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1. A case of T-cell acute lymphoblastic leukemia in retroviral gene therapy for ADA-SCID

2. FLT3L governs the development of partially overlapping hematopoietic lineages in humans and mice

3. Severe hematopoietic stem cell inflammation compromises chronic granulomatous disease gene therapy

4. T cell dynamics and response of the microbiota after gene therapy to treat X-linked severe combined immunodeficiency

5. Long-term outcomes of lentiviral gene therapy for the β-hemoglobinopathies: the HGB-205 trial

6. INSPIIRED: A Pipeline for Quantitative Analysis of Sites of New DNA Integration in Cellular Genomes

7. INSPIIRED: Quantification and Visualization Tools for Analyzing Integration Site Distributions

8. Retrieval of vector integration sites from cell-free DNA

9. A DL-4- and TNFα-based culture system to generate high numbers of nonmodified or genetically modified immunotherapeutic human T-lymphoid progenitors

11. Single-cell analysis of FOXP3 deficiencies in humans and mice unmasks intrinsic and extrinsic CD4+ T cell perturbations

12. Transient mTOR inhibition rescues 4-1BB CAR-Tregs from tonic signal-induced dysfunction

16. Late-onset enteric virus infection associated with hepatitis (EVAH) in transplanted SCID patients

18. OC 9 - HOMOZYGOUS CBL MUTATION IN B LYMPHOCYTES AFTER CBL-DRIVEN JMML IMPAIRS B CELL MATURATION, FUNCTION AND ANTIBACTERIAL IMMUNITY

19. Single-cell analysis reveals the continuum of human lympho-myeloid progenitor cells

20. Human kidney-derived hematopoietic stem cells can support long-term multilineage hematopoiesis

21. Genotoxic Signature in Cord Blood Cells of Newborns Exposed In Utero to a Zidovudine-Based Antiretroviral Combination

25. Long-Term Follow-up Study after Lentiviral Hematopoietic Stem/Progenitor Cell Gene Therapy for Wiskott - Aldrich Syndrome

26. Clinical Results of the Drepaglobe Trial for Sickle Cell Disease Patients

27. Outcomes Following Gene Therapy in Patients With Severe Wiskott-Aldrich Syndrome

30. A Modified γ-Retrovirus Vector for X-Linked Severe Combined Immunodeficiency

33. A combination of cyclophosphamide and interleukin-2 allows CD4+ T cells converted to Tregs to control scurfy syndrome

34. Monoubiquitination and endocytosis direct [gamma]-secretase cleavage of activated Notch receptor

35. The Notch ligand Delta1 is sequentially cleaved by an ADAM protease and [gamma]-secretase

36. CD28 costimulatory domain protects against tonic signaling-induced functional impairment in CAR-Tregs

37. Single cell analysis of FOXP3 deficiencies in humans and mice unmasks intrinsic and extrinsic CD4+ T cell perturbations

38. Clonal tracking in gene therapy patients reveals a diversity of human hematopoietic differentiation programs

39. Heterogeneity of human lympho-myeloid progenitors at the single cell level

40. Dynamics of Thymus-Colonizing Cells during Human Development

41. Occurrence of myelodysplastic syndrome in 2 patients with reticular dysgenesis

42. Additional file 2: of T cell dynamics and response of the microbiota after gene therapy to treat X-linked severe combined immunodeficiency

43. Extensive multilineage analysis in patients with mixed chimerism after allogeneic transplantation for sickle cell disease: insight into hematopoiesis and engraftment thresholds for gene therapy

45. Single-cell analysis of FOXP3 deficiencies in humans and mice unmasks intrinsic and extrinsic CD4+T cell perturbations

46. Single-cell analysis reveals the continuum of human lympho-myeloid progenitor cells

47. Single cell assays unveil functional and transcriptional heterogeneity of human hemopoietic lympho-myeloid progenitors

48. INSPIIRED: A Pipeline for Quantitative Analysis of Sites of New DNA Integration in Cellular Genomes

49. INSPIIRED: Quantification and Visualization Tools for Analyzing Integration Site Distributions

50. a Diversity of Human Hematopoietic Differentiation Programs Identified through In Vivo Tracking of Hematopoiesis in Wiskott-Aldrich Syndrome Patients

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