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List of works by Yoshiro Koda

A - 61C and C - 101G hp gene promoter polymorphisms are, respectively, associated with ahaptoglobinaemia and hypohaptoglobinaemia in Ghana

scientific article published on 01 November 2003

A biochemical and genetic study on all non-synonymous single nucleotide polymorphisms of the gene encoding human deoxyribonuclease I potentially relevant to autoimmunity.

scientific article published on 22 April 2010

A fatal case of hyperthermia due to tricyclic antidepressant intoxication

scientific article published on 01 October 2000

A founder deletion of corneodesmosin gene is prevalent in Japanese patients with peeling skin disease: Identification of 2 new cases

article

A novel Myc-target gene, mimitin, that is involved in cell proliferation of esophageal squamous cell carcinoma.

scientific article

A novel myc target gene, mina53, that is involved in cell proliferation

scientific journal article

Activation of tyrosine hydroxylase by micromolar concentrations of calcium in digitonin-permeabilized adrenal medullary cells

scientific article published on 01 July 1987

An Alu-mediated large deletion of the FUT2 gene in individuals with the ABO-Bombay phenotype.

scientific article published in January 2000

An autopsy case of subarachnoid hemorrhage due to ruptured cerebral aneurysm associated with polycystic kidney disease caused by a novel PKD1 mutation.

scientific article published on 2 July 2014

Ancient origin of the null allele se(428) of the human ABO-secretor locus (FUT2).

scientific article published in March 2000

Associations of protein tyrosine phosphatase nonreceptor 22 (PTPN22) gene polymorphisms with susceptibility to Graves' disease in a Japanese population.

scientific article published in June 2008

Changing transcription start sites in H-type alpha(1,2)fucosyltransferase gene (FUT1) during differentiation of the human erythroid lineage

scientific article

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 ⬇️

scientific article published on July 1, 2011

DNA sequence variation of the human ABO-secretor locus ( FUT2) in New Guinean populations: possible early human migration from Africa.

scientific article published on 3 September 2003

Denaturing high-performance liquid chromatography-based genotyping and genetic variation of FUT2 in Sri Lanka.

scientific article

Detection of G to A missense mutation of Lewis-negative gene by PCR on genomic DNA

scientific article published on 01 January 1994

Detection of T to G mutation at position 59 in the Lewis gene by mismatch polymerase chain reaction

scientific article published on 01 January 1995

Discoveries and application of prostate-specific antigen, and some proposals to optimize prostate cancer screening

scientific article published on 10 May 2016

Distinct single nucleotide polymorphism pattern at the FUT2 promoter among human populations

scientific article published on 02 September 2007

Distribution of 42-bp variable tandem repeat polymorphism of the cold-induced autoinflammatory syndrome 1 (CIAS1) gene in eight human populations ⬇️

scientific article published on October 28, 2010

Distribution of H type 1 and of H type 2 antigens of ABO blood group in different cells of human submandibular gland

scientific article published on 01 January 1998

Enhanced expression of interleukin-18 and its receptor in idiopathic pulmonary fibrosis

scientific article published on 12 August 2004

Ethnic variation in genotype frequencies of delta-aminolevulinic acid dehydratase (ALAD).

scientific article published on 17 September 2009

Evaluation of point-of-care testing of C-reactive protein in forensic autopsy cases

scientific article published on 26 January 2014

Evidence for recent positive selection at the human AIM1 locus in a European population.

scientific article

Expression of Mina53, a product of a Myc target gene in mouse testis.

scientific article

Extensive polymorphism of the FUT2 gene in an African (Xhosa) population of South Africa

scientific article

Extremely high prevalence of DNASE1*1 allele in African populations

scientific article published on 01 March 2008

FUT2 polymorphism in Latin American populations

scientific article published on 16 February 2020

Fatal subarachnoid hemorrhage complicating actinomycotic meningitis.

scientific article

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 ⬇️

scientific article published on February 2, 2011

Five novel missense mutations of the Lewis gene (FUT3) in African (Xhosa) and Caucasian populations in South Africa

scientific article

Four intracranial injury cases with peripapillary scleral hemorrhage-Reconsidering the mechanism of hemorrhage

scientific article published on 09 June 2017

Functional and genetic survey of all known single-nucleotide polymorphisms within the human deoxyribonuclease I gene in wide-ranging ethnic groups

scientific article published on 16 January 2011

Genetic determinants of circulating haptoglobin concentration

scientific article published on 18 March 2019

Genetic factors associated with serum haptoglobin level in a Japanese population

scientific article published on 12 March 2014

Genetic variation of FUT2 in Ovambos, Turks, and Mongolians.

scientific article published on 18 April 2008

Genetic variation of FUT2 in a Ghanaian population: identification of four novel mutations and inference of balancing selection.

scientific article

Genetic variation of FUT2 in a Peruvian population: identification of a novel LTR-mediated deletion and characterization of 4 nonsynonymous single-nucleotide polymorphisms

scientific article published on 08 April 2019

Gln222Arg (A2317G) polymorphism in the deoxyribonuclease I gene exhibits ethnic and functional differences

scientific article published on 01 January 2009

Global analysis of genetic variation in human arsenic (+3 oxidation state) methyltransferase (AS3MT)

scientific article published on 22 November 2009

Global analysis of single nucleotide polymorphisms in the exons of human deoxyribonuclease I-like 1 and 2 genes.

scientific article published in October 2010

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 dow

scientific article

HMGB1: A new marker for estimation of the postmortem interval ⬇️

scientific article published on January 1, 2010

Haptoglobin genotype and diabetic microangiopathies in Japanese diabetic patients

scientific article published on 01 July 2002

Haptoglobin genotyping of Vietnamese: global distribution of HP del, complete deletion allele of the HP gene

article

Haptoglobin polymorphism in Mongolian population: comparison of the two genotyping methods

scientific article published on 12 August 2009

Haptoglobin promoter polymorphism rs5472 as a prognostic biomarker for peptide vaccine efficacy in castration-resistant prostate cancer patients.

scientific article published in October 2015

Heterozygosity for two novel null alleles of the KEL gene causes the Kell-null phenotype in a Japanese woman.

scientific article published in April 2002

High prevalence of an anti-hypertriglyceridemic variant of the MLXIPL gene in Central Asia ⬇️

scientific article published on September 22, 2011

High-resolution melting analysis for detection of fusion allele of FUT2

scientific article published on 31 October 2020

IL-18 gene polymorphism confers susceptibility to the development of anti-GAD65 antibody in Graves' disease

scientific article published on 01 February 2006

Interleukin-13 gene polymorphisms confer the susceptibility of Japanese populations to Graves' disease

scientific article published on 13 October 2004

Lack of association of interleukin-18 gene polymorphisms with susceptibility of Japanese populations to Graves' disease or Graves' ophthalmopathy

scientific article published on 01 March 2006

Mina53 as a potential prognostic factor for esophageal squamous cell carcinoma.

scientific article

Missense mutation of FUT1 and deletion of FUT2 are responsible for Indian Bombay phenotype of ABO blood group system

scientific article

Molecular mechanisms of Lewis antigen expression.

scientific article

Mutant alleles associated with late-onset ornithine transcarbamylase deficiency in male patients have recurrently arisen and have been retained in some populations

article published in 2009

Myocardial "elektive disseminierte Parenchymnekrose" revisited

scientific article published on 01 September 1999

N-acetylglucosamine-phosphate mutase genotype and diabetic microvascular complications.

scientific article published in May 2003

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.

scientific article published on 19 October 2011

Polymorphic trial in oxidative damage of arsenic exposed Vietnamese.

scientific article published on 16 August 2011

Polymorphisms of eight STR loci in Chinese and African (Xhosa)populations.

scientific article published in February 2002

Population differences of two coding SNPs in pigmentation-related genes SLC24A5 and SLC45A2

scientific article

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)

scientific article published on 01 July 1999

Rapid Detection of Haptoglobin Gene Deletion in Alkaline-Denatured Blood by Loop-Mediated Isothermal Amplification Reaction ⬇️

scientific article published on May 1, 2011

Sec1-FUT2-Sec1 hybrid allele generated by interlocus gene conversion.

scientific article published on 7 December 2007

Selective quantification of human DNA by real-time PCR of FOXP2.

scientific article

Sequence analysis of human TRPV6 suggests positive selection outside Africa

scientific article published on 25 January 2009

Serum haptoglobin correlates positively with cholesterol and triglyceride concentrations in an obese Mongolian population

scientific article published on 08 March 2020

Simple and sensitive method for identification of human DNA by allele-specific polymerase chain reaction of FOXP2.

scientific article published on 24 April 2009

Structure and Expression of the Gene Encoding Secretor‐Type Galactoside 2‐α‐l‐fucosyltransferase (FUT2) ⬇️

scientific article (publication date: 15 June 1997)

TaqMan real-time polymerase chain reaction for detection of SEC1-FUT2 hybrid alleles: identification of novel hybrid allele.

scientific article

TaqMan-based real-time PCR for genotyping common polymorphisms of haptoglobin (HP1 and HP2)

scientific article published on 11 September 2008

TaqMan-based real-time polymerase chain reaction for detection of FUT2 copy number variations: identification of novel Alu-mediated deletion

scientific article published on 29 September 2010

The Haptoglobin-Gene Deletion Responsible for Anhaptoglobinemia ⬇️

scientific article published on February 1, 1998

The distribution of haptoglobin-gene deletion (Hp del) is restricted to East Asians

scientific article published on 01 October 2007

The fusion gene at the ABO-secretor locus (FUT2): absence in Chinese populations

scientific article published on 01 January 1999

The haptoglobin promoter polymorphism rs5471 is the most definitive genetic determinant of serum haptoglobin level in a Ghanaian population

scientific article published on 22 May 2018

The polymorphisms of fucosyltransferases

scientific article published on 01 March 2001

Three-base deletion and one-base insertion of the alpha(1,4)galactosyltransferase gene responsible for the P phenotype.

scientific article

Two novel FUT3 alleles responsible for Lewis-null phenotypes in Sri Lanka

scientific article published on 01 October 2004

Veratridine-induced phosphorylation and activation of tyrosine hydroxylase, and synthesis of catecholamines in cultured bovine adrenal medullary cells

scientific article published on 01 June 1989

c-myc induces autophagy in rat 3Y1 fibroblast cells.

scientific article published on June 2003

cis-unsaturated fatty acids stimulate catecholamine secretion, tyrosine hydroxylase and protein kinase C in adrenal medullary cells

scientific article published on 01 January 1989

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