A Targeted Genetic Association Study of the Rare Type of Osteomyelitis von Yahara, H., Horita, S., Yanamoto, S., Kitagawa, Y., Asaka, T., Yoda, T., Morita, K., Michi, Y., Takechi, M., Shimasue, H., Maruoka, Y., Kondo, E., Kusukawa, J., Tsujiguchi, H., Sato, T., Kannon, T., Nakamura, H., Tajima, A., Hosomichi, K., Yahara, K.

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Correction of the HLA-DQB104:01:01 sequence at position 79 in exon 1 von Okudaira, Y., Hosomichi, K., Ozaki, Y., Shiina, T., Mitsunaga, S.

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A toddler with phylloid-type pigmentary mosaicism and ambiguous genitalia resulting from trisomy 14 induced by a der(Y)t(Y;14) von Romero, V. I., Pozo, J. C., Saenz, S., Llamos-Paneque, A., Liehr, T., Hosomichi, K., Tajima, A.

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The HLA genomic loci map: expression, interaction, diversity and disease von Shiina, Takashi, Hosomichi, Kazuyoshi, Inoko, Hidetoshi, Kulski, Jerzy K

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Bulk-boundary propagator in Liouville theory on a disc von Hosomichi, Kazuo

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3073Leveraging transcriptome sequencing for detecting novel disease-related pathways using human cardiac sarcoidosis myocardium biopsies von Yoshida, S, Nomura, A, Tada, H, Sakata, K, Nakanishi, C, Fujino, N, Hosomichi, K, Tajima, A, Takamura, M

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Escape hematopoiesis by HLA-B5401-lacking hematopoietic stem progenitor cells in men with acquired aplastic anemia von Elbadry, Mahmoud I, Mizumaki, Hiroki, Hosokawa, Kohei, Espinoza, J Luis, Nakagawa, Noriharu, Chonabayashi, Kazuhisa, Yoshida, Yoshinori, Katagiri, Takamasa, Hosomichi, Kazuyoshi, Zaimoku, Yoshitaka, Imi, Tatsuya, Nguyen, Mai Anh Thi, Fujii, Youichi, Tajima, Atsushi, Ogawa, Seishi, Takenaka, Katsuto, Akashi, Koichi, Nakao, Shinji

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A frequent nonsense mutation in exon 1 across certain HLA-A and -B alleles in leukocytes of patients with acquired aplastic anemia von Mizumaki, Hiroki, Hosomichi, Kazuyoshi, Hosokawa, Kohei, Yoroidaka, Takeshi, Imi, Tatsuya, Zaimoku, Yoshitaka, Katagiri, Takamasa, Anh Thi Nguyen, Mai, Cao Tran, Dung, Ibrahim Yousef Elbadry, Mahmoud, Chonabayashi, Kazuhisa, Yoshida, Yoshinori, Takamatsu, Hiroyuki, Ozawa, Tatsuhiko, Azuma, Fumihiro, Kishi, Hiroyuki, Fujii, Yoichi, Ogawa, Seishi, Tajima, Atsushi, Nakao, Shinji

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Positional effects of polymorphisms in probe-target sequences on genoplot images of oligonucleotide microarrays von Cui, T L, Nakaoka, H, Akiyama, K, Kamura, H, Hosomichi, K, Bae, J, Cheong, H, Shin, H, Yada, T, Inoue, I

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Exome resequencing combined with linkage analysis identifies novel PTH1R variants in primary failure of tooth eruption in Japanese von Yamaguchi, Tetsutaro, Hosomichi, Kazuyoshi, Narita, Akira, Shirota, Tatsuo, Tomoyasu, Yoko, Maki, Koutaro, Inoue, Ituro

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Super-Liouville theory with boundary von Fukuda, Takeshi, Hosomichi, Kazuo

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Correction of the HLA‐DQB1 04:01:01 sequence at position 79 in exon 1 von Okudaira, Y., Hosomichi, K., Ozaki, Y., Shiina, T., Mitsunaga, S.

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3102Comprehensive genotyping and phenotyping in patients with severe hypercholesterolemia von Tada, H., Nomura, A., Teramoto, R., Hosomichi, K., Kawashiri, M., Nohara, A., Mabuchi, H., Tajima, A., Yamagishi, M.

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Diversity analysis of transcribed MHC class IIβ loci in Japanese quail von Asaji, S, Suzuki, S, Ishige, T, Hosomichi, K, Shiina, T, Hara, H, Hirano, T, Hanzawa, K

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P4020 Diversity analysis of transcribed MHC class IIβ loci in Japanese quail von Asaji, S., Suzuki, S., Ishige, T., Hosomichi, K., Shiina, T., Hara, H., Hirano, T., Hanzawa, K.

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Comparative Genomic Analysis of Two Avian (Quail and Chicken) MHC Regions von Shiina, Takashi, Shimizu, Sayoko, Hosomichi, Kazuyoshi, Kohara, Sakae, Watanabe, Seiki, Hanzawa, Kei, Beck, Stephan, Kulski, Jerzy K, Inoko, Hidetoshi

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Association Between Serum 25-Hydroxyvitamin D Concentrations, CDX2 Polymorphism in Promoter Region of Vitamin D Receptor Gene, and Chronic Pain in Rural Japanese Residents von Suzuki, Keita, Tsujiguchi, Hiromasa, Hara, Akinori, Pham, Oanh Kim, Miyagi, Sakae, Nguyen, Thao Thi Thu, Nakamura, Haruki, Suzuki, Fumihiko, Kasahara, Tomoko, Shimizu, Yukari, Yamada, Yohei, Kambayashi, Yasuhiro, Tsuboi, Hirohito, Sato, Takehiro, Kannon, Takayuki, Hosomichi, Kazuyoshi, Tajima, Atsushi, Takamura, Toshinari, Nakamura, Hiroyuki

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Sustained clonal hematopoiesis by HLA-lacking hematopoietic stem cells without driver mutations in aplastic anemia von Imi, Tatsuya, Katagiri, Takamasa, Hosomichi, Kazuyoshi, Zaimoku, Yoshitaka, Hoang Nguyen, Viet, Nakagawa, Noriharu, Tajima, Atsushi, Yoshizato, Tetsuichi, Ogawa, Seishi, Nakao, Shinji

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Multiple common and rare variants of ABCG2 cause gout von Higashino, Toshihide, Takada, Tappei, Nakaoka, Hirofumi, Toyoda, Yu, Stiburkova, Blanka, Miyata, Hiroshi, Ikebuchi, Yuki, Nakashima, Hiroshi, Shimizu, Seiko, Kawaguchi, Makoto, Sakiyama, Masayuki, Nakayama, Akiyoshi, Akashi, Airi, Tanahashi, Yuki, Kawamura, Yusuke, Nakamura, Takahiro, Wakai, Kenji, Okada, Rieko, Yamamoto, Ken, Hosomichi, Kazuyoshi, Hosoya, Tatsuo, Ichida, Kimiyoshi, Ooyama, Hiroshi, Suzuki, Hiroshi, Inoue, Ituro, Merriman, Tony R, Shinomiya, Nariyoshi, Matsuo, Hirotaka

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A toddler with phylloid-type pigmentary mosaicism and ambiguous genitalia resulting from trisomy 14 induced by a der(Y)t(Y;14) von Romero, V I, Pozo, J C, Saenz, S, Llamos-Paneque, A, Liehr, T, Hosomichi, K, Tajima, A

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