about
Missense mutation of FUT1 and deletion of FUT2 are responsible for Indian Bombay phenotype of ABO blood group systemPopulation differences of two coding SNPs in pigmentation-related genes SLC24A5 and SLC45A2Five novel missense mutations of the Lewis gene (FUT3) in African (Xhosa) and Caucasian populations in South AfricaChanging transcription start sites in H-type alpha(1,2)fucosyltransferase gene (FUT1) during differentiation of the human erythroid lineageExtensive polymorphism of the FUT2 gene in an African (Xhosa) population of South AfricaA novel myc target gene, mina53, that is involved in cell proliferationDNA sequence variation of the human ABO-secretor locus ( FUT2) in New Guinean populations: possible early human migration from Africa.Three-base deletion and one-base insertion of the alpha(1,4)galactosyltransferase gene responsible for the P phenotype.Mina53 as a potential prognostic factor for esophageal squamous cell carcinoma.Evidence for recent positive selection at the human AIM1 locus in a European population.Denaturing high-performance liquid chromatography-based genotyping and genetic variation of FUT2 in Sri Lanka.Molecular mechanisms of Lewis antigen expression.Discoveries and application of prostate-specific antigen, and some proposals to optimize prostate cancer screening.Simple and sensitive method for identification of human DNA by allele-specific polymerase chain reaction of FOXP2.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 dowA novel Myc-target gene, mimitin, that is involved in cell proliferation of esophageal squamous cell carcinoma.c-myc induces autophagy in rat 3Y1 fibroblast cells.A biochemical and genetic study on all non-synonymous single nucleotide polymorphisms of the gene encoding human deoxyribonuclease I potentially relevant to autoimmunity.Heterozygosity for two novel null alleles of the KEL gene causes the Kell-null phenotype in a Japanese woman.N-acetylglucosamine-phosphate mutase genotype and diabetic microvascular complications.Ethnic variation in genotype frequencies of delta-aminolevulinic acid dehydratase (ALAD).Genetic variation of FUT2 in Ovambos, Turks, and Mongolians.Genetic variation of FUT2 in a Ghanaian population: identification of four novel mutations and inference of balancing selection.Polymorphisms of eight STR loci in Chinese and African (Xhosa)populations.Polymorphic trial in oxidative damage of arsenic exposed Vietnamese.Associations of protein tyrosine phosphatase nonreceptor 22 (PTPN22) gene polymorphisms with susceptibility to Graves' disease in a Japanese population.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.Global analysis of single nucleotide polymorphisms in the exons of human deoxyribonuclease I-like 1 and 2 genes.Sec1-FUT2-Sec1 hybrid allele generated by interlocus gene conversion.Ancient origin of the null allele se(428) of the human ABO-secretor locus (FUT2).An Alu-mediated large deletion of the FUT2 gene in individuals with the ABO-Bombay phenotype.Fatal subarachnoid hemorrhage complicating actinomycotic meningitis.An autopsy case of subarachnoid hemorrhage due to ruptured cerebral aneurysm associated with polycystic kidney disease caused by a novel PKD1 mutation.Haptoglobin promoter polymorphism rs5472 as a prognostic biomarker for peptide vaccine efficacy in castration-resistant prostate cancer patients.Expression of Mina53, a product of a Myc target gene in mouse testis.TaqMan real-time polymerase chain reaction for detection of SEC1-FUT2 hybrid alleles: identification of novel hybrid allele.Selective quantification of human DNA by real-time PCR of FOXP2.Haptoglobin genotyping of Vietnamese: global distribution of HP del, complete deletion allele of the HP geneMutant alleles associated with late-onset ornithine transcarbamylase deficiency in male patients have recurrently arisen and have been retained in some populationsGlobal analysis of genetic variation in human arsenic (+3 oxidation state) methyltransferase (AS3MT)
P50
Q28249182-574BCCB4-4D68-4EB3-848A-3BE87C8A5F23Q28252679-6F5822A9-B5D7-4944-84B5-41819311F881Q28279542-DC8120D7-E61C-4D38-87F6-02E7351AA3EDQ28284412-E6C0FB7D-A035-4D1F-8F56-4DEEB63D1E65Q28284474-B2224739-CC9E-46F1-B0B8-E638FBF2F461Q28564890-6DED1FBC-703A-444F-ACE1-59BBA10F9578Q33194079-C5347610-DFBA-4EF6-AF63-24E9F8E157F7Q34118680-99D2DC06-A745-4522-AE3C-20BB3F327A9CQ34366268-C20C5D09-2F4E-4F67-A6A0-C57C8CE226B5Q34450971-085BAE44-E635-4F8D-B509-71093B1C078DQ34478684-7C2A7083-5B5F-4686-9CD4-0B5BF19C0A6BQ36157494-5B385DB3-DABF-4318-AB43-E3984320E173Q36907999-A7A48958-3547-4984-82F6-907DFB7E6CADQ38381585-B2B93874-961C-47EB-BD68-28A081D91D1DQ40437409-5450159D-EE29-48FC-A308-0B3E4DAB4D44Q40445617-981C77A1-639F-421C-A6BC-E4F1F9AC8DB7Q40638488-BD984915-77AA-4AB0-9138-DEE7C0924700Q43086615-8CCDC38A-5329-476C-BDA1-3396D4EFE904Q43936473-5D8F894F-040D-436E-83CD-7FC34BA239D5Q44444559-7E6F94C9-AC71-4E68-B037-00357773CD6FQ44645902-39EDA20E-63CA-4170-8835-19E0832CD581Q46160104-8760C978-11CE-4091-9C66-EEE791421135Q46192834-51C04779-7E18-480C-B147-C7703FA8DE88Q46285091-407F3EFC-1CC5-4446-AE3E-56C82D21B794Q46471966-416DC634-FBE3-4C30-8DD7-16A455E98E19Q46519883-B3985FE0-B9AB-460E-AB2B-557A4835E2F2Q46819916-2278DDC6-913B-432A-B18D-8B42213B9D2EQ46859750-EA57806A-947E-42BC-B483-DDED48B957CDQ46859883-07C34DA6-10D3-4E1A-AB9F-4216587DCA83Q47644378-96C5F56A-99BB-442C-AD54-8410F6210116Q47830177-19FFCD3E-FAC8-4FBA-B5A1-72D72F2C53ACQ48258588-21902B4B-6E37-4EF0-B81A-CF631D1B23EDQ48660948-5CA07779-A705-4DF3-ACB8-CA5ACC5A49D1Q52912696-642631E0-9C70-4E95-A055-430627C05970Q53632753-3B46B787-15A1-4724-AC2E-0959D40ADBB4Q54293301-FD5EA494-9F69-45F7-99C5-B25B640897BFQ54343839-2CDF54FA-95E9-46AA-AC1A-9F210DA5E695Q56670091-88F46FC1-3148-4510-BA0B-B4A4C9813002Q57563199-F6F6ED6B-9BE3-471E-A671-85F9EF209CE8Q59423387-AD65CA60-2701-4DAB-9347-DCDB44217A11
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Y Koda
@ast
Y Koda
@en
Y Koda
@es
Y Koda
@nl
type
label
Y Koda
@ast
Y Koda
@en
Y Koda
@es
Y Koda
@nl
prefLabel
Y Koda
@ast
Y Koda
@en
Y Koda
@es
Y Koda
@nl
P106
P1153
7005121055
P31
P496
0000-0003-1368-0116