ライフサイエンスコーパス: anterolateral

1 he section) were as follows: anterior 11.9%, anterolateral 15.8%, inferolateral 7.0%, inferior 24.3%,

2 s of procedures: (1) minor resections in the anterolateral (2, 3, 4b, 5, and 6) or (2) posterosuperio

3 olated MV operations were performed using an anterolateral 6 cm 4th intercostal space small-incision.

4 Cervical spine vertebroplasty from anterolateral access seems to be a safe, effective and b

5 Procedures were performed from anterolateral access, under local anesthesia, under x-ra

6 was to evaluate the method of treatment from anterolateral access.

7 z-scores were significantly more negative in anterolateral (AL) and mesial (M) regions on the operate

8 thway, including the middle-lateral (ML) and anterolateral (AL) belt regions of the auditory cortex,

9 der visual cortical areas lateromedial (LM), anterolateral (AL), posteromedial (PM), and anteromedial

10 key higher visual areas (lateromedial [LM], anterolateral [AL], and posteromedial [PM]) for percepti

11 However, the advantage of RMLR for the anterolateral(AL) (segments II, III, IVb, V and VI) segm

12 RC) is subdivided into functionally distinct anterolateral (alERC) and posteromedial (pmERC) subregio

13 somatosensory areas, and the medial (MM) and anterolateral (ALM) motor areas, single-neuron activity

14 Two types of complete disk displacement, anterolateral and anterior, occurred frequently in patie

15 bepicardial regions of the right ventricular anterolateral and apical regions.

16 extended to involve the distal and proximal anterolateral and inferior walls.

17 odal regions in posterior inferior parietal, anterolateral and medial temporal and medial prefrontal

18 or cruciate ligament (aACL and pACL) and the anterolateral and posteromedial bundles of the posterior

19 Anterolateral and posteromedial PM areas were 19.9+/-7 c

20 The number of anterolateral and posteromedial PM heads was 2.7+/-0.7 a

21 oint between the mitral annulus commissures [anterolateral and posteromedial] and z-axis directed tow

22 tex, with the former being generated in more anterolateral and the latter in more posteromedial parts

23 In particular, comprehension is dependent on anterolateral and ventral left temporal regions, as sugg

24 r visual areas (HVAs: LM (lateromedial), AL (anterolateral), and PM (posteromedial)) in mice of both

25 by 66% to 81% in the anteroseptal, anterior, anterolateral, and lateral regions (P < .05).

26 cementless THA through a minimally-invasive anterolateral approach.

27 l groups embedded within an undifferentiated anterolateral area (BSTal) that architectonically resemb

28 l levels of mouse visual cortex (area 17 and anterolateral area [AL]) and then determining the relati

29 cleus and the subcommissural zone and caudal anterolateral area of the BST - cell groups involved in

30 Of the three belt areas the anterolateral area shows the highest degree of specifici

31 r "L5 feedback") in higher visual areas, AL (anterolateral area) and PM (posteromedial area), display

32 dorsal area, dorsomedial nucleus, and caudal anterolateral area, and it moderately innervates the BST

33 cleus (BSTfu) and also innervates the caudal anterolateral area, anterodorsal area, rhomboid nucleus,

34 s (primary visual cortex, lateromedial area, anterolateral area, rostrolateral area, anteromedial are

35 treated with stellate-ganglion block at the anterolateral aspect of the C6 vertebra on the right sid

36 in nonhuman primates have characterized the anterolateral auditory pathway as a processing hierarchy

37 The small barrels in rat anterolateral barrel subfield and all barrel hollows in

38 n resulted in overlapping activations at the anterolateral belt and Wernicke's area, where the respon

39 When comparing these responses with those in anterolateral belt region of the auditory cortex, which

40 RP, and activation generated EPSCs in dorsal anterolateral BNST neurons that elicited two cell-type-s

41 ent views emphasize the contributions of the anterolateral BNST region in anxiety, accumulating data

42 We report here that neurons of the dorsal anterolateral BNST respond to glutamatergic synaptic inp

43 icted low-frequency cortical region near the anterolateral border of the primary auditory cortex, and

44 rophin releasing factor (CRF) neurons in the anterolateral cell group of the bed nucleus of the stria

45 The anterolateral cluster represents a lineage derived from

46 y or diagonally was investigated in cases of anterolateral cordotomy and in a case of thrombosis of t

47 e pattern consisted of late activation in an anterolateral corridor of the RA, and a second pattern c

48 s of diaphragm muscle were obtained from the anterolateral costal regions of the stimulated and inact

49 mplexity increasing along a posteromedial-to-anterolateral direction in core and lateral belt and alo

50 efined clusters located in the anteromedial, anterolateral, dorsal, and basoposterior brain, respecti

51 Functional connectivity between the anterolateral EC and the anterior-temporal (AT) memory n

52 lowed an anterior-to-posterior gradient, and anterolateral EC showed stronger temporal drift than pos

53 ns that are most closely associated with the anterolateral EC, which specifically affects memory in t

54 ns that are most closely associated with the anterolateral EC, which specifically affects memory in t

55 ic mitral regurgitation, at end systole, the anterolateral edge of the central scallop was displaced

56 nonprimary auditory cortex, overlapping the anterolateral end of Heschl's gyrus.

57 -oxygen-level-dependent fMRI activity in the anterolateral entorhinal (a homolog of the LEC in rodent

58 fically associated with increased FC between anterolateral entorhinal cortex (alEC) and dentate gyrus

59 etition suppression activity specifically in anterolateral entorhinal cortex (alEC) and hippocampus,

60 ogy first appears in the transentorhinal and anterolateral entorhinal cortex (alEC) in the aging brai

61 oral regions, namely in perirhinal (PrC) and anterolateral entorhinal cortex (alErC) in the medial te

62 liest in brain regions that overlap with the anterolateral entorhinal cortex (alERC).

63 es suggest that tau deposition starts in the anterolateral entorhinal cortex (EC) with normal aging,

64 es suggest that tau deposition starts in the anterolateral entorhinal cortex (EC) with normal aging,

65 is related to hyperconnectivity between the anterolateral entorhinal cortex and DG/CA3.

66 te early neurodegeneration of the perirhinal/anterolateral entorhinal cortex to impaired familiarity

67 the early primitive streak was seen from the anterolateral epiblast.

68 sual area, MT), and faces (middle fundus and anterolateral face patches in inferotemporal cortex - ar

69 whether the lateromedial field (LM) and the anterolateral field (AL), which are the principal target

70 ed the magnitude of hypertrophy in the basal anterolateral free wall (by 20+/-6%; P=0.001), as well a

71 ignificant regional conduction delays in the anterolateral free wall of the RV outflow tract of BS pa

72 ental LV hypertrophy largely confined to the anterolateral free wall, posterior septum, or apex, whic

73 nodes (receivers of influence) were found in anterolateral frontal, superior parietal, and superior t

74 ose that are already within the anterior and anterolateral funiculi and those that are crossing the c

75 Furthermore, we could detect an anterolateral gradient of WCS onset within one recording

76 The anterolateral group of the bed nuclei of the stria termi

77 The anterolateral group of the bed nucleus of the stria term

78 trol network (central amygdalar nucleus, BST anterolateral group, descending paraventricular hypothal

79 minated in one particular non-primary field, anterolateral Heschl's gyrus, and were suppressed when s

80 and location in parallel anterior "what" (in anterolateral Heschl's gyrus, anterior superior temporal

81 wer suppression decreased with distance from anterolateral HG throughout superior temporal cortex, an

82 in posteromedial HG, a non-primary field in anterolateral HG was characterized by high spontaneous a

83 We also observed that, in anterolateral HG, the power of high gamma responses to p

84 Compared to posteromedial HG, responses from anterolateral HG-an auditory belt field-exhibited longer

85 fied a cortical network comprising the right anterolateral hippocampus-a region modulating the hypoth

86 striatum dorsale and hyperstriatum ventrale, anterolateral hyperstriatum adjacent to the vallecula, c

87 rtebrates, the peptidergic somata lie in the anterolateral hypothalamus.

88 nts (12 ankles) with arthroscopically proved anterolateral impingement and in 19 control subjects (20

89 l MR imaging of the ankle is insensitive for anterolateral impingement.

90 , the central cardiac region in one, and the anterolateral-inferior fundal border in one.

91 ntral arborisations in the ventral neuropil (anterolateral interneurones 1-6, ALIN1-ALIN6) and those

92 the anterior ectosylvian visual area and the anterolateral lateral suprasylvian visual area, as well

93 splaced from CTL by 2.9+/-0.23 mm toward the anterolateral left ventricle and 2.5+/-0.12 mm toward th

94 Coronary occlusion produced stunning of the anterolateral left ventricle that resolved over 24 hours

95 EPCM was sutured to the anterolateral left ventricular wall, which included the

96 ons may disrupt projections from M3, whereas anterolateral lesions may disrupt projections from M1 an

97 of the split in contact with the globe at an anterolateral location, suggesting an inadequate posteri

98 e undetected areas of wall thickening in the anterolateral LV free wall (17 to 20 mm), which resulted

99 sment of LV hypertrophy, particularly in the anterolateral LV free wall, and represents a powerful su

100 The infarctions were localized to the anterolateral LV wall.

101 The nonvolitional technique of bilateral anterolateral magnetic stimulation of the phrenic nerves

102 Besides the generally identified groups of anterolateral, medial, and posterolateral neurons within

103 precursors were observed migrating from the anterolateral mesoderm in living embryos from 16 to 28 h

104 %) patients had abnormal electrograms in the anterolateral mitral annulus and/or MAD area.

105 entered on the face/mouth motor field of the anterolateral motor cortex (ALM) revealed that FSNs fire

106 c sequence branching signals occurred in the anterolateral motor cortex and M1TJ.

107 Photoinhibition of anterolateral motor cortex impaired corrections, which r

108 ibit preparatory activity similar to that in anterolateral motor cortex prior to reward acquisition.

109 Neural activity in anterolateral motor cortex reflected upcoming, ongoing a

110 ion variables were weakly represented in the anterolateral motor cortex, a region necessary for gener

111 tency suppression of preparatory activity in anterolateral motor cortex.

112 By contrast, the tongue 'premotor' (anterolateral motor) cortex(3-10) encoded latent variabl

113 ood-sampling algorithm on recovery-corrected anterolateral myocardial regions of interest.

114 Patterning of the anterolateral neural plate (telencephalon) may be regula

115 sting that FGF8 regulates the development of anterolateral neural plate derivatives.

116 reas the spatial selectivity was better than anterolateral neurons.

117 in the hypothalamus, the pretectum, and the anterolateral optic tectum.

118 l 6 basal segments (anteroseptal, P=0.01 and anterolateral, P<0.001).

119 h arrhythmia foci being mapped at either the anterolateral papillary muscle or posteromedial papillar

120 cle level; also, in 1 patient, attachment of anterolateral papillary muscle with the lateral free wal

121 nd septally (5.8+/-1.5 mm, P<0.001), and the anterolateral papillary tip underwent greater septal-lat

122 ceived forceps-like process systems from the anterolateral part of the third ventricle.

123 Projection neurons of the anterolateral pathway are attractive therapeutic targets

124 The anterolateral pathway consists of ascending spinal tract

125 However, the organizational logic of the anterolateral pathway remains poorly understood.

126 fourth pattern defines two other nuclei, the anterolateral periolivary nucleus (rostral) and the post

127 g the left and right LUS aeration scores and anterolateral pleural line abnormalities, had an area un

128 clinical VAs (N=29 posteromedial PM and N=6 anterolateral PM).

129 omedial portion of Heschl's gyrus (HGPM) and anterolateral portion of Heschl's gyrus (HGAL), planum t

130 L/pACL) and the posterior cruciate ligament (anterolateral/posteromedial; aPCL/pPCL) were analyzed.

131 te (dACC), right dorsolateral, and bilateral anterolateral prefrontal (alPFC) cortices.

132 ssociated with increasing myelination in the anterolateral prefrontal cortex, which showed stabilized

133 Conversely, stimulation of anterolateral prefrontal sites, often considered crucial

134 rate that the functional organization of the anterolateral processing pathway in humans is largely co

135 ing evidence supports the hypothesis that an anterolateral processing pathway mediates sound identifi

136 1 had normal tests, but the other developed anterolateral Q waves.

137 of sensory loss following transection of the anterolateral quadrant of the cord consists of a narrow

138 ted by stimulation sites that were both more anterolateral (r = .51, p < .01) and more negatively cor

139 fication of a late-activated corridor in the anterolateral RA.

140 s (diameter 25-40 mu m) are clustered in the anterolateral region of the eighth abdominal neuromere,

141 in the inferobasal region, 9 (39.1%) in the anterolateral region, 4 (17.4%) in the RVOT, and 6 (26.1

142 in the inferobasal region, 12 (26.6%) in the anterolateral region, 8 (17.7%) in the RV outflow tract

143 e midpart of the mitral annulus and near the anterolateral region; 3) increased posterior mitral leaf

144 Electrograms were recorded from the anterolateral right atrium, His bundle position, and cor

145 mostly because of a significant delay in the anterolateral right ventricular outflow tract.

146 ally and 0.9+/-0.6 mm apically away from the anterolateral scallop; such displacement correlated with

147 pontine parabrachial nucleus and targets its anterolateral sector (BNST-AL).

148 lusion led to hypokinesia of the anterior or anterolateral segments of the myocardium.

149 Hex-expressing cells reveals an anterior and anterolateral shift from their distal epiblast position.

150 icular apex) of the posterior leaflet on the anterolateral side (eg, 7.0 versus 6.2 mm), which is ana

151 rized by the formation of new bone along the anterolateral spinal column at four adjacent vertebral b

152 nstrate that functional connectivity between anterolateral superior temporal cortex and right anterio

153 nguage deficits associated with altered left anterolateral superior temporal cortex connectivity in a

154 h comprehension in normal subjects with left anterolateral superior temporal cortex connectivity in a

155 normal narrative speech comprehension, left anterolateral superior temporal cortex displayed positiv

156 We compared the organization of left anterolateral superior temporal cortex functional connec

157 onnectivity and with local activation in the anterolateral superior temporal cortex.

158 ty of a key speech-processing region in left anterolateral superior temporal cortex.

159 frontal gyrus and homotopic cortex in right anterolateral superior temporal cortex.

160 with the degree of disruption of left-right anterolateral superior temporal cortical connectivity an

161 functional connection between left and right anterolateral superior temporal cortices.

162 nferiorly, extending to the pelvis along the anterolateral surface of the psoas muscle; and laterally

163 of the paravertebral ganglia, located on the anterolateral surface of the vertebral body.

164 The anterolateral system (ALS) is a major ascending pathway

165 2a::Cre mouse line has been shown to capture anterolateral system (ALS) projection neurons.

166 Anterolateral system (ALS) spinal projection neurons are

167 Anterolateral system (AS) neurons transmit pain signals

168 timodal 'wide dynamic range' neurones of the anterolateral system.

169 enhanced or depressed during arousal via the anterolateral system.

170 of structural deficit, revealed significant anterolateral temporal atrophy (especially on the left),

171 semantic dementia have prominent atrophy in anterolateral temporal cortex and also have significant

172 mine the consequences of focal damage to the anterolateral temporal cortex for the operation of this

173 enial cortices with predominately medial and anterolateral temporal cortex.

174 tations in entorhinal, medial prefrontal and anterolateral temporal cortices via the hippocampal form

175 gion critical to semantic processing, is the anterolateral temporal lobe, especially on the left.

176 own to be severely impaired by damage to the anterolateral temporal lobe.

177 g the medial prefrontal cortex, amygdala and anterolateral temporal lobe.

178 NTLE patients demonstrated seizure onset in anterolateral temporal neocortex on electroencephalograp

179 asurements of skin-to-muscle depth (STMD) at anterolateral thigh and anterior thigh were performed.

180 than AAI needle length (15.02 mm), using the anterolateral thigh as the recommended administration si

181 Evidence of the anterolateral thigh fascia lata (ALTFL) rescue flap tech

182 the oral cavity or skin, reconstructed with anterolateral thigh or osteocutaneous fibula free flaps.

183 rapy, delivered via ice cup massage over the anterolateral thigh.

184 otomy in 227, partial sternotomy in 349, and anterolateral thoracotomy in 241.

185 complete sternotomy, partial sternotomy, and anterolateral thoracotomy, respectively.

186 tial sternotomy, and 42 (18 and 90) days for anterolateral thoracotomy.

187 organized somatotopically, with hand fibers anterolateral to foot fibers, not anteromedial as is cur

188 verlapping layer VI-to-II sequence and in an anterolateral to posteromedial gradient [the transverse

189 nd flipped over position on the cranial base anterolateral to the foramen magnum.

190 neurons that resides in the tuberal region, anterolateral to the neuroanatomical core of the VMH.

191 SAHS have excess fat deposition, especially anterolateral to the upper airway when compared with con

192 t in control subjects was localized to areas anterolateral to the upper airway, the differences were

193 irth sequence of gastrulation into a spatial anterolateral-to-posteromedial arrangement.

194 egions of Pf as well as the posteromedial to anterolateral topographic gradient of increasing Pf proj

195 presentation of somatosensory stimuli in the anterolateral tract, the principal pathway transmitting

196 increased perfusion defect of the apical and anterolateral wall at day 28 post-myocardial infarction.

197 tk have significant [18F]-FHBG uptake in the anterolateral wall compared with background signal in co

198 Shortening FRPs in the anterolateral wall of the ventricle increased the amplit

199 selectively depressed left ventricular (LV) anterolateral wall strain (LWS) and right ventricular (R

200 base (versus apex), the inferoseptum (versus anterolateral wall), and the subendocardium (versus sube

201 in components were typically greatest in the anterolateral wall, increased toward the apex, and incre

202 the left ventricular posterobasal (68%) and anterolateral walls (58%).

203 ocardial probe accumulation, was seen in the anterolateral walls of the infarcted mice but not in the