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51. Editing central memory T-lymphocyte specificity for safe and effective adoptive immunotherapy of leukaemia

52. Loss of mismatched HLA as a mechanism of leukemia immune escape in family haploidentical and unrelated HSCT: updated analysis of 113 transplants from alternative donors

53. Transplantation Outcome By Disease Risk and Donor Type over Time: An Analysis of 100,000 Allogeneic Stem Cell Transplantation on Behalf of the Acute Leukemia Working Party of the EBMT

54. Cell-Specific Transcriptional Regulatory Domains Attract Gamma Retroviral Integration in the Human Genome

55. Leukemic Dendritic Cells Expand Central Memory T Lymphocytes From HCT Donors Able to React against the Original Leukemia in Vitro and In Vivo

56. GENOMIC LOSS OF MISMATCHED HLA IN LEUKEMIA IS A MAJOR MECHANISM OF IN VIVO ESCAPE FROM T CELL IMMUNOSURVEILLANCE FOLLOWING HAPLOIDENTICAL HEMATOPOIETIC STEM CELL TRANSPLANTATION

57. Loss of Mismatched HLA as a Mechanism of Leukemia Immune Escape in Family Haploidentical and Unrelated HSCT: Analysis of 103 Transplants From Alternative Donors

59. Immune Reconstitution and Immune Correlates of Clinical Outcome in Acute Leukemia Patients Treated with Haploidentical stem cell transplantation

60. Thiotepa-cyclophosphamide high-dose immunosuppressive therapy with autologous haematopoietic stem cell transplantation in aggressive forms of multiple sclerosis: results in 9 patients

62. Rapamycin-based GvHD prophylaxis after T-cell replete unmanipulated haploidentical peripheral stem cell transplantation for advanced leukaemias: preliminary results of the TrRaMM study

64. SECOND ALLOGENEIC STEM CELL TRANSPLANTATION AS SALVAGE TREATMENT IN RELAPSED HAEMATOLOGICAL MALIGNANCIES: FEASIBILITY AND OUTCOME IN 26 PATIENTS

66. Trapianto di cellule staminali ematopoietiche

67. Suicide gene therapy of GvHD fully preserves immunocompetence after haploidentical hemopoietic cell transplantation

68. Targeted disruption of t cell receptor genes using engineered zinc finger protein nucleases

69. Immunostimulatory leukemic dendritic cells can efficiently expand leukemia-reactive T cells from HSCT donors

72. T Cell Receptor Gene Transfer into Early Differentiated Lymphocytes by Lentiviral Vectors for Safe and Effective Adoptive Immune Therapy of Leukemia

73. REQUIREMENTS FOR RETROVIRAL TARGETING OF A SUICIDE GENE TO ALLOREACTIVE SELF-RENEWING MEMORY LYMPHOCYTES FOR ADOPTIVE IMMUNOTHERAPY OF LEUKEMIA

74. Efficient differentiation of primary and secondary acute myeloid leukaemias into functionally competent leukaemic dendritic cells to improve graft-versus-leukemia effect

75. Efficient differentiation of primary and secondary acute myeloid leukemias into functionally competent leukemic dendritic cells to improve the graft versus leukemia effect

77. TK007 phase II study final analysis. Genetically modified donor lymphocytes abate transplant related mortality and increase leukaemia-free survival providing early immune reconstitution after haploidentical haematopoietic stem cell transplantation

78. Direct antigen presentation by leukemic dendritic cells promotes expansion of allogeneic leukemia-reactive T lymphocytes

81. SUICIDE GENE TRANSFER INTO DONOR LYMPHOCYTES ALLOWS EARLY AND EFFECTIVE IMMUNE-RECONSTITUTION AFTER FAMILY HAPLOIDENTICAL HEMATOPOIETIC STEM CELL TRANSPLANTATION FOR LEUKEMIAS: RESULTS OF THE TK007 STUDY

82. Genomic Loss of the Mismatched HLA Locus in Leukemia Is a Major Mechanism of in Vivo Escape from T Cell Immunosurveillance Following Haploidentical HSCT

83. Targeting of a therapeutic suicide gene to human alloreactive memory T-cells with stem-cell features requires IL-7 and IL-15

84. The effect of donor-recipient KIR ligand incompatibility after haploidentical hematopoietic stem cell transplantation is overruled by biological characteristics of early reconstituting NK cells with impaired graft versus leukemia activity

85. Suicide gene therapy with central memory human T lymphocytes for a graft-versus-leukemia effect and control of graft-versus-host disease

87. Temporal, quantitative and functional characteristics of Single-KIR positive alloreactive NK cell recovery account for impaired graft versus leukemia activity after haploidentical HSCT

88. High alloreactive potential of suicide gene expressing central memory T lymphocytes cultured with homeostatic Gamma-chain cytokines for the cure of hematological malignancies

89. Infusions of HSV-TK engineered donor lymphocytes promote the expansion of host-restricted viral-specific T lymphocytes and protect patients undergoing haploidentical stem cell transplantation from infectious mortality

90. Impaired GvL potential of natural killer cells early reconstituting following haploidentical HSCT

91. Rapid and effective immune reconstitution with HSV-TK engineered donor lymphocyte add-backs after Haplo-HSCT

92. High alloreactive potential of central memory T-lymphocytes expressing a suicide gene for the cure of hematologic malignancies

93. Haematopoietic chimerism after T-cell depleted stem cell transplantation: early detection of host chimerism by patient-specific HLA alleles analysis is a sensitive marker for relapse of high-risk haematologic malignancies

94. Foscarnet is an effective pre-emptive treatment of cytomegalovirus reactivation after T-cell depleted haploidentical stem cell transplantation

96. Infusions of HSV-TK genetically modified donor lymphocytes enable a wider use of partially mismatched allogeneic transplantation by reducing infection related mortality and improving survival in high risk acute leukemia

97. Secondary SOLID Tumors after Allogeneic STEM CELL Transplantation: A CROSS-Sectional Evaluation in 260 Adults at 1-Year Follow-up

99. Suicide gene therapy of graft-versus-host disease induced by central memory human T lymphocytes

100. Engraftment of CD34+ haplo-identical allogeneic cells after a non-TBI conditioning and ATG Fresenius: a single-centre experience in 30 patients

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