カジ旅勝てない

文字サイズを大きくする English and Other Languages 代表: 03-3416-0181 ／ 予約センター（病院）: 03-5494-7300 〈月～金曜日（祝祭日を除く）9時〜17時〉 交通案内 お問い合わせ 取材・撮影について サイト内検索 調達情報 患者・ご家族の方へ 病院の紹介 医師・スタッフ紹介 外来受診のご案内 入院のご案内 救急受診のご案内 セカンドオピニオン外来のご案内 妊娠・出産をお考えの方 子どもと家族への支援 病気に関する情報 医療関係者の方へ 患者紹介・医療連携 小児集中治療室（PICU)への転院・搬送 新生児集中治療室（NICU）への転送・搬送 母体搬送 各診療部門の紹介 医療機器の共同利用について 医療型短期入所施設 もみじの家について 医療連携登録医の皆さまへ 研究者・企業の方へ 研究所について 研究所の概要 各研究部門の紹介 研究業績(年報) 臨床研究センターについて 臨床研究センターの概要 各部門の紹介 治験について 事業・実績 ご寄付について ご寄付のお申し込み 遺贈・相続財産からのご寄付 税制上の優遇措置 寄付について よくあるご質問 ご寄付いただいた方々 寄付金の使途 採用・研修 採用・募集 見学・短期研修 セミナー・学習会 研修用動画 国立成育医療研究センターについて 理事長挨拶 役員紹介 理念と方針 沿革 広報活動 情報公開 主な取り組み 研究開発監理部 サイト内検索 患者・ご家族の方へ 病院の紹介 医師・スタッフ紹介 外来受診のご案内 入院のご案内 救急受診のご案内 セカンドオピニオン外来のご案内 妊娠・出産をお考えの方 子どもと家族への支援 病気に関する情報 医療関係者の方へ 患者紹介・医療連携 小児集中治療室（PICU)への転院・搬送 新生児集中治療室（NICU）への転送・搬送 母体搬送 各診療部門の紹介 医療機器の共同利用について 医療型短期入所施設 もみじの家について 医療連携登録医の皆さまへ 研究者・企業の方へ 研究所について 臨床研究センターについて ご寄付について ご寄付のお申し込み 遺贈・相続財産からのご寄付 税制上の優遇措置 寄付について よくあるご質問 ご寄付いただいた方々 寄付金の使途 採用・研修 採用・募集 見学・研修 セミナー・学習会 研修用動画 当センターについて 理事長挨拶 役員紹介 理念と方針 沿革 広報活動 情報公開 主な取り組み 施設から探す 病院 研究所 臨床研究センター 調達情報 アクセス・交通案内 お問い合わせ サイトマップ English and Other Languages トップ > 研究者・企業の方へ > 研究所について > 各研究部門の紹介 > 周産期病態研究部 周産期病態研究部 研究部紹介 胎児と胎児付属物（胎盤）の発生・分化異常や、それに伴う周産期（妊娠後期から新生児早期まで）の病気の解明を目指しています。分子生物学的手法に加え、ゲノム・エピゲノムの観点から病態を理解し、ポストゲノムシークエンス時代の、新たな周産期医療に資する研究成果を目標としています。 周産期ゲノミクス研究室、胎児発育研究室、母性管理研究室の三研究室が中心となって、生殖細胞の形成から出生に至るまで、広く母体と胎児（新生児）と胎盤に関する研究を行っています。 オリジナルWebサイトはこちら --> 研究内容 周産期の異常は、母子双方に対して緊急かつ集学的な医療介入が必要になります。しかし、周産期に起こる疾患の詳細なメカニズムは未解明な点が多く、早期の診断や根治的な治療法が確立されていない疾患が数多くあります。また、特に異常のない妊娠経過に見えても、胎児期の環境（母体の栄養状態など）が不良の場合、出生後も長期にわたり児の遺伝子発現状態に影響を与えることがわかってきました。さらに、胎児期の環境に起因する長期の影響が成人期にもおよび、生活習慣病等の発症リスクになりうる可能性も指摘されています。そのため、「周産期病態」の研究は成育医療に止まらず、生涯にわたる健康を左右する重要な課題といえます。これらの背景を踏まえ、本研究部は、周産期に起こる疾患の直接の病因病態を解明すること、そして適切な診断治療法を開発することを目的とします。この目標を達成するために我々は、大きく二つのアプローチで研究に臨んでいます。第一に、実際の症例から頂いた試料（治療の過程で必要とされる採血検査の少量の余剰など）を用い、異常妊娠症例を、特に分子生物学的・遺伝学的手法で解析しています。第二に、異常妊娠症例解析から得られた知見の詳細を再検証するために、培養細胞やモデル動物を用いて解析しています。これら二つの中核プロジェクトに加え、DNAマイクロアレイ技術や大規模超高速DNA塩基配列解析（次世代シークエンサー）などを積極的に応用し、先進的なヒト異常妊娠の病因病態解明、診断法開発を目指しています。また、国内20カ所以上の医療機関および研究機関と連携して、希少疾患の分子遺伝学的診断情報と研究を進めています。 スタッフ 周産期病態研究部 梅澤 明弘（部長・併任）秦 健一郎（シニアフェロー） 周産期ゲノミクス研究室 中林 一彦（室長） 胎児発育研究室 河合 智子（室長） 母性管理研究室 山口 晃史（室長・併任） 部室員 冨川 順子（研究員）大西 英理子（研究員）石渡 啓介伊東 紀子大科 恭子緒方 広子嘉村 浩美川崎 範子木下 史織蘇 哲民谷口 公介田山 千春長尾　健長谷川 慶太藤井 達也堀 あすか右田 王介宮本 義孝山村 倫啓 業績 2024 Yamato G, Tsumura Y, Muramatsu H, Shimada A, Imaizumi T, Tsukagoshi H, Kaburagi T, Shiba N, Yamada Y, Deguchi T, Kawai T, Terui K, Ito E, Watanabe K, Hayashi Y. Cytokine profiling in 128 patients with transient abnormal myelopoiesis: a report from the JPLSG TAM-10 trial. Blood Adv. 2024 May 1:bloodadvances.2023011628. doi: 10.1182/bloodadvances.2023011628. Epub ahead of print. Kawai T, Kinoshita S, Takayama Y, Ohnishi E, Kamura H, Kojima K, Kikuchi H, Terao M, Sugawara T, Migita O, Kagami M, Isojima T, Yamaguchi Y, Wakui K, Ohashi H, Shimizu K, Mizuno D, Okamoto N, Fukushima Y, Takada F, Kosaki K, Takada S, Akutsu H, Ura K, Nakabayashi K, Hata K. Loss of function in NSD2 causes DNA methylation signature similar to that in Wolf-Hirschhorn syndrome. Genet Med Open. doi: 10.1016/j.gimo.2024.101838 Muranishi Y, Kobori Y, Katoh-Fukui Y, Tamaoka S, Hattori A, Osaka A, Okada H, Nakabayashi K, Hata K, Kawai T, Ogata-Kawata H, Iwahata T, Saito K, Kon M, Shinohara N, Fukami M : Systematic molecular analyses for 115 karyotypically normal men with isolated non-obstructive azoospermia. Hum Reprod. 2024 Mar 20:deae057. doi: 10.1093/humrep/deae057. Online ahead of print. En A, Takemoto K, Yamakami Y, Nakabayashi K, Fujii M : Upregulated expression of lamin B receptor increases cell proliferation and suppresses genomic instability: implications for cellular immortalization. FEBS J. 2024 Mar 11. doi: 10.1111/febs.17113. Online ahead of print. Kinoshita S, Kojima K, Ohnishi E, Takayama Y, Kikuchi H, Takada S, Nakabayashi K, Kawai T, Hata K : Loss of NSD2 causes dysregulation of synaptic genes and altered H3K36 dimethylation in mice. Front Genet. 2024 Feb 14;15:1308234. doi: 10.3389/fgene.2024.1308234. eCollection 2024. Takahashi F, Baba T, Christianto A, Yanai S, Lee-Okada HC, Ishiwata K, Nakabayashi K, Hata K, Ishii T, Hasegawa T, Yokomizo T, Choi MH, Morohashi KI : Development of sexual dimorphism of skeletal muscles through the adrenal cortex, caused by androgen-induced global gene suppression. Cell Rep. 2024;43:113715. doi: 10.1016/j.celrep.2024.113715. Epub 2024 Feb 1. Rengifo Rojas C, Cercy J, Perillous S, Gonthier-Guéret C, Montibus B, Maupetit-Méhouas S, Espinadel A, Dupré M, Hong CC, Hata K, Nakabayashi K, Plagge A, Bouschet T, Arnaud P, Vaillant I, Court F : Biallelic non-productive enhancer-promoter interactions precede imprinted expression of Kcnk9 during mouse neural commitment. HGG Adv. 2024;5:100271. doi: 10.1016/j.xhgg.2024.100271. Online ahead of print. Takeuchi I, Tanase-Nakao K, Ogawa A, Sugawara T, Migita O, Kashima M, Yamazaki T, Iguchi A, Naiki Y, Uchiyama T, Tamaoki J, Maeda H, Shimizu H, Kawai T, Taniguchi K, Hirata H, Kobayashi M, Matsumoto K, Naruse K, Hata K, Akutsu H, Kato T, Narumi S, Arai K, Ishiguro A : Congenital anaemia associated with loss-of-function variants in DNA polymerase epsilon 1. J Med Genet. 2024;61:239-243. doi: 10.1136/jmg-2023-109444. Takeuchi I, Tanase-Nakao K, Ogawa A, Sugawara T, Migita O, Kashima M, Yamazaki T, Iguchi A, Naiki Y, Uchiyama T, Tamaoki J, Maeda H, Shimizu H, Kawai T, Taniguchi K, Hirata H, Kobayashi M, Matsumoto K, Naruse K, Hata K, Akutsu H, Kato T, Narumi S, Arai K, Ishiguro A : Congenital anaemia associated with loss-of-function variants in DNA polymerase epsilon 1. J Med Genet. 2024;61:239-243. doi: 10.1136/jmg-2023-109444. 2023 Kawai Y, Watanabe Y, Omae Y, Miyahara R, Khor SS, Noiri E, Kitajima K, Shimanuki H, Gatanaga H, Hata K, Hattori K, Iida A, Ishibashi-Ueda H, Kaname T, Kanto T, Matsumura R, Miyo K, Noguchi M, Ozaki K, Sugiyama M, Takahashi A, Tokuda H, Tomita T, Umezawa A, Watanabe H, Yoshida S, Goto YI, Maruoka Y, Matsubara Y, Niida S, Mizokami M, Tokunaga K : Exploring the genetic diversity of the Japanese population: Insights from a large-scale whole genome sequencing analysis. PLoS Genet. 2023;19:e1010625. doi: 10.1371/journal.pgen.1010625. eCollection 2023 Dec. Miyamoto S, Hirakawa T, Noguchi Y, Urushiyama D, Miyata K, Baba T, Yotsumoto F, Yasunaga S, Nakabayashi K, Hata K, Nakagawa W, Otsuka T, Nozawa Y, Furuhata I, Mikasa J : Physical Properties of Ultrafine Bubbles Generated Using a Generator System. In Vivo. 2023 Nov-Dec;37(6):2555-2563. doi: 10.21873/invivo.13363. Yoshida T, Matsubara K, Ogata-Kawata H, Miyado M, Ishiwata K, Nakabayashi K, Hata K, Kageyama I, Tamaoka S, Shimada Y, Fukami M, Sasaki S : Variations in gender identity and sexual orientation of university students. Sex Med. 2023;11:qfad057. doi: 10.1093/sexmed/qfad057. eCollection 2023 Oct. Miyamoto S, Hirakawa T, Noguchi Y, Urushiyama D, Miyata K, Baba T, Yotsumoto F, Yasunaga S, Nakabayashi K, Hata K, Nakagawa W, Otsuka T, Nozawa Y, Furuhata I, Mikasa J : Physical Properties of Ultrafine Bubbles Generated Using a Generator System. In Vivo. 2023;37:2555-2563. doi: 10.21873/invivo.13363. Uchiyama T, Kawai T, Nakabayashi K, Nakazawa Y, Goto F, Okamura K, Nishimura T, Kato K, Watanabe N, Miura A, Yasuda T, Ando Y, Minegishi T, Edasawa K, Shimura M, Akiba Y, Sato-Otsubo A, Mizukami T, Kato M, Akashi K, Nunoi H, Onodera M : Myelodysplasia after clonal hematopoiesis with APOBEC3-mediated CYBB inactivation in retroviral gene therapy for X-CGD. Mol Ther. Mol Ther. 2023;31:3424-3440. doi: 10.1016/j.ymthe.2023.09.004. Epub 2023 Sep 13. Oshina K, Kuroda K, Nakabayashi K, Tomikawa J, Kitade M, Sugiyama R, Hata K, Itakura A.: Gene expression signatures associated with chronic endometritis revealed by RNA sequencing. Front Med (Lausanne). 2023;10:1185284. doi: 10.3389/fmed.2023.1185284. eCollection 2023. Yoshida K, Nishi K, Ishikura S, Matsumoto T, Nakabayashi K, Yazaki R, Ohshima T, Suenaga M, Shirasawa S, Tsunoda T.: Inhibitory Effect of Pyra-Metho-Carnil on Cancer Spheroid Growth Through Decrease in Glycolysis-associated Molecules. Anticancer Res. 2023;43:3717-3726. doi: 10.21873/anticanres.16556. Tamaoka S, Fukuda A, Nakabayashi K, Matsubara K, Ogata-Kawata H, Muranishi Y, Hata K, Kato-Fukui Y, Sakamoto S, Kasahara M, Fukami M.: Rare sequence variants associated with the risk of non-syndromic biliary atresia. Hepatol Res. 2023;53:1134-1141. doi: 10.1111/hepr.13946. Epub 2023 Aug 2. Kamihara Y, Ozawa K, Muromoto J, Sugibayashi R, Wada S, Shibata Y, Hori A, Hasegawa F, Hata K, Sago H.: Clinical features of fetal hydrothorax associated with mucopolysaccharidosis-VII. J Obstet Gynaecol Res. 2023;49:2538-2543. doi: 10.1111/jog.15744. Epub 2023 Jul 19. Hasegawa K, Nakabayashi K, Ishiwata K, Kasuga Y, Hata K, Tanaka M.: A capture methyl-seq protocol with improved efficiency and cost-effectiveness using pre-pooling and enzymatic conversion. BMC Res Notes. 2023;16:141. doi: 10.1186/s13104-023-06401-3. Kawai T, Iwasaki Y, Ogata-Kawata H, Kamura H, Nakamura K, Hata K, Takano T, Nakabayashi K. : Identification of a KDM6A somatic mutation responsible for Kabuki syndrome by excluding a conflicting KMT2D germline variant through episignature analysis. Eur J Med Genet. 2023;66:104806. doi: 10.1016/j.ejmg.2023.104806. Epub 2023 Jun 27. Yasuda T, Uchiyama T, Watanabe N, Ito N, Nakabayashi K, Mochizuki H, Onodera M : Peripheral immune system modulates Purkinje cell degeneration in Niemann-Pick disease type C1. Life Sci Alliance. 2023;6:e202201881. doi: 10.26508/lsa.202201881. Print 2023 Sep. Hasegawa K, Kumasaka N, Nakabayashi K, Kamura H, Maehara K, Kasuga Y, Hata K, Tanaka M : Genome-wide association study of preterm birth and gestational age in a Japanese population. Hum Genome Var. 2023;10:19. doi: 10.1038/s41439-023-00246-9. Katoh-Fukui Y, Hattori A, Zhang R, Terao M, Takada S, Nakabayashi K, Hata K, Yamada Y, Matsuura N, Fukami M : Chromosomal microdeletion leading to pituitary gigantism through hormone-gene overexpression. Hum Mol Genet. 2023 Jul 4;32(14):2318-2325. doi: 10.1093/hmg/ddad053. Yoshida M, Nakabayashi K, Yang W, Sato-Otsubo A, Tsujimoto SI, Ogata-Kawata H, Kawai T, Ishiwata K, Sakamoto M, Okamura K, Yoshida K, Shirai R, Osumi T, Kiyotani C, Shioda Y, Terashima K, Ishimaru S, Yuza Y, Takagi M, Arakawa Y, Imamura T, Hasegawa D, Inoue A, Yoshioka T, Ito S, Tomizawa D, Koh K, Matsumoto K, Kiyokawa N, Ogawa S, Manabe A, Niwa A, Hata K, Yang JJ, Kato M : Prevalence of pathogenic variants in cancer-predisposing genes in second cancer after childhood solid cancers. Cancer Med. 2023 May;12(10):11264-11273. doi: 10.1002/cam4.5835. Epub 2023 Apr 6. Fukui K, Amari S, Yotani N, Kosaki R, Hata K, Kosuga M, Sago H, Isayama T, Ito Y : A Neonate with Mucopolysaccharidosis Type VII with Intractable Ascites. AJP Rep. 2023;13:e25-e28. doi: 10.1055/a-2028-7784. eCollection 2023 Jan. Asahina Y, Tahara U, Aoki S, Nakabayashi K, Tateishi C, Hayashi D, Amagai M, Tsuruta D, Kubo A : Two sporadic cases of childhood-onset Hailey-Hailey disease with superimposed mosaicism. Eur J Hum Genet. 2023 Jun;31(6):716-720. doi: 10.1038/s41431-023-01316-w. Epub 2023 Mar 15. Shirai R, Osumi T, Keino D, Nakabayashi K, Uchiyama T, Sekiguchi M, Hiwatari M, Yoshida M, Yoshida K, Yamada Y, Tomizawa D, Takae S, Kiyokawa N, Matsumoto K, Yoshioka T, Hata K, Hori T, Suzuki N, Kato M : Minimal residual disease detection by mutation-specific droplet digital PCR for leukemia/lymphoma. Int J Hematol. 2023 Jun;117(6):910-918. doi: 10.1007/s12185-023-03566-2. Epub 2023 Mar 3. Tamaoka S, Saito K, Yoshida T, Nakabayashi K, Tatsumi K, Kawamura T, Matsuzaki T, Matsubara K, Ogata-Kawata H, Hata K, Kato-Fukui Y, Fukami M : Exome-based genome-wide screening of rare variants associated with the risk of polycystic ovary syndrome. Reprod Med Biol. 2023 Feb 23;22(1):e12504. doi: 10.1002/rmb2.12504. eCollection 2023 Jan-Dec. Onizuka M, Imanishi T, Harada K, Aoyama Y, Amaki J, Toyosaki M, Machida S, Kikkawa E, Yamada S, Nakabayashi K, Hata K, Higashimoto K, Soejima H, Ando K : Donor cord blood aging accelerates in recipients after transplantation. Sci Rep. 2023 Feb 14;13(1):2603. doi: 10.1038/s41598-023-29912-2. Nakabayashi K, Yamamura M, Haseagawa K, Hata K. Reduced Representation Bisulfite Sequencing (RRBS). Methods Mol Biol. 2023;2577:39-51. doi: 10.1007/978-1-0716-2724-2_3. PMID: 36173564 2022 Okazaki Y, Taniguchi K, Miyamoto Y, Kinoshita S, Nakabayashi　K, Kaneko K, Hamada H, Satoh T, Murashima A, Hata　K : Glucocorticoids increase the risk of preterm premature rupture of membranes possibly by inducing ITGA8 gene expression in the amnion. Placenta. 2022 Aug 18;128:73-82. doi: 10.1016/j.placenta.2022.07.012. Online ahead of print. Saito S, Ono N, Sasaki T, Aoki S, Kosaki K, Kuze B, Nakabayashi　K, Amagai M, Kubo A : Neurofibromatosis type 2 with mild Pierre-Robin sequence showing a heterozygous chromosome 22q12 microdeletion encompassing NF2 and MN1. J Hum Genet. 2022 Aug 15. doi: 10.1038/s10038-022-01068-3. Online ahead of print. Ito Y, Kamide T, Taniguchi K, Sato T, Yamamura M, Konishi A, Takahashi K, Kishi H, Hata　K, Samura O, Okamoto A : Pregnancy Outcome and Postnatal Chromosome Analysis of the Cord Blood and Chorionic Villi in Two Cases after Intrauterine Transfer of Mosaic Aneuploid Blastocysts. Case Rep Obstet Gynecol. 2022 Jul 19;2022:1763948. doi: 10.1155/2022/1763948. eCollection 2022. Yoshida K, Nishi K, Ishikura S, Nakabayashi　K, Yazaki R, Ohshima T, Suenaga M, Shirasawa S, Tsunoda T : Cancer Spheroid Proliferation Is Suppressed by a Novel Low-toxicity Compound, Pyra-Metho-Carnil, in a Context-independent Manner. Anticancer Res. 2022;42:3993-4001. doi: 10.21873/anticanres.15895. Kawashima S, Yuno A, Sano S, Nakamura A, Ishiwata K, Kawasaki T, Hosomichi K, Nakabayashi　K, Akustu H, Saitsu H, Fukami M, Usui T, Ogata T, Kagami M : Familial pseudohypoparathyroidism type 1B caused by an SVA retrotransposon insertion on the GNAS locus. J Bone Miner Res. 2022 Jul 20. doi: 10.1002/jbmr.4652. Online ahead of print. Tsuruta S, Kawasaki T, Machida M, Iwatsuki K, Inaba A, Shibata S, Shindo T, Nakabayashi　K, Hakamada K, Umezawa A, Akutsu H : Development of Human Gut Organoids With Resident Tissue Macrophages as a Model of Intestinal Immune Responses. Cell Mol Gastroenterol Hepatol. 2022;14(3):726-729.e5. doi: 10.1016/j.jcmgh.2022.06.006. Epub 2022 Jun Shirai R, Osumi T, Sato-Otsubo A, Nakabayashi　K, Ishiwata K, Yamada Y, Yoshida M, Yoshida K, Shioda Y, Kiyotani C, Terashima K, Tomizawa D, Takasugi N, Takita J, Miyazaki O, Kiyokawa N, Yoneda A, Kanamori Y, Hishiki T, Matsumoto K, Hata　K, Yoshioka T, Kato M : Quantitative assessment of copy number alterations by liquid biopsy for neuroblastoma. Genes Chromosomes Cancer, 2022;61:662-669. doi: 10.1002/gcc.23073. Hori A, Migita O, Isogawa N, Takada F, Hata　K : A novel TP63 variant in a patient with ankyloblepharon-ectodermal defect-cleft lip/palate syndrome and Rapp-Hodgkin syndrome-like ectodermal dysplasia. Hum Genome Var. 2022;9:17. doi: 10.1038/s41439-022-00186-w. Aoki S, Higashimoto K, Hidaka H, Ohtsuka Y, Aoki S, Mishima H, Yoshiura KI, Nakabayashi　K, Hata　K, Yatsuki H, Hara S, Ohba T, Katabuchi H, Soejima H : Aberrant hypomethylation at imprinted differentially methylated regions is involved in biparental placental mesenchymal dysplasia. Clin Epigenetics, 2022;14:64. doi: 10.1186/s13148-022-01280-0. Kyodo R, Takeuchi I, Narumi S, Shimizu H, Hata　K, Yoshioka T, Tanase-Nakao K, Shimizu T, Arai K : Novel biallelic mutations in the DUOX2 gene underlying very early-onset inflammatory bowel disease: A case report. Clin Immunol. 2022;238:109015. doi: 10.1016/j.clim.2022.109015. Epub 2022 Apr 14. Nakajima K, Suzuki H, Yamamoto M, Yamamoto T, Kawai T, Nakabayashi　K, Hata　K, Kosaki K, Nakajima H, Sano S, Kubo A : A familial case of periodontal Ehlers-Danlos syndrome lacking skin extensibility and joint hypermobility with a missense mutation in C1R. J Dermatol. 2022;49:714-718. doi:10.1111/1346-8138.16372. 2021 Kasuga Y, Kawai T, Miyakoshi K, Hori A, Tamagawa M, Hasegawa K, Ikenoue S, Ochiai D, Saisho Y, Hida M, Tanaka M, Hata K : DNA methylation analysis of cord blood samples in neonates born to gestational diabetes mothers diagnosed before 24 gestational weeks. BMJ Open Diabetes Res Care. 2022;10:e002539. doi: 10.1136/bmjdrc-2021-002539. Yamato G, Kawai T, Shiba N, Ikeda J, Hara Y, Ohki K, Tsujimoto SI, Kaburagi T, Yoshida K, Shiraishi Y, Miyano S, Kiyokawa N, Tomizawa D, Shimada A, Sotomatsu M, Arakawa H, Adachi S, Taga T, Horibe K, Ogawa S, Hata K, Hayashi Y : Genome-wide DNA Methylation Analysis in Pediatric Acute Myeloid Leukemia. Blood Adv.2022;6:3207-3219. doi: 10.1182/bloodadvances.2021005381. Sato-Otsubo A, Osumi T, Yoshida M, Iguchi A, Fukushima T, Nakabayashi K, Ogawa S, Hata K, Kato M : Genomic analysis of two rare cases of pediatric Ph-positive T-ALL. Pediatr Blood Cancer. 2022;69:e29427. doi: 10.1002/pbc.29427. Epub 2021 Oct 31. Akahane K, Kimura S, Miyake K, Watanabe A, Kagami K, Yoshimura K, Shinohara T, Harama D, Kasai S, Goi K, Kawai T, Hata K, Kiyokawa N, Koh K, Imamura T, Horibe K, Look AT, Minegishi M, Sugita K, Takita J, Inukai T : Association of allele-specific methylation of the ASNS gene with asparaginase sensitivity and prognosis in T-ALL. Blood Adv. 2022;6:212-224. doi: 10.1182/bloodadvances.2021004271. Orimo K, Tamari M, Takeda T, Kubo T, Rückert B, Motomura K, Sugiyama H, Yamada A, Saito K, Arae K, Kuriyama M, Hara M, Soyka MB, Ikutani M, Yamaguchi S, Morimoto N, Nakabayashi K, Hata K, Matsuda A, Akdis CA, Sudo K, Saito H, Nakae S, Tamaoki J, Tagaya E, Matsumoto K, Morita H : Direct platelet adhesion potentiates group 2 innate lymphoid cell functions. Allergy. 2022;77:843-855. doi: 10.1111/all.15057. Epub 2021 Aug 24. Morita M, Takeuchi I, Kato M, Migita O, Jimbo K, Shimizu H, Yoshimura S, Tomizawa D, Shimizu T, Hata K, Ishiguro A, Arai K : Intestinal outcome of bone marrow transplantation for monogenic inflammatory bowel disease. Pediatr Int. 2022;64:e14750. doi: 10.1111/ped.14750. Epub 2021 Jun 25. Nishiyama M, Wada S, Hasegawa F, Uehara Y, Ozaki M, Hata K, Ito Y, Sago H : Confined placental mosaicism of trisomy 6 detected through genome-wide NIPT was associated with placental abruption. Clin Case Rep. 2021 Dec 5;9:e05155. doi: 10.1002/ccr3.5155. eCollection 2021 Dec. Uchiyama T, Takahashi S, Nakabayashi K, Okamura K, Edasawa K, Yamada M, Watanabe N, Mochizuki E, Yasuda T, Miura A, Kato M, Tomizawa D, Otsu M, Ariga T, Onodera M : Nonconditioned ADA-SCID gene therapy reveals ADA requirement in the hematopoietic system and clonal dominance of vector-marked clones. Mol Ther Methods Clin Dev. 2021 Oct 16;23:424-433. doi: 10.1016/j.omtm.2021.10.003. eCollection 2021 Dec 10. 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Yoshida M, Nakabayashi K, Yang W, Sato-Otsubo A, Tsujimoto SI, Ogata-Kawata H, Kawai T, Ishiwata K, Sakamoto M, Okamura K, Yoshida K, Shirai R, Osumi T, Moriyama T, Nishii R, Takahashi H, Kiyotani C, Shioda Y, Terashima K, Ishimaru S, Yuza Y, Takagi M, Arakawa Y, Kinoshita A, Hino M, Imamura T, Hasegawa D, Nakazawa Y, Okuya M, Kakuda H, Takasugi N, Inoue A, Ohki K, Yoshioka T, Ito S, Tomizawa D, Koh K, Matsumoto K, Sanada M, Kiyokawa N, Ohara A, Ogawa S, Manabe A, Niwa A, >Hata K, Yang JJ, Kato M : NUDT15 variants confer high incidence of second malignancies in children with acute lymphoblastic leukemia. Blood Adv. 2021;5:5420-5428. doi: 10.1182/bloodadvances.2021005507. Hori A, Ogata-Kawata H, Sasaki A, Takahashi K, Taniguchi K, Migita O, Kawashima A, Okamoto A, Sekizawa A, Sago H, Takada F, Nakabayashi K, Hata K : Improved library preparation protocols for amplicon sequencing-based noninvasive fetal genotyping for RHD-positive D antigen-negative alleles. BMC Res Notes. 2021;14:380. doi: 10.1186/s13104-021-05793-4. Urushiyama D, Ohnishi E, Suda W, Kurakazu M, Kiyoshima C, Hirakawa T, Miyata K, Yotsumoto F, Nabeshima K, Setoue T, Nagamitsu S, Hattori M, Hata K, Miyamoto S : Vaginal microbiome as a tool for prediction of chorioamnionitis in preterm labor: a pilot study. Sci Rep. 2021;11:18971. doi: 10.1038/s41598-021-98587-4. Shirai R, Osumi T, Sato-Otsubo A, Nakabayashi K, Mori T, Yoshida M, Yoshida K, Kohri M, Ishihara T, Yasue S, Imamura T, Endo M, Miyamoto S, Ohki K, Sanada M, Kiyokawa N, Ogawa S, Yoshioka T, Hata K, Takagi M, Kato M : Genetic features of B-cell lymphoblastic lymphoma with TCF3-PBX1. Cancer Rep (Hoboken).2022;5:e1559. doi: 10.1002/cnr2.1559. Takano T, Ota H, Ohishi H, Hata K, Furukawa R, Nakabayashi K : Clinical Reports Adult acampomelic campomelic dysplasia and disorders of sex development due to a reciprocal translocation involving chromosome 17q24.3 upstream of the SOX9 gene. Eur J Med Genet . 2021;64:104332. doi: 10.1016/j.ejmg.2021.104332. Yoshikawa K, Kiyoshima C, Hirakawa T, Urushiyama D, Fukagawa S, Izuchi D, Sanui A, Kurakazu M, Miyata K, Nomiyama M, Setoue T, Nagamitsu S, Nabeshima K, Hata K, Yasunaga S, Miyamoto S : Diagnostic predictability of miR-4535 and miR-1915-5p expression in amniotic fluid for foetal morbidity of infection. Placenta. 2021;114:68-75. doi: 10.1016/j.placenta.2021.08.059. Yoshida M, Tomizawa D, Yoshimura S, Osumi T, Nakabayashi K, Ogata-Kawata H, Ishiwata K, Sato-Otsubo A, Kimura Y, Ito S, Matsumoto K, Deguchi T, Kiyokawa N, Yoshioka T, Hata K, Kato M : Genetic features of precursor B-cell phenotype Burkitt leukemia with IGH-MYC rearrangement. Cancer Rep (Hoboken).2022;5:e1545. doi: 10.1002/cnr2.1545. Hashimoto S, Nagai M, Nishi K, Ishikura S, Nakabayashi K, Yazaki R, Ohshima T, Suenaga M, Shirasawa S, Tsunoda T : Growth Suppression of Cancer Spheroids With Mutated KRAS by Low-toxicity Compounds from Natural Products. Anticancer Res. 2021;41:4061-4070. doi: 10.21873/anticanres.15207. Kasuga Y, Kawai T, Miyakoshi K, Saisho Y, Tamagawa M, Hasegawa K, Ikenoue S, Ochiai D, Hida M, Tanaka M, Hata K : Epigenetic Changes in Neonates Born to Mothers With Gestational Diabetes Mellitus May Be Associated With Neonatal Hypoglycaemia. Front Endocrinol (Lausanne). 2021;12:690648. doi: 10.3389/fendo.2021.690648. Ito N, Tsukamoto K, Taniguchi K, Takahashi K, Okamoto A, Aoki H, Otera-Takahashi Y, Kitagawa M, Ogata-Kawata H, Morita H, Hata K,Nakabayashi K : Isolation and characterization of fetal nucleated red blood cells from maternal blood as a target for single cell sequencing-based non-invasive genetic testing. Reprod Med Biol. 2021 Jun 14;20(3):352-360. doi: 10.1002/rmb2.12392. Ichiyama T, Kuroda K, Nagai Y, Urushiyama D, Ohno M, Yamaguchi T, Nagayoshi M, Sakuraba Y, Yamasaki F, Hata K, Miyamoto S, Itakura A, Takeda S, Tanaka A : Analysis of vaginal and endometrial microbiota communities in infertile women with a history of repeated implantation failure. Reprod Med Biol. 2021;20:334-344. doi: 10.1002/rmb2.12389. Ohki K, Kiyokawa N, Watanabe S, Iwafuchi H, Nakazawa A, Ishiwata K, Ogata-Kawata H, >Nakabayashi K, Okamura K, Tanaka F, Fukano R, Hata K, Mori T, Moriya Saito A, Hayashi Y, Taga T, Sekimizu M, Kobayashi R; Japan Children's Cancer Study Group (JCCG) : Characteristics of genetic alterations of peripheral T-cell lymphoma in childhood including identification of novel fusion genes: the Japan Children's Cancer Group (JCCG). Br J Haematol. 2021;194:718-729. doi: 10.1111/bjh.17639. Kawashima S, Hattori A, Suzuki E, Matsubara K, Toki M, Kosaki R, Hasegawa Y, Nakabayashi K, Fukami M, Kagami M : Methylation status of genes escaping from X-chromosome inactivation in patients with X-chromosome rearrangements. Clin Epigenetics. 2021;13:134. doi: 10.1186/s13148-021-01121-6. Kagami M, Hara-Isono K, Matsubara K, Nakabayashi K, Narumi S, Fukami M, Ohkubo Y, Saitsu H, Takada S, Ogata T : ZNF445: a homozygous truncating variant in a patient with Temple syndrome and multilocus imprinting disturbance. Clin Epigenetics. 2021;13:119. Kiyoshima C, Shirasu N, Urushiyama D, Fukagawa S, Hirakawa T, Yoshikawa K, Izuchi D, Miyata K, Kurakazu M, Yotsumoto F, Hiromatsu K, Nomiyama M, Eiji O, Hirose S, Ogura Y, Hayashi T, Hata K, Nabeshima K, Yasunaga S, Miyamoto S : MicroRNAs miR-4535 and miR-1915-5p in amniotic fluid as predictive biomarkers for chorioamnionitis. Future Sci OA. 2021;7:FSO686. doi: 10.2144/fsoa-2021-0006. Aoki S, Hirata Y, Kawai T, Nakabayashi K, Hata K, Suzuki H, Kosaki K, Amagai M, Kubo A : Frequent FGFR3 and Ras Gene Mutations in Skin Tags or Acrochordons. J Invest Dermatol. 2021;141:2756-2760.e8. doi: 10.1016/j.jid.2021.03.028. Epub 2021 Apr 30. Sun S, Yano S, Nakanishi MO, Hirose M, Nakabayashi K,Hata K, Ogura A, Tanaka S : Maintenance of mouse trophoblast stem cells in KSR-based medium allows conventional 3D culture. J Reprod Dev. 2021;67:197-205. doi: 10.1262/jrd.2020-119. Kashima K, Kawai T, Nishimura R, Shiwa Y, Urayama KY, Kamura H, Takeda K, Aoto S, Ito A, Matsubara K, Nagamatsu T, Fujii T, Omori I, Shimizu M, Hyodo H, Kugu K, Matsumoto K, Shimizu A, Oka A, Mizuguchi M, Nakabayashi K, Hata K, Takahashi N : Identification of epigenetic memory candidates associated with gestational age at birth through analysis of methylome and transcriptional data. Sci Rep. 2021;11:3381. doi: 10.1038/s41598-021-83016-3. Hana T, Ogiwara H, Migita O, Nakabayashi K, Hata K, Morota N : Deleterious fibronectin type III-related gene variants may induce a spinal extradural arachnoid cyst: an exome sequencing study of identical twin cases. Childs Nerv Syst. 2021;37:2329-2334. doi: 10.1007/s00381-021-05137-4. Taniguchi K, Inoue M, Arai K, Uchida K, Migita O, Akemoto Y, Hirayama J, Takeuchi I, Shimizu H, Hata K : Novel TNFAIP3 microdeletion in a girl with infantile-onset inflammatory bowel disease complicated by a severe perianal lesion. Hum Genome Var. 2021;8:1. doi: 10.1038/s41439-020-00128-4. Shiiya C, Aoki S, Nakabayashi K, Hata K, Amagai M, Kubo A. Linear and disseminated porokeratosis in one family showing identical and independent second hits in MVD among skin lesions, respectively: A proof of concept study. Br J Dermatol. 2021;184:1209-1212. Yamazawa K, Inoue T, Sakemi Y, Nakashima T, Yamashita H, Khono K, Fujita H, Enomoto K, Nakabayashi K, Hata K, Nakashima M, Matsunaga T, Nakamura A, Matsubara K, Ogata T, Kagami M : Loss of imprinting of the human-specific imprinted gene ZNF597 causes prenatal growth retardation and dysmorphic features: implications for phenotypic overlap with Silver-Russell syndrome. J Med Genet. 2021;58:427-432. Ishizuka T, Fujioka K, Mori I, Takeda T, Fuwa M, Ikeda T, Taguchi K, Morita H, Nakabayashi K, Niizeki H : Primary hypertrophic osteoarthropathy with severe arthralgia identified by gene mutation of SLCO2A1. Mod Rheumatol Case Rep. 2021 Jul;5(2):404-408. doi: 10.1080/24725625.2020.1861744. 2020 Nohara K, Nakabayashi K, Okamura K, Suzuki T, Suzuki S, Hata K : Gestational arsenic exposure induces site-specific DNA hypomethylation in active retrotransposon subfamilies in offspring sperm in mice. Epigenetics Chromatin. 2020;13:53. Ishizuka T, Fujioka K, Mori I, Takeda T, Fuwa M, Ikeda T, Taguchi K, Morita H,Nakabayashi K, Niizeki H : Primary hypertrophic osteoarthropathy with severe arthralgia identified by gene mutation of SLCO2A1. Mod Rheumatol Case Rep. 2021 Jul;5(2):404-408. doi: 10.1080/24725625.2020.1861744. Nohara K, Nakabayashi K, Okamura K, Suzuki T, Suzuki S, Hata K : Gestational arsenic exposure induces site-specific DNA hypomethylation in active retrotransposon subfamilies in offspring sperm in mice. Epigenetics Chromatin. 2020;13:53. Yoshida MA, Imoto J, Kawai Y, Funahashi S, Minei R, Akizuki Y, Ogura A, Nakabayashi K, Yura K, Ikeo K : Genomic and Transcriptomic Analyses of Bioluminescence Genes in the Enope Squid Watasenia scintillans. Mar Biotechnol (NY). 2020;22:760-771. Ishikura S, Nakabayashi K, Nagai M, Tsunoda T, Shirasawa S : ZFAT binds to centromeres to control noncoding RNA transcription through the KAT2B-H4K8ac-BRD4 axis. Nucleic Acids Res. 2020;48:10848-10866. Fujita H, Sasaki T, Miyamoto T, Akutsu SN, Sato S, Mori T, Nakabayashi K, Hata K, Suzuki H, Kosaki K, Matsuura S, Matsubara Y, Amagai M, Kubo A : Premature aging syndrome showing random chromosome number instabilities with CDC20 mutation. Aging Cell. 2020;19:e13251. Hara-Isono K, Matsubara K, Fuke T, Yamazawa K, Satou K, Murakami N, Saitoh S,Nakabayashi K, Hata K, Ogata T, Fukami M, Kagami M : Genome-wide methylation analysis in Silver-Russell syndrome, Temple syndrome, and Prader-Willi syndrome. Clin Epigenetics. 2020;12:159. Kubota Y, Seki M, Kawai T, Isobe T, Yoshida M, Sekiguchi M, Kimura S, Watanabe K, Sato-Otsubo A, Yoshida K, Suzuki H, Kataoka K, Fujii Y, Shiraishi Y, Chiba K, Tanaka H, Hiwatari M, Oka A, Hayashi Y, Miyano S, Ogawa S, Hata K, Tanaka Y, Takita J : Comprehensive genetic analysis of pediatric germ cell tumors identifies potential drug targets. Commun Biol. 2020;3:544 Hayakawa M, Tahara U, Ono N, Aoki S, Kawai T, Nakabayashi K, Hata K, Amagai M, Kubo A : Nagashima-type palmoplantar keratosis caused by biallelic maternal mutation of SERPINB7 with segmental uniparental disomy of chromosome 18q. J Dermatol. 2020;47:e453-e454. Tahara U, Ono N, Aoki S, Kawai T, Nakabayashi K, Hata K, Amagai M, Kubo A : Case of autosomal recessive woolly hair/hypotrichosis with a homozygous c.736T>A mutation of LIPH caused by maternal uniparental disomy of chromosome 3. J Dermatol. 2020;47:e393-e394. Takahashi K, Sato T, Nishiyama M, Sasaki A, Taniguchi K, Migita O, Wada S, Hata K, Sago H : Monochorionic Diamniotic Twins of Discordant External Genitalia With 45,X/46,XY Mosaicism. Mol Genet Genomic Med. 2020;e1382. Oiso N, Kubo A, Shimizu A, Suzuki H, Kosaki K, Chikugo T, Nakabayashi K, Hata K, Yanagihara S, Ishikawa O, Matsubara Y, Amagai M, Kawada A : Epidermodysplasia verruciformis without progression to squamous cell carcinomas in an elderly man: α-human papillomavirus infection in the evolving verruca. Int J Dermatol. 2020;59:e334-e336. Sekiguchi M, Seki M, Kawai T, Yoshida K, Yoshida M, Isobe T, Hoshino N, Shirai R, Tanaka M, Souzaki R, Watanabe K, Arakawa Y, Nannya Y, Suzuki H, Fujii Y, Kataoka K, Shiraishi Y, Chiba K, Tanaka H, Shimamura T, Sato Y, Sato-Otsubo A, Kimura S, Kubota Y, Hiwatari M, Koh K, Hayashi Y, Kanamori Y, Kasahara M, Kohashi K, Kato M, Yoshioka T, Matsumoto K, Oka A, Taguchi T, Sanada M, Tanaka Y, Miyano S, Hata K, Ogawa S, Takita J : Integrated multiomics analysis of hepatoblastoma unravels its heterogeneity and provides novel druggable targets. NPJ Precis Oncol. 2020;4:20. Yagi M, Kabata M, Tanaka A, Ukai T, Ohta S, Nakabayashi K, Shimizu M, Hata K, Meissner A, Yamamoto T, Yamada Y : Identification of distinct loci for de novo DNA methylation by DNMT3A and DNMT3B during mammalian development. Nat Commun. 2020;11:3199. Kinjo K, Nagasaki K, Muroya K, Suzuki E, Ishiwata K, Nakabayashi K, Hattori A, Nagao K, Nozawa RS, Obuse C, Miyado K, Ogata T, Fukami M, Miyado M : Rare variant of the epigenetic regulator SMCHD1 in a patient with pituitary hormone deficiency. Sci Rep. 2020;10:10985. Sato T, Ito Y, Samura O, Aoki H, Uchiyama T, Okamoto A, Hata K : Direct Assessment of Single-Cell DNA Using Crudely Purified Live Cells: A Proof of Concept for Noninvasive Prenatal Definitive Diagnosis. J Mol Diagn. 2020;22:132-140 Taniguchi K, Kawai T, Kitawaki J, Tomikawa J, Nakabayashi K, Okamura K, Sago H, Hata K : Epitranscriptomic profiling in human placenta: N6-methyladenosine modification at the 5'-untranslated region is related to fetal growth and preeclampsia. FASEB J. 2020;34:494-512 Sato T, Kojima T, Samura O, Kawaguchi S, Nakamura A, Nakajima M, Tanuma-Takahashi A, Nakabayashi K, Hata K, Ikegawa S, Nishimura G, Okamoto A, Yamada T : Two unrelated pedigrees with achondrogenesis type 1b carrying a Japan-specific pathogenic variant in SLC26A2. Am J Med Genet A. 2020;182:735-739 Takano T, Nakabayashi K, Ota H, Arai Y, Kamura H, Hata K : Tetrasomy 21 pter→q21.3 due to an extra +dic(21;21)mat in a severely psychomotor-retarded female patient without Down syndrome phenotype. Eur J Med Genet. 2020;63:103824 Tomikawa J, Takada S, Okamura K, Terao M, Ogata-Kawata H, Akutsu H, Tanaka S, Hata K, Nakabayashi K : Exploring trophoblast-specific Tead4 enhancers through chromatin conformation capture assays followed by functional screening. Nucleic Acids Res. 2020;48:278-289 Kimura S, Seki M, Kawai T, Goto H, Yoshida K, Isobe T, Sekiguchi M, Watanabe K, Kubota Y, Nannya Y, Ueno H, Shiozawa Y, Suzuki H, Shiraishi Y, Ohki K, Kato M, Koh K, Kobayashi R, Deguchi T, Hashii Y, Imamura T, Sato A, Kiyokawa N, Manabe A, Sanada M, Mansour MR, Ohara A, Horibe K, Kobayashi M, Oka A, Hayashi Y, Miyano S, >Hata K, Ogawa S, Takita J : DNA methylation-based classification reveals difference between pediatric T-cell acute lymphoblastic leukemia and normal thymocytes. Leukemia. 2020;34:1163-1168 Inoue T, Nakamura A, Iwahashi-Odano M, Tanase-Nakao K, Matsubara K, Nishioka J, Maruo Y, Hasegawa Y, Suzumura H, Sato S, Kobayashi Y, Murakami N, Nakabayashi K, Yamazawa K, Fuke T, Narumi S, Oka A, Ogata T, Fukami M, Kagami M : Contribution of Gene Mutations to Silver-Russell Syndrome Phenotype: Multigene Sequencing Analysis in 92 Etiology-Unknown Patients. Clin Epigenetics. 2020;12:86. Tanaka K, Nakabayashi K, Kawai T, Tanigaki S, Matsumoto K, Hata K, Kobayashi Y : Gene expression and DNA methylation changes in BeWo cells dependent on tumor necrosis factor-α and insulin-like growth factor-I. Hum Cell. 2020;33:37-46. (Correction to: Gene expression and DNA methylation changes in BeWo cells dependent on tumor necrosis factor-α and insulin-like growth factor-I. Hum Cell. 2020;33:294) Takeuchi I, Kawai T, Nambu M, Migita O, Yoshimura S, Nishimura K, Yoshioka T, Ogura M, Kyodo R, Shimizu H, Ito S, Kato M, Onodera M, Hata K, Matsubara Y, Arai K : X-linked Inhibitor of Apoptosis Protein Deficiency Complicated With Crohn's Disease-Like Enterocolitis and Takayasu Arteritis: A Case Report. Clin Immunol. 2020;217:108495. Fukuda T, Hiraide T, Yamoto K, Nakashima M, Kawai T, Yanagi K, Ogata T, Saitsu H : Exome reports A de novo GNB2 variant associated with global developmental delay, intellectual disability, and dysmorphic features. Eur J Med Genet. 2020;63:103804 Narumi-Kishimoto Y, Ozawa H, Yanagi K, Kawai T, Okamura K, Hata K, Kaname T, Matsubara Y : A Novel EFTUD2 Mutation Identified an Adult Male With Mandibulofacial Dysostosis Guion-Almeida Type. Clin Dysmorphol. 2020;29:186-188. 研究所について 研究所の概要 所長挨拶 副所長挨拶 概要 各研究部門の紹介 研究業績(年報) 臨床研究センターについて 臨床研究センターの概要 各部門の紹介 治験について 事業・実績 研究者・企業の方へ 研究所について 臨床研究センターについて ダイバーシティ・男女共同参画推進 治験について 臨床研究の計画・実施のご相談 製剤開発室 ページトップへ戻る サイトマップソーシャルメディア個人情報保護方針著作権とリンク特定商取引法に基づく表示 〒157-8535 東京都世田谷区大蔵2-10-1　電話：03-3416-0181　FAX：03-3416-2222 © National Center for Child Health and Development All rights reserved.