Musashi Ichimaru-Kubiura
Saga, 8498501, Japan
Last Updated: 09/26/2026
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Found 11 publications
Beckwith-Wiedemann spectrum exhibiting a 46,XY karyotype caused by genome-wide paternal uniparental heterodisomy: a case report.
Journal: Human genomics
Published: March 21, 2026
Variants of NLRP genes encoding subcortical maternal complex components are linked to biparental placental mesenchymal dysplasia.
Journal: Human genomics
Published: March 23, 2025
Establishment of DNA methylation during primate germ cell development.
Journal: Nature communications
Published: March 22, 2025
Identification of responsible sequences which mutations cause maternal H19-ICR hypermethylation with Beckwith-Wiedemann syndrome-like overgrowth.
Journal: Communications biology
Published: August 07, 2024
DNMT1 can induce primary germ layer differentiation through de novo DNA methylation.
Journal: Genes to cells : devoted to molecular & cellular mechanisms
Published: February 17, 2024
Whole-exome sequencing reveals causative genetic variants for several overgrowth syndromes in molecularly negative Beckwith-Wiedemann spectrum.
Journal: Journal of medical genetics
Published: September 07, 2023
mRNA-based generation of marmoset PGCLCs capable of differentiation into gonocyte-like cells.
Journal: Stem cell reports
Published: August 23, 2022
Evidence for divergence of DNA methylation maintenance and a conserved inhibitory mechanism from DNA demethylation in chickens and mammals.
Journal: Genes & genomics
Published: December 17, 2020
Cyclic DNA remethylation following active demethylation at euchromatic regions in mouse embryonic stem cells.
Journal: Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology
Published: August 03, 2020
A two-dimensional multiwell cell culture method for the production of CYP3A4-expressing hepatocyte-like cells from HepaRG cells.
Journal: Pharmacology research & perspectives
Published: July 03, 2020
Showing 1-11 of 11
Last Updated: 09/26/2026