Tsuneyama H - Search Results

1

Anemic Disease of the Newborn With Little Increase in Hemolysis and Erythropoiesis Due to Maternal Anti-Jr^a: A Case Study and Review of the Literature.

Katsuragi S, Ohto H, Yoshida A, Otake A, Tsuneyama H, Ogasawara K, Isa K, Ikeda T. Katsuragi S, et al. Among authors: tsuneyama h. Transfus Med Rev. 2019 Jul;33(3):183-188. doi: 10.1016/j.tmrv.2019.03.002. Epub 2019 Apr 26. Transfus Med Rev. 2019. PMID: 31227265 Review.

2

First case of hemolytic disease of the newborn due to anti-Ula antibodies.

Sakuma K, Suzuki H, Ohto H, Tsuneyama H, Uchikawa M. Sakuma K, et al. Among authors: tsuneyama h. Vox Sang. 1994;66(4):293-4. doi: 10.1111/j.1423-0410.1994.tb00332.x. Vox Sang. 1994. PMID: 8079454

3

Three episodes of delayed hemolytic transfusion reactions due to multiple red cell antibodies, anti-Di, anti-Jk and anti-E.

Yasuda H, Ohto H, Yamaguchi O, Sakuma S, Suzuki T, Mita M, Tsuneyama H, Uchikawa M. Yasuda H, et al. Among authors: tsuneyama h. Transfus Sci. 2000 Oct;23(2):107-12. doi: 10.1016/s0955-3886(00)00074-6. Transfus Sci. 2000. PMID: 11035271

4

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

Takahashi Y, Isa K, Sano R, Nakajima T, Kubo R, Takahashi K, Kominato Y, Tsuneyama H, Ogasawara K, Uchikawa M. Takahashi Y, et al. Among authors: tsuneyama h. Vox Sang. 2014 Feb;106(2):167-75. doi: 10.1111/vox.12077. Epub 2013 Sep 2. Vox Sang. 2014. PMID: 23992526

5

Novel alleles of Lan- in Japanese populations.

Tanaka M, Yamamuro Y, Takahashi J, Ogasawara K, Osabe T, Tsuneyama H, Enomoto T, Watanabe S, Uchikawa M, Tadokoro K, Tani Y. Tanaka M, et al. Among authors: tsuneyama h. Transfusion. 2014 May;54(5):1438-9. doi: 10.1111/trf.12540. Epub 2014 Jan 9. Transfusion. 2014. PMID: 24400966 No abstract available.

6

Anti-KANNO: a novel alloantibody against a red cell antigen of high frequency.

Kawabata K, Uchikawa M, Ohto H, Yasuda H, Tsuneyama H, Tsuchida H, Ito S. Kawabata K, et al. Among authors: tsuneyama h. Transfus Med Rev. 2014 Jan;28(1):23-8. doi: 10.1016/j.tmrv.2013.12.001. Epub 2013 Dec 16. Transfus Med Rev. 2014. PMID: 24485899

7

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.

Takahashi Y, Isa K, Sano R, Nakajima T, Kubo R, Takahashi K, Kominato Y, Michino J, Masuno A, Tsuneyama H, Ito S, Ogasawara K, Uchikawa M. Takahashi Y, et al. Among authors: tsuneyama h. Vox Sang. 2014 Aug;107(2):171-80. doi: 10.1111/vox.12136. Epub 2014 Mar 6. Vox Sang. 2014. PMID: 24602004

8

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

Onodera T, Sasaki K, Tsuneyama H, Isa K, Ogasawara K, Satake M, Tadokoro K, Uchikawa M. Onodera T, et al. Among authors: tsuneyama h. Vox Sang. 2014 May;106(4):382-4. doi: 10.1111/vox.12117. Vox Sang. 2014. PMID: 24877238

9

ABO chimerism with a minor allele detected by the peptide nucleic acid-mediated polymerase chain reaction clamping method.

Sano R, Takahashi Y, Nakajima T, Yoshii M, Kubo R, Takahashi K, Kominato Y, Takeshita H, Yasuda T, Tsuneyama H, Uchikawa M, Isa K, Ogasawara K. Sano R, et al. Among authors: tsuneyama h. Blood Transfus. 2014 Jul;12(3):431-4. doi: 10.2450/2014.0162-13. Epub 2014 Jan 2. Blood Transfus. 2014. PMID: 24887221 Free PMC article. No abstract available.

10

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

Toyoda C, Suzuki Y, Tsuneyama H, Onodera T, Masuno A, Yabe R, Ogasawara K, Okuda M, Nakajima K, Uchikawa M. Toyoda C, et al. Among authors: tsuneyama h. Transfus Med. 2014 Oct;24(5):286-91. doi: 10.1111/tme.12146. Epub 2014 Sep 2. Transfus Med. 2014. PMID: 25180691

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