Sentence examples for rat to identify from inspiring English sources

We performed in vivo phage display in the stroke prone spontaneously hypertensive rat, a cardiovascular disease model, and the normotensive Wistar Kyoto rat to identify cardiac targeting peptides, and then assessed each in the context of viral gene delivery.

First, a pathologist reviewed the gross tumor tissue blocks in paraffin that was processed from rat 9 the reference rat, to identify and delineate the viable portion of the tumor by its macroscopic morphology, and the delineation was validated using microscopic examination of the associated H&E stains (Fig. 3).

In the past, we used a specific nomenclature in the rat to identify MCH neuron sub-populations [23]: MCH type A neurons for spinally MCH projecting cells, and MCH type B neurons for MCH/CART cortically projecting cells [13],[13],[13].

Next, we used the Recombination Analysis Tool (RAT) to identify possible recombination events in the genomes of the four types of mitochondria.

The hormonal effects of TT were evaluated in primates, rabbits and rats to identify its usefulness in the management of ED [54].

Firstly, we implanted the Matrigel, a carrier of basement membrane matrix, into the abdominal skin of rats to identify the relevant components of the NGF-P-FAK signaling pathway related to angiogenesis.

As vasoregression developed in the second month of life in TGR rats, to identify the genes involved in vasoregression, we compared 3-month old TGR and control rats with these groups at 1-month of age, i.e. at the onset of neurodamage.

The aim of the present study was to characterize the expression pattern of newly identified PDEs (PDE7-PDE11) in lung tissue and primary PASMCs from control and MCT-PH rats to identify potential therapeutic targets in the PDE family that are involved in the pathogenesis of PAH.

Proliferative activity was not varied The results on SU reinforce the validity of Pirc rats to identify chemopreventive products.

We chose to compare muscles from 15-month-old adult and 32-month-old aged FBN rats to identify primary markers of sarcopenia.

We first wanted to assess cartilage turnover levels in normal Sprague Dawley rats, to identify the age at which the turnover stabilizes.