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1 DC and myeloid development using a series of radiation chimeras.
2 h tissue-specific targeted mouse mutants and radiation chimeras.
3 CD4:CD8 phenotype could be reconstituted in radiation chimeras.
4 that deletion is efficient in reconstituted radiation chimeras and is B cell, CD28, inducible costim
5 dependent autoimmune manifestations shown by radiation chimeras and thymic transplants in nude mice,
9 sms in HSV-2 tk- OVA clearance was tested in radiation chimeras by adoptive transfer of wild-type or
12 (mCMV) using VIP-knockout (VIP-KO) mice and radiation chimeras engrafted with syngenic VIP-KO hemato
17 for B-1-cell tolerance, we generated GalT-/- radiation chimeras in which CR1/CR2 was expressed on eit
18 Early virus clearance was demonstrated in radiation chimeras in which IFN-gammaR expression was li
22 mouse skin allograft model and an allogeneic radiation chimera model to examine the role of MHC Ags i
23 y normal bone marrow environment using mixed radiation chimeras, NKAP deletion results in HSC failure
25 s of Sle1 are completely reconstituted in B6 radiation chimeras receiving B6.NZMc1 bone marrow but no
26 ith genetic ablation of CTLA-4, we have used radiation chimeras reconstituted with a mixture of CTLA-
27 failure and lethality is cell intrinsic, as radiation chimeras reconstituted with inducible Mx1-cre
33 NFR1/RelA-deficient embryonic tissues and of radiation chimeras suggest that the dependence on RelA i
35 sent study, we used Bambi-deficient mice and radiation chimeras to evaluate the function of this rece
36 tudy we have used PECAM-1-deficient mice and radiation chimeras to investigate the function of this r
40 nd that peripheral deletion was defective in radiation chimeras with non-functional tissue FasL, rega
41 tablished model of atherosclerosis, creating radiation chimeras with NZM2410-derived, lupus-susceptib
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