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ATM-serine 1981 and CHEK2-threonine 68 phosphorylation was highest one hour after irradiation and declined subsequently, staying above steady-state level six hours later.
Protein and fluorescence levels were highest one hour p.i., but the amount of native LigA decreased significantly (from 5.95-fold to 4.04-fold), while the fluorescence level produced by the PAG reporter strain remained constant (from 2.07-fold to 2.03-fold).
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Turn on high for one hour and then set to low for about six hours.
In the SE + PEEP group, the AFC rate was higher at one hour than at subsequent time points and higher than in the SE group (45.4% vs. 19.4% at one hour, P < 0.05).
No side effects were observed, except for a high drowsiness one hour after the administration of cannabis oil (p<0.01).
When fasted animals were then given the opportunity to eat, oxyntomodulin levels in the blood increased within 20 minutes, and remained high for one hour.
Incubation of the eluted LVs in the high salt buffer for one hour on ice resulted in a significant reduction of infectivity by 16.0 ± 6.4%.
Subsequently all groups were rested in basal glucose for 30 minutes, and stimulated with high glucose for one hour prior to collection of samples for insulin assay.
Others observed a reduction by 50% of infectious retroviral particles when exposed to high salt for one hour at room temperature [ 32].
Compound 4 (650 mg, 1.04 mmol) and 4- dimethylamino pyridine (205 mg, 1.68 mmol) were weighed into an oven dried flask containing a magnetic stirring bar and were dried over potassium hydroxide under high vacuum for one hour.
Triflate 4a (300 mg, 0.397 mmol), 18-crown-6 (210 mg, 0.794 mmol) and potassium trifluoroacetate (333 mg, 2.19 mmol) were weighed into an oven dried flask containing a magnetic stirring bar and dried over potassium hydroxide under high vacuum for one hour.
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