ライフサイエンスコーパス: unilateral lesion

1 animals with both callosal transections and unilateral lesions.

2 affected and unaffected breast of women with unilateral lesions.

3 We found that of 68 focal unilateral lesions, 40% were associated with contralater

4 Unilateral lesions also suppressed c-fos expression in t

5 language organization and susceptibility to unilateral lesions and to investigate the contribution o

6 function (the paretic forelimb in rats with unilateral lesions), animals were trained with their non

7 Although the workup and management of unilateral lesions are well established, limited informa

8 Thus bilateral or unilateral lesions circumscribed surgically within the O

9 go a workup similar to that in patients with unilateral lesions, differences in their natural history

10 Rats with unilateral-lesions displayed a CTA by rejecting the sacc

11 In keeping with past results, unilateral lesions disrupted lordosis responses to contr

12 s smaller than that of the sham-operated and unilateral lesioned groups, but significant conditioned

13 Compared with shams, rats with unilateral lesions had a greater rate of acquisition and

14 system in rats with neglect resulting from a unilateral lesion in AGm, followed by treatment with age

15 the role of this upregulation, we performed unilateral lesion in mice lacking one allele of the Gnal

16 s pallidus (GP), superimposed on the earlier unilateral lesion in substantia nigra (SN) with 6-hydrox

17 oducing contralateral rotations in rats with unilateral lesion in the nigrostriatal region induced by

18 We studied the effects of a restricted, unilateral lesion in the portion of the optic tectum tha

19 eve food pellets was studied in 55 rats with unilateral lesions in the dorsal spinal cord at the C1/2

20 However, in six rabbits with unilateral lesions in the RN, or with bilateral lesions

21 ed contextual fear memory, whereas rats with unilateral lesions in the same hemisphere displayed inte

22 onditioned fear to tone and context, whereas unilateral lesions induced partial impairments with no l

23 Infants with unilateral lesions initially had responses after TMS of

24 We hypothesized that unilateral lesions made at birth may affect synaptic phy

25 Although the focus is on the effects of unilateral lesions made ipsilateral to stimulation sites

26 with broader cortical blindness produced by unilateral lesion of all contiguous visual cortical area

27 Rats were given a unilateral lesion of anterior CeN and a unilateral lesio

28 ned rats was poorer than that of rats with a unilateral lesion of either structure or with a symmetri

29 Furthermore, unilateral lesion of hypoglossal afferents greatly dimin

30 for a few days or several weeks following a unilateral lesion of the cuneate nucleus, the source of

31 en a unilateral lesion of anterior CeN and a unilateral lesion of the DLS, made either ipsilateral (c

32 resentations in area 3b within weeks after a unilateral lesion of the dorsal column in squirrel monke

33 A complete unilateral lesion of the dorsal column somatosensory pat

34 ix adult monkeys (Macaca mulatta) received a unilateral lesion of the lateral corticospinal tract (CS

35 oro-Gold (FG) into the thalamus, and a small unilateral lesion of the lateral projection reduced the

36 nection procedure that combined a selective, unilateral lesion of the nucleus accumbens core and infu

37 In addition, unilateral lesion of the vagus reduced Fos expression in

38 Following a unilateral lesion of the visual cortex (cortical areas 1

39 Nine days following unilateral lesioning of the entorhinal cortex, S100B was

40 as measured in four rhesus monkeys following unilateral lesioning of the optic tract combined with tr

41 We compared the effect of unilateral lesioning of the sciatic nerve or unilateral

42 After unilateral lesions of adult BFC, responses of neurons in

43 Fifth, unilateral lesions of ALa yield behavioral disturbances

44 In anaesthetized rats with unilateral lesions of around 70% of the Phox2b(+)TH(-) n

45 tion performance by assessing the effects of unilateral lesions of basal forebrain cholinergic neuron

46 The animals were prepared with unilateral lesions of both the vPFC and vHC, either in t

47 Unilateral lesions of CA3 cells using ibotenate, which a

48 Marmoset monkeys with unilateral lesions of either the antOFC or vlPFC were sc

49 reased in the ipsilateral striatum following unilateral lesions of either the left or right SN.

50 Unilateral lesions of LMN did not abolish HD cells in AD

51 ession, the rat received either bilateral or unilateral lesions of LMN.

52 Specifically, the effects of unilateral lesions of nigrostriatal DA neurons on oral d

53 Monkeys with crossed unilateral lesions of prefrontal cortex and inferior tem

54 Unilateral lesions of PT nearly eliminated NPY+ fibers i

55 Compared with controls, rats with unilateral lesions of RSP and POR on opposite sides of t

56 Unilateral lesions of substantia nigra pars compacta neu

57 am, ipsilaterally, or contralaterally placed unilateral lesions of the ABL and accumbens and were tra

58 Importantly, unilateral lesions of the ACC (including some of medial

59 of the Acb, Acb shell, Acb core, and Amy, or unilateral lesions of the Amy after training but before

60 of these two structures, achieved by crossed unilateral lesions of the amygdala in one hemisphere and

61 teral lesions of the VM cortex or with right unilateral lesions of the amygdala or the right insular

62 Patients with unilateral lesions of the antero-ventral part of the ant

63 Unilateral lesions of the AV3V region suppressed c-fos e

64 In Experiment 1, rats received unilateral lesions of the BLA and were implanted with ca

65 In another experiment, hamsters given unilateral lesions of the CeA and infusions of D-Phe CRF

66 d a turning syndrome somewhat reminiscent of unilateral lesions of the dopaminergic nigro-striatal pa

67 In monkeys with chronic unilateral lesions of the dorsal columns and expanded ch

68 hemispheric deficits produced as a result of unilateral lesions of the entire vibrissa representation

69 ection after either one-stage or progressive unilateral lesions of the entorhinal area.

70 adult rats (120-200 gm), specifically after unilateral lesions of the entorhinal cortex (EC), and th

71 Adult rats received unilateral lesions of the entorhinal cortex to induce co

72 Unilateral lesions of the forelimb area of the sensorimo

73 We have found that unilateral lesions of the forelimb region of the sensori

74 Rats were given unilateral lesions of the medial auditory thalamus or a

75 Numerous observations in patients with unilateral lesions of the medial temporal lobe (MTL) and

76 Extensive unilateral lesions of the medullary corticospinal fibres

77 Connections between them were interrupted by unilateral lesions of the mPFC and amygdala, but on oppo

78 Rats received unilateral lesions of the nucleus basalis and were infus

79 Patients with unilateral lesions of the OFC and of the ACC and/or medi

80 uter layers of the adult olfactory bulb into unilateral lesions of the rat corticospinal tract (CST)

81 iment 1, homing pigeons (Columba livia) with unilateral lesions of the right or left HF were trained

82 an essential role, we examined patients with unilateral lesions of the rostral prefrontal cortex.

83 Unilateral lesions of the RVL reduced the evoked blood p

84 he dorsal striatum was reduced 2 weeks after unilateral lesions of the SN with 6-hydroxydopamine.

85 Rats received unilateral lesions of the SNc and lesions of the CeA in

86 Rats then received unilateral lesions of the whole dorsal striatum or restr

87 We describe data showing that unilateral lesions of VS enhance neural representations

88 In animals with unilateral lesions only, nonparetic forelimb training wo

89 We have studied the effects of a unilateral lesion placed in the STN in predominantly hem

90 In contrast, posttraining bilateral and unilateral lesions produced significant deficits in the

91 by the dopamine (DA) agonist apomorphine in unilateral lesioned rats.

92 pinized and 6-hydroxydopamine (OHDA)-induced unilateral lesioned rats.

93 When tested, unilateral-lesioned rats displayed a CTA by rejecting th

94 Unilateral lesions restricted to the basolateral amygdal

95 nding others' emotions, by showing that even unilateral lesions result in deficits in both accuracy a

96 neural responses are used, consistently with unilateral lesion studies.

97 After unilateral lesions, the firing properties of HD cells in

98 ceptual mechanisms are maximally impaired by unilateral lesions to the temporal and parietal cortex.

99 However, unilateral lesions to this system in various species are

100 s of the brain were compared over time after unilateral lesioning treatments.

101 Neglect after a unilateral lesion was measured as the tendency to make e

102 Unilateral lesions were made by injection of ibotenic ac

103 Mice with unilateral lesions were then challenged with l-dopa (lev

104 19.6% [22 of 112]) (P = .003) compared with unilateral lesions, while rates of hyperaldosteronism we

105 ic bilateral sensorimotor cortex lesions, or unilateral lesions, with or without callosal transection