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Better understanding of strain and location-dependant variation in murine GTMs has obvious implications for the use of animals as experimental models.
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Various studies using PCR-DGGE and cluster analyses of human [16], [17] and murine GTMs [18], [19] for example, have indicated the occurrence of host-specific predominant mucosa-associated and luminal bacterial community profiles.
Evidence is emerging to suggest a considerable degree of individuality and temporal stability within human and murine GTMs.
The peptide sequence and production of the murine hybridoma has been described [[6]].
The effect of Helicobacter infections on murine reproduction has not been well studied.
Murine MRJ has been shown to be essential for murine placental development [ 4].
Neff, F. et al. Rapamycin extends murine lifespan but has limited effects on aging.
The human and murine data have been compiled and mapped in Supplementary Figure 3.
The rare reports of transformation reported for murine MSCs have not been noted for human.
Primers for murine Prdm1, Bcl6, and Tbx21; primers for murine Eomes; and primers for murine Tcf7 have been reported previously.
As yet, murine aortic grafts have merely been monitored histopathologically.
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