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pneumoniae were detected in tissue lysate from control (vehicle-inoculated) mice (n = 2)

We observed a significant decrease in MMP-2 activity and a significant increase in MMP-9 activity in GGC-treated cells, suggestive of the differential effect of GGC and increased GSH on MMPs

Pramlintide was generally well-tolerated and approximately 90% of the pramlintide-treated subjects were able to escalate to the highest dose of 240 g three times a day

(155) found that a molecular driver of early onset IBD, specifically CD, is the recessive inheritance of NOD2 alleles, most likely a consequence of impaired NOD2 protein activity