ライフサイエンスコーパス: fusiform

1 tant visual cues in social perception (right fusiform).

2 hippocampus, parahippocampus, thalamus, and fusiform.

3 get-evoked activation decreases in the right fusiform.

4 y related to cortical thickness in the right fusiform.

5 aped abdominal aortic aneurysms (SaAAAs) and fusiform abdominal aortic aneurysms (FuAAAs) regarding p

6 ing thoracic aortic aneurysms (n=10 total, 5 fusiform and 5 saccular) underwent 3-dimensional reconst

7 This analysis reveals a network of fusiform and anterior temporal areas that carry informat

8 from the undiseased portion) and small SMCs (fusiform and growing in multilayers, from the undiseased

9 ateral sulcus, in a region lying between the fusiform and lingual gyri.

10 s well as increases in the precuneus and the fusiform and lingual gyrus.

11 etween the posterior cingulate and both left fusiform and medial frontal gyri.

12 rCBF in the right parahippocampus, thalamus, fusiform and middle temporal gyri, as well as the left a

13 al prefrontal, posterior cingulate, temporal fusiform and occipitotemporal cortex.

14 gender, race, and emotion categories in the fusiform and orbitofrontal cortices were stereotypically

15 roups showed differential hypo-activation of fusiform and posterior temporo-occipital junctional cort

16 Besides fusiform and saccular aneurysms that can thrombose, SA/C

17 yma such as in the ventromedial nucleus were fusiform and showed a bipolar morphology.

18 e and emotion processing including amygdala, fusiform, and insula.

19 ivation to SS in the precentral, prefrontal, fusiform, and posterior cingulate cortices before CBT-I.

20 ion neurons have been described: multipolar, fusiform, and pyramidal.

21 hinner cortex in various frontal regions and fusiform, and reduced FA in inferior longitudinal fascic

22 us, hippocampus, posterior cingulate cortex, fusiform, and visual cortex (P < .05 significance thresh

23 aortic repair (1993-2013), predominantly for fusiform aneurysm (n = 144), saccular aneurysm (n = 94),

24 form dilations of cerebral vessels and giant fusiform aneurysm in supraclinoid segment of the interna

25 In advanced cases, formation of a fusiform aneurysm is possible.

26 es of the circle of Willis coexisting with a fusiform aneurysm of the basilar artery.

27 domain or the kinase activation loop in 4/6 fusiform aneurysms (and 0/38 saccular aneurysms; Fisher'

28 , 178 aneurysms) with unruptured saccular or fusiform aneurysms or recurrent aneurysms after previous

29 n the internal carotid artery were included; fusiform aneurysms, infundibulae, and vascular segments

30 e a significantly higher normalized PWS than fusiform aneurysms.

31 olgi-impregnated neurons had round or ovoid, fusiform, angular, and polygonal cell bodies (10-30 mum

32 ss) of the right inferior parietal and right fusiform areas was shown to play a key role in ET charac

33 How does face-selectivity in the fusiform arise in development, and why does it develop s

34 05 [0.02], P = .07, P for interaction = .04; fusiform: beta>50 [SE], 0.09 [0.03], P = .002, beta</=50

35 t the swollen ER bodies were derived from ER fusiform bodies.

36 uatic locomotion, including development of a fusiform body and reduction of hindlimbs [8-11], but the

37 (FFA), occipital face area (OFA), amygdala, fusiform body area (FBA), retrosplenial complex (RSC) an

38 ing the extrastriate body area (EBA) and the fusiform body area (FBA).

39 ns in the bilateral cerebellum and bilateral fusiform body-area, with power suppression during a more

40 s have shown that in normal hearing animals, fusiform cell activity can be modulated by activation of

41 ned, and the two motifs combined to modulate fusiform cell output and acoustic-driven responses.

42 ereas deep afterhyperpolarizations following fusiform cell spike trains potently inhibited stellate c

43 onstrate increased synchrony and bursting of fusiform cell spontaneous firing, which correlate with f

44 artwheel cell) and principal output neurons (fusiform cell) were compared before and after manipulati

45 synapses on bushy cells (AN-BC synapses) and fusiform cells (AN-FC synapses) and PF synapses on FC (P

46 mably reflecting direct excitatory inputs to fusiform cells and an indirect inhibitory input to fusif

47 eveal that 5-HT exerts a potent influence on fusiform cells by altering their intrinsic properties, w

48 rm cells and an indirect inhibitory input to fusiform cells from the granule cell-cartwheel cell syst

49 , a reduction in KCNQ2/3 channel activity in fusiform cells in noise-exposed mice by 4 days after exp

50 taneous firing (hyperactivity) is induced in fusiform cells of the dorsal cochlear nucleus (DCN) foll

51 several higher auditory stations but not in fusiform cells of the dorsal cochlear nucleus (DCN), key

52 In fusiform cells of the dorsal cochlear nucleus, excitator

53 Optogenetically activated populations of fusiform cells reliably enhanced interneuron excitabilit

54 e of increased synchrony and bursting in DCN fusiform cells suggests that a neural code for phantom s

55 stellate cells were more strongly coupled to fusiform cells than to other stellate cells.

56 o suppress tinnitus-related hyperactivity of fusiform cells using the cholinergic agonist, carbachol.

57 we show that excitatory projection neurons (fusiform cells) and inhibitory stellate interneurons of

58 nitus, we recorded spontaneous activity from fusiform cells, the principle neurons of the DCN, in nor

59 gic axon terminals increased excitability of fusiform cells.

60 n dorsal cochlear nucleus principal neurons, fusiform cells.

61 a novel mechanism in the pathophysiology of fusiform cerebral aneurysms and suggest a potential role

62 vident in both face-selective regions of the fusiform cortex and domain-general regions of the prefro

63 ial expressions in amygdala, as well as left fusiform cortex and right middle frontal gyrus (cluster-

64 We found that mid-fusiform cortex is the first brain region sensitive to l

65 isorders, for example, aberrant amygdala and fusiform cortex structure and function occurring in the

66 This unique sensitivity of mid-fusiform cortex to sub-lexical and lexical characteristi

67 Thinner left inferior temporal and right fusiform cortex were associated with the UNC13A single n

68 lume in the hippocampus, parahippocampus and fusiform cortex, and a white-matter index for the fornix

69 including the amygdala, anterior insula, and fusiform cortex, even after accounting for prescan state

70 n manifested in neural patterns of the right fusiform cortex.

71 al discriminability in lateral occipital and fusiform cortices, suggesting that activation patterns w

72 was detected in right inferior temporal and fusiform cortices, which correlated negatively with CGG

73 ors thereof within the medial prefrontal and fusiform cortices.

74 these measures but increased the density of fusiform DCX cells per section.

75 Both round and fusiform DCX-immunoreactive (DCX-ir) cells were found in

76 esent a rare case of a patient with multiple fusiform dilations of cerebral vessels and giant fusifor

77 only occurring, and 'other types', including fusiform/dolichoectatic, dissecting, serpentine, posttra

78 Individuals with LOX variants had fusiform enlargement of the root and ascending thoracic

79 in the occipital and temporal lobe, and the fusiform face area (FFA) and anterior temporal lobe play

80 houses enhanced the sensory responses in the fusiform face area (FFA) and parahippocampal place area

81 Mirroring the arrangement of human regions fusiform face area (FFA) and PPA (which are adjacent to

82 gory-selective visual regions, including the fusiform face area (FFA) and the parahippocampal place a

83 sulcus (pSTS) and its connectivity with the fusiform face area (FFA) during eye contact with a speak

84 presenting architectural styles included the fusiform face area (FFA) in addition to several scene-se

85 brain -i.e. face patches in monkeys and the fusiform face area (FFA) in humans.

86 The fusiform face area (FFA) is a region of human cortex tha

87 The fusiform face area (FFA) is a well-studied human brain r

88 The fusiform face area (FFA) is thought to be a computationa

89 the amplitude of gamma oscillations, in the fusiform face area (FFA) of individuals diagnosed with A

90 e fMRI responses in the right face-selective fusiform face area (FFA) was closely associated with ind

91 ng hypothesis, this dedifferentiation in the fusiform face area (FFA) was driven by increased activat

92 functional network connectivity of the left fusiform face area (FFA) with the hippocampus and inferi

93 dial category-selective areas, including the fusiform face area (FFA), occipital face area (OFA), amy

94 A gaze processing network comprising fusiform face area (FFA), superior temporal sulcus, amyg

95 r superior temporal sulcus (pSTS) and to the fusiform face area (FFA), using a searchlight approach t

96 nd race of faces, it remains unclear whether fusiform face area (FFA)-the portion of fusiform gyrus t

97 retation of domain-specific regions like the fusiform face area (FFA).

98 160-ms recruitment of the category-sensitive fusiform face area (FFA).

99 ells the story behind our first paper on the fusiform face area (FFA): how we chose the question, dev

100 ivers and nonperceivers were observed in the fusiform face area and extrastriate visual cortex.

101 Positive connectivity to the right fusiform face area and negative connectivity to left fro

102 han responses to nonsymmetrical views in the fusiform face area and superior temporal sulcus, but not

103 network defined by connectivity to the right fusiform face area and to left frontal regions.

104 Damage to the right fusiform face area can disrupt the ability to recognize

105 iarity in the model, whereas activity in the fusiform face area covaries with the prediction error pa

106 nitude of repetition suppression (RS) in the Fusiform Face Area is influenced by the probability of r

107 ce the neural response to faces in the right fusiform face area or right occipital face area.

108 The fusiform face area responds selectively to faces and is

109 cial identity and provides evidence that the fusiform face area responds with distinct patterns of ac

110 The ventral temporal fusiform face area showed sensitivity to fearful express

111 ctional connectivity between the ACC and the fusiform face area that was disrupted by stress odors un

112 nd unexpected face and house stimuli in the "fusiform face area" (FFA) could be well-described as a s

113 ncluding the "proto" occipital face area and fusiform face area) and scene selectivity (including the

114 Similar results were also found in the fusiform face area, a face-selective perceptual processi

115 In the fusiform face area, a face-space coding model with sigmo

116 ccur without normal functioning of the right fusiform face area, an area proposed to mediate greeble

117 (PPA) compared with adjacent regions (e.g., fusiform face area, FFA) within the temporal visual cort

118 al areas, including the occipital face area, fusiform face area, lateral occipital cortex, mid fusifo

119 connectivity of the social brain (amygdala, fusiform face area, orbital-frontal regions).

120 we show that (1) the VWFA, compared with the fusiform face area, shows higher connectivity to left-he

121 decisions, respectively, particularly in the fusiform face area.

122 network defined by connectivity to the right fusiform face area.

123 osia, only 29 of which intersected the right fusiform face area.

124 -down control descending from the ACC to the fusiform face area.

125 es were behaviorally relevant in the brain's fusiform face area.

126 well as in the face-sensitive occipital and fusiform face areas.

127 a representation of face orientation in the fusiform face-selective area (FFA).

128 ten assume uniform aortic wall thickness and fusiform geometry.

129 entorhinal cortical thickness, greater right fusiform gyral activity during emotional face processing

130 posterior cingulate (cue-alpha) and the left fusiform gyri (item-gamma).

131 P < .05) and FA values in the cerebellum and fusiform gyri (P < .05).

132 ipital complex, the parahippocampal, and the fusiform gyri did not predict target presence, while hig

133 p deprivation caused decreased activation in fusiform gyri for angry faces and decreased ratings of h

134 amygdala, hippocampus, parahippocampal, and fusiform gyri in 30 of 31 subjects compared with normal

135 t posterior hippocampus, parahippocampal and fusiform gyri, and predominantly left hemisphere extra-t

136 ial/pulvinar nuclei of the thalamus, and the fusiform gyri, as well as the medial and lateral dorsal

137 -wise differences in the cuneus, lingual and fusiform gyri, middle occipital lobe, inferior parietal

138 stimuli resulted in greater deactivation in fusiform gyri, possibly reflecting greater suppression o

139 eam, particularly the inferior occipital and fusiform gyri, remained selective despite showing only 9

140 icularly strong in the inferior temporal and fusiform gyri, two areas important for object recognitio

141 in visual areas, particularly the bilateral fusiform gyri.

142 were identified in the inferior frontal and fusiform gyri.

143 the inferior frontal, inferior parietal, and fusiform gyri; the precuneus; and the dorsomedial prefro

144 parahippocampus (0.032 vs 0.037; p<0.0001), fusiform gyrus (0.036 vs 0.041; p<0.0001), inferior temp

145 0.001), anterior vermis (40%, P < 0.001) and fusiform gyrus (20%, P < 0.001) compared with controls o

146 iculum, and entorhinal cortex), and anterior fusiform gyrus (corrected P < .05; uncorrected P = .001)

147 s (Cohen's d=-0.293; P=1.71 x 10(-21)), left fusiform gyrus (d=-0.288; P=8.25 x 10(-21)) and left ros

148 lts, particularly those anchored in the left fusiform gyrus (FFG) (the visual word form area).

149 ition is linked to dopamine (DA) activity in fusiform gyrus (FFG).

150 le of face-selective neural responses of the fusiform gyrus (FG) in face perception in a patient impl

151 Recent research indicates that the human fusiform gyrus (FG), which is a hominoid-specific struct

152 tients with lesions in the VTC including the fusiform gyrus (FG).

153 show that the strength of rsFC between left fusiform gyrus (L-FG) and higher-order language systems

154 - left intraparietal sulcus (L.IPS) and left fusiform gyrus (L.FFG).

155 s (p(uncorrected) < 0.05, SBC = -0.32), left fusiform gyrus (P(FDR) < 0.01, SBC = -0.51).

156 ctivity, was correlated with GMV in the left fusiform gyrus (r = -0.19, P(uncorrected) = 0.049) and r

157 contact modulated BOLD activity in the right fusiform gyrus (rFG) and left inferior occipital gyrus (

158 tinct behaviors are constructed in the right fusiform gyrus (rFG).

159 zed beta coefficient (SBC) = -0.26) and left fusiform gyrus (SBC = -0.25) in sample 1 were replicated

160 e right anterior cingulate cortex), and left fusiform gyrus (SDM estimate = -0.146; P = .003).

161 uperior Temporal Gyrus (t=1.403, p=0.00780), Fusiform Gyrus (t=1.26), and Parahippocampal Gyrus (t=1.

162 nterior cytoarchitectonic areas (e.g., areas fusiform gyrus [FG]1-FG4) and another that contains a se

163 l thickness in the right parahippocampal and fusiform gyrus across both time points was found in both

164 was inversely correlated with the change in fusiform gyrus activation in the fasted state but not in

165 d connections to the occipital lobe from the fusiform gyrus along with longer association fibers that

166 modulation of the afferent connections from fusiform gyrus and AMG to VPFC.

167 ault mode network, superior parietal lobule, fusiform gyrus and anterior insula.

168 s in the pars orbitalis, paracentral lobule, fusiform gyrus and inferior temporal gyrus was lowest in

169 Differences were prominent in the fusiform gyrus and lateral temporal lobe.

170 d with less perfusion in the right occipital/fusiform gyrus and left subgenual ACC.

171 sociated with decreased FC between the right fusiform gyrus and left superior occipital cortex.

172 ion and the ankle DF/PF tasks, the bilateral fusiform gyrus and middle temporal gyrus, right inferior

173 effects within right amygdala, hippocampus, fusiform gyrus and orbitofrontal cortex.

174 mygdala and orbitofrontal cortex and between fusiform gyrus and orbitofrontal cortex.

175 l sulcus encoded response complexity and the fusiform gyrus and precuneus organized its activity acco

176 in right lateral occipital cortex and right fusiform gyrus and sources in a control region (left V1)

177 in ReHo between the two bands were found in fusiform gyrus and superior frontal gyrus (slow-4> slow-

178 hippocampus, dorsolateral prefrontal cortex, fusiform gyrus and superior frontal gyrus-583 subjects)

179 Fusiform gyrus and temporal pole cortical thickness was

180 ted by visual semantic loops within the left fusiform gyrus and that these neural processes may be me

181 uced and increased fMRI responses in the mid-fusiform gyrus and the lateral occipital cortex, respect

182 in the left inferior prefrontal cortex, the fusiform gyrus and the medial temporal lobe including bo

183 amage to the inferior temporal gyrus, to the fusiform gyrus and to a white matter network including t

184 l resolution imaging techniques identify the fusiform gyrus as subserving processing of invariant fac

185 of the salience network; and a subregion of fusiform gyrus associated with face perception.

186 temporal gyrus, superior temporal gyrus, and fusiform gyrus during memory encoding reduced odds of re

187 Clinically, the ability to recruit the fusiform gyrus during the task in noise was negatively c

188 in dorsomedial prefrontal cortex (DMPFC) and fusiform gyrus emphasized a human-nonhuman distinction.

189 regions (temporal pole for word matching and fusiform gyrus for face matching).

190 Face-selective neural responses in the human fusiform gyrus have been widely examined.

191 The fusiform gyrus is an important region implicated in such

192 ese findings indicate that the right lateral fusiform gyrus is critically involved in object recognit

193 The fusiform gyrus is understood to be involved in the proce

194 The large fusiform gyrus library (117 subjects) with high sequenci

195 ortical dysfunction in the temporal lobe and fusiform gyrus may be related to epileptic activity in I

196 fMRI revealed that the left fusiform gyrus may facilitate the production of backward

197 bust face-selective responses in the lateral fusiform gyrus of individual blind participants during h

198 work and that a right anterior region of the fusiform gyrus plays a central role within the informati

199 Although prior research suggests that fusiform gyrus represents the sex and race of faces, it

200 The right fusiform gyrus showed adaptation to faces (not objects)

201 ons, the lateral section of the right middle fusiform gyrus showed the largest face-selective respons

202 The mid fusiform gyrus showed the strongest, earliest response a

203 ateral occipito-temporal sulcus and adjacent fusiform gyrus shows maximal selectivity for words and h

204 the visual word-form area (part of the left fusiform gyrus specialized for printed words); and persi

205 esion also extended laterally to involve the fusiform gyrus substantially.

206 wer spectra in the primary visual cortex and fusiform gyrus that are maximally discriminative of data

207 ther fusiform face area (FFA)-the portion of fusiform gyrus that is functionally-defined by its prefe

208 eralized hyperactivation in the amygdala and fusiform gyrus that was subject to intersession habituat

209 Reduced right parahippocampal and fusiform gyrus thickness are familial trait markers for

210 ediated the association with inattention and fusiform gyrus thickness mediated the association with i

211 found positive correlations between the left fusiform gyrus to amygdala connectivity and different st

212 , and may serve in concert with amygdala and fusiform gyrus to modulate visual attention toward motiv

213 es modulated unidirectional connections from fusiform gyrus to orbitofrontal cortex.

214 ced modulation of connectivity from the left fusiform gyrus to the left amygdala and from the right a

215 ophy of the bilateral temporal poles and the fusiform gyrus were associated with prosopagnosia in rtv

216 ing, whereas PrC, anterior HC, and posterior fusiform gyrus were recruited during discrimination lear

217 ocampal gyrus, left orbitofrontal cortex and fusiform gyrus whereas patients with left hippocampal sc

218 ed fMRI to measure neural responses from the fusiform gyrus while subjects observed a rapid stream of

219 cortical thickness (maximum Cohen's d (left fusiform gyrus) = -0.33).

220 s placed over high-order visual areas (e.g., fusiform gyrus) showed both effects of spatial and objec

221 s in orthographic processing circuits (i.e., fusiform gyrus) was predictive of smaller gains in fluen

222 h brain regions with foveal tendencies (e.g. fusiform gyrus), and activations of layer-units with sel

223 as well as the insula, cingulate cortex, and fusiform gyrus, a regional distribution that was nearly

224 cus functional connectivity localized to the fusiform gyrus, a visual processing region also identifi

225 la, middle occipital, anterior cingulate and fusiform gyrus, amygdala, striatum, pulvinar, and substa

226 We found that activity in the fusiform gyrus, an area associated with the processing o

227 ate cortex, superior temporal gyrus, insula, fusiform gyrus, and caudate nucleus.

228 ippocampus, parahippocampal gyrus, amygdala, fusiform gyrus, and choroid plexus but not in other brai

229 rome group was found in the cingulate gyrus, fusiform gyrus, and frontal cortex in response to all fa

230 ed decreased activity in the right amygdala, fusiform gyrus, and inferior occipital gyrus compared wi

231 eral temporal lobe, including temporal pole, fusiform gyrus, and insula, and extending into occipital

232 ctivation patterns within the visual cortex, fusiform gyrus, and lateral temporal lobe.

233 lts showed that the visual cortex, bilateral fusiform gyrus, and right parahippocampal gyrus were act

234 more consistent activation of the amygdala, fusiform gyrus, and thalamus than emerging adults, who s

235 ly increased in temporal regions, insula and fusiform gyrus, consistent with those areas known to be

236 with ASD had lower FC than TC in cerebellum, fusiform gyrus, inferior occipital gyrus and posterior i

237 ed abnormal hyperactivation in the amygdala, fusiform gyrus, insula, anterior cingulate cortex, and d

238 flood in the Parahippocampal Gyrus, and Left Fusiform Gyrus, of those afflicted with AN.

239 the left parahippocampal gyrus and the left fusiform gyrus, recruited during facial expression proce

240 gyrus and bilateral middle/inferior temporal/fusiform gyrus, respectively) that showed reversed effec

241 laims have been made, and within the lateral fusiform gyrus, they are restricted to a small area (200

242 as the amygdala, hippocampus, temporal pole, fusiform gyrus, visual primary cortex, and motor areas (

243 wed that repetition suppression in bilateral fusiform gyrus, was selectively correlated with priming

244 cal area in the collateral sulcus and medial fusiform gyrus, which was place-selective according to b

245 us, left temporoparietal junction, and right fusiform gyrus, with patients showing relative hypoactiv

246 l gyrus, left parahippocampal gyrus and left fusiform gyrus.

247 ween higher-level language areas and the mid fusiform gyrus.

248 onse profiles such as the lateral and medial fusiform gyrus.

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

250 the downstream face-selective region in the fusiform gyrus.

251 tex at the junction of the right lingual and fusiform gyrus.

252 9557 in the right occipital cortex and right fusiform gyrus.

253 t posterior hippocampus, parahippocampus and fusiform gyrus.

254 hesis in relation to face selectivity in the fusiform gyrus.

255 redict functional activation to faces in the fusiform gyrus.

256 tion following a lesion to the right lateral fusiform gyrus.

257 olor, and place selectivity that tracked the fusiform gyrus/collateral sulcus.

258 ties in the right temporal pole and anterior fusiform gyrus; while in the Alzheimer's disease group,

259 , ventral IPS, lateral occipital region, and fusiform gyrus], which was accompanied by activation tha

260 Left fusiform habituation in female participants was directly

261 tual aneurysm model of 6 cm wide x 6 cm long fusiform hyper-elastic anisotropic design.

262 ewis-Sumner syndrome patients had multifocal fusiform hypertrophy in the nerve trunks.

263 ection neurons were multipolar, globular, or fusiform in shape.

264 diagnosis interaction was found in the left fusiform/inferior temporal cortex: participants with aut

265 to represent the information being encoded (fusiform/lateral occipital cortex), they each exerted op

266 uron numbers as well as the total numbers of fusiform (migrating) and round (differentiating) DCX neu

267 gic features, such as wide neck, large size, fusiform morphology, incorporation of side branches, and

268 Furthermore, fusiform myocyte-like cells forming reticulated pathways

269 Fusiform neurons were located rostrally, in the anterome

270 A urease-negative, fusiform, novel bacterium named Helicobacter saguini was

271 more bilateral or right-sided inferotemporal/fusiform object recognition network, which remained rela

272 eous fibrillar echotexture; grade 2, a focal fusiform or diffuse enlarged tendon; and grade 3, a hypo

273 ions and sad faces modulating unidirectional fusiform-orbitofrontal connections.

274 orm face area, lateral occipital cortex, mid fusiform, parahippocampal place area, and extending supe

275 GA-HRP into the anteromedian nucleus labeled fusiform premotor neurons within the OPt, as well as mul

276 t 5-HT directly enhances the excitability of fusiform principal cells via activation of two distinct

277 in superior frontal lobe, cingulate cortex, fusiform, putamen, and medial temporal lobe.

278 y a region within the left occipito-temporal/fusiform region (L-OT/F) often referred to as the visual

279 his is consistent with an involvement of the fusiform region in both early and midlatency face-proces

280 These analyses confirm a role for the right fusiform region in early to midlatency responses consist

281 he N/M170-as having a major generator in the fusiform region; however, this evoked component is not b

282 rior and superior parietal, hippocampus, and fusiform regions was stronger in individuals older than

283 posterior hippocampal, parahippocampal, and fusiform regions, as well as a posterior neocortical VOI

284 e ventral aspects of the form pathway (e.g., fusiform regions, ventral extrastriate body area) are no

285 mFus-faces and pFus-faces (mid and posterior fusiform, respectively)].

286 Interestingly, for fusiform rust disease-resistance traits, Bayes Cpi, Baye

287 Fusiform rust is controlled by few genes of large effect

288 o predict polygenic (height) and oligogenic (fusiform rust resistance) traits in a structured breedin

289 e and motile circular shape to a contractile fusiform shape show changes in the location of the sarco

290 umbrella cells a subapical pool of discoidal/fusiform-shaped vesicles (DFVs) undergoes Rab11a-depende

291 Fusiform-shaped, retrogradely labeled cells fell within

292 Additionally, we identified the posterior fusiform site (pFUS) as causally the most relevant node

293 corded multiunit spontaneous activity in the fusiform soma layer (FSL) of the DCN in control and tone

294 olved in sensory processing and integration (fusiform, somatosensory cortex, and thalamus), salience

295 al in predicting face selectivity within the fusiform, suggesting a possible mechanistic architecture

296 n one object-selective region, the posterior fusiform sulcus, and a strong sensitivity to these rever

297 ontains a tertiary, longitudinal sulcus (mid-fusiform sulcus, MFS) that bisects the FG into lateral a

298 Trichodesmium forms macroscopic, fusiform (tufts), spherical (puffs) and raft-like coloni

299 knockout in vivo led to the accumulation of fusiform vesicles in mouse urothelial superficial umbrel

300 the hinge areas in the uroplakin-delivering fusiform vesicles, as well as at the apical surface; and