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M Uchikawa

Showing results (41-50 of 59) with videos related to

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The Biochemical Journal|July 15, 1989
Studies on the defect which causes absence of decay accelerating factor (DAF) from the peripheral blood cells of an individual with the Inab phenotypeC G Tate, M Uchikawa, M J Tanner, et al.
Vox Sanguinis|November 4, 2015
Presence of nucleotide substitutions in the ABO promoter in individuals with phenotypes A3 and B3K Isa, Y Yamamuro, K Ogasawara, et al.
Vox Sanguinis|September 3, 2013
Deletion of the RUNX1 binding site in the erythroid cell-specific regulatory element of the ABO gene in two individuals with the Am phenotypeY Takahashi, K Isa, R Sano, et al.
Transfusion Medicine (Oxford, England)|September 3, 2014
Production of human monoclonal anti-Jk3, recognising an epitope including the Jk(a) /Jk(b) polymorphic site of the Kidd glycoproteinC Toyoda, Y Suzuki, H Tsuneyama, et al.
Cytogenetic and Genome Research|November 12, 2003
Gene arrangement at the Rhesus blood group locus of chimpanzees detected by fiber-FISHY Suto, Y Ishikawa, H Hyodo, et al.
Medical Microbiology and Immunology|October 1, 1995
Prevalence of Borna disease virus RNA in peripheral blood mononuclear cells from blood donorsM Kishi, T Nakaya, Y Nakamura, et al.
Human Genetics|June 1, 1996
Extensive polymorphism of ABO blood group gene: three major lineages of the alleles for the common ABO phenotypesK Ogasawara, M Bannai, N Saitou, et al.
American Journal of Medical Genetics|December 26, 2001
Two cases of mosaic RhD blood-group phenotypes and paternal isodisomy for chromosome 1O Miyoshi, R Yabe, K Wakui, et al.
Transfusion|November 29, 2001
E variants found in Japanese and c antigenicity alteration without substitution in the second extracellular loopK Kashiwase, Y Ishikawa, H Hyodo, et al.
Blood|October 1, 1996
Molecular genetic analysis of variant phenotypes of the ABO blood group systemK Ogasawara, R Yabe, M Uchikawa, et al.
Pageof 6

Showing results (41-50 of 59) with videos related to

Sort By:
Pageof 6
The Biochemical Journal|July 15, 1989
Studies on the defect which causes absence of decay accelerating factor (DAF) from the peripheral blood cells of an individual with the Inab phenotypeC G Tate, M Uchikawa, M J Tanner, et al.
Vox Sanguinis|November 4, 2015
Presence of nucleotide substitutions in the ABO promoter in individuals with phenotypes A3 and B3K Isa, Y Yamamuro, K Ogasawara, et al.
Vox Sanguinis|September 3, 2013
Deletion of the RUNX1 binding site in the erythroid cell-specific regulatory element of the ABO gene in two individuals with the Am phenotypeY Takahashi, K Isa, R Sano, et al.
Transfusion Medicine (Oxford, England)|September 3, 2014
Production of human monoclonal anti-Jk3, recognising an epitope including the Jk(a) /Jk(b) polymorphic site of the Kidd glycoproteinC Toyoda, Y Suzuki, H Tsuneyama, et al.
Cytogenetic and Genome Research|November 12, 2003
Gene arrangement at the Rhesus blood group locus of chimpanzees detected by fiber-FISHY Suto, Y Ishikawa, H Hyodo, et al.
Medical Microbiology and Immunology|October 1, 1995
Prevalence of Borna disease virus RNA in peripheral blood mononuclear cells from blood donorsM Kishi, T Nakaya, Y Nakamura, et al.
Human Genetics|June 1, 1996
Extensive polymorphism of ABO blood group gene: three major lineages of the alleles for the common ABO phenotypesK Ogasawara, M Bannai, N Saitou, et al.
American Journal of Medical Genetics|December 26, 2001
Two cases of mosaic RhD blood-group phenotypes and paternal isodisomy for chromosome 1O Miyoshi, R Yabe, K Wakui, et al.
Transfusion|November 29, 2001
E variants found in Japanese and c antigenicity alteration without substitution in the second extracellular loopK Kashiwase, Y Ishikawa, H Hyodo, et al.
Blood|October 1, 1996
Molecular genetic analysis of variant phenotypes of the ABO blood group systemK Ogasawara, R Yabe, M Uchikawa, et al.
Pageof 6