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 e to production in sperm upon contacting egg jelly.

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

8 ibuted to the uneven distribution of cardiac jelly.

9 ion by preventing sperm from penetrating the jelly.

10 ccumulation of its protein occurs in locular jelly.

11 lar matrix components comprising the cardiac jelly.

12 to observe transformation products in royal jelly.

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

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

15 4 and Adamts5 proteases that degrade cardiac jelly.

16 ciated with premature degradation of cardiac jelly.

17 similar rheological behaviour to commercial jelly.

18 t convert stored pollen and honey into royal jelly.

19 is widely used to manufacture ice cream and jellies.

20 alternatively, evolved convergently in comb jellies.

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

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

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

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

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

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

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

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

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

30 Royal jelly and other glandular secretions are the primary foo

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

54 The jelly coat contains three morphologically distinct layer

55 The jelly coat contains three morphologically distinct layer

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

97 from several different creatures, including jelly fish.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

120 oligosaccharides were observed in the three jelly layers.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

135 Jelly palm fruit were generally rich in phenolic content

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

199 ny other structures previously classified as jelly rolls.

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

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

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

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

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

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

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

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

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

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

210 The egg jelly that encapsulates amphibian eggs is essential for

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

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

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

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

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

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

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

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

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

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

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

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

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

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