ライフサイエンスコーパス: lateral

1 steering wheel variability (p = 0.0001) and lateral acceleration variability (p < .0001) relative to

2 ing from neurons that provide input from the lateral accessory lobe (LAL) to the noduli (NO).

3 inin-immunostained tangential neurons of the lateral accessory lobe cluster were also immunoreactive

4 tum (medial accumbens shell, accumbens core, lateral accumbens shell) and showed complex and heteroge

5 nce of vision on the ability to map frontal, lateral and back space has not been investigated.

6 neurons project axon collaterals to both the lateral and medial NTS subdivisions.

7 in subregions of both the ventral posterior lateral and posterior (PO) nuclei, forming a pair of rec

8 sents with a preferential involvement of the lateral and postero-lateral basal LV and is associated m

9 Terminal fields were densest in the lateral and ventrolateral periaqueductal gray (PAG), lat

10 ntial involvement of the lateral and postero-lateral basal LV and is associated mostly with variants

11 e optic gland and the peduncle, optic, dorso-lateral, basal, subvertical, frontal, magnocellular, and

12 g the first 3 days of acute coma, increasing lateral brain displacement is associated with worsening

13 DRO1 in regulating auxin-mediated changes in lateral branch angle.

14 We found that stalk width, number of lateral branches (tillers), and branching of the inflore

15 s required for the control of organ size and lateral branching.

16 With the discovery of lateral budding in 'Kolteria novifilia' and the capabili

17 mal caruncle and an oblique line joining the lateral canthus and the subnasal point would successfull

18 that the 5 mum-thick membranes are stable at lateral cell sizes of 5 mm by 20 mm.

19 R: R(2) = 0.86; T1weighted: not measurable), lateral center-edge angle of Wiberg (SWMR: R(2) = 0.88;

20 Sharp's angle, Tonnis angle, lateral center-edge angle of Wiberg and caput-collum-dia

21 trocorticographic (ECoG) activity across the lateral cerebral cortex as people heard and then mentall

22 and specific cis-interactions contribute to lateral clustering on lipid bilayers.

23 The IR lateral compartment and SR medial compartment significan

24 ovide input into the CX, especially from the lateral complex (LX), the superior protocerebrum, the po

25 FM labeling of lateral cristae in tmc double mutants revealed the prese

26 t vertical acoustic confinement releases the lateral design of freedom, and enables negligible cross-

27 ould be promoted by anisotropically enhanced lateral diffusion of oxygen along the midplane and by ju

28 permeability for small molecules and a slow lateral diffusion of proteins.

29 Lateral dimensions and separation were resolved down to

30 designable periodic arrangements and tunable lateral dimensions at the predesignated spatial location

31 leads to nonuniform growths along different lateral directions to form six-pointed Au nanostars.

32 Maximum lateral displacement during the first 3 days of coma was

33 ring pyocin contraction: tail fibres trigger lateral dissociation of baseplate triplexes; the dissoci

34 -public distinction is reflected in a medial-lateral division of prefrontal cortex - with lateral fro

35 everal novel corticofugal targets (i.e., the lateral dorsal nucleus, submedial nucleus) previously un

36 ly by private companies proposing to utilize lateral drilling technology to excavate boreholes for SN

37 l pulmonary artery occlusion pressure were a lateral e'-wave greater than 8 (for a left ventricular e

38 nting; rearward folding of the pinna's upper-lateral edge exhibited such differences only during refl

39 The lateral entorhinal cortex (LEC) projects to BLA where it

40 ing of the PttCLE47 gene expression affected lateral expansion of stems and decreased apical height g

41 l NW striking fault and then ruptured a left-lateral fault to the surface.

42 Suprapatellar effusion and reduced lateral femoral cartilage thickness were more prevalent

43 bril binding by both sHSPs and for mediating lateral fibril-fibril association, which sequesters pref

44 The Aspergillus Galactomannan Lateral Flow Assay (LFA) is a rapid test for the diagnos

45 then we validated a proof of concept for the lateral flow assay (LFA).

46 A new lateral flow assay (LFA, Sona, IMMY, Norman OK) improves

47 red blood cells (RBCs) through a no-reaction lateral flow assay (nrLFA) device.

48 of low-titer cryptococcal antigen (CrAg) by lateral flow assay is frequently uncertain.

49 ease of use, low cost and quick operation of lateral flow assays (LFA) have made them some of the mos

50 semiquantitative cryptococcal antigen (CrAg) lateral flow assays (LFAs) have been developed, but thei

51 Lateral flow assays (LFAs) represent a class of diagnost

52 by the CrAgSQ (IMMY) and CryptoPS (Biosynex) lateral flow assays.

53 ommercially available soy allergen detection lateral flow devices (LFDs).

54 Focusing on the widely used, low-cost lateral flow format as an exemplar, we achieve a detecti

55 e S1 domain of the spike protein (S1), and a lateral flow immunoassay (LFI) based on full-length spik

56 Lateral flow immunoassay paper strips quantitatively mea

57 OVID-19-related symptoms were verified and a lateral flow immunoassay test that detected SARS-CoV-2 i

58 e transcription-RPA technique coupled with a lateral flow immunochromatographic assay (CTV-RT-RPA-LFI

59 mping", to successfully conduct a commercial lateral flow immunochromatographic assay for tetanus ant

60 computerized tomography (CT) scan, RT-qPCR, lateral flow immunochromatographic strip (LFICS) for dia

61 we circumvent this problem by introducing a lateral flow plasmonic biosensor (LFPB) based on gold-vi

62 dies against SARS-CoV-2 was assessed using a lateral flow point-of-care test, the WONDFO SARS-CoV-2 A

63 tests, there are many other applications for lateral flow strip technology.

64 We discuss how this lateral flow test device can be an effective tool to det

65 esent an effort to develop and calibrate the lateral flow test devices for the detection of a bed bug

66 es in plasma is generally performed by rapid lateral flow test strips that lack quantitative results

67 asma separation membranes (PSM) coupled with lateral flow tests (low volume).

68 Lateral flow urine lipoarabinomannan (LAM) tests could o

69 Unlike other lateral flow-based assays (LFAs) involving the utilizati

70 , and 100% specific and 97% sensitive with a lateral-flow readout.

71 menable to multiplexed detection in a single lateral-flow strip incorporating an internal control for

72 following repeated mild TBI (rmTBI) using a lateral fluid percussion injury model.

73 movement (perking) differed according to the lateral focus of attention only during voluntary orienti

74 d in APOE epsilon4+group (left cingulate and lateral frontal and parietal regions p<0.01, threshold-f

75 between early encoding processes that engage lateral frontal and sensory regions to successfully enco

76 h, we identified a small cluster in the left lateral frontal lobe where children with greater upper-b

77 lateral division of prefrontal cortex - with lateral frontal pole (FPl) supporting the context-depend

78 ontoparietal lobes, in addition to scattered lateral frontal, parietal, and temporal areas.

79 d set-shifting provide evidence for atypical lateral frontoparietal and midcingulo-insular network ac

80 found robust face-selective responses in the lateral fusiform gyrus of individual blind participants

81 cessary for face-selectivity to arise in the lateral fusiform gyrus.

82 r promotes neural progenitor identity in the lateral ganglionic eminence (LGE), despite upregulating

83 sistently observe membrane thinning near the lateral gate for all proteins.

84 shows that the energy necessary to open the lateral gate in BamA/TamA varies by species, but is alwa

85 We also see occasional spontaneous lateral gate opening and sliding of the beta-strands at

86 uster assembly, one of which was acquired by lateral gene transfer from Chlamydiae.

87 that project to the pretectum (PT), ventral lateral geniculate nucleus (vLGN) or parabigeminal nucle

88 Even though the lateral geniculate nucleus of the thalamus (LGN) is asso

89 The lateral geniculate nucleus was only modulated by 3 to 9%

90 Likewise, the superior colliculus, dorsal lateral geniculate nucleus, and the posterior nucleus of

91 ied was the physical inversion of the dorsal lateral geniculate nucleus, as well as the lateral poste

92 in ongoing spiking activity in subcortical (lateral geniculate nucleus, LGN) and cortical (area MT)

93 al vapor deposition (CVD) is limited by slow lateral growth rates, which result in a tendency for non

94 reduces the nucleation density and promotes lateral growth.

95 The lateral habenula (LHb) is hyperactive in depression, and

96 off, accompanied by increased firing in the lateral habenula (LHb) that contributes to downstream ac

97 both approach and avoidance behavior via the lateral habenula.

98 pplications in oxide-electronic devices, the lateral homogeneity of such samples must be considered a

99 The lateral horn, the insect analog of the mammalian cortica

100 paraventricular hypothalamic nucleus (PVH), lateral hypothalamic area, and central nucleus of the am

101 Activation of LS(Nts) terminals in the lateral hypothalamus (LH) also decreases food intake.

102 n-concentrating hormone (MCH) neurons in the lateral hypothalamus (LH), which regulate REM sleep init

103 successfully withheld licking responses, but lateral hypothalamus (LH)-projecting neurons were more a

104 oject from the central amygdala (CeA) to the lateral hypothalamus (LH)] mediates avoidance of stress-

105 send convergent projections into the caudal lateral hypothalamus (LHA) encompassing the parasubthala

106 eters of one-dimensional carbon nanotube and lateral infinity of two-dimensional graphene.

107 dendrites of neighboring cells in support of lateral information exchange.

108 Lateral inhibition is a fundamental feature of circuits

109 f particular odorants.SIGNIFICANCE STATEMENT Lateral inhibition is a key feature of circuitry in many

110 ty between projection neurons, feedback, and lateral inhibition of these axons by a large population

111 The model predicted that in the absence of lateral inhibition, two-dimensional rhizoid cell groups

112 These can be larger than those formed with lateral inhibition.

113 jections act via mechanisms such as surround/lateral inhibition.

114 roaches capable of detecting and quantifying lateral interactions between proteins on membranes.

115 mproved model is presented, which shows that lateral ion currents lead to an accumulation of ions at

116 Lateral labia and medial tympaniform membranes consist o

117 ndependent pathway to regulate the growth of lateral leaflets.

118 r complex, superior olivary nuclear complex, lateral lemniscus, inferior colliculus, medial geniculat

119 Early in this pathway, in the lateral line ganglia, neurons respond almost exclusively

120 sory feedback pathways to the electrosensory lateral line lobe (ELL).

121 Information about water flow, detected by lateral line organs, is critical to the behavior and sur

122 lar architecture for the zebrafish posterior lateral line primordium, an experimentally tractable mod

123 These proteins also form transient lateral links connecting neighboring stereocilia during

124 novel sounds from speakers at four different lateral locations while the participants silently read a

125 reproductive anatomy of both sexes and their lateral mating behavior coevolved.

126 aque monkeys (Macaca mulatta), we found that lateral MD neurons carrying CD signals discharged before

127 The segregation of lipids into lateral membrane domains has been extensively studied.

128 basal domains, which comes at the expense of lateral membrane height in MDCK cells.

129 ) and K(ATP) channels to the ICD, but not to lateral membranes.

130 oliferative CP state and exhibit directional lateral migration.

131 he role of submesoscale fronts in generating lateral mixing, a mechanism which has been hypothesized

132 upt decrease in the free-energy barriers for lateral mobility of outer-spherically adsorbed Mg(2+).

133 n the membrane, whereas RhoA regulates their lateral mobility, allowing the emergence of the apical d

134 d mainly by significant contractility of the lateral more than the medial compartment of the inferior

135 n of primary motor cortex (wMC) and anterior lateral motor cortex (ALM).

136 Whereas lateral movement of proteins in this lipid bilayer is po

137 that the M(w) 6.5 event initiated on a right-lateral NW striking fault and then ruptured a left-later

138 found that TMS over object-selective cortex (lateral occipital complex) selectively impaired object r

139 s by targeting hippocampal interactions with lateral occipital cortex (LOC).

140 d found a larger N2 component for shape over lateral-occipital electrodes (250-400 ms), which also in

141 an underlying model or goods space and that lateral OFC is only required for normal behavior when th

142 p-down feedback as chemogenetic silencing of lateral OFC neurons disrupted reversal learning, as well

143 ty reflecting initial task learning, whereas lateral OFC neurons responded saliently and transiently

144 t identified an asymmetrical response of the lateral OFC to reward in both species.

145 ce, monitored the activity of neurons of the lateral OFC using two-photon calcium imaging and investi

146 The dynamic interaction of lateral OFC with sensory cortex thus implements computat

147 ses revealed a distinct engagement of S1 and lateral OFC, with S1 neural activity reflecting initial

148 We also found that lateral olivocochlear (LOC) efferent fibres re-form func

149 Compared with those undergoing the lateral or posterior approach, patients undergoing an an

150 opensity-score matched patients undergoing a lateral or posterior approach, the 2993 matched patients

151 omedial prefrontal "reward" network, and the lateral orbitofrontal "nonreward" network.

152 und in three other frontal cortical regions: lateral orbitofrontal cortex (orbital part of area 12 [1

153 Posterior lateral orbitofrontal cortex specifically detected rare

154 the dorsolateral prefrontal cortex, and the lateral orbitofrontal cortex, significantly moderated th

155 then received tumor removal surgery through lateral orbitotomy and histopathology confirmed a pleomo

156 ilayers and improve our understanding of the lateral organization in plasma membranes with higher com

157 Small solutes have been shown to alter the lateral organization of cell membranes and reconstituted

158 d (bilayer size, chain conformational order, lateral packing, lipid phase, and morphology) and the pr

159 h weaker, expression enrichment of the adult lateral parabrachial is also found with genes from indep

160 and ventrolateral periaqueductal gray (PAG), lateral parabrachial nucleus (LPB), caudal pressor area,

161 c receptor (Htr2c)-expressing neurons in the lateral parabrachial nucleus (LPBN(Htr2c) neurons) inhib

162 The lateral parabrachial nucleus (lPBN) is a major target of

163 The ventral lateral parietal cortex (VLPC) shows robust activation d

164 ting an interconnected network with numerous lateral paths both within, and particularly across, thes

165 ns to the ventromedial hypothalamus (VMH) or lateral periaqueductal gray (lPAG) drives escape behavio

166 eficient mice, although it is reduced in the lateral periodontium (gums) of neonatal Magel2-deficient

167 The contact area determines the lateral physical resolution of the measurement, and cons

168 The lateral plate mesoderm (LPM) forms the progenitor cells

169 The question remains whether the lateral portals or cytosolic constriction conduct ions u

170 The lateral position of the particle beam then is flexibly c

171 l lateral geniculate nucleus, as well as the lateral posterior and pulvinar nuclei in the domestic fe

172 Lateral posterior nucleus (LP) of thalamus, the rodent h

173 out high channel count recordings in dorsal-lateral prefrontal cortex (dlPFC; 768 electrodes) while

174 nnections between anterior cingulate cortex, lateral prefrontal cortex and anterior striatum.

175 d with CUD by using RNA sequencing of dorsal-lateral prefrontal cortex neurons.

176 Here, we show that the lateral prefrontal cortex of non-human primates contains

177 These results suggest that the lateral prefrontal cortex plays a key role in inferring

178 a frequency at which they synchronize across lateral prefrontal cortex, anterior cingulate cortex and

179 art of area 12 [12o]), cingulate cortex, and lateral prefrontal cortex.

180 ), is regulated by neurons in the medial and lateral preoptic area of the hypothalamus.

181 and local interneurons (LNs), which provide lateral processing within the AL.

182 previously undescribed small neuropil of the lateral protocerebrum.

183 previously undescribed small neuropil of the lateral protocerebrum.

184 giving rise to SOT are identified, i.e., the lateral Pt-Co asymmetry as well as out-of-plane injected

185 e nanoribbons (GNRs) are challenging because lateral quantum confinement and many-electron interactio

186 Group differences were not found in the more lateral quartiles.

187 The mean lateral rectus recession was 8.2 +/- 1.1 mm, and the mea

188 aled in Nissl-stained sections, of which the lateral regions of the EC display denser AChE staining t

189 Utilizing collimation, 3.6x greater lateral resolution beyond the Fresnel zone limit was ach

190 The lateral resolution is comparable to that of linear struc

191 ensitivity of infrared spectroscopy with the lateral resolution of scanning probe microscopy, allowin

192 d that frontal RFs require spectral cues and lateral RFs require ILDs.

193 the first known case of the participation of lateral rim cells in a sub-retinal pigment shield in an

194 separate cell type, but by extensions of the lateral rim pigment cells that penetrate gaps in the BM.

195 ty of MUS is dispensable for its function in lateral root development.

196 the double mutant occur mainly at stage I of lateral root development.

197 superoxide concentration and ROS-stimulated lateral root emergence.

198 , which produce no flavonols, have increased lateral root emergence.

199 nt with opposite effects of these mutants on lateral root emergence.

200 nvestigated this paradigm during Arabidopsis lateral root formation, when the lateral root primordia

201 uch as phyllotaxis, flower morphogenesis, or lateral root initiation, have been extensively studied,

202 Arabidopsis lateral root formation, when the lateral root primordia (LRP) must traverse three overlyi

203 n which increased level of kaempferol in the lateral root primordia of tt7-2 reduces superoxide conce

204 and MUSTACHES-LIKE (MUL), are overlapped in lateral root primordia.

205 ck function and the subsequent initiation of lateral root primordia.

206 SA, the gravitropic set-point angle (GSA) of lateral roots (LRs), auxin levels and auxin transport.

207 etin biosynthesis, formed reduced numbers of lateral roots and tt7-2 had elevated levels of kaempfero

208 The development of lateral roots requires multiple mechanisms that act toge

209 atdro1 primary and lateral roots showed impairment in establishing an auxin

210 atdro1 lateral roots were able to respond to exogenous auxin an

211 s to examine the ferret temporal region: the lateral rostral suprasylvian sulcal area.

212 degenerative diseases, including amyotrophic lateral sclerosis (ALS) and Alzheimer's disease (AD).

213 ues of Alzheimer's disease (AD), amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD

214 ism in UNC13A is associated with amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD

215 The most common genetic cause of amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD

216 t common known genetic cause for amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD

217 Amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD

218 pansions (HREs) in C9orf72 cause amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD

219 he two compounds in persons with amyotrophic lateral sclerosis (ALS) are not known.

220 Amyotrophic lateral sclerosis (ALS) is a fatal disease involving mot

221 Amyotrophic lateral sclerosis (ALS) is a multifactorial, multisystem

222 Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease c

223 rontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS) is incompletely understood.

224 dividuals who are diagnosed with amyotrophic lateral sclerosis (ALS) today face the same historically

225 he RNA-binding protein FUS cause amyotrophic lateral sclerosis (ALS), a devastating neurodegenerative

226 D), stroke, Parkinson's disease, Amyotrophic lateral sclerosis (ALS), and other neuroinflammatory con

227 utrient metabolism is altered in amyotrophic lateral sclerosis (ALS), as early as childhood, suggesti

228 d as a susceptibility factor for amyotrophic lateral sclerosis (ALS), but results are conflicting and

229 approach, we selected a model of amyotrophic lateral sclerosis (ALS), in which astrocytes expressing

230 us system (CNS) diseases such as amyotrophic lateral sclerosis (ALS), multiple sclerosis, and Parkins

231 on-invasive ventilation (NIV) in amyotrophic lateral sclerosis (ALS), the question of enteral nutriti

232 ppaB activity in pathogenesis of amyotrophic lateral sclerosis (ALS), we generated transgenic mice wi

233 In addition, expression of an amyotrophic lateral sclerosis (ALS)-associated superoxide dismutase

234 al lobar degeneration (FTLD) and amyotrophic lateral sclerosis (ALS).

235 potential therapeutic target in amyotrophic lateral sclerosis (ALS).

236 the commonest cause of familial amyotrophic lateral sclerosis (ALS).

237 are highly conserved features in amyotrophic lateral sclerosis (ALS).

238 rts of individuals with sporadic amyotrophic lateral sclerosis (ALS).

239 euroinflammation is important in amyotrophic lateral sclerosis (ALS).

240 degenerative diseases, including amyotrophic lateral sclerosis (ALS).

241 the most common genetic cause of amyotrophic lateral sclerosis (ALS)/frontotemporal dementia (FTD).

242 jority of patients with sporadic amyotrophic lateral sclerosis (up to 97%) and a substantial proporti

243 f72 in normal physiology, and in amyotrophic lateral sclerosis and frontotemporal degeneration.

244 tive diseases, including C9orf72 Amyotrophic Lateral Sclerosis and Frontotemporal Dementia (ALS/FTD).

245 e of frontotemporal dementia and amyotrophic lateral sclerosis and no mutation in known amyotrophic l

246 Frontotemporal dementia and amyotrophic lateral sclerosis are clinically and pathologically over

247 t the corticofugal hypothesis of amyotrophic lateral sclerosis experimentally.

248 ecline in the total score on the Amyotrophic Lateral Sclerosis Functional Rating Scale-Revised (ALSFR

249 Amyotrophic Lateral Sclerosis Functional Rating Scale-Revised item s

250 ative genes and risk factors for amyotrophic lateral sclerosis have been identified.

251 Amyotrophic lateral sclerosis is the most common degenerative disord

252 lerosis and no mutation in known amyotrophic lateral sclerosis or dementia genes.

253 the multiple roles of kinases in amyotrophic lateral sclerosis pathogenesis.

254 eration (p = 1.76 x 10(-08) with amyotrophic lateral sclerosis).

255 's disease, Alzheimer's disease, amyotrophic lateral sclerosis, and Huntington's disease.

256 l phenotypes (Alzheimer disease, amyotrophic lateral sclerosis, depression, insomnia, intelligence, n

257 rodegenerative diseases, such as amyotrophic lateral sclerosis, frontotemporal lobar degeneration, an

258 d mSOD1 might play a role in the amyotrophic lateral sclerosis-linked aggregation of SOD1.

259 to the onset and progression of amyotrophic lateral sclerosis.

260 eases, including Parkinson's and amyotrophic lateral sclerosis.

261 causing Parkinson's disease and amyotrophic lateral sclerosis/frontotemporal dementia/myopathy, resp

262 could determine that cholesterol facilitated lateral segregation most with the SMs that had 16 carbon

263 ional connectivity within the sensory-motor, lateral sensory-motor, auditory, salience, and subcortic

264 eously recorded from rat CA1 and caudodorsal lateral septum in rat during a rewarded navigation task

265 are members of a gene family that regulates lateral shoot orientation in plants.

266 The formation of any lateral shoots at the grafted sites were studied in two

267 gers pathological Cx43 redistribution to the lateral sides of cardiomyocytes (remodeling).

268 e improvements it is still limited in yield, lateral size and contamination.

269 rtunities for high-quality SCHPFs with large lateral size and controllable thickness that may find wi

270 to patterned arrays that span the membrane's lateral size.

271 ssion of the Smp/beta-catenin pathway in the lateral skeletal precursor cells, and does not influence

272 capability of those snakes which suffer high lateral slipping of the body.

273 netization in a two-phase bulk magnet with a lateral spatial resolution of 50 nm.

274 zation of CMU1 and CMU2, thus regulating the lateral stability of cortical microtubules.

275 nocular region in V1 of albino rats includes lateral striate cortex, being therefore about 25% larger

276 eward-evoked dopamine release in the ventral lateral striatum (VLS), but not in the ventral medial st

277 In contrast, the lateral striatum supported both types of memories if the

278 he NI to the visual hyperpallium, and to the lateral striatum.

279 nucleus of the trapezoid body (MNTB) to the lateral superior olive (LSO) this spontaneous activity g

280 rgical approach compared with a posterior or lateral surgical approach was associated with a small bu

281 logopenic progressive aphasia and medial and lateral temporal lobe for typical Alzheimer's disease.

282 ithin the visual cortex, fusiform gyrus, and lateral temporal lobe.

283 al frontal lobes, parahippocampal gyrus, and lateral temporal neocortex were at least twice as likely

284 ime, RD, FA, and AD values of the dorsal and lateral tracts on the injured side closely tracked measu

285 e found that both lesioned dorsal and intact lateral tracts on the lesion side exhibited prominent di

286 requires a high activation energy barrier in lateral tubulin-tubulin interactions.

287 onnections to relay ipsilateral eye input to lateral V1 in Long Evans rats is a consequence of the ex

288 nregulation of candidate ion channels in the lateral ventral neurons (LNvs) and show that the hyperpo

289 We show that lateral ventral neurons (LNvs) need I(h) to fire action

290 NTF), and the implantation of eMSCs into the lateral ventricle activated relevant pathways associated

291 .001), white matter (26 mL; P < .001), mean lateral ventricles (2.2 mL; P < .001), and mean summated

292 that patients had significant enlargement of lateral ventricles (F(1,59) = 48.89; p < 0.001) and redu

293 1.14; p = 0.036; CVR, 1.30; p < 0.001), and lateral ventricles (VR, 1.56; p = 0.004).

294 hesus macaques had persistent enlargement of lateral ventricles, smaller volumes and altered function

295 ture suggests that impairments in medial and lateral VPFC regions and their connections may be import

296 of VTA TH neurons, we identified medial and lateral VTA TH neuron activity profiles during self-admi

297 es, places, characters) were most salient in lateral VTC, whereas category representations (e.g., cor

298 side of the nostril sulcus representing the lateral wall is funnel-like.

299 ependymal cells that line the bottom and the lateral walls of the third ventricle.

300 rs at I409C/R410C, in close proximity to the lateral windows, and L402C/L403C, at the cytosolic ends