ライフサイエンスコーパス: motor region

1 l prefrontal cortex, functions as a visceral motor region.

2 iii) elicit stronger effects of TMS on these motor regions.

3 corticography was recorded over auditory and motor regions.

4 rocal interactions with temporal and frontal motor regions.

5 piratory modulation, with highest density in motor regions.

6 as actions are produced by modality-specific motor regions.

7 these deep-layer cells also target brainstem motor regions.

8 s, lateral frontal cortex, and somatosensory/motor regions.

9 densely connected with other frontal cortex motor regions.

10 ngulate gyrus and right sensorimotor and pre-motor regions.

11 2% identity to MYO3 across the motor and non-motor regions.

12 g frontal and parietal areas [10, 11], other motor regions [12-15], and also the existence of multise

13 Consistent with prior data, the cortical motor regions activated during the motor task showed gre

14 s also densely connected with frontal cortex motor regions, albeit to a lesser extent than the M1 gra

15 well established in humans for language and motor regions and correlate with handedness.

16 mal anticorrelation between dorsal attention/motor regions and default-mode/frontoparietal regions, p

17 between the left precentral gyrus and other motor regions, and between Broca's and Wernicke's areas.

18 actions between auditory, somatosensory, and motor regions, and the hemispheric lateralization patter

19 One metastate is associated with sensory and motor regions, and the other involves areas related to h

20 Secondary motor regions are less efficient at generating motor out

21 cted by an associative account, responses in motor regions are observed for novel and/or abstract vis

22 rdless of age group, stronger coupling among motor regions, as well as between language/speech region

23 in striatal areas but also in extrastriatal "motor" regions, bilaterally.

24 nnectivity among a bilateral network of core motor regions comprising M1, lateral premotor cortex, an

25 and inter-hemispheric interactions among key motor regions constitute an important pathophysiological

26 the cortex concentrated in visual and somato-motor regions, distinct from the pattern of intersubject

27 d the activation and interaction of cortical motor regions during simple, internally paced and extern

28 and the increased activation in the cortical motor regions during the dopamine-replete state was posi

29 s task have revealed selective activation of motor regions during the perception of 'natural' versus

30 Truncation mutants lacking the motor region failed to localize to filopodial tips but s

31 The divergent non-motor regions flanking the ATPase domain are critical in

32 did not consistently distinguish sensory and motor regions from paralimbic and association regions: (

33 Each motor region has unique terminations in the ipsilateral

34 overy in a number of primary and non-primary motor regions in all patients, but no session effects we

35 movement-related activation in ipsilesional motor regions in chronic subcortical stroke patients.

36 Crucially, however, distinct motor regions in the precentral gyrus sparked by articul

37 Overall, the forelimb motor region included: (1) a large caudal forelimb area

38 ves the SMA and cortical regions outside the motor regions, including prefrontal and parietal regions

39 The enzyme was found in motor regions, including the dorsal motor nucleus of the

40 These activations in motor regions may possibly reflect volitional effort to

41 These molecules share a conserved motor region of approximately 340 amino acids, which is

42 dyslexics relative to the controls in a pre-motor region of Broca's area (BA 6/44).

43 The general structural features of the motor region of myosin superfamily members are now well

44 ivity between frontal cortical areas and the motor region of the striatum as a putative substrate for

45 ucleus is a specialized autonomic-projecting motor region of the striatum, whereas the lateral and an

46 ic carrot DNA, DcKRP120-1, homologous to the motor region of tobacco TKRP125.

47 models N-terminal scaffolding and C-terminal motor regions of DnaB to produce a clear break in the he

48 blood oxygen level dependent signal of three motor regions of interest in each hemisphere.

49 d with a unique gene expression signature in motor regions of the brain implicated in neurodegenerati

50 nitive-behavioural dysfunction affecting non-motor regions of the brain.

51 I, and VIII bilaterally corresponding to the motor regions of the cerebellum (z score = 3.96 and 3.42

52 rain correlates of stuttering are the speech-motor regions of the non-dominant (right) cerebral hemis

53 ally, it is thought that action selection in motor regions originates from a competitive process that

54 ed a buildup of choice-selective activity in motor regions over time reflecting the integrated sensor

55 , fast spindles (13.5-15 Hz) at task-related motor regions predicted overnight enhancement in procedu

56 gined transformations to the equation or the motor region reflecting manual programming.

57 in the proportion of activated voxels in any motor region (relative to the total number of activated

58 evels, including auditory, sensorimotor, and motor regions, suggesting the representation of sensorim

59 tions between basal ganglia circuits and the motor regions that directly control performance.

60 in several identical primary and nonprimary motor regions that is independent of time after stroke.

61 r expression in the cerebellum and striatum, motor regions that may contribute to the improved behavi

62 PMd and remote right-hemispheric and mesial motor regions that was only present during arbitrary vis

63 e, sport novices recruit lower-level sensory-motor regions, thought to support the instantiation of m

64 ral cingulate (M3) and caudal cingulate (M4) motor regions through the corona radiata (CR), internal

65 onal gradients extending from perceptual and motor regions to cortical areas representing more abstra

66 k together with right-hemispheric and mesial motor regions to sustain visuomotor mapping performed wi

67 and raphespinal innervation to the cervical motor region was promoted by C'ase plus transplant.

68 ansient synchronization between auditory and motor regions was observed.

69 sions positive for p62 immunostaining in non-motor regions were strongly over-represented in the C9OR

70 ndings suggest that PPTg input to downstream motor regions, where it can be integrated with other rel

71 molecular basis for the function of the non-motor regions within the context of full-length MCAK is

72 We hypothesized that recruitment of motor regions would shift from primary to secondary moto