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順天堂大学大学院研究基盤センター
大学院医学研究科研究基盤センター共同研究・研修室(T) 附属研究施設一覧へ

メンバーの業績


 

2023

  1. Mizoue, Y., Ikeda, T., Ikegami, T., Riabets, O., Oishi, Y., Tobita, M., Akutsu, H., Hattori, K., Heissig, B., Koide, H. The stem cell transcription factor ZFP296 transforms NIH3T3 cells and promotes anchorage-independent growth of cancer cells. Int. J. Dev. Biol. 67, 147-153 (2023)
  2. Hashimoto, R., Koide, H., Katoh, Y. Long-term glucocorticoid treatment increases CD204 expression by activating the MAPK pathway and enhances modified LDL uptake in murine macrophages. J. Pharmacol. Sci. 151, 46-53 (2023)
  3. Hashimoto, R., Koide, H., Katoh, Y. MEK inhibitors increase the mortality rate in mice with LPS-induced inflammation through IL-12-NO signaling. Cell Death Discov. 9, 374 (2023)
  4. Nishio, H., Niba, ETE., Saito, T., Okamoto, K., Takeshima, Y., Awano, H. Spinal Muscular Atrophy: The Past, Present, and Future of Diagnosis and Treatment. Int. J. Mol. Sci. 24, 11939 (2023)
  5. Matsuzawa, M., Ando, T., Fukase, S., Kimura, M., Kume, Y., Ide, T., Izawa, K., Kaitani, A., Hara, M., Nakamura, E., Kamei, A., Matsuda, A., Nakano, N., Maeda, K., Tada, N., Ogawa, H., Okumura, K., Murakami, A., Ebihara, N., Kitaura, J. The protective role of conjunctival goblet cell mucin sialylation. Nat. Commun. 14, 1417 (2023)
  6. Nagata, K., Araumi, S., Ando, D., Ito, N., Ando, M., Ikeda, Y., Takahashi, M., Noguchi, S., Yasuda, Y., Nakano, N., Ando, T., Hara, M., Yashiro, T., Hachisu, M., Nishiyama, C. Kaempferol suppresses the activation of mast cells by modulating the expression of FcεRI and SHIP1.Int. J. Mol. Sci. 24, 5997 (2023)

2022

  1. Noguchi, Y., Bo, R., Nishio, H., Matsumoto, H., Matsui, K., Yano, Y., Sugawara, M., Ueda, G., Wijaya, YOS., Niba, ETE., Shinohara, M., Bouike, Y., Takeuchi, A., Okamoto, K., Saito, T., Shimomura, H., Lee, T., Takeshima, Y., Iijima, K., Nozu, K., Awano, H. PCR-Based Screening of Spinal Muscular Atrophy for Newborn Infants in Hyogo Prefecture, Japan. Genes. 13, 2110 (2022)
  2. Niba, ETE., Nishio, H., Wijaya, YOS., Ar Rochmah, M., Takarada, T., Takeuchi, A., Kimizu, T., Okamoto, K., Saito, T., Awano, H., Takeshima, Y., and Shinohara, M. Stability and oligomerization of mutated SMN protein determine clinical severity of spinal muscular atrophy. Genes. 13, 205 (2022)
  3. Wijaya, YOS., Niba, ETE., Nishio, H., Okamoto, K., Awano, H., Saito, T., Takeshima, Y., Shinohara, M. High concentration or combined treatment of antisense oligonucleotides for spinal muscular atrophy perturbed SMN2 splicing in patient fibroblasts. Genes. 13, 685 (2022)

2021

  1. Ikeda, Y., Kaga, M., Koide, H., and Ikeda, S. A novel deletion mutation in the ATP2C1 gene in a case of generalized Hailey-Hailey disease possibly aggravated by scabies infection. J. Dermatol. 48, e178-179 (2021)
  2. Kamijo, S., Hara, M., Suzuki, M., Nakae, S., Ogawa, H., Okumura, K., and Takai, T. Innate IL-17A enhances IL-33-independent skin eosinophilia and IgE response on subcutaneous papain sensitization. J. Invest. Dermatol. 141, 105-113 (2021)
  3. Yoneyama, T., Nakano, N., Hara, M., Yamada, H., Izawa, K., Uchida, K., Kaitani, A., Ando, T., Kitaura, J., Ohtsuka, Y., Ogawa, H., Okumura, K., and Shimizu, T. Notch signaling contributes to the establishment of sustained unresponsiveness to food allergens by oral immunotherapy. J. Allergy Clin. Immunol. 147, 1063-1076 (2021)
  4. Yashiro, T., Yamamoto, M., Araumi, S., Hara, M., Yogo, K., Uchida, K., Kasakura, K., and Nishiyama, C. PU.1 and IRF8 modulate activation of NLRP3 inflammasome via regulating its expression in human macrophages. Front. Immunol. 12, 649572 (2021)
  5. Nakano, N., Saida, K., Hara, M., Izawa, K., Ando, T., Kaitani, A., Kasakura, K., Yashiro, T., Nishiyama, C., Ogawa, H., Kitaura, J., and Okumura, K. Mucosal mast cell-specific gene expression is promoted by interdependent action of Notch and TGF-β signaling. J. Immunol. 207, 3098-3106 (2021)
  6. Niba, ETE., Awano, H., Lee, T., Takeshima, Y., Shinohara, M., Nishio, H., and Matsuo, M. Dystrophin Dp71 subisoforms localize to the mitochondria of human cells. Life. 11, 978 (2021)
  7. Niba, ETE., Nishio, H., Wijaya, YOS., Lai, PS., Tozawa, T., Chiyonobu, T., Yamadera, M., Okamoto, K., Awano, H., Takeshima, Y., Saito, T., and Shinohara, M. Clinical phenotypes of spinal muscular atrophy patients with hybrid SMN gene. Brain Dev. 43, 294-302 (2021)
  8. Niba, ETE, Wijaya, YOS., Awano, H., Taniguchi, N., Takeshima, Y., Nishio, H., and Shinohara, M. DBS screening for glycogen storage disease type 1a: detection of c.648G>T mutation in G6PC by combination of modified competitive oligonucleotide priming-PCR and melting curve analysis. Int J Neonatal Screen. 7, 79 (2021)
  9. Kimizu, T., Ida, S., Okamoto, K., Awano, H., Niba, ETE., Wijaya, YOS., Okazaki, S., Shimomura, H., Lee, T., Tominaga, K., Nabatame, S., Saito, T., Hamazaki, T., Sakai, N., Saito, K., Shintaku, H., Nozu, K., Takeshima, Y., Iijima, K., Nishio, H., and Shinohara, M. Spinal muscular atrophy: diagnosis, incidence, and newborn screening in Japan. Int J Neonatal Screen. 7, 45 (2021)
  10. Wijaya, YOS., Är Rochmah, M., Niba, ETE., Morisada, N., Noguchi, Y., Hidaka, Y., Ozasa, S., Inoue, T., Shimazu, T., Takahashi, Y., Tozawa, T., Chiyonobu, T., Inoue, T., Shiroshita, T., Yokoyama, A., Okamoto, K., Awano, H., Takeshima, Y., Saito, T., Saito, K., Nishio, H., and Shinohara, M. Phenotypes of SMA patients retaining SMN1 with intragenic mutation. Brain Dev. 43, 745-758 (2021)
  11. Wijaya, YOS., Nishio, H., Niba, ETE., Shiroshita, T., Kato, M., Bouike, Y., Tode, C., Ar Rochmah, M., Harahap, NIF., Nurputra, DK., Okamoto, K., Saito, T., Takeuchi, A., Lai, PS., Yamaguchi, S., and Shinohara, M. Dried blood spot screening system for spinal muscular atrophy with allele-specific polymerase chain reaction and melting peak analysis. Genet Test Mol Biomarkers. 25, 293-301 (2021)
  12. Wijaya, YOS., Nishio, H., Niba, ETE., Okamoto, K., Shintaku, H., Takeshima, Y., Saito, T., Shinohara, M., and Awano, H. Detection of spinal muscular atrophy patients using dried saliva spots. Genes. 12, 1621 (2021)
  13. Wijaya, YOS., Niba, ETE., Yabushita, R., Bouike, Y., Nishio, H., and Awano, H. Glycogen storage disease type Ia screening using dried blood spots on filter paper: application of COP-PCR for detection of the c.648G>T G6PC gene mutation. Kobe J Med Sci. 67, E71-E78 (2021)

2020

  1. Xiao, Y., Mo, W., Jia, H., Yuc, D., Qiud, Y., Jiao, Y., Zhu, W., Koide, H., Cao, J., and Zhang, S. Ionizing radiation induces cutaneous lipid remolding and skin adipocytes confer protection against radiation-induced skin injury. J. Dermatol. Sci. 97, 152-160 (2020)
  2. Hashimoto, R., Kakigi, R., Miyamoto, Y., Nakamura, K., Itoh, S., Daida, H., Okada, T., and Katoh, Y. JAK-STAT-dependent regulation of scavenger receptors in LPS-activated murine macrophages. Eur. J. Pharmacol. 871, 172940 (2020)
  3. Eshima, H., Tamura, Y., Kakehi, S., Kakigi, R., Hashimoto, R., Funai, K., Kawamori, R., and Watada, H. A chronic high-fat diet exacerbates contractile dysfunction with impaired intracellular Ca²⁺ release capacity in the skeletal muscle of aged mice. J. Appl. Physiol. (1985) 128, 1153 (2020)
  4. Joshi, S., Kitagawa, A., Jacob, C., Hashimoto, R., Dhagia, V., Ramesh, A., Zheng, C., Zhang, H., Jordan, A., Waddell, I., Leopold, J., Hu, C., McMurtry, I., D'Alessandro, A., Stenmark, K., and Gupte, S. Hypoxic activation of glucose-6-phosphate dehydrogenase controls the expression of genes involved in the pathogenesis of pulmonary hypertension through the regulation of DNA methylation. Am. J. Physiol. Lung Cell Mol. Physiol. 318, L773 (2020)
  5. Hashimoto, R., Lanier, G., Dhagia, V., Joshi, S., Jordan, A., Waddell, I., Tuder, R., Stenmark, K., Wolin, M., McMurtry, I., and Gupte, S. Pluripotent hematopoietic stem cells augment α-adrenergic receptor-mediated contraction of pulmonary artery and contribute to the pathogenesis of pulmonary hypertension. Am. J. Physiol. Lung Cell Mol. Physiol. 318, L386 (2020)
  6. Niba, ETE., Awano, H., Nagai, M., Taniguchi, M., Itoh, K., Nishimura, N., Iijima, K., Nishio, H., and Matsuo, M. Pilocytic astrocytoma tissue from a 25-year-old patient with Duchenne muscular dystrophy expresses the DMD transcript but not protein. Clin Res Pediatr. 3, 1-9 (2020)
  7. Rochmah, MA., Wijaya, YOS., Harahap, NIF., Tode, C., Takeuchi, A., Ohuchi, K., Shimazawa, M., Hara, H., Funato, M., Saito, T., Saito, K., Lai, PS., Awano, H., Shinohara, M., Nishio, H., and Niba ETE. Phosphoethanolamine elevation in plasma of spinal muscular atrophy type 1 patients. Kobe J Med Sci. 66, E1-E11 (2020)
  8. Wijaya, YOS., Purevsuren, J., Harahap, NIF., Niba, ETE., Bouike, Y., Nurputra, DK., Rochmah, MA., Thursina, C., Hapsara, S., Yamaguchi, S., Nishio, H., and Shinohara, M. Assessment of spinal muscular atrophy carrier status by determining SMN1 copy number using dried blood spots. Int J Neonatal Screen. 6, 43 (2020)

2019

  1. Shoji, Y., Takamura, H., Ninomiya, I., Fushida, S., Tada, Y., Yokota, T., Ohta, T., and Koide, H. The embryonic stem cell-specific transcription factor ZFP57 promotes liver metastasis of colorectal cancer. J. Surg. Res. 237, 22-29 (2019)
  2. Maruyama, N., Takai, T., Kamijo, S., Suchiva, P., Ohba, M., Takeshige, T., Suzuki, M., Hara, M., Matsuno, K., Harada, S., Harada, N., Nakae, S., Sudo, K., Okuno, T., Yokomizo, T., Ogawa, H., Okumura, K., and Ikeda, S. Cyclooxygenase inhibition in mice heightens adaptive- and innate-type responses against inhaled protease allergen and IL-33. Allergy 74, 2237-2240 (2019)
  3. Yoshikawa, S., Oh-Hora, M., Hashimoto, R., Nagao, T., Peters, L., Egawa, M., Ohta, T., Miyake, K., Adachi, T., Kawano, Y., Yamanishi, Y., and Karasuyama, H.  Pivotal role of STIM2, but not STIM1, in IL-4 production by IL-3-stimulated murine basophils.  Sci. Signal. 12, eaav2060 (2019)
  4. Hashimoto, R., Miyamoto, Y., Itoh, S., Daida, H., Okada, T., and Katoh, Y.  Phorbol 12-myristate 13-acetate (PMA) suppresses high Ca²⁺-enhanced adipogenesis in bone marrow stromal cells.  J. Physiol. Sci. 69, 741 (2019)
  5. Niba, ETE., Ar Rochmah, M., Harahap, NIF., Awano, H., Morioka, I., Iijima, K., Takeshima, Y., Saito, T., Saito, K., Takeuchi, A., Lai, PS., Bouike, Y., Matsuo, M., Nishio, H., and Shinohara, M. Spinal muscular atrophy: new screening system with real-time mCOP-PCR and PCR-RFLP for SMN1 deletion. Kobe J Med Sci. 65, E44-E48 (2019)
  6. Niba, ETE., Ar Rochmah, M., Harahap, NIF., Awano, H., Morioka, I., Iijima, K., Takeshima, Y., Saito, T., Saito, K., Takeuchi, A., Lai, PS., Bouike, Y., Matsuo, M., Nishio, H., and Shinohara, M. Spinal muscular atrophy: Advanced version of screening system with real-time mCOP-PCR and PCR-RFLP for SMN1 deletion. Kobe J Med Sci. 65, E49-E53 (2019)
  7. Takeuchi, A., Tode, C., Nishino, M., Wijaya, YOS., Niba, ETE., Awano, H., Takeshima, Y., Saito, T., Saito, K., Lai, PS., Bouike, Y., Nishio, H., and Shinohara, M. Newborn Screening for Spinal Muscular Atrophy: DNA Preparation from Dried Blood Spot and DNA Polymerase Selection in PCR. Kobe J Med Sci. 65, E95-E99 (2019)
  8. Shinohara, M., Niba, ETE., Wijaya, YOS., Takayama, I., Mitsuishi, C., Kumasaka, S., Kondo, Y., Takatera, A., Hokuto, I., Morioka, I., Ogiwara, K., Tobita, K., Takeuchi, A., and Nishio, H.; SMA-NBS PILOT STUDY GROUP. A novel system for spinal muscular atrophy screening in newborns: Japanese pilot study. Int J Neonatal Screen. 5, 41 (2019)
  9. Takeuchi, A., Tode, C., Nishino, M., Wijaya, YOS., Niba, ETE., Awano, H., Takeshima, Y., Saito, T., Saito, K., Lai, PS., Bouike, Y., Nishio, H., and Shinohara, M. Newborn screening for spinal muscular atrophy: DNA preparation from dried blood spot and DNA polymerase selection in PCR. Kobe J Med Sci. 65, E95-E99 (2019)
  10. Wijaya, YOS., Niba, ETE., Ar Rochmah, M., Harahap, NIF., Awano, H., Takeshima, Y., Saito, T., Saito, K., Takeuchi, A., Lai, PS., Bouike, Y., Nishio, H., and Shinohara, M. Nested PCR amplification may secure DNA template quality and quantity in real- time mCOP-PCR screening for SMA. Kobe J Med Sci. 65, E54-E58 (2019)

2018

  1. Kinjo, T., Sun, C., Ikeda, T., Ikegami, T., Tada, Y., Akagi, T., Yokota, T., and Koide, H. Platelet-derived growth factor-C functions as a growth factor in mouse embryonic stem cells and human fibrosarcoma cells. Cell. Mol. Biol. Lett. 23, 8 (2018)
  2. Kadoguchi, T., Shimada, K., Koide, H., Miyazaki, T., Shiozawa, T., Takahashi, S., Aikawa, T., Ouchi, S., Kitamura, K., Sugita, Y., Hamad, A.S., Kunimoto, M., Sato-Okabayashi, Y., Akita, K., Isoda, K., and Daida, H. Possible role of NADPH oxidase 4 in angiotensin II-induced muscle wasting in mice. Front. Physiol. 9, 340 (2018)
  3. Kawaguchi, T., Niba, ETE., Rani, AQM., Onishi, Y., Koizumi, M., Awano, H., Matsumoto, M., Nagai, M., Yoshida, S., Sakakibara, S., Maeda, N., Sato, O., Nishio, H., and Matsuo, M. Detection of dystrophin Dp71 in human skeletal muscle using an automated capillary Western assay system. Int J Mol Sci. 19, 1546 (2018)
  4. Harahap, NIF., Niba, ETE., Ar Rochmah, M., Wijaya, YOS., Saito, T., Saito, K., Awano, H., Morioka, I., Iijima, K., Lai, PS., Motsuo, M., Nishio, H., and Shinohara, M. Intron-retained transcripts of the spinal muscular atrophy genes, SMN1 and SMN2. Brain Dev. 40, 670-677 (2018)

2017

  1. Kometani, M., Yoneda, T., Demura, M., Koide, H., Nishimoto, K., Mukai, K., Gomez-Sanchez, C.E., Akagi, T., Yokota, T., Horike, S.I., Karashima, S., Miyamori, I., Yamagishi, M., and Takeda, Y. Cortisol overproduction results from DNA methylation of CYP11B1 in hypercortisolemia. Sci. Rep. 7, 11205 (2017)
  2. Nagaoka, M., Yashiro, T., Uchida, Y., Ando, T., Hara, M., Arai, H., Ogawa, H., Okumura, K., Kasakura, K., and Nishiyama, C. The orphan nuclear receptor NR4A3 is involved in the function of dendritic cells. J. Immunol. 199, 2958-2967 (2017)
  3. Yashiro, T., Kasakura, K., Oda, Y., Kitamura, N., Inoue, A., Nakamura, S., Yokoyama, H., Fukuyama, K., Hara, M., Ogawa, H., Okumura, K., Nishiyama, M., and Nishiyama, C. The hematopoietic cell-specific transcription factor PU.1 is critical for expression of CD11c. Int. Immunol. 29, 87-94 (2017)
  4. Kawauchi, T., Ishimaru, K., Nakamura, Y., Nakano, N., Hara, M., Ogawa, H., Okumura, K., Shibata, S., and Nakao, A. Clock-dependent temporal regulation of IL-33/ST2-mediated mast cell response. Allergol. Int. 66, 472-478 (2017)
  5. Honjo, A., Nakano, N., Yamazaki, S., Hara, M., Uchida, K., Kitaura, J., Nishiyama, C., Yagita, H., Ohtsuka, Y., Ogawa, H., Okumura, K., and Shimizu, T. Pharmacologic inhibition of Notch signaling suppresses food antigen-induced mucosal mast cell hyperplasia. J. Allergy Clin. Immunol. 139, 987-996 (2017)
  6. Niba, ETE., Ar Rochmah, M., Harahap, NIF., Awano, H., Morioka, I., Iijima, K., Saito, T., Saito, K., Takeuchi, A., Lai, PS., Bouike, Y., Nishio, H., and Shinohara, M. SMA diagnosis: Detection of SMN1 deletion with real-time mCOP-PCR system using fresh blood DNA. Kobe J Med Sci. 63, E80-E83 (2017)
  7. Niba, ETE., Yamanaka, R., Rani, AQM., Awano, H., Matsumoto, M., Nishio, H., and Matsuo, M. DMD transcripts in CRL-2061 rhabdomyosarcoma cells show high levels of intron retention by intron-specific PCR amplification. Cancer Cell Int. 17, 58 (2017)
  8. Niba, ETE., Nishida, A., Tran, VK., Vu, DC., Matsumoto, M., Awano, H., Lee, T., Takeshima, Y., Nishio, H., and Matsuo, M. Cryptic splice activation but not exon skipping is observed in minigene assays of dystrophin c.9361+1G>A mutation identified by NGS. J Hum Genet. 62, 531-537 (2017)
  9. Ar Rochmah, M., Harahap, NIF., Niba, ETE., Nakanishi, K., Awano, H., Morioka, I., Iijima, K., Saito, T., Saito, K., Lai, PS., Takeshima, Y., Takeuchi, A., Bouike, Y., Okamoto, M., Nishio, H., and Shinohara, M. Genetic screening of spinal muscular atrophy using a real-time modified COP-PCR technique with dried blood-spot DNA. Brain Dev. 39, 774-782 (2017)
  10. Ar Rochmah, M., Shima, A., Harahap, NIF., Niba, ETE., Morisada, N., Yanagisawa, S., Saito, T., Kaneko, K., Saito, K., Morioka, I., Iijima, K., Lai, PS., Bouike, Y., Nishio, H., and Shinohara, M. Gender effects on the clinical phenotype in Japanese patients with spinal muscular atrophy. Kobe J Med Sci. 63, E41-E44 (2017)
  11. Shinohara, M., Ar Rochmah, M., Nakanishi, K., Harahap, NIF., Niba, ETE., Saito, T., Saito, K., Takeuchi, A., Bouike, Y., and Nishio, H. New, improved version of the mCOP-PCR screening system for detection of spinal muscular atrophy Gene (SMN1) deletion. Kobe J Med Sci. 63, E37-E40 (2017)

2016

  1. Uranishi, K., Akagi, T., Koide, H., and Yokota, T.  Esrrb directly binds to Gata6 promoter and regulates its expression with Dax1 and Ncoa3.  Biochem. Biophys. Res. Commun.  478, 1720-1725 (2016)
  2. Tabe, Y., Hatanaka, Y., Nakashiro, M., Sekihara, K., Yamamoto, S., Matsushita, H., Kazuno, S., Fujimura, T., Ikegami, T., Nakanaga, K., Matsumoto, H., Ueno, T., Aoki, J., Yokomizo, T., Konopleva, M., Andreeff, M., Miida, T., Iwabuchi, K., and Sasai, K. Integrative genomic and proteomic analyses identifies glycerol-3-phosphate acyltransferase as a target of low-dose ionizing radiation in EBV infected-B cells. Int. J. Radiat. Biol. 92, 24-34(2016)
  3. Someya, A., Ikegami, T., Sakamoto, K., and Nagaoka, I. Glucosamine Downregulates the IL-1 beta-Induced Expression of Proinflammatory Cytokine Genes in Human Synovial MH7A Cells by O-GlcNAc Modification-Dependent and - Independent Mechanisms. PLoS One. 11, e0165158 (2016)
  4. Suzuki, M., Hara, M., Ichikawa, S., Kamijo, S., Nakazawa, T., Hatanaka, H., Akiyama, K., Ogawa, H., Okumura, K., and Takai, T. Presensitization to Ascaris antigens promotes induction of mite-specific IgE upon mite antigen inhalation in mice. Allergol. Int. 65, 44-51 (2016)
  5. Shimura, S., Takai, T., Iida, H., Maruyama, N., Ochi, H., Kamijo, S., Nishioka, I., Hara, M., Matsuda, A., Saito, H., Nakae, S., Ogawa, H., Okumura, K., and Ikeda, S. Epicutaneous allergic sensitization by cooperation between allergen protease activity and mechanical skin barrier damage in mice. J. Invest. Dermatol. 136, 1408-1417 (2016)
  6. Kamijo, S., Suzuki, M., Hara, M., Shimura, S., Ochi, H., Maruyama, N., Matsuda, A., Saito, H., Nakae, S., Suto, H., Ichikawa, S., Ikeda, S., Ogawa, H., Okumura, K., and Takai, T. Subcutaneous allergic sensitization to protease allergen is dependent on mast cells but not IL-33: Distinct mechanisms between subcutaneous and intranasal routes. J. Immunol. 196, 3559-3569 (2016)
  7. Miura, R., Kasakura, K., Nakano, N., Hara, M., Maeda, K., Okumura, K., Ogawa, H., Yashiro, T., and Nishiyama, C. Role of PU.1 in MHC class II expression via CIITA transcription in plasmacytoid dendritic cells. PLoS One. 11, e0154094 (2016)
  8. Yashiro, T., Hara, M., Ogawa, H., Okumura, K., and Nishiyama, C. Critical role of transcription factor PU.1 in the function of the OX40L/TNFSF4 promoter in dendritic cells. Sci. Rep. 6, 34825 (2016)
  9. Nishida, A., Yasuno, S., Takeuchi, A., Awano, H., Lee, T., Niba, ET., Fujimoto, T., Itoh, K., Takeshima, Y., Nishio, H., and Matsuo, M. HEK293 cells express dystrophin Dp71 with nucleus-specific localization of Dp71ab. Histochem Cell Biol. 146, 301-309 (2016)

2015

  1. Akagi, T., Kuure, S., Uranishi, K., Koide, H., Costantini, F., and Yokota, T. ETS-related transcription factors ETV4 and ETV5 are involved in proliferation and induction of differentiation-associated genes in ES cells. J. Biol. Chem. 290, 22460-22473 (2015)
  2. Tada, Y., Yamaguchi, Y., Kinjo, T., Song, X., Akagi, T., Takamura, H., Ohta, T., Yokota, T., and Koide, H. The stem cell transcription factor ZFP57 induces IGF2 expression to promote anchorage-independent growth in cancer cells. Oncogene 34, 752-760 (2015)
  3. Kanai, D., Ueda, A., Akagi, T., Yokota, T., and Koide, H. Oct3/4 directly regulates expression of E2F3a in mouse embryonic stem cells. Biochem. Biophys. Res. Commun. 459, 374-378 (2015)
  4. Nakano, N., Nishiyama, C., Yagita, H., Hara, M., Motomura, Y., Kubo, M., Okumura, K., and Ogawa, H. Notch signaling enhances FcεRI-mediated cytokine production by mast cells through direct and indirect mechanisms. J. Immunol. 194, 4535-4544 (2015)
  5. Ishiyama, K., Yashiro, T., Nakano, N., Kasakura, K., Miura, R., Hara, M., Kawai, F., Maeda, K., Tamura, N., Okumura, K., Ogawa, H., Takasaki, Y., and Nishiyama, C. Involvement of PU.1 in NFATc1 promoter function in osteoclast development. Allergol. Int. 64, 241-247 (2015)
  6. Yamazaki, S., Nakano, N., Honjo, A., Hara, M., Maeda, K., Nishiyama, C., Kitaura, J., Ohtsuka, Y., Okumura, K., Ogawa, H., and Shimizu, T. The transcription factor Ehf is involved in TGF-β-induced suppression of FcεRI and c-kit expression and FcεRI-mediated activation in mast cells. J. Immunol. 195, 3427-3435 (2015)
  7. Nishida, A., Minegishi, M., Takeuchi, A., Awano, H., Niba, ET., and Matsuo, M. Neuronal SH-SY5Y cells use the C-dystrophin promoter coupled with exon 78 skipping and display multiple patterns of alternative splicing including two intronic insertion events. Hum Genet. 134, 993-1001 (2015)
  8. Nishida, A., Minegishi, M., Takeuchi, A., Niba, ET., Awano, H., Lee, T., Iijima, K., Takeshima, Y., and Matsuo, M. Tissue- and case-specific retention of intron 40 in mature dystrophin mRNA. J Hum Genet. 60, 327-333 (2015)

2014

  1. Yamaguchi, Y., Takamura, H., Tada, Y., Akagi, T., Oyama, K., Miyashita, T., Tajima, H., Kitagawa, H., Fushida, S., Yokota, T., Ohta, T., and Koide, H. Nanog positively regulates Zfp57 expression in mouse embryonic stem cells. Biochem. Biophys. Res. Commun. 453, 817-820 (2014)
  2. Doe, K., Nozawa, K., Hiruma, K., Yamada, Y., Matsuki, Y., Nakano, S., Ogasawara, M., Nakano, H., Ikeda, T., Ikegami, T., Fujishiro, M., Kawasaki, M., Ikeda, K., Amano, H., Morimoto, S., Ogawa, H., Takamori, K., Sekigawa, I. and Takasaki, Y. Antibody against chromatin assembly factor-1 is a novel autoantibody specifically recognized in systemic lupus erythematosus. Lupus 23, 1031-1041 (2014)
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