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1 e and should, therefore, be considered fully histocompatible.
4 us group of patients each of whom received a histocompatible bone marrow transplant from a sibling, i
5 A-affected C3H/HeJ mice induced hair loss in histocompatible C3H/OuJ mice (four of 13) and normal C3H
7 enesis (pES cells) are a potential source of histocompatible cells and tissues for transplantation.
10 re generated in vivo by immunizing mice with histocompatible dendritic cells that had been exposed to
16 lood, Locatelli et al compare the results of histocompatible family donor bone marrow and cord blood
18 hat the forced intrathymic administration of histocompatible HSCs can sustain long-term thymopoiesis
20 model in which two genetically different yet histocompatible kidneys are chronically and simultaneous
25 cells with defined epitope specificity into histocompatible mice and the subsequent detection of the
26 cific Th1 cells alone did not protect BALB/c histocompatible mice, indicating that additional immune
28 at underwent transplantation with syngeneic (histocompatible) or allogeneic (histoincompatible) T lym
30 ne cell-based rejection that operates within histocompatible pairs and that maximal allogeneic respon
35 tation is not feasible due to age, lack of a histocompatible sibling, co-morbidities, or by patient c
37 include the need for efficient derivation of histocompatible stem cells and the zoonotic risk inheren
38 ating an unlimited supply of rejuvenated and histocompatible stem cells for the treatment of cardiac
39 d exogenous HSCs into unconditioned congenic histocompatible strains of mice, we show that approximat
40 ortin 1 and hepcidin responses in mice given histocompatible T cells, whereas mice given histoincompa
47 ame apparent that neither knockout strain is histocompatible with the putative control and that the p