ライフサイエンスコーパス: IML

1 y(styrenesulfonate)/poly(ethylenimine) as an IML was initially found to be 3.40%.

2 ork reports the design and fabrication of an IML using a simple solution process.

3 (A) receptor-mediated innervation of OML and IML interneurons also displayed significant differences

4 Both OML and IML interneurons received a direct excitatory monosynapt

5 rmediolateral cell column (IML) of L5-S1 and IML and medial gray of T13-L2, respectively, was activat

6 ing at the inner ML (IML)/(OML) interface as IML sprouts into the denervated zone.

7 dense in the intermediolateral cell column (IML) and intercalated nucleus, regions containing retrog

8 ocated in the intermediolateral cell column (IML) and lamina X (the central autonomic area), regions

9 d GABA in the intermediolateral cell column (IML) as detected by electron microscopy.

10 eurons of the intermediolateral cell column (IML) at all ages.

11 eurons in the intermediolateral cell column (IML) of L5-S1 and IML and medial gray of T13-L2, respect

12 minals in the intermediolateral cell column (IML) that synapse on SPNs and use the inhibitory neurotr

13 levels of the intermediolateral cell column (IML) were labeled by 4 days.

14 l SPNs in the intermediolateral cell column (IML) were recorded in urethane/chloralose-anesthetized r

15 ojects to the intermediolateral cell column (IML).

16 eurons in the intermediolateral cell column (IML).

17 instead of in the intermediolateral column (IML) of the spinal cord.

18 cation to form the intermediolateral column (IML).

19 ettled to form the intermediolateral column (IML); the rest migrated medially to locations between th

20 ntermediolateral nucleus of the spinal cord (IML).

21 udy thus paves way to develop such efficient IMLs for more efficient tandem solar cells.

22 rent sizes and graphene quantum dot embedded IML.

23 d were especially dense in the ventral horn, IML and medial gray.

24 ynthase-ir profiles) or GABA-ir dendrites in IML, and terminals immunoreactive for both VGLUT3 and GA

25 L interneurons but predominantly shunting in IML interneurons.

26 ically in the ipsilateral intermediolateral (IML) cell column of the spinal cord and several brainste

27 jects to cells within the intermediolateral (IML) cell column of the thoracic cord and the sacral par

28 tatory projections to the intermediolateral (IML) cell column.

29 etic nucleus (SPN) of the intermediolateral (IML) regions of L6-S1 spinal cord segments in rats.

30 8 hours, were transported to the ipsilateral IML in the caudal half of the last cervical and first th

31 and the lateral internal medullary lamina (L-IML).

32 The L-IML group exhibited an intermediate level of impairment.

33 ns of the lateral internal medullary lamina (IML) or ibotenic acid lesions of the lateral intralamina

34 ansparent and conductive intermediate layer (IML).

35 The inner molecular layer (IML) displayed a corresponding volumetric expansion in r

36 of the dentate gyrus inner molecular layer (IML) is a pathophysiological process that may facilitate

37 fibers (MF) into the inner molecular layer (IML) of the fascia dentata (FD).

38 s with isolated mediastinal lymphadenopathy (IML) are a common presentation to physicians, and medias

39 Consistent with ongoing maturation, IML interneurons displayed lower input resistances and m

40 e located in the outer ML (OML) or inner ML (IML).

41 tion of FAC1 immunostaining at the inner ML (IML)/(OML) interface as IML sprouts into the denervated

42 Rats with ILN, but not IML, lesions were impaired in acquiring an initial and 5

43 e right T4 spinal intermediolateral nucleus (IML) immediately increased ipsilateral brown adipose tis

44 The percentages of IML-projecting neurons containing 5-HT(1A)R-ir were 49%

45 Two subtypes of IML neurons were originally described by Ramon y Cajal,

46 Furthermore, only IML interneurons also received significant synaptic inpu

47 nied by a corresponding increase in relative IML volume.

48 R, Matlab and SAS/IML code for implementing lossless data reduction is fre

49 A program written in SAS/IML is available from the authors on request.

50 olabeled for 5-HT(1A)R-ir and 5-HT, and some IML-projecting neurons in the RVLM were doubly immunolab

51 Moreover, some IML-projecting neurons in the PPR and RPa were doubly im

52 correlation between aberrant supragranular (IML) mossy fiber sprouting and increased densities of AM

53 The increases in BAT SNA evoked by T4 IML microinjections of NMDA (12 pmol) were significantly

54 han the response to NMDA alone) following T4 IML microinjections of 5-HT (100 pmol to 2 nmol, but not

55 hydroxytryptamine (5-HT, 2 nmol) into the T4 IML increased BAT SNA (peak: +342% of control) at a long

56 evoked by microinjection of NMDA into the T4 IML was reversed by microinjection of methysergide (600

57 ction of methysergide (600 pmol) into the T4 IML.

58 ction of methysergide (600 pmol) into the T4 IML.

59 iminution of FAC1 staining in the OML as the IML sprouted into the denervated zone and revealed that

60 t migrated medially to locations between the IML and the central canal.

61 lin transgenic mice were located in both the IML and near the central canal.

62 tead of migrating dorsolaterally to form the IML.

63 ndicular to radial glial fibers, to form the IML.

64 microscopy, 54% of the axon terminals in the IML (n = 1,337 terminals) were TTC immunolabeled (TTC(+)

65 with GluR1 subunit protein densities in the IML (R=0.784, P<0.0093).

66 of VAChT-positive cholinergic fibers in the IML after EC damage, along with no change in the OML.

67 that the cells expressing MC4-R mRNA in the IML and DMV were autonomic preganglionic neurons as cell

68 ays post-infection, labeling was seen in the IML and lamina X in T12-L1 segments, and in medullary ra

69 Electron microscopy in the IML and lamina X revealed that these puncta were presyna

70 close apposition to serotonin fibers in the IML and medial gray.

71 ansmission onto SPNs and interneurons in the IML and that A1Rs may play a protective role on neurons

72 The use of Ag-NPs in the IML has been shown to lengthen the life time of electron

73 sities of AMPA GluR1 subunit proteins in the IML of the FD.

74 In the IML of the HS group, despite the losses of granule cells

75 that those AT1R-immunopositive cells in the IML were sympathetic preganglionic neurones, while those

76 esser extent) postsynaptic structures in the IML, as well as the luminal membrane of endothelial cell

77 argets of spiny, granule-like neurons in the IML, termed semilunar granule cells (SGCs).

78 , an infection of GABAergic terminals in the IML.

79 beled with rhodamine beads injected into the IML of adult male rats.

80 ng deficits and that extensive damage to the IML or ILN has no detectable effects on retrograde or an

81 .e., supraspinal neurons that project to the IML) were identified near the ventral medullary surface;

82 sy fiber sprouting, which was limited to the IML, the increased GluR1 stainings were distributed thro

83 gration during migration from the OML to the IML.

84 distinct patterns of infectivity within the IML of thoracolumbar and SPN of lumbosacral segments con

85 l labeling was found throughout the thoracic IML suggesting that the PAG modulates sympathetic functi

86 localized 5-HT(1A)R immunoreactivity (ir) to IML-projecting neurons that were retrogradely labeled wi

87 inical trial of 77 consecutive patients with IML from 5 centers between April 2009 and March 2011.

88 edictive value of EBUS-TBNA in patients with IML were 92% (95% CI, 83-95%) and 40% (95% CI, 12-74%),

89 aving initial investigation in patients with IML.

90 rtex, 3) the commissural/associational zone (IML) immediately adjacent to the granule cell layer, and

91 ny other neuropil profiles within this zone; IML staining was rare and restricted to large apical den