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The immunosuppressed mouse model was induced by cyclophosphamide.
A subcutaneous xenograft nude mouse model was established.
An encephalitis mouse model was established via intracranial HV administration.
Liver-injured mouse model was established by CCl4 injection.
A nude mouse model was utilized to demonstrate the osteoinductive potential of the scaffold in vivo.
Their Veloc-Immune mouse model was an idea which evolved during a "think tank" meeting.
DMP1-Tg mouse model was created with Gateway, a bacteriophage-based homologous recombination method by Cyagen Bioscience Inc. (Guangzhou, China).
The only problem encountered with the PDX mouse model was engraftment latency in some animals of the first passage.
S89G-DMP1 knock-in point mutation mouse model was created with homologous recombination method by Beijing Biocytogen Co., Ltd, China.
These conditions are similar to previous studies in which this mouse model was used [4, 5, 21, 22].
In the present study, the mouse model was infected with S. aureus to cause mammary gland inflammation.
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