ライフサイエンスコーパス: dopaminergic agonist

コーパス検索結果 (１語後でソート)

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1 The experiment examined the influence of a dopaminergic agonist (amphetamine) and an antagonist (ha

2 ce, which can be ameliorated by the indirect dopaminergic agonist, amphetamine, has been demonstrated

3 onjunction with pharmacological fMRI using a dopaminergic agonist and an antagonist.

4 nd this organization is influenced by both a dopaminergic agonist and an antagonist.

5 psychiatric disorders commonly treated with dopaminergic agonists and antagonists.

6 tor activity in the presence or absence of a dopaminergic agonist (apomorphine) or an atypical antips

7 r phosphoinositide hydrolysis in response to dopaminergic agonist, apparently by coupling to a Gq-lik

8 controlled pharmacological fMRI study with a dopaminergic agonist (bromocriptine) and antagonist (sul

9 absent or blunted responses to stimulant and dopaminergic agonist drugs, in conjunction with near-com

10 rs contribute to the beneficial influence of dopaminergic agonists for the protection and restoration

11 etic pulses of glutamate, GABA, dopamine and dopaminergic agonists locally, onto layer 5 pyramidal ne

12 Application of the dopaminergic agonist quinpirole to cotransfected cells i

13 present study challenge the prediction that dopaminergic agonists reduce STN activity predominantly

14 Treatment of GH4-121 cells with a dopaminergic agonist resulted in activation of PLD in bo

15 uence contributes to the effects of indirect dopaminergic agonists such as D-amphetamine on striatal

16 Three distinct classes of drugs: dopaminergic agonists (such as D-amphetamine), serotoner

17 Dopaminergic agonists, such as pramipexole, appear to ha

18 The stimulation of PLD by dopaminergic agonists took place in the absence of any d

19 by measuring striatal c-Fos expression after dopaminergic agonist treatment at postnatal day 4 (P4) t

20 icantly lower in short photoperiod mice, and dopaminergic agonist treatment rescued the photopic ligh

21 utant mice were relieved using ropinirole, a dopaminergic agonist widely used for RLS treatment.

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