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Mice were monitored daily for neurological impairment at which time they were killed and brains were removed to evaluate for tumor development.
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This report describes the research results that the cathode catalyst after a 9000 h cell operation has been removed to evaluate the O2 reduction reaction (ORR) and H2O2 generation amount during the ORR.
Organs and plasma are removed to evaluate inflammation and oxidative stress by q-RT-PCR, insulinemia by ELISA test and insulin pathway by Western blot.
At the end of the collection period for hepatic bile the intestine was removed to evaluate contractile responses of smooth muscle [ 9].
The animals were sacrificed at 2, 4, and 8 weeks; the surrounding tissue along with the implant was removed to evaluate biocompatibility and biodegradability by histologic analysis and GPC, respectively.
After mouse euthanasia, esophagus, stomach and cecum were aseptically removed to evaluate C. albicans colonization.
Since insulin injections prevent an accurate measure of endogenous insulin and glucose levels, the 2 OB/D subjects treated with insulin were removed prior to evaluating insulin resistance with the HOMA.
The trigeminal ganglion (TG) and cervical spinal cord (CSC) ipsilateral to the formalin injection and medulla-pons in toto of each animal were removed and processed to evaluate expression levels of the genes encoding for c-Fos (c-fos), TRPA1 (Trpa1), CGRP (Calca) and SP (PPT-A).
Thoracic and abdominal aortas were removed in order to evaluate VC, by von Kossa staining and calcium content quantification, respectively.
Similarly rRNA- and tRNA-related clusters were removed by evaluating the genomic localization of their elements, relative to genes encoding stable RNAs.
At the specified times, rats were sacrificed and leg muscles were removed and evaluated.
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CEO of Professional Science Editing for Scientists @ prosciediting.com