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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.Clinical Science (London, England : 1979)|June 1, 1987
Multiple forms of immunoreactive renin in human adrenocortical tumour tissue from patients with primary aldosteronismK Mizuno, M Ojima, S Hashimoto, 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.Journal of Medicine|January 1, 1987
A hitherto unreported case of 21-hydroxylase deficiency associated with Bartter's syndrome and a balanced 6-9 translocationR Yabe, K Mizuno, M Ojima, et al.Nihon Naibunpi Gakkai Zasshi|August 20, 1986
[A case of 21-hydroxylase deficiency and Bartter's syndrome associated with a balanced 6-9 translocation]R Yabe, K Mizuno, M Ojima, et al.Life Sciences|November 10, 1986
Biochemical evidence for existence of immunoreactive renin in human prolactinoma tissueK Mizuno, M Ojima, Y Kusano, 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.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.Vox Sanguinis|February 24, 2018
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<sub>m</sub> and A<sub>1</sub> B<sub>m</sub> phenotypesK Ogasawara, T Miyazaki, S Ito, 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.Pageof 3