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1. International retrospective study of allogeneic hematopoietic cell transplantation for activated PI3K-delta syndrome

3. Detailed analysis of Japanese patients with adenosine deaminase 2 deficiency reveals characteristic elevation of type II interferon signature and STAT1 hyperactivation

4. Hematopoietic Cell Transplantation with Reduced Intensity Conditioning Using Fludarabine/Busulfan or Fludarabine/Melphalan for Primary Immunodeficiency Diseases

5. Helix‐to‐Disc Conversion of Thia[6]helicenes into Coronenes Facilitated by Sulfur Oxidation and Fluorination.

10. Hematopoietic stem cell transplantation for progressive combined immunodeficiency and lymphoproliferation in patients with activated phosphatidylinositol-3-OH kinase δ syndrome type 1

11. Dysregulation of Epstein-Barr Virus Infection in Hypomorphic ZAP70 Mutation

14. Case Report: The leopard sign as a potential characteristic of chronic granulomatous disease-associated colitis, unrelated to colitis severity

16. Hematopoietic stem cell transplantation in 29 patients hemizygous for hypomorphic IKBKG/NEMO mutations

17. Abnormal hematopoiesis and autoimmunity in human subjects with germline IKZF1 mutations

18. Haploinsufficiency of TNFAIP3 (A20) by germline mutation is involved in autoimmune lymphoproliferative syndrome

19. Clinical and Immunological Characterization of ICF Syndrome in Japan

20. Comprehensive molecular diagnosis of Epstein–Barr virus-associated lymphoproliferative diseases using next-generation sequencing

23. Phosphatase and tensin homolog (PTEN) mutation can cause activated phosphatidylinositol 3-kinase δ syndrome–like immunodeficiency

24. Robust and highly efficient hiPSC generation from patient non-mobilized peripheral blood-derived CD34+ cells using the auto-erasable Sendai virus vector

26. Hematopoietic Stem Cell Transplantation for XIAP Deficiency in Japan

28. A case of autoimmune enteropathy with CTLA4 haploinsufficiency

29. Novel compound heterozygous variants in the SLC39A7 gene in a Japanese girl with B-cell deficiency.

30. Successful ruxolitinib administration for a patient with steroid‐refractory idiopathic pneumonia syndrome following hematopoietic stem cell transplantation: A case report and literature review

31. Additional file 5 of Robust and highly efficient hiPSC generation from patient non-mobilized peripheral blood-derived CD34+ cells using the auto-erasable Sendai virus vector

32. Additional file 3 of Robust and highly efficient hiPSC generation from patient non-mobilized peripheral blood-derived CD34+ cells using the auto-erasable Sendai virus vector

33. Additional file 4 of Robust and highly efficient hiPSC generation from patient non-mobilized peripheral blood-derived CD34+ cells using the auto-erasable Sendai virus vector

34. Somatic mutation in RUNX1 underlies mucocutaneus inflammatory manifestations

36. Heterozygous OAS1 gain-of-function variants cause an autoinflammatory immunodeficiency

37. Cytomegalovirus Laryngitis in Primary Combined Immunodeficiency Diseases

38. Autosomal recessive complete STAT1 deficiency caused by compound heterozygous intronic mutations

39. Additional file 1 of Robust and highly efficient hiPSC generation from patient non-mobilized peripheral blood-derived CD34+ cells using the auto-erasable Sendai virus vector

40. Additional file 2 of Robust and highly efficient hiPSC generation from patient non-mobilized peripheral blood-derived CD34+ cells using the auto-erasable Sendai virus vector

41. Additional file 1: of Robust and highly efficient hiPSC generation from patient non-mobilized peripheral blood-derived CD34+ cells using the auto-erasable Sendai virus vector

42. High‐throughput analysis revealed the unique immunoglobulin gene rearrangements in plasmacytoma‐like post‐transplant lymphoproliferative disorder

43. Prominent dermal Langerhans cells in an Omenn syndrome patient with a novel mutation in theIL 2 RGgene

44. Epstein-Barr Virus-Associated γδ T-Cell Lymphoproliferative Disorder Associated With Hypomorphic IL2RG Mutation

46. B-lymphoblastic lymphoma with TCF3-PBX1 fusion gene

47. Infantile-onset primary alveolar proteinosis with hypogammaglobulinemia caused by heterozygous mutations of 2′-5′-oligoadenylate synthase 1

48. Flow cytometry-based diagnosis of primary immunodeficiency diseases

50. Hematopoietic stem cell transplantation for pulmonary alveolar proteinosis associated with primary immunodeficiency disease

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