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1 of MDS/AML (RR = 1.8; P =.12) compared with bone marrow grafts.
2 radiated mice receiving fully MHC-mismatched bone marrow grafts.
3 rs of T cells in unmanipulated PBSCs than in bone marrow grafts.
4 nts receiving blood transfusions or organ or bone marrow grafts.
5 n of allogeneic, xenogeneic and missing self bone-marrow grafts.
6 he primary host barrier cells that recognize bone marrow grafts bearing hematopoietic histocompatibil
8 al studies, we added mature donor T cells to bone marrow grafts combined with heart grafts, and compa
13 sk [RR] = 1.4; P < .0001), blood cell versus bone marrow grafts in patients age 18 to 39 years (RR =
14 neous pregnancy and healthy childbirth after bone marrow grafting is relatively rare due to irradiati
15 24 weeks after transplantation, and hCD34(+) bone marrow grafts of primary recipients could reconstit
16 agalTCR T cells in arrbetagal mice by use of bone marrow grafts, or double-transgenic mice, also gave
17 Because T cells and NK cells are critical in bone marrow graft rejection, our purpose was to examine
20 nd older versus age 18 to 39 years receiving bone marrow grafts (RR = 1.44; P = .0005), CML versus AM
21 isease (GVHD) was lower with T-cell-depleted bone marrow grafts; T-cell-depleted grafts were not asso
22 oreover, these data support the results from bone marrow grafts that circulating CD11b+ cells can ent
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