249 results on '"Onodera, Masafumi"'
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2. Melting temperature mapping method in children: Rapid identification of pathogenic microbes
3. A novel mucopolysaccharidosis type II mouse model with an iduronate-2-sulfatase-P88L mutation
4. Myelodysplasia after clonal hematopoiesis with APOBEC3-mediated CYBB inactivation in retroviral gene therapy for X-CGD
5. Enhanced osteoblastic differentiation of parietal bone in a novel murine model of mucopolysaccharidosis type II
6. Corrigendum to “Enhanced osteoblastic differentiation of parietal bone in a novel murine model of mucopolysaccharidosis type II” [Molecular Genetics and Metabolism Reports Vol. 37, December 2023, 101021]
7. Severe Liver Disorder Following Liver Transplantation in STING-Associated Vasculopathy with Onset in Infancy
8. A Distinct Feature of T Cell Subpopulations in a Patient with CHARGE Syndrome and Omenn Syndrome
9. Melting temperature mapping method in children: Rapid identification of pathogenic microbes
10. Chromosomal translocation t(11;14) and p53 deletion induced by the CRISPR/Cas9 system in normal B cell-derived iPS cells
11. Foxo in T Cells Regulates Thermogenic Program through Ccr4/Ccl22 Axis
12. Lipid peroxidation and the subsequent cell death transmitting from ferroptotic cells to neighboring cells
13. Prospective Study of Live Attenuated Vaccines for Patients with Nephrotic Syndrome Receiving Immunosuppressive Agents
14. A prospective study of allogeneic transplantation from unrelated donors for chronic granulomatous disease with target busulfan-based reduced-intensity conditioning
15. Peripheral immune system modulates Purkinje cell degeneration in Niemann–Pick disease type C1
16. Ferroptosis model system by the re-expression of BACH1
17. Colonic Pro-inflammatory Macrophages Cause Insulin Resistance in an Intestinal Ccl2/Ccr2-Dependent Manner
18. Haploinsufficiency of A20 caused by a novel nonsense variant or entire deletion of TNFAIP3 is clinically distinct from Behçet’s disease
19. Safety and efficacy of elapegademase in patients with adenosine deaminase deficiency: A multicenter, open‐label, single‐arm, phase 3, and postmarketing clinical study.
20. National Survey on Clinical Practice of Gene Therapy using Adeno-associated Virus Vector ―The Actual Status and Hurdle on Clinical Practice in Gene Therapy for Spinal Muscular Atrophy―
21. Attempts to Induce t(11;14) during Redifferentiation of Normal B Cell-Derived Ips Cells to Study Myeloma-Initiating Cells
22. LBODP008 Gene Therapy For Congenital Adrenal Hyperplasia With AAV Vectors Into Fibroblasts, IPS Cells And Model Mice
23. Persistent Impairment of T-Cell Regeneration in a Patient with Activated PI3K δ Syndrome
24. Adeno-Associated Virus-Mediated Gene Therapy for Patients' Fibroblasts, Induced Pluripotent Stem Cells, and a Mouse Model of Congenital Adrenal Hyperplasia
25. X‐linked agammaglobulinemia complicated with pulmonary aspergillosis
26. Fecal Calprotectin Rise in Chronic Granulomatous Disease-Associated Colitis
27. Curative haploidentical BMT in a murine model of X-linked chronic granulomatous disease
28. Outcomes in Two Japanese Adenosine Deaminase-Deficiency Patients Treated by Stem Cell Gene Therapy with No Cytoreductive Conditioning
29. Interstitial Lung Disease with Multiple Microgranulomas in Chronic Granulomatous Disease
30. Nonconditioned ADA-SCID gene therapy reveals ADA requirement in the hematopoietic system and clonal dominance of vector-marked clones
31. Normal B Cell-Derived iPSCs Capable of Inducing RAS Mutants and Aid to Explore Myeloma-Initiating Cells
32. Production of therapeutic iduronate‐2‐sulfatase enzyme with a novel single‐stranded RNA virus vector
33. Basiliximab treatment for steroid-resistant rejection in pediatric patients following liver transplantation for acute liver failure
34. Prospective Study of Allogeneic Hematopoietic Stem Cell Transplantation with Post-Transplantation Cyclophosphamide and Antithymocyte Globulin from HLA-Mismatched Related Donors for Nonmalignant Diseases
35. Evaluation methods for biodistribution, safety and efficacy of gene therapy products
36. X-linked inhibitor of apoptosis protein deficiency complicated with Crohn's disease-like enterocolitis and Takayasu arteritis: A case report
37. Digenic mutations in ALDH2 and ADH5 impair formaldehyde clearance and cause a multisystem disorder, AMeD syndrome
38. Chromosomal Translocation t(11;14) Induced By the Cre-Loxp System in Normal B Cell-Derived Ips Cells for the Study of Myeloma-Initiating Cells
39. A Distinct Feature of T Cell Subpopulations in a Patient with CHARGE Syndrome and Omenn Syndrome
40. Aspects of Gene Therapy Products Using Current Genome-Editing Technology in Japan
41. Bacillus Calmette-Guérin (BCG) Infections at High Frequency in Both AR-CGD and X-CGD Patients Following BCG Vaccination
42. A chemical genomics-aggrephagy integrated method studying functional analysis of autophagy inducers
43. Introduction of Chromosomal Translocation t(11; 14) and a p53 Deletion into Normal B Cell-Derived iPSCs to Elucidate the Cellular Origin of Myeloma Cells
44. Bacillus Calmette-Guérin (BCG) Infections at High Frequency in Both AR-CGD and X-CGD Patients Following BCG Vaccination.
45. Additional file 1: of Haploinsufficiency of A20 caused by a novel nonsense variant or entire deletion of TNFAIP3 is clinically distinct from Behçet’s disease
46. Additional file 2: of Haploinsufficiency of A20 caused by a novel nonsense variant or entire deletion of TNFAIP3 is clinically distinct from Behçet’s disease
47. A chemical genomics-aggrephagy integrated method studying functional analysis of autophagy inducers.
48. Infectivity Assessment of Recombinant Adeno-Associated Virus and Wild-Type Adeno-Associated Virus Exposed to Various Diluents and Environmental Conditions
49. Establishment of immunity against Epstein‐Barr virus infection in a patient with CHARGE/complete DiGeorge syndrome after peripheral blood lymphocyte transfusion
50. Thymitis in chronic granulomatous disease
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