Uchikawa M - Search Results

1

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: uchikawa m. Vox Sang. 2014 May;106(4):382-4. doi: 10.1111/vox.12117. Vox Sang. 2014. PMID: 24877238

2

Asian-type DEL (RHD*DEL1) with an allo-anti-D: A paradoxical observation in a healthy multiparous woman.

Ohto H, Ito S, Srivastava K, Ogiyama Y, Uchikawa M, Nollet KE, Flegel WA. Ohto H, et al. Among authors: uchikawa m. Transfusion. 2023 Aug;63(8):1601-1611. doi: 10.1111/trf.17465. Epub 2023 Jul 19. Transfusion. 2023. PMID: 37465939 Free PMC article.

3

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: uchikawa m. Vox Sang. 1994;66(4):293-4. doi: 10.1111/j.1423-0410.1994.tb00332.x. Vox Sang. 1994. PMID: 8079454

4

Extensive polymorphism of ABO blood group gene: three major lineages of the alleles for the common ABO phenotypes.

Ogasawara K, Bannai M, Saitou N, Yabe R, Nakata K, Takenaka M, Fujisawa K, Uchikawa M, Ishikawa Y, Juji T, Tokunaga K. Ogasawara K, et al. Among authors: uchikawa m. Hum Genet. 1996 Jun;97(6):777-83. doi: 10.1007/BF02346189. Hum Genet. 1996. PMID: 8641696

5

Molecular genetic analysis of variant phenotypes of the ABO blood group system.

Ogasawara K, Yabe R, Uchikawa M, Saitou N, Bannai M, Nakata K, Takenaka M, Fujisawa K, Ishikawa Y, Juji T, Tokunaga K. Ogasawara K, et al. Among authors: uchikawa m. Blood. 1996 Oct 1;88(7):2732-7. Blood. 1996. PMID: 8839869 Free article.

6

Serological analysis of monoclonal anti-E and -e with Japanese E/e variant red cells.

Uchikawa M, Toyoda C, Shinozaki K, Suzuki Y, Tsuneyama H, Juji T. Uchikawa M, et al. Transfus Clin Biol. 1996;3(6):387-9. doi: 10.1016/s1246-7820(96)80050-4. Transfus Clin Biol. 1996. PMID: 9018795

7

Molecular cloning and characterization of decay-accelerating factor deficiency in Cromer blood group Inab phenotype.

Wang L, Uchikawa M, Tsuneyama H, Tokunaga K, Tadokoro K, Juji T. Wang L, et al. Among authors: uchikawa m. Blood. 1998 Jan 15;91(2):680-4. Blood. 1998. PMID: 9427725 Free article.

8

A new high-molecular-weight glycophorin C variant with a duplication of exon 2 in the glycophorin C gene.

Uchikawa M, Tsuneyama H, Onodera T, Murata S, Juji T. Uchikawa M, et al. Transfus Med. 1997 Dec;7(4):305-9. doi: 10.1046/j.1365-3148.1997.d01-36.x. Transfus Med. 1997. PMID: 9510930

9

Different alleles cause an imbalance in A2 and A2B phenotypes of the ABO blood group.

Ogasawara K, Yabe R, Uchikawa M, Bannai M, Nakata K, Takenaka M, Takahashi Y, Juji T, Tokunaga K. Ogasawara K, et al. Among authors: uchikawa m. Vox Sang. 1998;74(4):242-7. Vox Sang. 1998. PMID: 9691405

10

Polymorphisms of RhD(Va) and a new RhD(Va)-like variant found in Japanese individuals.

Hyodo H, Ishikawa Y, Kashiwase K, Ogawa A, Watanabe Y, Tsuneyama H, Toyoda C, Uchikawa M, Akaza T, Fujii T, Kozuma S, Taketani Y, Juji T. Hyodo H, et al. Among authors: uchikawa m. Vox Sang. 2000;78(2):122-5. doi: 10.1159/000031162. Vox Sang. 2000. PMID: 10765149

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