56 results on '"Mizutani, Shuki"'
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2. Current state of therapeutic development for rare cancers in Japan, and proposals for improvement
3. Clinical and biological features of paediatric acute myeloid leukaemia ( AML ) with primary induction failure in the Japanese Paediatric Leukaemia/Lymphoma Study Group AML ‐05 study
4. Sequential use of second-generation tyrosine kinase inhibitors following imatinib therapy in pediatric chronic myeloid leukemia: A report from the Japanese Pediatric Leukemia/Lymphoma Study Group
5. Fludarabine, cytarabine, granulocyte colony-stimulating factor and idarubicin for relapsed childhood acute myeloid leukemia
6. Flow cytometric analysis as an additional predictive tool of treatment response in children with chronic-phase chronic myeloid leukemia treated with imatinib
7. Outcome of relapsed core binding factor acute myeloid leukemia in children: A result from the Japanese Pediatric Leukemia/Lymphoma Study Group (JPLSG) AML-05R study
8. Salvage therapy for children with relapsed or refractory Philadelphia chromosome-positive acute lymphoblastic leukemia
9. EWSR 1/ ELF 5induces acute myeloid leukemia by inhibiting p53/p21 pathway
10. Genomic analysis of clonal origin of Langerhans cell histiocytosis following acute lymphoblastic leukaemia
11. Leukostasis in Children and Adolescents with Chronic Myeloid Leukemia: Japanese Pediatric Leukemia/Lymphoma Study Group
12. Transient abnormal myelopoiesis in non-Down syndrome neonate
13. Partial rescue of mucopolysaccharidosis type VII mice with a lifelong engraftment of allogeneic stem cells in utero
14. FOXL2 transcriptionally repressesSf1expression by antagonizing WT1 during ovarian development in mice
15. Two novelHSD3B2missense mutations with diverse residual enzymatic activities for Δ5-steroids
16. Roles of AML1/RUNX1 in T-cell malignancy induced by loss of p53
17. Artemis-dependent DNA double-strand break formation at stalled replication forks
18. Ataxia telangiectasia mutated-dependent regulation of topoisomerase II alpha expression and sensitivity to topoisomerase II inhibitor
19. Expression of angiogenesis-related factors and inflammatory cytokines in placenta and umbilical vessels in pregnancies with preeclampsia and chorioamnionitis/funisitis
20. Functional studies of a novel Germline p53 splicing mutation identified in a patient with Li–Fraumeni‐Like syndrome
21. Two preterm infants with late onset circulatory collapse induced by levothyroxine sodium
22. Caffeine yields aneuploidy through asymmetrical cell division caused by misalignment of chromosomes
23. Soluble TWEAK is markedly elevated in hemophagocytic lymphohistiocytosis
24. Fortuitous detection of a submicroscopic deletion at 1q25 in a girl with Cornelia‐de Lange syndrome carrying t(5;13)(p13.1;q12.1) by array‐based comparative genomic hybridization
25. Clinical and molecular cytogenetic characterization of two patients with non‐mutational aberrations of the FMR2 gene
26. Common gene expression signatures in t(8;21)- and inv(16)-acute myeloid leukaemia
27. Features and outcome of neonatal leukemia in Japan: Experience of the Japan Infant Leukemia Study Group
28. Analysis of serum granulysin in patients with hematopoietic stem-cell transplantation: Its usefulness as a marker of graft-versus-host reaction
29. Detection of cryptic chromosome aberrations in a patient with a balanced t(1;9)(p34.2;p24) by array‐based comparative genomic hybridization
30. Novel adopted immunotherapy for mixed chimerism after unrelated cord blood transplantation in Omenn syndrome
31. Ataxia‐telangiectasia‐mutated dependent phosphorylation of Artemis in response to DNA damage
32. Analysis of serum soluble CD40 ligand (sCD40L) in the patients undergoing allogeneic stem cell transplantation: platelet is a major source of serum sCD40L
33. Allogeneic hematopoietic stem cell transplantation for seven children with X‐linked hyper‐IgM syndrome: A single center experience
34. Coagulopathy in a patient with X-linked hyper-IgM syndrome who developed Kaposi's sarcoma
35. Expression of Cyclin-dependent Kinase Inhibitor p27/Kipl and AP-1 Coactivator p38/Jabl Correlates with Differentiation of Embryonal Rhabdomyosarcoma
36. Risk‐directed treatment of infant acute lymphoblastic leukaemia based on early assessment of MLL gene status: results of the Japan Infant Leukaemia Study (MLL96)
37. Activation of an ataxia telangiectasia mutation-dependent intra-S-phase checkpoint by anti-tumour drugs in HL-60 and human lymphoblastoid cells
38. Abnormalities of the p53 gene in juvenile myelomonocytic leukaemia
39. Clonal dissemination of T-lymphocytes inscid mice from familial hemophagocytic lymphohistiocytosis
40. Clonal and non-clonal karyotypically abnormal cells in haemophagocytic lymphohistiocytosis
41. Pyothorax-associated pleural lymphoma. A case evolving from T-cell-rich lymphoid infiltration to overt B-cell lymphoma in association with Epstein-Barr virus
42. A novel 203 kD aberrant BCR-ABL product in a girl with Philadelphia chromosome positive acute lymphoblastic leultaemia
43. A long‐term suppression by α‐interferon of Philadelphia chromosome in children with chronic myelogenous leukemia
44. bcl-2 Gene Rearrangement Analysis of Japanese Follicular Lymphomas by Polymerase Chain Reaction in Formalin-fixed, Paraffin-embedded Tissue Specimens
45. Carrier Detection in Agammaglobulinemia by X Chromosome Inactivation Analysis
46. Molecular studies of chronic myelogenous leukemia using the polymerase chain reaction
47. Malignant Cell Detection in Burkitt's Lymphoma Using Third-complementarity-determining Region (CDRIII), Clone-specific Probe Developed by Sequencing DNA from Stored Slides
48. MOLECULAR ANALYSIS OF BCR/ABL PRODUCTS IN A CASE OF MYELODYSPLASTIC SYNDROME WITH LATE APPEARING PHILADELPHIA CHROMOSOME
49. Mixed Blasts Crisis Following Extramedullary Involvement with the Cytogenetic Evidence of Clonal Evolutions Philadelphia Chromosome-Positive Chronic Myelocytic Leukemia
50. Human Lymphocytes Receptors for Measles Virus
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