Sentence examples for mouse was infused from inspiring English sources

DR1 mice (n = 10 for each group) were immunized with CII/CFA, and on day 23 after immunization, when arthritis was established, each mouse was infused intravenously with 5 × 105 cells of either Vβ8, Vβ14+ T cells or Vβ8, Vβ14- T cells.

Furthermore, a separate group of NOD/Scid mice was infused with TCRγδ/NK-depleted, FACS-sorted DNCD3 splenocytes (5×105 cells/mouse) isolated from 14 day-old NOD females followed by co-infusion of diabetogenic cells (5×105 cells/mouse) 1 month later.

For this, a group of NOD/Scid mice was infused with in vitro CFSE-labeled DNCD3 splenic cells (5×106 cells/mouse) that were FACS-sorted from a pool of 14 day-old NOD female mice, and 7 days later the CFSE+ cells were harvested from the spleen and pancreas of recipient mice and the cell cycle division was measured by FACS in the CD3-gated population.

1.0 μL of virus suspension or saline solution (sham mice) was infused to the CA1 region of the hippocampus (−2.0 mm AP, ±1.7 mm ML, −2.0 mm DV to bregma) according to the Paxinos and Watson mouse brain atlas (1998).

The irradiated mice were infused with a mix of hematopoietic stem cells, of which half expressed PrP and half didn't.

Vehicle mice were infused only with physiological solution, whereas control mice with recombinant human IgG1 Fc only.

To determine the role of TNF in the bone loss induced by PTH, WT and TNF−/− mice were infused with cPTH for 2 weeks.

To evaluate the precision of measurements of dead cells in fresh samples, NOD mice were infused with 5×107 PKH-labeled dead autologous splenocytes.

To examine if TLR4 is necessary for the detection of LPS in the endometrium, WT and Tlr4−/− mice were infused intrauterine with 100 µl of vehicle or 100 µg ultrapure LPS from E. coli O111 B4.

To see whether FGF19v also exhibited reduced ability to induce hepatocyte proliferation in vivo, mice were infused with FGF19, FGF19v (1 ng/h) or vehicle control by osmotic mini-pump.

Groups of 1 2 month-old NOD/Scid female mice were infused i.p. with either diabetogenic spleen cells from hyperglycemic NOD mice (control diabetes), or FACS-sorted DNCD3 splenic cells, or co-infused with FACS-sorted DNCD3 splenic cells and diabetogenic cells, or TCRγδ /NK-depleted, FACS-sorted DNCD3 splenic cells from young NOD or NON.NOD (control) mice.