Exact(3)
Ning et al. [68] have observed that diosgenin could significantly reduce the pathological expression and degree of myocardial ischemia, reduce myocardial infarction, dilate the coronary arteries, increase myocardial blood supply, and improve the function of vascular endothelial cells in the acute dog experimental myocardial ischemia model.
To study the effect of oral treatment with PD200347, a gabapentinoid (GBP), on osteoarthritis (OA) progression and OA mediators, matrix metalloproteases (MMPs) and the inducible form of nitric oxide synthase (iNOS) expression in a dog experimental model of OA.
This is supported by a previous report in a dog experimental OA model (anterior cruciate ligament model) showing that the protective effect of SrRan was associated with a reduction in the levels of pro-catabolic factors such as proteases and cytokines (IL-1β) in the diseased tissues [ 31].
Similar(57)
However, all dogs (experimental and control groups) had a slight increase in the firmness of the testes on palpation from 24 hours PI and until PI days 3-7.
Generally, trained dogs, including search and rescue dogs, look at humans less than untrained dogs in experimental paradigms requiring dogs to solve a problem such as opening a container (Marshall-Pescini et al. 2009, 2008; Prato-Previde et al. 2008).
The reason for the differing results of the two studies is unclear but the use of different species (e.g., man versus dog) and experimental preparations (eg, in vitro versus in vivo) may be, at least in part, responsible.
There are no approved antimicrobials for the treatment of LD in dogs and because it is difficult to induce clinical disease in dogs by experimental infection, the optimal use of available antibiotics and duration of treatment are unknown [ 1].
can safely protect adult dogs against experimental challenge inoculation with infective heartworm larvae for a period of 12 months.
Paradoxically, not only nociceptors, but non-neuronal cells, including keratinocytes express full length TRPV1 mRNA, while patient dogs and experimental animals that underwent topical treatment or anatomically targeted molecular surgery have shown neither obvious behavioral, nor pathological side effects.
This was also found in dogs with experimental hydrocephalus [ 20].
Starting in the summer of 1923, Dunkin began to create purpose-bred dogs for experimental work on distemper.
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