Motoko Unoki

Tokyo, Japan

Last Updated: 09/26/2026

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Found 28 publications

Cutting-edge insights into DNA methylation maintenance.

Cutting-edge insights into DNA methylation maintenance.

Journal: Genes & genetic systems

Published: September 17, 2025

Missense substitutions in the BTB domain of ZBTB24 can lead to protein instability and cause ICF2 syndrome.

Missense substitutions in the BTB domain of ZBTB24 can lead to protein instability and cause ICF2 syndrome.

Journal: Human molecular genetics

Published: June 25, 2025

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

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

Journal: Genes & genetic systems

Published: June 11, 2025

A deletion at the X-linked ARHGAP36 gene locus is associated with the orange coloration of tortoiseshell and calico cats.

A deletion at the X-linked ARHGAP36 gene locus is associated with the orange coloration of tortoiseshell and calico cats.

Journal: Current biology : CB

Published: December 23, 2024

Inhibitory effects of extracts from Eucalyptus gunnii on α-synuclein amyloid fibrils.

Inhibitory effects of extracts from Eucalyptus gunnii on α-synuclein amyloid fibrils.

Journal: Bioscience, biotechnology, and biochemistry

Published: June 15, 2024

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

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

Journal: Frontiers in immunology

Published: June 08, 2024

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

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

Journal: Frontiers in immunology

Published: March 22, 2024

The maternal protein NLRP5 stabilizes UHRF1 in the cytoplasm: implication for the pathogenesis of multilocus imprinting disturbance.

The maternal protein NLRP5 stabilizes UHRF1 in the cytoplasm: implication for the pathogenesis of multilocus imprinting disturbance.

Journal: Human molecular genetics

Published: March 15, 2024

Long-read sequencing reveals novel isoform-specific eQTLs and regulatory mechanisms of isoform expression in human B cells.

Long-read sequencing reveals novel isoform-specific eQTLs and regulatory mechanisms of isoform expression in human B cells.

Journal: Genome biology

Published: February 05, 2024

Long-read sequencing reveals the complex structure of extra dic(21;21) chromosome and its biological effects.

Long-read sequencing reveals the complex structure of extra dic(21;21) chromosome and its biological effects.

Journal: Human genetics

Published: April 12, 2023

UHRF1 is essential for proper cytoplasmic architecture and function of mouse oocytes and derived embryos.

UHRF1 is essential for proper cytoplasmic architecture and function of mouse oocytes and derived embryos.

Journal: Life science alliance

Published: January 06, 2023

The UHRF protein family in epigenetics, development, and carcinogenesis.

The UHRF protein family in epigenetics, development, and carcinogenesis.

Journal: Proceedings of the Japan Academy. Series B, Physical and biological sciences

Published: October 10, 2022

Showing 1-12 of 28

Last Updated: 09/26/2026