Y. Miyawaki

发表

A possible mechanism for Inv22‐related F8 large deletions in severe hemophilia A patients with high responding factor VIII inhibitors

T. Murate, T. Matsushita, A. Takagi, 2012, Journal of thrombosis and haemostasis : JTH.

Down-regulation of PROS1 Gene Expression by 17β-Estradiol via Estrogen Receptor α (ERα)-Sp1 Interaction Recruiting Receptor-interacting Protein 140 and the Corepressor-HDAC3 Complex*

T. Murate, H. Saito, A. Takagi, 2010, The Journal of Biological Chemistry.

Thrombosis from a prothrombin mutation conveying antithrombin resistance

Y. Miyawaki, 2013 .

Ribavirin-induced intracellular GTP depletion activates transcription elongation in coagulation factor VII gene expression.

T. Murate, H. Saito, A. Takagi, 2013, The Biochemical journal.

Life‐threatening hemorrhage and prolonged wound healing are remarkable phenotypes manifested by complete plasminogen activator inhibitor‐1 deficiency in humans

T. Terao, J. Takamatsu, N. Kanayama, 2011, Journal of thrombosis and haemostasis : JTH.

Severe hemophilia A in a Japanese female caused by an F8-intron 22 inversion associated with skewed X chromosome inactivation

T. Naoe, T. Murate, Koji Yamamoto, 2010, International journal of hematology.

Thrombosis from a prothrombin mutation conveying antithrombin resistance.

T. Naoe, T. Murate, H. Saito, 2012, The New England journal of medicine.

A novel ENG mutation causing impaired co-translational processing of endoglin associated with hereditary hemorrhagic telangiectasia.

T. Murate, H. Saito, T. Matsushita, 2012, Thrombosis research.

A novel missense mutation causing abnormal LMAN1 in a Japanese patient with combined deficiency of factor V and factor VIII

T. Murate, H. Saito, T. Matsushita, 2009, American journal of hematology.

Impaired secretion of carboxyl-terminal truncated factor VII due to an F7 nonsense mutation associated with FVII deficiency.

T. Naoe, T. Murate, T. Matsushita, 2010, Thrombosis research.