ライフサイエンスコーパス: medial

1 of the CRS-induced structural remodeling of medial amygdala (MeA) stellate neurons.

2 nals from the PV MOB to the anterior part of medial amygdala (MeA).

3 n regions (for example, the locus coeruleus, medial amygdala and paraventricular nucleus), implicatin

4 nd that CIC activity in the hypothalamus and medial amygdala modulates social interactions.

5 rm an intrinsic network (referred to as the "medial amygdala network") that supports social functioni

6 d stronger intrinsic connectivity within the medial amygdala network.

7 e nucleus accumbens shell, and moderately to medial amygdala, locus coeruleus and solitary tract, con

8 y numbers, which were mainly observed in the medial amygdala/bed nucleus of the stria terminalis to l

9 Aortic medial amyloid is the most prevalent amyloid found to da

10 pallium, expressing all genes, includes the medial and dorsomedial cortices, and the majority of the

11 nd lateral horn through dual pathways termed medial and lateral antennal lobe tracts (m-ALT and l-ALT

12 ented in patterns of neural activity in both medial and lateral parts of the orbitofrontal cortex (OF

13 In conclusion, medial and lateral plantar nerve injuries did not occur

14 single minimally invasive technique, and the medial and lateral plantar nerve lesions were scrupulous

15 arge distance between the FHL tendon and the medial and lateral plantar nerves.

16 r-subject correlations in insula, cingulate, medial and lateral prefrontal, superior temporal, and su

17 y of electrophysiological properties between medial and lateral SNc neurons modulated by cholinergic

18 s represented in motor cortex areas that are medial and posterior relative to ALM, including vibrissa

19 physis below the right femoral head, with a medial and posterior slip of the right femoral head.

20 parts of the thalamus, including the ventral medial and ventral anterior-lateral nuclei.

21 eys, we discovered a network centered in the medial and ventrolateral prefrontal cortex that is exclu

22 amus into four subnuclei (anterior, lateral, medial, and posterior).

23 Medial apoptosis and proliferation were both significant

24 ion from previously uncharted regions of the medial arcopallium and a minor projection from the caudo

25 MMAN input is organized across the lateral-medial axis whereas NIf input is organized across the ro

26 ts; however, APOE epsilon4 rendered only the medial (beta = -0.22, P = .03) and lateral (beta = -0.08

27 idergic (GABAergic) neurotransmission in the medial CeA and the sensitivity of GABAergic synapses to

28 anced GABAergic neurotransmission within the medial CeA in LgA rats, which was blocked with SB-334867

29 tionships, indicating that the brainstem and medial cerebellar structures were functionally spared.

30 ABSTRACT: It is well known that the medial cerebellum controls saccadic speed and accuracy.

31 ally connected to a focal area in the dorsal medial cerebellum.

32 erior lateral color patch) and AMC (anterior medial color patch), while presenting images of objects

33 Specifically, medial cytokinin promotes auxin biosynthesis components

34 Medial DA neurons received predominantly GABAergic curre

35 rvicellular portion of the ventral posterior medial division, VPMpc) of mice and the thalamic termina

36 he division plane in newborn cells to ensure medial division.

37 RMED7 (PIN7)-mediated auxin efflux from, the medial domain.

38 made up of two lateral valve domains and two medial domains, which retain meristematic properties and

39 s that the adaptations in infralimbic cortex-medial dorsal thalamus circuitry observed after stress r

40 tes offered by the Puelles school includes a medial, dorsal, lateral, and ventral pallium.

41 D1-expressing neurons in the medial DS (DMS) were recruited during fear extinction, a

42 he effects of P301L hTau transduction in the medial EC (MEC) of mice on tau phosphorylation and accum

43 lycans (CSPGs) on apical surfaces of palatal medial edge epithelial (MEE) cells were necessary for pa

44 Overall, our work demonstrates that medial entorhinal activity plays an especially important

45 Here we show that ripple bursts in CA1 and medial entorhinal cortex (MEC) are temporally associated

46 The medial entorhinal cortex (MEC) contains specialized neur

47 The medial entorhinal cortex (mEC) has been identified as a

48 ABSTRACT: The medial entorhinal cortex (mEC) is strongly involved in s

49 We demonstrate that medial entorhinal cortex (mEC) neurons from the mouse mo

50 hing is known about Kv2 channel functions in medial entorhinal cortex (mEC) neurons, which are involv

51 k, we consider the question of cell types in medial entorhinal cortex (MEC), a region likely to be in

52 mutation on layer II stellate neurons of the medial entorhinal cortex (mEC), which transmit excitator

53 ine levels and locus coeruleus fibres in the medial entorhinal cortex and dentate gyrus, with no fran

54 lls in the hippocampus and grid cells in the medial entorhinal cortex have different codes for space.

55 The spatial receptive fields of neurons in medial entorhinal cortex layer II (MECII) and in the hip

56 he effect of large-scale inactivation of the medial entorhinal cortex on temporal, as well as spatial

57 the locus coeruleus prior to accrual in the medial entorhinal cortex or hippocampus, and tau patholo

58 pyramidal neurons from acute slices of mouse medial entorhinal cortex, we find that subthreshold inpu

59 elated with noradrenergic innervation in the medial entorhinal cortex.

60 y, primary visual, rostrolateral visual, and medial entorhinal cortices send projections only to the

61 Medial entorhinal inactivation produced a specific defic

62 areas of PS patterning and growth as well as medial epithelial seam dissolution during palatal fusion

63 Together, this study establishes the medial extended amygdala as a major neural substrate reg

64 Seventeen lesions occurred in the medial femoral condyle, two occurred in the lateral femo

65 these sites, including descending inhibitory medial forebrain bundle fibers, induces both feeding and

66 ort the view that striatal neurons integrate medial frontal activity and are consistent with drift-di

67 ivity was correlated with and dependent upon medial frontal activity.

68 activation in two anterior nodes of the DMN (medial frontal and superior frontal) in the non-rest ple

69 we investigate a novel strategy to normalize medial frontal brain activity by stimulating cerebellar

70 Twenty minutes of inphase stimulation over medial frontal cortex (MFC) and right lateral prefrontal

71 ad attenuated delta activity (1-4 Hz) in the medial frontal cortex (MFC) during interval timing.

72 vioral mechanisms of reward signaling by the medial frontal cortex (MFC) have not been resolved.

73 ractions among orbital frontal cortex (OFC), medial frontal cortex (MFC), and amygdala are thought to

74 Orbitofrontal cortex (OFC), medial frontal cortex (MFC), and amygdala mediate stimul

75 rom a hierarchical organization of posterior medial frontal cortex and its interaction with the basal

76 We recorded single neurons in the human medial frontal cortex and medial temporal lobe while sub

77 associated with increased activation in the medial frontal cortex beneath the anode; showing a posit

78 l circuits and provides insight into how the medial frontal cortex exerts top-down control of cogniti

79 atal ramping activity are disrupted when the medial frontal cortex is inactivated.

80 is of such flexibility, we recorded from the medial frontal cortex of nonhuman primates trained to pr

81 However, activity in the posterior medial frontal cortex was elevated in AN following punis

82 mission in the cingulate region of the mouse medial frontal cortex, an associative region that mature

83 signals explains fMRI responses in posterior-medial frontal cortex.

84 nctional delta rhythms between 1-4 Hz in the medial frontal cortex.

85 neurons are correlated with activity of the medial frontal cortex.

86 e precuneus, temporal parietal junction, and medial frontal cortices, there were large differences in

87 Past work has implicated medial frontal neurons expressing D1 dopamine receptors

88 Descending facial lobe projections to the medial funicular nucleus were also noted.

89 us; lateral noradrenergic neurons in the LC; medial GABAergic neurons in the pontine central gray; ve

90 rth disrupts interneuron neurogenesis in the medial ganglionic eminence (MGE) and, more importantly,

91 nic precursors of GABAergic neurons from the medial ganglionic eminence (MGE) into adult mouse spinal

92 rons are the two major subtypes generated by medial ganglionic eminence (MGE) progenitors.

93 opment, several cIN subtypes derive from the medial ganglionic eminence (MGE), a transient ventral te

94 uired for the differentiation of a subset of medial ganglionic eminence (MGE)-derived neurons, but ar

95 tical interneurons that are derived from the medial ganglionic eminence, as most studies have examine

96 we compared interneuronal progenitors in the medial ganglionic eminences (MGEs), lateral ganglionic e

97 The flow of auditory information through the medial geniculate body (MGB) is regulated, in part, by c

98 es of neurons in the ventral division of the medial geniculate body (MGBv).

99 arallel thalamocortical projections from the medial geniculate nucleus (MGN).

100 e habenulopeduncular pathway consists of the medial habenula (MHb), its output tract, the fasciculus

101 itionally, IL-18 is produced in the brain in medial habenula neurons, which project IL-18-containing

102 f Broca, and the nucleus basalis of Meynert, medial habenular nucleus, zona incerta, neurosecretory a

103 teral nucleus, the torus semicircularis, the medial hindbrain, and the thalamus, and the flow of info

104 JQ1 ameliorates AngII-induced hypertension, medial hypertrophy and inflammation in vivo in mice.

105 s of the thalamus was primarily contacted by medial hypothalamic areas as well as the zona incerta an

106 Here, ninety-seven patients with medial KOA and thirty-eight asymptomatic participants we

107 e and the 3D kinematic gait of patients with medial KOA remains unclear.

108 Patients with medial KOA were divided into early, moderate, and severe

109 antify elastic properties of sound producing medial labia (ML).

110 subdivided along the anterior-posterior and medial-lateral axes by microdissections.

111 ferentially along the anterior-posterior and medial-lateral axes of the chick tectum using microarray

112 ation of circular fibres, oriented along the medial-lateral axis.

113 rent anterior-posterior, dorsal-ventral, and medial-lateral coordinates that we interpret as cell typ

114 ptic puncta, neuronal processes also exhibit medial-lateral territories at both developmental stages

115 of a 5.4 kDa protein called medin within the medial layer of large arteries.

116 ctography of the corticospinal tract and the medial lemniscus was performed with diffusion tensor ima

117 lear neurons, whose axons course through the medial longitudinal fasciculus (MLF), and neurons in the

118 ated by a group of five afferent nuclei (the Medial Magnocellular nucleus of the Anterior Nidopallium

119 l nerve was examined at 4 cm proximal to the medial malleolus with gray-scale ultrasonography and SWE

120 age damage induced by destabilization of the medial meniscus (DMM) OA-inducing surgery in mice.

121 udy, we performed the destabilization of the medial meniscus (DMM) surgery at 12-week-old mice to ind

122 mouse models such as destabilization of the medial meniscus (DMM) used for evaluating disease-modify

123 e differentiated into two nuclear complexes, medial (MHb) and lateral habenula (LHb).

124 tions with the adjacent endoderm control the medial movement of cardiomyocytes, a process referred to

125 sembly are periodic pulses of junctional and medial myosin II that result in progressively stronger c

126 strong expression of Vax1 in ectoderm of the medial nasal processes, the upper lip remained intact in

127 a are enriched on neuronal somata and in the medial neuropil.

128 rodent barrel cortex (BC) and the posterior medial nucleus of the thalamus (POm).

129 channels can be activated in neurons of the medial nucleus of the trapezoid body (MNTB) of the audit

130 The calyx of Held synapse in the mammalian medial nucleus of the trapezoid body (MNTB) plays an imp

131 r glycinergic or GABAergic inhibition to the medial nucleus of the trapezoid body (MNTB) specific to

132 bitory connections in the mammalian CNS: the medial nucleus of the trapezoid body to lateral superior

133 eus bushy cells and principal neurons in the medial nucleus of the trapezoid body.

134 4 most significant clusters appeared in the medial occipital and posterior cingulate cortex (each le

135 er, DLB showed greater hypometabolism in the medial occipital lobe, orbitofrontal cortex, anterior te

136 the frontal cortex and high toward the caudo-medial (occipital) pole.

137 Auditory responses occur in the medial octavolateral nucleus, the torus semicircularis,

138 and regional reductions in frontal regions (medial OFC and superior frontal gyrus) and primary and h

139 e inhibitory efferent input from cholinergic medial olivocochlear (MOC) neurons originating in the br

140 t only one rostral or caudal location within medial or lateral HVC, and each HVC location receives co

141 es during value-guided learning, whereas the medial orbitofrontal cortex (often referred to as ventro

142 and modulated the food-related signal in the medial orbitofrontal cortex (P=0.01) and nucleus accumbe

143 tially associated with nucleus accumbens and medial orbitofrontal cortex activity, whereas distress w

144 mpaired credit assignment, whereas damage to medial orbitofrontal cortex meant that patients were mor

145 The lizard medial pallium, expressing all genes, includes the media

146 The VMS receives inputs from medial pallium-originated limbic structures (e.g., the m

147 with reduced cortical thickness in frontal, medial parietal and occipital regions.

148 sterior parietal cortex, this highlights the medial parietal cortex as a target site for transforming

149 his view and, given its direct output to the medial part of the central amygdala and the hypothalamic

150 intercalated masses (IM), which inhibit the medial part of the central amygdalar nucleus (CeM).

151 s were injected into the taste thalamus (the medial parvicellular portion of the ventral posterior me

152 by PNA-binding proteins that block entry to medial pathways.

153 y into the prelimbic (PLmPFC) or infralimbic medial PFC (ILmPFC).

154 estigate these, we assessed the influence of medial PFC (mPFC) activity on spatial learning and hippo

155 elective mTORC1 inhibitor rapamycin into the medial PFC (mPFC) blocks the antidepressant behavioral a

156 irectional interactions between mouse MD and medial PFC (mPFC), with MD-to-mPFC supporting working me

157 emodeling and dendritic spine density in the medial PFC.

158 m the thoracic notum as well as the expected medial, pleural series of axillary sclerites.

159 The medial portion had lower CO activity and fewer ITD-sensi

160 ow that the signals measured from the monkey medial posterior parietal cortex are valid for correctly

161 dies on decoding reach trajectories from the medial posterior parietal cortex, this highlights the me

162 d transient rise in glutamate cycling in the medial prefronal cortex (mPFC) of awake rats as measured

163 The medial prefrontal - anterior cingulate cortex appears mo

164 ons from the claustrum-insular region to the medial prefrontal and anterior cingulate cortex of the c

165 redictions and the errors thereof within the medial prefrontal and fusiform cortices.

166 h affirmative sentences, negated ones led to medial prefrontal and more widespread motor source activ

167 ctivity between the ventral striatum and the medial prefrontal and parietal cortices and between the

168 The medial prefrontal areas 32, 24, 14, and 25 (mPFC) form p

169 Medial prefrontal connections were restricted mainly to

170 addition, infusing CPP into the infralimbic medial prefrontal cortex (IL-mPFC), a structure implicat

171 A brain network comprising the medial prefrontal cortex (mPFC) and amygdala plays impor

172 ring adolescence decreased n-3 PUFAs in both medial prefrontal cortex (mPFC) and nucleus accumbens, i

173 ition center (PMC), locus coeruleus (LC) and medial prefrontal cortex (mPFC) during cystometry in una

174 Brain activity in medial prefrontal cortex (MPFC) during exposure to persu

175 holine receptor is an important modulator of medial prefrontal cortex (mPFC) functions, such as the w

176 In humans and rodents, the medial prefrontal cortex (mPFC) has been implicated in s

177 Dysfunction of the medial prefrontal cortex (mPFC) has been linked to the c

178 els of gamma-aminobutyric acid (GABA) in the medial prefrontal cortex (mPFC) have been reported in an

179 how that reduced cholinergic transmission in medial prefrontal cortex (mPFC) impaired appetitive trac

180 verely disrupts the columnar organization of medial prefrontal cortex (mPFC) in a transcription- and

181 w gamma coupling between the hippocampus and medial prefrontal cortex (mPFC) is augmented in a geneti

182 into either the infralimbic division of the medial prefrontal cortex (mPFC) or the basolateral amygd

183 onic contributions of two direct hippocampal-medial prefrontal cortex (mPFC) pathways, one arising in

184 that dopaminergic pathway projecting to the medial prefrontal cortex (mPFC) suppresses stress suscep

185 neuropathic pain.SIGNIFICANCE STATEMENT The medial prefrontal cortex (mPFC) undergoes major reorgani

186 rdinated neural activity in the hippocampus, medial prefrontal cortex (mPFC), and amygdala.

187 le food showed decreased TAAR1 levels in the medial prefrontal cortex (mPFC), and RO5256390 microinfu

188 d gene expression studies both implicate the medial prefrontal cortex (mPFC), particularly deep-layer

189 leus accumbens (NAcc), the amygdala, and the medial prefrontal cortex (mPFC), which form an intrinsic

190 sulting in decreased 5HTergic innervation of medial prefrontal cortex (mPFC).

191 ain intrinsic functional connectivity in the medial prefrontal cortex (mPFC).

192 enual anterior cingulate cortex (sgACC), and medial prefrontal cortex (mPFC).

193 within telencephalic structures such as the medial prefrontal cortex (mPFC).

194 p x time interaction effect was found in the medial prefrontal cortex (mPFC)/anterior cingulate corte

195 lium-originated limbic structures (e.g., the medial prefrontal cortex [mPFC]), and the VLS receives i

196 twork seed, and two connections (between the medial prefrontal cortex and both the right superior par

197 ivity involving the caudate nucleus, insula, medial prefrontal cortex and other domain-specific regio

198 ative modulation of connectivity between the medial prefrontal cortex and the posterior cingulate cor

199 The involvement of the temporal pole-medial prefrontal cortex circuit in a model highly predi

200 ents, while abnormalities in a temporal pole-medial prefrontal cortex circuit might speak to the soci

201 s a 3-6 Hz oscillatory signature, with BLA-->medial prefrontal cortex directionality signaling the re

202 hat the cortical sources in sensorimotor and medial prefrontal cortex even distinguished between pred

203 network as in the healthy control group, the medial prefrontal cortex had a "hyperregulatory" effect

204 ges and transcriptional abnormalities in the medial prefrontal cortex of immune-challenged and contro

205 The exaggerated influence of the medial prefrontal cortex on the posterior cingulate cort

206 duced synaptic plasticity in the hippocampal-medial prefrontal cortex pathway.

207 The medial prefrontal cortex plays a key role in higher orde

208 that neural patterns in the hippocampus and medial prefrontal cortex represented the featural overla

209 irus-driven expression of progranulin in the medial prefrontal cortex reverses social dominance defic

210 eal-time activity of associative inputs from medial prefrontal cortex to dorsomedial striatum and sen

211 l bonding, how a functional circuit from the medial prefrontal cortex to nucleus accumbens is dynamic

212 contribution of neural projections from the medial prefrontal cortex to the dorsal periaqueductal gr

213 Although the prelimbic cortex (PL, part of medial prefrontal cortex) has been implicated in social

214 d lower WM volume bilaterally in orbital and medial prefrontal cortex, and greater GM volume in poste

215 This network comprises the hippocampus, medial prefrontal cortex, and left angular gyrus, among

216 f neural regions, including the hippocampus, medial prefrontal cortex, and left angular gyrus.

217 fected sites included the brainstem, ventral medial prefrontal cortex, and superior temporal lobe, mo

218 ntal cortex and inferior frontal gyrus), the medial prefrontal cortex, and the dorsal anterior cingul

219 ward and emotional-regulation brain regions (medial prefrontal cortex, cingulate cortex, and insula)

220 h a particular focus on sex differences, the medial prefrontal cortex, social reward, social isolatio

221 The medial prefrontal cortex, which has a central role in se

222 oted aversive learning, while an independent medial prefrontal cortex-projecting ensemble extinguishe

223 he rTPJ with ventral and dorsal parts of the medial prefrontal cortex.

224 rneurons on pyramidal layer 5 neurons in the medial prefrontal cortex.

225 viors include the amygdala, hippocampus, and medial prefrontal cortex.

226 ve network including the hippocampus and the medial prefrontal cortex.

227 actions between a core 'self network' (e.g., medial prefrontal cortex; mPFC), a cognitive control net

228 Upstream, medial prefrontal cortical projections provide gamma-rhy

229 ar projections to the anterior cingulate and medial prefrontal cortices.

230 ations in the task-related spike activity of medial prefrontal neurons correspond with increased acti

231 ed behavioral data, ensemble recordings from medial premotor cortex (MPC) in macaque monkeys, and com

232 While the medial preoptic area (MPOA) is known to be critical for

233 The medial preoptic area (mPOA), an essential node for socia

234 iors occur in a variety of mammals, with the medial preoptic nucleus (POM) and the ventromedial hypot

235 First, overlapping regions in medial pSTG exhibited significant sensitivity to both cu

236 nucleus, zona incerta, lateral posterior and medial pulvinar nuclei, nucleus limitans, pretectal area

237 e, bilateral projection to the region of the medial rectus C-group motoneurons.

238 n produced similar short-term alterations in medial rectus motoneuron firing pattern, which were more

239 ase for the mechanism of compensation on the medial rectus motoneuron.

240 Medial rectus motoneurons receive two main pontine input

241 projection onto some of the A- and B- group medial rectus motoneurons that supply singly innervated

242 otor physiology, single-unit recordings from medial rectus motoneurons were obtained in the control s

243 the MLF or the ATD pathway on the firing of medial rectus motoneurons, as well as the plastic mechan

244 yes, we injected retrograde tracers into the medial rectus muscle of the cat, a highly visual nonprim

245 with injection of retrograde tracer into the medial rectus muscle.

246 -responsive neurons in the ventral posterior medial region (VPM) respond to visual stimuli.

247 ively.SIGNIFICANCE STATEMENT The lateral and medial regions of the orbitofrontal cortex are cytoarchi

248 Rhythmic medial septal (MS) GABAergic input coordinates cortical

249 Medial septal inputs to the hippocampal system are cruci

250 re seen in the olfactory tubercle, striatum, medial septal nucleus, vertical and horizontal limbs of

251 entify GABAergic projection neurons from the medial septum (MS) as the major afferents to dentate PV

252 nucleus (SCN) that paralleled changes in the medial septum and hippocampus, but not in other neural s

253 Critically, at P12, inactivation of the medial septum eliminates theta in both structures.

254 However, the precise contributions of the medial septum's cholinergic neurones to these functions

255 ergic neurons) across its different regions (medial septum, diagonal band, magnocellular preoptic are

256 GABAergic cells in the DG and project to the medial septum.

257 f GCs with activity patterns governed by the medial septum.

258 s topographically forming a lateral core and medial shell arrangement of cortical regions.

259 The medial SN connects with limbic striatal and cortical reg

260 We show that astrocytes in the medial subdivision of the central amygdala (CeM) determi

261 ontal gyrus, the lateral substantia, and the medial substantia in PD patients.

262 tuning.SIGNIFICANCE STATEMENT Neurons in the medial superior olive (MSO) play a unique role in sound

263 d model of a binaural brainstem nucleus, the medial superior olive (MSO), that accounts qualitatively

264 ingle-unit activity recorded from the dorsal medial superior temporal (MSTd) and ventral intraparieta

265 array recordings from the motion-processing medial temporal (MT) area of anesthetized male marmosets

266 iking responses of individual neurons in the medial temporal lobe (MTL) are attenuated, delayed, and

267 The medial temporal lobe (MTL) contains "concept cells" that

268 Given the critical role of the medial temporal lobe (MTL) in episodic memory, age-relat

269 loid (Abeta) and tau proteins and atrophy of medial temporal lobe (MTL) structures crucial to memory

270 There has been interest in the idea that medial temporal lobe (MTL) structures might be especiall

271 ogical data indicate that tau tangles in the medial temporal lobe (MTL) underlie episodic-memory impa

272 he activity of neuronal ensembles within the medial temporal lobe (MTL).

273 iduals with notably focal involvement of the medial temporal lobe and a slow steady progression, like

274 haviour relationships (i.e. episodic memory: medial temporal lobe and angular gyrus; semantic memory:

275 tions between rather than within the visual, medial temporal lobe and default mode networks, whereas

276 with localised volume loss in the thalamus, medial temporal lobe and temporal neocortex.

277 gs establish further parallels between human medial temporal lobe epilepsy and a naturally occurring

278 ent in the early-onset group, and more focal medial temporal lobe loss in the late-onset group.

279 urons in the human medial frontal cortex and medial temporal lobe while subjects held up to three ite

280 elatively less pronounced involvement of the medial temporal lobe, abnormal cerebrospinal fluid amylo

281 a nigra and ventral tegmental area (SN/VTA), medial temporal lobe, or subsequent memory performance.

282 ories, and less sparse than elsewhere in the medial temporal lobe.

283 e individuals are endowed with occipital and medial temporal reflexes that generate a greater fluency

284 1451 uptake than the probable DLB group, and medial temporal uptake completely distinguished AD demen

285 The medial temporal-lobe system is essential for the formati

286 The average arterial percent medial thickness (control, 6.9; HF-PH, 11.0; PVOD, 15.0)

287 PASP correlated with arterial percent medial thickness (r=0.41) and arterial %IT (r=0.35) but

288 ificant after adjusting for arterial percent medial thickness and %IT and did not vary by HF type.

289 wedge insoles (LWIs) on the stresses in the medial tibial cartilage by combining musculoskeletal (MS

290 onger than those in area 1 and extended in a medial to lateral direction.

291 oid core of medium-sized Bar neurons located medial to the locus coeruleus (LC).

292 e ligand pdgfaa is expressed in the endoderm medial to the pdgfra-expressing myocardial precursors.

293 The Golgi is composed of a stack of cis, medial, trans cisternae that are biochemically distinct.

294 The severe group had more medial translation than the asymptomatic groups.

295 ral femoral condyle, and one occurred in the medial trochlea.

296 chlear morphology (sulcus angle, lateral and medial trochlear inclination, and trochlear angle) and S

297 on selectively inhibited dopamine neurons in medial VTA, which were most impacted by CMS.

298 CB-EPCs show reduced vasoactivity, increased medial wall thickness, increased calcification and apopt

299 ripe is required for patterning and also for medial wing disc growth, at least in the posterior compa

300 al nucleus of the ventral telencephalon, the medial zone of the dorsal telencephalon, preoptic area a