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1. Generation of human induced pluripotent stem cell lines derived from four Rett syndrome patients with MECP2 mutations

2. Efficient deletion of microRNAs using CRISPR/Cas9 with dual guide RNAs

4. Pre-existing cross-reactive neutralizing activity against SARS-CoV-2 and seasonal coronaviruses prior to the COVID-19 pandemic (2014-2019) with limited immunity against recent emerging SARS-CoV-2 variants, Vietnam

6. Actual conditions for returning home after hospitalization among older patients receiving home medical care in Japan: OHCARE Study

9. bBase editing of key residues in the BCL11A-XL-specific zinc finger domains de-represses fetal globin expression

10. Complete suspension culture of human induced pluripotent stem cells supplemented with suppressors of spontaneous differentiation

11. Complete suspension culture of human induced pluripotent stem cells supplemented with suppressors of spontaneous differentiation

12. Efficient repair of human genetic defect by CRISPR/Cas9 mediated interlocus gene conversion

13. Complete suspension culture of human induced pluripotent stem cells supplemented with suppressors of spontaneous differentiation

17. Jdp2 is a spatiotemporal transcriptional activator of the AhR via the Nrf2 gene battery

18. Restoring tumor immunogenicity with dendritic cell reprogramming

23. Editing the core region in HPFH deletions alters fetal and adult globin expression for treatment of β-hemoglobinopathies

24. High-efficiency editing in hematopoietic stem cells and the HUDEP-2 cell line based on in vitro mRNA synthesis

25. Chemically defined cytokine-free expansion of human haematopoietic stem cells

30. A specific G9a inhibitor unveils BGLT3 lncRNA as a universal mediator of chemically induced fetal globin gene expression

31. Efficient and error-free correction of sickle mutation in human erythroid cells using prime editor-2

32. Deficiency of ribosomal protein S26, which is mutated in a subset of patients with Diamond Blackfan anemia, impairs erythroid differentiation

33. Abstract A40: Restoring tumor immunogenicity with dendritic cell reprogramming

34. Elucidation of the Role of FAM210B in Mitochondrial Metabolism and Erythropoiesis

35. Altered Transcription By GATA1 Impairs Autophagy and Prevents Ferroptosis in X-Linked Sideroblastic Anemia

36. A pseudovirus-based platform to measure neutralizing antibodies in Mexico using SARS-CoV-2 as proof-of-concept

38. ANTXR1 Regulates Erythroid Cell Proliferation and Differentiation through wnt/β-Catenin Signaling Pathway In Vitro and in Hematopoietic Stem Cell

39. Exploring the mechanistic link between SF3B1 mutation and ring sideroblast formation in myelodysplastic syndrome

40. Erythroid lineage-specific lentiviral RNAi vectors suitable for molecular functional studies and therapeutic applications

41. Transmembrane Protein ANTXR1 Regulates γ-Globin Expression by Targeting the Wnt/β-Catenin Signaling Pathway

42. First pseudovirus-based assay to measure virus-elicited neutralizing antibodies in Mexico: proof-of-concept with SARS-CoV-2

43. Editing the core region in HPFH deletions alters fetal and adult globin expression for treatment of β-hemoglobinopathies

44. Clinical and molecular features of patients with COL1‐related disorders: Implications for the wider spectrum and the risk of vascular complications

47. Precise modelling and correction of a spectrum of β-thalassemic mutations in human erythroid cells by base editors

48. Congenital sideroblastic anemia model due to ALAS2 mutation is susceptible to ferroptosis

49. HMGB1-mediated restriction of EPO signaling contributes to anemia of inflammation

50. Induction of Fetal Hemoglobin by Introducing Natural Hereditary Persistence of Fetal Hemoglobin Mutations in the γ-Globin Gene Promoters for Genome Editing Therapies for β-Thalassemia

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