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Mechanisms of Development
|
August 29, 2000
Zebrafish mutations in Gli-mediated hedgehog signaling lead to lens transdifferentiation from the adenohypophysis anlage
H Kondoh, M Uchikawa, H Yoda, et al.
British Journal of Haematology
|
October 1, 1989
Studies on the sensitivity to complement-mediated lysis of erythrocytes (Inab phenotype) with a deficiency of DAF (decay accelerating factor)
A H Merry, V I Rawlinson, M Uchikawa, et al.
Vox Sanguinis
|
September 5, 2015
Weak D alleles in Japanese: a c.960G>A silent mutation in exon 7 of the RHD gene that affects D expression
K Ogasawara, K Sasaki, K Isa, et al.
Vox Sanguinis
|
April 14, 2015
A novel DO null allele with a c.268C>T (p.Gln90Stop) mutation in Japanese
T Onodera, H Tsuneyama, K Ogasawara, et al.
Immunogenetics
|
June 12, 2001
Recombination and gene conversion-like events may contribute to ABO gene diversity causing various phenotypes
K Ogasawara, R Yabe, M Uchikawa, et al.
Transfusion Medicine (Oxford, England)
|
May 2, 2002
Recombinant forms of glycophorin C as a tool for characterization of epitopes for new murine monoclonal antibodies with anti-glycophorin C specificity
E Jaskiewicz, M Czerwinski, M Uchikawa, et al.
Vox Sanguinis
|
June 6, 2000
D(Va) category phenotype and genotype in Japanese families
T J Legler, V Wiemann, H Ohto, et al.
Transfusion Science
|
October 18, 2000
Three episodes of delayed hemolytic transfusion reactions due to multiple red cell antibodies, anti-Di, anti-Jk and anti-E
H Yasuda, H Ohto, O Yamaguchi, et al.
Vox Sanguinis
|
May 31, 2014
JK null alleles identified from Japanese individuals with Jk(a−b−) phenotype
T Onodera, K Sasaki, H Tsuneyama, et al.
Vox Sanguinis
|
February 12, 2009
Application of bead array technology to simultaneous detection of human leucocyte antigen and human platelet antigen antibodies
K Fujiwara, K Shimano, H Tanaka, et al.
Page
of 6
Search research articles
Search
Showing results (21-30 of 59) with videos related to
Sort By:
Page
of 6
Mechanisms of Development
|
August 29, 2000
Zebrafish mutations in Gli-mediated hedgehog signaling lead to lens transdifferentiation from the adenohypophysis anlage
H Kondoh, M Uchikawa, H Yoda, et al.
British Journal of Haematology
|
October 1, 1989
Studies on the sensitivity to complement-mediated lysis of erythrocytes (Inab phenotype) with a deficiency of DAF (decay accelerating factor)
A H Merry, V I Rawlinson, M Uchikawa, et al.
Vox Sanguinis
|
September 5, 2015
Weak D alleles in Japanese: a c.960G>A silent mutation in exon 7 of the RHD gene that affects D expression
K Ogasawara, K Sasaki, K Isa, et al.
Vox Sanguinis
|
April 14, 2015
A novel DO null allele with a c.268C>T (p.Gln90Stop) mutation in Japanese
T Onodera, H Tsuneyama, K Ogasawara, et al.
Immunogenetics
|
June 12, 2001
Recombination and gene conversion-like events may contribute to ABO gene diversity causing various phenotypes
K Ogasawara, R Yabe, M Uchikawa, et al.
Transfusion Medicine (Oxford, England)
|
May 2, 2002
Recombinant forms of glycophorin C as a tool for characterization of epitopes for new murine monoclonal antibodies with anti-glycophorin C specificity
E Jaskiewicz, M Czerwinski, M Uchikawa, et al.
Vox Sanguinis
|
June 6, 2000
D(Va) category phenotype and genotype in Japanese families
T J Legler, V Wiemann, H Ohto, et al.
Transfusion Science
|
October 18, 2000
Three episodes of delayed hemolytic transfusion reactions due to multiple red cell antibodies, anti-Di, anti-Jk and anti-E
H Yasuda, H Ohto, O Yamaguchi, et al.
Vox Sanguinis
|
May 31, 2014
JK null alleles identified from Japanese individuals with Jk(a−b−) phenotype
T Onodera, K Sasaki, H Tsuneyama, et al.
Vox Sanguinis
|
February 12, 2009
Application of bead array technology to simultaneous detection of human leucocyte antigen and human platelet antigen antibodies
K Fujiwara, K Shimano, H Tanaka, et al.
Page
of 6