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

10. Author Correction: Pluripotent stem cell model of Shwachman–Diamond syndrome reveals apoptotic predisposition of hemoangiogenic progenitors

15. Improvement of multilineage hematopoiesis in hematopoietic stem cell-transferred c-kit mutant NOG-EXL humanized mice

16. Pluripotent stem cell model of Shwachman–Diamond syndrome reveals apoptotic predisposition of hemoangiogenic progenitors

20. Involvement of mTOR pathway in neurodegeneration in NSF-related developmental and epileptic encephalopathy

21. A disease-specific iPS cell resource for studying rare and intractable diseases

22. A concise in vitro model for evaluating interactions between macrophage and skeletal muscle cells during muscle regeneration

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

26. Data from Specific Antileukemic Activity of PD0332991, a CDK4/6 Inhibitor, against Philadelphia Chromosome–Positive Lymphoid Leukemia

27. Supplementary Figure from Specific Antileukemic Activity of PD0332991, a CDK4/6 Inhibitor, against Philadelphia Chromosome–Positive Lymphoid Leukemia

28. Supplementary Table from Specific Antileukemic Activity of PD0332991, a CDK4/6 Inhibitor, against Philadelphia Chromosome–Positive Lymphoid Leukemia

29. Involvement of mTOR pathway in neurodegeneration in NSF-related developmental and epileptic encephalopathy

34. Induced pluripotent stem cells from CINCA syndrome patients as a model for dissecting somatic mosaicism and drug discovery

35. Unique multipotent cells in adult human mesenchymal cell populations

36. Recapitulation of pro-inflammatory signature of monocytes with ACVR1A mutation using FOP patient-derived iPSCs

39. Identification of a High‐Frequency Somatic NLRC4 Mutation as a Cause of Autoinflammation by Pluripotent Cell–Based Phenotype Dissection

50. Down syndrome-related transient abnormal myelopoiesis is attributed to a specific erythro-megakaryocytic subpopulation with GATA1 mutation

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