In vitro generation of functional murine heart organoids via FGF4 and extracellular matrix von Lee, Jiyoung, Sutani, Akito, Kaneko, Rin, Takeuchi, Jun, Sasano, Tetsuo, Kohda, Takashi, Ihara, Kensuke, Takahashi, Kentaro, Yamazoe, Masahiro, Morio, Tomohiro, Furukawa, Tetsushi, Ishino, Fumitoshi

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Inborn errors of immunity with eosinophilia von Okamoto, Keisuke, Morio, Tomohiro

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Noncoding RNA transcription at enhancers and genome folding in cancer von Isoda, Takeshi, Morio, Tomohiro, Takagi, Masatoshi

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Haploinsufficiency of A20 causes autoinflammatory and autoimmune disorders von Kadowaki, Tomonori, Ohnishi, Hidenori, Kawamoto, Norio, Hori, Tomohiro, Nishimura, Kenichi, Kobayashi, Chie, Shigemura, Tomonari, Ogata, Shohei, Inoue, Yuzaburo, Kawai, Tomoki, Hiejima, Eitaro, Takagi, Masatoshi, Imai, Kohsuke, Nishikomori, Ryuta, Ito, Shuichi, Heike, Toshio, Ohara, Osamu, Morio, Tomohiro, Fukao, Toshiyuki, Kanegane, Hirokazu

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AIOLOS Variants Causing Immunodeficiency in Human and Mice von Yamashita, Motoi, Morio, Tomohiro

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International Union of Immunological Societies: 2017 Primary Immunodeficiency Diseases Committee Report on Inborn Errors of Immunity von Picard, Capucine, Bobby Gaspar, H., Al-Herz, Waleed, Bousfiha, Aziz, Casanova, Jean-Laurent, Chatila, Talal, Crow, Yanick J., Cunningham-Rundles, Charlotte, Etzioni, Amos, Franco, Jose Luis, Holland, Steven M., Klein, Christoph, Morio, Tomohiro, Ochs, Hans D., Oksenhendler, Eric, Puck, Jennifer, Tang, Mimi L. K., Tangye, Stuart G., Torgerson, Troy R., Sullivan, Kathleen E.

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The 2017 IUIS Phenotypic Classification for Primary Immunodeficiencies von Bousfiha, Aziz, Jeddane, Leïla, Picard, Capucine, Ailal, Fatima, Bobby Gaspar, H., Al-Herz, Waleed, Chatila, Talal, Crow, Yanick J., Cunningham-Rundles, Charlotte, Etzioni, Amos, Franco, Jose Luis, Holland, Steven M., Klein, Christoph, Morio, Tomohiro, Ochs, Hans D., Oksenhendler, Eric, Puck, Jennifer, Tang, Mimi L. K., Tangye, Stuart G., Torgerson, Troy R., Casanova, Jean-Laurent, Sullivan, Kathleen E.

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Tocilizumab in systemic juvenile idiopathic arthritis in a real-world clinical setting: results from 1 year of postmarketing surveillance follow-up of 417 patients in Japan von Yokota, Shumpei, Itoh, Yasuhiko, Morio, Tomohiro, Origasa, Hideki, Sumitomo, Naokata, Tomobe, Minako, Tanaka, Kunihiko, Minota, Seiji

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Synergistic effect of combined PI3 kinase inhibitor and PARP inhibitor treatment on BCR/ABL1-positive acute lymphoblastic leukemia cells von Hiroki, Haruka, Akahane, Koshi, Inukai, Takeshi, Morio, Tomohiro, Takagi, Masatoshi

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Use of a Comprehensive Polymerase Chain Reaction System for Diagnosis of Ocular Infectious Diseases von Sugita, Sunao, MD, PhD, Ogawa, Manabu, MD, PhD, Shimizu, Norio, PhD, Morio, Tomohiro, MD, PhD, Ohguro, Nobuyuki, MD, PhD, Nakai, Kei, MD, PhD, Maruyama, Kazuichi, MD, PhD, Nagata, Kenji, MD, Takeda, Atsunobu, MD, PhD, Usui, Yoshihiko, MD, PhD, Sonoda, Koh-Hei, MD, PhD, Takeuchi, Masaru, MD, PhD, Mochizuki, Manabu, MD, PhD

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Inborn errors of immunity-recent advances in research on the pathogenesis von Yamashita, Motoi, Inoue, Kento, Okano, Tsubasa, Morio, Tomohiro

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Autosomal recessive complete STAT1 deficiency caused by compound heterozygous intronic mutations von Sakata, Sonoko, Tsumura, Miyuki, Matsubayashi, Tadashi, Karakawa, Shuhei, Kimura, Shunsuke, Tamaura, Moe, Okano, Tsubasa, Naruto, Takuya, Mizoguchi, Yoko, Kagawa, Reiko, Nishimura, Shiho, Imai, Kohsuke, Le Voyer, Tom, Casanova, Jean-Laurent, Bustamante, Jacinta, Morio, Tomohiro, Ohara, Osamu, Kobayashi, Masao, Okada, Satoshi

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The extended phenotype of LPS-responsive beige-like anchor protein (LRBA) deficiency von Gámez-Díaz, Laura, MSc, August, Dietrich, cand. MD, Stepensky, Polina, MD, Revel-Vilk, Shoshana, MD, MSc, Seidel, Markus G., MD, Noriko, Mitsuiki, MD, Morio, Tomohiro, MD, PhD, Worth, Austen J.J., MD, PhD, Blessing, Jacob, MD, PhD, Van de Veerdonk, Frank, MD, PhD, Feuchtinger, Tobias, MD, Kanariou, Maria, MD, PhD, Schmitt-Graeff, Annette, MD, Jung, Sophie, DD, PhD, Seneviratne, Suranjith, MD, PhD, Burns, Siobhan, MD, Belohradsky, Bernd H., MD, Rezaei, Nima, MD, PhD, Bakhtiar, Shahrzad, MD, Speckmann, Carsten, MD, Jordan, Michael, MD, Grimbacher, Bodo, MD

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Anti-nuclear matrix protein 2 antibody-positive inflammatory myopathies represent extensive myositis without dermatomyositis-specific rash von Ichimura, Yuki, Konishi, Risa, Shobo, Miwako, Inoue, Sae, Okune, Mari, Maeda, Akemi, Tanaka, Ryota, Kubota, Noriko, Matsumoto, Isao, Ishii, Akiko, Tamaoka, Akira, Shimbo, Asami, Mori, Masaaki, Morio, Tomohiro, Kishi, Takayuki, Miyamae, Takako, Tanboon, Jantima, Inoue, Michio, Nishino, Ichizo, Fujimoto, Manabu, Nomura, Toshifumi, Okiyama, Naoko

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A variant in human AIOLOS impairs adaptive immunity by interfering with IKAROS von Yamashita, Motoi, Kuehn, Hye Sun, Okuyama, Kazuki, Okada, Satoshi, Inoue, Yuzaburo, Mitsuiki, Noriko, Imai, Kohsuke, Takagi, Masatoshi, Kanegane, Hirokazu, Takeuchi, Masahiro, Shimojo, Naoki, Tsumura, Miyuki, Padhi, Aditya K., Zhang, Kam Y. J., Boisson, Bertrand, Casanova, Jean-Laurent, Ohara, Osamu, Rosenzweig, Sergio D., Taniuchi, Ichiro, Morio, Tomohiro

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Targeting Poly(ADP)ribose polymerase in BCR/ABL1-positive cells von Hiroki, Haruka, Ishii, Yuko, Piao, Jinhua, Namikawa, Yui, Masutani, Mitsuko, Honda, Hiroaki, Akahane, Koshi, Inukai, Takeshi, Morio, Tomohiro, Takagi, Masatoshi

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Copy number alteration analysis for neuroblastoma using droplet digital polymerase chain reaction von Ishii, Yuko, Sato‐Otsubo, Aiko, Takita, Junko, Morio, Tomohiro, Takagi, Masatoshi

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Functional characterization of a germline ETV6 variant associated with inherited thrombocytopenia, acute lymphoblastic leukemia, and salivary gland carcinoma in childhood von Yoshino, Hiroshi, Nishiyama, Yohei, Kamma, Hiroshi, Chiba, Tomohiro, Fujiwara, Masachika, Karaho, Takehiro, Kogashiwa, Yasunao, Morio, Tomohiro, Yan, Kunimasa, Bessho, Fumio, Takagi, Masatoshi

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Gain-of-function IKBKB mutation causes human combined immune deficiency von Cardinez, Chelisa, Miraghazadeh, Bahar, Tanita, Kay, da Silva, Elizabeth, Hoshino, Akihiro, Okada, Satoshi, Chand, Rochna, Asano, Takaki, Tsumura, Miyuki, Yoshida, Kenichi, Ohnishi, Hidenori, Kato, Zenichiro, Yamazaki, Masahide, Okuno, Yusuke, Miyano, Satoru, Kojima, Seiji, Ogawa, Seishi, Andrews, T Daniel, Field, Matthew A, Burgio, Gaetan, Morio, Tomohiro, Vinuesa, Carola G, Kanegane, Hirokazu, Cook, Matthew C

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Recurrent Acute Abdomen as the Main Manifestation of Hereditary Angioedema von Iwanami, Keiichi, Okano, Tsubasa, Ohara, Osamu, Morio, Tomohiro

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