Tomohiko Sato

Mechanism of KIT gene regulation by GATA1 lacking the N-terminal domain in Down syndrome–related myeloid disorders

R. Kanezaki, T. Toki, E. Ito, 2022, Scientific Reports.

Dyserythropoietic anaemia with an intronic GATA1 splicing mutation in patients suspected to have Diamond‐Blackfan anaemia

S. Miyano, S. Ogawa, Kenichi Yoshida, 2022, EJHaem.

BRAF V600E-positive cells as molecular markers of bone marrow disease in pediatric Langerhans cell histiocytosis

H. Kanegane, R. Kanezaki, T. Toki, 2022, Haematologica.

Early-onset Marfan syndrome with a novel missense mutation: A case report.

T. Toki, K. Terui, Toru Takahashi, 2023, Journal of Cardiology Cases.