業績リスト
臨床教室との共同研究
原著論文  Original Research Papers  / 英文 English
Unoki, M., Velasco, G., Kori, S., Arita, K., Daigaku, Y., Au Yeung, W.K., Fujimoto, A., Ohashi, H., Kubota, T., Miyake, K. & Sasaki, H.
Novel compound heterozygous mutations in UHRF1 are associated with atypical immunodeficiency-centromeric instability-facial anomalies (ICF) syndrome with distinctive genome-wide DNA hypomethylation.
Hum. Mol. Genet. (Online publication).

Yano, S. Ishiuchi, T., Abe, S., Namekawa, S.H., Huang, G., Ogawa, Y. & Sasaki, H.
Histone H3K36me2 and H3K36me3 form a chromatin platform essential for DNMT3A-dependent DNA methylation in mouse oocytes.
Nat. Commun. 13, 4440 (2022).
PubMed

Inatomi, T., Matsuda, S., Ishiuchi, T., Do, Y., Nakayama, N., Abe, S., Kasho, K., Wanrooij, S., Nakada, K., Ichiyanagi, K., Sasaki, H., Yasukawa, T. & Kang. D.
TFB2M and POLRMT are essential for mammalian mitochondrial DNA replication.
Biochim. Biophys. Acta - Mol. Cell Res. 1869, 119167 (2022)
PubMed

Haratake, N., Hu, Q., Okamoto, T., Jogo, T., Toyokawa, G., Kinoshita, F., Takenaka, T., Tagawa, T., Iseda, N., Itoh, S., Yamada, Y., Oda, Y., Shimokawa, M., Kikutake, C., Suyama, M., Unoki, M., Sasaki, H. & Mori, M.
Identification of SLC38A7 as a prognostic marker and potentially targetable driver gene of lung squamous cell carcinoma.
Ann. Surg. 274, 500-507 (2021)
PubMed

Morikawa, T., Ohishi, H., Kosaka, K., Shimojo T., Nagano, A., Taniguchi, I., Fujioka, R., Moriyama, K., Unoki, M., Takahashi, M., Nakao, M., Izumi, Y., Bamba, T., Sasaki, H., Miura, S. & Shibata, H.
Ddhd1 knockout mouse as a model of locomotive and physiological abnormality in familial spastic paraplegia.
Biosci. Rep. 41, BSR20204171 (2021)
PubMed

Unoki, M., Sharif, J., Saito, Y., Velasco, G., Francastel, C., Koseki, H. & Sasaki, H.
CDCA7 and HELLS suppress DNA:RNA hybrid-associated DNA damage at pericentromeric repeats.
Sci. Rep. 10, 17865 (2020)
PubMed

Hiramoto, T., Tahara, M., Liao, J., Soda, Y., Miura, Y., Kurita, R., Hamana, H., Inoue K., Kohara, H., Hijikata, Y., Okano, S., Yamaguchi, Y., Oda, Y., Ichiyanagi, K., Toh, H., Sasaki, H., Kishi, H., Ryo, A., Muraguchi, A., Takeda, M. & Tani, K.
Non-transmissible MV vector with segmented RNA genome establishes different types of iPSCs from hematopoietic cells.
Mol. Ther. 28, 129-141 (2020)
PubMed

Inoguchi, Y., Ichiyanagi, K., Ohishi, H., Maeda, Y., Sonoda, N., Ogawa, Y., Inoguchi, T. & Sasaki, H.
Poorly controlled diabetes during pregnancy and lactation activates the Foxo1 pathway and causes glucose intolerance in adult offspring.
Sci. Rep. 9, 10181 (2019)
PubMed

Kubo, N., Harada, T., Shiraishi, Y., Nosaki, K., Nakagaki, N., Takeshita, M., Ouchi, H., Iwama, E., Tanaka, K., Okamoto, I., Sasaki, H. & Nakanishi, Y.
Identification of genomic alterations acquired during treatment with EGFR-TKIs in non-small cell lung cancer.
Anticancer Res. 39, 671-677 (2019)
PubMed

Kamae, C., Imai, K., Kato, T., Okano, T., Honma, K., Nakagawa, N., Yeh, T. W., Noguchi, E., Ohara, A., Shigemura, T., Takahashi, H., Takakura, S., Hayashi, M., Honma, A., Watanabe, S., Shigemori, T., Ohara, O., Sasaki, H., Kubota, T., Morio, T., Kanegae, H. & Nonoyama, S.
Clinical and immunological characterization of ICF syndrome in Japan.
J. Clin. Immunol. 38, 927-937 (2018)
PubMed

Hidaka, N., Iwama, E., Kubo, N., Harada, T., Miyawaki, K., Tanaka, K., Okamoto, I., Baba, E., Akashi, K., Sasaki, H. & Nakanishi, Y.
Most T790M mutations are present on the same EGFR allele as activating mutations in patients with non-small cell lung cancer.
Lung Cancer 108, 75-82 (2017)
PubMed

Thijssen, P.E., Ito, Y., Grillo, G., Wang, J., Velasco, G., Nitta, H., Unoki, M., Yoshihara, M., Suyama, M., Sun, Y., Lemmers, R.J.L.F., de Greef, J.C., Gennery, A., Picco, P., Kloeckener-Gruissem, B., Gungor, T., Reisli, I., Picard, C., Kebaili, K., Roquelaure, B., Iwai, T., Kondo, I., Kubota, T., van Ostaijen-Ten Dam, M.M., van Tol, M.J.D., Weemaes, C., Francastel, C., van der Maarel, S.M. & Sasaki. H.
Mutations in CDCA7 and HELLS cause immunodeficiency-centromeric instability-facial anomalies syndrome.
Nat. Commun. 6, 7870 (2015)
PubMed

Yokomizo, H., Inoguchi, T., Sonoda, N., Sakaki, Y., Maeda, Y., Inoue, T., Hirata, E., Takei, R., Ikeda, N., Fujii, M., Fukuda, K., Sasaki, H. & Takayanagi, R.
Maternal high fat diet induces insulin resistance and deterioration of pancreatic β cell function in adult offspring with gender differences in mice.
Am. J. Physiol. Endocrinol. Metab. 306, E1163-1175 (2014)
PubMed

Nitta, H., Unoki, M., Ichiyanagi, K., Kosho, T., Shigemura, T., Takahashi, H., Velasco, G., Francastel, C., Picard, C., Kubota, T. & Sasaki, H.
Three novel ZBTB24 mutations identified in Japanese and Cape Verdean type 2 ICF syndrome patients.
J. Hum. Genet. 58, 455-460 (2013)
PubMed

Fukasawa, M., Kimura, M., Morita, S., Matsubara, K., Yamanaka, S., Endo, C., Sakurada, A., Sato, M., Kondo, T., Horii, A., Sasaki, H. & Hatada, I.
Microarray analysis of promoter methylation in lung cancers.
J. Hum. Genet. 51, 368-374, (2006)
PubMed

Hatada, I., Fukasawa, M., Kimura, M., Morita, S., Yamada, K., Yoshikawa, T., Yamanaka, S., Endo, C., Sakurada, A., Sato, M., Kondo, T., Horii, A., Ushijima, T. & Sasaki, H.
Genome-wide profiling of promoter methylation in human.
Oncogene 25, 3059-3064 (2006)
PubMed

Cerrato, F., Sparago, A., Zou, X., Dean, W., Bruggemann, M., Sasaki, H., Reik, W. & Riccio, A.
The two domain hypothesis in Beckwith-Wiedemann syndrome: autonomous imprinting of the telomeric domain of the distal chromosome 7 cluster.
Hum. Mol. Genet. 14, 503-511 (2005)
PubMed

Kubota, T., Furuumi, H., Kamoda, T., Iwasaki, N., Tobita, N., Fujiwara, N., Goto, Y., Matsui, A., Sasaki, H. & Kajii, T.
ICF syndrome in a girl with DNA hypomethylation but without detectable DNMT3B mutation.
Am. J. Med. Genet. 129A, 290-293 (2004)
PubMed

Shirohzu, H., Kubota, T., Kumazawa, A., Sado, T., Chijiwa, T., Inagaki, K., Suetake, I., Tajima, S., Wakui, K., Miki, Y., Hayashi, M., Fukushima, Y. & Sasaki, H.
Three novel DNMT3B mutations in Japanese patients with ICF syndrome.
Am. J. Med. Genet. 112, 31-37 (2002)
PubMed

Kurosawa, K., Sasaki, H., Sato, Y., Yamanaka, M., Shimizu, M., Ito, Y., Okuyama, T., Matsuo, M., Imaizumi, K., Kuroki, Y. & Nishimura, G.
Paternal UPD14 is responsible for a distinctive malformation complex.
Am. J. Med. Genet. 110, 268-272 (2002)
PubMed

Hamatani, T., Sasaki, H., Ishihara, K., Hida, N., Maruyama, T., Yoshimura, Y., Hata, J. & Umezawa, A.
Epigenetic mark sequence of the H19 gene in human sperm.
Biochim. Biophys. Acta 1518, 137-144 (2001)
PubMed

Mizuno, S., Chijiwa, T., Okamura, T., Akashi, K., Fukumaki, Y., Niho, Y. & Sasaki, H.
Expression of DNA methyltransferases DNMT1, 3A and 3B in normal hematopoiesis and in acute and chronic myelogenouse leukemia.
Blood 97, 1172-1179 (2001)
PubMed

Kira, J., Koyanagi, Y., Yamada, T., Itoyama, Y., Goto, I., Yamamoto, M., Sasaki, H. & Sakaki, Y.
Increased HTLV-I-associated myelopathy: a quantitative PCR study.
Ann. Neurol. 29, 194-201 (1991)
PubMed

原著論文  Original Research Papers / 和文 Japanese
池松秀之, 鄭湧, 白根健次郎, 藤英博, 佐々木裕之, 松本信也, 野田望, 堀田多恵子, 内海健, 康東天
2014/15年流行期に患者より分離されたインフルエンザA/H3N2, Bウイルスのノイラミニダーゼ遺伝子と薬剤感受性との関連についての検討
福岡医学雑誌 107, 98-104 (2016)

池松秀之, 鄭湧, 白根健次郎, 藤英博, 佐々木裕之, 古賀結, 浦田美秩代, 堀田多恵子, 内海健, 康東天
2013/14流行期に患者より分離されたインフルエンザA/H1N1pdm09, A/H3N2, Bウイルスのノイラミニダーゼ遺伝子と薬剤感受性との関連についての検討
福岡医学雑誌 106, 231-239 (2015)
PubMed

池松秀之, 鄭湧, 白根健次郎, 藤英博, 佐々木裕之, 古賀結, 浦田美秩代, 堀田多恵子, 内海健, 康東天
2011/12及び2012/13年インフルエンザ流行期に患者より分散されたA/H3N2型ウイルス96株のNA遺伝子配列と薬剤感受性との関連についての検討
福岡医学雑誌 106, 16-22 (2015)
PubMed

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