ライフサイエンスコーパス: heteroreceptor

1 well as neurons of the respiratory network (heteroreceptors).

2 as a presynaptic inhibitory autoreceptor and heteroreceptor.

3 EpoR and betacR comprise a tissue-protective heteroreceptor.

4 modulate dopamine transmission via mGluR2/3 heteroreceptors.

5 and post-synaptic serotonergic receptors and heteroreceptors.

6 However, distinct heteroreceptors acting during adulthood are involved in

7 ptor activity without also changing 5-HT(1B) heteroreceptor activity.

8 In contrast, 5-HT(1A) heteroreceptors affect responses to forced swim stress,

9 Co-activation of the heteroreceptor also resulted in synergistic increases in

10 central 2alpha-adrenergic autoreceptors, and heteroreceptors and is an antagonist of serotonin 5-HT2

11 ibits dual functionality as autoreceptor and heteroreceptor, and this enables H3Rs to modulate the hi

12 e induction of signaling from p185(neu).EGFR heteroreceptor assemblies requires the ectodomain for li

13 r, these data suggest that mGlu7 serves as a heteroreceptor at inhibitory synapses in area CA1 and th

14 one on GABA(B) presynaptic autoreceptors and heteroreceptors because blocking GABA(B) receptors produ

15 t dopamine stimulation by cocaine enhances a heteroreceptor complex formation between dopamine D2 rec

16 We define therein an axonal D1 heteroreceptor component, apparently mediating volume ne

17 al mice to differentiate autoreceptor versus heteroreceptor effects of 8-OH-DPAT on hypoglossal nerve

18 ur results demonstrate that forebrain 5-HT1B heteroreceptors expressed during an early postnatal peri

19 he cells while enhancing postsynaptic 5-HT1A heteroreceptor expression in nonserotonergic neurons.

20 effect of activation of downstream 5-HT(1a) heteroreceptors from that of autoreceptors.

21 ift in the balance between dopamine auto and heteroreceptor function may contribute to the therapeuti

22 s in raphe nuclei without affecting 5-HT(1A) heteroreceptors, generating mice with higher (1A-High) o

23 ve previously shown that ETPs expressing the heteroreceptor (HR) comprising IL-4Ralpha and IL-13Ralph

24 The IL-4Ralpha/IL-13Ralpha1 heteroreceptor (HR) serves both IL-4 and IL-13 cytokines

25 13, namely the IL-4Ralpha/IL-13Ralpha1 (13R) heteroreceptor (HR), is compromised and determined wheth

26 hese compartments, m2 receptors appear to be heteroreceptors, i.e., they are associated predominantly

27 g Th2 programs, IL-4 is captured by the IL-4 heteroreceptor (IL-4Ralpha/IL-13Ralpha1) expressed on de

28 s chain associates with IL-4Ralpha to form a heteroreceptor (IL-4Ralpha/IL-13Ralpha1) that marks the

29 othesis that mGluR4a serves as a presynaptic heteroreceptor in the globus pallidus, where it may play

30 As heteroreceptors in GABAergic terminals in the same lamin

31 (dorsal raphe nucleus) and local inhibition (heteroreceptors in projection areas).

32 mechanisms of activation of presynaptic NMDA heteroreceptors in the rat central nervous system.

33 eurons by presynaptic muscarinic and GABA(B) heteroreceptors in the spinal cord probably contributes

34 ) and a 5-HT1A agonist, and dependent on the heteroreceptor interface.

35 cific D2R knock-out mice, we uncover that D2 heteroreceptors located on non-DAergic medium spiny neur

36 Activation of D2 heteroreceptors, located on STN axon terminals, provides

37 um, the presynaptic GABA-B autoreceptors and heteroreceptors may exhibit distinct receptor-effector c

38 utyric acid type B (GABA-B) autoreceptor and heteroreceptor-mediated inhibition to the sulfhydryl alk

39 This D2 heteroreceptor-mediated mechanism is more efficient in t

40 the expression of an IL-4Ralpha/IL-13Ralpha1 heteroreceptor on Th1 cells.

41 the C1 area of the RVL function primarily as heteroreceptors on presynaptic axons and terminals of no

42 ty, and its control by presynaptic auto- and heteroreceptors on presynaptic terminals.

43 ndently manipulate 5-HT(1A) autoreceptor and heteroreceptor populations.

44 roughout the brain that overlaps with 5-HT1B heteroreceptors (receptors located on non-serotonergic n

45 icated in autoregulation and also may play a heteroreceptor role in regulation of the output of the d

46 (a brain area with high expression of 5-HT1A heteroreceptors sensitive to cholinergic effects on affe

47 5-HT release throughout the brain and (2) a heteroreceptor that mediates inhibitory responses to rel

48 ells rapidly produce IL-4 which utilizes the heteroreceptor to drive apoptosis of Th1 cells, thus yie

49 (1B) receptors function as autoreceptors and heteroreceptors to exert presynaptic inhibition of trans

50 ha1, leading to an unusual expression of the heteroreceptor, which will serve as a death marker for t