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メンバーの業績
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2023
- 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)
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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)
- 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)
- 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)
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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)
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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
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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)
- 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)
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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
- 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)
- 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)
- 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)
- 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)
- 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)
- 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)
- 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)
- 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)
- 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)
- 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)
- 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)
- 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)
- 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
- 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)
- 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)
- 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.
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- 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)
- 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)
- 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)
- 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)
- 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
- 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)
- 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)
- 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)
- 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)
- 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)
- 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)
- 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)
- 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)
- 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)
- 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
- 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)
- 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)
- 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)
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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
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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)
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Ogawa, H., Okumura, K., Kasakura, K., and Nishiyama, C. The orphan nuclear
receptor NR4A3 is involved in the function of dendritic cells. J.
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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)
- 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)
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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)
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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)
- 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)
- 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
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Takeuchi, A., Bouike, Y., Okamoto, M., Nishio, H., and Shinohara, M. Genetic
screening of spinal muscular atrophy using a real-time modified COP-PCR
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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)
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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
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2016
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directly binds to Gata6 promoter and regulates its expression with Dax1 and
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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
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N., Matsuda, A., Saito, H., Nakae, S., Suto, H., Ichikawa, S., Ikeda, S.,
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PLoS One. 11, e0154094 (2016)
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Critical role of transcription factor PU.1 in the function of the OX40L/TNFSF4
promoter in dendritic cells. Sci. Rep. 6, 34825
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Fujimoto, T., Itoh, K., Takeshima, Y., Nishio, H., and Matsuo, M. HEK293 cells
express dystrophin Dp71 with nucleus-specific localization of Dp71ab.
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2015
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Yokota, T. ETS-related transcription factors ETV4 and ETV5 are involved in
proliferation and induction of differentiation-associated genes in ES
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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)
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directly regulates expression of E2F3a in mouse embryonic stem cells.
Biochem. Biophys. Res. Commun. 459, 374-378 (2015)
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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)
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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
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C., Kitaura, J., Ohtsuka, Y., Okumura, K., Ogawa, H., and Shimizu, T. The
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2014
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H. Nanog positively regulates Zfp57 expression in mouse embryonic stem
cells. Biochem. Biophys. Res. Commun. 453, 817-820
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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)
- Nakamura, Y., Nakano, N., Ishimaru, K., Hara, M., Ikegami, T.,
Tahara, Y., Katoh, R., Ogawa, H., Okumura, K., Shibata, S., Nishiyama, C., and
Nakao, A. Circadian regulation of allergic reactions by the mast cell clock in
mice. J. Allergy Clin. Immunol. 133, 568-575 (2014)
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J., Kamijo, S., Hara, M., Ushio, H., Baba, T., Hiramatsu, K., Ikeda,
S., Ogawa, H., and Okumura, K. TSLP expression induced via Toll-like receptor
pathways in human keratinocytes. Methods Enzymol.
535, 371-387 (2014)
- Kiatsurayanon, C., Niyonsaba, F., Smithrithee, R., Akiyama, T., Ushio, H.,
Hara, M., Okumura, K., Ikeda, S., Ogawa, H. Host defense
(Antimicrobial) peptide, human β-defensin-3, improves the function of the
epithelial tight-junction barrier in human keratinocytes. J.
Invest. Dermatol. 134, 2163-2173 (2014)
- Inage, E., Kasakura, K., Yashiro, T., Suzuki, R., Baba, Y., Nakano, N.,
Hara, M., Tanabe, A., Oboki, K., Matsumoto, K., Saito, H., Niyonsaba,
F., Ohtsuka, Y., Ogawa, H., Okumura, K., Shimizu, T., and Nishiyama, C.
Critical roles for PU.1, GATA1, and GATA2 in the expression of human FcεRI on
mast cells: PU.1 and GATA1 transactivate FCER1A, and GATA2 transactivates
FCER1A and MS4A2. J. Immunol. 192, 3936-3946 (2014)
- Aihara, Y., Oh-oka, K., Kondo, N., Sharma, J., Shrestha, N.C., Ishimaru, K.,
Hara, M., Yamagata, Z., Nakao, A. Residential area, birth order, and
dietary habit may influence TSLP levels in colostrum: comparative study
between Japan and Nepal. Allergol. Int. 63, 283-285
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- Koide, H. Embryonic stem cells and oncogenes. in
Pluripotent Stem Cell Biology - Advances in Mechanisms, Methods
and Models (Craig S. Atwood & Sivan Vadakkadath Meethal
eds.) pp 41-61, InTech (2014)
- Aihara, Y., Oh-oka, K., Kondo, N., Sharma, J., Ishimaru, K., Hara,
M., Yamagata, Z., and Nakao, A. Comparison of colostrum TGF-β2
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- Niba, ET., Tran, VK., Tuan-Pham, le A., Vu, DC., Nguyen, NK., Ta,
VT., Tran, TH., Lee, T., Takeshima, Y., and Matsuo, M. Targeted
next-generation sequencing reveals a homozygous nonsense mutation in CAPN3
that causes limb-girdle muscular dystrophy type 2A first in Vietnam.
J Mol Biomark Diagn. 5, 1000194 (2014).
- Niba, ET., Tran, VK., Tuan-Pham, le A., Vu, DC., Nguyen, NK., Ta,
VT., Tran, TH., Lee, T., Takeshima, Y., and Matsuo, M. Validation of ambiguous
MLPA results by targeted next-generation sequencing reveals a nonsense
mutation in the DMD gene. Clin Chim Acta. 436,
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