ライフサイエンスコーパス: cotransmission

1 s reduced, enabling a selective focus on the cotransmission.

2 to incorporate the concept of 5-HT/glutamate cotransmission.

3 in dopamine neurons are capable of glutamate cotransmission.

4 ional variation in dopamine-neuron glutamate cotransmission.

5 urons has increased, but less is known about cotransmission.

6 elease D-serine, enabling glutamate/D-serine cotransmission.

7 lateral dendrites and soma-centered ACh/GABA cotransmission.

8 gic and neuropeptidergic (Penk, Cartpt, Vgf) cotransmission and 571 estrogen-regulated transcripts.

9 such as multi-component synaptic potentials, cotransmission, and neuromodulation with obvious potenti

10 ophrenia resilience phenotype, and glutamate cotransmission appears to be important in attribution of

11 us, a reduction in dopamine neuron glutamate cotransmission appears to mediate significant components

12 ransmission were unaffected, while glutamate cotransmission at phasic firing frequencies was reduced,

13 Neurotrophins regulate sympathetic neuron cotransmission by modulating the activity-dependent rele

14 as accumulated in the past four decades, and cotransmission by multiple neurotransmitters from the sa

15 ostganglionic firing mediated by peptidergic cotransmission can provide a basis for heterosynaptic in

16 Fast glutamate and gamma-aminobutyric acid cotransmission convey discrete patterns of dopamine neur

17 ma-aminobutyric acid (GABA) or glutamatergic cotransmission during development and physiological func

18 Heretofore, in all examples of cotransmission, each released neurotransmitter acted on

19 haplotypes of alleles at nearby loci and the cotransmission from parent to offspring that reveal diff

20 GABA and DA cotransmission from SACs to ETCs may play a key role in

21 More recently, cotransmission has been recognised in the central nervou

22 Specifically, neurons used for cotransmission have terminals that contain few DCVs and

23 Here, we provide evidence for functional cotransmission in a neuromuscular system of Aplysia.

24 erential, yet synergistic, roles of ACh-GABA cotransmission in motion sensitivity and direction selec

25 ghlight a significant role of glutamate/GABA cotransmission in regulating the input-output dynamics o

26 Together with evidence for glutamate cotransmission in serotonergic raphe neurons and noradre

27 Peptidergic cotransmission in the ganglia can increase arterial tens

28 n this issue of Neuron the first instance of cotransmission in which two neurotransmitters act on the

29 ly, our analyses conclusively show clonemate cotransmission into ants, and, as such, we find support

30 proteins, demonstrating that suppression of cotransmission is actively modulated.

31 The role for this neurotransmitter cotransmission is poorly understood.

32 e present results suggest that glutamatergic cotransmission may be the rule for central monoaminergic

33 simple one-locus, two-phenotype gene-culture cotransmission model to compute the effect of genetic nu

34 se but also in dopamine neuron connectivity, cotransmission, modulation, and activity.

35 Our study shows the cotransmission of DENV-3 lineages through a complex diss

36 Cotransmission of diverse pathogens by the aggressively

37 Thus, cotransmission of dopamine and noradrenaline with either

38 To examine cotransmission of genetic and linguistic variation withi

39 wed parallel evolutionary trajectories, with cotransmission of genetic and linguistic variation.

40 gs provide physiological significance of the cotransmission of glutamate/GABA by SuM neurons in the D

41 However, recombination prevents the reliable cotransmission of interacting gene combinations and can

42 Specifically, cotransmission of larval clonemates from a snail first h

43 : evolution of reduced genomes in symbionts, cotransmission of partners, and obligate coexistence bet

44 rried paternal mitochondrial DNA, indicating cotransmission of plastids and mitochondria in the same

45 rphisms linked to the rf3 locus demonstrated cotransmission of rf3 and Rf3 alleles through heterozygo

46 d add another dimension to understanding the cotransmission of substance P and CGRP by primary affere

47 NPs, indicating a single origin and maternal cotransmission of the cms-T mitochondria and plastids to

48 V-1 and HCMV MTCT occurs in infancy, and the cotransmission of these viruses may occur via infant oro

49 e CCK(+)VGluT3(+)INT-mediated GABA/glutamate cotransmission onto principal cells in adult mice using

50 d the effects of either permanently blocking cotransmission or modifying the GABA/glutamate ratio on

51 est has focused on the mechanisms underlying cotransmission, plasticity and differential control of c

52 sion of GGI by GGII spirochetes declined and cotransmission predominated.

53 nscriptional restriction of fast transmitter cotransmission provides a mechanism allowing reversible

54 While soma-localized ACh/GABA cotransmission showed depression of the GABA component w

55 ave shown that the action of GABA and ACh in cotransmission spatially clustered near the soma play a

56 r, the molecular mechanism of HIV-1 and HCMV cotransmission through the oral mucosa and its role in M

57 ate (VGLUT3) and use acetylcholine/glutamate cotransmission to regulate striatal functions.

58 In nicotine, peptidergic cotransmission was enhanced in the ganglia, and repetiti

59 After some early hints, cotransmission was proposed in 1976 and the 'chemical co

60 gain insights into the physiological role of cotransmission, we measured peptide release from cell B1

61 To elucidate the behavioral role of the cotransmission, we targeted the glutamate-recycling enzy

62 ne the function of dopamine neuron glutamate cotransmission, which likely involves transmission of pr

63 can release multiple neuroactive substances (cotransmission) whose identities can even change over ti

64 heir genomes into one protein coat, ensuring cotransmission with each other and virtually eliminating