Rchr
J-GLOBAL ID:202001012067178810   Update date: Jan. 31, 2024

Nomaru Hiroko

ノウマル ヒロコ | Nomaru Hiroko
Research theme for competitive and other funds  (3):
  • 2021 - 2024 Downstream genes of signaling pathways implicated in human cardiovascular diseases: in vivo significance and regulatory mechanisms
  • 2019 - 2022 胸部大血管および心室筋形成における細胞分化の分子機構
  • 2010 - 2012 fosB遺伝子産物による脳ゲノムの機能制御機構の解明
Papers (12):
  • Masashi Ugawa, Yoko Kawamura, Keisuke Toda, Kazuki Teranishi, Hikari Morita, Hiroaki Adachi, Ryo Tamoto, Hiroko Nomaru, Keiji Nakagawa, Keiki Sugimoto, et al. In silico-labeled ghost cytometry. eLife. 2021. 10
  • Hiroko Nomaru, Yang Liu, Christopher De Bono, Dario Righelli, Andrea Cirino, Wei Wang, Hansoo Song, Silvia E Racedo, Anelisa G Dantas, Lu Zhang, et al. Single cell multi-omic analysis identifies a Tbx1-dependent multilineage primed population in murine cardiopharyngeal mesoderm. Nature communications. 2021. 12. 1. 6645-6645
  • S Boku, T Izumi, S Abe, T Takahashi, A Nishi, H Nomaru, Y Naka, G Kang, M Nagashima, A Hishimoto, et al. Copy number elevation of 22q11.2 genes arrests the developmental maturation of working memory capacity and adult hippocampal neurogenesis. Molecular psychiatry. 2018. 23. 4. 985-992
  • Tingwei Guo, Alexander Diacou, Hiroko Nomaru, Donna M McDonald-McGinn, Matthew Hestand, Wolfram Demaerel, Liangtian Zhang, Yingjie Zhao, Francisco Ujueta, Jidong Shan, et al. Deletion size analysis of 1680 22q11.2DS subjects identifies a new recombination hotspot on chromosome 22q11.2. Human molecular genetics. 2018. 27. 7. 1150-1163
  • Tingwei Guo, Gabriela M Repetto, Donna M McDonald McGinn, Jonathan H Chung, Hiroko Nomaru, Christopher L Campbell, Anna Blonska, Anne S Bassett, Eva W C Chow, Elisabeth E Mlynarski, et al. Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the GPR98 Locus on 5q14.3. Circulation. Cardiovascular genetics. 2017. 10. 5
more...
MISC (4):
Professional career (1):
  • 博士(医学) (九州大学)
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