ライフサイエンスコーパス: lemniscal

1 exhibited the postsynaptic relationships of lemniscal afferents.

2 uclei exhibited the morphology of ascending "lemniscal" afferents.

3 s (SpVc) and the dorsal column nucleus-based lemniscal and cortical pathway.

4 ly, for the formation of the whisker-related lemniscal and cortical structures.

5 he corticothalamic system suggests that both lemniscal and extralemniscal auditory thalamic nuclei re

6 ther rapidly changing stimuli unaffected, in lemniscal and nonlemniscal (but not polysensory) subdivi

7 ion appeared differentially affected in aged lemniscal and nonlemniscal MGB.

8 Our findings indicate that lemniscal and nonlemniscal nuclei are indeed different i

9 pattern of PV/CB staining that distinguishes lemniscal and nonlemniscal pathways.

10 species and are related to the functions of lemniscal and nonlemniscal somatosensory pathways.

11 Our results indicate that both lemniscal and nonlemniscal TC afferents play a role in i

12 te body (MGBv and MGBm) respectively are the lemniscal and nonlemniscal thalamic auditory nuclei.

13 differences in the nature and plasticity of lemniscal and paralemniscal information processing.

14 investigated the synaptic properties of the lemniscal and paralemniscal input to VPm and POm.

15 through two glutamatergic routes called the lemniscal and paralemniscal pathways via the ventral pos

16 nct classes of thalamocortical input via the lemniscal and paralemniscal pathways, the former via ven

17 Our data suggest that the lemniscal and paralemniscal projections should not be th

18 tinuations of, respectively, the subcortical lemniscal and paralemniscal systems conveying somatosens

19 longing to two major somatosensory pathways (lemniscal and paralemniscal) and explored the way in whi

20 sory cortex via two major parallel pathways, lemniscal and paralemniscal.

21 Slow, inexorable progression of lemniscal and thalamocortical axonal withdrawal is a neu

22 visual, auditory/vestibular, somatosensory (lemniscal), and proprioceptive (spinocerebellar) systems

23 es some neurons of the parabrachial, lateral lemniscal, and deep cerebellar nuclei, in addition to ce

24 ral subdivision of the MGN (MGv; the primary/lemniscal auditory pathway).

25 laterally and the somatosensory and auditory lemniscal axons are transected unilaterally on the day o

26 Examination of trigeminal lemniscal axons in dcc knockout mice revealed absence of

27 fic excitatory synapses, competition between lemniscal (barrel) and non-lemniscal (septal) processing

28 eurons, whereas it caused less adaptation in lemniscal cells.

29 y being an information route parallel to the lemniscal channel.

30 abeled cells localized ventromedially in the lemniscal division, i.e., the ventral subdivision of the

31 ble overlay on the more obligatory system of lemniscal feedforward type responses.

32 sformation of sensory representations in the lemniscal (high-fidelity) auditory thalamocortical netwo

33 an be transmitted to the amygdala via either lemniscal (i.e., LG --> V1, V2 --> TE2/PR) or non-lemnis

34 scal (i.e., LG --> V1, V2 --> TE2/PR) or non-lemniscal (i.e., LP --> V2, TE2/PR) thalamo-cortico-amyg

35 of the cuneate nucleus, the source of medial lemniscal (ML) axons carrying information from the contr

36 Lemniscal neurons are narrowly frequency tuned and provi

37 Lemniscal neurons most faithfully encoded stimuli when t

38 t of auditory nuclei projections and lateral lemniscal nuclear projections in embryonic rats, respect

39 entral nuclei of the trapezoid body, lateral lemniscal nuclei, and inferior colliculus.

40 the majority of projections from the lateral lemniscal nuclei, did not label in these experiments, in

41 In the lemniscal nuclei, most neurons contained low levels of G

42 emporal cortex, nucleus sagulum, and lateral lemniscal nuclei.

43 ditory-evoked response originates in the non-lemniscal pathway and not in cortical areas of the rat b

44 teral thalamus, resulting in a bilateral PrV lemniscal pathway at P0.

45 ed that the spike rates in neurons along the lemniscal pathway from receptors to cortex, which includ

46 bed the normal development of the trigeminal lemniscal pathway in the mouse.

47 Stimulation of the lemniscal pathway produced class 1, or "driver," respons

48 Here we find that neurons along the lemniscal pathway robustly encode rhythmic whisking on a

49 ese layer I projections represent a separate lemniscal pathway to the molecular layer or arise as col

50 In the mouse, thalamic relay synapses of the lemniscal pathway undergo extensive remodelling during t

51 Our data suggest that, unlike the lemniscal pathway, the paralemniscal one is not homogeno

52 have impaired development of the trigeminal-lemniscal pathway.

53 of these levels of the dorsal column-medial lemniscal pathway.

54 ving direct inputs from the primary sensory (lemniscal) pathway show the greatest decrement in synchr

55 where the thalamic input is dominated by the lemniscal projection.

56 eurons giving rise to the principal sensory (lemniscal) projections to the IC, i.e., those from the c

57 rthermore, increasing the intensity sharpens lemniscal receptive field profile as adaptation progress

58 eled thalamic synapses observed, 10-29% were lemniscal (RL) type synapses in VPL; 60-70% were cortico

59 tors to responses of thalamic relay cells to lemniscal (sensory) input in thalamic slices studied wit

60 mpetition between lemniscal (barrel) and non-lemniscal (septal) processing streams, and regulation of

61 ern had inputs from a variety of olivary and lemniscal sources, notably the contralateral lateral sup

62 SSA neurons were confined to the non-lemniscal subdivisions and exhibited broad receptive fie

63 Ascending lemniscal substrates are characterized by cascading exci

64 d developmental refinement of whisker relay (lemniscal) synapses in the thalamus in mice deficient of

65 l chemosense apparently relies on the medial lemniscal system to guide this chemically driven feeding

66 some engaging, predominantly, the ascending "lemniscal," taste pathway, a circuit associated with hig

67 Hence, monosynaptic excitatory lemniscal TC connections onto layer 4 do not behave unif

68 er-crossing areas, was closely examined: the lemniscal thalamocortical (TC) pathway.

69 l type differences in their relationships to lemniscal versus paralemniscal pathways.