The Molecular Biology Society of Japan

[4P-0139] Oct motif mutations in Beckwith-Wiedemann syndrome patients disturb the induction of DNA demethylation and maintenance of hypomethylation on the H19-ICR

〇Shuichi Kubo1, Chihiro Murata1, Hanayo Okamura1, Taku Sakasegawa1, Sakurai chiye1, Kiyotaka Hatsuzawa1, Naohiro Hori1 (1.Div. of Mol Biol. Sri., Grad. Sch. of Med., Univ. of Tottori)

DNA Demethylation, Sox-Oct motif, Beckwith-Wiedemann syndrome, Imprinting, H19-ICR

This archive has moved to the member page of The Molecular Biology Society of Japan.
Members can access the abstracts via links at the member page of the sites.
Please feel free to contact the journal offices for any inquiries.

Password