ライフサイエンスコーパス: gracile

1 resentation of the distal hindlimb in dorsal gracile.

2 f the present study was to establish whether gracile afferents to the inferior olive are topographica

3 e most lateral part of rDAO, whereas lateral gracile also targets more medial parts.

4 o demonstrate that projecting neurons in the gracile and cuneate nuclei express predominantly the Glu

5 onally present in nucleus solitarius and the gracile and cuneate nuclei.

6 from the midthoracic spinal cord ends in the gracile and cuneate nuclei.

7 the caudal end only received input from the gracile and cuneate nuclei.

8 ddle Paleolithic early modern humans being a gracile anomalous outlier.

9 standing how environmental changes disrupted gracile australopith niches.

10 Canals of gracile Australopithecus, and possibly Homo habilis, fal

11 For example, gracile axonal dystrophy (gad) mutant mice, which harbor

12 4) and gracile axonal dystrophy (GAD).

13 The skeleton was that of an adult man with a gracile build and severe scoliosis of the thoracic spine

14 keleton of modern Homo sapiens is relatively gracile compared with other hominoids and earlier homini

15 In the rat and monkey, the gracile, cuneate and spinal trigeminal nuclei all projec

16 Projections from the gracile, cuneate and spinal trigeminal nuclei were label

17 lla oblongata, with labelled neurones in the gracile, cuneate and spinal trigeminal nuclei.

18 c protein showed few oligodendrocytes in the gracile fasciculus at lumbar levels at birth.

19 central processes of sensory neurons in the gracile fasciculus of genetically diabetic BB rats, we h

20 Lesions that damaged only the gracile fasciculus or a small percentage of the cuneate

21 intense involvement of the posterior column (gracile fasciculus) in the thoracolumbar spinal cord, a

22 eption (the dorsal spinocerebellar tract and gracile fasciculus).

23 al intermediate septum or the midline of the gracile fasciculus, respectively; 2) terminating primari

24 e most cursorial of these fossils are small, gracile forms often grouped together as the Sphenosuchia

25 In gracile fossil adult hominins that lived between approxi

26 ately 35,000 years ago that people with more gracile, fully modern morphology make their appearance.

27 principally composed of the cuneate (CN) and gracile (GN) nuclei.

28 GRACILE (growth retardation, aminoaciduria, cholestasis,

29 was related to the dorsoventral locus of the gracile injection site: gracile injections centred dorsa

30 Gracile injections centred dorsally also resulted in mor

31 ventral locus of the gracile injection site: gracile injections centred dorsally produced the largest

32 f-shaped teeth, a beak-like lower jaw, long, gracile limbs, and a quadrupedal stance.

33 vely demonstrates that Alioramus is a small, gracile, long-snouted carnivore that deviates from other

34 ry with populations that evolved from modern gracile morphology in Africa 130,000-160,000 years ago.

35 re sacrifice did not affect the frequency of gracile NAD in controls or diabetics.

36 expected marked increase in the frequency of gracile NAD; however, substantial numbers of dystrophic

37 er seen within the hypoglossal, cuneate, and gracile nuclei at this time point.

38 projections of sensory neurons to medullary gracile nuclei in aged animals and man, and in a number

39 ated to the cell-cluster architecture of the gracile nuclei in sections processed for cytochrome oxid

40 The sensory terminals in the gracile nuclei provide a simple, well-characterized expe

41 y cutaneous afferents to terminations in the gracile nuclei.

42 The gracile nucleus (GN) and lateral part of rostral dorsal

43 Responses of neurons in the gracile nucleus (NG) of female rats to tactile and visce

44 osomal vacuolization, axonal swelling in the gracile nucleus and impaired neuromotor coordination.

45 horase reactivity was neither altered in the gracile nucleus and mNTS of non-acupoint stimulated rats

46 that EA ST 36 induces nNOS expression in the gracile nucleus and mNTS, and enhanced nNOS-NO in the nu

47 rimary afferent terminals in the ipsilateral gracile nucleus and spinal dorsal horn in three nerve in

48 primarily in the dorsal, lateral rim of the gracile nucleus and the medial rim of the cuneate nucleu

49 reactivity are consistently increased in the gracile nucleus and the mNTS by EA ST 36.

50 dorsal root ganglia, lumbar spinal cord and gracile nucleus at 2, 6 and 14 weeks after sciatic nerve

51 ion and the caudal region of the ipsilateral gracile nucleus compared to the side with intact sciatic

52 us, but was not altered in the contralateral gracile nucleus compared with sham-treated rats (P < 0.0

53 immunopositive terminals in spinal cord and gracile nucleus displayed morphological characteristics

54 oked c-fos expression in the dorsal horn and gracile nucleus following either sciatic nerve section o

55 Previous studies have shown that the gracile nucleus in postsynaptic dorsal column pathway pl

56 d single-unit recording was performed in the gracile nucleus in urethane-anesthetized rats to examine

57 atic nerve axotomy on nNOS expression in the gracile nucleus in young compared to aged rats.

58 viors of the female rat, suggesting that the gracile nucleus is a component of neural systems that co

59 owever, Abeta-evoked c-fos expression in the gracile nucleus may be under some other control since it

60 l-arginine-derived nitric oxide (NO) in the gracile nucleus modifies the hypotensive responses to el

61 in young rats, and is also increased in the gracile nucleus neurons of intact aged rats.

62 cells were also increased in the ipsilateral gracile nucleus of rats with EA stimulation.

63 medial portion of the dorsal horn and in the gracile nucleus of the brainstem on the side ipsilateral

64 o reveal the somatotopic organization of the gracile nucleus of the dorsal column-trigeminal complex,

65 crease in nNOS expression in the ipsilateral gracile nucleus of young rats, which is still seen in ol

66 tes results in fewer dystrophic axons in the gracile nucleus than in age-matched controls.

67 Estimates for the gracile nucleus were higher (80%).

68 NADPHd containing neurons in the ipsilateral gracile nucleus were moderately increased by axotomy ove

69 into one hindpaw in rats, and neurons in the gracile nucleus were recorded 2-8 days later.

70 In the gracile nucleus, at all survival times, an increased dis

71 lls in the rostral region of the ipsilateral gracile nucleus, but was not altered in the contralatera

72 ted in terminals of injured afferents in the gracile nucleus, CGRP was expressed in between 32 and 68

73 uneate nucleus or the dorsomedial rim of the gracile nucleus, respectively; and 3) ascending bilatera

74 gray, area postrema, pontine raphe nucleus, gracile nucleus, spinal trigeminal nucleus, and spinal c

75 in the dorso-medial medulla, ventral to the gracile nucleus, termed the matrix region.

76 In the gracile nucleus, virtually all puncta labeled for CTB ap

77 g the rostrocaudal length of the ipsilateral gracile nucleus.

78 inated in a mediolateral sequence within the gracile nucleus.

79 labeled axons ascend from this region to the gracile nucleus.

80 transmit visceral nociceptive signals to the gracile nucleus.

81 in subunit B revealed aberrant expansions of gracile projections into the cuneate and, in one case, e

82 or biotinylated dextran amine were made into gracile, resulting in anterograde labelling often distri

83 nt surfaces in combination with a relatively gracile skeleton (i.e., lower bone mass for our body siz

84 ciency, whereas in the Finnish patients with GRACILE syndrome complex III activity was within the nor

85 rgan failure (complex III deficiency and the GRACILE syndrome).

86 e in the BCS1L gene in Finnish patients with GRACILE syndrome, as well as five different mutations in

87 tations cause complex III deficiency and the GRACILE syndrome, which in neonates are lethal condition

88 ization was obtained, suggesting that medial gracile targets only the most lateral part of rDAO, wher

89 lay a more severe axonal degeneration of the gracile tract of the medulla and spinal cord than had be

90 nctions in the maintenance of neurons of the gracile tract, NTS and AP.