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For example, in the cases of the heart-muscle cells and pancreatic cells mentioned above, dosing them with leptin keeps them healthy.
Both anti-oestrogens could reduce the effects of E2 on proliferation in all the risk groups but their effects were rather more variable presumably because the serum drug levels achieved with the above dosing schedules were not sufficient to overcome the high plasma E2 levels reached after treatment with the 2 mg E2 pellet.
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Additional groups of rats given tRA at the above doses were also subcutaneously injected with ethinyl estradiol (EE) at a dose of 0.6 μg per rat per day.
In marked contrast, the vasopressor responses to exogenous noradrenaline or methoxamine were not inhibited by the above doses of NaHS or its vehicle.
Subsequently, the responses to the above doses of the isometheptene enantiomer were elicited again 15 min after administration of the aforementioned compounds.
Subsequently, using a 25G Quincke needle, hyperbaric bupivacaine (2.2 mL) mixed with the above doses of fentanyl was administered at the L3/4 interspace into the spinal subarachnoid space.
For serial passage of primary spheres, the primary spheres were treated with PSP for the above doses for 72 h and subsequently collected, dissociated with trypsin, and resuspended in DMEM/F12 medium with the above supplements.
Females continued to drink U-containing water at the above doses through gestation.
In the OLE, all subjects received pancreatin at the above dose.
After 24 h rectal temperature was recorded and corresponding groups was injected with above doses.
In DOX + SMI group, DOX of the above doses was injected i.p. within two weeks.
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