KBTBD11, encoding a novel PPARγ target gene, is involved in NFATc1 proteolysis by interacting with HSC70 and HSP60 von Watanabe, Kazuhisa, Matsumoto, Ayumi, Tsuda, Hidetoshi, Iwamoto, Sadahiko

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Genome-wide DNA methylation status of Mongolians exhibits signs of cellular stress response related to their nomadic lifestyle von Inaba, Yuta, Iwamoto, Sadahiko, Nakayama, Kazuhiro

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ILDR2 stabilization is regulated by its interaction with GRP78 von Watanabe, Kazuhisa, Nakayama, Kazuhiro, Ohta, Satoshi, Matsumoto, Ayumi, Tsuda, Hidetoshi, Iwamoto, Sadahiko

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Probiotics suppress nonalcoholic steatohepatitis and carcinogenesis progression in hepatocyte-specific PTEN knockout mice von Arai, Naoshi, Miura, Kouichi, Aizawa, Kenichi, Sekiya, Mariko, Nagayama, Manabu, Sakamoto, Hirotsugu, Maeda, Hiroshi, Morimoto, Naoki, Iwamoto, Sadahiko, Yamamoto, Hironori

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Lack of GPR180 ameliorates hepatic lipid depot via downregulation of mTORC1 signaling von Yoshida, Ken, Yokota, Kazuha, Watanabe, Kazuhisa, Tsuda, Hidetoshi, Matsumoto, Ayumi, Mizukami, Hiroaki, Iwamoto, Sadahiko

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N4BP2L1 interacts with dynactin and contributes to GLUT4 trafficking and glucose uptake in adipocytes von Watanabe, Kazuhisa, Matsumoto, Ayumi, Tsuda, Hidetoshi, Iwamoto, Sadahiko

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Kbtbd11 gene expression in adipose tissue increases in response to feeding and affects adipocyte differentiation von Watanabe, Kazuhisa, Yoshida, Ken, Iwamoto, Sadahiko

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Association of HLA-DPB1, NLRP10, OVOL1, and ABCC11 with the axillary microbiome in a Japanese population von Kutsuwada, Yukinobu, Yokota, Kazuha, Yoshida, Ken, Tsuda, Hidetoshi, Watanabe, Kazuhisa, Matsumoto, Ayumi, Iwamoto, Sadahiko

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Two cases of DYNC1H1 mutations with intractable epilepsy von Matsumoto, Ayumi, Kojima, Karin, Miya, Fuyuki, Miyauchi, Akihiko, Watanabe, Kazuhisa, Iwamoto, Sadahiko, Kawai, Kensuke, Kato, Mitsuhiro, Takahashi, Yukitoshi, Yamagata, Takanori

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Circadian-relevant genes are highly polymorphic in autism spectrum disorder patients von Yang, Zhiliang, Matsumoto, Ayumi, Nakayama, Kazuhiro, Jimbo, Eriko F, Kojima, Karin, Nagata, Koh-ichi, Iwamoto, Sadahiko, Yamagata, Takanori

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Unfavorable switching of skewed X chromosome inactivation leads to Menkes disease in a female infant von Matsumoto, Ayumi, Kano, Shintaro, Kobayashi, Natsumi, Matsuki, Mitsuru, Furukawa, Rieko, Yamagishi, Hirokazu, Yoshinari, Hiroki, Nakata, Waka, Wakabayashi, Hiroko, Tsuda, Hidetoshi, Watanabe, Kazuhisa, Takahashi, Hironori, Yamagata, Takanori, Matsumura, Takayoshi, Osaka, Hitoshi, Mori, Harushi, Iwamoto, Sadahiko

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Seasonal effects of UCP1 gene polymorphism on visceral fat accumulation in Japanese adults von Nakayama, Kazuhiro, Miyashita, Hiroshi, Yanagisawa, Yoshiko, Iwamoto, Sadahiko

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Sin3A-associated protein, 18 kDa, a novel binding partner of TRIB1, regulates MTTP expression [S] von Makishima, Saho, Boonvisut, Supichaya, Ishizuka, Yuumi, Watanabe, Kazuhisa, Nakayama, Kazuhiro, Iwamoto, Sadahiko

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Investigation of Maternal Diet and FADS1 Polymorphism Associated with Long-Chain Polyunsaturated Fatty Acid Compositions in Human Milk von Niwa, Sakurako, Kawabata, Terue, Shoji, Kumiko, Ogata, Hiromitsu, Kagawa, Yasuo, Nakayama, Kazuhiro, Yanagisawa, Yoshiko, Iwamoto, Sadahiko, Tatsuta, Nozomi, Asato, Kaname, Arima, Takahiro, Yaegashi, Nobuo, Nakai, Kunihiko

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Influence of AHRR Pro189Ala polymorphism on kidney functions von Nakayama, Kazuhiro, Saito, Shinichi, Watanabe, Kazuhisa, Miyashita, Hiroshi, Nishijima, Fuyuhiko, Kamo, Yoshie, Tada, Koji, Ishizuka, Satoshi, Niwa, Toshimitsu, Iwamoto, Sadahiko, Shimizu, Hidehisa

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Identification of deleterious rare variants in MTTP, PNPLA3, and TM6SF2 in Japanese males and association studies with NAFLD von Boonvisut, Supichaya, Yoshida, Ken, Nakayama, Kazuhiro, Watanabe, Kazuhisa, Miyashita, Hiroshi, Iwamoto, Sadahiko

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Kbtbd11 contributes to adipocyte homeostasis through the activation of upstream stimulatory factor 1 von Watanabe, Kazuhisa, Yokota, Kazuha, Yoshida, Ken, Matsumoto, Ayumi, Iwamoto, Sadahiko

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TRIB1 downregulates hepatic lipogenesis and glycogenesis via multiple molecular interactions von Ishizuka, Yuumi, Nakayama, Kazuhiro, Ogawa, Ayumi, Makishima, Saho, Boonvisut, Supichaya, Hirao, Atsushi, Iwasaki, Yusaku, Yada, Toshihiko, Yanagisawa, Yoshiko, Miyashita, Hiroshi, Takahashi, Masafumi, Iwamoto, Sadahiko

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Novel BEST1 mutation in autosomal recessive bestrophinopathy in Japanese siblings von Yamada, Rika, Takagi, Rina, Iwamoto, Sadahiko, Shimada, Shoichi, Kakehashi, Akihiro

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ZNF70, a novel ILDR2-interacting protein, contributes to the regulation of HES1 gene expression von Watanabe, Kazuhisa, Nakayama, Kazuhiro, Ohta, Satoshi, Tago, Kenji, Boonvisut, Supichaya, Millings, Elizabeth J., Fischer, Stuart G., LeDuc, Charles A., Leibel, Rudolph L., Iwamoto, Sadahiko

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