Prevalence of and risk factors for non-alcoholic fatty liver disease in a non-obese Japanese population, 2011–2012 by Nishioji, Kenichi, Sumida, Yoshio, Kamaguchi, Mai, Mochizuki, Naomi, Kobayashi, Masao, Nishimura, Takeshi, Yamaguchi, Kanji, Itoh, Yoshito

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BATF2 inhibits immunopathological Th17 responses by suppressing Il23a expression during Trypanosoma cruzi infection by Kitada, Shoko, Kayama, Hisako, Okuzaki, Daisuke, Koga, Ritsuko, Kobayashi, Masao, Arima, Yasunobu, Kumanogoh, Atsushi, Murakami, Masaaki, Ikawa, Masahito, Takeda, Kiyoshi

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Autosomal recessive complete STAT1 deficiency caused by compound heterozygous intronic mutations by 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 Impact of PNPLA3 rs738409 Genetic Polymorphism and Weight Gain ≥10 kg after Age 20 on Non-Alcoholic Fatty Liver Disease in Non-Obese Japanese Individuals by Nishioji, Kenichi, Mochizuki, Naomi, Kobayashi, Masao, Kamaguchi, Mai, Sumida, Yoshio, Nishimura, Takeshi, Yamaguchi, Kanji, Kadotani, Hiroshi, Itoh, Yoshito

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Human gain-of-function STAT1 mutation disturbs IL-17 immunity in mice by Tamaura, Moe, Satoh-Takayama, Naoko, Tsumura, Miyuki, Sasaki, Takaharu, Goda, Satoshi, Kageyama, Tomoko, Hayakawa, Seiichi, Kimura, Shunsuke, Asano, Takaki, Nakayama, Manabu, Koseki, Haruhiko, Ohara, Osamu, Okada, Satoshi, Ohno, Hiroshi, Kobayashi, Masao

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Impact of graft-versus-host disease on the clinical outcome of allogeneic hematopoietic stem cell transplantation for non-malignant diseases by Umeda, Katsutsugu, Imai, Kohsuke, Yanagimachi, Masakatsu, Yabe, Hiromasa, Kobayashi, Masao, Takahashi, Yoshiyuki, Kajiwara, Michiko, Yoshida, Nao, Cho, Yuko, Inoue, Masami, Hashii, Yoshiko, Atsuta, Yoshiko, Morio, Tomohiro

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NBS1 I171V variant underlies individual differences in chromosomal radiosensitivity within human populations by Tomioka, Keita, Miyamoto, Tatsuo, Akutsu, Silvia Natsuko, Yanagihara, Hiromi, Fujita, Kazumasa, Royba, Ekaterina, Tauchi, Hiroshi, Yamamoto, Takashi, Koh, Iemasa, Hirata, Eiji, Kudo, Yoshiki, Kobayashi, Masao, Okada, Satoshi, Matsuura, Shinya

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Monogenic mutations differentially affect the quantity and quality of T follicular helper cells in patients with human primary immunodeficiencies by Ma, Cindy S., PhD, Wong, Natalie, BSc Hons, Rao, Geetha, MSc, Avery, Danielle T., BApplSci, Torpy, James, MPhil, Hambridge, Thomas, BSc Hons, Bustamante, Jacinta, MD, PhD, Okada, Satoshi, MD, PhD, Stoddard, Jennifer L., BS, Deenick, Elissa K., PhD, Pelham, Simon J., MSc, Payne, Kathryn, BSc Hons, Boisson-Dupuis, Stéphanie, PhD, Puel, Anne, PhD, Kobayashi, Masao, MD, PhD, Arkwright, Peter D., FRCPCH, DPhil, Kilic, Sara Sebnem, MD, El Baghdadi, Jamila, PhD, Nonoyama, Shigeaki, MD, PhD, Minegishi, Yoshiyuki, MD, PhD, Mahdaviani, Seyed Alireza, MD, Mansouri, Davood, MD, Bousfiha, Aziz, MD, Blincoe, Annaliesse K., BHB, MBChB, French, Martyn A., MB ChB, MD, FRACP, FRCPath, FRCP, Hsu, Peter, FRACP, PhD, Campbell, Dianne E., FRACP, PhD, Stormon, Michael O., MBBS, FRACP, Wong, Melanie, MBBS, PhD, FRACP, FRCPA, Adelstein, Stephen, MBBCh, PhD, FRACP, FRCPA, Smart, Joanne M., MBBS, FRACP, Fulcher, David A., MBBS, PhD, FRACP, FRCPA, Cook, Matthew C., MBBS, PhD, FRACP, FRCPA, Phan, Tri Giang, MBBS, PhD, FRACP, FRCPA, Stepensky, Polina, MD, Boztug, Kaan, MD, Kansu, Aydan, MD, İkincioğullari, Aydan, MD, Baumann, Ulrich, MD, Beier, Rita, MD, Roscioli, Tony, FRACP, PhD, Ziegler, John B., MD, FRACP, Gray, Paul, FRACP, Picard, Capucine, MD, PhD, Grimbacher, Bodo, MD, Warnatz, Klaus, MD, PhD, Holland, Steven M., MD, Casanova, Jean-Laurent, MD, PhD, Uzel, Gulbu, MD, Tangye, Stuart G., PhD

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Downregulation of endothelial nitric oxide synthase (eNOS) and endothelin-1 (ET-1) in a co-culture system with human stimulated X-linked CGD neutrophils by Nakamura-Utsunomiya, Akari, Tsumura, Miyuki, Okada, Satoshi, Kawaguchi, Hiroshi, Kobayashi, Masao

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Bone marrow transplantation from a human leukocyte antigen-mismatched unrelated donor in a case with C1q deficiency associated with refractory systemic lupus erythematosus by Matsumura, Risa, Mochizuki, Shinji, Maruyama, Natsuki, Morishita, Yusuke, Kawaguchi, Hiroshi, Okada, Satoshi, Tsumura, Miyuki, Kaji, Shunsaku, Shimizu, Junya, Shimada, Akira, Kobayashi, Masao

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Abnormal hematopoiesis and autoimmunity in human subjects with germline IKZF1 mutations by Hoshino, Akihiro, MD, PhD, Okada, Satoshi, MD, PhD, Yoshida, Kenichi, MD, PhD, Nishida, Naonori, MD, PhD, Okuno, Yusuke, MD, PhD, Ueno, Hiroo, MD, Yamashita, Motoi, MD, Okano, Tsubasa, MD, Tsumura, Miyuki, PhD, Nishimura, Shiho, MD, Sakata, Sonoko, MD, Kobayashi, Masao, MD, PhD, Nakamura, Haruna, MD, Kamizono, Junji, MD, PhD, Mitsui-Sekinaka, Kanako, MD, Ichimura, Takuya, MD, Ohga, Shouichi, MD, PhD, Nakazawa, Yozo, MD, PhD, Takagi, Masatoshi, MD, PhD, Imai, Kohsuke, MD, PhD, Shiraishi, Yuichi, MD, PhD, Chiba, Kenichi, BA, Tanaka, Hiroko, BS, Miyano, Satoru, PhD, Ogawa, Seishi, MD, PhD, Kojima, Seiji, MD, PhD, Nonoyama, Shigeaki, MD, PhD, Morio, Tomohiro, MD, PhD, Kanegane, Hirokazu, MD, PhD

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Phosphatase and tensin homolog ( PTEN ) mutation can cause activated phosphatidylinositol 3-kinase δ syndrome–like immunodeficiency by Tsujita, Yuki, MD, Mitsui-Sekinaka, Kanako, MD, Imai, Kohsuke, MD, PhD, Yeh, Tzu-Wen, MSc, Mitsuiki, Noriko, MD, PhD, Asano, Takaki, MD, Ohnishi, Hidenori, MD, PhD, Kato, Zenichiro, MD, PhD, Sekinaka, Yujin, MD, Zaha, Kiyotaka, MD, Kato, Tamaki, MD, PhD, Okano, Tsubasa, MD, Takashima, Takehiro, MD, Kobayashi, Kaoru, MD, PhD, Kimura, Mitsuaki, MD, PhD, Kunitsu, Tomoaki, MD, Maruo, Yoshihiro, MD, PhD, Kanegane, Hirokazu, MD, PhD, Takagi, Masatoshi, MD, PhD, Yoshida, Kenichi, MD, PhD, Okuno, Yusuke, MD, PhD, Muramatsu, Hideki, MD, PhD, Shiraishi, Yuichi, PhD, Chiba, Kenichi, BA, Tanaka, Hiroko, BSc, Miyano, Satoru, PhD, Kojima, Seiji, MD, PhD, Ogawa, Seishi, MD, PhD, Ohara, Osamu, PhD, Okada, Satoshi, MD, PhD, Kobayashi, Masao, MD, PhD, Morio, Tomohiro, MD, PhD, Nonoyama, Shigeaki, MD, PhD

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Examination time as a quality indicator of screening upper gastrointestinal endoscopy for asymptomatic examinees by Kawamura, Takuji, Wada, Hironori, Sakiyama, Naokuni, Ueda, Yuki, Shirakawa, Atsushi, Okada, Yusuke, Sanada, Kasumi, Nakase, Kojiro, Mandai, Koichiro, Suzuki, Azumi, Kamaguchi, Mai, Morita, Atsuhiro, Nishioji, Kenichi, Tanaka, Kiyohito, Mochizuki, Naomi, Uno, Koji, Yokota, Isao, Kobayashi, Masao, Yasuda, Kenjiro

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Molecular mechanism and structural basis of gain-of-function of STAT1 caused by pathogenic R274Q mutation by Fujiki, Ryoji, Hijikata, Atsushi, Shirai, Tsuyoshi, Okada, Satoshi, Kobayashi, Masao, Ohara, Osamu

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Effects of idursulfase enzyme replacement therapy for Mucopolysaccharidosis type II when started in early infancy: Comparison in two siblings by Tajima, Go, Sakura, Nobuo, Kosuga, Motomichi, Okuyama, Torayuki, Kobayashi, Masao

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Prospective validation of the provisional entity of refractory cytopenia of childhood, proposed by the World Health Organization by Hama, Asahito, Hasegawa, Daisuke, Manabe, Atsushi, Nozawa, Kazue, Narita, Atsushi, Muramatsu, Hideki, Kosaka, Yoshiyuki, Kobayashi, Masao, Koh, Katsuyoshi, Takahashi, Yoshiyuki, Watanabe, Kenichiro, Ohara, Akira, Ito, Masafumi, Kojima, Seiji

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Paroxysmal nocturnal hemoglobinuria and telomere length predicts response to immunosuppressive therapy in pediatric aplastic anemia by Narita, Atsushi, Muramatsu, Hideki, Sekiya, Yuko, Okuno, Yusuke, Sakaguchi, Hirotoshi, Nishio, Nobuhiro, Yoshida, Nao, Wang, Xinan, Xu, Yinyan, Kawashima, Nozomu, Doisaki, Sayoko, Hama, Asahito, Takahashi, Yoshiyuki, Kudo, Kazuko, Moritake, Hiroshi, Kobayashi, Masao, Kobayashi, Ryoji, Ito, Etsuro, Yabe, Hiromasa, Ohga, Shouichi, Ohara, Akira, Kojima, Seiji

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NOTCH1 pathway activating mutations and clonal evolution in pediatric T‐cell acute lymphoblastic leukemia by Kimura, Shunsuke, Seki, Masafumi, Yoshida, Kenichi, Shiraishi, Yuichi, Akiyama, Masaharu, Koh, Katsuyoshi, Imamura, Toshihiko, Manabe, Atsushi, Hayashi, Yasuhide, Kobayashi, Masao, Oka, Akira, Miyano, Satoru, Ogawa, Seishi, Takita, Junko

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Inherited CARD9 Deficiency in a Child with Invasive Disease Due to Exophiala dermatitidis and Two Older but Asymptomatic Siblings by Imanaka, Yusuke, Taniguchi, Maki, Doi, Takehiko, Tsumura, Miyuki, Nagaoka, Rie, Shimomura, Maiko, Asano, Takaki, Kagawa, Reiko, Mizoguchi, Yoko, Karakawa, Shuhei, Arihiro, Koji, Imai, Kohsuke, Morio, Tomohiro, Casanova, Jean-Laurent, Puel, Anne, Ohara, Osamu, Kamei, Katsuhiko, Kobayashi, Masao, Okada, Satoshi

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Characteristics of gastric cancer in negative test of serum anti-Helicobacter pylori antibody and pepsinogen test: a multicenter study by Kiso, Mariko, Yoshihara, Masaharu, Ito, Masanori, Inoue, Kazuhiko, Kato, Katsuaki, Nakajima, Shigemi, Mabe, Katsuhiro, Kobayashi, Masao, Uemura, Naomi, Yada, Tomoyuki, Oka, Masashi, Kawai, Takashi, Boda, Tomoyuki, Kotachi, Takahiro, Masuda, Kazuhiko, Tanaka, Shinji, Chayama, Kazuaki

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