ライフサイエンスコーパス: medial

1 ithin 10 angstrom of the distal [4Fe-4S] and medial [3Fe-4S] clusters, to cysteine (C), allows site-s

2 opamine binding across the ventral striatum (medial accumbens shell, accumbens core, lateral accumben

3 while memory under starvation is mediated by medial alpha'/beta' neurons.

4 he accessory olfactory bulb to the posterior medial amygdala-that is necessary for all behavioural re

5 duction to abduction averaged 1.1 +/- 0.2 mm medial and 1.1 +/- 0.2 mm anterior to the globe's geomet

6 ical distribution of CINs originating in the medial and caudal GEs at different time points.

7 lamus, and the fusiform gyri, as well as the medial and lateral dorsal and ventral prefrontal regions

8 There was also loss of cells in the medial and lateral mammillary nuclei in the hypothalamus

9 Hypoactivation was found in the medial and lateral prefrontal regions, most pronounced d

10 degrees C(6), is regulated by neurons in the medial and lateral preoptic area of the hypothalamus.

11 l lobe for logopenic progressive aphasia and medial and lateral temporal lobe for typical Alzheimer's

12 ewed literature suggests that impairments in medial and lateral VPFC regions and their connections ma

13 r photometry recordings showed DA neurons in medial and lateral VTA have distinct activity profiles d

14 photometry of VTA TH neurons, we identified medial and lateral VTA TH neuron activity profiles durin

15 Focusing on area 14, lying on the medial and orbital surfaces of the gyrus rectus, this st

16 correlation between NT-proBNP and GMD in the medial and posterior cingulate cortex but also in precun

17 catheter tip into the OA distal third versus medial and proximal thirds (P = 0.04) and a mean cathete

18 was locally delayed, almost tenfold, between medial and trans Golgi cisterna.

19 A/Glu was significantly reduced in the right medial anterior and right medial posterior thalamus of C

20 orrelated with general symptoms in the right medial anterior thalamus, as well as with disorganizatio

21 substantia nigra and then progressed to more medial areas of this region.

22 deactivation mainly encompassing lateral or medial associative neocortical areas.

23 isplay denser AChE staining than that of the medial banks.

24 with the decrease in MKRN3 expression in the medial basal hypothalamus of mice before the initiation

25 vating PAG-projecting neurons in the central-medial boundary zone of the amygdala (Amg(C/M-PAG) neuro

26 gher involvement of sensorimotor regions and medial brain structures.

27 2a1/Vgat) and are distributed largely in the medial CeA subdivision.

28 ermis output neurons in the mouse fastigial (medial cerebellar) nucleus, we identify five major class

29 t contractility of the lateral more than the medial compartment of the inferior rectus (IR) in both e

30 The IR lateral compartment and SR medial compartment significantly co-relaxed when binocul

31 nd GMD across the whole frontal and parietal medial cortex reflecting the consequence of HF onto the

32 d a role for the hippocampus and a Posterior Medial cortical network in signaling event boundaries.

33 beled expression in CeL and central amygdala medial division (CeM).

34 More precisely, in these cases the medial dorsal cutaneous nerve got injured during the fas

35 ive neurons, from PV-positive neurons in the medial dorsal thalamic nucleus, and from SOM-positive ne

36 ircuit from superior colliculus (SC) through medial-dorsal nucleus of the thalamus (MD) to frontal ey

37 alamocortical connections in the ipsilateral medial-dorsal thalamic nuclei.

38 a medial subpopulation (dorsal region of the medial DR) had increased.

39 zebrafish (the enamel organ) is derived from medial endoderm, as hitherto assumed based on position d

40 d influence on the population of intimal and medial endothelial, macrophage, and smooth muscle cell f

41 haracteristic loss of layer 3 neurons in the medial entorhinal area (MEA) that underlies seizure deve

42 enetic stimulation of BLA projections to the medial entorhinal cortex (mEC) enhances the consolidatio

43 Grid cell modules in the medial entorhinal cortex (MEC) express activity patterns

44 firing rate coding properties of neurons in medial entorhinal cortex (MEC) in a mouse model of tauop

45 The interplay between hippocampus and medial entorhinal cortex (mEC) is of key importance for

46 al neurons from slice preparations of rodent medial entorhinal cortex (MEC), but their functional rol

47 theta' waves and interacts strongly with the medial entorhinal cortex (MEC).

48 correct errors in path integration in mouse medial entorhinal cortex (MEC).

49 f spatial location and movement speed in the medial entorhinal cortex during the 'active' theta state

50 regions/layers in the dorsal hippocampus and medial entorhinal cortex of rats during exploration.

51 network activity from the hippocampus to the medial entorhinal cortex.

52 Here, we find that neurons of the mouse medial (fastigial) cerebellar nuclei (mCbN), which fire

53 MIV-711 significantly reduced medial femoral bone area progression (P = 0.002 for 100

54 002 for 100 mg/d and 0.004 for 200 mg/d) and medial femoral cartilage thinning (P = 0.023 for 100 mg/

55 resulting from excessive inward remodeling, medial fibrosis, and thrombosis.

56 ion and its membrane diffusion parameters in medial forebrain bundle axonal tracts connecting midbrai

57 In contrast, beta-band power within medial frontal areas was selectively attenuated when par

58 initiation and increased beta-bursting over medial frontal areas with movement cancellation.

59 is linked to decreased alpha oscillation in medial frontal channels.

60 The medial frontal cortex has been linked to voluntary actio

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

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

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

64 like internal-state-related variables in the medial frontal gyrus in both healthy subjects and smoker

65 inent gray matter hypoplasia was observed in medial frontal regions, the inferior olives, and the cer

66 oked by Ca(2+) spikes and describe resulting medial-frontal EEG on a male macaque monkey.

67 uced CTh/CSA in more restricted areas of the medial frontoparietal lobes, in addition to scattered la

68 ere, we show that Prdm16 expression in mouse medial ganglionic eminence (MGE) progenitors is required

69 ice lacking ALK4 in GABAergic neurons of the medial ganglionic eminence (MGE) showed marked deficits

70 GABA on apoptosis is mediated by inputs from medial ganglionic eminence (MGE)-derived but not caudal

71 i.e., the anterior entopeduncular area-basal medial ganglionic eminence of mammals).

72 We deleted mouse Nf1 from the medial ganglionic eminence, which gives rise to both oli

73 tem cells within the ventricular zone of the medial ganglionic eminence.

74 ring voluntary isometric contractions of the medial gastrocnemius (MG) muscle in chronic stroke survi

75 ndex (color power Doppler ultrasound) of the medial gastrocnemius (MG) muscle on either paretic or no

76 ation was significantly decreased in paretic medial gastrocnemius (MG) muscles compared to non-pareti

77 the same extent (P > .05) as the soleus and medial gastrocnemius.

78 ivity is observed in auditory cortex and the medial geniculate body of the thalamus in the absence of

79 lex, lateral lemniscus, inferior colliculus, medial geniculate body, and auditory cortex all being in

80 re principal neurons that can project to the medial geniculate nucleus.

81 rneurons electrically coupled to the central medial giant fiber (MGF), the command-like interneuron f

82 The medial habenula (MHb) is a phylogenetically-conserved ep

83 alpha3* nAChRs are densely expressed by medial habenula (mHb) neurons, which project almost excl

84 We find five subtypes of neurons in the medial habenula (MHb) that are organized into anatomical

85 n of cell populations that comprise both the medial habenular (MHb) and lateral habenular (LHb) subre

86 Electrophysiological recordings from medial habenular neurons revealed that GPR139 signaling

87 ncoding of sensory and motor features in the medial hypothalamic-brainstem instinctive network.SIGNIF

88 have identified neuronal populations in the medial hypothalamus and brainstem that encode defensive

89 The posterior and medial IC exhibited resembling connectivity patterns, wh

90 que sulcus running from lateral (surface) to medial (inside).

91 prefer therapeutic surgical weakening of the medial IR in the hypotropic eye.

92 ntly more cartilage volume reductions in the medial knee compartment and patella for participants wit

93 private-public distinction is reflected in a medial-lateral division of prefrontal cortex - with late

94 The medial layer of the aorta can also be subject to abnorma

95 nd loss of smooth muscle cells (SMCs) in the medial layer of the aortic wall.

96 rimental OA following destabilisation of the medial meniscus (DMM) and after acute cartilage injury a

97 rance and distribution were evaluated in the medial meniscus transection model of OA (5-, 10-, and 15

98 processes, whereas beta-band activity within medial motor areas reflects deliberate re-aiming.

99 ect axon collaterals to both the lateral and medial NTS subdivisions.

100 gyrus (PoCG) and between the dorsal/ventral medial nucleus and insula in the less frequent connectiv

101 ubtypes of cerebellar nuclear neurons of the medial nucleus are controlled by Purkinje cells, the sol

102 the presynaptic calyces to the postsynaptic medial nucleus of the trapezoid body (MNTB) neurons.

103 cinergic sound localization pathway from the medial nucleus of the trapezoid body (MNTB) to the later

104 Is) on spontaneous glutamate release in the medial nucleus of the trapezoid body (MNTB), an auditory

105 the encoding of acoustic information by the medial nucleus of trapezoid body, the most prominent sou

106 ascular meniscal cells and chondrocytes from medial OA knee joints (n = 10).

107 l cells derived from the lateral meniscus in medial OA patients have chondrogenic capacity in vitro a

108 ementia risk scores in parietal, frontal and medial occipital cortices, (3) with higher UPDRS-III sco

109 nier offsets, by contrast, occurred first at medial occipital electrodes, with responses at later tim

110 tion of GABAergic synaptic transmission onto medial OFC (mOFC), but not lateral OFC (lOFC) neurons.

111 Medial olivocochlear (MOC) efferent neurons in the brain

112 of a sustained sound.SIGNIFICANCE STATEMENT Medial olivocochlear (MOC) neurons are the final stage o

113 ripheral compression per se, rather than the medial olivocochlear reflex, could facilitate noise adap

114 tory peripheral compression, rather than the medial olivocochlear reflex, could facilitate noise adap

115 d the same mean level and both activated the medial olivocochlear reflex.

116 y and highly fluctuating noises activate the medial olivocochlear reflex; and (3) adaptation occurs e

117 Thus, enhancement of the medial olivocochlear system could be a viable strategy t

118 r to their respective sites of origin in the medial or caudal GE.

119 evaluation of patients >7 years old who had medial or lateral rectus muscle surgery at the Universit

120 tion pattern along the rostrocaudal axis for medial- or caudal-born CINs.

121 ntal cortex/superior frontal gyrus, and left medial orbitofrontal cortex.

122 the prefrontal cortex, temporal cortex, and medial orbitofrontal cortex.

123 s, MFS) that bisects the FG into lateral and medial parallel gyri.

124 large cohort of patients (n = 50), from the medial parietal cortex (MPC) and the medial temporal lob

125 oreactivity in the OB that was denser in the medial part (medOB), where processes were observed close

126 Crucially, we found that the medial part of PMC, putatively covering the supplementar

127 bumin-positive interneurons (PVIs) in dorsal-medial PFC (dmPFC) prior to an active bout, or a bout in

128 Unbiased mRNA expression profiling in the medial PFC (mPFC) of maternally separated (MS) pups iden

129 n the brain affects synaptic function in the medial PFC (mPFC).

130 hat the dorsal, prelimbic (PL) region of the medial PFC aids active avoidance in situations requiring

131 icroglia-mediated neuronal remodeling in the medial PFC, and subsequent behavioral and cognitive cons

132 icroglia-mediated neuronal remodeling in the medial PFC.

133 sed colony-stimulating factor (CSF)-1 in the medial PFC.

134 and hippocampal regions in a core posterior medial (PM) brain network.

135 r tau deposition in AT than in the posterior-medial (PM) memory network.

136 2 spots in the ventral PMC and 1 spot in the medial PMC, corresponding approximately to the ventral P

137 lar nucleus of the anterior nidopallium, and medial portion of the dorsolateral thalamic nucleus (DLM

138 e MFI was reported to be concentrated in the medial portion of the muscles in all participants, the m

139 s show that V. cholerae colonizes mainly the medial portion of the small intestine and that both the

140 duced in the right medial anterior and right medial posterior thalamus of CHR relative to HC groups.

141 s with disorganization symptoms in the right medial posterior thalamus.

142 tual choice, rather than on dorsolateral and medial prefrontal areas involved in several forms of cog

143 sex information is represented in the dorsal medial prefrontal cortex (dmPFC) across excitatory and i

144 s responsivity, with a prominent role of the medial prefrontal cortex (mPFC) and basolateral amygdala

145 ctures involved in emotional regulation, the medial prefrontal cortex (mPFC) and basolateral amygdala

146 as neuronal atrophy and synaptic loss in the medial prefrontal cortex (mPFC) and hippocampus.

147 nt anatomic and functional relay between the medial prefrontal cortex (mPFC) and the hippocampus (HPC

148 ven modularity-based parcellation of the rat medial prefrontal cortex (mPFC) combined with seed-based

149 Finally, gene expression analysis in the medial prefrontal cortex (mPFC) for a subset of genes pr

150 x differences in learned fear inhibition and medial prefrontal cortex (mPFC) function.

151 he glutamatergic system and its receptors in medial prefrontal cortex (mPFC) has been implicated in m

152 bic (PL) and infralimbic (IL) regions of the medial prefrontal cortex (mPFC) have been implicated in

153 e role of the Medial Temporal Lobe (MTL) and Medial Prefrontal Cortex (mPFC) in these processes, but

154 Using targeted medial prefrontal cortex (mPFC) infusions, these effects

155 Low miR-218 expression in the medial prefrontal cortex (mPFC) is a consistent trait of

156 Here, we demonstrated the medial prefrontal cortex (mPFC) is a site of learning-in

157 n between the ventral hippocampus (vHPC) and medial prefrontal cortex (mPFC) is known to be necessary

158 ectively modulate activity in neurons of the medial prefrontal cortex (mPFC) projecting to the nucleu

159 lutamatergic axon terminals arising from the medial prefrontal cortex (mPFC) to the dorsal raphe nucl

160 that the core empathy network including the medial prefrontal cortex (mPFC) was more engaged for eve

161 tivity on principal glutamatergic neurons in medial prefrontal cortex (mPFC) without any effect on gl

162 reas, the orbitofrontal cortex (OFC) and the medial prefrontal cortex (mPFC), as mice learned olfacto

163 0-80 Hz) brain oscillatory activities in the medial prefrontal cortex (mPFC), basolateral amygdala (B

164 A) dopamine (DA) neurons that project to the medial prefrontal cortex (mPFC), but not to nucleus accu

165 these inhibitory neurons, especially in the medial prefrontal cortex (mPFC), have been found in diff

166 We also tested performance in a medial prefrontal cortex (mPFC)-dependent rule-shifting

167 theta phase coupling between hippocampus and medial prefrontal cortex (mPFC).

168 , but not glutamate principle neurons in the medial prefrontal cortex (mPFC).

169 Parallel evidence, however, shows that the medial prefrontal cortex (mPFC; a critical node of the n

170 es neuronal atrophy and synaptic loss in the medial prefrontal cortex (PFC), and this leads to behavi

171 The functional anatomy of the medial prefrontal cortex and basal ganglia has been exte

172 rd-linked effective connectivity between the medial prefrontal cortex and basal ganglia related to de

173 ala (CeA) and gene expression changes in the medial prefrontal cortex and CeA from the same animals u

174 appears to be necessary to the stability of medial prefrontal cortex and hippocampal cell assembly f

175 n contrast, boundary-evoked responses in the medial prefrontal cortex and middle temporal gyrus incre

176 erlap between transcriptional alterations in medial prefrontal cortex and nucleus accumbens in human

177 n two brain regions implicated in depression-medial prefrontal cortex and nucleus accumbens-of humans

178 ypically involved in spatial navigation: the medial prefrontal cortex and the right entorhinal cortex

179 This review uses the example of amygdala-medial prefrontal cortex circuitry development to illust

180 and medial secondary motor subregions of the medial prefrontal cortex have heterogeneous responses to

181 owing weaning leads to a failure to activate medial prefrontal cortex neurons projecting to the poste

182 RNAs found to alter in expression within the medial prefrontal cortex of FKBP5 knockout mice were sel

183 STATEMENT The hippocampal formation and the medial prefrontal cortex of mammals represent the surrou

184 for SST interneuron-evoked disinhibition of medial prefrontal cortex output neurons and recruitment

185 of social-affective brain regions, with the medial prefrontal cortex playing a central role in the i

186 gulate cortex, temporoparietal junction, and medial prefrontal cortex promotes honesty, particularly

187 where photoactivation of SNAP-mGluR2 in the medial prefrontal cortex reversibly modulates working me

188 We acquired dorsolateral/medial prefrontal cortex samples from individuals with A

189 Second, event-related directed medial prefrontal cortex to basal ganglia effective conn

190 nes on layer II/III pyramidal neurons of the medial prefrontal cortex via CXCR4-dependent stimulation

191 trength of others' opinions in the posterior medial prefrontal cortex when opinions are disconfirming

192 the rostral anterior cingulate gyrus of the medial prefrontal cortex while monkeys expressed context

193 population of non-VIP ChAT(+) neurons in the medial prefrontal cortex with a distinct developmental o

194 scular endothelial cells) cells of cortical (medial prefrontal cortex) and subcortical (hippocampus)

195 (ventral hippocampus, nucleus accumbens, and medial prefrontal cortex) of susceptible, resilient, and

196 amate microdialysis in nucleus accumbens and medial prefrontal cortex, and ex vivo striatal dopamine

197 Activity in the orbitofrontal cortex, medial prefrontal cortex, and putamen represented the re

198 as targeted on the posteromedial cortex, the medial prefrontal cortex, and the cingulum.

199 circuit, that includes the amygdala, ventral medial prefrontal cortex, and ventral striatum, has subs

200 imbalance in several key regions, namely the medial prefrontal cortex, basolateral amygdala, hippocam

201 tioned context cues evolves over time in the medial prefrontal cortex, but not in animals that cannot

202 of cellular redox status, are reduced in the medial prefrontal cortex, striatum, and thalamus in schi

203 The medial prefrontal cortex, the hippocampus, and the thala

204 Coma patients displayed significantly lower medial prefrontal cortex-posteromedial cortex functional

205 The machine learning medial prefrontal cortex-posteromedial cortex multimodal

206 nit mRNA levels in the nucleus accumbens and medial prefrontal cortex.

207 that underlies remote memory storage in the medial prefrontal cortex.

208 basal ganglia and other regions such as the medial prefrontal cortex.

209 ncreased cortical thickness in the bilateral medial prefrontal cortex.

210 ate into myelinating oligodendrocytes in the medial prefrontal cortex.

211 etween participants and each agent recruited medial prefrontal cortex/pregenual anterior cingulate (p

212 us (and for disorganized schizotypy, also in medial prefrontal cortex; all false discovery rate-corre

213 Whereas higher levels of medial prefrontal cortical glutamate were associated wit

214 activity of midbrain dopamine neurons and of medial prefrontal cortical neurons.

215 iated by cells in entorhinal and (in humans) medial prefrontal cortices, which maintain their co-acti

216 Right medial prefrontal volume and surface area were positivel

217 suggest that specialized coordination in the medial prefrontal-amygdala network underlies social-deci

218 or oestrogen receptor 1 (ESR1) in either the medial preoptic area (MPOA) or the ventromedial hypothal

219 The medial preoptic nucleus (MPN) and ventrolateral part of

220 reward state and with opioid markers in the medial preoptic nucleus (mPOA).

221 MCs, termed degradative SMCs, compromise the medial properties and function of the aortic wall by enh

222 atient required a second embolization of the medial rectal artery and two required surgery.

223 The most commonly biopsied EOM was the medial rectus (44.4%).

224 Medial rectus (MR) lever arms averaged 12.0 +/- 0.2 mm a

225 agnosis of secondary exotropia who underwent medial rectus advancement surgery by a single surgeon.

226 s recession was 8.2 +/- 1.1 mm, and the mean medial rectus muscle resection was 6.7 +/- 0.9 mm.

227 Sustained GDNF treatment of one medial rectus muscle resulted in a measurable misalignme

228 Contrary to traditional teaching, medial rectus muscle surgery was not more likely to indu

229 istency, irregularity, and adherences to the medial rectus muscle.

230 GDNF, releasing 2 ug/day for 90 days, on one medial rectus muscle.

231 uscular junction number was unaltered in the medial rectus muscles, but were significantly reduced in

232 antly decreased in treated and contralateral medial rectus muscles.

233 reated with resection and advancement of the medial rectus.

234 r 2/3 pyramidal neurons in the cingulate and medial secondary motor subregions of the medial prefront

235 The medial septum (MS) is critical in theta generation by tw

236 MHb and its sole identified GABA input, the medial septum and nucleus of the diagonal band (MSDB).

237 hese effects were observed in BFCNs from the medial septum diagonal band and horizontal diagonal band

238 y neurons (D1-MSNs) in the nucleus accumbens medial shell (NAcmSh), and with lateral hypothalamus (LH

239 ons of a glutamate AMPA antagonist (DNQX) in medial shell of nucleus accumbens (NAc) can cause either

240 equired for AMPA-blocking microinjections in medial shell to induce either positively-valenced 'desir

241 This combination of medial SMC loss with marked increases in non-SMC aortic

242 Medial SMCs proliferate broadly to thicken the media, af

243 ifen required the presence of the underlying medial smooth muscle cells.

244 downstream brain regions such as the dorsal medial striatum (DMS) that encode action plans necessary

245 teral striatum (VLS), but not in the ventral medial striatum.

246 reas the number of serotonergic neurons in a medial subpopulation (dorsal region of the medial DR) ha

247 r cortex/supplementary motor cortex and left medial superior frontal gyrus.

248 Neurons in the medial superior olive (MSO) detect 10 us differences in

249 In the medial superior olive (MSO), these refinements generate

250 rience.SIGNIFICANCE STATEMENT Neurons in the medial superior olive, an ultra-fast coincidence detecto

251 Neurons in the medial superior olive, with their large bilateral dendri

252 rophysiology of the middle temporal (MT) and medial superior temporal (MST) areas.

253 ed to the largest disparity scale in macaque medial temporal area and to the estimated size of the re

254 rhinal volumes predicted degeneration in the medial temporal cortex, recapitulating a prior influenti

255 Medial temporal cortical thicknesses were not correlated

256 The IT projects directly to the medial temporal lobe (MTL) [19], where neurons respond s

257 umulating evidence points to the role of the Medial Temporal Lobe (MTL) and Medial Prefrontal Cortex

258 disrupted functional integration across the medial temporal lobe (MTL) subsystem of the default netw

259 ICANCE STATEMENT By recording from the human medial temporal lobe (MTL) while subjects recall items e

260 rom the medial parietal cortex (MPC) and the medial temporal lobe (MTL), structures known to be engag

261 The representational formats of medial temporal lobe and neocortex are sufficient to det

262 rability in women is not just limited to the medial temporal lobe and significantly contributed to gr

263 ons for future experience within neocortical-medial temporal lobe circuits.

264 related to a loss of structural stability in medial temporal lobe connectivity in a way that matched

265 Medial temporal lobe epilepsy (TLE) is the most common f

266 ngs were signal abnormalities located in the medial temporal lobe in 16 of 37 patients (43%; 95% conf

267 drawing on new insights into the role of the medial temporal lobe in auditory cognition.

268 ive persistently active neurons in the human medial temporal lobe phase lock to ongoing slow-frequenc

269 lt was robust against various thresholds and medial temporal lobe regions defining elevated tau.

270 Recordings from the medial temporal lobe, including the hippocampus, reveal

271 europathology was extensive and involved the medial temporal lobe, the diencephalon, cerebral cortex,

272 revealing a mechanism by which IEDs disrupt medial temporal lobe-dependent declarative memory retrie

273 itofrontal cortex and a key component of the medial temporal lobe-prefrontal cortex circuit.

274 ation areas first and then propagates to the medial temporal lobe.

275 breakdown of the BBB in the hippocampus and medial temporal lobe.

276 sleep also activates epileptic activities in medial temporal regions.

277 Despite removal of medial temporal structures, more than one-third of patie

278 of the hippocampus and immediately adjacent medial-temporal cortex by delivering theta-burst transcr

279 The hippocampus and surrounding medial-temporal-lobe (MTL) structures are critical for b

280 Synapses from the posterior medial thalamic nucleus to edge TRN cells evoke slower,

281 ctive pain, such as parabrachial nucleus and medial thalamic nucleus, as well as sensory-discriminati

282 n which pulmonary arteries narrow because of medial thickening and occlusion by neointimal lesions, r

283 uding increased right ventricular pressures, medial thickening, neointimal lesion formation, elastin

284 nd higher cartilage volume reductions on the medial tibia when runners wore a shoe that maximized the

285 as significantly higher in the heel than the medial tip, and females had more dopamine than males.

286 to RFA reduced recovery of reaching, damage medial to HL reduced recovery of hindlimb placing, and d

287 In vitro, ectopic HCLCs emerged in regions medial to inner HCs as well as in the stria vascularis.

288 al measures of MFI in four quartiles (Q1-Q4; medial to lateral) at cervical levels C4 through C7 were

289 rostrocaudal axis of origin is related to a medial-to-lateral axis of termination.

290 Lateral labia and medial tympaniform membranes consist of an extracellular

291 particularly dense in the dorsal tegmentum, medial vestibular nuclei and lateral parabrachial nucleu

292 ct activity profiles during fear extinction: medial VTA activity more closely reflected RPE, while la

293 ral level of domains (e.g., places), whereas medial VTC was also organized at the level of specific c

294 In both lateral and medial VTC, domain-level and category-level structure de

295 ed visual representations across lateral and medial VTC.

296 ences in representations between lateral and medial VTC.

297 he domain of places) were equally salient in medial VTC.

298 side of the nostril sulcus representing the medial wall of the nostril is rectangular, whereas the s

299 etuses treated with placebo had an increased medial wall thickness of peripheral pulmonary vessels (4

300 ng shh-GFP positive radial glia cells in the medial zone of the dorsal telencephalon (i.e., the teleo