ライフサイエンスコーパス: medial frontal cortex

1 ly in the anterior and not posterior OFC (or medial frontal cortex).

2 how these functions are parcelled out in the medial frontal cortex.

3 reased interaction between retrosplenial and medial frontal cortex.

4 he right anterior cingulate cortex and right medial frontal cortex.

5 btained with TMS over the right DLPFC or the medial frontal cortex.

6 al decreases in amygdala, temporal pole, and medial frontal cortex.

7 o main types of pyramidal cells in the mouse medial frontal cortex.

8 es of layer 5 pyramidal neurons in the mouse medial frontal cortex.

9 s in deep layer pyramidal cells in the mouse medial frontal cortex.

10 taset of human single neuron recordings from medial frontal cortex.

11 signals explains fMRI responses in posterior-medial frontal cortex.

12 nctional delta rhythms between 1-4 Hz in the medial frontal cortex.

13 neurons are correlated with activity of the medial frontal cortex.

14 res in the precuneus, inferior parietal, and medial frontal cortex.

15 to find evidence for "new" regions in human medial frontal cortex.

16 ivity between midbrain locomotor regions and medial frontal cortex.

17 on in a nearby but more anterior part of the medial frontal cortex.

18 t 40-70 Hz gamma oscillation in the aged rat medial frontal cortex.

19 ninvasive dc electrical stimulation over the medial-frontal cortex.

20 20 min of noninvasive brain stimulation over medial-frontal cortex.

21 ft P < 0.001; right P < 0.001 corrected) and medial frontal cortex (+/-18, 42, 32; left P < 0.001; ri

22 addition to anterior cingulate cortex within medial frontal cortex, a group of subcortical structures

23 related with atrophy of the anterior rostral medial frontal cortex, a region associated with theory o

24 gnals increased in anterior cingulate cortex/medial frontal cortex (ACC/MFC), a brain region previous

25 We found that medial frontal cortex activity associated with action mo

26 One hour after bilateral injury to the medial frontal cortex, adult male rats were given inject

27 mission in the cingulate region of the mouse medial frontal cortex, an associative region that mature

28 The medial frontal cortex and adjacent orbitofrontal cortex

29 Excitotoxic lesions of the medial frontal cortex and anterior cingulate cortex in r

30 d all the behavioral changes associated with medial frontal cortex and anterior cingulate cortex lesi

31 campus from the thalamus, septal nuclei, and medial frontal cortex and from reductions in the conduct

32 iates the control signal originated from the medial frontal cortex and implements the behavioral swit

33 rom a hierarchical organization of posterior medial frontal cortex and its interaction with the basal

34 for a hierarchical organization of posterior medial frontal cortex and its interaction with the BG, w

35 We recorded single neurons in the human medial frontal cortex and medial temporal lobe while sub

36 lationship between structure and function in medial frontal cortex and offers a strategy for testing

37 g primary neuronal cultures derived from the medial frontal cortex and striatum of in utero saline- a

38 ciated with neuroimaging changes in specific medial frontal cortex and subcortical structures, sugges

39 apping regions of the prefrontal cortex, the medial frontal cortex and the orbitofrontal cortex, must

40 y to have less cortical thinning of the left medial frontal cortex and the right middle temporal cort

41 nits) recorded in the hippocampus, amygdala, medial frontal cortex and ventral temporal cortex of neu

42 trol, supported by the orbitofrontal cortex, medial frontal cortex and ventrolateral frontal cortex,

43 ssociated with the rat sensory-motor cortex, medial frontal cortex, and amygdalar regions.

44 ding the inferior frontal junction, superior medial frontal cortex, and bilateral insula, temporally

45 nd 2) the supplementary motor area, superior medial frontal cortex, and putamen-brain circuits respec

46 in S than in C in the lateral hypothalamus, medial frontal cortex, and striatum.

47 ngulate cortex, dorsolateral frontal cortex, medial frontal cortex, and subcortical structures.

48 In medial frontal cortex, anterior insula/frontal operculum

49 The medial frontal cortex appeared to have an important role

50 ychological states, suggesting subregions of medial frontal cortex are functionally heterogeneous.

51 acaques were least likely to branch to other medial frontal cortex areas compared to perigenual ACC (

52 e the agranular orbital cortex and agranular medial frontal cortex (areas 24, 32, and 25).

53 the left prefrontal cortex and the superior medial frontal cortex before participants (N = 62, 24 ma

54 associated with increased activation in the medial frontal cortex beneath the anode; showing a posit

55 ron, Bari et al. (2019) show that neurons in medial frontal cortex, but not a nearby premotor area, e

56 cts was reliably observed when we stimulated medial-frontal cortex, but when we stimulated posterior

57 Although damage to the medial frontal cortex causes profound decision-making im

58 brain areas related to anticipation of pain (medial frontal cortex, cerebellum), attention to pain (d

59 egions in BDD, by sparser bottom-up striatum-medial frontal cortex connectivity in MDD, and by sparse

60 by two separate circuits, one originating in medial frontal cortex controlling emotional expressions,

61 formation maintained in the dorsolateral and medial frontal cortex depends on the context in which it

62 currently a debate as to whether the dorsal medial frontal cortex (dMFC) merely detects or actively

63 ppocampus --> dorsal striatum --> insula --> medial frontal cortex, dorsolateral prefrontal cortex, a

64 The medial frontal cortex enables performance monitoring, in

65 ystem and its target areas, the striatum and medial frontal cortex, especially the anterior cingulate

66 l circuits and provides insight into how the medial frontal cortex exerts top-down control of cogniti

67 Although the medial frontal cortex exhibits a sensitivity to reaction

68 presupplementary motor area (pre-SMA) in the medial frontal cortex has a function in switching from a

69 In humans, the medial frontal cortex has been implicated in the supervi

70 The medial frontal cortex has been linked to voluntary actio

71 Neurons in medial frontal cortex have been found to distinguish bet

72 l cell type and the 5-HT(2A) receptor in the medial frontal cortex have essential roles in psilocybin

73 ty and enhanced FC between the brainstem and medial frontal cortex, highlighting the dynamic role of

74 We found that TMS over the medial-frontal cortex impairs the processing of angry, b

75 Recent work on the role of the medial frontal cortex in cognition and its involvement i

76 The role of the medial frontal cortex in cognition continues to generate

77 y studies have reported abnormalities of the medial frontal cortex in depressive illness; however, th

78 Activation of medial frontal cortex in fMRI studies is associated with

79 ctural remodeling of dendritic spines in the medial frontal cortex in mice.

80 Moreover, selective atrophy within the medial frontal cortex in older adults predicted a tempor

81 To investigate the role of the primate medial frontal cortex in planning and controlling multip

82 isions in humans and implicate the posterior-medial frontal cortex in this process.

83 n-regulated using noninvasive stimulation of medial-frontal cortex in the human brain.

84 Lesions of the medial frontal cortex (in rats) or lateral prefrontal co

85 A principal function of the medial frontal cortex, in particular the anterior cingul

86 Areas in human medial frontal cortex, including areas associated with h

87 Lesion of the medial frontal cortex, including the anterior cingulate

88 lowing both types of trials in the posterior medial frontal cortex, including the anterior midcingula

89 and from thalamic neurons projecting to the medial frontal cortex indicated that this phenomenon ori

90 mentary motor area (pre-SMA), an area in the medial frontal cortex involved in movement planning and

91 hese two violent subject groups in which the medial frontal cortex is compromised in antisocial perso

92 These results imply that medial frontal cortex is important for allowing the anim

93 The medial frontal cortex is important for goal-directed beh

94 atal ramping activity are disrupted when the medial frontal cortex is inactivated.

95 Information processing in the medial frontal cortex is often said to be modulated in p

96 tal fasciculus) and cortical gray matter (in medial frontal cortex, left insula, Heschl's gyrus, and

97 ft dorsolateral prefrontal cortex, bilateral medial frontal cortex, left supplementary motor area, le

98 of impairment identical to that of rats with medial frontal cortex lesions: they were selectively imp

99 superior colliculus also labeled neurons in medial frontal cortex, likely in premotor cortex.

100 Together, these findings suggest that medial frontal cortex maintains separate predictive mode

101 of experiments to elucidate the role of rat medial frontal cortex (MFC) (including prelimbic, infral

102 We show that medial frontal cortex (MFC) activity is predictive of fu

103 Twenty minutes of inphase stimulation over medial frontal cortex (MFC) and right lateral prefrontal

104 This process depends on the medial frontal cortex (MFC) and the medial temporal lobe

105 teral prefrontal cortex (dlPFC), followed by medial frontal cortex (mFC) and then by orbitofrontal co

106 With the medial frontal cortex (MFC) centrally implicated in seve

107 stimulus-triggered 4 Hz oscillations in the medial frontal cortex (MFC) during interval timing tasks

108 ad attenuated delta activity (1-4 Hz) in the medial frontal cortex (MFC) during interval timing.

109 The medial frontal cortex (MFC) enables executive control by

110 escribe how common brain networks within the medial frontal cortex (MFC) facilitate adaptive behavior

111 Influential theories of Medial Frontal Cortex (MFC) function suggest that the MF

112 The rat medial frontal cortex (MFC) has been implicated in allow

113 The medial frontal cortex (MFC) has been shown to play an im

114 ulate cortex (ACC) and adjacent areas of the medial frontal cortex (MFC) have been implicated in moni

115 vioral mechanisms of reward signaling by the medial frontal cortex (MFC) have not been resolved.

116 revious work showed that inactivation of the medial frontal cortex (MFC) impairs interval timing and

117 from the medial temporal lobe (MTL) and the medial frontal cortex (MFC) in neurosurgical patients pe

118 esonance spectroscopy studies of GABA in the medial frontal cortex (MFC) in patients with schizophren

119 The functional organization of human medial frontal cortex (MFC) is a subject of intense stud

120 Medial frontal cortex (MFC) is crucial when actions have

121 Here we show that the primate medial frontal cortex (MFC)(7) is involved in making new

122 between licking and reward signaling by the medial frontal cortex (MFC), a key cortical region for r

123 ractions among orbital frontal cortex (OFC), medial frontal cortex (MFC), and amygdala are thought to

124 Orbitofrontal cortex (OFC), medial frontal cortex (MFC), and amygdala mediate stimul

125 ctions of the orbitofrontal cortex (OFC) and medial frontal cortex (MFC), with OFC being essential fo

126 ons that monitor performance, especially the medial frontal cortex (MFC).

127 iability in glutamatergic metabolites in the medial frontal cortex (MFC, glutamate: CVR = 0.15, p < 0

128 s by drink interactions were observed in the medial frontal cortex (MFC; P for interaction < .001) an

129 ly (e.g., frontal pole, paracingulate gyrus, medial frontal cortex, middle/superior temporal gyrus, p

130 Thus, primate medial frontal cortex might mediate the behavioral effec

131 sent study quantified the changes in how rat medial frontal cortex neurons respond to the same action

132 In the present study, ensembles of medial frontal cortex neurons were recorded from rats tr

133 te to contribute to movement cancellation in medial frontal cortex of macaque monkeys.

134 we recorded electroencephalogram (EEG) over medial frontal cortex of macaques performing a stop sign

135 ut not alpha4 mRNA levels, were lower in the medial frontal cortex of mice with a genetic deletion of

136 is of such flexibility, we recorded from the medial frontal cortex of nonhuman primates trained to pr

137 f projection neurons and interneurons of the medial frontal cortex of the dopamine D(1) receptor null

138 lation (TMS) over the left or right DLPFC or medial frontal cortex on random number generation in hea

139 scranial magnetic stimulation (TMS) over the medial-frontal cortex or over a control site (mid-line p

140 Medial frontal cortex persistent activity, on the other

141 role of 2 cortical subregions, the prelimbic medial frontal cortex (PL) and lateral orbitofrontal cor

142 vidence highlights the role of the posterior medial frontal cortex (pMFC) in social conformity and co

143 We show that a region of the posterior-medial frontal cortex (pMFC) uniquely explains trial-wis

144 The posterior medial frontal cortex (pMFC), a key area for monitoring

145 calize this integration process in posterior-medial frontal cortex (pMFC).

146 of DMN including posterior cingulate cortex, medial frontal cortex, posterior inferior parietal lobul

147 (2) An anterior subdivision of medial frontal cortex [pre-supplementary motor area (SMA

148 show that a peri-choice signal generated in medial frontal cortex provides a source of input to this

149 t transcranial direct current stimulation of medial-frontal cortex provides causal control over the e

150 eral prefrontal cortex (r = 0.41, P < 0.05), medial frontal cortex (r = 0.40, P < 0.05) and lentiform

151 ey reflect deficient computation of value in medial frontal cortex, rather than deficient reward pred

152 ood flow in the dorsal-lateral, orbital, and medial frontal cortex relative to the unpleasant conditi

153 The activations in the medial frontal cortex replicate findings in previous TOM

154 del prediction driven by connectivity in the medial frontal cortex, salience network, motor regions,

155 First, high-beta power in the medial frontal cortex showed opposite modulations separa

156 First, high beta power in the medial frontal cortex showed opposite modulations well s

157 poral, frontal, and parietal lobes and right medial-frontal cortex) showed lesser growth in diabetes,

158 the left prefrontal cortex and the superior medial frontal cortex (SMFC) modulated performance, with

159 the efficacy of left prefrontal and superior medial frontal cortex (SMFC) stimulation to modulate per

160 cerebellar hemisphere); a different region (medial frontal cortex, "supplementary motor area") showe

161 ases in dendritic spine density in the mouse medial frontal cortex that are driven by an elevated rat

162 pically preceded by slow-ramping activity in medial frontal cortex that begins around two seconds bef

163 tic sulcal morphological organization of the medial frontal cortex that can be traced from Old World

164 Schizophrenia involves abnormalities in the medial frontal cortex that lead to cognitive deficits.

165 onkeys and humans have shown activity in the medial frontal cortex that reflects dynamic control and

166 minately in the anterior lateral frontal and medial frontal cortex, that was specifically activated b

167 ysis demonstrated significant changes in the medial frontal cortex, the left and right paracingulate

168 ison subjects was seen in three regions: the medial frontal cortex, the right lateral prefrontal cort

169 n extensive neural network that included the medial frontal cortex, the superior frontal cortex, the

170 Within the medial frontal cortex, the supplementary eye field (SEF)

171 compound-B retention was first noted in the medial frontal cortex, then the precuneus, lateral front

172 The activity of most neurons in the medial frontal cortex tiled progress to goal, akin to ho

173 cluding the right inferior frontal gyrus and medial frontal cortex, to attentional capture, response

174 prefrontal cortex, and possibly the superior medial frontal cortex, to process two decision-making op

175 ychological states to discrete subregions in medial frontal cortex using relatively unbiased data-dri

176 rigenual anterior cingulate cortex, anterior medial frontal cortex, ventromedial prefrontal cortex, a

177 pathways from their activation volumes to 1) medial frontal cortex via forceps minor and uncinate fas

178 ins, sulcal morphological variability of the medial frontal cortex was assessed in Old World monkeys

179 However, activity in the posterior medial frontal cortex was elevated in AN following punis

180 in the absence of lesions to the lateral or medial frontal cortex, we conclude that a functional con

181 asively passing direct current through human medial-frontal cortex, we could enhance the event-relate

182 His hippocampi and medial frontal cortex were significantly more active dur

183 e and mirrored by fMRI signal changes in the medial frontal cortex, where activation also varied with

184 We recorded single neurons in the human medial frontal cortex while subjects performed two tasks

185 epresentation of predicted perception in the medial frontal cortex, while human subjects decided whet

186 The finding of increased beta-bursting over medial frontal cortex with movement cancellation in huma

187 ates x, y, z = -7, -71, 18; F = 7.55), right medial frontal cortex (x, y, z = 7, 59, 12; F = 8.53), r

188 posterior cingulate cortex/precuneus and the medial frontal cortex yielded optimal group separation a