Exact(1)
These variations, for which we provide some prominent examples for different parts of skin from children and adult humans as well as from newborn and adult rats, indicate a close association of the specific cellular localization of GS with different functional and structural features of skin.
Similar(59)
After treatment with Cd at doses of 3.0, 3.5 and 4.5 mg/kg, the hepatic and renal accumulation of Cd was significantly lower in the WI rats than in the Fischer rats, indicating a kinetic mechanism for the observed strain differences in Cd toxicity.
Assessment of brain ketone metabolism in rats indicated a 7 to 8 fold increase in 11C-acetoacetate under ketone dietary treatment [86, 87].
Not so for the injected rats: They showed about one-fourth the freezing behavior of uninjected rats, indicating a much weaker memory, Miller and Sweatt report online today in Neuron.
A decreased E/A ratio in immunized rats indicated a diastolic dysfunction.
In addition, the lowest plasma cholesterol value was found in PP rats, indicating a long-term impact of the maternal metabolic status on these parameters.
In concordance with our results another study of the same group showed a reduced daily food intake over a two-week ICV treatment period with IL-6 in rats indicating a different pattern of response between rats and mice [46].
However, the maximal caffeine-induced increase of [Ca2+]i in SUS+Rec-3 d rats was similar to that obtained in CON-28 d rats, indicating a complete recovery of ryanodine-sensitive Ca2+ releases in cerebral VSMCs (Fig. 4 and Fig. 6Ab).
Stress-induced ventricular arrhythmias were reduced by about a half following GF injection, while no changes were observed in untreated rats, indicating a protective effect of local delivery of cytokines.
The co-localization of OX1R INS in the pancreas of normal Wistar rats indicates a functional role for OX1R in the regulation of insulin metabolism and consequently that of glucose.
This impairment was not observed in mesenteric arteries of GLO-I transgenic rats indicating a specific intracellular methylglyoxal effect.
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