ライフサイエンスコーパス: supplementary motor area

1 coactivation of the primary motor cortex and supplementary motor area.

2 cal motor scores and brain metabolism in the supplementary motor area.

3 connectivity between anterior cingulate and supplementary motor area.

4 neuron activity was recorded from the caudal supplementary motor area.

5 e primary motor cortex than with that of the supplementary motor area.

6 ing Broca's area, the premotor area, and the supplementary motor area.

7 esial premotor areas, probably including the supplementary motor area.

8 ), the lateral premotor cortex and bilateral supplementary motor area.

9 l cortex and cerebellum, and medially in the supplementary motor area.

10 y within the dACC and spreading into the pre-supplementary motor area.

11 cific locus at the ventral border of the pre-supplementary motor area.

12 mporary goals, which may be monitored by the supplementary motor area.

13 tive conditions increased activations in the supplementary motor area.

14 ight lateral prefrontal cortex and bilateral supplementary motor area.

15 classified more reliably, especially in the supplementary motor area.

16 (VLPFC)/insula, inferior frontal cortex, and supplementary motor area.

17 s region with the anterior cingulate and pre-supplementary motor area.

18 ecially between the primary motor cortex and supplementary motor area.

19 ophy of superior lateral premotor cortex and supplementary motor area.

20 anatomical bundle, and overlapping with the supplementary motor area.

21 y be due to disconnection from cingulate and supplementary motor areas.

22 ity in the lentiform nuclei, cerebellum, and supplementary motor areas.

23 ing Broca's area as well as the premotor and supplementary motor areas.

24 emotor, dorsolateral prefrontal and anterior supplementary motor areas.

25 s and mesial premotor regions, including the supplementary motor areas.

26 y reduced neural response to laughter in the supplementary motor area, a premotor region thought to f

27 We argue here for the engagement of supplementary motor areas across a variety of sound cate

28 All patients showed greater relative supplementary motor area activation than did the normal

29 ve ipsilateral premotor cortex and bilateral supplementary motor area activity.

30 lism of superior lateral premotor cortex and supplementary motor area, although there was some variab

31 ding the left and right presupplementary and supplementary motor area and anterior cingulate cortex.

32 e temporal cortex, and medial regions in the supplementary motor area and anterior cingulate.

33 e inhibition meta-analysis, showing that the supplementary motor area and basal ganglia were underact

34 g the primary motor cortex, premotor cortex, supplementary motor area and basal ganglia.

35 nnectivity between amygdala and motor areas (supplementary motor area and cerebellum) was enhanced.

36 sensorimotor cortex, dorsal premotor cortex, supplementary motor area and cerebellum.

37 erses, at least partially, the impairment of supplementary motor area and dorsal prefrontal cortex ac

38 ed that it would also concomitantly increase supplementary motor area and dorsal prefrontal cortex ac

39 esponse including structural connectivity to supplementary motor area and functional anticorrelation

40 The supplementary motor area and inferior frontal cortex act

41 al primary sensorimotor and premotor cortex, supplementary motor area and ipsilateral cerebellar cort

42 BOLD activation in right premotor cortex and supplementary motor area and left hippocampus and with i

43 lysis, our results suggest motor output from supplementary motor area and left primary motor cortex a

44 ied to the scalp overlying the region of the supplementary motor area and over other positions, inclu

45 ctional connectivity at rest between the pre-supplementary motor area and prefrontal cortex were prop

46 The results also showed that supplementary motor area and putamen/globus pallidus reg

47 Supplementary motor area and right dorsal prefrontal cor

48 Relative increases in activation of the supplementary motor area and right dorsal prefrontal cor

49 re condition, accompanied by increased right supplementary motor area and temporoparietal junction ac

50 ptom-related motor planning and body schema (supplementary motor area and temporoparietal junction).

51 arietal lobules, the frontal eye fields, the supplementary motor area and the anterior insulae.

52 and recruited more areas, including the pre-supplementary motor area and the bilateral posterior lob

53 A network involving supplementary motor area and the caudal portion of dorsa

54 omponent of this network originates from the supplementary motor area and the cingulate motor areas o

55 sensorimotor cortex, dorsal premotor cortex, supplementary motor area and the inferior parietal corte

56 d significantly with activations in the left supplementary motor area and the left medial parietal co

57 ional connectivity network included the left supplementary motor area and the prefrontal, inferior pa

58 Moreover, foci in the right rostral supplementary motor area and the right inferior parietal

59 The pre-supplementary motor area and the rostral portion of the

60 By contrast, separate signals in supplementary motor area and ventromedial prefrontal cor

61 ction), pain processing (anterior insula and supplementary motor area), and identification of emotion

62 left lateral orbitofrontal cortex and right supplementary motor area, and also dissociated abnormali

63 orks, including the inferior frontal cortex, supplementary motor area, and anterior cingulate cortex

64 bition in the right inferior frontal cortex, supplementary motor area, and anterior cingulate cortex,

65 e bilateral putamen, anterior-dorsal insula, supplementary motor area, and anterior cingulate cortex.

66 etwork, including right angular gyrus, right supplementary motor area, and bilateral cerebellum, yiel

67 erior frontal gyrus, left anterior cingulate/supplementary motor area, and bilateral posterior cingul

68 frontal cortex, superior temporal gyrus, and supplementary motor area, and bilaterally in the medial

69 ated to changes in grey matter volume in pre-supplementary motor area, and changes in its underlying

70 A significant proportion of neurons in supplementary motor area, and hippocampus and environs,

71 ITG), left postcentral gyrus/precuneus, left supplementary motor area, and left lingual gyrus were id

72 t hemisphere, including sensorimotor cortex, supplementary motor area, and rostral inferior parietal

73 hibition engages the inferior frontal gyrus, supplementary motor area, and striatum.

74 afferents from the primary motor cortex, the supplementary motor area, and the caudal subdivision of

75 sensorimotor cortex, inferior-frontal gyrus, supplementary motor area, and the cerebellum.

76 zed by hypermetabolism of the basal ganglia, supplementary motor area, and the cerebellum.

77 cortex, the insula bilaterally, the midline supplementary motor area, and the medial parietal cortex

78 eys composed of bilateral premotor cortices, supplementary motor area, and the right inferior frontal

79 , and anterior PFC, lateral premotor cortex, supplementary motor area, and the striatum are involved

80 orsal premotor cortex, supplementary and pre-supplementary motor areas, and planum temporale), b) dom

81 icle (SLF) to dorsal area 6, area 9, and the supplementary motor area; and via the cingulate fascicle

82 lateral premotor area, orbitofrontal cortex, supplementary motor area, anteior cingulate gyrus) and p

83 with significantly reduced activation in the supplementary motor area, anterior cingulate and midcing

84 The supplementary motor area appears important for productio

85 the ventral lateral premotor cortex, and the supplementary motor area are essential for the voluntary

86 ulation (the anterior insula, cerebellum and supplementary motor area) arguably because the reading r

87 ases in the dorsal midbrain, cerebellum, and supplementary motor area, as well as reductions in motor

88 the dorsal anterior cingulate cortex and the supplementary motor area, as well as the insula, which w

89 e superior motor cortex, premotor cortex and supplementary motor area at loci similar to those detect

90 x (Brodmann area [BA] 4), bilaterally in the supplementary motor area (BA 6), and in the right anteri

91 g the anterior cingulate cortex (BA 24), the supplementary motor area (BA 6), and the precuneus, enco

92 organized with a sharp transition around the supplementary motor area between fast (13-15 Hz) centrop

93 f interest, as well as activation within the supplementary motor area, brainstem, and inferior fronta

94 ficantly correlated with the activity of the supplementary motor area but not with that of the primar

95 of the mesial premotor system, including the supplementary motor area, but also by enhancing informat

96 hin the anterior insula and presupplementary/supplementary motor areas, carried behavioral consequenc

97 ation, including dorsal premotor cortex, pre-supplementary motor area, cerebellum, and basal ganglia

98 creases in rCBF were significantly higher in supplementary motor area, cingulate cortex, and dorsolat

99 tivation in the medial prefrontal cortex and supplementary motor area, cingulate gyrus, cuneus and oc

100 sk-related activation in regions such as the supplementary motor area, cingulate motor areas, premoto

101 otor cortex, premotor and prefrontal cortex, supplementary motor areas, cingulate sulcus, temporal lo

102 ngs showed abnormal primary motor cortex and supplementary motor area co-activation with increasing c

103 observed increased activation in the insula, supplementary motor area, dorsolateral prefrontal cortex

104 ity between the right amygdala and the right supplementary motor area during both fearful versus neut

105 volving dorsal anterior cingulate cortex and supplementary motor area encoded the difference between

106 revealed that Broca's area and the left pre-supplementary motor area evoked distinct neural activity

107 vity between the left premotor area and left supplementary motor area, for both the left and the righ

108 Although the supplementary and pre-supplementary motor areas have been intensely investigat

109 pling increase of prefrontal cortex with the supplementary motor area, i.e. the mesial premotor loop.

110 (i) the mesial premotor loop comprising the supplementary motor area; (ii) the lateral premotor loop

111 uired from the parietal-occipital cortex and supplementary motor area in all subjects.

112 xels (>80%) at 3.0 T, with activation in the supplementary motor area in the 3.0-T data that was not

113 n primates indicating a critical role of the supplementary motor area in the organization of forthcom

114 e mesial frontocentral cortex (including the supplementary motor area) in the organization of sequent

115 Stimulation over the supplementary motor area induced accuracy errors only in

116 in the thalamus, anterior cingulate cortex, supplementary motor area, inferior parietal lobe, and do

117 al and lateral to the hand area, as well the supplementary motor area, insula, putamen, and cerebellu

118 Stimulation over the supplementary motor area interfered with the organizatio

119 r cortex (BA 4a), bilateral premotor cortex, supplementary motor area, intraparietal sulcus, dorsolat

120 d function (increased brain activity in left supplementary motor area, left parahippocampal gyrus, an

121 onization, including increased activation in supplementary motor area, left premotor area, right thal

122 ortex, bilateral medial frontal cortex, left supplementary motor area, left thalamus, left cerebellar

123 Abnormal anatomical connectivity of the supplementary motor area may contribute to the susceptib

124 t lateral prefrontal, insula, cingulate, and supplementary motor area network.

125 Finally, compared with the supplementary motor area, neurons in the presupplementar

126 n GABA neurotransmitter concentration in the supplementary motor area of the human brain.

127 ex, the ventral lateral premotor cortex, the supplementary motor area on the medial wall, and the ros

128 feedback connections from putamen to the pre-supplementary motor area (Pcorrected = 0.020) and primar

129 We suggest that supplementary and pre-supplementary motor areas play a role in facilitating sp

130 Inputs from the pre-supplementary motor area (pre-SMA) and inferior frontal

131 where thalamic neurons projecting to the pre-supplementary motor area (pre-SMA) are located relative

132 terior inferior frontal gyrus (pIFG) and pre-supplementary motor area (pre-SMA) with M1 at rest.

133 cture and functional connectivity of the pre-supplementary motor area (pre-SMA), assessed with magnet

134 ed with the accumulated gains, including pre-supplementary motor area (pre-SMA), inferior frontal gyr

135 by a higher increase in DA levels in the pre-supplementary motor area (pre-SMA).

136 re was an enhancement of activity in the pre-supplementary motor area (pre-SMA).

137 eral prefrontal cortex (VLPFC) and the (pre)-supplementary motor area (pre-SMA/SMA) have dissociable

138 us; and, (2) posterior cingulate cortex with supplementary motor area, precentral gyrus, and postcent

139 network, including the primary motor cortex, supplementary motor area, premotor area and superior par

140 sing the putamen, caudate nucleus, thalamus, supplementary motor area, premotor cortex, and dorsolate

141 control and motivation to act, including the supplementary motor area, premotor cortex, primary motor

142 l previous monkey findings and show that the supplementary motor area, premotor, and the right prefro

143 f right inferior frontal cortex (r-IFC), pre-supplementary motor area (preSMA), and the subthalamic n

144 on of effective connectivity between the pre-supplementary motor area, primary motor cortex and putam

145 or areas] and the medial motor cortex [MMCx; supplementary motor area proper (SMA), pre-SMA and foot

146 ment decision making and a posterior region (supplementary motor area proper) directly involved in mo

147 contrast, activation in dorsal striatum and supplementary motor areas reflects subjects' choice prob

148 et al. (2016) report that neurons in the pre-supplementary motor area represent the frequency of tact

149 The supplementary motor area represents the anatomical link

150 rea, left ventral premotor cortex, posterior supplementary motor area, right superior part of the cer

151 ircuit and disconnection between the rostral supplementary motor area, rostral cingulate motor area a

152 ther with disconnections between the rostral supplementary motor area, rostral cingulate motor area a

153 Akinesia is linked to hypoactivation of the supplementary motor area secondary to insufficient thala

154 a different region (medial frontal cortex, "supplementary motor area") showed greater activity durin

155 Task dependent BOLD activity in the supplementary motor area (SMA) and dorsolateral premotor

156 food cues in orbitofrontal cortex (OFC) and supplementary motor area (SMA) and less deactivation bel

157 mpal gyrus, with covarying reductions in the supplementary motor area (SMA) and orbitofrontal cortex.

158 ch as anterior cingulate and insular cortex, supplementary motor area (SMA) and parietal operculum (P

159 the dACC is selective for pain, whereas the supplementary motor area (SMA) and pre-SMA are specifica

160 The supplementary motor area (SMA) and pre-SMA are widely co

161 rupt profile change where the border between supplementary motor area (SMA) and pre-SMA is expected.

162 te nucleus (CN), cingulate motor area (CMA), supplementary motor area (SMA) and primary sensorimotor

163 ed by greater activation in the thalamus and supplementary motor area (SMA) and reduced connectivity

164 e during time perception including the right supplementary motor area (SMA) and right pre-SMA and bas

165 ed during simple manual movement, namely the supplementary motor area (SMA) and the cingulate motor a

166 Here we examined the connection between supplementary motor area (SMA) and the hand area of the

167 as on the medial wall of the hemisphere, the supplementary motor area (SMA) and the pre-SMA.

168 studies in normal humans have shown that the supplementary motor area (SMA) and the primary motor cor

169 of spinal termination of efferents from the supplementary motor area (SMA) and the two caudal cingul

170 ing across the primary motor cortex (M1) and supplementary motor area (SMA) by inspecting the positiv

171 inferior frontal, inferior premotor, insula, supplementary motor area (SMA) complex, striatum, and st

172 Neural signals in the supplementary motor area (SMA) correlate with the intens

173 ogram (EEG) over motor, pre-motor cortex and supplementary motor area (SMA) during action observation

174 eft dorsolateral prefrontal cortex (PFC) and supplementary motor area (SMA) during emotion regulation

175 oscillations significantly increased in the supplementary motor area (SMA) during post-training comp

176 ivity of the primary motor cortex and caudal supplementary motor area (SMA) during volitional movemen

177 nce of basal ganglia, prefrontal cortex, and supplementary motor area (SMA) for timing.

178 ential studies in man suggest a role for the supplementary motor area (SMA) in movement preparation,

179 The supplementary motor area (SMA) is frequently involved by

180 The supplementary motor area (SMA) makes a crucial contribut

181 tivity of individual neurons recorded in the supplementary motor area (SMA) of monkeys during a seria

182 dies in man have identified the premotor and supplementary motor area (SMA) of the cortex as being of

183 We recorded from the supplementary motor area (SMA) of two monkeys as they ex

184 We determined that the supplementary motor area (SMA) plays an important role i

185 and premotor cortex bilaterally, also in the supplementary motor area (SMA) predominantly in the left

186 e right dorsal premotor cortex (rPMd) or the supplementary motor area (SMA) prior to the TS at variou

187 y processing risk costs and midcingulate and supplementary motor area (SMA) processing effort costs.

188 uted pattern; more extensive activity in the supplementary motor area (SMA) proper that extended into

189 In contrast, M1 and supplementary motor area (SMA) showed more integrative s

190 Here we report neuronal activity in the supplementary motor area (SMA) that is correlated with b

191 ections from the digit representation in the supplementary motor area (SMA) to the PMd and PMv are st

192 the basal ganglia, motor cortex area 4, and supplementary motor area (SMA) using functional magnetic

193 prising M1, lateral premotor cortex, and the supplementary motor area (SMA) were assessed using dynam

194 tor area (PMD), ventral premotor area (PMV), supplementary motor area (SMA), and frontal eye field (F

195 tor area (PMD), ventral premotor area (PMV), supplementary motor area (SMA), and frontal eye field (F

196 l cortex, the supplementary eye field (SEF), supplementary motor area (SMA), and pre-SMA have been im

197 e dorsal oculomotor area (OMD; area 8b), the supplementary motor area (SMA), and somatosensory cortex

198 1), injected isotope tracers into M1 and the supplementary motor area (SMA), and studied projections

199 in neuronal firing rate, particularly in the supplementary motor area (SMA), as the reported time of

200 OLD response than did heavy drinkers in left supplementary motor area (SMA), bilateral parietal lobul

201 ions with the primary motor cortex (M1), the supplementary motor area (SMA), cingulate motor areas, s

202 ctivity between the primary motor area (M1), supplementary motor area (SMA), dorsal premotor cortex (

203 Activations within the supplementary motor area (SMA), frontal operculum, middl

204 he primary somatosensory cortex (S1) and the supplementary motor area (SMA), in both patient populati

205 y when the actions are familiar; and (2) the supplementary motor area (SMA), involved in active motor

206 number of frontal areas, including the left supplementary motor area (SMA), left dorsal premotor cor

207 MDr) divisions, ventral premotor area (PMV), supplementary motor area (SMA), presupplementary motor a

208 medial premotor system, including the caudal supplementary motor area (SMA), the left putamen, and th

209 ter connectivity between the putamen and the supplementary motor area (SMA), the premotor cortex (PMC

210 thalamus (THAL), ventral-striatum (VS), and supplementary motor area (SMA), using both mediator anal

211 that, if an individual has more GABA in the supplementary motor area (SMA)--a region previously asso

212 onstrate that GABA concentrations within the supplementary motor area (SMA)--a region strongly associ

213 ed rCBF change in the thalamus, midbrain and supplementary motor area (SMA).

214 ions were found in the contralateral PMv and supplementary motor area (SMA).

215 (M1), primary somatosensory cortex (S1), and supplementary motor area (SMA).

216 sly recorded pairs of neurons in the macaque supplementary motor area (SMA).

217 sensory area (S1), premotor cortex (PMC) and supplementary motor area (SMA).

218 ck to the cerebral cortex, in particular the supplementary motor area (SMA).

219 , parietal and paracingulate cortex, and the supplementary motor area (SMA).

220 portion of area 46, area ProM, CMAr, and the supplementary motor area (SMA).

221 tional significant increases in the anterior supplementary motor area (SMA)/cingulate.

222 or subdivision of medial frontal cortex [pre-supplementary motor area (SMA)] was activated, which cou

223 tralateral thalamus, ipsilateral cerebellum, supplementary motor area (SMA)]; however, the TD group s

224 resting motor network between right and left supplementary motor areas (SMA) was elevated after train

225 n the right dorso-lateral prefrontal cortex, supplementary motor areas (SMA), the right premotor area

226 ons) located on the right medial wall in the supplementary motor area ('SMA proper').

227 nterest: the prefrontal cortex, motor cortex/supplementary motor area, somatosensory cortex, temporal

228 These regions as well as supplementary motor area, striatum and the hippocampus h

229 s such as medial superior frontal gyrus (pre-supplementary motor area/supplementary eye field), dorso

230 ateral STG, precentral and postcentral gyri, supplementary motor area, supramarginal gyrus, posterior

231 eased activation in a smaller cluster in the supplementary motor area survived comparison with the ps

232 resentation in the primary motor cortex; the supplementary motor area; the inferior lateral premotor

233 fluence from the right amygdala to the right supplementary motor area to happy stimuli (P < 0.05) wit

234 two components in dorsal premotor cortex and supplementary motor areas, two regions that may be impor

235 furthermore, the increased activation in the supplementary motor area was abuse specific.

236 on circuit in the superior parietal lobe and supplementary motor area was activated in response to th

237 r insula and the presupplementary motor area/supplementary motor area was associated with a greater d

238 les, including a left inferior frontal gyrus/supplementary motor area, which was most strongly connec

239 g task blocks was present in the caudate and supplementary motor area, while sustained negative activ

240 Coactivation in the motor cortex and supplementary motor area with increasing cognitive load

241 ected) in the left premotor cortex and right supplementary motor area, with concomitant reduction in