ライフサイエンスコーパス: ventral

1 n upper versus lower body, and dorsal versus ventral abdominal depots.

2 characterized by increases in FC between NAc-ventral ACC for environmental, NAc-thalamus for physical

3 f the dorsal ACC in motor evaluation and the ventral ACC in affective and contextual memory.

4 ations and horizontal cells along the dorsal-ventral and central-peripheral axes of the retina.

5 For example, the ventral and dorsal CA1 regions critically support social

6 revealed a differential sensitivity between ventral and dorsal cardiac lymphatics to the effects of

7 ge domains align with existing models on the ventral and dorsal pathways for language processing.

8 ansitions were anatomically localized to the ventral and dorsal respiratory groups, respectively.

9 coded in mPFC, but with opposite sign in its ventral and dorsal subdivisions.

10 elated activity is represented in a diffuse, ventral and dorsal system in the posterior parietal regi

11 ty-defined 3D shape is processed in both the ventral and the dorsal visual stream.

12 In the primate thalamus, the parvocellular ventral anterior nucleus (VApc) and the centromedian nuc

13 The neuro-oncological ventral antigen 2 (NOVA2) protein is a major factor regu

14 The ventral astrocyte in particular, whose territory can ext

15 s and change in the connectivity between the ventral attention and cognitive networks.

16 subdivisions are positively correlated with ventral attention and somatomotor networks and negativel

17 with the within-network connectivity of the ventral attention network (VAN), the dorsal attention ne

18 mscribed by specific functional systems (the ventral attention network) and cytoarchitectonic classes

19 efault Mode Network, Frontoparietal Network, Ventral Attention Network, and the Limbic Network-with p

20 network-dorsal attention network (VAN-DAN), ventral attention network- somatosensory network (VAN-SM

21 SMN) and the between-network connectivity of ventral attention network-dorsal attention network (VAN-

22 etwork- somatosensory network (VAN-SMN), and ventral attention network-visual network (VAN-VN).

23 ks, the DMN and visual, limbic, auditory and ventral attention networks, and between the fronto-parie

24 x hormones and within-network integration in Ventral Attention, Dorsal Attention, and SomatoMotor Net

25 ow that BMP signaling establishes the dorsal-ventral axis in some mollusks.

26 de to the mollusks, suggests that the dorsal-ventral axis is patterned via Activin/Nodal signaling.

27 orsal morphogen gradient patterns the dorsal-ventral axis of the early Drosophila embryo, and we foun

28 of the transcription factor Dorsal in dorsal-ventral axis patterning of Drosophila embryos.

29 radient's conserved role in embryonic dorsal-ventral axis patterning.

30 rn astrocytes were found all along the dorso-ventral axis, counting however for only 11% of newborn c

31 through enhancer sog_Distal along the dorso-ventral axis, we hypothesized Opa's role is more general

32 as a conserved role in patterning the dorsal-ventral body axis.

33 The closure of the embryonic ventral body wall in amniotes is an important morphogene

34 novel population of GABAergic neurons in the ventral brainstem, distinguished by prodynorphin express

35 reased DAT surface expression selectively in ventral, but not dorsal, striatum.

36 istribution in DAergic terminals from female ventral, but not dorsal, striatum.

37 Here, we show that activity in the ventral CA1 (vCA1) hippocampal projections to the basal

38 While recent studies have indicated that ventral CA1 (vCA1) projection neurons are functionally d

39 increased dendritic spine maturation in the ventral CA1 hippocampal subregion.

40 Patch-clamp recordings of ventral CA1 pyramidal cells 24 h after a single systemic

41 rties in the vHipp with resultant changes in ventral CA1 that indirectly increases neuronal excitabil

42 ults from an earlier requirement for Tbx1 in ventral cardiac LEC progenitors.

43 to and are essential for the development of ventral cardiac lymphatics.

44 d greater neural activation in the bilateral ventral caudate and the nucleus accumbens during reward

45 actively on the underlying matrix toward the ventral cell center through the dynamic shortening of my

46 We propose that the ventral circuit defines behavioral goals, and the dorsal

47 The ventral circuit, that includes the amygdala, ventral med

48 Previous studies suggest that ventral cochlear nucleus bushy cells may be putative neu

49 Compared to other ventral cochlear nucleus output neurons, bushy cells sho

50 ating in the posterior slope (PS) (T6I), the ventral complex (T6II), and the ventrolateral protocereb

51 ted to production of CSF-cNs and reach their ventral destinations during first postnatal weeks.

52 findings suggest that MCs in the dorsal and ventral DG differ in the distribution of their axonal pr

53 ally been assumed that MCs in the dorsal and ventral DG have similar patterns of termination in the i

54 epletion results in short flagella, aberrant ventral disk organization, loss of the funis, defective

55 The ventral division (vLGN) connects subcortically, sending

56 connects to cortex to serve form vision; the ventral division (vLGN) projects subcortically to sensor

57 o promote HSC emergence predominantly in the ventral domain of the dorsal aorta.

58 ified from hemogenic endothelium (HE) in the ventral dorsal aorta (VDA), support lifelong hematopoies

59 ges a distributed neuronal population within ventral, dorsal and pontine network compartments.

60 s expressed in the caudal embryo in a dorsal-ventral (DV) gradient across all three germ layers, incl

61 ver, extramedullary neurons originating from ventral epidermis in cephalochordates (and presumably in

62 duces ectopic deformations in the dorsal and ventral epithelia of Drosophila embryos.

63 lls, resulting in a significant reduction in ventral extension and overall CVP area.

64 found that a group of neurons targeting the ventral fan-shaped body (ventral P-FNs) are robustly tun

65 hibitory interneurons (cINs) are born in the ventral forebrain and migrate into cortex, where their n

66 neurons implicated in social behavior in the ventral forebrain and show that Syt2a is colocalized wit

67 identified FMR1 targets in human dorsal and ventral forebrain neural progenitors and excitatory and

68 ging pattern showed volume loss of the right ventral frontal area and the left temporal lobe, which r

69 Ventral furrow formation, the first step in Drosophila g

70 he evolution of asymmetry between dorsal and ventral hemitrichia.

71 ity of the Abdominal Hernia-Q (AHQ), a novel ventral hernia (VH) patient-reported outcomes measure (P

72 acy of the bioscaffold is evaluated in a rat ventral hernia model.

73 Ventral hernia repair(VHR) is one of the most commonly p

74 coronary artery bypass grafting, colectomy, ventral hernia repair, lower extremity vascular bypass,

75 te 18% of patients operated on for a primary ventral hernia, but consensus is lacking on the manageme

76 , of whom 2113 underwent repair of a primary ventral hernia.

77 r is the definitive treatment for incisional ventral hernias but is often deferred if the perceived r

78 ired to coordinate growth between dorsal and ventral hindgut domains to regulate the extension of the

79 estingly, the absence of Wnt activity in the ventral hindgut is crucial for proper hindgut morphogene

80 ectopic stabilization of beta-catenin in the ventral hindgut via gain- or loss-of-function mutations

81 excitatory afferent pathways, we showed that ventral hippocampal (vHipp) input alone enhances palatab

82 Ventral hippocampal CA1 (vCA1) projections to the amygda

83 Both dorsal and ventral hippocampus (dH and vH) project to the NAc, but

84 sociated with increased synaptic strength of ventral hippocampus (VH) excitatory synapses onto D1 med

85 , nucleus accumbens (NAc) afferents from the ventral hippocampus (vHIP) are implicated in stress-indu

86 Comparing synaptic properties of ventral hippocampus (vHipp), basolateral amygdala (BLA)

87 examined the impact of connections from the ventral hippocampus (vHipp,) basolateral amygdala (BLA)

88 Theta-frequency communication between the ventral hippocampus (vHPC) and medial prefrontal cortex

89 RNA-seq of the ventral hippocampus (vHpc) highlights that E2-dependent

90 al learning involves connections between the ventral hippocampus and the prelimbic cortex in rodents

91 ertal EE also prevented hyperactivity in the ventral hippocampus but did not prevent hyperactivity in

92 behavioral paradigm that requires intact PFC-ventral hippocampus connectivity.

93 rticolimbic interneurons impacts on mPFC and ventral hippocampus functional connectivity before and a

94 n regions regulating reward and anxiety, the ventral hippocampus is uniquely poised to translate the

95 iated by normalizing excessive firing in the ventral hippocampus without affecting anxiety-like behav

96 ) EE on DA neurons, pyramidal neurons in the ventral hippocampus, and projection neurons in the basol

97 addition, adult male KO mice showed reduced ventral hippocampus-mPFC-evoked potentials and an augmen

98 irect excitatory input from the intermediate/ventral hippocampus.

99 processing of afferent information from the ventral hippocampus.

100 In addition, we found that ventral hypothalamic cells were more prominent in female

101 ent MLL1 inhibition caused a durable loss of ventral identity, resulting in the generation of neurons

102 t landmark-based targeting techniques of the ventral intermediate nucleus and demonstrate the role of

103 kground MRI-guided focused US thalamotomy of ventral intermediate nucleus of the thalamus is a treatm

104 tation of standard MRI sequences is that the ventral intermediate nucleus, dentatorubrothalamic tract

105 ular control and somatomotor networks in the ventral intermediate thalamus (motor integration zones),

106 Neural responses in the ventral intraparietal area are modulated by the task ref

107 orms during eye morphogenesis by asymmetric, ventral invagination.

108 f the hard cortical bone, also known as the "ventral lamina", covering the neural elements of the spi

109 , late-born V3 INs became fate-restricted to ventral laminae and displayed mostly descending and loca

110 ic cells that project to the pretectum (PT), ventral lateral geniculate nucleus (vLGN) or parabigemin

111 The ventral lateral parietal cortex (VLPC) shows robust acti

112 reased reward-evoked dopamine release in the ventral lateral striatum (VLS), but not in the ventral m

113 reases reward-evoked dopamine release in the ventral lateral striatum.

114 ients have abnormal connectivity between the ventral lateral/posterolateral nucleus (VL/VPL) and post

115 nction in regulating the elongation of showy ventral ligules that play a major role in pollinator att

116 control, and under SPL7, somatosensory PSC, ventral LOC and cerebellar control.SIGNIFICANCE STATEMEN

117 ed that the axonal projections of dorsal and ventral MCs differ.

118 tcentral gyrus (PoCG) and between the dorsal/ventral medial nucleus and insula in the less frequent c

119 ventral circuit, that includes the amygdala, ventral medial prefrontal cortex, and ventral striatum,

120 ntral lateral striatum (VLS), but not in the ventral medial striatum.

121 luding the dorsal vagal complex, A5, rostral ventral medulla, A1, and midline raphe, as well as sympa

122 cortical actin waves that travel across the ventral membrane of oversized, multinucleated Dictyostel

123 vity increase before gastrulation and induce ventral mesoderm formation.

124 ically project to cholinergic neurons of the ventral MHb.

125 The in vivo firing patterns of ventral midbrain dopamine neurons are controlled by affe

126 In cultures of striatum or ventral midbrain, CHL1 was also closely associated with

127 driven by a particular vulnerability of the ventral motor neurons of the spinal cord to decreased SM

128 To do so, we performed ventral neck surgery in 21 C57BL/6J male mice, divided i

129 The Drosophila ventral nerve cord (VNC) receives and processes descendi

130 adult thoracic and abdominal neuromeres, the ventral nerve cord (VNC), to provide an anatomical descr

131 d neuroblasts reactivate from quiescence and ventral nerve cord glia expand their membranes.

132 trients and PI3-kinase activation, brain and ventral nerve cord neuroblasts reactivate from quiescenc

133 set of commissural neurons in the developing ventral nerve cord produces defasciculated axon bundles

134 nergic motor neurons (MNs) in the C. elegans ventral nerve cord to select and maintain their unique t

135 e cuticle from DBL-1-expressing cells in the ventral nerve cord.

136 e E (Inpp5e), ridge top (rdg), with expanded ventral neural cell fates at E10.5.

137 s and by notochord and floorplate cells, and ventral neural cells are patterned by the activities of

138 factors, giving Hh a broader role in dorsal-ventral neural patterning.

139 ion of candidate ion channels in the lateral ventral neurons (LNvs) and show that the hyperpolarizati

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

141 After establishment by sonic hedgehog, ventral NSC identity became independent of this morphoge

142 orsal action observation network (AON) and a ventral object recognition pathway.

143 erior temporal lobe, affecting primarily the ventral, occipito-temporal, lexical route.

144 sual word recognition across the entire left ventral occipitotemporal cortex.

145 Ventral P-FNs did not generate a 'map' of airflow direct

146 Imaging experiments suggest that ventral P-FNs inherit their airflow tuning from neurons

147 Silencing ventral P-FNs prevented flies from selecting appropriate

148 urons targeting the ventral fan-shaped body (ventral P-FNs) are robustly tuned for airflow direction.

149 gions (limbic striatum, globus pallidus, and ventral pallidum (9-14%; p < 0.04) in humans and Islands

150 The ventral pallidum (VP) is a central node in the reward sy

151 The ventral pallidum (VP) is a key hub in the reward system

152 The ventral pallidum (VP) is a key node in the neural circui

153 The ventral pallidum (VP) is a key structure in the reward s

154 The ventral pallidum (VP) is a major component of the BG lim

155 ied outcome history-based RPE signals in the ventral pallidum (VP), a basal ganglia region functional

156 (2020) dissect the function of the enigmatic ventral pallidum and elegantly demonstrate positive and

157 Here we reveal synaptic properties in the ventral pallidum, a central hub of reward circuits, that

158 ucleus, and from SOM-positive neurons in the ventral pallidum.

159 omplex [preBotC], ventral respiratory group, ventral parafacial region [pF(V) ] and pF(L) ), nucleus

160 d craniofacial hypoplasia, especially in the ventral part of the skull and the mandible, and rostrall

161 The ventral pathway computes the identity of an object; the

162 e of Wnt/betacatenin signaling in the dorsal/ventral patterning of amphioxus embryo.

163 lation when it was applied to 2 spots in the ventral PMC and 1 spot in the medial PMC, corresponding

164 dial PMC, corresponding approximately to the ventral PMC and the dorsal portion of the supplementary

165 rtico-cortical interactions between premotor ventral (PMv)-motor cortex (M1), anterior inferior parie

166 Here we show that a dorsal-ventral polarized supracellular F-actin network, running

167 by promoting cell division in the distal and ventral portion of the limb.

168 inhibitory interneurons are generated in its ventral portion.

169 Class I ventral posterior dendritic arborisation (c1vpda) propri

170 The ventral posterior hypothalamus (VPH) is an anatomically

171 tical (TC) neurons in subregions of both the ventral posterior lateral and posterior (PO) nuclei, for

172 located in the central core-connect with the ventral posterior nucleus, the primary somatosensory tha

173 idline and paramedian anterior, central, and ventral posterior skull base.

174 well as sensory-discriminative pain, such as ventral posteromedial thalamic nuclei.

175 onflict- and value-related regions, only the ventral pre-supplementary motor area (or dorsal anterior

176 as well as the medial and lateral dorsal and ventral prefrontal regions.

177 e accompanied by white matter changes in the ventral prefrontal tract, although the integrity of the

178 namely, the uncinate fasciculus, fornix, and ventral prefrontal tract, showed structural changes afte

179 y interconnecting somatosensory (S1, S2) and ventral premotor (PMv) network in primates.

180 Inferior frontal gyrus (IFG), ventral premotor cortex (PMv) and inferior parietal lobu

181 ior intraparietal area, the hand area of the ventral premotor cortex, and the primary motor cortex is

182 xcitatory-inhibitory balance in perilesional ventral premotor cortex.

183 nctionally interconnecting somatosensory and ventral premotor network in non-human primates.

184 ilar role in neurogenesis in both dorsal and ventral progenitor lineages and, if so, whether it regul

185 Overall the phenotype of the ventral prostate (VP) and mammary gland (MG) in ERbeta(c

186 in severe pigmentation defects in dorsal and ventral regions of the mouse skin.

187 MCs in dorsal and ventral regions were labeled selectively with Cre-depend

188 rgic and GABAergic neurons were found in the ventral respiratory column (Botzinger and preBotzinger C

189 otzinger and preBotzinger Complex [preBotC], ventral respiratory group, ventral parafacial region [pF

190 In addition, true S-cones in the ventral retina form clusters, which may augment synaptic

191 ipolar cells (SCBCs) are also skewed towards ventral retina, with wiring patterns matching the distri

192 Ventral root avulsion leads to severe motoneuron degener

193 Following reimplantation of lumbar ventral roots, timed GDNF-gene therapy enhanced motoneur

194 When the ventral route is damaged, as in the case of neurodegener

195 r waste expulsion, contains bilateral dorsal-ventral sarcomeres.

196 nferior frontal and supramarginal regions; a ventral semantic network involving anterior middle tempo

197 ine cortical regions, whereas the dorsal and ventral shell project to the cortical motor system and t

198 fect where the urethral opening forms on the ventral side of the penis.

199 responses in dorsal stream areas compared to ventral stream areas.

200 owed an interconnected set of regions in the ventral stream processing faces or bodies, but is has be

201 ced functional connectivity along dorsal and ventral stream regions mediating phonological and other

202 e fasciculus in semantic processing, and for ventral-stream pathways in language production.

203 Together, our data reveal that ventral striatal and midbrain reward networks form a rei

204 symptoms demonstrates adaptations in insula-ventral striatal circuitry and metabolic regulatory horm

205 In study 2, this specific prefrontal-ventral striatal dysfunction was associated with fewer d

206 d prominently to the "salience" network, the ventral striatal/ventromedial prefrontal "reward" networ

207 This was driven entirely by DeltaBP(ND) in ventral striatum (-34 +/- 14% in CHR, -20 +/- 12% in HC;

208 metry to measure dopamine binding across the ventral striatum (medial accumbens shell, accumbens core

209 sion-making, the orbitofrontal cortex (OFC), ventral striatum (VS), and dorsal striatum (DS), while m

210 ly, we observe that SRPEs are encoded in the ventral striatum (VS).

211 ic (PL) PFC, basolateral amygdala (BLA), and ventral striatum (VS).

212 functional magnetic resonance imaging (fMRI) ventral striatum activation during reward anticipation (

213 results are consistent with findings in the ventral striatum and amygdala and show that this monosyn

214 Ventral striatum and dopaminergic midbrain neurons form

215 d systems (dopamine, opioid peptides) in the ventral striatum and from the between-system recruitment

216 Dopamine levels in the ventral striatum are elevated following exposure to stre

217 ., face-selective areas) and hippocampus and ventral striatum increased as a function of RPE value (d

218 The ventral striatum is believed to encode the subjective va

219 In the ventral striatum of CHL1-deficient mice, levels of phosp

220 pathway" medium spiny neurons (iMSNs) in the ventral striatum of D2R knockout mice, this mutant resto

221 the dorsal anterior cingulate cortex and the ventral striatum that negatively correlated with increas

222 s is accompanied by enhanced activity in the ventral striatum when curiosity or hunger was elicited,

223 were also found in the prefrontal cortex and ventral striatum which, although of smaller amplitude, w

224 he core hubs of the brain reward system (the ventral striatum), better reward learning in the Probabi

225 ive reinforcement-related prediction errors (ventral striatum), but also aversive processing (insular

226 gdala, ventral medial prefrontal cortex, and ventral striatum, has substantial connectivity with the

227 e anterior limb of the internal capsule, the ventral striatum, the subthalamic nucleus, and a midbrai

228 n of information, involving the left lateral ventral striatum.

229 ight ventromedial prefrontal cortex and left ventral striatum.

230 nin, tryptophan-hydroxylase-2 (TPH2), in the ventral subnucleus of the dorsal raphe nucleus (DRv).

231 ivity between the inferior frontal gyrus and ventral subthalamic nucleus.

232 nd lowest in the midbrain/pons and along the ventral surface of the brain.

233 elective responses to faces clustered in the ventral TC, which responded increasingly strongly to mar

234 neural activities of dopamine neurons in the ventral tegmental area (DA(VTA) neurons).

235 ke projections to the substantia nigra (SN), ventral tegmental area (VTA) and ventrolateral-ventromed

236 antly, however, while phasic activity of the ventral tegmental area (VTA) contributes to reinforcemen

237 Here, we demonstrated that the ventral tegmental area (VTA) dopamine (DA) neurons that

238 Static measures included assessing ventral tegmental area (VTA) dopamine cell number and vo

239 The ventral tegmental area (VTA) has dopamine, GABA, and glu

240 CSA) by directly injecting nicotine into the ventral tegmental area (VTA) in mice.

241 ressing neurons and their projections to the ventral tegmental area (VTA) in the reinstatement of coc

242 tonergic input from the dorsal raphe (DR) to ventral tegmental area (VTA) influences vulnerability to

243 The ventral tegmental area (VTA) is a major source of dopami

244 that HDAC2, but not HDAC1, inhibition in the ventral tegmental area (VTA) is sufficient to normalize

245 Dopamine neurons of the ventral tegmental area (VTA) regulate reward association

246 reas as follows: dorsal raphe nucleus (DRN), ventral tegmental area (VTA), or rostromedial tegmentum

247 ause significant neuroadaptations within the ventral tegmental area (VTA), with alterations in gene e

248 ed with core regions of the SMN, whereas the ventral tegmental area (VTA)-related mesocorticolimbic p

249 ion within many brain regions, including the ventral tegmental area (VTA).

250 We used in vivo fiber photometry in the ventral tegmental area and measured phasic dopamine resp

251 mbic dopamine system-which originates in the ventral tegmental area and projects to the striatum-has

252 Inhibiting both ventral tegmental area and substantia nigra pars compact

253 Importantly, profilin 2 knockdown in the ventral tegmental area did not affect anxiety behavior.

254 hat raphe nucleus serotonin neurons activate ventral tegmental area dopamine neurons via glutamate co

255 r, activation of dopaminergic neurons in the ventral tegmental area following mating was impaired in

256 In marked contrast, activating all ventral tegmental area GABA neurons resulted in a unifor

257 mpared the results with global activation of ventral tegmental area GABA neurons, which will activate

258 e nuclei, substantia nigra pars compacta and ventral tegmental area homologs, superficial mamillary a

259 elivery to stimulate dopamine neurons of the ventral tegmental area of freely moving mice in a condit

260 locked D2R desensitization in neurons in the ventral tegmental area of the brain.

261 whereas markers specific to the neighboring ventral tegmental area were virtually undetected.

262 hippocampus, anterior cingulate cortex, and ventral tegmental area.

263 ain areas projecting to the substantia nigra/ventral tegmental area.

264 iated genes in the adult and fetal raphe and ventral tegmental areas.

265 The ventral telencephalon acts as an instructive tissue, but

266 c integration sites in the preoptic area and ventral telencephalon.

267 Human ventral temporal cortex (VTC) is critical for visual rec

268 sensitive to haptic perception and the left ventral temporal cortex (VTC) to size.

269 is a fundamental ability supported by human ventral temporal cortex (VTC).

270 reconsideration of the sulcal patterning in ventral temporal cortex across hominoids, as well as rev

271 Task-related activity in the ventral thalamus, a major target of basal ganglia output

272 bulb, basal telencephalon, preoptic nuclei, ventral thalamus, posterior tuberculum, and locus coerul

273 across the paraventricular hypothalamus and ventral thalamus, supressing their activity during the m

274 is not uniform, as dopamine neurons from the ventral tier are lost more rapidly than those of the dor

275 They also had larger ventral tissue bridges (Deltamedian=0.80, 95% CI 0.20 to

276 Spared ventral tissue bridges could serve as neuroimaging bioma

277 tional inference tree analysis revealed that ventral tissue bridges' width (<=2.1 or >2.1 mm) at 1 mo

278 Larger width of ventral tissue bridges-a proxy for spinothalamic tract f

279 PT and vLGN are primarily located in layers ventral to the SGS.

280 evelopmental analysis reveals a progressive, ventral-to-dorsal maturation of telencephalic meninges.

281 l tongue (42,106 vs 53,493 um(2), p < 0.01), ventral tongue (30,793 vs 39,095 um(2), *p < 0.05)) comp

282 The resulting anterior-posterior and dorsal-ventral transcriptional maps provided a powerful resourc

283 ases of neuron differentiation, such as soma ventral translocation and axonal targeting.

284 he more famously studied reinforced pathway (ventral value pathway; VVP), interface with prefrontal r

285 nd functionally dissociated dorsal (dDG) and ventral (vDG) adult canine DG were comparatively examine

286 nd Hox gene regulation of trachealess (trh), ventral veinless (vvl), and cut (ct), key genes involved

287 neuronal subtypes that partition dorsal and ventral visual circuits by differential Wnt signalling t

288 s (DCNNs) and cascade of regions along human ventral visual cortex.

289 re nodes and more variably in other parts of ventral visual cortex.

290 ew-is a mid-level processing stage along the ventral visual pathway of the macaque monkey.

291 irst object-specific processing stage in the ventral visual pathway, just as area MT is the first mot

292 y with the putative VWFA than other adjacent ventral visual regions that also show foveal bias, and (

293 Area LM, akin to primate ventral visual stream areas, showed higher selectivity f

294 sparity processing in LM, resembling primate ventral visual stream areas.

295 ate brains typically have regions within the ventral visual stream that are selectively responsive to

296 category-specific computational hubs in the ventral visual stream with the distributed cortical memo

297 harpens neural representation throughout the ventral visual stream, generating suppressed sensory res

298 global encoding similarity), particularly in ventral visual stream.

299 tifies complex and multifactorial origins of ventral wall defects and has important implications for

300 by caudally-polarized motile cilia along the ventral wall of the central canal.