All Stories

  1. Application of immortalized human erythroid progenitor cell line in serologic tests to detect red blood cell alloantibodies

    Article • Transfusion, September 2018, Wiley

    Dr Kenichi Ogasawara

  2. The B allele with a 5·8 kb deletion in intron 1 of the ABO gene is the major allele in Japanese individuals with Bm and A1 Bm phenotypes

    Article • Vox Sanguinis, February 2018, Wiley

    Dr Kenichi Ogasawara

  3. Silent KEL alleles identified from Japanese individuals with the Ko phenotype

    Article • Vox Sanguinis, December 2017, Wiley

    Dr Kenichi Ogasawara, makoto uchikawa

  4. Mutations of theKLF1gene detected in Japanese with the In(Lu) phenotype

    Article • Transfusion, February 2017, Wiley

    Dr Kenichi Ogasawara

  5. Prevalence ofRHDalleles in Japanese individuals with weak D phenotype: Identification of 20 newRHDalleles

    Article • Vox Sanguinis, May 2016, Wiley

    Dr Kenichi Ogasawara

  6. Weak D alleles in Japanese: a c.960G>A silent mutation in exon 7 of theRHDgene that affects D expression

    Article • Vox Sanguinis, September 2015, Wiley

    Dr Kenichi Ogasawara

  7. Molecular basis for D− Japanese: identification of novel DEL and D− alleles

    Article • Vox Sanguinis, May 2015, Wiley

    Dr Kenichi Ogasawara

  8. A novelDOnull allele with a c.268C>T (p.Gln90Stop) mutation in Japanese

    Article • Vox Sanguinis, April 2015, Wiley

    Dr Kenichi Ogasawara

  9. A newABCG2null allele with a 27-kb deletion including the promoter region causing the Jr(a−) phenotype

    Article • Transfusion, December 2014, Wiley

    Dr Kenichi Ogasawara

  10. Production of human monoclonal anti-Jk3, recognising an epitope including the Jka/Jkbpolymorphic site of the Kidd glycoprotein

    Article • Transfusion Medicine, September 2014, Wiley

    Dr Kenichi Ogasawara

  11. JKnull alleles identified from Japanese individuals with Jk(a−b−) phenotype

    Article • Vox Sanguinis, December 2013, Wiley

    Dr Kenichi Ogasawara