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Case Reports in Rheumatology|January 30, 2019
A Case of Sporadic Blau Syndrome with an Uncommon Clinical CourseMiyoko Imayoshi, Yoshiyasu Ogata, Shuichi Yamamoto
The Journal of Biological Chemistry|February 14, 2003
Fes tyrosine kinase promotes survival and terminal granulocyte differentiation of factor-dependent myeloid progenitors (32D) and activates lineage-specific transcription factorsJynho Kim, Yoshiyasu Ogata, Ricardo A Feldman
Pediatrics International : Official Journal of the Japan Pediatric Society|February 18, 2017
Nasal hemophilic pseudotumor in a patient with mild hemophilia A and allergic rhinitisYoshiyasu Ogata, Mikio Monji, Keita Kai, et al.
Blood Cells, Molecules & Diseases|March 9, 2004
The Fes tyrosine kinase: a signal transducer that regulates myeloid-specific gene expression through transcriptional activationJynho Kim, Yoshiyasu Ogata, Humayra Ali, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|August 5, 2025
Cytokine-Induced Cytotoxicity and Extracellular Matrix Abnormalities in Hepatocytes Derived From RAD50-Interacting Protein 1-Deficient Induced Pluripotent Stem CellsYumeng Zhang, Yoshiyasu Ogata, Satomi Nadanaka, et al.
American Journal of Hematology|September 3, 2005
Partial tandem duplication of MLL gene in acute myeloid leukemia with translocation (11;17)(q23;q12-21)Shuichi Yamamoto, Masanori Nishi, Kazuto Taniguchi, et al.
Journal of Human Genetics|September 12, 2025
Functional analysis of novel and recurrent RINT1 variants in patients with infantile liver dysfunctionTaiga Aoki, Ayano Inui, Yoshiyasu Ogata, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|November 19, 2019
Perioperative safety and haematostatic efficacy of a new bypassing agent pd-FVIIa/FX (Byclot) in haemophilia patients with high-responding type inhibitorsRie Shirayama, Hideyuki Takedani, Yushi Chikasawa, et al.
Journal of Human Genetics|September 24, 2005
Mutations of syntaxin 11 and SNAP23 genes as causes of familial hemophagocytic lymphohistiocytosis were not found in Japanese peopleKen Yamamoto, Eiichi Ishii, Hisanori Horiuchi, et al.
Blood|January 6, 2005
Genetic subtypes of familial hemophagocytic lymphohistiocytosis: correlations with clinical features and cytotoxic T lymphocyte/natural killer cell functionsEiichi Ishii, Ikuyo Ueda, Ryutaro Shirakawa, et al.
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