Sentence examples for bone marrow cell transfer from inspiring English sources

To test for successful adoptive bone marrow cell transfer, Tlr3 expression in peripheral blood leukocytes from reconstituted mice was determined 6 weeks after reconstitution using quantitative real-time PCR analysis before proceeding with infection.

A similar observation was made when PECAM-1−/ PECAM-1−/row cells were transferred into PECAM-1−/− mice, suggesting that deletion of PECAM-1 on either the bone marrow precellsr cells or the vasculature is sufficient to lead to observed phenotype, consistent were loss of homophilic intransferredbetween PECAM-1 expressed on HSC and the bone marrow vasculature.

Interestingly, protection against tumour development was restored when MMP-8-containing bone marrow cells were transferred back into these animals (Balbin et al, 2003).

One mouse from the group of animals transplanted with the relapse sample was killed at day 106 and bone marrow cells were transferred to secondary recipients (10 cells per mice).

Furthermore, culture medium obtained from the damaged osteocytes could induce TRACP-positive cells in bone marrow cell culture.

BMC: bone marrow cell.

Therefore, Tcra−/− Relb+/+ bone marrow cells were adoptively transferred into lethally irradiated Tcra−/− Relb−/− (Tcra−/−→Tcra−/− Relb−/−) or Tcra−/− Relb+/− (Tcra−/−→Tcra−/− Relb+/−) recipient mice.

In these experiments, donor female Tcra−/− bone marrow cells were adoptively transferred to male recipients, so efficient thymus reconstitution by donor cells could be ascertained by the presence of X-chromosome-specific genomic sequences, as detected by PCR, and the absence of Y-chromosome-specific sequences in thymocytes from chimeric recipient mice (Figure S10B).

Since the resistance of LTβR deficient mice to ECM development was not corrected by wild-type bone marrow reconstitution, the data suggest that LTβR expression on radioresistant, stromal probably endothelial cells determines the sensitivity to ECM and bone marrow cells from LTβR can not transfer ECM resistance to sensitive wild-type mice.

Irrespective of the genotype of the transferred bone marrow cells, PI3Kγ−/− recipient mice exhibited similar inflammation at the site of infarction (Figure 3E).

To distinguish between a role of erythrocyte and endothelial DARC to EAE pathogenesis, we generated reciprocal bone marrow chimeras by transferring bone marrow cells from Darc−/− C57BL/6 mice into lethally irradiated wild-type C57BL/6 mice and vice versa.