Ogasawara K - 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: ogasawara k. Vox Sang. 2014 May;106(4):382-4. doi: 10.1111/vox.12117. Vox Sang. 2014. PMID: 24877238

2

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. Hum Genet. 1996 Jun;97(6):777-83. doi: 10.1007/BF02346189. Hum Genet. 1996. PMID: 8641696

3

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. Blood. 1996 Oct 1;88(7):2732-7. Blood. 1996. PMID: 8839869 Free article.

4

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. Vox Sang. 1998;74(4):242-7. Vox Sang. 1998. PMID: 9691405

5

Recombination and gene conversion-like events may contribute to ABO gene diversity causing various phenotypes.

Ogasawara K, Yabe R, Uchikawa M, Nakata K, Watanabe J, Takahashi Y, Tokunaga K. Ogasawara K, et al. Immunogenetics. 2001 Apr;53(3):190-9. doi: 10.1007/s002510100315. Immunogenetics. 2001. PMID: 11398963

6

A new blood group system, RHAG: three antigens resulting from amino acid substitutions in the Rh-associated glycoprotein.

Tilley L, Green C, Poole J, Gaskell A, Ridgwell K, Burton NM, Uchikawa M, Tsuneyama H, Ogasawara K, Akkøk CA, Daniels G. Tilley L, et al. Among authors: ogasawara k. Vox Sang. 2010 Feb;98(2):151-9. doi: 10.1111/j.1423-0410.2009.01243.x. Epub 2009 Sep 8. Vox Sang. 2010. PMID: 19744193

7

Expression of ABO blood-group genes is dependent upon an erythroid cell-specific regulatory element that is deleted in persons with the B(m) phenotype.

Sano R, Nakajima T, Takahashi K, Kubo R, Kominato Y, Tsukada J, Takeshita H, Yasuda T, Ito K, Maruhashi T, Yokohama A, Isa K, Ogasawara K, Uchikawa M. Sano R, et al. Among authors: ogasawara k. Blood. 2012 May 31;119(22):5301-10. doi: 10.1182/blood-2011-10-387167. Epub 2012 Mar 9. Blood. 2012. PMID: 22408256 Free article. Clinical Trial.

8

Mutation of the GATA site in the erythroid cell-specific regulatory element of the ABO gene in a Bm subgroup individual.

Nakajima T, Sano R, Takahashi Y, Kubo R, Takahashi K, Kominato Y, Tsukada J, Takeshita H, Yasuda T, Uchikawa M, Isa K, Ogasawara K. Nakajima T, et al. Among authors: ogasawara k. Transfusion. 2013 Nov;53(11 Suppl 2):2917-27. doi: 10.1111/trf.12181. Epub 2013 Apr 8. Transfusion. 2013. PMID: 23560502

9

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: ogasawara k. Vox Sang. 2014 Feb;106(2):167-75. doi: 10.1111/vox.12077. Epub 2013 Sep 2. Vox Sang. 2014. PMID: 23992526

10

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: ogasawara k. Transfusion. 2014 May;54(5):1438-9. doi: 10.1111/trf.12540. Epub 2014 Jan 9. Transfusion. 2014. PMID: 24400966 No abstract available.

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