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

Vox sanguinis, 2015-11, Vol.109 (4), p.359-365

2015

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

Vox sanguinis, 2016-02, Vol.110 (2), p.179-184

2016

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The KANNO blood group system

Immunohematology, 2022-12, Vol.38 (4), p.119

2022

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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 A1Bm phenotypes

Vox sanguinis, 2018-05, Vol.113 (4), p.393-396

2018

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Prevalence of RHD alleles in Japanese individuals with weak D phenotype: Identification of 20 new RHD alleles

Vox sanguinis, 2016-10, Vol.111 (3), p.315-319

2016

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Deletion of the RUNX1 binding site in the erythroid cell-specific regulatory element of the ABO gene in two individuals with the Am phenotype

Vox sanguinis, 2014-02, Vol.106 (2), p.167-175

2014

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Blood group B gene is barely expressed in in vitro erythroid culture of Bm-derived CD34+ cells without an erythroid cell-specific regulatory element

Vox sanguinis, 2015-04, Vol.108 (3), p.302-309

2015

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Presence of nucleotide substitutions in the ABO promoter in individuals with phenotypes A3 and B3

Vox sanguinis, 2016-04, Vol.110 (3), p.285-287

2016

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Silent KEL alleles identified from Japanese individuals with the Ko phenotype

Vox sanguinis, 2018-04, Vol.113 (3), p.290-296

2018

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Silent KEL alleles identified from Japanese individuals with the K o phenotype

Vox sanguinis, 2018-04, Vol.113 (3), p.290-296

2018

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Presence of nucleotide substitutions in transcriptional regulatory elements such as the erythroid cell-specific enhancer-like element and the ABO promoter in individuals with phenotypes A3 and B3, respectively

Vox sanguinis, 2014-08, Vol.107 (2), p.171-180

2014

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The B allele with a 5·8 kb deletion in intron 1 of the ABO gene is the major allele in Japanese individuals with B m and A 1 B m phenotypes

Vox sanguinis, 2018-05, Vol.113 (4), p.393-396

2018

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A novel DO null allele with a c.268C>T (p.Gln90Stop) mutation in Japanese

Vox sanguinis, 2015-08, Vol.109 (2), p.191-193

2015

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A 3·0-kb deletion including an erythroid cell-specific regulatory element in intron 1 of the ABO blood group gene in an individual with the Bm phenotype

Vox sanguinis, 2015-04, Vol.108 (3), p.310-313

2015

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Involvement of Sox1, 2 and 3 in the early and subsequent molecular events of lens induction

Development (Cambridge), 1998-07, Vol.125 (13), p.2521-2532

1998

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Application of bead array technology to simultaneous detection of human leucocyte antigen and human platelet antigen antibodies

Vox sanguinis, 2009-04, Vol.96 (3), p.244-251

2009

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JK null alleles identified from Japanese individuals with Jk(a−b−) phenotype

Vox sanguinis, 2014-05, Vol.106 (4), p.382-384

2014

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Production of human monoclonal anti-Jk3, recognising an epitope including the Jk(a) /Jk(b) polymorphic site of the Kidd glycoprotein

Transfusion medicine (Oxford, England), 2014-10, Vol.24 (5), p.286-291

2014

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Receptor Specificities of Human Respiroviruses

Journal of Virology, 2001-05, Vol.75 (10), p.4604-4613

2001

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Neogenin regulates neuronal survival through DAP kinase

Cell death and differentiation, 2008-10, Vol.15 (10), p.1593-1608

2008

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A new blood group system, RHAG: three antigens resulting from amino acid substitutions in the Rh-associated glycoprotein

Vox sanguinis, 2010-02, Vol.98 (2), p.151-159

2010

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A new blood group system, RHAG: three antigens resulting from amino acid substitutions in the Rh‐associated glycoprotein

Vox sanguinis, 2010-02, Vol.98 (2), p.151-159

2010

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Functional Analysis of Chicken Sox2 Enhancers Highlights an Array of Diverse Regulatory Elements that Are Conserved in Mammals

Developmental cell, 2003-04, Vol.4 (4), p.509-519

2003

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Pairing SOX off: with partners in the regulation of embryonic development

Trends in Genetics, 2000-04, Vol.16 (4), p.182-187

2000

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Molecular genetic analysis of variant phenotypes of the ABO blood group system

Blood, 1996-10, Vol.88 (7), p.2732-2737

1996

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

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

The KANNO blood group system

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 A1Bm phenotypes

Prevalence of RHD alleles in Japanese individuals with weak D phenotype: Identification of 20 new RHD alleles

Deletion of the RUNX1 binding site in the erythroid cell-specific regulatory element of the ABO gene in two individuals with the Am phenotype

Blood group B gene is barely expressed in in vitro erythroid culture of Bm-derived CD34+ cells without an erythroid cell-specific regulatory element

Presence of nucleotide substitutions in the ABO promoter in individuals with phenotypes A3 and B3

Silent KEL alleles identified from Japanese individuals with the Ko phenotype

Silent KEL alleles identified from Japanese individuals with the K o phenotype

Presence of nucleotide substitutions in transcriptional regulatory elements such as the erythroid cell-specific enhancer-like element and the ABO promoter in individuals with phenotypes A3 and B3, respectively

The B allele with a 5·8 kb deletion in intron 1 of the ABO gene is the major allele in Japanese individuals with B m and A 1 B m phenotypes

A novel DO null allele with a c.268C>T (p.Gln90Stop) mutation in Japanese

A 3·0-kb deletion including an erythroid cell-specific regulatory element in intron 1 of the ABO blood group gene in an individual with the Bm phenotype

Involvement of Sox1, 2 and 3 in the early and subsequent molecular events of lens induction

Application of bead array technology to simultaneous detection of human leucocyte antigen and human platelet antigen antibodies

JK null alleles identified from Japanese individuals with Jk(a−b−) phenotype

Production of human monoclonal anti-Jk3, recognising an epitope including the Jk(a) /Jk(b) polymorphic site of the Kidd glycoprotein

Receptor Specificities of Human Respiroviruses

Neogenin regulates neuronal survival through DAP kinase

A new blood group system, RHAG: three antigens resulting from amino acid substitutions in the Rh-associated glycoprotein

A new blood group system, RHAG: three antigens resulting from amino acid substitutions in the Rh‐associated glycoprotein

Functional Analysis of Chicken Sox2 Enhancers Highlights an Array of Diverse Regulatory Elements that Are Conserved in Mammals

Pairing SOX off: with partners in the regulation of embryonic development

Molecular genetic analysis of variant phenotypes of the ABO blood group system

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