This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. We have shown that genetic engineering of autologous stem cells to induce molecular chimerism can be used to establish B cell tolerance in mice. To determine whether a similar approach could be used in Rhesus macaques, we investigated whether induction of molecular chimerism could affect production of antibodies specific for the epitope Gal alpha1-3Gal beta 1-4GlcNAc-R (alpha Gal)
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