DDSを用いた粘膜ワクチンの増強効果 von 成戸, 卓也, 横田, 俊平

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P-86. ddPCRを用いたABO血液型による造血細胞移植後キメリズム検査法の確立 von 柳町昌克, 成戸卓也, 松本尚也, 廣瀬綾菜, 宮川直将, 慶野大, 浜之上聡, 岩崎史記, 横須賀とも子, 後藤裕明

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高IgD症候群のMVK遺伝子異常と新しい治療法の導入 von 成戸, 卓也

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Direct effect of interleukin-6 (IL-6) on growth plate chondrocytes von 中島, 章子, 成戸, 卓也, 宮前, 多佳子, 今川, 智之, 森, 雅亮, 横田, 俊平

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Direct effect of interleukin-6（IL-6）on growth plate chondrocytes von 中島章子, 成戸卓也, 宮前多佳子, 今川智之, 森雅亮, 横田俊平

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21.川崎病患者に特異的な血漿中の低分子量タンパク質の検出と同定 von 田口宏美, 成戸卓也, 今川智之, 森 雅亮, 川崎博史, 横田俊平, 平野 久

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Toll-Like Receptor 9 Plays a Pivotal Role in Angiotensin II-Induced Atherosclerosis von Fukuda, Daiju, Nishimoto, Sachiko, Aini, Kunduziayi, Tanaka, Atsushi, Nishiguchi, Tsuyoshi, Kim-Kaneyama, Joo-Ri, Lei, Xiao-Feng, Masuda, Kiyoshi, Naruto, Takuya, Tanaka, Kimie, Higashikuni, Yasutomi, Hirata, Yoichiro, Yagi, Shusuke, Kusunose, Kenya, Yamada, Hirotsugu, Soeki, Takeshi, Imoto, Issei, Akasaka, Takashi, Shimabukuro, Michio, Sata, Masataka

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Novel human mutation and CRISPR/Cas genome-edited mice reveal the importance of C-terminal domain of MSX1 in tooth and palate development von Mitsui, Silvia Naomi, Yasue, Akihiro, Masuda, Kiyoshi, Naruto, Takuya, Minegishi, Yoshiyuki, Oyadomari, Seiichi, Noji, Sumihare, Imoto, Issei, Tanaka, Eiji

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Simultaneous Detection of Both Single Nucleotide Variations and Copy Number Alterations by Next-Generation Sequencing in Gorlin Syndrome von Morita, Kei-ichi, Naruto, Takuya, Tanimoto, Kousuke, Yasukawa, Chisato, Oikawa, Yu, Masuda, Kiyoshi, Imoto, Issei, Inazawa, Johji, Omura, Ken, Harada, Hiroyuki

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KH-type splicing regulatory protein is involved in esophageal squamous cell carcinoma progression von Fujita, Yuji, Masuda, Kiyoshi, Hamada, Junichi, Shoda, Katsutoshi, Naruto, Takuya, Hamada, Satoshi, Miyakami, Yuko, Kohmoto, Tomohiro, Watanabe, Miki, Takahashi, Rizu, Tange, Shoichiro, Saito, Masako, Kudo, Yasusei, Fujiwara, Hitoshi, Ichikawa, Daisuke, Tangoku, Akira, Otsuji, Eigo, Imoto, Issei

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Detection of 1p36 deletion by clinical exome-first diagnostic approach von Watanabe, Miki, Hayabuchi, Yasunobu, Ono, Akemi, Naruto, Takuya, Horikawa, Hideaki, Kohmoto, Tomohiro, Masuda, Kiyoshi, Nakagawa, Ryuji, Ito, Hiromichi, Kagami, Shoji, Imoto, Issei

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Novel CLCN7 compound heterozygous mutations in intermediate autosomal recessive osteopetrosis von Okamoto, Nana, Kohmoto, Tomohiro, Naruto, Takuya, Masuda, Kiyoshi, Komori, Takahide, Imoto, Issei

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Genome-first approach diagnosed Cabezas syndrome via novel CUL4B mutation detection von Okamoto, Nobuhiko, Watanabe, Miki, Naruto, Takuya, Matsuda, Keiko, Kohmoto, Tomohiro, Saito, Masako, Masuda, Kiyoshi, Imoto, Issei

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