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1. Assessing the efficacy of target adaptive sampling long-read sequencing through hereditary cancer patient genomes

2. High-dose cytarabine induction therapy and flow cytometric measurable residual disease monitoring for children with acute myeloid leukemia

4. Genome-wide DNA methylation analysis in pediatric acute myeloid leukemia

5. High DOCK1 expression identifies a distinct prognostic subgroup of pediatric acute myeloid leukemia: Results of the Japanese Pediatric Leukemia/Lymphoma Study Group AML‐05 trial.

6. NUDT15 variants confer high incidence of second malignancies in children with acute lymphoblastic leukemia

8. High-dose cytarabine induction therapy and flow cytometric measurable residual disease monitoring for children with acute myeloid leukemia

12. Optimizing transplantation procedures through identification of prognostic factors in second remission for children with acute myeloid leukemia with no prior history of transplant

13. Distinct αβ double-negative T cells discriminate between autoimmune lymphoproliferative syndrome and RAS-associated lymphoproliferative disease

14. Prevalence of pathogenic variants in cancer‐predisposing genes in second cancer after childhood solid cancers

16. Data from Recurrent RARB Translocations in Acute Promyelocytic Leukemia Lacking RARA Translocation

17. Supplementary Information from Recurrent RARB Translocations in Acute Promyelocytic Leukemia Lacking RARA Translocation

18. Prognostic Factors in Children with Acute Myeloid Leukemia Receiving the First Hematopoietic Stem Cell Transplantation in Second Remission

19. Evaluation of High-Dose Cytarabine Induction Therapy and Flow Cytometric Measurable Residual Disease Monitoring for Children with De Novo Acute Myeloid Leukemia: A Report from the JPLSG-AML-12 Trial

21. Low NUDT15 expression levels due to biallelicNUDT15variants and 6‐mercaptopurine intolerance

22. A phase III clinical trial evaluating efficacy and safety of minimal residual disease-based risk stratification for children with acute myeloid leukemia, incorporating a randomized study of gemtuzumab ozogamicin in combination with post-induction chemotherapy for non-low-risk patients (JPLSG-AML-20)

26. Low NUDT15 expression levels due to biallelic NUDT15 variants and 6‐mercaptopurine intolerance.

27. phase III clinical trial evaluating efficacy and safety of minimal residual disease-based risk stratification for children with acute myeloid leukemia, incorporating a randomized study of gemtuzumab ozogamicin in combination with post-induction chemotherapy for non-low-risk patients (JPLSG-AML-20)

31. Comparison of clonazepam and levetiracetam in children for prevention of busulfan-induced seizure in hematopoietic stem cell transplantation

32. Evaluation of High-Dose Cytarabine Induction Therapy and Flow Cytometric Measurable Residual Disease Monitoring for Children with De NovoAcute Myeloid Leukemia: A Report from the JPLSG-AML-12 Trial

33. Acute promyelocytic leukemia with a cryptic insertion of RARA into TBL1XR1

34. A novel KMT2A‐ACTN2 fusion in infant B‐cell acute lymphoblastic leukemia

35. Whole transcriptome sequencing reveals a KMT2A‐USP2 fusion in infant acute myeloid leukemia

37. NUDT15variants confer high incidence of second malignancies in children with acute lymphoblastic leukemia

38. Recurrent RARB Translocations in Acute Promyelocytic Leukemia Lacking RARA Translocation

39. SomaticMECOMmosaicism in a patient with congenital bone marrow failure without a radial abnormality

41. Clinical Courses of Two Pediatric Patients with Acute Megakaryoblastic Leukemia Harboring the CBFA2T3-GLIS2 Fusion Gene

42. Metabolic Reprogramming By PRDM16 Drives Cytarabine Resistance in Acute Myeloid Leukemia

45. Association of isochromosome (7)(q10) in Shwachman–Diamond syndrome with the severity of cytopenia.

46. Apnoea, dyspnoea and wheezing in primary lower respiratory infections due to human rhinovirus in Japanese infants

47. A Cryptic NUP214-ABL1Fusion in B-cell Precursor Acute Lymphoblastic Leukemia

50. Optimizing transplantation procedures through identification of prognostic factors in second remission for children with acute myeloid leukemia with no prior history of transplant.

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