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2. Statistically and functionally fine-mapped blood eQTLs and pQTLs from 1,405 humans reveal distinct regulation patterns and disease relevance

3. Usage Patterns of GlucoNote, a Self-Management Smartphone App, Based on ResearchKit for Patients With Type 2 Diabetes and Prediabetes

6. KRAS G12 mutations as adverse prognostic factors in KMT2A-rearranged acute myeloid leukemia

9. Inhibition of TOPORS ubiquitin ligase augments the efficacy of DNA hypomethylating agents through DNMT1 stabilization

12. Mechanisms of action and resistance in histone methylation-targeted therapy

13. Publisher Correction: Statistically and functionally fine-mapped blood eQTLs and pQTLs from 1,405 humans reveal distinct regulation patterns and disease relevance

16. Molecular taxonomy of myelodysplastic syndromes and its clinical implications

20. Quantification of escape from X chromosome inactivation with single-cell omics data reveals heterogeneity across cell types and tissues

24. Evolutionary histories of breast cancer and related clones

30. Mitotic perturbation is a key mechanism of action of decitabine in myeloid tumor treatment

32. Postazacitidine clone size predicts long-term outcome of patients with myelodysplastic syndromes and related myeloid neoplasms

33. Implications of TP53 allelic state for genome stability, clinical presentation and outcomes in myelodysplastic syndromes

34. Identification of the ultrahigh-risk subgroup in neuroblastoma cases through DNA methylation analysis and its treatment exploiting cancer metabolism

36. DOCK2 is involved in the host genetics and biology of severe COVID-19

40. Pseudouridine-modified tRNA fragments repress aberrant protein synthesis and predict leukaemic progression in myelodysplastic syndrome

42. The whole blood transcriptional regulation landscape in 465 COVID-19 infected samples from Japan COVID-19 Task Force

43. Multi-omics analysis defines highly refractory RAS burdened immature subgroup of infant acute lymphoblastic leukemia

44. Patient-specific MDS-RS iPSCs define the mis-spliced transcript repertoire and chromatin landscape of SF3B1-mutant HSPCs

45. Two novel high-risk adult B-cell acute lymphoblastic leukemia subtypes with high expression of CDX2 and IDH1/2 mutations

46. Common progenitor origin for Rosai–Dorfman disease and clear cell sarcoma.

47. Sexual transmission of HTLV‐1 resulting in uveitis with short‐term latency and low proviral load.

48. Modelling and drug targeting of a myeloid neoplasm with atypical 3q26/MECOM rearrangement using patient‐specific iPSCs.

49. Whole-genome landscape of adult T-cell leukemia/lymphoma

50. Germ line DDX41 mutations define a unique subtype of myeloid neoplasms

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