Hasil Pencarian - Ayumi Matsumoto

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  1. 1
    KBTBD11, encoding a novel PPARγ target gene, is involved in NFATc1 proteolysis by interacting with HSC70 and HSP60

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

    Diterbitkan 2022-11-01
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  2. 2
    N4BP2L1 interacts with dynactin and contributes to GLUT4 trafficking and glucose uptake in adipocytes

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

    Diterbitkan 2021-11-01
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  3. 3
    Kbtbd11 contributes to adipocyte homeostasis through the activation of upstream stimulatory factor 1

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

    Diterbitkan 2019-11-01
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  4. 4
    A novel upstream transcription factor 1 target gene N4bp2l1 that regulates adipogenesis

    A novel upstream transcription factor 1 target gene N4bp2l1 that regulates adipogenesis oleh Kazuhisa Watanabe, Kazuha Yokota, Ken Yoshida, Ayumi Matsumoto, Sadahiko Iwamoto

    Diterbitkan 2019-12-01
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  5. 5
    ILDR2 stabilization is regulated by its interaction with GRP78

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

    Diterbitkan 2021-04-01
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  6. 6
    Lack of GPR180 ameliorates hepatic lipid depot via downregulation of mTORC1 signaling

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

    Diterbitkan 2023-02-01
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  7. 7
    LIN7A depletion disrupts cerebral cortex development, contributing to intellectual disability in 12q21-deletion syndrome.

    LIN7A depletion disrupts cerebral cortex development, contributing to intellectual disability in 12q21-deletion syndrome. oleh Ayumi Matsumoto, Makoto Mizuno, Nanako Hamada, Yasuyuki Nozaki, Eriko F Jimbo, Mariko Y Momoi, Koh-ichi Nagata, Takanori Yamagata

    Diterbitkan 2014-01-01
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  8. 8
    Single cell RNA sequencing uncovers cellular developmental sequences and novel potential intercellular communications in embryonic kidney

    Single cell RNA sequencing uncovers cellular developmental sequences and novel potential intercellular communications in embryonic kidney oleh Isao Matsui, Ayumi Matsumoto, Kazunori Inoue, Yusuke Katsuma, Seiichi Yasuda, Karin Shimada, Yusuke Sakaguchi, Masayuki Mizui, Jun-ya Kaimori, Yoshitsugu Takabatake, Yoshitaka Isaka

    Diterbitkan 2021-01-01
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  9. 9
    A case of congenital fiber‐type disproportion syndrome presenting dilated cardiomyopathy with ACTA1 mutation

    A case of congenital fiber‐type disproportion syndrome presenting dilated cardiomyopathy with ACTA1 mutation oleh Ayumi Matsumoto, Hidetoshi Tsuda, Sadahiro Furui, Masako Kawada‐Nagashima, Tatsuya Anzai, Mitsuru Seki, Kazuhisa Watanabe, Kazuhiro Muramatsu, Hitoshi Osaka, Sadahiko Iwamoto, Ichizo Nishino, Takanori Yamagata

    Diterbitkan 2022-09-01
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  10. 10
    Hepatic phosphate uptake and subsequent nerve-mediated phosphaturia are crucial for phosphate homeostasis following portal vein passage of phosphate in rats

    Hepatic phosphate uptake and subsequent nerve-mediated phosphaturia are crucial for phosphate homeostasis following portal vein passage of phosphate in rats oleh Seiichi Yasuda, Kazunori Inoue, Isao Matsui, Ayumi Matsumoto, Yusuke Katsuma, Hiroki Okushima, Atsuhiro Imai, Yusuke Sakaguchi, Jun-ya Kaimori, Ryohei Yamamoto, Masayuki Mizui, Yoshitaka Isaka

    Diterbitkan 2023-04-01
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  11. 11
    Genome‐Wide Association Study of Lean Nonalcoholic Fatty Liver Disease Suggests Human Leukocyte Antigen as a Novel Candidate Locus

    Genome‐Wide Association Study of Lean Nonalcoholic Fatty Liver Disease Suggests Human Leukocyte Antigen as a Novel Candidate Locus oleh Ken Yoshida, Kazuha Yokota, Yukinobu Kutsuwada, Kazuhiro Nakayama, Kazuhisa Watanabe, Ayumi Matsumoto, Hiroshi Miyashita, Seik‐soon Khor, Katsushi Tokunaga, Yosuke Kawai, Masao Nagasaki, Sadahiko Iwamoto

    Diterbitkan 2020-08-01
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  12. 12
    Red cell distribution width and renal outcome in patients with non-dialysis-dependent chronic kidney disease.

    Red cell distribution width and renal outcome in patients with non-dialysis-dependent chronic kidney disease. oleh Sayoko Yonemoto, Takayuki Hamano, Naohiko Fujii, Karin Shimada, Satoshi Yamaguchi, Ayumi Matsumoto, Keiichi Kubota, Nobuhiro Hashimoto, Tatsufumi Oka, Masamitsu Senda, Yusuke Sakaguchi, Isao Matsui, Yoshitaka Isaka

    Diterbitkan 2018-01-01
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  13. 13
    Recurrent membranous nephropathy with a possible alteration in the etiology: a case report

    Recurrent membranous nephropathy with a possible alteration in the etiology: a case report oleh Ayumi Matsumoto, Isao Matsui, Keiji Mano, Hitoshi Mizuno, Yusuke Katsuma, Seiichi Yasuda, Karin Shimada, Kazunori Inoue, Takashi Oki, Tadashi Hanai, Keiko Kojima, Tetsuya Kaneko, Yoshitaka Isaka

    Diterbitkan 2021-07-01
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  14. 14
    Renoprotection by long‐term low‐dose tolvaptan in patients with heart failure and hyponatremia

    Renoprotection by long‐term low‐dose tolvaptan in patients with heart failure and hyponatremia oleh Tatsufumi Oka, Takayuki Hamano, Tomohito Ohtani, Yohei Doi, Karin Shimada, Ayumi Matsumoto, Satoshi Yamaguchi, Nobuhiro Hashimoto, Masamitsu Senda, Yusuke Sakaguchi, Isao Matsui, Kei Nakamoto, Fusako Sera, Shungo Hikoso, Yasushi Sakata, Yoshitaka Isaka

    Diterbitkan 2021-12-01
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  15. 15
    Unfavorable switching of skewed X chromosome inactivation leads to Menkes disease in a female infant

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

    Diterbitkan 2024-01-01
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  16. 16
    Integrative Analyses of De Novo Mutations Provide Deeper Biological Insights into Autism Spectrum Disorder

    Integrative Analyses of De Novo Mutations Provide Deeper Biological Insights into Autism Spectrum Disorder oleh Atsushi Takata, Noriko Miyake, Yoshinori Tsurusaki, Ryoko Fukai, Satoko Miyatake, Eriko Koshimizu, Itaru Kushima, Takashi Okada, Mako Morikawa, Yota Uno, Kanako Ishizuka, Kazuhiko Nakamura, Masatsugu Tsujii, Takeo Yoshikawa, Tomoko Toyota, Nobuhiko Okamoto, Yoko Hiraki, Ryota Hashimoto, Yuka Yasuda, Shinji Saitoh, Kei Ohashi, Yasunari Sakai, Shouichi Ohga, Toshiro Hara, Mitsuhiro Kato, Kazuyuki Nakamura, Aiko Ito, Chizuru Seiwa, Emi Shirahata, Hitoshi Osaka, Ayumi Matsumoto, Saoko Takeshita, Jun Tohyama, Tomoko Saikusa, Toyojiro Matsuishi, Takumi Nakamura, Takashi Tsuboi, Tadafumi Kato, Toshifumi Suzuki, Hirotomo Saitsu, Mitsuko Nakashima, Takeshi Mizuguchi, Fumiaki Tanaka, Norio Mori, Norio Ozaki, Naomichi Matsumoto

    Diterbitkan 2018-01-01
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