ライフサイエンスコーパス: lateral

1 PCDD/F congeners that are substituted in the lateral 2, 3, 7, and 8 positions are the most toxic, rem

2 2FG structure, which supports an alternating lateral access mechanism for LPS extraction.

3 es and plasma membranes, as well as on their lateral accumulation in lipid rafts.

4 umulate in dendritic spines of the adult rat lateral amygdala (LA) during consolidation of aversive p

5 Although long-term potentiation (LTP) in the lateral amygdala (LA) plays an essential role in auditor

6 ld denervation developed interval decline in lateral and inferior segments (diff-SEP -82 to -99) comp

7 of objects (predators, conspecifics) in the lateral and posterior visual fields, respectively.

8 ing collateral cardinal, spinal, superficial lateral and superficial intersegmental lymphatics.

9 ween the two groups was observed towards the lateral and the posterior sides of prostate.

10 nd that sniffing is accompanied by prominent lateral and vertical deflections of the nose, i.e., twit

11 he Puelles school includes a medial, dorsal, lateral, and ventral pallium.

12 d interfacial structure consists of a ridged lateral arrangement of adsorbed water molecules hydrogen

13 ided along the anterior-posterior and medial-lateral axes by microdissections.

14 ally along the anterior-posterior and medial-lateral axes of the chick tectum using microarray based

15 f circular fibres, oriented along the medial-lateral axis.

16 only the medial (beta = -0.22, P = .03) and lateral (beta = -0.08, P = .03) temporal regions, subcor

17 The z-disc is a structural component at the lateral borders of the sarcomere and is important for me

18 2011, a global dataset for the cirrus cloud lateral boundary (CCLB) was established.

19 in both the continental U.S. domain and from lateral boundary conditions that lead to the largest red

20 of architectures, depending on the number of lateral branches, internode elongation and phyllotaxy.

21 r, reproductive organs develop on very short lateral branches.

22 We showed that these lateral buds resulted from mislocalization of DivIVA, a

23 en microtubules undergo dynamic instability, lateral captures predominate even in the absence of rota

24 umnar neuropil domains (ventromedial, ventro-lateral, centromedial, central, centrolateral, dorsomedi

25 Our work establishes that MLIs in the lateral cerebellum are broadly activated during movement

26 Lateral chest radiograph demonstrated lytic destruction

27 and two anterior color patches ALC (anterior lateral color patch) and AMC (anterior medial color patc

28 lor patches, middle color patch CLC (central lateral color patch), and two anterior color patches ALC

29 Furthermore, if the orientation bias of lateral connections is very strong, or if inhibition is

30 Peloruside acts primarily at lateral contacts and has an effect on the "seam" of hete

31 diment deficit may result in drowning and/or lateral contraction.

32 terior-posterior, dorsal-ventral, and medial-lateral coordinates that we interpret as cell types.

33 anising centres (ncMTOCs) along the anterior/lateral cortex.

34 We found that lateral crosslinking activities have a much greater effe

35 eached a steady state where line tension and lateral crowding balanced.

36 bstrates by a hydrophobic interface confined lateral crystal growth method.

37 as the opposite where visual PSPs invade the lateral dendrite (LD).

38 f tranverse diffusion through the tissue and lateral diffusion and exchange with skin appendages is p

39 crowding, and molecular interactions deviate lateral diffusion from the expected random walks.

40 RFM image sequences, to account for both the lateral diffusion of molecules at the membrane and the c

41 how interactions between cellular pathways, lateral diffusion of proteins between synapses, and chlo

42 ree-dimensional photonic crystals to grow to lateral dimensions of 1 cm ( 30,000 of unit cells) and

43 those in area 1 and extended in a medial to lateral direction.

44 Ncad+ MCAs exhibit rapid lateral dispersal prior to penetration of three-dimensio

45 thic chip with 128 multiplexed deterministic lateral displacement devices containing 1.5 million mic

46 Our findings show relative longitudinal and lateral displacements of helical turns related to constr

47 entral ganglia by axons in the anterior- and lateral-dorsal nerve branches, and that sensitization in

48 match of Pb and IrTe2, which produces strong lateral electronic modulation of hexagonal symmetry and

49 As a component of the SC lateral element, SYCP3 has a critical role in defining t

50 inal cortex (PRC), which in turn projects to lateral entorhinal cortex (LEC).

51 Expansion of ARF3 expression into lateral epidermal cells in a TAS3 ta-siRNA-insensitive m

52 sin-II-dependent force anisotropy within the lateral epidermis, and stiffness anisotropy within the f

53 oach is implemented to limit the vapor phase lateral expansion over the heat transfer surface and act

54 surplus may result in vertical growth and/or lateral expansion, while a sediment deficit may result i

55 e nanoribbons in solution and found that the lateral extension results in decrease of their electroni

56 resolution of better than 15 mum over a 1-mm lateral field of view through the entire depth of an int

57 A lateral flow assay (LFA) can provide a rapid and cost-ef

58 Nucleic acid hybridization-based lateral flow assay (LFA) holds great potential to addres

59 A rapid, semi-quantitative lateral flow assay (LFA) was developed to screen the oxy

60 ndly test conditions, we evaluated two rapid lateral flow assays (LFA) for detection of Mycobacterium

61 materials is critical for the development of lateral flow assays and analytical devices based on pape

62 and capture DNA probe were performed on the lateral flow biosensor.

63 robe was immobilized on the test zone of the lateral flow biosensor.

64 metal detection on well-spot C-microPAD and lateral flow C-microPAD.

65 integration of active, chemical valves into lateral flow devices, using a scalable, single-step, wea

66 n and 6-FAM, which are then easily read on a lateral flow dipstick, upon which these products are imm

67 e, we reported a rapid and multiple-targeted lateral flow immunoassay (LFIA) system for the detection

68 With the use of a traditional sandwich lateral flow immunoassay, a portable imaging device, and

69 A novel lateral flow immunochromatographic device (LFD) was eval

70 s tailored to enhance a popular dual-antigen lateral flow malaria RDT that targets Plasmodium falcipa

71 Finally, lateral flow strips with a streptavidin capture test lin

72 NA extraction and enrichment into a low cost lateral flow-based test.

73 tep to step adjustments in postural sway and lateral foot placement positively correlated with those

74 ateral prefrontal cortex (rVLPFC) and the bi-lateral frontal eye field (FEF).

75 e-demand (MD) network, comprising regions of lateral frontal, insular, dorsomedial frontal, and parie

76 Foxp2 and ectopic persistence of the dorsal lateral ganglionic eminence marker Sp8.

77 s in the medial ganglionic eminences (MGEs), lateral ganglionic eminences (LGEs), and caudal ganglion

78 The aqueous cavity and lateral gate are reminiscent of features of protein-cond

79 oviding the first experimental evidence of a lateral gate in TamA: a structural element implicated in

80 phocholine (DMPC) liposomes, suggesting that lateral gating of the BamA barrel and/or hybrid barrel f

81 omplexa, is likely to have been obtained via lateral gene transfer from a prokaryote.

82 ecorded evoked responses in the mouse dorsal lateral geniculate nucleus (dLGN; thalamic relay for cor

83 , instructive changes in the firing of mouse lateral geniculate nucleus (LGN) neurons, leading to inc

84 t receptive field property of neurons in the lateral geniculate nucleus (LGN) of the dorsal thalamus,

85 the visual system passes through the dorsal lateral geniculate nucleus (LGN), where nerve signals or

86 As in other carnivores, the dorsal lateral geniculate nucleus consisted of three main layer

87 to promote anatomical recovery in the dorsal lateral geniculate nuclues (dLGN) from long-term MD star

88 KEY POINTS: The lateral habenula (LHb) has been implicated in regulation

89 The lateral habenula (LHb) is a brain structure receiving in

90 Lesions of dorsal column or lateral habenula (LHb) prevented the inhibitory effects

91 Furthermore, we showed that the lateral habenula (LHb) receives direct synaptic input fr

92 into two nuclear complexes, medial (MHb) and lateral habenula (LHb).

93 esults are consistent with the view that the lateral habenula establishes inhibitory relationships be

94 orientation) and one oriented with the medio-lateral hand axis (Across orientation).

95 and growth dynamics of highly anisotropic 2D lateral heterojunctions between pseudo-1D ReS2 and isotr

96 Surprisingly, the results reveal that ReS2 lateral heterojunctions to WS2 produce well-oriented (hi

97 tions or by stitching them laterally to form lateral heterojunctions via direct growth.

98 olayer WS2 /WS2(1-x) Se2x /WS2 multijunction lateral heterostructure via direct growth by chemical va

99 ansition metal dichalcogenides region in the lateral heterostructure with low-energy exciton resonanc

100 be incurred at the interfacial regions of a lateral heterostructure.

101 l control over the growth of two-dimensional lateral heterostructures at such extreme dimensions has

102 e technological potential of atomically thin lateral heterostructures in optoelectronic applications.

103 The lateral hypothalamic hypocretin/orexin (HCRT) system has

104 Damage to the lateral hypothalamus (LH) causes profound physical inact

105 However, the lateral hypothalamus (LH) is also a key reward-control l

106 uced alterations in sleep, we focused on the lateral hypothalamus (LH).

107 to be identified.SIGNIFICANCE STATEMENT The lateral hypothalamus (LHA) regulates motivated feeding b

108 to the mesolimbic dopamine circuit from the lateral hypothalamus and dorsal raphe nucleus and define

109 rease HS content and sulfation levels in the lateral hypothalamus and that HS contributes to the regu

110 Gamma-rhythmic input to the lateral hypothalamus from somatostatin-positive lateral

111 A new study suggests that the lateral hypothalamus may also participate in the formati

112 -aminobutyric-acid)-releasing neurons of the lateral hypothalamus, which promote the transition to wa

113 ughput and high sensitivity and permitting a lateral image resolution down to approximately 2.5 mum f

114 pposite changes in the septum (decrease) and lateral (increase) wall.

115 ws sensory organ segregation by antagonizing lateral induction and promoting commitment to the non-se

116 mally diverted from this fate and increasing lateral induction produces misshapen or fused sensory or

117 er-surround receptive fields, a prototype of lateral inhibition between neighboring sensory cells in

118 toreceptor interactions were consistent with lateral inhibition mediated by retinal horizontal cells

119 Cell fate determination by lateral inhibition via Notch/Delta signalling has been e

120 to cone signals is horizontal-cell-mediated lateral inhibition, which imparts a spatially antagonist

121 se results, we propose that FtsA antagonizes lateral interactions between FtsZ protofilaments, and th

122 crescentus FtsZ as an intrinsic regulator of lateral interactions between protofilaments in vitro Fts

123 lies of AOB mitral cells are synchronized by lateral interactions through chemical and electrical syn

124 We show that Even-skipped lateral interneurons (ELs) are sensory processing intern

125 decades, neurophysiological responses in the lateral intraparietal area (LIP) have received extensive

126 g technique were implanted into the anterior-lateral left ventricular wall in C57BL/6J (allogeneic mo

127 lic remodeling index (RVESRI) was defined by lateral length divided by septal height.

128 Channelrhodopsin (ChR2) expressed in ear and lateral line hair cells and acquired high-speed videos o

129 elopment, morphogenesis, and polarity in the lateral line of Danio rerio and the embryo of Caenorhabd

130 Detection of water motion by the lateral line relies on mechanotransduction complexes at

131 imilarly, HCs in neuromasts of the zebrafish lateral line system are generated as pairs, and two sibl

132 spikes) in hair-cell afferent neurons of the lateral line.

133 At lateral locations there was a central-eccentric location

134 ing behaviors such as oblique, vertical, and lateral lunging.

135 hycardia substrate concentrated to the basal lateral LV, with marked epicardial predominance.

136 vity; and (4) latest activation at the basal lateral LV.

137 survival compared to those with LGE and high lateral MAPSE (log-rank P < .0001).

138 th late gadolinium enhancement (LGE) and low lateral MAPSE had significantly reduced survival compare

139 IP2(S227E) rescued Eps15 localization at the lateral membrane and reestablished single-lumen cyst for

140 ery, Eps15 and pS227-FIP2 colocalized at the lateral membrane.

141 t of gastrulation and is concentrated in the lateral mesoderm and ectoderm at the neurula stage.

142 When seeded as individual cells, lateral migration and cell-cell junction formation prece

143 leton, especially microtubules, restrict the lateral mobility of AtHIR1 at the plasma membrane and fa

144 aces in real time via high-speed non-contact lateral molecular force microscopy.

145 igh actin-ezrin intensity area restricts the lateral movement of BCRs upon stimulation, consequently

146 be used to better leverage the differential lateral movement of particles with different sizes as th

147 urons in the laterodorsal tegmental nucleus; lateral noradrenergic neurons in the LC; medial GABAergi

148 e inactivating the central, basolateral, and lateral nuclei of the amygdala selectively strengthened

149 ncipal neurons per case were selected in the lateral nucleus and traced using Neurolucida software in

150 converge on post-synaptic neurons within the lateral nucleus of the amygdala (LA).

151 ring both encoding and retrieval, the AG and lateral occipital complex (LOC) became functionally conn

152 The lateral occipital complex (LOC) can represent shape fait

153 mulus onset, face-selective sources in right lateral occipital cortex and right fusiform gyrus and so

154 of the orbitofrontal cortex (OFC), only the lateral OFC represents the elemental nutritive attribute

155 In the north, the small lateral offset between the surface and mantle traces of

156 gle of tissue between the lateral rectus and lateral orbital wall and the superior rectus and the orb

157 en with BPD exhibited higher activity in the lateral orbitofrontal and dorsolateral prefrontal cortic

158 Recent work in macaques has suggested the lateral orbitofrontal cortex (lOFC) is relatively more c

159 ts), the lower was their D2-type BPND in the lateral orbitofrontal cortex, an important region in val

160 The lateral ordering improves as the growth rate is increase

161 udy, a GmCLV1A mutant (F-S562L) with altered lateral organ development, and two mutants of GmNARK, is

162 GED, a key gene involved in the sculpting of lateral organs in several model species, we identified i

163 gesting that the two peptides adopt distinct lateral packing of the diffracting units.

164 with the Nr4a2-labeled subplate cells in the lateral pallium at the site of the future insular cortex

165 Thus, the region of the lateral pallium was misidentified in the quadripartite m

166 mPFC]), and the VLS receives inputs from the lateral pallium-originated areas (e.g., the insula) [5,

167 ch hitherto was considered to arise from the lateral pallium.

168 d that glutamatergic neurons in the external lateral parabrachial nucleus (PBel) play a critical role

169 4-275; P < .001) in the posterior cingulate, lateral parietal, hippocampal, and parahippocampal corti

170 nd that the CDt innervated the caudal-dorsal-lateral part of the substantia nigra pars reticulata (cd

171 tterns of neural activity in both medial and lateral parts of the orbitofrontal cortex (OFC), only th

172 s that the previously subdominant, conserved lateral patch had become immunodominant for individuals

173 recall of memory B cells that recognized the lateral patch, the principal exposed epitope that did no

174 erties of a particular chordotonal organ-the lateral pentascolopidial (lch5) organ of Drosophila larv

175 ers to ketamine showed increased GBCr in the lateral PFC, caudate, and insula.

176 These changes were associated with increase lateral PFC-STN coherence and altered STN neuronal spiki

177 Lateral plant organs, particularly leaves, initiate at t

178 In conclusion, medial and lateral plantar nerve injuries did not occur more freque

179 ce between the FHL tendon and the medial and lateral plantar nerves.

180 g. neural tube, axial and paraxial mesoderm, lateral plate, ectoderm, endoderm) to drive axis morphog

181 rve fibers terminate in a restricted central-lateral portion of the nucleus of the solitary tract (nT

182 uggest that dechlorination of PCDD/Fs at the lateral positions is facile if not preferred in these en

183 ttern-based signatures of reward identity in lateral posterior OFC were modulated after selective dev

184 ymptomatic LV dysfunction had higher odds of lateral precordial T-wave inversions (odds ratio, 18.4;

185 confidence interval, 1.21-4.01; P=0.01) and lateral precordial T-wave inversions (odds ratio, 9.87;

186 of the route to the goal, bilateral inferior lateral prefrontal activity scales with the planning dem

187 nd MDD non-suicides (MDD, N=9) in the dorsal lateral prefrontal cortex (Brodmann Area 9) of sudden de

188 The lateral prefrontal cortex (LPFC) is essential for higher

189 The lateral prefrontal cortex (LPFC) plays a central role in

190 the ventral intraparietal area (VIP) and the lateral prefrontal cortex (PFC) of rhesus monkeys.

191 ical regions including the striatum, insula, lateral prefrontal cortex and anterior cingulate in resp

192 behavioural and EEG study, we focused on the lateral prefrontal cortex including dorsal and ventral p

193 erior frontal gyrus, or via damage to dorsal lateral prefrontal cortex regions, resulting in deterior

194 orrelations in insula, cingulate, medial and lateral prefrontal, superior temporal, and superior pari

195 Increasing the outward chain lateral pressure in the bilayer, through addition of lam

196 a case of an isolated fracture of the right lateral pterygoid plate by a penetrating foreign body (w

197 presence of a triangle of tissue between the lateral rectus and lateral orbital wall and the superior

198 that the stereotypical misinnervation of the lateral rectus by fibers of the oculomotor nerve in DRS

199 to temporally precise motor commands for the lateral rectus eye muscle.

200 in secondary aberrant misinnervation of the lateral rectus muscle by the oculomotor nerve.

201 able to nocturnal animals, but pronounced in lateral regions of the eye where images move quickly [4]

202 light-induced water splitting with improved lateral resolution is achieved.

203 Images of beads prove a near-isotropic lateral resolution of sub-100 nm.

204 To achieve spatially invariant lateral resolution, propagation-invariant sinusoidal fri

205 n biological systems with better than 10 mum lateral resolution.

206 l the mechanism of recognition of the ZEDIII lateral ridge by VH3-23/VK1-5 antibodies.

207 ntified a mutant that overcomes the block of lateral root (LR) formation under osmotic stress.

208 During lateral root (LR) formation, new LR meristems are specif

209 f the five ethylene receptors, ETR1 controls lateral root and root hair initiation and elongation and

210 AtLAZY2 and AtLAZY4 determined lateral root branch angle.

211 what extent the environmental regulation of lateral root development is a product of cell-type prefe

212 Floral organ abscission and lateral root emergence are both accompanied by cell-wall

213 d endodermal cells, rather than the sites of lateral root emergence, mediates the transport of apopla

214 attern of prebranch sites, an early stage in lateral root formation characterized by a stably maintai

215 regulator KIP-RELATED PROTEIN2 and ABERRANT LATERAL ROOT FORMATION4, resulting in a mass of cells wi

216 t3plt5plt7 triple mutants, the morphology of lateral root primordia (LRP), the auxin response gradien

217 gering new formative divisions that generate lateral root primordia (LRP).

218 nd adventitious buds (UABs) on the crown and lateral roots.

219 N1) are mutated in patients with amyotrophic lateral sclerosis (ALS) [5, 6].

220 glected symptom in patients with amyotrophic lateral sclerosis (ALS) although it is reported by most

221 reviously found in patients with amyotrophic lateral sclerosis (ALS) and developmental delay, intelle

222 (STRs), such as those that cause amyotrophic lateral sclerosis (ALS) and fragile X syndrome, is chall

223 ous tissue of most cases of both amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD

224 the most common genetic cause of amyotrophic lateral sclerosis (ALS) and frontotemporal dementia, tho

225 en linked to the pathogenesis of amyotrophic lateral sclerosis (ALS) and frontotemporal dementia.

226 involved in the pathogenesis of Amyotrophic Lateral Sclerosis (ALS) and Frontotemporal Lobar Dementi

227 In trying to model FUS-amyotrophic lateral sclerosis (ALS) in mouse it is clear that FUS is

228 Amyotrophic lateral sclerosis (ALS) is a devastating and incurable n

229 Amyotrophic lateral sclerosis (ALS) is a heterogeneous degenerative

230 Amyotrophic lateral sclerosis (ALS) is a multifactorial lethal motor

231 Amyotrophic lateral sclerosis (ALS) is debilitating neurodegenerativ

232 Amyotrophic lateral sclerosis (ALS) may be associated with low body

233 identify reliable biomarkers of amyotrophic lateral sclerosis (ALS), a progressive neurodegenerative

234 cord injury, multiple sclerosis, amyotrophic lateral sclerosis (ALS), and Alzheimer's disease.

235 he most common cause of familial amyotrophic lateral sclerosis (ALS), but the mechanisms underlying r

236 bar affect (PBA) is prevalent in amyotrophic lateral sclerosis (ALS), but there is limited informatio

237 neuromuscular disorders, such as amyotrophic lateral sclerosis (ALS), end life via respiratory failur

238 of FUS inclusions is promoted by amyotrophic lateral sclerosis (ALS)-linked mutations, but the cellul

239 adult-onset degenerative disease amyotrophic lateral sclerosis (ALS).

240 rly neuropathological feature of amyotrophic lateral sclerosis (ALS).

241 of the neurodegenerative disease amyotrophic lateral sclerosis (ALS).

242 a role in the pathophysiology of amyotrophic lateral sclerosis (ALS).

243 ed astrocyte and mouse models of amyotrophic lateral sclerosis (ALS).

244 nal fluid (CSF) of patients with amyotrophic lateral sclerosis (ALS).

245 gene are causative for familial amyotrophic lateral sclerosis (fALS).

246 OD1 mutations linked to familial amyotrophic lateral sclerosis (fALS/SOD1).

247 the most common genetic cause of amyotrophic lateral sclerosis and frontotemporal dementia (C9ALS/FTD

248 commonest known genetic cause of amyotrophic lateral sclerosis and frontotemporal dementia.

249 otypes for C. elegans models for amyotrophic lateral sclerosis and Parkinson's disease, and show a pa

250 and alpha-synuclein, involved in amyotrophic lateral sclerosis and Parkinson's disease, respectively,

251 and to motor unit dismantling in amyotrophic lateral sclerosis at late disease stage.

252 nnervation, which degenerates in amyotrophic lateral sclerosis from the early disease stage.

253 es in the cerebrospinal fluid of amyotrophic lateral sclerosis patients in early disease stage.

254 cipients had cancer, 79 (8%) had amyotrophic lateral sclerosis, 44 (4.5%) had lung disease, 26 (2.6%)

255 cal diseases, including ataxias, amyotrophic lateral sclerosis, nucleotide expansion disorders (Fried

256 gated whether spread of a mutant amyotrophic lateral sclerosis-associated cytosolic superoxide dismut

257 OPTN, E50K and M98K, but not an amyotrophic lateral sclerosis-associated mutant, E478G, induced cell

258 esignated HTB1M) of two familial amyotrophic lateral sclerosis-linked SOD1 mutants, SOD1(G93A) and SO

259 disease, muscular dystrophy, and amyotrophic lateral sclerosis.

260 nd the later stages can resemble amyotrophic lateral sclerosis.

261 outcome of the motor function in amyotrophic lateral sclerosis.

262 n (MSPd) that is associated with amyotrophic lateral sclerosis.

263 FUS and pathology of FUS-related amyotrophic lateral sclerosis.

264 signaling function implicated in amyotrophic lateral sclerosis.

265 e properties approved for use in amyotrophic lateral sclerosis.

266 disease, Huntington disease, and amyotrophic lateral sclerosis.

267 opsis The novel role of BdMUTE in specifying lateral SCs appears linked to its acquisition of cell-to

268 rongly tilts the Hawaiian plume and leads to lateral separation between high- and low-pressure melt s

269 eral hypothalamus from somatostatin-positive lateral septum cells evokes food approach without affect

270 la to the anterior hypothalamus and then the lateral septum to modulate aggression associated with ma

271 ections provide gamma-rhythmic inputs to the lateral septum; these inputs are causally associated wit

272 viewed records of 551 patients who underwent lateral sinus augmentation at Tufts University School of

273 associated with hemorrhage in patients with lateral sinus DAVFs than does CVR, and thus may offer gu

274 From 1995 to 2016, 163 cases of lateral sinus DAVFs were included and divided into hemor

275 ortical venous reflux (CVR) in patients with lateral sinus dural arteriovenous fistulas (DAVFs).

276 ation of the time-dependent evolution of the lateral size and thickness of the nanoprisms, enabled by

277 SiNSs) with thickness approximately 4 nm and lateral size of several micrometers, based on the intrin

278 Control of lateral size, aggregation state (single vs. few layers)

279 ss of 100 nm to 2.5 [Formula: see text]m and lateral sizes from [Formula: see text]m(2) to [Formula:

280 five-atom-thick, beta-In2Se3 nanosheets with lateral sizes tunable from approximately 300 to approxim

281 self-administration had on firing in dorsal lateral striatum (DLS), a brain area known to be involve

282 plateau, forcing the development of the left-lateral strike-slip Haiyuan fault south of the northern

283 on and enhanced inhibitory synapses from the lateral subdivision of the central amygdala via A2A rece

284 the medial nucleus of the trapezoid body to lateral superior olive glycinergic synapse, and the bask

285 loops can effectively bind the Abeta fibril lateral surface around the same 13-16 region.

286 ffusion for kinetochore capture, both to the lateral surface of a microtubule and at or near its end.

287 known as superantigens (SAgs), which engage lateral surfaces of major histocompatibility class II mo

288 d high-frequency theta power are seen across lateral temporal lobe recording sites and persist throug

289 N+, 1.19 [0.11]), less severe atrophy of the lateral temporal lobe, and lower mean (SD) cerebrospinal

290 ncta, neuronal processes also exhibit medial-lateral territories at both developmental stages with en

291 teleosts, which included localization to the lateral tuberal nucleus (NLT), the putative homolog of t

292 scale mantle convection, are likely to cause lateral variations in the back-arc mantle temperature.

293 similarity between the posterior-dorsal and lateral-ventral regions was corroborated by a multivaria

294 The lateral ventricle (LV) is a preferential location for br

295 hat infusion of 100 ng of HIV-1 Tat into the lateral ventricle of yellow fluorescent protein-expressi

296 ll maintenance and neurogenesis in the adult lateral ventricle subventricular zone and dentate gyrus.

297 ippocampus, pallidum, putamen, thalamus, and lateral ventricle).

298 distinct localization within the mouse brain-lateral ventricle.

299 ds: this local current crowding enhances the lateral void growth and coalescence.

300 nvolved the subepicardial layer inferior and lateral wall in 154 patients (41%; IL group), the midwal