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You searched for: Author/Creator Shiraishi, Yuichi

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1. Acquisition of monosomy 7 and a RUNX1 mutation in Pearson syndrome. Issue 2 (16th November 2020)

2. Alteration of the immune environment in bone marrow from children with recurrent B cell precursor acute lymphoblastic leukemia. Issue 1 (29th November 2021)

3. ASXL2 mutations are frequently found in pediatric AML patients with t(8;21)/ RUNX1‐RUNX1T1 and associated with a better prognosis. Issue 5 (14th February 2017)

5. Clinical utility of target capture‐based panel sequencing in hematological malignancies: A multicenter feasibility study. Issue 9 (17th July 2020)

6. Constitutional abnormalities of IDH1 combined with secondary mutations predispose a patient with Maffucci syndrome to acute lymphoblastic leukemia. Issue 12 (24th May 2017)

7. Description of longitudinal tumor evolution in a case of multiply relapsed clear cell sarcoma of the kidney. Issue 2 (29th December 2021)

8. Diagnostic utility of integrated analysis of exome and transcriptome: Successful diagnosis of Au‐Kline syndrome in a patient with submucous cleft palate, scaphocephaly, and intellectual disabilities. Issue 9 (26th June 2020)

9. Distinct gene alterations with a high percentage of myeloperoxidase-positive leukemic blasts in de novo acute myeloid leukemia. (February 2018)

10. Dysregulation of Epstein-Barr Virus Infection in Hypomorphic ZAP70 Mutation. (19th April 2018)