresponding - Real-time PCR-based detection of the Alu-mediated deletion of FUT2 (sedel2).
Yoshiro Koda
Legal medicine (Tokyo, Japan), 30 Oct. 2021, [Reviewed]
Last, Corresponding - Rapid detection of phenotypes Bombay sedel and nonsecretor rs200157007 SNP (302C > T) by real-time PCR-based methods
Mikiko Soejima; Yoshiro Koda
Scientific Reports, 22 Jul. 2021, [Reviewed]
Last, Corresponding - 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, [Reviewed]
Last, Corresponding - Estimation of secretor status of ABO antigens by high-resolution melting analysis of rs601338 (428G > A)
Mikiko Soejima; Yoshiro Koda
Clinica Chimica Acta, 01 Jun. 2021, [Reviewed]
Last, Corresponding - Survey and characterization of nonfunctional alleles of FUT2 in a database
Mikiko Soejima; Yoshiro Koda
Scientific Reports, 04 Feb. 2021, [Reviewed]
Last, Corresponding - High-resolution melting analysis for detection of fusion allele of FUT2
Mikiko Soejima; Yoshiro Koda
Electrophoresis, 01 Feb. 2021, [Reviewed]
Last, Corresponding - Detection of helium in a fire victim: A case report
Mikiko Soejima; Naoko Tanaka; Toru Oshima; Hiroshi Kinoshita; Yoshiro Koda
Forensic Science International, Jan. 2021, [Reviewed]
Last, Corresponding - Estimation of Lewis-negative alleles by high-resolution melting analysis of three tag SNPs of FUT3
Mikiko Soejima; Yoshiro Koda
Vox Sanguinis, 2021, [Reviewed]
Last, Corresponding - Haptoglobin polymorphisms in Latin American populations
Mikiko Soejima; Yoshiro Koda
Scientific Reports, 01 Dec. 2020, [Reviewed]
Last, Corresponding - Effect of tolvaptan on renal involvement in patients with autosomal dominant polycystic kidney disease according to different gene mutations.
Moriyama T; Nakayama Y; Soejima M; Yokota Y; Ota K; Ito S; Kodama G; Nakamura N; Kurokawa Y; Yano J; Ueda U; Takamiya Y; Kaida Y; Hazama T; Shibata R; Koda Y; Fukami K
Clinical and experimental nephrology, 03 Nov. 2020, [Reviewed] - ADPKD遺伝子変異別にみた総腎容量に対するトルバプタンの効果
森山 智文; 中山 陽介; 副島 美貴子; 甲斐田 裕介; 柴田 了; 神田 芳郎; 深水 圭
日本腎臓学会誌, Jul. 2020 - FUT2 polymorphism in Latin American populations
Mikiko Soejima; Yoshiro Koda
Clinica Chimica Acta, 01 Jun. 2020, [Reviewed]
Last, Corresponding - 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]
Last, Corresponding - Genetic determinants of circulating haptoglobin concentration
Nabila Kazmi; Yoshiro Koda; Ndeye Coumba Ndiaye; Sophie Visvikis-Siest; Matthew J Morton; Tom R Gaunt; Ian Galea
Clinica Chimica Acta, Jul. 2019, [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, [Reviewed]
Last, Corresponding - ADPKD患者における遺伝子変異と脳血管合併症との関連について
森山 智文; 副島 美貴子; 神田 芳郎; 深水 圭
日本腎臓学会誌, May 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]
Last, Corresponding - Four intracranial injury cases with peripapillary scleral hemorrhage—Reconsidering the mechanism of hemorrhage
Oshima, T.; Yoshikawa, H.; Koda, Y.; Ohtani, M.; Tsukamoto, S.; Mimasaka, S.
Legal Medicine, 2017, [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, [Reviewed] - Discoveries and application of prostate-specific antigen, and some proposals to optimize prostate cancer screening
Tokudome, S.; Ando, R.; Koda, Y.
Cancer Management and Research, 2016
Last - Haptoglobin promoter polymorphism rs5472 as a prognostic biomarker for peptide vaccine efficacy in castration-resistant prostate cancer patients
Araki, H.; Pang, X.; Komatsu, N.; Soejima, M.; Miyata, N.; Takaki, M.; Muta, S.; Sasada, T.; Noguchi, M.; Koda, Y.; Itoh, K.; Kuhara, S.; Tashiro, K.
Cancer Immunology, Immunotherapy, 01 Dec. 2015, [Reviewed] - Haptoglobin genotyping of Vietnamese: Global distribution of HPdel, complete deletion allele of the HP 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]
Last, Corresponding - 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]
Last, Corresponding - 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]
Last, Corresponding - Evaluation of point-of-care testing of C-reactive protein in forensic autopsy cases
Mikiko Soejima; Yoshiro Koda
FORENSIC SCIENCE INTERNATIONAL, Apr. 2014, [Reviewed]
Last, Corresponding - 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]
Last, Corresponding - 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]
Last, Corresponding - 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.; Yoshimoto, J.; Tanabe, S.; Koda, Y.
Transfusion, Jun. 2012, [Reviewed]
Last, Corresponding - 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, [Reviewed] - 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
Haruo Takeshita; Junko Fujihara; Misuzu Ueki; Reiko Iida; Yoshiro Koda; Mikiko Soejima; Isao Yuasa; Hideaki Kato; Tamiko Nakajima; Yoshihiko Kominato; Toshihiro Yasuda
DNA AND CELL BIOLOGY, Jan. 2012, [Reviewed] - High prevalence of an anti-hypertriglyceridemic variant of the MLXIPL gene in Central Asia
Kazuhiro Nakayama; Yoshiko Yanagisawa; Ayumi Ogawa; Yuumi Ishizuka; Lkhagvasuren Munkhtulga; Phitaya Charupoonphol; Somjit Supannnatas; Stevenson Kuartei; Ulziiburen Chimedregzen; Yoshiro Koda; Takafumi Ishida; Yasuo Kagawa; Sadahiko Iwamoto
Journal of Human Genetics, 21 Dec. 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, [Reviewed] - Identification of novel Alu-mediated deletion by TaqMan-based real-time PCR method
SOEJIMA Mikiko; KODA Yoshiro
DNA多型, 30 May 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]
Last, Corresponding - 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]
Last, Corresponding - Functional and Genetic Survey of All Known Single-Nucleotide Polymorphisms Within the Human Deoxyribonuclease I Gene in Wide-Ranging Ethnic Groups
Junko Fujihara; Misuzu Ueki; Toshihiro Yasuda; Reiko Iida; Mikiko Soejima; Yoshiro Koda; Kaori Kimura-Kataoka; Hideaki Kato; Arturo Panduro; Miki Tongu; Haruo Takeshita
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] - EVALUATION OF TWO REAL-TIME PCR METHODS FOR DETECTION OF HP^
, A RISK MUTATION FOR ANAPHYLACTIC SHOCK, BEFORE TRANSFUSION
KODA Yoshiro; SOEJIMA Mikiko; KAWANO Hiroyuki; EGASHIRA Kouichi; SAGAWA Kimitaka
日本輸血学細胞治療学会誌, 25 Feb. 2011, [Reviewed]
Lead, Corresponding - 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, [Reviewed] - Polymorphic trial in oxidative damage of arsenic exposed Vietnamese
Fujihara, J.; Soejima, M.; Yasuda, T.; Koda, Y.; Kunito, T.; Iwata, H.; Tanabe, S.; Takeshita, H.
Toxicology and Applied Pharmacology, 2011, [Reviewed] - 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, [Reviewed] - 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, [Reviewed] - 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, [Reviewed]
Last, Corresponding - 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 - VII DNA多型の臨床応用 3.脂質代謝に関わる転写因子MLXIPLの遺伝的多様性とその人類生物学的意義
中山一大; 柳沢佳子; 後藤孝也; 山中一央; 小川歩美; 岩本禎彦; LKHAGVASUREN Munkhtulga; 神田芳郎; 石田貴文; 香川靖雄
DNA多型, 2010 - HMGB1: A new marker for estimation of the postmortem interval
Kiyoshi Kikuchi; Ko-ichi Kawahara; Kamal Krishna Biswas; Takashi Ito; Salunya Tancharoen; Naoto Shiomi; Yoshiro Koda; Fumiyo Matsuda; Yoko Morimoto; Yoko Oyama; Kazunori Takenouchi; Naoki Miura; Noboru Arimura; Yuko Nawa; Shinichiro Arimura; Meng Xiao Jie; Binita Shrestha; Masahiro Iwata; Kentaro Mera; Hisayo Sameshima; Yoshiko Ohno; Ryuichi Maenosono; Yutaka Tajima; Hisaaki Uchikado; Terukazu Kuramoto; Kenji Nakayama; Minoru Shigemori; Yoshihiro Yoshida; Teruto Hashiguchi; Ikuro Maruyama
Experimental and Therapeutic Medicine, Jan. 2010, [Reviewed] - Mutant alleles associated with late-onset ornithine transcarbamylase deficiency in male patients have recurrently arisen and have been retained in some populations
Sanae Numata; Yoshiro Koda; Kenji Ihara; Tomo Sawada; Yoshiyuki Okano; Toshinobu Matsuura; Fumio Endo; Han-Wook Yoo; Jose A Arranz; Vicente Rubio; Bendicht Wermuth; Nicholas Ah Mew; Mendel Tuchman; Jason R Pinner; Edwin P Kirk; Makoto Yoshino
Journal of Human Genetics, Jan. 2010, [Reviewed] - Global analysis of genetic variation in human arsenic (+ 3 oxidation state) methyltransferase (AS3MT)
Fujihara, J.; Soejima, M.; Yasuda, T.; Koda, Y.; Agusa, T.; Kunito, T.; Tongu, M.; Yamada, T.; Takeshita, H.
Toxicology and Applied Pharmacology, 2010, [Reviewed] - 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, [Reviewed] - 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, [Reviewed]
Last, Corresponding - Simple and Sensitive Method for Identification of Human DNA by Allele-Specific Polymerase Chain Reaction of FOXP2
Hiroshige, K.; Soejima, M.; Nishioka, T.; Kamimura, S.; Koda, Y.
Journal of Forensic Sciences, Jul. 2009, [Reviewed] - Identification of an ethnic-specific variant (V207M) of the KCNQ1 cardiac potassium channel gene in sudden unexplained death and implications from a knock-in mouse model
Hajime Nishio; Masayoshi Kuwahara; Hirokazu Tsubone; Yoshiro Koda; Takako Sato; Shinya Fukunishi; Akiyoshi Tamura; Koichi Suzuki
INTERNATIONAL JOURNAL OF LEGAL MEDICINE, May 2009, [Reviewed] - Genetic variation of FUT3 in Ghanaians, Caucasians, and Mongolians
Mikiko Soejima; Lkhagvasuren Munkhtulga; Sadahiko Iwamoto; Yoshiro Koda
TRANSFUSION, May 2009, [Reviewed]
Last, Corresponding - Sequence Analysis of Human TRPV6 Suggests Positive Selection Outside Africa
Mikiko Soejima; Hidenori Tachida; Yoshiro Koda
BIOCHEMICAL GENETICS, Feb. 2009, [Reviewed]
Last, Corresponding - 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, [Reviewed] - TaqMan-Based Real-Time PCR for Genotyping Common Polymorphisms of Haptoglobin (HP1 and HP2)
Mikiko Soejima; Yoshiro Koda
CLINICAL CHEMISTRY, Nov. 2008, [Reviewed]
Last, Corresponding - 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, [Reviewed]
Last, Corresponding - 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, [Reviewed] - Associations of protein tyrosine phosphatase nonreceptor 22 (PTPN22) gene polymorphisms with susceptibility to Graves' disease in a Japanese population
Michiko Ichimura; Hiroo Kaku; Tomoka Fukutani; Hirohisa Koga; Tokunori Mukai; Ikuyo Miyake; Kentaro Yamada; Yoshiro Koda; Yuji Hiromatsu
THYROID, Jun. 2008, [Reviewed] - Rapid real-time PCR detection of HPdel directly from diluted blood samples
Mikiko Soejima; Yoshiro Koda
CLINICAL CHEMISTRY, Jun. 2008, [Reviewed]
Last, Corresponding - Sec1-FUT2-Sec1 hybrid allele generated by interlocus gene conversion
Mikiko Soejima; Junko Fujihara; Haruo Takeshita; Yoshiro Koda
TRANSFUSION, Mar. 2008, [Reviewed]
Last, Corresponding - 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; 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 - Distinct single nucleotide polymorphism pattern at the FUT2 promoter among human populations
Mikiko Soejima; Yoshiro Koda
ANNALS OF HEMATOLOGY, Jan. 2008, [Reviewed]
Last, Corresponding - Extremely high prevalence of DNASE1* 1 allele in African populations
Takeshita, H.; Fujihara, J.; Soejima, M.; Koda, Y.; Yasuda, T.; Nakajima, T.
Cell Biochemistry and Function, 2008, [Reviewed] - Genetic variation of FUT2 in Ovambos, Turks, and Mongolians
Soejima, M.; Nakajima, T.; Fujihara, J.; Takeshita, H.; Koda, Y.
Transfusion, 2008, [Reviewed]
Last, Corresponding - The distribution of haptoglobin-gene deletion (Hp(del)) is restricted to East Asians
Mikiko Soejima; Yoshiro Koda; Junko Fujihara; Haruo Takeshita
TRANSFUSION, Oct. 2007, [Reviewed]
Corresponding - 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, [Reviewed]
Last, Corresponding - Population differences of two coding SNPs in pigmentation-related genes SLC24A5 and SLC45A2
Mikiko Soejima; Yoshiro Koda
INTERNATIONAL JOURNAL OF LEGAL MEDICINE, Jan. 2007, [Reviewed]
Last, Corresponding - 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, [Reviewed]
Last - Lack of association of interleukin-18 gene polymorphisms with susceptibility of Japanese populations to Graves' disease or Graves' ophthalmopathy
T Mukai; Y Hiromatsu; M Ichimura; T Fukutani; H Kaku; Miyake, I; S Shoji; Y Koda; T Bednarczuk
THYROID, Mar. 2006, [Reviewed] - IL-18 gene polymorphism confers susceptibility to the development of anti-GAD65 antibody in Graves' disease
Y Hiromatsu; T Mukai; H Kaku; Miyake, I; M Ichimura; T Fukutani; H Nakayama; K Takata; Y Imamura; S Shoji; K Yamada; Y Koda; T Bednarczuk
DIABETIC MEDICINE, Feb. 2006, [Reviewed] - 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, [Reviewed] - 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, [Reviewed]
Last, Corresponding - Denaturing high-performance liquid chromatography-based genotyping and genetic variation of FUT2 in Sri Lanka
M Soejima; Y Koda
TRANSFUSION, Dec. 2005, [Reviewed]
Last, Corresponding - Molecular mechanisms of Lewis antigen expression
Mikiko Soejima; Yoshiro Koda
Legal Medicine, Jul. 2005
Last, Corresponding - Glucose-dependent insulinotropic polypeptide (GIP) stimulation of pancreatic beta-cell survival is dependent upon phosphatidylinositol 3-kinase (PI3K)/protein kinase B (PKB) signaling, inactivation of the forkhead transcription factor Foxo1, and down-regulation of bax expression
SJ Kim; K Winter; C Nian; M Tsuneoka; Y Koda; CHS McIntosh
JOURNAL OF BIOLOGICAL CHEMISTRY, Jun. 2005, [Reviewed] - 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, [Reviewed]
Last - 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, [Reviewed]
Last, Corresponding - Interleukin-13 gene polymorphisms confer the susceptibility of Japanese populations to Graves' disease
Y Hiromatsu; T Fukutani; M Ichimura; T Mukai; H Kaku; H Nakayama; Miyake, I; S Shoji; Y Koda; T Bednarczuk
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, Jan. 2005, [Reviewed] - Mina53 as a potential prognostic factor for esophageal squamous cell carcinoma
M Tsuneoka; H Fujita; N Arima; K Teye; T Okamura; H Inutsuka; Y Koda; K Shirouzu; H Kimura
CLINICAL CANCER RESEARCH, Nov. 2004, [Reviewed] - 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, [Reviewed] - Two novel FUT3 alleles responsible for Lewis-null phenotypes in Sri Lanka
M Soejima; H Kimura; Y Koda
TRANSFUSION, Oct. 2004, [Reviewed]
Last, Corresponding - 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, [Reviewed] - 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, [Reviewed]
Lead - Enhanced expression of interleukin-18 and its receptor in idiopathic pulmonary fibrosis
Kitasato, Y.; Hoshino, T.; Okamoto, M.; Kato, S.; Koda, Y.; Nagata, N.; Kinoshita, M.; Koga, H.; Yoon, D.-Y.; Asao, H.; Ohmoto, H.; Koga, T.; Rikimaru, T.; Aizawa, H.
American Journal of Respiratory Cell and Molecular Biology, 2004, [Reviewed] - Increased expression of a Myc target gene Mina53 in human colon cancer
K Teye; M Tsuneoka; N Arima; Y Koda; Y Nakamura; Y Ueta; K Shirouzu; H Kimura
AMERICAN JOURNAL OF PATHOLOGY, Jan. 2004, [Reviewed] - 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, [Reviewed] - 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, [Reviewed]
Lead - N-acetylglucosamine-phosphate mutase genotype and diabetic microvascular complications [2]
H. Pang; Y. Koda; S. I. Yamagishi; S. Amano; Y. Inagaki; T. Okamoto; K. Yamada; H. Kimura
Diabetic Medicine, 01 May 2003, [Reviewed] - 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, [Reviewed] - Fatal subarachnoid hemorrhage complicating actinomycotic meningitis
Koda, Y.; Seto, Y.; Takeichi, S.; Kimura, H.
Forensic Science International, 2003, [Reviewed]
Lead - c-myc induces autophagy in rat 3Y1 fibroblast cells.
Tsuneoka M; Umata T; Kimura H; Koda Y; Nakajima M; Kosai K; Takahashi T; Takahashi Y; Yamamoto A
Cell Struct Funct., 2003, [Reviewed] - 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, [Reviewed] - 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, [Reviewed]
Lead - 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, [Reviewed]
Last - 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, [Reviewed] - 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, [Reviewed] - 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] - Distinctive distribution of AIM1 polymorphism among major human populations with different skin color
K Nakayama; S Fukamachi; H Kimura; Y Koda; A Soemantri; T Ishida
JOURNAL OF HUMAN GENETICS, 2002, [Reviewed] - 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, [Reviewed]
Lead - 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, [Reviewed] - 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, [Reviewed]
Lead - 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, [Reviewed] - The polymorphisms of fucosyltransferases
Yoshiro Koda; Mikiko Soejima; Hiroshi Kimura
Legal Medicine, 2001, [Reviewed]
Lead - A fatal case of hyperthermia due to tricyclic antidepressant intoxication
FUJITANI Noboru; KODA Yoshiro; OKAMURA Torahiko; HATTORI Hideki; KIMURA Hiroshi
Leg Med (Tokyo), 01 Oct. 2000, [Reviewed] - 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, [Reviewed] - 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, [Reviewed]
Lead - 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, [Reviewed]
Lead - 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, [Reviewed]
Lead - 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, [Reviewed] - Myocardial "elektive disseminierte Parenchymnekrose" revisited
FUJITANI Noboru; KODA Yoshiro; ONISHI Shunzo; KIMURA Hiroshi
Leg Med (Tokyo), 01 Sep. 1999, [Reviewed] - 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, [Reviewed] - 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, [Reviewed] - 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, [Reviewed] - 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, [Reviewed] - 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, [Reviewed] - 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, [Reviewed]
Lead - 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, [Reviewed] - 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, [Reviewed] - 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, [Reviewed] - The haptoglobin-gene deletion responsible for anhaptoglobinemia
Y Koda; M Soejima; N Yoshioka; H Kimura
AMERICAN JOURNAL OF HUMAN GENETICS, Feb. 1998, [Reviewed]
Lead - Distribution of H type 1 and of H type 2 antigens of ABO blood group in different cells of human submandibular gland
YH Liu; N Fujitani; Y Koda; H Kimura
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, Jan. 1998, [Reviewed] - 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, [Reviewed]
Lead - 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, [Reviewed]
Lead - 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, [Reviewed]
Lead - 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, [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] - 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, [Reviewed]
Lead - 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.
Japanese Journal of Legal Medicine, 1996, [Reviewed] - DETECTION OF T-MUTATION TO G-MUTATION AT POSITION-59 IN THE LEWIS GENE BY MISMATCH POLYMERASE CHAIN-REACTION
Y KODA; M SOEJIMA; H KIMURA
INTERNATIONAL JOURNAL OF LEGAL MEDICINE, Jun. 1995, [Reviewed]
Lead - 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, [Reviewed]
Lead - ANALYSIS OF LEWIS FUCOSYL-TRANSFERASE GENES FROM THE HUMAN GASTRIC-MUCOSA OF LEWIS-POSITIVE AND LEWIS-NEGATIVE INDIVIDUALS
Y KODA; H KIMURA; E MEKADA
BLOOD, Nov. 1993, [Reviewed]
Lead - RUBINSTEIN-TAYBI SYNDROME WITH THYMIC HYPOPLASIA
H KIMURA; Y ITO; Y KODA; Y HASE
AMERICAN JOURNAL OF MEDICAL GENETICS, May 1993, [Reviewed] - VERATRIDINE CAUSES THE CA-2+-DEPENDENT INCREASE IN DIACYLGLYCEROL FORMATION AND TRANSLOCATION OF PROTEIN-KINASE-C TO MEMBRANES IN CULTURED BOVINE ADRENAL-MEDULLARY CELLS
Y UEZONO; A WADA; N YANAGIHARA; H KOBAYASHI; T MIZUKI; T TERAO; Y KODA; F IZUMI
NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, Jul. 1992, [Reviewed] - PROTEIN-KINASE-C IN HUMAN PHEOCHROMOCYTOMA
Y KODA; Y UEZONO; H KOBAYASHI; F IZUMI; H INATOMI; Y YAMADA; T OKAMURA
NEUROSCIENCE LETTERS, Jun. 1991, [Reviewed]
Lead - SUBTYPES OF PROTEIN-KINASE-C IN RAT CEREBRAL MICROVESSELS
H KOBAYASHI; T MIZUKI; Y KODA; M OKAZAKI; A KUROIWA; F IZUMI
EXPERIENTIA, Mar. 1991, [Reviewed] - INHIBITORY EFFECT OF OKADAIC ACID ON CARBACHOL-EVOKED SECRETION OF CATECHOLAMINES IN CULTURED BOVINE ADRENAL-MEDULLARY CELLS
N YANAGIHARA; Y TOYOHIRA; Y KODA; A WADA; F IZUMI
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, Jan. 1991, [Reviewed] - PURIFICATION AND CHARACTERIZATION OF CALMODULIN-DEPENDENT MULTIFUNCTIONAL PROTEIN-KINASE FROM SMOOTH-MUSCLE - ISOLATION OF CALDESMON KINASE
M IKEBE; S REARDON; GC SCOTTWOO; ZH ZHOU; Y KODA
BIOCHEMISTRY, Dec. 1990, [Reviewed] - PROTEIN KINASE-C SUBTYPES IN TISSUES DERIVED FROM NEURAL CREST
Y KODA; H KOBAYASHI; T MIZUKI; M OKAZAKI; Y UEZONO; N YANAGIHARA; A WADA; F IZUMI
BRAIN RESEARCH, Jun. 1990, [Reviewed]
Lead - VERATRIDINE-INDUCED PHOSPHORYLATION AND ACTIVATION OF TYROSINE-HYDROXYLASE, AND SYNTHESIS OF CATECHOLAMINES IN CULTURED BOVINE ADRENAL-MEDULLARY CELLS
Y UEZONO; N YANAGIHARA; A WADA; Y KODA; K YOKOTA; H KOBAYASHI; F IZUMI
NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, Jun. 1989, [Reviewed] - CIS-UNSATURATED FATTY-ACIDS STIMULATE CATECHOLAMINE SECRETION, TYROSINE-HYDROXYLASE AND PROTEIN KINASE-C IN ADRENAL-MEDULLARY CELLS
Y KODA; A WADA; N YANAGIHARA; Y UEZONO; F IZUMI
NEUROSCIENCE, Feb. 1989, [Reviewed]
Lead, Corresponding - ACTIVATION OF TYROSINE-HYDROXYLASE BY MICROMOLAR CONCENTRATIONS OF CALCIUM IN DIGITONIN-PERMEABILIZED ADRENAL-MEDULLARY CELLS
N YANAGIHARA; Y UEZONO; Y KODA; A WADA; F IZUMI
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, Jul. 1987, [Reviewed]
- 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 - 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 - Analysis of the promoter region of a rat α(1, 2)fucosyltransferase gene(Futa)
SOEJIMA Mikiko; KODA Yoshiro; KIMURA Hiroshi
日本分子生物学会年会プログラム・講演要旨集, 01 Dec. 1998 - Hemizygous haptoglobin gene deletion is a cause of familial anhaptoglobinemia
Koda, Y.; Soejlma, M.; Ktmura, H.
Japanese Journal of Human Genetics, 1997 - ACTIVATION OF TYROSINE-HYDROXYLASE BY MICROMOLAR CONCENTRATIONS OF CA IN LEAKY ADRENAL-MEDULLARY CELLS AND PC12 CELLS
N YANAGIHARA; Y UEZONO; Y KODA; A WADA; F IZUMI
JAPANESE JOURNAL OF PHARMACOLOGY, 1986 - CALCIUM-ION AND THE RELEASE OF CATECHOLAMINES - EXPERIMENTS IN LEAKY ADRENAL-MEDULLA CELLS AND CHROMAFFIN GRANULES
F IZUMI; Y TOYOHIRA; Y KODA; Y UEZONO; N YANAGIHARA; A WADA
JAPANESE JOURNAL OF PHARMACOLOGY, 1986
- Legal medicine for medical sutudent
久保真一他, Joint work, 12章 遺伝子多型と血液型 他
南山堂, Apr. 2024
9784525190279 - 研究の公正性、信頼性を確保するために - 利益相反について
神田芳郎, Single work
Journal of Clinical Rehabilitation, Jun. 2016 - 倫理とは何か ― 人を対象とした医学研究倫理について
神田芳郎, Single work
Journal of Clinical Rehabilitation, Mar. 2016 - ハプトグロビン欠損症
副島美貴子、神田芳郎, Contributor
別冊日本臨牀 新領域別症候群シリーズ No.20 先天性代謝異常症候群(第2版)下、日本臨牀社, Dec. 2012 - 現代人の進化
J. K. プリチャード (翻訳者 神田 芳郎), Contributor
日経サイエンス, Feb. 2011 - e-ラーニング
Johnn A. Dent/Ronald M. Harden (鈴木康之/錦織宏監訳、神田芳郎訳者), Contributor
医学教育の理論と実践(篠原出版新社), Mar. 2010 - 血液型多型とDNA多型
田中宣幸他, Contributor
学生のための法医学改訂6版 南山堂, Nov. 2006 - 無ハプトグロビン血症,低ハプトグロビン血症
神田芳郎、副島美貴子、木村博司, Contributor
別冊日本臨牀日本臨床 先天代謝異常症候群 遺伝子解析の進歩と成果 日本臨床社, May 1998 - Anhaptoglobinemia and hypohaptoglobinemia
Y. Koda; M. Soejima; H. Kimura
1998
- Apr. 2021
- 教務委員
Apr. 2017 - Mar. 2019 - 教務委員長
Apr. 2013 - Mar. 2017 - 久留米大学医学教育ワークショップ実行委員長
Aug. 2012 - 教務委員
Apr. 2005 - Mar. 2011 - 久留米大学医学教育ワークショップ実行委員
Aug. 2010 - 久留米大学医学教育ワークショップ実行委員
Aug. 2008 - 学生のための法医学改訂6版 分担執筆
01 Nov. 2006 - 久留米大学医学教育ワークショップ実行委員
Aug. 2006 - 久留米大学テュートリアル教育委員
Apr. 2003 - Mar. 2005
- 1999 - Present
日本輸血・細胞治療学会 - 1997 - Present
日本分子生物学会 - 1996 - Present
日本人類遺伝学会 - Jan. 1991 - Present
日本法医学会 - 2003 - 2012
European Society of Human Genetics - 2000 - 2011
Society for Molecular Biology and Evolution
- Development of a method to investigate the global spread of HPdel, a gene that causes adverse transfusion reactions
Grant-in-Aid for Scientific Research (C)
Kurume University
01 Apr. 2025 - 31 Mar. 2028 - Usefulness of nucleic acid amplification in search for responsible bacteria for sepsis.
Grant-in-Aid for Scientific Research (C)
Kurume University
Apr. 2022 - Mar. 2025 - Does the obesity affect the relationship between serum haptoglobin and cholesterol levels?
Grant-in-Aid for Scientific Research (C)
Kurume University
01 Apr. 2020 - 31 Mar. 2023 - How the ABO antigens acquire the expression on the red blood cells ?
Grant-in-Aid for Scientific Research (C)
Kurume University
01 Apr. 2018 - 31 Mar. 2022 - Is haptoglobin one of possible predictive markers for complications or prognosis after intracranial hemorrhage?
Grant-in-Aid for Scientific Research (C)
Kurume University
01 Apr. 2017 - 31 Mar. 2020 - Established of Prevention or Prediction of Clinical outcome in Cerebrovascular disease by Haptoglobin-genotyping
Grant-in-Aid for Scientific Research (C)
Kurume University
01 Apr. 2016 - 31 Mar. 2019 - Searching of genetic polymorphisms affecting the serum haptoglobin concentration.
Grant-in-Aid for Scientific Research (C)
Kurume University
01 Apr. 2014 - 31 Mar. 2017 - Two approaches for identification of SNPs associated with ridge counts of human finger prints.
Grant-in-Aid for Scientific Research (C)
Kurume University
01 Apr. 2013 - 31 Mar. 2016 - Development of assay system of biochemical markers by TaqMan protein quantification method useful for forensic diagnosis.
Grant-in-Aid for Challenging Exploratory Research
Kurume University
2011 - 2012 - 入浴中急死の病態解明と予防対策の検討
2012 - Analysis of polymorphisms and association study of FUT2 and FUT3, regulating synthesis of Lewis blood group antigens.
Grant-in-Aid for Scientific Research (C)
Kurume University
2009 - 2011 - Search for polymorphisms of genes regulating population-specific morphological traits and functional analyses
Grant-in-Aid for Scientific Research (A)
Kurume University
2009 - 2011 - 輸血副作用の原因遺伝子ハプトグロビン欠失アリルの迅速簡便な診断法の確立と輸血前診断への臨床応用
2008 - 2010 - Analyses of polymorphisms in the FUT2 and FUT3 and mechanism of synthesis of Lewis blood group antigens
Grant-in-Aid for Scientific Research (C)
Kurume University
2006 - 2007 - Analysis of Myc-target gene, Mina53 in cells and in a body
Grant-in-Aid for Scientific Research (C)
Kurume University
2004 - 2005 - Haplotype analysis of polymorphic genes and its forensic application
Grant-in-Aid for Scientific Research (B)
Kurume University
2004 - 2005 - Analysis of Functions and Domains of A Novel Cell Proliferation Relating Protein Meu-2
Grant-in-Aid for Scientific Research (C)
KURUME UNIVERSITY
2002 - 2003 - Allelic variation of the human ABO secretor locus (FUT2) in the world wide populations
Grant-in-Aid for Scientific Research (C)
KURUME UNIVERSITY
2002 - 2003 - Progress in the biological science of ABO blood group system -a pioneer work in legal medicine-
Grant-in-Aid for Scientific Research (A)
TOYAMA MEDICAL AND PHARMACEUTICAL UNIVERSITY
2001 - 2003 - Analyses of SNPs on various human gene loci and their forensic applications
Grant-in-Aid for Scientific Research (C)
KURUME UNIVERSITY
2001 - 2002 - 日本人集団における疾患感受性遺伝子ハプロタイプ解析とその応用
2002 - Analysis of the DNA sequence variation of the fucosyltransferase genes
Grant-in-Aid for Scientific Research (C)
Dept. of Forensic Medicine, Kurume University School of Medicine
1999 - 2000 - Distribution of race-specific null alleles of the FUT2 in Africa, European and Asian populations.
Grant-in-Aid for Scientific Research (B).
Dept. of Forensic Medicine, Kurume University School of Medicine
1998 - 1999 - Expression and immunohistochemical studies of alpha (1,2) fucosyltransferases
Grant-in-Aid for Scientific Research (C)
Kurume University School of Medicine
1997 - 1998 - フコシルトランスフェラーゼ遺伝子の多型性について
1998 - α (1, 2) フコシルトランスフェラーゼ遺伝子の分子進化
1995 - Molecular analysis for genetic polymorphism
1991 - Regulation of the expression of ABO related histo-blood group antigens.
1991
