48 results on '"Nishimukai, Hiroaki"'
Search Results
2. Application of fragment analysis based on methylation status mobility difference to identify vaginal secretions
3. The global distribution of the p.R1193Q polymorphism in the SCN5A gene
4. A simple identification method for vaginal secretions using relative quantification of Lactobacillus DNA
5. Rare alleles of the ABO blood group system in two European populations
6. A hypervariable STR polymorphism in the complement factor I (CFI) gene: Asian-specific alleles
7. Suballeles of the ABO Blood Group System in a Japanese Population
8. Molecular basis of complement factor I (CFI) polymorphism: one of two polymorphic suballeles responsible for CFI A is Japanese-specific
9. Variation of interleukin 8 − 251 A > T polymorphism in worldwide populations and intra-ethnic differences in Japanese populations
10. DNA polymorphisms and haplotypes in the 5′-upstream region of the ABO blood group gene
11. HERC1 polymorphisms: population-specific variations in haplotype composition
12. Distribution of abo genotypes and allele frequencies in a korean population
13. Lyonization pattern of normal human nails
14. Immunohistochemical detection of truncated APC protein in sporadic human colorectal adenomas and adenocarcinomas
15. Genotyping of ABO blood groups by PCR and RFLP analysis of 5 nucleotide positions
16. A simple and versatile authenticity assay of coffee products by single-nucleotide polymorphism genotyping
17. Molecular bases for human complement C7 polymorphisms, C7*3 and C7*4
18. Haplotypes in the 5′-upstream region, exons 3 and 4, and introns 2 and 3 of the ABO blood group gene
19. Typing of the nt343C>T (R95X) allele of the C9 gene by PCR-SSP and the allele frequency of R95X in five ethnic populations
20. Polymorphisms of Serum Proteins in Japanese Patients with Vascular Diseases: I. Factor XIIIB, Plasminogen and Complement Types in Primary Varicose Veins
21. A New Complement Factor B Variant (BF S075) in Japanese
22. Complement C6 and C7 Polymorphisms in Japanese Patients with Chronic Glomerulonephritis
23. Three Japanese Families with Members Carrying C7 Silent Allele (C7*Q0): Possibility for an Association between C7*Q0 and C6*B
24. I (C3b/C4b Inactivator) Typing by Agarose Gel Isoelectric Focusing and Immunoblotting Technique
25. Polymorphism of Plasminogen in Healthy Individuals and Patients with Cerebral Infarction
26. C3 Variants in Japanese
27. C6 Polymorphism in Japanese: Typing by Agarose Gel Isoelectric Focusing-Immunofixation
28. A hypervariable STR polymorphism in the CFI gene: Mutation rate and no linkage disequilibrium with FGA
29. Distribution of OCA2∗481Thr and OCA2∗615Arg, associated with hypopigmentation, in several additional populations
30. A Japanese-specific allele in the GALNT11 gene
31. Lyonization pattern of normal human nails
32. A hypervariable STR polymorphism in the complement factor I (CFI) gene: Asian-specific alleles
33. Identification of human blood with hybridoma-derived antibody to human immunoglobulin G.
34. Variation of interleukin 8 −251 A>T polymorphism in worldwide populations and intra-ethnic differences in Japanese populations
35. Short tandem repeat typing in exon 1 of the androgen receptor gene
36. A-Elute alleles of the ABO blood group system in Japanese
37. ICA and organ-specific autoantibodies among Japanese patients with early-onset insulin-dependent diabetes mellitus — the JDS study
38. Immunogenetics of early-onset insulin-dependent diabetes mellitus among the Japanese: HLA, Gm, BF, GLO, and organ-specific autoantibodies — the J.D.S. study
39. HEREDITARY DEFICIENCY OF THE THIRD COMPONENT OF COMPLEMENT IN TWO SISTERS WITH SYSTEMIC LUPUS ERYTHEMATOSUS-LIKE SYMPTOMS.
40. Two New Slow-Moving Variants of Human Serum Albumin.
41. Genetic Polymorphism of Plasminogen: A New Basic Variant (PLG B) and Population Study in Japanese.
42. Genetic Polymorphism of the Seventh Component of Complement: A New Variant.
43. I(C3b/C4b Inactivator) Typing by Agarose Gel Isoelectric Focusing and Immunoblotting Technique.
44. Purification and partial characterization of aldehyde dehydrogenase from human erythrocytes
45. Single nucleotide polymorphisms in the human complement C6 and C7 genes
46. Purification and partial characterization of aldehyde dehydrogenase from human erythrocytes
47. A novel C3 allotype C3'F02' has an amino acid substitution that may inhibit IC3b synthesis and cause C3-hypocohplehentehia
48. Mouse C7 is regulated by the heat-stable antigen on erythrocyte
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