ライフサイエンスコーパス: fissure

1 and upslanting versus downslanting palpebral fissures).

2 rms an isolated pocket medial to the Sylvian fissure.

3 e, 41.2% for haemorrhoids and 57.1% for anal fissure.

4 haryngeal foramen separated from the metotic fissure.

5 for haemorrhoids and 41 presented with anal fissure.

6 ne in both nasal and temporal sectors of the fissure.

7 xin A (BTA) in the treatment of chronic anal fissure.

8 a relationship to the closed embryonic optic fissure.

9 re promising agents in the treatment of anal fissure.

10 ting in concert surrounding the left sylvian fissure.

11 degrees , and 0 degrees ) sectors of the lid fissure.

12 nd subicular regions through the hippocampal fissure.

13 ns displayed a spatial preference toward the fissure.

14 ssected (LCM) tissue from the margins of the fissure.

15 way in directing proper closure of the optic fissure.

16 tioning of the ventral plexus in the choroid fissure.

17 e left cerebral hemisphere along the Sylvian fissure.

18 heres, short temporal lobe, and long sylvian fissure.

19 ription factor Pax2 and closure of the optic fissure.

20 having branches that reached the hippocampal fissure.

21 esulted in the abnormal closure of the optic fissure.

22 that this fissure was the superior accessory fissure.

23 ach to the left portal vein at the umbilical fissure.

24 expression in the anterior tip of the optic fissure.

25 rms at its inferior part, known as the optic fissure.

26 ng its most distinctive feature, the Sylvian fissure.

27 along the dentate gyrus, subiculum, CA1 and fissure.

28 ns and one unexpected cluster in the lateral fissure.

29 nergy needed to open the 6-7 August eruptive fissure.

30 frontal bossing, and down-slanting palpebral fissures.

31 tical access to regions situated within deep fissures.

32 and MEC using microprisms inserted into the fissures.

33 of the right lung with no visible interlobar fissures.

34 ing to the diagnosis of haemorrhoids or anal fissures.

35 ritical for regulating formation of specific fissures.

36 which are subsequently further subdivided by fissures.

37 indistinct occipital sinuses and cerebellar fissures.

38 e basement membrane specifically at emerging fissures.

39 ow set ears, and downward slanting palpebral fissures.

40 commonly aggregate near osteoarthritic (OA) fissures.

41 (3) cisterns are continuous with prevascular fissures.

42 ld hypertelorism, and downslanting palpebral fissures.

43 ques, which may be accompanied by purpura or fissuring.

44 a minor increase in the incidence of plaque fissuring.

45 issure width - 0.044-0.127; index of Sylvian fissure - 0.036-0.085; index of insular cistern width -

46 ard the hilus and delimited by a hippocampal fissure; 2) nonperiventricular adult neurogenesis; and 3

47 Thirty-four patients had 36 accessory fissures (26 right, 10 left).

48 fissures (36%), downward slanting palpebral fissures (32%), and lagophthalmos (28%).

49 on (60%), abnormal upward slanting palpebral fissures (36%), downward slanting palpebral fissures (32

50 dysmorphic features include small palpebral fissures, a wide nasal bridge and nose, micrognathia, an

51 Most strikingly, the base of each fissure acts as a boundary for gc precursor dispersion,

52 Anal fissure (AF) is regarded as a common problem, but there

53 ior-posterior axis into lobules separated by fissures, allowing the large number of cells needed for

54 nction of the cell's soma location along the fissure-alveus axis of the cell layer.

55 yed and/or incomplete closure of the ventral fissure, an excess of mesenchymal cells in the vitreous

56 0(+) endothelium was seen in the hippocampal fissure and cortical blood vessels, notably from P14, sh

57 fferential expression analysis between optic fissure and dorsal retinal tissue resulted in the detect

58 also appeared in cortices along the lateral fissure and intraparietal sulcus.

59 ax2 in coordinating the closure of the optic fissure and optic disc specification, which is necessary

60 ng both in normal closure of the human optic fissure and pathogenesis of coloboma.

61 vity leads to a failure to close the choroid fissure and progressive expansion of retinal tissue into

62 for 38 gyral regions, including the sylvian fissure and temporal and postcentral gyri, by using magn

63 cted from the margins of the zebrafish optic fissure and the opposing dorsal retina before (32 hours

64 rity) include cortex in and near the Sylvian fissure and the precentral gyrus.

65 that highlight distinct differences between fissured and intact cartilage surfaces.

66 ease in the total amount of surface which is fissured and thus leads to the conclusion that the surfa

67 Fbw7-deficient cerebella showed supranumeral fissures and aberrant progenitor cell migration.

68 A close topographic relationship of vitreous fissures and cisterns to the underlying vasculature of t

69 r zone in regulating formation of additional fissures and for extensive cerebellar growth.

70 e descendents to regulate formation of three fissures and for general growth of the cerebellum.

71 he N lineage cells that separate to form the fissures and lateral ectodermal and mesodermal derivativ

72 ic disorder characterized by small palpebral fissures and other craniofacial malformations, often wit

73 stern Elysium, but seas and lakes from these fissures and previous water flooding events were presume

74 correct diagnosis, while hyperkeratosis and fissures and ridges were independent risk markers of der

75 caused by atherosclerotic plaque rupture or fissuring and subsequent occlusive or subocclusive throm

76 l nerve leaves the braincase via the metotic fissure) and homoplastic characters.

77 (central, peripheral, or abutting pleura or fissures), and attenuation (solid, calcified, or subsoli

78 st that there is delayed fusion of the optic fissure, and inner nuclear layer abnormalities indicate

79 neocortex just anterior to the main vertical fissure, and precisely locating it as we do here is usef

80 ula and other regions surrounding the rhinal fissure, and the medial prefrontal cortex.

81 the neural tube, body wall, face, and optic fissure, and they also display defects in lung and heart

82 The presentation of painful defecation, anal fissures, and macroscopic blood in stools was highly sug

83 to other brain regions situated within deep fissures, and opens up these regions for study at cellul

84 ad articular cartilage contour irregularity, fissures, and/or thinning.

85 ss hippocampal layers and was largest at the fissure; and (3) a low-frequency rhythm with largest amp

86 ular nose; long, narrow upslanting palpebral fissures; and large, fleshy low-set ears.

87 round the temporal lobe and interhemispheric fissure, anterior-posterior stretch in the frontal and o

88 3.4] for >/= 4 partners), and report of anal fissures (aOR, 2.3 [95% CI, 1.1-4.8]) were associated wi

89 sional reconstruction shows that major brain fissures appear while most of the cerebral surface remai

90 rly located near the fundus of the calcarine fissure, approximately 25 mm away from the most posterio

91 al quality than those with unconsolidated or fissured aquifers, highlighting the vulnerability of the

92 Prevascular vitreous fissures are an almost universal feature of human eyes.

93 egulate the formation of a normal pattern of fissures are poorly understood.

94 lts suggest that subarachnoid clots in sulci/fissures are sufficient to induce spreading depolarizati

95 Enthesis microdamage (fissuring) as well as vascular and reparative changes we

96 of angular stomatitis (AS), ie, thinning or fissuring at the mouth angles, increased 6-fold from Dec

97 likely that residual iris is trapped in the fissure between the artificial iris and the anterior cha

98 isrupts human cortex surrounding the Sylvian fissure bilaterally including "Broca's area," the primar

99 es were observed in cortical and hippocampal fissure blood vessels, showing maximum density at P7, bu

100 Fourteen patients required surgery for anal fissure (Botox +/- fissurectomy 8; LIS 6).

101 centric hilum, longitudinal fissure, lack of fissure branching, fissure ratio, and maximum granule si

102 ebrows, hypertelorism, downslanted palpebral fissures, broad nasal base, long smooth philtrum and ful

103 rphism with coarse face, upslanted palpebral fissures, broad nasal tip, and wide mouth, developmental

104 s and lateral bank of the anterior calcarine fissure but was not characterized fully.

105 Complications of chronic anal fissure (CAF) treatments are prompting interest in lower

106 a large lipid core, endothelial denudation, fissured cap, severe stenosis, or combinations of these

107 e clusters and explained 16% of variation in fissure caries in molar teeth but little variation in ot

108 h failure to close the neural tube and optic fissure, causing exencephaly and retinal coloboma, commo

109 ye development is the closure of the choroid fissure (CF), a transient structure in the ventral optic

110 art, imbibing water, increasing swelling and fissuring--characteristic manifestations of osteoarthros

111 a loss-of-function leads to lack of choroid fissure closure (known as a coloboma), a loss of optic n

112 formation, resulting from a failure in optic fissure closure (OFC) and causing visual impairment.

113 taging and unique anatomical detail of optic fissure closure (OFC) in the embryonic chick, including

114 r MITF in regulating processes such as optic-fissure closure and bone development or homeostasis, whi

115 basis of the presence or absence of an optic fissure closure defect (OFCD); those with OFCD were furt

116 (noi(tu29a) and gup(m189); congenital optic fissure closure defects).

117 ax2, the mechanism of the failure of choroid fissure closure is associated with a cell fate switch fr

118 JNK to regulate BMP4 expression during optic fissure closure is conserved in Drosophila during dorsal

119 Our results show that proper optic fissure closure relies on Wnt8b suppression by Foxg1 in

120 Optic fissure closure requires precise orchestration in timing

121 profile global gene expression during optic fissure closure using laser capture microdissected (LCM)

122 To test the hypothesis that optic fissure closure was apoptosis-dependent, the anti-apopto

123 the embryologic and molecular basis of optic fissure closure with clinical observations in patients w

124 s of ventral optic cup formation and choroid fissure closure, and that bcl6a is a direct target of Va

125 Pitx2, a gene required for normal optic fissure closure, is dramatically downregulated in the pe

126 zinc finger proteins Nlz1 and Nlz2 in normal fissure closure.

127 closer to a molecular understanding of optic fissure closure.

128 cantly less solute adsorption at surfaces of fissures compared to adjacent intact surfaces of damaged

129 phic evidence of emphysema heterogeneity and fissure completeness was associated with an enhanced res

130 On frontal radiographs, presence of this fissure correlated with a curvilinear band of atelectasi

131 the surface ahead of the main liquid-filled fissure could be the origin of many precursor eruptions.

132 A plume of water vapour escapes from fissures crossing the south polar region of the Saturnia

133 ications, such as those with small palpebral fissures, deep-set eyes, corneal basement membrane dystr

134 ulation of signaling by Fz5 and Fz8 in optic fissure/disc formation and progenitor expansion.

135 laps with Fz5 in the neural retina and optic fissure/disc.

136 The optic fissure does not close in late VAD embryos, and severe f

137 scle, which contracts to close the palpebral fissure during blinking.

138 esulting from incomplete fusion of the optic fissure during development.

139 ene networks underlying closure of the optic fissure during vertebrate eye development are poorly und

140 ng of the right eyelid with narrow palpebral fissure, dysarthria, anisocoria (narrower pupil on the r

141 step in substrate disintegration, elongated fissures emerge which develop into coniform cracks as di

142 both groups and included upslanted palpebral fissures, epicanthus, telecanthus, a wide nasal bridge a

143 Here we show that the massive 2014-2015 fissure eruption in Holuhraun, Iceland, reduced the size

144 Dyke growth was slowed down by an effusive fissure eruption near the end of the dyke.

145 anule cell precursors located at the base of fissures fail to undergo cell shape changes required for

146 Ultimately the ventral fissure fails to close resulting in coloboma.

147 The average strike-dimension of volcanic fissures/feeder-dykes in Etna is about 2.7 km.

148 e data on the size distributions of volcanic fissures/feeder-dykes, crater cones, dyke thicknesses, a

149 omy in mineralized arthropods from Paleogene fissure fillings and demonstrate the value of these foss

150 il tarsiid from the middle-Eocene Shanghuang fissure-fillings in southern Jiangsu Province, China.

151 Fissures, fistulas, abscesses, and anal canal stenosis a

152 res lateral internal sphincterotomy for anal fissure, fistulotomy, and ileal pouch reconstruction can

153 ithin the aquifer and indicated small-medium fissure flows to be the dominant pathway, delivering 52-

154 In addition, the positioning and timing of fissure formation are altered.

155 nsplantation experiments that Tbx18 controls fissure formation in the late stages of somite maturatio

156 ntact N lineage cells at or near the time of fissure formation, ablation experiments suggest that the

157 ing correlates spatially and temporally with fissure formation, and that Gli2 is the main activator d

158 ts, including ectopic neurons and defects in fissure formation, Bergmann glia organization and baseme

159 astically alters the timing and placement of fissure formation, the migration and positioning of gran

160 glia-basement membrane adhesion required for fissure formation.

161 ese contacts are not required for initiating fissure formation.

162 ng vertebrate eye morphogenesis, a transient fissure forms at its inferior part, known as the optic f

163 The Sylvian fissure forms by the relative overgrowth of the frontal

164 and impedes the lateral edges of the choroid fissure from meeting and fusing.

165 f the basal ganglia, widening of the Sylvian fissures, fronto-temporal atrophy and severe spongiform

166 A failure in optic fissure fusion during development can lead to blinding m

167 consistent with a role in facilitating optic fissure fusion during vertebrate eye development.

168 nd cellular mechanisms that facilitate optic fissure fusion remain elusive.

169 highly differentially expressed across optic fissure fusion, with a resultant ocular coloboma phenoty

170 f), during (48 hpf) and after (56 hpf) optic fissure fusion.

171 Closure of the optic fissure has been well characterized and many genetic alt

172 ct in to control growth and/or patterning of fissures has not been determined.

173 The primary end point was fissure healing after 3 months.

174 iate domains of conflicting synergy models - fissures impacting all aspects of combination therapy di

175 h signaling results in formation of an extra fissure in a position conserved in rat.

176 eps of fusion are: widening of a hydrophobic fissure in bilayers for stalk formation, splay within th

177 o avoid surgery for haemorrhoids and/or anal fissure in Crohn's disease (CD) patients is still curren

178 dal plate, the otic capsules and the metotic fissure in gnathostomes.

179 The midposterior fundus of the Sylvian fissure in the human brain is central to the cortical pr

180 surgical treatment of haemorrhoids and anal fissures in CD patients over a period of 8 years.

181 tegral to determining the distinct number of fissures in each species.

182 ular to the walls of vertical synsedimentary fissures in microbial reefs.

183 een devoted to neighborhood inequalities and fissures in the civic infrastructure that potentially ch

184 Importantly, the pattern of the remaining fissures in the mutants corresponds to the first fissure

185 Anal fissures in women who report never having had anal inter

186 We observe early biochemical patterns of fissuring in cartilage that define future onset of OA.

187 t common changes were cell clustering and/or fissuring (in 76% of entheses).

188 l to undergo cell shape changes required for fissure initiation.

189 ved in SW generation surrounding the lateral fissure (insula, superior temporal, parietal, middle fro

190 is and today consists primarily of assessing fissure integrity (FI).

191 with frequent axonal projections across the fissure into the CA1 and subicular regions.

192 The lava erupted from a fissure, inundated the channels, and drained downstream

193 bsence of Tbr2, formation of the hippocampal fissure is abnormal, leading to aberrant development of

194 ), a cortical vestibular area in the sylvian fissure, is not responsive to optic flow.

195 located at the posterior end of the sylvian fissure, is strongly interconnected with PIVC, and recei

196 aracteristics (eccentric hilum, longitudinal fissure, lack of fissure branching, fissure ratio, and m

197 Incomplete fusion of the optic fissure leads to ocular coloboma, a congenital eye defec

198 Mean palpebral fissure, levator function, and margin reflex distance we

199 o the cingulate sulcus (CiS) and the lateral fissure (LF), is conserved across the primates studied a

200 cessory fissures were manifested by a normal fissure line; two, by slight thickening or minimal linea

201 Disruption of a plaque, ulceration, tears, fissures, lipid-rich or fibrous lesions, and luminal or

202 re-sized ice particles from a series of warm fissures located near its south pole.

203 1 (NTN1) is precisely expressed in the chick fissure margin during fusion but is immediately downregu

204 the basal lamina does not occur at the optic fissure margin.

205 sition was transiently enriched in the human fissure margins during OFC at days 41-44.

206 f human OFC in which epithelial cells at the fissure margins undergo a transient epithelial-to-mesenc

207 ls, the primary site for the fusion of optic fissure margins, FAT1 is localized at earliest cell-cell

208 Apoptosis was not observed in the human fissure margins.

209 differ with respect to caries: (C1) pit and fissure molar surfaces, (C2) mandibular anterior surface

210 ontology categories in the context of optic fissure morphogenesis and highlight interesting transcri

211 profiled global gene expression during optic fissure morphogenesis by transcriptome analysis of tissu

212 irst observed in the posterior aspect of the fissure moving anteriorly to the frontal lobe and latera

213 both abduction and adduction, with palpebral fissure narrowing and globe retraction in adduction.

214 Most affected eyes had lid fissure narrowing and retraction in adduction.

215 otemporal suture and medially by the orbital fissure; none extended above the lesser sphenoid wing.

216 cular thalamic nucleus (RTN) and the primary fissure of the cerebellum of the posthypoxic animals.

217 ized growth in regions bordering the Sylvian fissure of the frontal, parietal and temporal lobes.

218 ts with a prospectively identified accessory fissure of the lower lobe were reviewed and correlated w

219 A shift of the fissures of both lungs in the basal direction was appare

220 ed of an elaborate set of folia separated by fissures of different lengths, remains largely unexplore

221 on inside a temperature gradient in pores or fissures of rocks.

222 riginates from defective fusion of the optic fissure (OF), a transient gap that forms during eye morp

223 ults from errors in the sealing of the optic fissure (OF), a transient structure at the bottom of the

224 uires timely and precise fusion of the optic fissure (OF).

225 parterial bronchi and absence of middle lobe fissure on CTscans suggesting heterotaxy syndrome.

226 Lobar segmentations delineated by major fissures on both CT scans were used to calculate the per

227 ema and a target lobe with intact interlobar fissures on CT of the thorax.

228 It is thought that the Cerberus Fossae fissures on Mars were the source of both lava and water

229 Eruptive fissures opened in the LERZ on 3 May, eventually extendi

230 nt or interventional procedure consisting of fissure opening with linear cutting staplers buttressed

231 acy of alginate staple-line reinforcement of fissure openings as compared with stapling alone, with o

232 ated with a failure in fusion of the choroid fissure or in some instances, more severe ventral optic

233 e peaks most often occurred over the Sylvian fissure or the upper bank of the posterior superior temp

234 me, is elevated in culprit lesions that have fissured or ruptured in patients with sudden death from

235 7.1%), and signs of fungal infection, cracks/fissures, or maceration between toes (36.3%); 30.9% had

236 Historically, the terms superior orbital fissure, orbital apex, and cavernous sinus have been use

237 symmetrical relative to the interhemispheric fissure, other regions express asymmetric patterns of re

238 in older patients; (2) prevascular vitreous fissures overly the retinal vessels; and (3) cisterns ar

239 enotypes in the lesions was less than in the fissure (p < 0.001) or buccal (p = 0.011) sites.

240 CA-to-OA ratio and proptosis (P<0.001), lid fissure (P = 0.004), and intraocular pressure (P<0.001).

241 correlated with proptosis (P<0.0001) and lid fissure (P<0.045).

242 ent dentition caries, as well as for pit-and-fissure- (PF) and smooth- (SM) surface caries.

243 Degenerative, eyewall-parallel fissure planes and their course were described for the f

244 The fissure planes were rare in younger eyes (12%) and signi

245 g ventilatory obstruction, and lesions along fissures predisposed patients to chest tube placement (P

246 eterogeneous emphysema and intact interlobar fissures produces significant improvements in lung funct

247 luding long, narrow and upslanting palpebral fissures, prominent nasal bridge, square dental arch and

248 arse facies, puffy eyelids, narrow palpebral fissures, prominent supraorbital ridges, a bulbous nose,

249 itudinal fissure, lack of fissure branching, fissure ratio, and maximum granule size) to each of 323

250 ynergy reveals the persistence of historical fissures regarding the appropriate domains of conflictin

251 mented epithelium (RPE) proliferation in the fissure region with concomitant acquisition of RPE cell

252 Chronic anal fissures remain a challenging condition.

253 idence that cell death is required for optic fissure remodelling.

254 urvive to birth, but fail to close the optic fissure (retinal coloboma).

255 rate the in situ distribution of biofilms on fissure rock faces using video documentation.

256 Fissure sealant (FS) and fluoride varnish (FV) are effec

257 alone (diet, plaque removal, fluorides, and fissure sealants).

258 The fissure-sealing of newly erupted molars is an effective

259 ark a stage at which the balance of the oral fissure shifted from mostly teeth to mostly baleen.

260 at times when geophysical models predict its fissures should be under tension and therefore may be wi

261 retina despite the presence of an open fetal fissure, showing that coloboma and retinal folding repre

262 ssion in the nasal and temporal edges of the fissure.SIGNIFICANCE STATEMENT Coloboma is an ocular dis

263 dysfunction (dry skin, less acidic skin, and fissured skin), and atopic dermatitis (AD) with a severe

264 alized antithrombotic efficacy at denuded or fissured stenotic high-risk lesions without systemic ble

265 nterior surfaces, (C3) posterior non-pit and fissure surfaces, (C4) maxillary anterior surfaces, and

266 tion, normalized mean surface intensities of fissured surfaces of injured explants were 6%, 40%, and

267 terface, allowing formation of the acellular fissure that defines the somite boundary.

268 nnections of the cortex dorsal to the rhinal fissure that includes the RAIC have been examined previo

269 ervations show eruptions from "tiger stripe" fissures that are sustained (although tidally modulated)

270 ures in the mutants corresponds to the first fissures that form during normal development.

271 he skull roof) but lacking a ventral cranial fissure, the presence of which is considered a derived f

272 st, concomitantly with the loss of branchial fissures, the acquisition of a feeding mechanism based o

273 stresses that would affect the width of the fissures; therefore, the quantity of water vapour releas

274 rieved from in vivo and assessed for surface fissure, thickness, density, chondrocyte numbers, collag

275 Failure of the optic fissure to close gives rise to an ocular disorder known

276 in zebrafish leads to a failure of the optic fissure to close, a phenotype which closely resembles th

277 CA1 appear to sprout across the hippocampal fissure to preferentially synapse onto early-born DGCs.

278 section with the lateral aspect of the major fissure toward the infrahilar region on the right and th

279 omprehensive analysis of the zebrafish optic fissure transcriptome and provides a valuable resource t

280 include a long, narrow nose, short palpebral fissures, type III syndactyly, and dental abnormalities

281 ng slices taken perpendicular to the Sylvian fissure, volumes of the hippocampus, amygdala, anterior

282 he human somatosensory cortex in the Sylvian fissure was examined using functional magnetic resonance

283 Otherwise, if the fissure was incomplete or the lung had an emphysematous

284 After 3 months healing of the fissure was noted in 32 of 74 (43%) patients in the dilt

285 ronchovascular structures revealed that this fissure was the superior accessory fissure.

286 We studied river-subsurface fissure water systems and identified Eukarya from a rive

287 thriving at 1.4 km depths in palaeometeoric fissure water up to 12,300 yr old in South African mines

288 o account for the development of the Sylvian fissure, we compared the growth of the frontotemporal op

289 c cup and stalk and the closure of the optic fissure were substantially rescued in these embryos.

290 lateral pleural puncture, and lesions along fissures were associated with higher [corrected] pneumot

291 Four of the 36 accessory fissures were manifested by a normal fissure line; two,

292 d distal vessels extending to the pleura and fissures were seen in 40 cases (82%) and 30 cases (61%),

293 CD200 was mainly observed in the hippocampal fissure, where GFAP(+) /CD200(+) astrocytes were also fo

294 the timing of initiation and positioning of fissures, whereas in upper rhombic lip-derived cells the

295 white matter caudal to the posterior sylvian fissure, which included the posterior supramarginal gyru

296 thin the expanding hemifusion diaphragm, and fissure widening initiating pore formation in a hemifusi

297 ern - 0.034-0.067; index of interhemispheric fissure width - 0.044-0.127; index of Sylvian fissure -

298 Homogeneous solid nodules, attached to a fissure with a lentiform or triangular shape, were class

299 y syndromes often involves plaque rupture or fissure with platelet aggregation.

300 The complex spatial association of the PCC fissure zone with the Liquine-Ofqui Fault zone was likel