ライフサイエンスコーパス: lobe

1 sula) compared to others (e.g. the occipital lobe).

2 ions, (ii) alpha-interface at the allosteric lobe.

3 the lesions were located in the right liver lobe.

4 nal were only found in the lateral occipital lobe.

5 e BBB in the hippocampus and medial temporal lobe.

6 lved lobe) and type of opacities within each lobe.

7 sociated with ripples in the medial temporal lobe.

8 nferior frontal gyrus, but not the occipital lobe.

9 odorant-responsive glomeruli in the antennal lobe.

10 .0020 mm/year, P = 0.0006) anterior temporal lobe.

11 and target every glomerulus in the antennal lobe.

12 nd localized beyond the ipsilateral temporal lobe.

13 of neural activity in the anterior temporal lobe.

14 with faster rates of atrophy in the temporal lobe.

15 cortex, fusiform gyrus, and lateral temporal lobe.

16 or the degree of parenchymal involvement per lobe.

17 t and then propagates to the medial temporal lobe.

18 ive degeneration in the frontal and temporal lobes.

19 issure of the frontal, parietal and temporal lobes.

20 ex morphologies and compositionally distinct lobes.

21 eas of the temporal, parietal, and occipital lobes.

22 s into other midline structures and cerebral lobes.

23 phatic drainage patterns of individual liver lobes.

24 vertical, frontal, magnocellular, and buccal lobes.

25 stly in the inferior aspect of the posterior lobes.

26 her MT in the bilateral frontal and parietal lobes.

27 Of the 414 operated thyroid lobes, 2.4% (n = 10) bled.

28 e neuronal diversity of the Drosophila optic lobe(3) and its connectome(4-6) are almost completely ch

29 nd affected mainly the branches of the lower lobe (30/41 [73.2%]).

30 strongest modulation in the medial temporal lobe (33 of 416) and in particular the right hippocampus

31 d exhibit more structurally complex antennal lobes [7-12].

32 ement with CT for findings in the left lower lobe (82.1%).

33 The origins of the posterior lobe, a recently evolved structure in some species of Dr

34 For every doubling in the inferior frontal lobe activation, angina frequency was increased by 13.7

35 nterior-most placode generates the endocrine lobe [adenohypophysis (ADH)] of the pituitary, a master

36 l neurodegeneration in the anterior temporal lobe, affecting primarily the ventral, occipito-temporal

37 l hemorrhage was noted in 3 left superior PV lobes after IRF.

38 The insect antennal lobe (AL) contains the first synapses of the olfactory s

39 ual differences are apparent across antennal lobe (AL) glomeruli (compact microcircuits corresponding

40 on and inhibition in the mosquito's antennal lobe (AL).

41 ly responsible for diencephalic and temporal lobe amnesia.

42 e correct lung and also to specific anatomic lobes among a diverse group of intubated patients with a

43 orbitofrontal cortex, inferomedial temporal lobe and cerebellum.

44 nderlie the common core symptoms of temporal lobe and diencephalic anterograde amnesia.SIGNIFICANCE S

45 the fissure moving anteriorly to the frontal lobe and laterally in the direction of the temporal pole

46 g and analysis to accurately measure global, lobe and millimetre scale growth trajectory patterns ove

47 representational formats of medial temporal lobe and neocortex are sufficient to determine both, mem

48 egions-of-interest including insula, frontal lobe and putamen in AD compared with controls, but no si

49 n is not just limited to the medial temporal lobe and significantly contributed to greater risk of fa

50 disorganization primarily involving frontal lobe and subcortical regions in nonpsychotic relatives m

51 associated with the developing genitalia of lobed and non-lobed species.

52 to the limbic system, whereas the occipital lobes and cerebellar hemispheres were unaffected.

53 volume increases in the temporal and limbic lobes and decrease in the superior temporal gyrus.

54 lyses of neural tissue (central brain, optic lobes and ommatidia) across development in two sympatric

55 FC between left and right inferior parietal lobes and right insular cortex.

56 TD participants in the frontal and temporal lobes and several sub-lobar regions previously associate

57 luding six distinct tracts between the optic lobes and the cerebrum.

58 onary involvement (by percentage of involved lobe) and type of opacities within each lobe.

59 igand: one weighted to the anterior temporal lobe, and another weighted to posterior temporo-parietal

60 d prediction signals in the insula, temporal lobe, and prefrontal cortex, while DA depletion affected

61 m, occipital, temporal, parietal and frontal lobes, and right hippocampus (p < 0.025 after family-wis

62 The pinnately lobed Aptian leaf fossil Mesodescolea plicata was origin

63 tergic and GABAergic deficits in the frontal lobe are potential targets for symptomatic drug treatmen

64 cal evidence that the mushroom body vertical lobes are necessary for retrieving visual memories for s

65 s are not only determined by medial temporal lobe areas, but essentially also by the neocortical regi

66 hat automatically segment the five pulmonary lobes, assign a CO-RADS score for the suspicion of COVID

67 The anterior temporal lobes (ATL) have become a key brain region of interest i

68 al outline that possesses a distinctly three lobed axis with an elevated central ridge and regularly

69 % CI -17.91, -3.79, p < 0.0125) and parietal lobes (B = -12.75, 95% CI -21.58, -3.91, p < 0.0125).

70 ere calculated in the neocortex and cortical lobes, basal ganglia (BG), hippocampi, and thalami.

71 of interest, especially the medial temporal lobe (beta=0.66-0.76, t=3.90-5.58, FDR-corrected p (p(FD

72 miR-298 varied in postmortem human temporal lobe between AD patients and age-matched non-AD controls

73 middle temporal areas, and anterior temporal lobe, but also parts of the control network as well as s

74 frontal cortex (MFC) and the medial temporal lobe, but it remains unknown how these structures implem

75 aggregates and neuronal loss in the temporal lobe, but primary age-related tauopathy lacks the requis

76 e medial diencephalon or the medial temporal lobes can result in profound anterograde amnesic syndrom

77 with non-lower lobe cancer, those with lower lobe cancer had a higher level of tumor markers (neuron-

78 Patients with lower lobe cancer had a lower proportion of adenocarcinoma his

79 Lower lobe cancer is associated with a higher all-cause mortal

80 hermore, compared to patients with non-lower lobe cancer, those with lower lobe cancer had a higher l

81 cases, 911 (39.8%) cases pertained to lower lobe cancers.

82 xperience within neocortical-medial temporal lobe circuits.

83 tangential neurons of the lateral accessory lobe cluster were also immunoreactive for GABA and the G

84 den was significantly reduced in the frontal lobe compared to the placebo group.

85 y system, projection neurons of the antennal lobe connect randomly to Kenyon cells of the mushroom bo

86 proportionally large volume of human frontal lobe connections is accompanied by a reduction in the pr

87 s of structural stability in medial temporal lobe connectivity in a way that matched proposed disease

88 tionary modifications affecting the temporal lobe connectivity pattern.

89 nnectivity and stronger hippocampal-temporal lobe connectivity.

90 nnectivity and stronger hippocampal-temporal lobe connectivity.

91 We propose that lobe contractile ring formation is locally inhibited by

92 ENT Frontal neural networks and the temporal lobes contribute to reward-guided learning in mammals.

93 pathologies in the hippocampus and temporal lobe cortex of drug-resistant temporal lobe epilepsy pat

94 hanism by which IEDs disrupt medial temporal lobe-dependent declarative memory retrieval processes.SI

95 fluctuates based on the particular stage of lobe development.

96 owever, how the organization of the temporal lobe differs across several anthropoid primates.

97 T-scan of abdomen showed enlarged left liver lobe due to the presence of large abscess cavity along w

98 s in the human neocortex and mesial temporal lobe during rhythmic onset seizures.

99 pathways to the electrosensory lateral line lobe (ELL).

100 Mesial temporal lobe epilepsy (MTLE) is a chronic neurological disorder

101 Mesial temporal lobe epilepsy (MTLE) is the most common form of focal, p

102 e included subjects with unilateral temporal lobe epilepsy (TLE) before (n = 29) or after (n = 56) an

103 Temporal lobe epilepsy (TLE) is characterized by recurrent seizur

104 Medial temporal lobe epilepsy (TLE) is the most common form of medicatio

105 hippocampal sclerosis are common in temporal lobe epilepsy (TLE), but little is known about the relat

106 temporal cortex samples of multiple temporal lobe epilepsy and non-epileptic subjects.

107 Individuals with temporal lobe epilepsy and normal MRI showed a similar pattern of

108 ogy were significantly activated in temporal lobe epilepsy brain samples, including the c-Jun N-termi

109 stochemical analysis of tissue from temporal lobe epilepsy cases revealed increased phosphorylation o

110 In temporal lobe epilepsy cases, hippocampal levels of phosphorylate

111 Temporal lobe epilepsy causes severe cognitive deficits, but the

112 Temporal lobe epilepsy is a complex neurological disease caused b

113 Temporal lobe epilepsy is the most common form of epilepsy in adu

114 boid and ramified cells from mesial temporal lobe epilepsy or peritumoral cortex tissue expressed P2Y

115 poral lobe cortex of drug-resistant temporal lobe epilepsy patients who underwent temporal lobe resec

116 Temporal lobe epilepsy represents a major cause of drug-resistant

117 healthy controls and 1249 patients: temporal lobe epilepsy with hippocampal sclerosis (n = 599), temp

118 th hippocampal sclerosis (n = 599), temporal lobe epilepsy with normal MRI (n = 275), genetic general

119 tonic-clonic seizures in a model of temporal lobe epilepsy, and rescued cognitive impairment and tran

120 ommon epilepsy syndromes, including temporal lobe epilepsy, extratemporal epilepsy, and genetic gener

121 ach for therapeutic intervention in temporal lobe epilepsy.

122 campal seizures in a mouse model of temporal lobe epilepsy.

123 human patients and animal models of temporal lobe epilepsy.

124 additional damage characteristic of temporal lobe epilepsy.

125 ppocampus, a region associated with temporal lobe epilepsy.

126 nitive impairment in drug-resistant temporal lobe epilepsy.

127 ons were ground-glass opacities (GGO) (59/70 lobes examined) and areas of consolidation (33/70).

128 The optic lobes exhibit the highest levels of polyploidy, associat

129 d directly inoculated into the mouse frontal lobe, exhibit striking differences in proliferative pote

130 rmal cells normally engulf and degrade large lobes extended by the PGCs [4].

131 nectivity between these regions and temporal lobe face patches.

132 the common ancestors to all sarcopterygians (lobe-finned fishes and tetrapods), in which Pax6 would b

133 We conclude that changes in lobe flexure occurred late in development, consistent wi

134 or posterior cortical atrophy, left temporal lobe for logopenic progressive aphasia and medial and la

135 sive aphasia and medial and lateral temporal lobe for typical Alzheimer's disease.

136 tau accumulation in the frontal and temporal lobes for all phenotypes and key regions of atrophy in t

137 orchestrated via auxin transport to control lobe formation and determine pavement cell shape.

138 The predictability of lobe formation in these cells allowed us to demonstrate

139 al shapes, reduction of vesicle circularity, lobe formation, and modulation of vesicle compactness.

140 ese young cells changes during the course of lobe formation, suggesting that these fluctuating auxin

141 ut not centralspindlin, is essential for PGC lobe formation.

142 aECM protein Dumpy is spatially expanded in lobe-forming species, connecting the posterior lobe to t

143 ns demonstrated connections to the occipital lobe from the fusiform gyrus along with longer associati

144 cigarette smokers.Methods: Whole right upper lobes from 12 human donors without pulmonary disease (6

145 s" and "representational" models of temporal lobe function is challenged.

146 show significant variation in integumentary lobe fusion and curvature.

147 Right lobe graft weight (764.8 + 145.46 vs 703.24 + 125.53 gra

148 Use of well-selected right lobe grafts (adequate future liver remnant in donor, GRW

149 Abnormalities within frontal lobe gray and white matter of bipolar disorder (BD) pati

150 were predominantly localized in the temporal lobe, however, sex differences in extra-temporal tau hig

151 abnormalities located in the medial temporal lobe in 16 of 37 patients (43%; 95% confidence interval

152 nsights into the role of the medial temporal lobe in auditory cognition.

153 ase and propagates up to the DNA recognition lobe in full-length CRISPR-Cas9.

154 brain tau deposition in the medial temporal lobe in MCI participants (r = 0.43 for early MCI and r =

155 ior frontal gyrus and left anterior temporal lobe in the process of flexible feature modulation durin

156 OP1/OP4 and 34 areas distributed across all lobes in stroke versus healthy adults.

157 hest CT and segments the lesions, lungs, and lobes in three dimensions, based on a dataset of 9749 ch

158 ied two new target glomeruli in the antennal lobe, in addition to the five known ones, and the ventro

159 s in tissue from human frontal and occipital lobes, in 11 cases with (M(age) = 79 +/- 7 years) and 5

160 estricted areas of the medial frontoparietal lobes, in addition to scattered lateral frontal, parieta

161 nal tau deposition in the bilateral temporal lobes including the entorhinal cortex.

162 Recordings from the medial temporal lobe, including the hippocampus, reveal the existence of

163 The geometric alignment of the lobes indicates that they were a co-orbiting binary that

164 larly require cAMP signaling in the antennal lobe inhibitory local interneurons.

165 volume of the frontal, temporal and parietal lobes, insula and whole brain.

166 the most primitive known seeds, with highly lobed integument and exposed nucellus.

167 larities identified between the Genomosperma lobed integument and floral organs, we propose that the

168 ocircuitry of agranular areas of the frontal lobe involved in cognitive control and responsible for e

169 s of the cavity, lung involvement, number of lobes involved, and the air-fluid levels in the two pati

170 Coma, temporal lobe involvement, hematoma volume, and electrographic se

171 ; CI, 1.36-17.57; p = 0.015); coma, temporal lobe involvement, intraparenchymal hemorrhage volume, an

172 ombined measures of the severity of lung and lobe involvement, quantifying both the extent of COVID-1

173 The inferior frontal lobe is an important area of the brain involved in the s

174 The frontal lobe is central to distinctive aspects of human cognitio

175 The medial temporal lobe is one of the most well-studied brain regions affec

176 versial whether a tumor located in the lower lobe is related with worse outcome of non-small cell lun

177 hat provide input from the lateral accessory lobe (LAL) to the noduli (NO).

178 The principle in right lobe living donor liver transplantation is to use "near-

179 and recipient outcomes in 623 primary right lobe living donor liver transplantations, using grafts w

180 e chest radiograph findings with correlating lobe ("lobe-specific" agreement) on CT was 87% versus 62

181 ferential lymphatic drainage patterns: Right lobe mainly to hepatoduodenal ligament lymph node 1 (LN1

182 gests that structural changes in the frontal lobe may have an indirect influence on age-related gener

183 e fact that each valve, secreted by 2 mantle lobes, may present antisymmetric ornamental patterns of

184 ly increased frequency of mushroom-body beta-lobe midline crossing, a metric of axonal guidance.

185 IT projects directly to the medial temporal lobe (MTL) [19], where neurons respond selectively to di

186 ce points to the role of the Medial Temporal Lobe (MTL) and Medial Prefrontal Cortex (mPFC) in these

187 The medial temporal lobe (MTL) is known as the locus of spatial coding and e

188 hippocampus and surrounding medial-temporal-lobe (MTL) structures are critical for both memory and s

189 ional integration across the medial temporal lobe (MTL) subsystem of the default network.

190 By recording from the human medial temporal lobe (MTL) while subjects recall items experienced in a

191 arietal cortex (MPC) and the medial temporal lobe (MTL), structures known to be engaged during face a

192 ography approach to demonstrate that frontal lobe networks, extending within and beyond the frontal l

193 olume in nearly all networks, except frontal lobe networks, where differences in grey matter were mor

194 g a continuous front in the Drosophila optic lobe neuroepithelium to produce neural stem cells (NSCs)

195 ingle species with significant variations in lobe number and fusion, reminiscent of floral developmen

196 The marked atrophy of the medial temporal lobe observed in AD patients may explain the increased f

197 rks, extending within and beyond the frontal lobes, occupy 66% of total brain white matter in humans

198 compensation allows tailoring of the maximum lobe of a propagation-invariant light field and promises

199 SR1 transmembrane segments 1 and 4 and the C-lobe of arrestin.

200 We covalently labeled each lobe of CaM (N and C) with fluorescent probes and used i

201 evolved morphological novelty, the posterior lobe of D. melanogaster.

202 cellular recording and staining in the optic lobe of intact animals.

203 al analyses of EEG recorded over the frontal lobe of macaque monkeys (one male, one female) performin

204 ne residues (Y954) located in the C-terminal lobe of the activator kinase domain was important to pot

205 Deep inside the temporal lobe of the brain, the hippocampus has a central role in

206 The G2 loop and switch I at the effector lobe of the catalytic domain exhibit large conformationa

207 ve lobula columnar (LC) neurons in the optic lobe of the fruit fly Drosophila melanogaster to charact

208 on, visible cysts were removed from the left lobe of the liver in nonanatomical resection and suspici

209 The study included 70 lung lobes of 14 patients who died of reverse-transcription p

210 of the transcriptomic diversity of the optic lobes of Drosophila.

211 nt rectangular neural network in the feeding lobes of Lobata (Mnemiopsis/Bolinopsis) but not in other

212 S LASSO uncovers a network spanning all four lobes of the brain.

213 The two lobes of the contact binary have closely aligned poles a

214 ideration of the geometry and mechanics of 2 lobes of the mantle, constrained both by the rigid shell

215 physically bridging the gap between the two lobes of the SBP.

216 By accepting electrons in both lobes of their empty p-orbital, they are capable of simu

217 ative overgrowth of the frontal and temporal lobes over the insula, corresponding to domains of highl

218 er olfactory epithelium (p = 0.071), frontal lobe (p < 0.001), or lungs (p = 0.037).

219 ntense stimulation was found in the parietal lobe (P2, P4, and P6 electrodes).

220 ysis moreover showed that the mesial frontal lobes, parahippocampal gyrus, and lateral temporal neoco

221 degeneration affecting the anterior temporal lobe, partial compensation appears to be possible by ove

222 active neurons in the human medial temporal lobe phase lock to ongoing slow-frequency (1-7 Hz) oscil

223 he same brain regions in the mesial temporal lobe, precuneus cortex, and angular gyrus.

224 uptake was evident in temporal and parietal lobes, precuneus, and posterior cingulate cortex.

225 ectivity between both temporal and occipital lobes predicted reading errors.

226 -glass opacities, consolidation, and a lower lobe predominance at CT.

227 and symmetric in 13 of 14 (93%), with lower lobe predominance in seven of 14 (50%).

228 x and a key component of the medial temporal lobe-prefrontal cortex circuit.

229 t the resulting imbalance of medial temporal lobe-prefrontal cortex connectivity partially mediated t

230 a-level rise and sediment supply that drives lobe progradation.

231 invasion of dorsal tracts into the temporal lobe provides a further specialization.

232 The right Anterior Temporal Lobe (rATL), putatively involved in semantic integration

233 position to the later pattern of debris-flow lobes reaching the present-day shelf edge.

234 ted inhibitory self-coupling within temporal lobe regions and excitatory projections between temporal

235 ainst various thresholds and medial temporal lobe regions defining elevated tau.

236 logical relationships primarily with frontal lobe regions, and their network-level alterations were a

237 ed on posterior parietal and medial temporal lobe regions, but the temporal dynamics of these regions

238 obe epilepsy patients who underwent temporal lobe resection (n = 19), in comparison with age- and reg

239 (n = 29) or after (n = 56) anterior temporal lobe resection and healthy volunteers (n = 124) comparab

240 ose who remained seizure-free after temporal lobe resection, normalizing the rate of atrophy to that

241 ct to the cortical motor system and temporal lobe, respectively.

242 5 +/- 6.1 for right upper, middle, and lower lobes, respectively (P < 0.001).

243 +/- 4.0 (P < 0.001) for left upper and lower lobes, respectively.

244 cortical development in males and females at lobe scales.

245 ciated with memory impairment after temporal lobe seizures.

246 enal ligament LN1 + LN2 concurrently; median lobe showed a more variable LN1/LN2 drainage pattern wit

247 e belonging to the non-classical small optic lobe (SOL) family of calpains, an important class of dev

248 as well in the brain region (in the temporal lobe) spatially separate from but most connected with it

249 th the developing genitalia of lobed and non-lobed species.

250 Lobe-specific agreement differed most between pulmonary

251 The lowest lobe-specific agreement for pulmonary ultrasound was nor

252 The highest lobe-specific agreement was for the finding of atelectas

253 CT findings when analyzed by both lung- and lobe-specific location among a diverse population of mec

254 radiograph findings with correlating lobe ("lobe-specific" agreement) on CT was 87% versus 62% (p <

255 d woman was diagnosed with a new right upper lobe stage I lung adenocarcinoma and underwent video-ass

256 r left upper lobectomy for remote left upper lobe stage IIIA adenocarcinoma and prior bilateral breas

257 elopment, which results in young plants with lobed stem outlines and a discontinuous distribution of

258 clear asymmetries exist within the temporal lobe structures subserving the core system and that the

259 Its two lenticular lobes suggest low-velocity accumulation of numerous smal

260 d insectivorous diets (transverse crests and lobes) suggests a varied faunivorous diet appropriate to

261 region in the left dorsal anterior temporal lobe supports object-color knowledge in both the blind a

262 Children were more often drug-free; temporal lobe surgeries had the best seizure outcomes; and a long

263 A temporal lobe tau PET meta-region of interest was used.

264 the memory system, centered on the temporal lobe that builds specific memory traces.

265 ior frontal gyrus and left anterior temporal lobe that related to our measures of feature modulation

266 requency on deltas with multiple self-formed lobes that scale with backwater hydrodynamics.

267 f the columnar organization of mushroom body lobes that, as shown in Drosophila and other hexapods, c

268 Within the antennal lobe, the CSDn differentially innervates each glomerulus

269 ets inhibitory local neurons in the antennal lobe, the CSDn has more distributed connectivity in the

270 s extensive and involved the medial temporal lobe, the diencephalon, cerebral cortex, basal ganglia,

271 In the Drosophila larval optic lobe, the generation of neural stem cells involves an ep

272 lfactory projections connecting the antennal lobe, the insect analog of the mammalian olfactory bulb,

273 d volume but greater right inferior temporal lobe thickness, surface area, and volume than the nondep

274 Subsequently, in the antennal lobe this representation is transformed into a dense and

275 s for synchronous discharges in the temporal lobe, though critical microcircuit-level detail is missi

276 neralization from the epileptogenic temporal lobe to broader brain networks in these patients.

277 toduodenal ligament lymph node 1 (LN1); left lobe to hepatoduodenal ligament LN1 + LN2 concurrently;

278 be-forming species, connecting the posterior lobe to the ancestrally derived aECM network.

279 The frontal cortex and temporal lobes together regulate complex learning and memory capa

280 ore active when "locked" onto Rsp5 via its N-lobe ubiquitin-binding surface and less active when they

281 [15, 17, 18] into the mushroom body vertical lobes (VLs) to selectively inhibit neural activity in th

282 nge in iron levels over time in the temporal lobe was associated with cognitive decline in individual

283 Blood flow to the inferior frontal lobe was evaluated as a ratio compared with whole brain

284 layers that make up the structure of its two lobes, we provide clues about the large-scale rheologica

285 R2* values in the temporal lobe were associated with longitudinal changes in Consor

286 ing-state absolute EEG powers in the frontal lobe were associated with wiser advising from the 2nd-,

287 ivariate responses in left anterior temporal lobe were predicted by degree of conceptual brightness m

288 erences between the methods in the left lung lobes were minor, with a mean difference of -0.4 +/- 4.4

289 a small cluster in the left lateral frontal lobe where children with greater upper-body muscular fit

290 of the C terminus of protein A to the apical lobe, which correlates well with the predicted structure

291 t ventral frontal area and the left temporal lobe, which represented a close mirror image of svPPA.

292 e changes in both hemispheres of the frontal lobe, which suggests that structural changes in the fron

293 chiometry; one TRPV6 tetramer binds both CaM lobes, which adopt a distinct head-to-tail arrangement.

294 been linked to major differences in temporal lobe white matter in humans compared with monkeys.

295 s global, while the second of (LSS, LHOS) is lobe-wise.

296 natomic association of the superior temporal lobe with other regions of whole-brain networks in patie

297 parison of refined 3D geologic models of the lobes with triaxial ellipsoids that suitably represent t

298 d in all brain regions, except the occipital lobe, with large effect sizes in the parietotemporal jun

299 cantly between PS and SPECT/CT in right lung lobes, with a mean difference of -8.2 +/- 3.8, 18.0 +/-

300 network hubs in both antero-mesial temporal lobes, with development of an abnormal excitatory fronto