Publications by authors named "Motoko Unoki"

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Missense substitutions in the BTB domain of ZBTB24 can lead to protein instability and cause ICF2 syndrome.
Or Givol, Ido S Han, Francesco Cecere, Liran Giladi, Noa Dotan-Glick, Motoko Unoki

Hum Mol Genet· December 2025

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Congenital diseases with defects in DNA methylation maintenance: focusing on ICF syndrome and multilocus imprinting disturbance.
Motoko Unoki

Genes Genet Syst· September 2025

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A deletion at the X-linked ARHGAP36 gene locus is associated with the orange coloration of tortoiseshell and calico cats.
Hidehiro Toh, Wan Kin Au Yeung, Motoko Unoki, Yuki Matsumoto, Yuka Miki

Curr Biol· June 2025

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Long-read sequencing reveals novel isoform-specific eQTLs and regulatory mechanisms of isoform expression in human B cells.
Yuya Nagura, Mihoko Shimada, Ryoji Kuribayashi, Ko Ikemoto, Hiroki Kiyose, Motoko Unoki

Genome Biol· May 2025

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Cutting-edge insights into DNA methylation maintenance.
Motoko Unoki

Genes Genet Syst· January 2025

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Inhibitory effects of extracts from Eucalyptus gunnii on α-synuclein amyloid fibrils.
Masatomo So, Misaki Ono, Shigeki Oogai, Minako Kondo, Kaede Yamazaki, Motoko Unoki

Biosci Biotechnol Biochem· October 2024

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The maternal protein NLRP5 stabilizes UHRF1 in the cytoplasm: implication for the pathogenesis of multilocus imprinting disturbance.
Motoko Unoki, Shuhei Uemura, Akihiro Fujimoto, Hiroyuki Sasaki

Hum Mol Genet· September 2024

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Corrigendum: Exploring the intersection of epigenetics, DNA repair, and immunology from studies of ICF syndrome, an inborn error of immunity.
Motoko Unoki

Front Immunol· June 2024

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Exploring the intersection of epigenetics, DNA repair, and immunology from studies of ICF syndrome, an inborn error of immunity.
Motoko Unoki

Front Immunol· May 2024

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Long-read sequencing reveals the complex structure of extra dic(21;21) chromosome and its biological effects.
Kugui Yoshida-Tanaka, Ko Ikemoto, Ryoji Kuribayashi, Motoko Unoki, Takako Takano

Hum Genet· September 2023

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UHRF1 is essential for proper cytoplasmic architecture and function of mouse oocytes and derived embryos.
Shuhei Uemura, Shoji Maenohara, Kimiko Inoue, Narumi Ogonuki, Shogo Matoba, Motoko Unoki

Life Sci Alliance· August 2023

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Novel compound heterozygous mutations in UHRF1 are associated with atypical immunodeficiency, centromeric instability and facial anomalies syndrome with distinctive genome-wide DNA hypomethylation.
Motoko Unoki, Guillaume Velasco, Satomi Kori, Kyohei Arita, Yasukazu Daigaku

Hum Mol Genet· April 2023

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The UHRF protein family in epigenetics, development, and carcinogenesis.
Motoko Unoki, Hiroyuki Sasaki

Proc Jpn Acad Ser B Phys Biol Sci· October 2022

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Identification of SLC38A7 as a Prognostic Marker and Potential Therapeutic Target of Lung Squamous Cell Carcinoma.
Naoki Haratake, Qingjiang Hu, Tatsuro Okamoto, Tomoko Jogo, Gouji Toyokawa, Motoko Unoki

Ann Surg· September 2021

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Chromatin remodeling in replication-uncoupled maintenance DNA methylation and chromosome stability: Insights from ICF syndrome studies.
Motoko Unoki

Genes Cells· June 2021

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Interplay between Histone and DNA Methylation Seen through Comparative Methylomes in Rare Mendelian Disorders.
Guillaume Velasco, Damien Ulveling, Sophie Rondeau, Pauline Marzin, Motoko Unoki

Int J Mol Sci· April 2021

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Ddhd1 knockout mouse as a model of locomotive and physiological abnormality in familial spastic paraplegia.
Takuya Morikawa, Hiroaki Ohishi, Kengo Kosaka, Tomofumi Shimojo, Akihiro Nagano, Motoko Unoki

Biosci Rep· February 2021

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CDCA7 and HELLS suppress DNA:RNA hybrid-associated DNA damage at pericentromeric repeats.
Motoko Unoki, Jafar Sharif, Yuichiro Saito, Guillaume Velasco, Claire Francastel

Sci Rep· October 2020

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Serine 298 Phosphorylation in Linker 2 of UHRF1 Regulates Ligand-Binding Property of Its Tandem Tudor Domain.
Satomi Kori, Tomohiro Jimenji, Toru Ekimoto, Miwa Sato, Fumie Kusano, Motoko Unoki

J Mol Biol· June 2020

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Characterization of genetic-origin-dependent monoallelic expression in mouse embryonic stem cells.
Hiroaki Ohishi, Wan Kin Au Yeung, Motoko Unoki, Kenji Ichiyanagi, Kei Fukuda

Genes Cells· January 2020

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Identification of ZBTB24 protein domains and motifs for heterochromatin localization and transcriptional activation.
Sharmin Aktar, Hiroyuki Sasaki, Motoko Unoki

Genes Cells· November 2019

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CDCA7 and HELLS mutations undermine nonhomologous end joining in centromeric instability syndrome.
Motoko Unoki, Hironori Funabiki, Guillaume Velasco, Claire Francastel, Hiroyuki Sasaki

J Clin Invest· January 2019

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Accurate estimation of 5-methylcytosine in mammalian mitochondrial DNA.
Shigeru Matsuda, Takehiro Yasukawa, Yuriko Sakaguchi, Kenji Ichiyanagi, Motoko Unoki

Sci Rep· April 2018

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Role of UHRF1 in de novo DNA methylation in oocytes and maintenance methylation in preimplantation embryos.
Shoji Maenohara, Motoko Unoki, Hidehiro Toh, Hiroaki Ohishi, Jafar Sharif

PLoS Genet· October 2017

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Corrigendum: Mutations in CDCA7 and HELLS cause immunodeficiency-centromeric instability-facial anomalies syndrome.
Peter E Thijssen, Yuya Ito, Giacomo Grillo, Jun Wang, Guillaume Velasco, Motoko Unoki

Nat Commun· June 2016

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