Takahashi J - Search Results

1

Expression analysis of human Rhesus blood group antigens by gene transduction into erythroid and non-erythroid cells.

Iwamoto S, Yamasaki M, Kawano M, Okuda H, Omi T, Takahashi J, Tani Y, Omine M, Kajii E. Iwamoto S, et al. Among authors: takahashi j. Int J Hematol. 1998 Oct;68(3):257-68. doi: 10.1016/s0925-5710(98)00072-3. Int J Hematol. 1998. PMID: 9846010

2

Isolation, characterization, and family study of DTI, a novel partial D phenotype affecting the fourth external loop of D polypeptides.

Omi T, Takahashi J, Seno T, Tanaka M, Hirayama F, Matsuo M, Ueda N, Obara K, Okuda H, Iwamoto S, Tani Y, Kajii E. Omi T, et al. Among authors: takahashi j. Transfusion. 2002 Apr;42(4):481-9. doi: 10.1046/j.1525-1438.2002.00082.x. Transfusion. 2002. PMID: 12076297

3

The genomic organization of the partial D category DVa: the presence of a new partial D associated with the DVa phenotype.

Omi T, Takahashi J, Tsudo N, Okuda H, Iwamoto S, Tanaka M, Seno T, Tani Y, Kajii E. Omi T, et al. Among authors: takahashi j. Biochem Biophys Res Commun. 1999 Jan 27;254(3):786-94. doi: 10.1006/bbrc.1998.0121. Biochem Biophys Res Commun. 1999. PMID: 9920819

4

The STR polymorphisms in intron 8 may provide information about the molecular evolution of RH haplotypes.

Fujiwara H, Okuda H, Omi T, Iwamoto S, Tanaka Y, Takahashi J, Tani Y, Minakami H, Araki S, Sato I, Kajii E. Fujiwara H, et al. Among authors: takahashi j. Hum Genet. 1999 Apr;104(4):301-6. doi: 10.1007/s004390050958. Hum Genet. 1999. PMID: 10369159

5

Reactivity of autoantibodies of autoimmune hemolytic anemia with recombinant rhesus blood group antigens or anion transporter band3.

Iwamoto S, Kamesaki T, Oyamada T, Okuda H, Kumada M, Omi T, Takahashi J, Tani Y, Omine M, Kajii E. Iwamoto S, et al. Among authors: takahashi j. Am J Hematol. 2001 Oct;68(2):106-14. doi: 10.1002/ajh.1161. Am J Hematol. 2001. PMID: 11559950 Free article.

6

Molecular characterization of weak D phenotypes by site-directed mutagenesis and expression of mutant Rh-green fluorescence protein fusions in K562 cells.

Kamesaki T, Iwamoto S, Kumada M, Omi T, Okuda H, Tanaka M, Takahashi J, Obara K, Seno T, Tani Y, Kajii E. Kamesaki T, et al. Among authors: takahashi j. Vox Sang. 2001 Nov;81(4):254-8. doi: 10.1046/j.1423-0410.2001.00118.x. Vox Sang. 2001. PMID: 11904002

7

Detection of Rh23 in the partial D phenotype associated with the D(Va) category.

Omi T, Okuda H, Iwamoto S, Kajii E, Takahashi J, Tanaka M, Tani Y, Fraser RH, Seno T. Omi T, et al. Among authors: takahashi j. Transfusion. 2000 Feb;40(2):256-8. doi: 10.1046/j.1537-2995.2000.40020256.x. Transfusion. 2000. PMID: 10686014 No abstract available.

8

A novel mutation in the RHD gene in Japanese individuals with weak D, encoding an amino acid change in the 11th transmembranous domain of the RhD protein.

Kamesaki T, Kumada M, Omi T, Okuda H, Iwamoto S, Takahashi J, Kimura K, Hirayama F, Kamata H, Obara K, Taniguchi M, Tani Y, Kajii E. Kamesaki T, et al. Among authors: takahashi j. Vox Sang. 2003 Feb;84(2):141. doi: 10.1046/j.1423-0410.2003.00274.x. Vox Sang. 2003. PMID: 12609022 No abstract available.

9

A new mutation detected in RhAG of a Japanese family with Rh(mod) syndrome may form a longer RhAG protein.

Kamesaki T, Iwamoto S, Kajii E, Takahashi J, Kimura K, Nakade T, Tani Y. Kamesaki T, et al. Among authors: takahashi j. Transfusion. 2002 Mar;42(3):383-4. doi: 10.1046/j.1537-2995.2002.00062.x. Transfusion. 2002. PMID: 11961248 No abstract available.

10

Treatment of McLeod phenotype chronic granulomatous disease with reduced-intensity conditioning and unrelated-donor umbilical cord blood transplantation.

Suzuki N, Hatakeyama N, Yamamoto M, Mizue N, Kuroiwa Y, Yoda M, Takahashi J, Tani Y, Tsutsumi H. Suzuki N, et al. Among authors: takahashi j. Int J Hematol. 2007 Jan;85(1):70-2. doi: 10.1532/IJH9706129. Int J Hematol. 2007. PMID: 17261504

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