ライフサイエンスコーパス: fringe

1 ate an oxic/anoxic interface and a capillary fringe.

2 CD release efficiency is further enhanced by Fringe.

3 thousand) were observed across the capillary fringe.

4 by the beta3N-acetylglucosaminyl transferase Fringe.

5 inctive segmentation and a filamentous fuzzy fringe.

6 chlorine CSIA depletions for VC at the plume fringe.

7 activity, which was highest in the capillary fringe.

8 any meters down to the groundwater capillary fringe.

9 cosamine added onto Notch in the presence of Fringe.

10 d, Manic fringe, Lunatic fringe, and Radical fringe.

11 diated by protein O-fucosyltransferase 1 and Fringe.

12 t do impair carbohydrate chain elongation by Fringe.

13 t partially via regulation of thickveins and fringe.

14 inhibition of Serrate-to-Notch signaling by Fringe.

15 aracterized 14 point mutations in Drosophila fringe.

16 ctivation by Serrate even in the presence of Fringe.

17 place within the lower part of the capillary fringe.

18 terface is created, often near the capillary fringe.

19 centrations in the vicinity of the capillary fringe.

20 moving air-water interfaces in the capillary fringe.

21 bove the saturated zone within the capillary fringe.

22 the ligule comprises an epidermally derived fringe.

23 ansducing them into distinctive interference fringes.

24 nocrystals with perfectly parallel, oriented fringes.

25 -fucosylated EGF repeats are modified by the Fringes.

26 ucosylated EGF repeat by all three mammalian Fringes.

27 m/s) and large (>25 microm) droplets in the fringes.

28 84 amino acids that are identical among all Fringes.

29 bserve coherent Rabi oscillations and Ramsey fringes.

30 cter of the Empire, even at its northernmost fringes.

31 ion to the formation of optical interference fringes.

32 t phenomena such as Rabi flopping and Ramsey fringes.

33 he signal interference from geometry-induced fringing.

34 nd secretion, with the N-terminus of radical fringe (a Golgi-resident protein).

35 iated by protein O-fucosyltransferase-1) and Fringe, a beta1,3-N-acetylglucosaminyltransferase that m

36 so regulates the glycosyltransferase Lunatic Fringe, a modulator of Notch signalling, maintaining its

37 ior SII region that borders the suprasylvian fringe--a region in which neurons have very large, and f

38 in TIRFM, often creates spatial interference fringes across the illuminated area.

39 Furthermore, loss of Fringe activity reduced the prevalence of the O-Fuc tris

40 tifs that are required for unique aspects of Fringe activity.

41 ure intensity changes in the Airy Disc First Fringe (ADFF) has been derived to follow the growth char

42 nct wave vectors giving rise to interference fringes analogous to two mechanical slits.

43 cally biodegrade AN and DPA in the capillary fringe and decrease the contaminant concentrations in th

44 are presented that demonstrate that radical fringe and lunatic fringe are expressed in the granulosa

45 s a set of four sequence motifs shared among Fringe and other putative beta1,3-glycosyltransferases.

46 identified pronephric expression of lunatic fringe and radical fringe that is temporally and spatial

47 t also leads to the degradation of the actin fringe and the formation of an aggregate of filamentous

48 le including biodegradation in the capillary fringe and unsaturated zone and clearly demonstrates tha

49 aneous degradation kinetics in the capillary fringe and unsaturated zone.

50 ntrations to low levels within the capillary fringe and unsaturated zone.

51 en applied to the visibility of interference fringes and predictability of paths within a two-alterna

52 LFNG (Lunatic Fringe) and MFNG (Manic Fringe) transfer N-acetylglucosa

53 have been identified, Manic fringe, Lunatic fringe, and Radical fringe.

54 observed in the published structure of Manic Fringe, and residues predicted to be involved in UDP-N-a

55 demonstrate that radical fringe and lunatic fringe are expressed in the granulosa cells of developin

56 resolution, propagation-invariant sinusoidal fringes are generated by a digital micromirror device.

57 No such fringes are observed for silver films grown on lightly d

58 These fringes are particularly problematic when imaging large

59 ect; for knee replacement, those in town and fringe areas had greater need.

60 hat for creating trapping potentials free of fringing artifacts it is important to go beyond the Four

61 ast and unlike Zernike phase plate images no fringing artifacts.

62 The transmission electron microscopy lattice fringes as well as the selected area electron diffractio

63 cles may be controlled by the cortical actin fringe at the pollen tube apex.

64 mense benefit in saving lives offer us a new fringe benefit: lessons in viral immunology.

65 rsican core protein, a proposed substrate of Fringe beta-1,3-N-acetylglucosaminyltransferases.

66 f several alpine glaciers in the Dry Valleys fringed by multiple cold-based drop moraines.

67 Today, the ice sheet is fringed by vulnerable floating ice shelves that buttress

68 ethods have been developed to minimize these fringes by modulating the TIRFM field during a frame cap

69 contaminant biodegradation in the capillary fringe can create a sink for nonvolatile contaminants.

70 ed that natural attenuation in the capillary fringe can prevent the migration of CB, 12DCB, and 14DCB

71 on of volatile contaminants in the capillary fringe can prevent vapor migration.

72 metry and surface plasmon resonance that the Fringe-catalyzed addition of GlcNAc to the O-fucose at T

73 We propose that this finding explains the Fringe-catalyzed enhancement of Notch-Delta signaling ob

74 Fringe catalyzes the addition of N-acetylglucosamine in

75 hat restrict Notch-Jagged signaling, such as Fringe, cis-inhibition, and increased production of Delt

76 These include the plume fringe concept, transport limitations, and transient con

77 We find universal scaling of the average fringe contrast with system size and temperature that de

78 Moreover, the full distribution of the fringe contrast, which is also equivalent to the full co

79 Therefore, each Fringe contributes to T and B cell development, and Frin

80 hese data support a model in which the actin fringe contributes to the focused secretion of pectin to

81 The fringes correspond to electronic states extending over t

82 to the posterior portion of the suprasylvian fringe, corresponding to area DZ of hearing, early-deafe

83 large or small scales using echo timing and fringe counting.

84 Histological analysis of the lunatic fringe-deficient ovary demonstrated aberrant folliculoge

85 ispersion (with and without DIF) and aerobic fringe degradation on the evolution of carbon and chlori

86 e observations argue against models in which Fringe-dependent glycosylation modulates Notch signaling

87 h receptors by their ligands is modulated by Fringe-dependent glycosylation.

88 ulation-frequency modulation (FF) and dorsal fringe (DF) areas.

89 he FF (F means frequency modulation), dorsal fringe (DF), and ventral fringe (VF) areas consist of "c

90 dies, the differential effects of Drosophila fringe (DFng) on Notch signaling are thought to result f

91 asymmetric effect of the glycosyltransferase Fringe, different outcomes are generated depending on wh

92 ton, in particular the apical cortical actin fringe, directs the flow of vesicles to the apical domai

93 Finally, together with the modulator lunatic fringe, Dll3 altered N signaling levels that were induce

94 And interestingly, Fringe domain in CHSY1 has this DDD motif.

95 CHSY1 contains a Fringe domain, and Fringe is well known for its regulati

96 Microdielectric spectroscopy with planar fringe-effect (FE) interdigital sensors is a useful meth

97 kness measurements of dielectric films using fringe-effect (FE) sensors is developed and experimental

98 l-plate method is to use the microdielectric fringe-effect (FE) sensors, which can be placed inside t

99 op a method in which the alternating voltage-fringing electric field formed between surface microelec

100 r, molecular adsorbates are polarized by the fringing electric fields radiating from the surface of a

101 The fringing electrical field, created by electrodes microfa

102 ly due to interaction of the object with the fringing electromagnetic field of the QCM.

103 nhance activation from Delta-like 1, Radical Fringe enhances signaling from both.

104 Fringe enzymes add N-acetylglucosamine to O-fucose and m

105 Fringe enzymes add N-acetylglucosamine to O-linked fucos

106 ther modified by Fringe, suggesting that the Fringe enzymes can differentiate between them.

107 n et al. show that modification of Notch2 by Fringe enzymes is critical to maturing B cells for acces

108 n individual O-fucosylated EGF repeat by the Fringe enzymes.

109 Perturbation of Fringe expression through morpholino antisense oligonucl

110 heries is US $37,500 per hectare of mangrove fringe, falling within the higher end of values previous

111 zes Dll4-Notch signaling in cells expressing Fringe family glycosyltransferases.

112 The Fringe family of beta1,3-N-acetylglucosaminyltransferase

113 etylglucosamine, catalyzed by members of the Fringe family, modulates Notch activity.

114 both electrostatic interlayer screening and fringe field effects.

115 zed by means of Overhauser DNP in the 0.35-T fringe field of a 1.5-T MR imaging magnet by using a cus

116 Utilizing a very large field-gradient in the fringe field of a magnet, stray-field-imaging (STRAFI) t

117 g with switchable diffraction angles using a fringe field switching (FFS) liquid crystal (LC) cell.

118 field focusing and screening effects of the fringing field.

119 Driving at a low-frequency electric field in fringe-field switching (FFS) mode can be one of the effi

120 ce charge, separation field in the FAIMS and fringe fields around the edges of the FAIMS electrodes.

121 rojecting tubular section, which prevents dc fringe fields from penetrating to the center of the mini

122 The model was then used to study fringe fields in a simple arrangement where a 0.5 mm (w)

123 riven primarily by gradients in the remanent fringe fields of a few nanometre-thick magnetic film.

124 lary; bulk of the ion loss was caused by the fringe fields.

125 Confocal images confirmed that the capillary fringe fluctuations affect colloid transport behavior.

126 Our results demonstrate that capillary fringe fluctuations are an effective means for colloid m

127 moving air-water interfaces during capillary fringe fluctuations by confocal microscopy.

128 Capillary fringe fluctuations due to changing water tables lead to

129 We simulated capillary fringe fluctuations in a glass-bead-filled column.

130 ut then were removed by subsequent capillary fringe fluctuations.

131 s that correspond to 16 genes, which include fringe (fng), a gene involved in ventral eye patterning,

132 ontrolled by the Notch (N)-modifying protein Fringe (Fng).

133 aerobic natural attenuation in the capillary fringe for preventing contaminant migration in the unsat

134 e amplitude, results in quantum interference fringes for n = 1 to 20 photon transitions.

135 In total internal reflection interference fringe FPR, interfering laser beams enter a 1.65-numerci

136 can influence Notch activation by preventing Fringe from blocking Notch-Serrate binding.

137 The position of the backscattered fringe from each capillary, which are in proximity or es

138 Lastly, we identify fringe function as a necessary effector for high fidelit

139 sistent with the spatial distribution of the Fringe function, the GlcA-extended form of the Fringe pr

140 ble heterozygous mouse models to examine the Fringe genes as potential modifiers of the Notch-mediate

141 e heterozygous for mutations in Jag1 and the Fringe genes display striking bile duct proliferation, w

142 The Fringe genes encode glycosyltransferases, which modify N

143 These findings suggest that the Fringe genes may regulate postnatal bile duct growth and

144 nt for both Jag1 and one of three paralogous Fringe genes: Lunatic (Lfng), Radical (Rfng), and Manic

145 iate signaling, but we propose that although fringe glycosylation does not reduce Jagged1 binding to

146 Our data support the idea that fringe glycosylation increases Delta1 binding to potenti

147 n the mucin-type and epidermal growth factor-fringe glycosylation pathways did not affect cytokinesis

148 ugh the expected disaccharide product of the Fringe glycosyltransferase, (GlcNAcbeta1-3)fucitol, was

149 ed1, underscoring the diversity of mammalian fringe glycosyltransferases in regulating signaling down

150 ligands, whose interactions can be tuned by Fringe glycosyltransferases.

151 orm of exotic self-expression in some social fringe groups, tattoos have left their maverick image be

152 The fringes have a period of 0.32 nm, which corresponds to t

153 ession delays for three transcripts [Lunatic fringe, Hes7/her1, and Notch-regulated-ankyrin-repeat-pr

154 ays, including Notch (Notch homolog 2, manic fringe homolog), growth factor (FGF intracellular-bindin

155 The Lytechinus variegatus Fringe homologue is expressed in both the signaling and

156 The fact that three Fringe homologues exist in mammals raises the question o

157 les of the modulation of Notch activation by Fringe homologues in boundary formation and in regulatin

158 schmann geometry by creating an interference fringe image on the interface with a polarizer-quartz we

159 s that are perpendicular to the interference fringe image, multiple bioaffinity adsorption measuremen

160 for the Notch signaling pathway and lunatic fringe in mammalian folliculogenesis.

161 this interferometer, we obtain interference fringes in a Mach-Zehnder geometry in an unmodified 200

162 h which-path information and high-visibility fringes in a single experiment.

163 The shift of the matter-wave fringes in a static electric field encodes the molecular

164 development, RFNG in B cell development, or Fringes in T and B cell activation are not identified.

165 atic [LFng], Manic [MFng], or Radical [RFng] Fringe) increased Delta1 binding and activation of Notch

166 re is also evidence that proximity to forest fringes increases malaria incidence, which implies the o

167 We found that lymph node fringes indeed contained physiological gradients of the

168 This modification of Notch by Fringe influences the binding of Notch ligands to Notch

169 While Lunatic and Manic Fringe inhibit Notch1 activation from Jagged1 and enhanc

170 ten-year discounted value of one hectare of fringe is >300 times the official cost set by the Mexica

171 that, similar to Manic and Lunatic, Radical fringe is also a fucose-specific beta1,3-N-acetylglucosa

172 Lunatic fringe is an important regulator of Notch signaling.

173 The substrate of Fringe is EGF-O-fucose and the transfer of fucose to Not

174 Fringe is highly conserved, and comparison among 18 diff

175 Taken together, the results show that Fringe is necessary both for maternal and zygotic Notch

176 Fringe is only distantly related to other glycosyltransf

177 contributes to T and B cell development, and Fringe is required for optimal in vitro stimulation of T

178 Upon complete growth inhibition, the actin fringe is the first actin cytoskeleton component to disa

179 CHSY1 contains a Fringe domain, and Fringe is well known for its regulation of Notch signali

180 -Notch1 signaling, possibly favored by Manic-Fringe, is specifically required for cardiac epithelial-

181 rodimerization of mutant Notch3 with Lunatic Fringe itself.

182 galactose (Gal) to the GlcNAc transferred by Fringe, JAG1-induced NOTCH signaling is not inhibited by

183 anteroposterior encroachment of alar lunatic fringe (L-fng) expression, and/or basal Shh signaling is

184 eins, whereas depletion of vimentin enhances Fringe levels to promote Dll4 signaling.

185 expressed otic genes such as NeuroD, Lunatic fringe (Lfng) and Six1 are shifted dorsally, whereas the

186 Lunatic fringe (Lfng) encodes a glycosyltransferase that modulat

187 We have investigated the role of Lunatic fringe (Lfng) expression during neurogenesis in the vert

188 In mice, lunatic fringe (Lfng) expression oscillates, and LFNG protein co

189 d Danio rerio, include an absence of lunatic fringe (lfng) expression within the presomitic mesoderm

190 e analyzed the reaction catalyzed by Lunatic Fringe (Lfng) in detail.

191 otch pathway and the Notch modulator Lunatic fringe (Lfng) play multiple roles during segmentation.

192 Lunatic Fringe (Lfng), a glycosyltransferase that enhances Notch

193 Here, we report that Lunatic fringe (Lfng), a key modifier of the Notch receptor, is

194 sion of the Notch target genes HEY1, lunatic fringe (LFNG), and ephrin-B2, reduced phosphorylation of

195 ial regulation of Notch receptors by Lunatic Fringe (Lfng), which encodes an O-fucosylpeptide 3-beta-

196 latory expression of genes including Lunatic fringe (Lfng).

197 Lunatic, Manic, and Radical Fringe (LFNG, MFNG, and RFNG) are N-acetylglucosaminyltr

198 The fringe-lipped bat, Trachops cirrhosus, uses prey-emitted

199 alian homologues have been identified, Manic fringe, Lunatic fringe, and Radical fringe.

200 Mammals have three Fringes: Lunatic, Manic, and Radical.

201 ty is limited by dipolar coupling from their fringing magnetic fields.

202 We investigated whether O-fucosylation or Fringe-mediated elongation of O-fucose on Notch3 is impa

203 porosity results, ellipsometry, interference fringes method (IFM), and focused ion beam (FIB) cross s

204 rt that an established Notch modifier, Manic Fringe (Mfng), is expressed in the putative endocrine pr

205 alone, and this combination phenocopies the fringe MO embryos.

206 Combined, these results suggest that Fringe modifications "mark" different regions in the Not

207 Fringe modifications at EGF8 and EGF12 enhanced Notch1 b

208 ified similar sites on Notch1, while Radical Fringe modified a subset.

209 We found that Lunatic and Manic Fringe modified similar sites on Notch1, while Radical F

210 Together, Serrate and Fringe modulate Notch activation to generate the proper

211 We also show that the Serrate antagonist, fringe, must temper Notch activity to insure that the ac

212 ) substrates show fine-structured electronic fringes near the silicon valence band edge as observed b

213 Lunatic fringe null female mice were found to be infertile.

214 rom Cripto, Notch receptor, Notch ligand, or Fringe null phenotypes.

215 Fringe O-fucose-beta1,3-N-acetylglucosaminyltransferases

216 Anatomic features including a capillary fringe (odds ratio [OR] = 5.3, P = .036) and immature le

217 the new method is to present stimuli on the fringe of awareness, such that it is more difficult for

218 widely established and exists on the current fringe of dengue transmission.

219 a wide range of care settings, and a smaller fringe of health care centers outside those systems.

220 and incremental personnel costs (salary and fringe of providers).

221 s then repopulated, because the cells on the fringe of the damage, which are no longer contact-inhibi

222 ved iron and manganese concentrations at the fringe of the methane plume show that oxidation is prima

223 he postsynaptic membrane, at the cytoplasmic fringe of the PSD.

224 howed that ATES mobilizes arsenic toward the fringe of the warm water bubble and the center of the co

225 Structures at or near the fringe of this network were compatible with flavin bindi

226 bon isotope pattern (-2 per thousand) at the fringes of a nondegrading PCE plume.

227 o risks pushing contemporary evo devo to the fringes of evolutionary biology because it does not desc

228 e extremes (conditions representative of the fringes of malaria transmission, where range expansions

229 ave high cultivation potential (e.g., in the fringes of the Amazon basin, in the Paraguayan Chaco, an

230 a impact model, especially over the epidemic fringes of the malaria distribution.

231 n-based estimates suggest that in the desert fringes of the Sahara, vectorial capacity would increase

232 Additionally, we observed an influence of Fringe on a Notch fragment including only 4 of its 36 EG

233 tylglucosamine as a basis for the effects of Fringe on Drosophila Notch-ligand binding.

234 s, but suggest that the inhibitory effect of Fringe on Jagged/Serrate mediated signaling involves oth

235 Moreover, the influences of OFUT1 and Fringe on Notch activation can be positive or negative,

236 e or region can account for the influence of Fringe on Notch-ligand binding.

237 to determine whether the variable effects of Fringes on Notch1 result from generation of unique glyco

238 that the hexagonal patterns and the parallel fringes originated from the same rotationally mismatched

239 ociated with the observation of interference fringes, particle behavior generally corresponds to the

240 sts that the contraction of the interference fringe pattern about the mid-latitude NAA transmitter is

241 ze of the transmitter nighttime interference fringe pattern has been determined, taking into account

242 The position of the fringe pattern in this image changes upon the adsorption

243 generate a sinusoidal high spatial frequency fringe pattern on specimen for lateral resolution enhanc

244 The dependence of the fringe pattern on the intensity of the central light-wav

245 can produce even the most elaborate optical fringe pattern.

246 g a unique, near-field microscopy technique, fringe patterns and nanoparticle motions are visualized

247 Moreover, the area of fringe patterns beneath the bubble increases with time.

248 Finally, Fringe perturbations result in more severe phenotypes th

249 sed for the stabilization and control of the fringe phase.

250 Together, these data suggest that Fringe plays a role in CADASIL pathophysiology.

251 ond O-fucose monosaccharide, indicating that Fringe preferentially modifies certain sites more than o

252 inge function, the GlcA-extended form of the Fringe product was enriched in the dorsal portion of the

253 ch1, Dll1, and Jag1, and their dependence on Fringe protein expression in mammalian cells.

254 Here, we report that expression of mammalian fringe proteins (Lunatic [LFng], Manic [MFng], or Radica

255 s guided by a multiple sequence alignment of Fringe proteins and solutions from docking an epidermal

256 Fringe proteins are beta3-N-acetylglucosaminyltransferas

257 Fringe proteins are O-fucose-specific beta-1,3 N-acetylg

258 conserved, and comparison among 18 different Fringe proteins from 11 different species identifies a c

259 Whereas Fringe proteins modify Notch receptors and strengthen th

260 at Dll1 and Jag1 can cis-inhibit Notch1, and Fringe proteins modulate these interactions in a way tha

261 stricted expression of the Notch ligands and Fringe proteins that both elicit the formation of the in

262 map to amino acids that are conserved among Fringe proteins, but not among other glycosyltransferase

263 Vimentin also suppresses expression of Fringe proteins, whereas depletion of vimentin enhances

264 the observed spatially varying interference fringe provides a useful measure for correcting image-di

265 DP Expedition 310 to Tahiti, and show that a fringing reef retreated upslope during postglacial sea-l

266 From size frequency data on Luhuitou fringing reef, Hainan, South China Sea, a matrix populat

267 cleractinian coral Pocillopora damicornis on fringing reefs around two Pacific remote islets with lar

268 ical growth on a subsiding foundation caused fringing reefs to transform into barrier reefs then atol

269 protein (AIP) localize to the cortical actin fringe region.

270 ermal growth factor (EGF) domains, OFUT1 and Fringe, regulate Notch signaling.

271 at transfer sugars to EGF domains, OFUT1 and Fringe, regulate Notch signaling.

272 The data are consistent with a Fringe-requiring Notch signal as one upstream component

273 oskeleton, because the apical cortical actin fringe resides in the same region as the alkaline band i

274 Rather than constituting a fringe science, pest management research for organic sys

275 igand-binding platform and are adjacent to a Fringe-sensitive residue that modulates Notch activity.

276 Fringe similarly modulated Notch-ligand cis interactions

277 t reporter system, that the 3'UTR of Lunatic Fringe strongly destabilizes transcripts, while transcri

278 EGF repeats of Notch are further modified by Fringe, suggesting that the Fringe enzymes can different

279 nd environmentally variable reef flat of the fringing Suleman Reef, Egypt, over 45-hour sampling peri

280 st cover (as a proxy for proximity to forest fringes) tends to be associated with higher malaria inci

281 ric expression of lunatic fringe and radical fringe that is temporally and spatially appropriate for

282 to the productive area in the mangrove-water fringe that is used as nursery and/or feeding grounds by

283 ciated with the displacement of interference fringes that are analyzed using an efficient spatiotempo

284 ration, and low attenuation in the capillary fringe), the respect of these empirical screening criter

285 actin turnover and new polymerization in the fringe, the tip-focused calcium gradient biases secretio

286 briefly stops growth while causing the actin fringe to completely disappear.

287 tein O-fucosyltransferase 1 is necessary for Fringe to function.

288 near genome and radiated from the TAD(cPcdh) fringes toward cis-regulatory sequences within the cPcdh

289 LFNG (Lunatic Fringe) and MFNG (Manic Fringe) transfer N-acetylglucosamine (GlcNAc) to O-fucos

290 Here, we address the role of the actin fringe using three different inhibitors of growth: brefe

291 modulation), dorsal fringe (DF), and ventral fringe (VF) areas consist of "combination-sensitive" neu

292 Fringe was initially described in Drosophila, and three

293 bserved at all measured flow velocities, and fringe washout progressively shattered reflectance and p

294 onship between the shift in the interference fringes (which measures the shift of the myosin heads sc

295 somite 0 requires the expression of lunatic fringe, which modifies the activation of the Notch signa

296 ed by, expression of the glycosyltransferase Fringe, which specifically modifies O-linked fucose.

297 is presented, which compensates for spatial fringes while simultaneously permitting rapid image acqu

298 of the beta3-N-acetylglucosaminyltransferase Fringe with Notch, we observed varying degrees of elonga

299 fferences in the biochemical behavior of the Fringes with regard to their in vitro enzymatic activiti

300 Parallel-line-like Moire fringes with similarly large periodicities were also obs

301 to 17% with the water table or its capillary fringe within plant rooting depths.