Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Ryuichi Yabe"'
Autor:
Naoko Watanabe-Okochi, Yumi Suzuki, Hatsue Tsuneyama, Ryuichi Yabe, Nelson-Hirokazu Tsuno, Kazunori Nakajima, Kana Sasaki, Kenichi Ogasawara, Makoto Uchikawa, Kazumi Isa
Publikováno v:
Vox Sanguinis. 115:756-766
Background The low-incidence antigen Sta of the MNS system is usually associated with the GP(B-A) hybrid molecule, which carries the 'N' antigen at the N terminus. The GP(A-A) molecule with trypsin-resistant M antigen has been found in a few St(a+) i
Autor:
Akira Oda, Takafumi Kimura, Kazumi Isa, Nelson Hirokazu Tsuno, Yumi Suzuki, Ryuichi Yabe, Kenichi Ogasawara, Makoto Uchikawa
Publikováno v:
TransfusionREFERENCES. 61(10)
BACKGROUND In this study, we identified a novel glycophorin variant (GP.MOT) in a Mia -positive Japanese blood donor. The proband with this glycophorin variant was discovered by antigen screening of samples from 475,493 Japanese blood donors using mo
Autor:
Ryuichi Yabe, Hatsue Tsuneyama, Kazumi Isa, Masahiro Satake, Go Kikuchi, Masayuki Shiba, Yukio Nakamura, Tadashi Nagai, Kenichi Ogasawara, Kenji Tadokoro, Ryo Kurita
Publikováno v:
Transfusion. 58:2675-2682
Background Antibody screening in pretransfusion tests is necessary to avoid critical complications of blood transfusion. Although red blood cells (RBCs) expressing relevant alloantigen(s) have been used for serologic antibody screening, little attent
Autor:
N. Yokoya, Yuji Hori, Toru Miyazaki, Makoto Uchikawa, Takayuki Enomoto, Shoichi Ito, Masahiro Satake, Kenichi Ogasawara, Ryuichi Yabe, M. Kumamoto, S. Watanabe
Publikováno v:
Vox Sanguinis. 113:393-396
Bm and A1 Bm phenotypes are the most frequent ABO variants in the Japanese population. The B antigen on Bm red blood cells is only detectable by adsorption and elution tests, and plasma B-transferase activity is usually detected at half or less level
Publikováno v:
The Proceedings of the Dynamics & Design Conference. 2022:106
Autor:
Masahiro Satake, Nelson-Hirokazu Tsuno, Kazumi Isa, Kenichi Ogasawara, Makoto Uchikawa, Yumi Suzuki, Ryuichi Yabe, Yuika Kikuchi
Publikováno v:
Vox Sanguinis. 114:171-173
We found an individual with weakened S antigen expression on red blood cells (RBCs) during routine blood grouping. The proband was typed S+s+ by polyclonal antibodies, but the RBCs demonstrated different reactivity with three monoclonal anti-S. The p
Autor:
Naoko, Watanabe-Okochi, Hatsue, Tsuneyama, Kazumi, Isa, Kana, Sasaki, Yumi, Suzuki, Ryuichi, Yabe, Nelson-Hirokazu, Tsuno, Kazunori, Nakajima, Kenichi, Ogasawara, Makoto, Uchikawa
Publikováno v:
Vox sanguinisReferences. 115(8)
The low-incidence antigen StAmong Japanese blood donors, we screened 24 292 individuals for the presence of St(a+) with trypsin-resistant 'N' antigen and 193 009 individuals for the presence of St(a+) with trypsin-resistant M antigen. The breakpoints
Autor:
Go, Kikuchi, Ryo, Kurita, Kenichi, Ogasawara, Kazumi, Isa, Hatsue, Tsuneyama, Yukio, Nakamura, Ryuichi, Yabe, Masayuki, Shiba, Kenji, Tadokoro, Tadashi, Nagai, Masahiro, Satake
Publikováno v:
Transfusion. 58(11)
Antibody screening in pretransfusion tests is necessary to avoid critical complications of blood transfusion. Although red blood cells (RBCs) expressing relevant alloantigen(s) have been used for serologic antibody screening, little attention has bee
Autor:
K. Ogasawara, Kazunori Nakajima, Hatsue Tsuneyama, Yumi Suzuki, A. Masuno, M. Okuda, Chizu Toyoda, T. Onodera, Makoto Uchikawa, Ryuichi Yabe
Publikováno v:
Transfusion Medicine. 24:286-291
SUMMARY Background and objectives The Kidd blood group system consists of polymorphic antigens, Jka (JK1) and Jkb (JK2), and a high-incidence antigen, Jk3. Anti-Jk3 is often observed in immunised Jk(a−b−) individuals. In this study, we aimed to e
Autor:
Makoto Uchikawa, Hatsue Tsuneyama, Ryuichi Yabe, K. Sasaki, M. Saito, Kazumi Isa, Kenichi Ogasawara, Masahiro Satake
Publikováno v:
Vox sanguinis. 111(3)
We identified 46 different RHD alleles from 226 Japanese individuals with weak D phenotype, 26 of which had been previously described and 20 that were novel. Among these weak D individuals, the alleles with c.960G>A, c.845G>A (RHD*15) or c.1013T>C (R