ライフサイエンスコーパス: jelly

1 % (fish and lemon) to 79% (peanut butter and jelly).

2 cells and the extracellular matrix (cardiac jelly).

3 and the extracellular matrix (termed cardiac jelly).

4 as Phacellophora camtschatica (the egg-yolk jelly).

5 CCD hives, normal hives, and imported royal jelly.

6 a constricted outflow tract, and no cardiac jelly.

7 e to production in sperm upon contacting egg jelly.

8 tons, is a major component of sea urchin egg jelly.

9 ibuted to the uneven distribution of cardiac jelly.

10 ion by preventing sperm from penetrating the jelly.

11 ccumulation of its protein occurs in locular jelly.

12 lar matrix components comprising the cardiac jelly.

13 and other ingredients such as honey or royal jelly.

14 yocardium are separated by so-called cardiac jelly.

15 t convert stored pollen and honey into royal jelly.

16 to observe transformation products in royal jelly.

17 was present in all honeys, as well as Royal Jelly.

18 hai and clover honeys, but absent from Royal Jelly.

19 4 and Adamts5 proteases that degrade cardiac jelly.

20 autopsy have been filled with a clear liquid jelly.

21 ciated with premature degradation of cardiac jelly.

22 (ARDS) and may have the appearance of liquid jelly.

23 similar rheological behaviour to commercial jelly.

24 secretion and ingestion of worker and royal jellies.

25 is widely used to manufacture ice cream and jellies.

26 alternatively, evolved convergently in comb jellies.

27 identifies sea urchin sperm receptor for egg jelly-3 (suREJ3) as a new member of the polycystin-1 fam

28 thod was applied to green tea (10) and royal jelly (8) samples.

29 esting these perturbations confirms the moon jellies' ability to recover their round shape from many

30 redominantly on the posterior surface of egg jelly-activated sperm, and peptides from the disintegrin

31 Other than jellies and jams, quince could be processed into various

32 The total silicon content in jellies and puddings did not exceed 0.36mg and 2.42mg/se

33 nalyzed: soups, main courses, coffee drinks, jellies and puddings.

34 te (5% weight/volume), with a solution of KY jelly and ascorbic acid (5% weight/volume).

35 trace-elements (TE) contents of honey, royal-jelly and beeswax from a historical Zn-Pb mining distric

36 d on natural extracts (green tea, soy, royal jelly and grapes) observing the appearance of new bioact

37 tor 10HDA-the major lipid component of royal jelly and hence a putative regulator of honeybee caste d

38 r depends on differential feeding with royal jelly and involves epigenomic modifications by DNA methy

39 different types of foodstuffs were analyzed: jelly and juice powder, jelly candy, jujube candy, hard

40 Royal jelly and other glandular secretions are the primary foo

41 es in the endocardium to degrade the cardiac jelly and prevent excessive trabeculation.

42 elopment and was associated with the locular jelly and seeds.

43 generating system by mixing a solution of KY jelly and sodium nitrite (5% weight/volume), with a solu

44 s of 694 various contaminants in honey, jam, jelly and syrup samples by ultrahigh-performance liquid

45 s not observed in materials unrelated to egg jelly and the response of sperm to egg jelly extract is

46 and aliphatic hydroxy acids typical of royal jelly and unsaturated dicarboxylic acids.

47 liary layer and then mechanically mixed with jelly, and applied to eggs as they progress down the ovi

48 ts in an absence of hyaluronan (HA), cardiac jelly, and endocardial cushions, a loss of vascular inte

49 rostructures such as myocardium, the cardiac jelly, and endocardium are presented.

50 ce in bee products like honey, pollen, royal jelly, and propolis.

51 that evaluated PA in honeys, pollens, royal jelly, and propolis.

52 logy is whether sponges or ctenophores (comb jellies) are the sister group to all other animals.

53 m cells (hUC-MSCs), originating in Wharton's jelly, are multipotent stem cells that home to damaged t

54 d function of neurons in cnidarians and comb jellies, as well as neuron-like cells in nerveless placo

55 nergy level of the resonance band of organic jelly, as a function of pH and density of the jelly, we

56 EZ Jelly, K-Y Jelly, Astroglide, and Conceptrol induced cytotoxicity i

57 sition of fibronectin protein in the cardiac jelly at E9.0 through E10.5 and in the outflow tract at

58 ochondrial DNA (mt-DNA) molecule of the moon jelly Aurelia aurita (Cnidaria, Scyphozoa) - the first m

59 Specifically, we focus on the moon jelly Aurelia aurita and the control of its energy-effic

60 ducts (bee pollen, propolis, honey and royal jelly) available in Turkey.

61 sented collections (e.g., of variously sized jelly beans or nuts) and required to answer with a vocal

62 We show in Drosophila that secreted Jelly belly (Jeb) and its receptor tyrosine kinase Anapl

63 The secreted protein Jelly belly (Jeb) is required for an essential signallin

64 We demonstrate that Alk and its ligand Jelly belly (Jeb) play a central role as an anterograde

65 We show that Jelly belly (Jeb) produced by R1-R6 axons interacts with

66 I3-kinase signaling during NR as its ligand, Jelly belly (Jeb), is constitutively expressed from a gl

67 We identified a novel gene, jelly belly (jeb), which is required for visceral mesode

68 n target recognition, including Sec15, DLAR, Jelly belly, and PTP69D.

69 ture of different receptor types in the comb jelly Beroe abyssicola-the voracious predator from North

70 meat loaf, milk chocolate with soft nougat, jelly, cake, and candies] at pork DNA concentrations of

71 ever, in response to some perturbations, the jellies can also adopt other stable body shapes, such as

72 tuffs were analyzed: jelly and juice powder, jelly candy, jujube candy, hard candy, ice cream syrup,

73 tability, and variability of the ANG and egg jelly coat (JC) communities were characterized and compa

74 ivating peptides, which diffuse from the egg jelly coat and interact with their receptor in the flage

75 The jelly coat contains three morphologically distinct layer

76 The jelly coat contains three morphologically distinct layer

77 in from the pentraxin superfamily in the egg jelly coat from the South American burrowing frog, Lepid

78 lectin binding properties of the individual jelly coat layers as a step in identifying jelly glycopr

79 The reactivity of 31 lectins with isolated jelly coat layers was examined with enzyme-linked lectin

80 n binding site distribution among and within jelly coat layers.

81 screte Triticum lectin binding moiety in the jelly coat near the first polar body as it is being give

82 ith mucin-type oligosaccharides from the egg jelly coat of the anuran Xenopus laevis.

83 e in its true discharge state penetrates the jelly coat of the egg.

84 The interaction of the lectin XL35 with the jelly coat protein (JCP) surrounding oocytes in Xenopus

85 dle must penetrate through a 30 microm thick jelly coat surrounding the egg and thus it must be suffi

86 ran Xenopus laevis are surrounded by a thick jelly coat that is required during fertilization.

87 Some lectins were localized in the jelly coat using confocal microscopy, which revealed sub

88 eggs consists of a vitelline envelope and a jelly coat.

89 alkaline sodium borohydride reduction of the jelly coating from the South African clawed toad, Xenopu

90 We report that a highly abundant jelly component, major royal jelly protein 3 (MRJP-3), a

91 eal for the manufacturing of dairy products, jellies, condensation protein, gelatin gel, bread, etc.

92 l sensor is acceptable in foodstuffs such as jellies, condiments, soft drinks, and candies.

93 Worker jelly consumed during the first 3 d of larval developmen

94 n both oral food challenge tests (OFCs) with jelly containing whole citron and lemon seeds, she had s

95 a, and severe abdominal pain after ingesting jelly containing yuzu (citrus junos) seeds and peel.Pric

96 hallenged by analyses of the genomes of comb jellies (Ctenophora), which, instead, found ctenophores

97 rge ciliary structures uniquely seen in comb jellies (ctenophores).(1)(,)(2)(,)(3) A comb plate is co

98 cardial-derived factors that support cardiac jelly deposition at the onset of valve formation.

99 Intracoronary infusion of Wharton's jelly derived mesenchymal stem cells significantly reduc

100 ntracoronary infusion of allogenic Wharton's jelly derived mesenchymal stem cells within 3-7 days of

101 WIST1 during transdifferentiation of Wharton jelly-derived MSC (WJ-MSC) into iEC.

102 ned medium of human umbilical cord Wharton's jelly-derived MSCs.

103 Jelly-DOM also favored the rapid growth and dominance of

104 t were rare in ambient waters, implying that jelly-DOM was channeled through a small component of the

105 When jelly-DOM was consumed it was shunted toward bacterial r

106 ease colloidal and dissolved organic matter (jelly-DOM), and could further influence the functioning

107 associated mutations in the receptor for egg jelly domain disrupt cleavage, abolish the ability of po

108 Both forms have a small receptor for egg jelly domain, a G-protein-coupled receptor proteolytic s

109 a process that requires the receptor for egg jelly domain.

110 in a highly organized manner in the cardiac jelly during heart looping.

111 Freshly oviposited jellied eggs were soaked in buffer, and the conditioned

112 occurs when sea urchin sperm contact the egg jelly (EJ) layer.

113 Sea urchin egg jelly (EJ) triggers sperm acrosome reaction (AR), an exo

114 During sea urchin fertilization, egg jelly (EJ) triggers the sperm acrosome reaction (AR) whi

115 event, is triggered by glycoproteins in egg jelly (EJ).

116 re Mnemiopsis leidyi The genome of this comb jelly encodes homologs of vertebrate ionotropic glutamat

117 Thus, the composition of cardiac jelly essential for myocardial morphogenesis is dynamica

118 demonstrated that a protein from Xenopus egg jelly exhibits sperm chemoattractant activity when assay

119 ide of the myocardium and within the cardiac jelly extending to the endocardial cell surfaces.

120 o egg jelly and the response of sperm to egg jelly extract is clearly chemotactic rather than chemoki

121 nd contact a glass capillary filled with egg jelly extract.

122 two-chamber bioassay device we find that egg jelly extracts are capable of stimulating sperm movement

123 However, how the jelly facilitates transfer of RNA is still unknown.

124 Such an energetic pathway between jelly-falls and N. norvegicus could become more importan

125 potentially high energetic contribution from jelly-falls highlights a possible role of gelatinous mat

126 We estimate that the energy input from jelly-falls may represent a significant contribution to

127 sh detritus to the seafloor, hereby known as jelly-falls.

128 ting that they are major constituents of the jelly fiber network.

129 from several different creatures, including jelly fish.

130 eted from the glands of honeybees into Royal Jelly, forming a complex with apalbumin1 capable of stim

131 Interestingly, royal jelly from colonies exposed to treated pollen contained

132 ining egg-laying behavior, egg size, and egg jelly function of 13 species of Central and South Americ

133 l jelly coat layers as a step in identifying jelly glycoproteins that may be essential in fertilizati

134 making it suitable for functional foods like jelly gummies (JG).

135 Here, we show that worker and royal jellies harbor robust RNA-binding activity.

136 to other basal metazoans, ctenophores (comb jellies) have both complex nervous and mesoderm-derived

137 y were enhanced degradation of gelatin-based jellies in vitro and an increase in the processing of a

138 he high-molecular mass components of the egg jelly in a calcium-dependent manner with specificity for

139 Microinjection of the virus into the cardiac jelly in the AV canal at stage-13 in vivo (ovo) revealed

140 Royalactin, a component of royal jelly, induces queen differentiation in honeybees.

141 ts, allowing the apparent leakage of cardiac jelly into the lumen.

142 gands achieve interaction across the cardiac jelly is not understood.

143 The origin of ctenophores (comb jellies) is obscured by their controversial phylogenetic

144 Jelly (J) and jelly with PE (JE) were stored at 4 degree

145 EZ Jelly, K-Y Jelly, Astroglide, and Conceptrol induced cyt

146 Each jelly layer also contains low-molecular-weight proteins

147 Each jelly layer is known to have specific functions in the f

148 Neutral oligosaccharides unique to jelly layer J3 and the combined layers J1+J2 had similar

149 ee jelly layers; however, two lectins showed jelly layer selectivity.

150 phorylation increases when sperm contact the jelly layer surrounding eggs.

151 o when sperm respond to contact with the egg jelly layer.

152 We have shown previously that the egg jelly layers are composed of a fibrous network of glycoc

153 Components of these egg jelly layers are necessary for the fertilization of the

154 Eggs which are stripped of their jelly layers are refractile to fertilization by sperm, b

155 eggs includes three morphologically distinct jelly layers designated J1, J2, and J3 from the innermos

156 ferential staining of individually dissected jelly layers shows that both J1 and J2 contain three hig

157 Although the jelly layers surrounding amphibian eggs are known to be

158 al oligosaccharide structures from different jelly layers were both unique and overlapping, while sul

159 oligosaccharides were observed in the three jelly layers.

160 tify the oligosaccharides from X. laevis egg jelly layers.

161 s tested showed some reactivity to all three jelly layers; however, two lectins showed jelly layer se

162 high structural transformability and unique jelly-like soft mechanical properties.

163 by cytoplasmic microtubules that behave as a jelly-like viscoelastic fluid.

164 All royal jelly liquid dietary supplements were positive for chlor

165 biological activities have been reported for jelly macromolecules in any vertebrate.

166 emonstration of a physiological role for egg jelly macromolecules in Xenopus fertilization.

167 of Has2, a crucial component of the cardiac jelly matrix.

168 the second to an outburst of the alien comb jelly Mnemiopsis leidyi; both shifts were triggered by i

169 djustment for confounders, both 2% lidocaine jelly (odds ratio [OR], 11.28; 95% CI, 3.39-37.46; P < 0

170 Allurin, a 21 kDa protein isolated from egg jelly of the frog Xenopus laevis, has previously been de

171 n, a sperm chemoattractant isolated from the jelly of Xenopus laevis eggs.

172 Chromatography of whole egg jelly on a Sephacryl 500 column resulted in isolation of

173 differentially organized within the cardiac jelly on the convex side and in the outer loop areas.

174 done simultaneously on the other arm with KY jelly only (placebo).

175 species of planktonic animals known as comb jellies or ctenophores, are capable of rapidly fusing in

176 Use of lidocaine jelly or Tetravisc may increase the risk of endophthalmi

177 : fruit salads, nectar preparation, jams and jellies, or export.

178 Smoke, fog, jelly, paints, milk and shaving cream are common everyda

179 Jelly palm fruit were generally rich in phenolic content

180 ical composition are desirable attributes in jelly palm fruit, none of the genotypes evaluated showed

181 on whether sponges (phylum Porifera) or comb jellies (phylum Ctenophora) are the sister group of all

182 Samples of jelly, popsicles, isotonic drinks, and food flavoring sa

183 The cardiac jelly produced by the myocardium was distributed in an u

184 gative, but the second oral ingestion of the jelly product at home caused another allergic reaction.

185 d boy experienced anaphylaxis after eating a jelly product for diet supplement containing erythritol

186 Prick test with the jelly product was negative, but the second oral ingestio

187 on by sperm, but the addition of solubilized jelly promotes fertilization.

188 r beekeeping products, such as pollen, royal jelly, propolis, and beeswax, are also vulnerable to PA

189 In this species, the Major Royal Jelly Protein (MRJP) family is required for all major as

190 highly abundant jelly component, major royal jelly protein 3 (MRJP-3), acts as an extracellular non-s

191 r proteins which constitute 30% of the total jelly protein are steadily released into the surrounding

192 oney, the most predominant being major royal jelly proteins (MRJPs).

193 ge-specific expansions of yellow/major royal jelly proteins and desaturases, and complete CpG DNA met

194 ion products, hexose sugars, and major royal jelly proteins supporting the hypothesis that the jars o

195 s bound to the REJ protein (receptor for egg jelly) purified from sperm.

196 e C-terminus, including the receptor for egg jelly (REJ) domain, all transmembrane domains, and the c

197 lycystic kidney disease and receptor for egg jelly related gene ( PKDREJ )], but unlike polycystin-1,

198 e effect of five common vaginal products (KY Jelly, Replens Silky Smooth lubricant, coconut oil, Repl

199 and zirconium oxide for green tea and royal jelly, respectively.

200 Moon jellies respond to perturbations to body shape, such as

201 Royal Jelly (RJ) is a natural substance produced by honeybees,

202 tify the major and minor sugars of 400 Royal Jellies (RJs).

203 omputations discriminated between Greek Key, Jelly Role, and Up and Down categories of antiparallel b

204 Although the central jelly roll architecture is conserved among the three det

205 Located within the mu1 jelly roll beta barrel domain, which is a known regulato

206 an additional change (V403A) within the mu1 jelly roll beta barrel domain.

207 ctral resolution is achieved through a novel jelly roll cell design, which allowed these studies to b

208 The loops connecting the strands of the jelly roll define the limited features of the surface.

209 ases form homotetramers, with the N-terminal jelly roll domain contributing to substrate selectivity.

210 The C-terminal beta-jelly roll domain did not bind insoluble collagen fiber,

211 ver, we found that the S. pombe Cnp3(CENP-C) jelly roll fold harbors an inner binding pocket that is

212 e-binding fold and to the recognition of the jelly roll fold in the capsid protein of a large variety

213 prevalent in capsids of dsDNA phages as the jelly roll fold is in eukaryotic viruses.

214 The beta-jelly roll fold observed has identical topology to those

215 als two seven-stranded beta sheets forming a jelly roll fold with unexpected structural similarity to

216 One architectural motif (beta-jelly roll fold) forms virtually the entire capsid (dist

217 The P-domain of ssKex2 has a novel jelly roll like fold consisting of nine beta strands and

218 s shown striking similarities, with the beta jelly roll motif observed across multiple evolutionarily

219 omparison of domains containing greek key or jelly roll motifs.

220 rall structure of Aly36B belongs to the beta-jelly roll scaffold, adopting a typical beta-sandwich fo

221 tranded anti-parallel beta-sandwich with the jelly roll topology found in many viruses.

222 The capsid protein has a beta-barrel "jelly roll" fold similar to that found in many diverse i

223 The capsid protein has a beta-barrel "jelly roll" motif similar to that found in many icosahed

224 The structure reveals a "beta-jelly roll" topology, with high degree of similarity to

225 e fold of the major capsid protein VP2 is a "jelly roll" with a beta-barrel motif similar to that fou

226 resent in other 2-OG oxygenases including a 'jelly roll' beta strand core and residues binding iron a

227 The artificial 'jelly roll' data set upon which the algorithm was tested

228 re localized within loops at one edge of the jelly roll, suggesting a distinct protein interaction su

229 Despite a common jelly roll-fold, these striking differences of the mode

230 the capsid protein fold is a canonical viral jelly roll.

231 most common capsid proteins, with the single jelly-roll (SJR) fold, appears to have evolved from a pa

232 e C-terminal portion of delta, which forms a jelly-roll beta barrel structure, regulates membrane pen

233 The structure reveals a jelly-roll beta-barrel fold comprising 17 beta-strands v

234 mains: an S domain, which adopts the typical jelly-roll beta-barrel fold, and a P1 domain, which form

235 many non-complement proteins, has a compact jelly-roll beta-sandwich fold similar to that of the mul

236 -neurexin binding interface that extends the jelly-roll beta-sandwich of LNS2 of neurexin-1 into neur

237 arvovirus ancestor from which they inherit a jelly-roll capsid protein and a superfamily 3 helicase.

238 etectable similarity with other viral double jelly-roll capsid proteins.

239 tailless icosahedral viruses with the double jelly-roll capsid proteins.

240 arms" of a subunit (extensions from its beta-jelly-roll core) associate with a neighboring pentamer.

241 asses 2 Ig folds (CNA(2) and CNA(3)) and one jelly-roll domain (XNA) each of which synthesizes a sing

242 l domain of the 30K MPs is homologous to the jelly-roll domain of the capsid proteins (CPs) of small

243 capsid protein (MCP) with a predicted double jelly-roll domain.

244 class MPs, which all share a similar single jelly-roll domain.

245 ermination revealed an NTD consisting of two jelly-roll domains interacting across each subunit inter

246 of these viruses consist of two consecutive jelly-roll domains, assembled into trimers, with pseudo

247 resolution; this assigns the MAM fold to the jelly-roll family and reveals extensive interactions bet

248 d transglycosidases that adopt a common beta-jelly-roll fold and are active on a range of terrestrial

249 hese structures revealed a typical GH11 beta-jelly-roll fold and detailed interaction networks betwee

250 The S domain adopts a jelly-roll fold commonly observed in small RNA viruses.

251 in at a resolution of 2.5 A, which reveals a jelly-roll fold typical of the TNF superfamily.

252 rotein of Sputnik is likely to have a double jelly-roll fold, although sequence alignments do not sho

253 ein, as occurs in many CBMs that display the jelly-roll fold, but is formed by the loops that link th

254 how that the protein displays a typical beta-jelly-roll fold.

255 The 2 capsid proteins with variant single jelly-roll folds form pentamers and hexamers which assem

256 However, the double jelly-roll major capsid protein (DJR-MCP), the hallmark

257 277) composed of 8,280 copies of the double jelly-roll major capsid protein (MCP) p72, arranged in t

258 he outer virus shell is composed of a double jelly-roll protein that can be found in many double-stra

259 pentameric capsomers consist of five single jelly-roll proteins.

260 not generate the isopeptide bond within the jelly-roll structure of XNA.

261 Given the prevalence of the signature jelly-roll topology in viral capsid proteins, we are int

262 The 23 kDa protein presents a jelly-roll topology, built up mainly by antiparallel bet

263 also occurs in other big icosahedral double jelly-roll viruses such as Adenovirus.

264 o eight-stranded, antiparallel beta-barrel, "jelly-roll" domains related by a pseudo-sixfold rotation

265 trimeric capsomers consist of three double "jelly-roll" major capsid proteins creating pseudohexamer

266 k at the capsid interior, an S domain with a jelly-roll, beta-barrel fold forming the continuous caps

267 subunits, each with two eight-stranded viral jelly rolls normal to the viral capsid, and putative mem

268 ny other structures previously classified as jelly rolls.

269 a common structural signature, in particular jelly-rolls.

270 ences in the electrophoretic profiles of the jelly samples when the proteins were extracted with an a

271 envinphos was determined in some fresh royal jelly samples, and no pesticide residues were detected i

272 Nine (eight of green tea and one of royal jelly) samples were found to be positive for pesticides

273 branching phyla, especially sponges and comb jellies (sea gooseberries), sit in the tree of life.

274 ast, allurin is not found within the tubular jelly-secreting glands or ducts that constitute a major

275 SpmSyn has been lost from comb jellies, some sponge species, and was lost from most fre

276 ion in different kinds of foodstuffs: solid jelly (strawberry and custard) powder samples and soft d

277 duction of a reduced-sugar pomegranate juice jelly supplemented with an aqueous extract of pomegranat

278 olved in fertilization, the receptor for egg jelly (suREJ).

279 Here we provide evidence that the jelly surrounding Xenopus laevis eggs releases a small d

280 of oligosaccharides is determined in the egg jelly surrounding Xenopus laevis eggs.

281 omato pastes, soups, sauces, desserts, jams, jellies, sweets and breakfast cereals.

282 illator, then, we use the molecule to make a jelly that acts as chain of oscillators with a fractal l

283 The egg jelly that encapsulates amphibian eggs is essential for

284 s are surrounded by investment layers of egg jelly that interact with the sperm immediately prior to

285 cular-weight "structural" glycoconjugates of jelly that remain after extraction of the diffusible com

286 an extracellular environment in the cardiac jelly that supports trabecular growth.

287 posed to exhibit a reduced amount of cardiac jelly, the extracellular matrix between the myocardial a

288 s after adding sperm in the presence of egg jelly to beads coated with recombinant receptor.

289 cells migrate collectively into the cardiac jelly to form a bilayered structure; subsequently, the c

290 myocytes extrude and expand into the cardiac jelly to form sheet-like projections.

291 into an extracellular matrix, called cardiac jelly, to form endocardial cushions.

292 V canal: to enhance formation of the cardiac jelly, to induce endocardial EMT and to pattern the AV m

293 binds the glycoprotein coat of the egg (egg jelly), triggering the acrosome reaction, which transfor

294 Energy jelly was consumed immediately after the consumption of

295 elly, as a function of pH and density of the jelly, we realize a logic gate, whose truth table is fin

296 ix stem (rUCMS) cells derived from Wharton's jelly were then administered intratumoral (i.t) or i.v.

297 early metazoan evolution is Ctenophora (comb jellies), which diverged very early from the animal stem

298 Jelly (J) and jelly with PE (JE) were stored at 4 degrees C over an 8w

299 cells (MSCs) from umbilical cord's Wharton's Jelly (WJ) on a molecular level, and potentially render

300 Jelly-Z is the first robot that utilized twisted and coi