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1. Aberrant X chromosomal rearrangement through multi‐step template switching during sister chromatid formation in a patient with severe hemophilia A. Issue 9 (5th July 2020)

3. Apparent synonymous mutation F9 c.87A>G causes secretion failure by in-frame mutation with aberrant splicing. Issue 179 (July 2019)

4. CLEC‐2 stimulates IGF‐1 secretion from podoplanin‐positive stromal cells and positively regulates erythropoiesis in mice. (20th April 2021)

5. Clinical conditions and risk factors for inhibitor‐development in patients with haemophilia: A decade‐long prospective cohort study in Japan, J‐HIS2 (Japan Hemophilia Inhibitor Study 2). Issue 5 (11th June 2022)

6. Diverse CD36 expression among Japanese population: defective CD36 mutations cause platelet and monocyte CD36 reductions in not only deficient but also normal phenotype subjects. Issue 5 (May 2015)

7. Diverse CD36 expression among Japanese population: defective CD36 mutations cause platelet and monocyte CD36 reductions in not only deficient but also normal phenotype subjects. Issue 5 (May 2015)

8. Essential role of a carboxyl‐terminal α‐helix motif in the secretion of coagulation factor XI. (10th February 2021)

9. F9 mRNA splicing aberration due to a deep Intronic structural variation in a patient with moderate hemophilia B. Issue 213 (May 2022)

10. Functional inhibition of MEF2 by C/EBP is a possible mechanism of leukemia development by CEBP‐IGH fusion gene. Issue 3 (27th November 2022)