Magnitude of the Screening Field for YBCO Coils von Yanagisawa, Y, Kominato, Y, Nakagome, H, Hu, R, Takematsu, T, Takao, T, Uglietti, D, Kiyoshi, T, Takahashi, M, Maeda, H

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Sequence analysis of ABO and its homologues is valid for species identification von Sano, R., Fukuda, H., Takahashi, Y., Takahashi, K., Kubo, R., Kobayashi, M., Fujihara, J., Takeshita, H., Kominato, Y.

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Presence of nucleotide substitutions in the ABO promoter in individuals with phenotypes A3 and B3 von Isa, K., Yamamuro, Y., Ogasawara, K., Yabe, R., Ogiyama, Y., Ito, S., Takahashi, Y., Kominato, Y., Sano, R., Uchikawa, M.

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Deletion of the RUNX1 binding site in the erythroid cell-specific regulatory element of the ABO gene in two individuals with the Am phenotype von Takahashi, Y., Isa, K., Sano, R., Nakajima, T., Kubo, R., Takahashi, K., Kominato, Y., Tsuneyama, H., Ogasawara, K., Uchikawa, M.

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Blood group B gene is barely expressed in in vitro erythroid culture of Bm-derived CD34+ cells without an erythroid cell-specific regulatory element von Sano, R., Nogawa, M., Nakajima, T., Takahashi, Y., Takahashi, K., Kubo, R., Kominato, Y., Yokohama, A., Tsukada, J., Yamao, H., Kishida, T., Ogasawara, K., Uchikawa, M.

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Presence of nucleotide substitutions in transcriptional regulatory elements such as the erythroid cell-specific enhancer-like element and the ABO promoter in individuals with pheno... von 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.

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ABO alleles are linked with haplotypes of an erythroid cell-specific regulatory element in intron 1 with a few exceptions attributable to genetic recombination von Nakajima, T., Sano, R., Takahashi, Y., Watanabe, K., Kubo, R., Kobayashi, M., Takahashi, K., Takeshita, H., Kominato, Y.

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A 3·0-kb deletion including an erythroid cell-specific regulatory element in intron 1 of the ABO blood group gene in an individual with the Bm phenotype von Sano, R., Kuboya, E., Nakajima, T., Takahashi, Y., Takahashi, K., Kubo, R., Kominato, Y., Takeshita, H., Yamao, H., Kishida, T., Isa, K., Ogasawara, K., Uchikawa, M.

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Reduction of blood group A antigen on erythrocytes in a patient with myelodysplastic syndrome harboring somatic mutations in RUNX1 and GATA2 von Hayakawa, Akira, Sano, Rie, Takahashi, Yoichiro, Okawa, Takafumi, Kubo, Rieko, Harada, Megumi, Fukuda, Haruki, Yokohama, Akihiko, Handa, Hiroshi, Kawabata‐Iwakawa, Reika, Tsuneyama, Hatsue, Tsukada, Junichi, Kominato, Yoshihiko

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Garlic Supplementation Increases Testicular Testosterone and Decreases Plasma Corticosterone in Rats Fed a High Protein Diet von Oi, Yuriko, Imafuku, Mika, Shishido, Chiaki, Iwai, Kazuo, Kominato, Yutaka, Nishimura, Syoji

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A single amino acid substitution can shift the optimum pH of DNase I for enzyme activity: biochemical and molecular analysis of the piscine DNase I family von Yasuda, T, Takeshita, H, Iida, R, Ueki, M, Nakajima, T, Kaneko, Y, Mogi, K, Kominato, Y, Kishi, K

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Post-traumatic cerebral infarction caused by thrombus in the middle cerebral artery von Hayakawa, Akira, Sano, Rie, Takahashi, Yoichiro, Fukuda, Haruki, Okawa, Takafumi, Kubo, Rieko, Takei, Hiroyuki, Komatsu, Takakazu, Tokue, Hiroyuki, Sawada, Yusuke, Oshima, Kiyohiro, Horioka, Kie, Kominato, Yoshihiko

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Human Hypoxic Signal Transduction through a Signature Motif in Hepatocyte Nuclear Factor 4 von Tsuchiya, Terumasa, Kominato, Yoshihiko, Ueda, Masatsugu

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Monocyte expression of the human prointerleukin 1 beta gene (IL1B) is dependent on promoter sequences which bind the hematopoietic transcription factor Spi-1/PU.1 von Kominato, Yoshihiko, Galson, Deborah L., Waterman, Wayne R., Webb, Andrew C., Auron, Philip E.

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Characterization of the human ABO gene promoter in erythroid cell lineage von Hata, Y., Kominato, Y., Yamamoto, F.-I., Takizawa, H.

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Presence of nucleotide substitutions in the ABO promoter in individuals with phenotypes A sub(3) and B sub(3) von Isa, K, Yamamuro, Y, Ogasawara, K, Yabe, R, Ogiyama, Y, Ito, S, Takahashi, Y, Kominato, Y, Sano, R, Uchikawa, M

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Presence of nucleotide substitutions in the ABO promoter in individuals with phenotypes A 3 and B 3 von Isa, K., Yamamuro, Y., Ogasawara, K., Yabe, R., Ogiyama, Y., Ito, S., Takahashi, Y., Kominato, Y., Sano, R., Uchikawa, M.

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Blood group B gene is barely expressed in in vitro erythroid culture of B m ‐derived CD34 + cells without an erythroid cell‐specific regulatory element von Sano, R., Nogawa, M., Nakajima, T., Takahashi, Y., Takahashi, K., Kubo, R., Kominato, Y., Yokohama, A., Tsukada, J., Yamao, H., Kishida, T., Ogasawara, K., Uchikawa, M.

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Reduced expression of human mismatch repair genes in adult T‐cell leukemia von Morimoto, Hiroaki, Tsukada, Junichi, Kominato, Yoshihiko, Tanaka, Yoshiya

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A 3.0-kb deletion including an erythroid cell-specific regulatory element in intron 1 of the ABO blood group gene in an individual with the B sub(m) phenotype von Sano, R, Kuboya, E, Nakajima, T, Takahashi, Y, Takahashi, K, Kubo, R, Kominato, Y, Takeshita, H, Yamao, H, Kishida, T, Isa, K, Ogasawara, K, Uchikawa, M

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