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We demonstrate that administration of cystamine, which is rapidly metabolized to cysteamine, could completely prevent HIT in the murine model.
Our preliminary data demonstrate that administration of NXY-059 (60 mg/kg/h for 24 h) ameliorates cortical infarction in rats subjected to permanent focal cerebral ischemia with 24 h survival.
Our findings demonstrate that administration of CDDO-MA reduced the striatal lesion volumes by more than 70%.
Notably, we demonstrate that administration of testosterone could largely rescue the hypogonadal and spermatogenetic defects in the mutant animal.
The results of this study demonstrate that administration of a selective kisspeptin antagonist profoundly suppressed pulsatile LH secretion in the rat.
Our data demonstrate that administration of gremlin siRNA plasmid to diabetic mice alleviated renal hypertrophy, cell proliferation and apoptosis, and subsequently suppressed collagen type IV accumulation and mesangial expansion, indicating beneficial effects of Gremlin inhibition on diabetic nephropathy.
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Several previous studies have demonstrated that administration of autologous bone marrow derived mononuclear cells (BMMNCs) improves cardiac function in patients after acute myocardial infarction (AMI).
One study has demonstrated that administration of anti-miR-200c-5p anti-miR-200c-5p anti-miR-200c-5p anti-miR-200c-5prespoligonucleotideinjury by inhibiting the downregulattenuatesual-spulmonaryy phosphatase 1 inflammatoryduced mouse model.
Initial results demonstrated that administration of BMP9 is capable of reversing PAH in these rodents.
The results of this study demonstrated that administration of 2 mg sublingual buprenorphine effectively reduced pain in patients with acute renal colic.
It has been demonstrated that administration of OHDHA increases the concentration of PUFAs-containing phospholipids (e.g. DHA or EPA-containing phospholipids).
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