ライフサイエンスコーパス: neurochemically

1 bdivisions that differ both anatomically and neurochemically.

2 reased activity may be due to the release of neurochemically active substances as a result of the pre

3 This relationship was both neurochemically and anatomically specific.

4 l, we demonstrate that impulsive animals are neurochemically and behaviorally more sensitive to heroi

5 d glucose can alter the electrical output of neurochemically and biophysically defined LH cells in mo

6 Vagal inputs to these neurochemically and topographically distinct enteric neu

7 d mesencephalic transplant can anatomically, neurochemically, and functionally reinstate the 6-OHDA-e

8 They are anatomically, developmentally, neurochemically, and functionally related to the basal g

9 oubly dissociated both neuroanatomically and neurochemically at the level of the nucleus accumbens.

10 e differential vulnerability of circuits and neurochemically by the vulnerability of neurons that dif

11 procedure to neuroanatomically localize and neurochemically characterize substrates in the VP that m

12 eritioneal administration of Fluorogold, and neurochemically characterized by simultaneous single- an

13 cral dorsal root ganglion (DRG) neurons were neurochemically characterized by using six neuronal mark

14 urons, the BF is in fact an anatomically and neurochemically complex structure.

15 neocortex, it is in fact an anatomically and neurochemically complex structure.

16 system in the zebrafish is anatomically and neurochemically complex, providing a substrate for auton

17 th multiple-labeling immunohistochemistry to neurochemically define these neurons and characterize th

18 Among the 10 neurochemically defined axonal populations, a significan

19 We found multiple neurochemically defined cell types, suggesting multiple

20 ar GABAAR subunit expression patterns within neurochemically defined cellular circuits of the mouse E

21 porting the participation of the receptor in neurochemically defined circuits integrating sensory cue

22 her with results regarding the birthdates of neurochemically defined classes of V ganglion cells, the

23 The striatum contains neurochemically defined compartments termed patches and

24 ontained GABA, and some expressed markers of neurochemically defined GABAergic subtypes, indicating t

25 alic proliferative zone (PZ) to give rise to neurochemically defined interneuron subgroups.

26 he upper and lower visual quadrants occupied neurochemically defined medial, central, lateral, and la

27 Thus, our results identify a neurochemically defined neural circuit through which D-F

28 ely distinguishes subgroups corresponding to neurochemically defined pathologies.

29 The neurochemically defined PLd was labeled by tracer inject

30 irrel monkeys, and macaque monkeys, we found neurochemically defined subdivisions within the medial v

31 valbumin, and nitric oxide synthase, we find neurochemically defined subdivisions within the MVe simi

32 istribution of these cells relative to other neurochemically defined subdivisions.

33 A and calbinin-D28k indicating that they are neurochemically different from the newly described vasop

34 for progression to dementia and in defining neurochemically differentiated subsets of MCI subjects.

35 hat GABAergic and cholinergic neurons define neurochemically distinct areas.

36 dissect the locomotor function of the three neurochemically distinct cell types within the MLR: glut

37 studies have identified two anatomically and neurochemically distinct cellular compartments within th

38 study demonstrates that muOR is expressed by neurochemically distinct classes of myenteric neurons th

39 the functional activation of neurons in the neurochemically distinct compartments of the striatum, t

40 Thus, morphologically and neurochemically distinct cSLR/AAA cholinergic neurons ex

41 s express Piezo2, and that these neurons are neurochemically distinct from corneal polymodal nocicept

42 ssical' GABAergic neurons of the cortex, are neurochemically distinct from LHA hcrt/orx and MCH cells

43 as been no systematic examination of whether neurochemically distinct interneuron classes undergo dif

44 t cells (BCs), we tested the hypothesis that neurochemically distinct interneuron populations are dif

45 c cholinergic specializations are present on neurochemically distinct interneuron subtypes in the hip

46 y, I propose that differential engagement of neurochemically distinct interneuron subtypes is a unify

47 s was located on somatodendritic surfaces of neurochemically distinct myenteric plexus neurons, while

48 Multiple neurochemically distinct pathways originate from these b

49 icate that intraperitoneal IL-1beta recruits neurochemically distinct pathways within the BSTov and C

50 rise multiple subsets of morphologically and neurochemically distinct phenotypes located at strategic

51 A neurochemically distinct population of koniocellular (K)

52 vity in 1a afferents is modulated by several neurochemically distinct populations of presynaptic neur

53 Overall, we found seven neurochemically distinct populations of principal neuron

54 y of these substances suggested at least two neurochemically distinct portions of NCL.

55 an ever-growing list of morphologically and neurochemically distinct spinal cord interneurons.

56 ides important morphological insights into a neurochemically distinct subclass of local-circuit inhib

57 Piezo2 expression occurs in a neurochemically distinct subpopulation of corneal affere

58 B5-I neurons and show that they belong to a neurochemically distinct subset.

59 Our findings demonstrate that multiple, neurochemically distinct types of hair cells are present

60 Two anatomically and neurochemically distinct zones within the vomeronasal or

61 previous evidence that these subregions are neurochemically distinct.

62 can be studied in isolation because they are neurochemically distinct.

63 ributed with respect to the functionally and neurochemically diverse cell populations of the ventral

64 LDT afferents arise from neurochemically diverse cell types and mediate multiple

65 ypothesized that the developing human IPN is neurochemically heterogeneous despite its cytological si

66 la oblongata (VLM) of the brainstem contains neurochemically heterogeneous neurons that have a critic

67 indicates that the receptor is located in a neurochemically heterogeneous population of small diamet

68 Because the DRN is neurochemically heterogeneous, dual immunoelectron micro

69 Because the DR is neurochemically heterogeneous, when possible, neurons we

70 t2(a) receptor exists on morphologically and neurochemically heterogenous neurones and is closely ass

71 lear that most of the avian telencephalon is neurochemically, hodologically, and functionally compara

72 e of how cholinergic neuromodulation acts on neurochemically identical but morphologically distinct i

73 AGB), we investigated kainate sensitivity of neurochemically identified cell populations within the s

74 able to up-regulate CREB phosphorylation in neurochemically identified gamma-aminobutyratergic neuro

75 on of the electrophysiological properties of neurochemically identified interneurons sampled in the s

76 896 (pNR1S896), or serine 890 (pNR1S890) in neurochemically identified neurons of the adult rat stri

77 An analysis of effects on neurochemically identified neurons revealed that 5-HT ne

78 vivo measured by juxtacellular recording of neurochemically identified neurons.

79 forming whole-cell patch-clamp recordings of neurochemically identified striatal neurons combined wit

80 h of which contained an inhibitory pause, in neurochemically identified ventral tegmental area (VTA)

81 d manipulate the activity of genetically and neurochemically identified VTA-projecting BNST neurons i

82 somes were discovered several decades ago as neurochemically identified zones in the striatum, yet te

83 transmission was not required to synchronize neurochemically induced membrane oscillations between el

84 No neurochemically-induced changes in EE were observed, nor

85 ematically mapped in a neuroanatomically and neurochemically interactive manner in the VP.

86 s fairly homogeneous cytoarchitecturally and neurochemically, it has been divided into distinct funct

87 Our data suggest that the PPN is neurochemically segregated, and such differences define

88 However, the role of TXNIP in neurochemically specific hypothalamic subpopulations and

89 al brain metabolism or blood flow as well as neurochemically specific pharmacological interventions,

90 These findings demonstrate robust, innate, neurochemically specific, and apparently heritable pheno

91 The loss of CB immunoreactivity was neurochemically specific.

92 , previously identified in human striatum as neurochemically unique domains of the accumbens and puta

93 Because interneurons are genetically and neurochemically unique from striatal projection neurons,

94 RN may be anatomically, morphologically, and neurochemically unique subdivisions of the gerbil DRN.