Uchikawa M - Search Results

1

Two cases of mosaic RhD blood-group phenotypes and paternal isodisomy for chromosome 1.

Miyoshi O, Yabe R, Wakui K, Fukushima Y, Koizumi S, Uchikawa M, Kajii T, Numakura C, Takahashi S, Hayasaka K, Niikawa N. Miyoshi O, et al. Among authors: uchikawa m. Am J Med Genet. 2001 Dec 1;104(3):250-6. Am J Med Genet. 2001. PMID: 11754053

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

3

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

4

Prevalence of RHD alleles in Japanese individuals with weak D phenotype: Identification of 20 new RHD alleles.

Isa K, Sasaki K, Ogasawara K, Saito M, Tsuneyama H, Yabe R, Uchikawa M, Satake M. Isa K, et al. Among authors: uchikawa m. Vox Sang. 2016 Oct;111(3):315-319. doi: 10.1111/vox.12413. Epub 2016 May 17. Vox Sang. 2016. PMID: 27183894

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

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. Among authors: uchikawa m. Immunogenetics. 2001 Apr;53(3):190-9. doi: 10.1007/s002510100315. Immunogenetics. 2001. PMID: 11398963

7

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_m and A₁ B_m phenotypes.

Ogasawara K, Miyazaki T, Ito S, Yabe R, Uchikawa M, Enomoto T, Yokoya N, Hori Y, Kumamoto M, Watanabe S, Satake M. Ogasawara K, et al. Among authors: uchikawa m. Vox Sang. 2018 May;113(4):393-396. doi: 10.1111/vox.12642. Epub 2018 Feb 23. Vox Sang. 2018. PMID: 29473176

8

Presence of nucleotide substitutions in the ABO promoter in individuals with phenotypes A3 and B3.

Isa K, Yamamuro Y, Ogasawara K, Yabe R, Ogiyama Y, Ito S, Takahashi Y, Kominato Y, Sano R, Uchikawa M. Isa K, et al. Among authors: uchikawa m. Vox Sang. 2016 Apr;110(3):285-7. doi: 10.1111/vox.12363. Epub 2015 Nov 3. Vox Sang. 2016. PMID: 26529276

9

Gene organization and rearrangements at the human Rhesus blood group locus revealed by fiber-FISH analysis.

Suto Y, Ishikawa Y, Hyodo H, Uchikawa M, Juji T. Suto Y, et al. Among authors: uchikawa m. Hum Genet. 2000 Feb;106(2):164-71. doi: 10.1007/s004390051024. Hum Genet. 2000. PMID: 10746557

10

GP.MOT: A novel glycophorin variant identified in a Japanese blood donor.

Oda A, Suzuki Y, Isa K, Ogasawara K, Yabe R, Kimura T, Uchikawa M, Tsuno NH. Oda A, et al. Among authors: uchikawa m. Transfusion. 2021 Oct;61(10):2825-2829. doi: 10.1111/trf.16535. Epub 2021 Aug 9. Transfusion. 2021. PMID: 34369596

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