戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 otely controls the release of Dilps into the hemolymph.
2 ehalose is the predominant sugar in mosquito hemolymph.
3 ounter the complement system in the mosquito hemolymph.
4 eas the WT lysozyme is secreted into the fly hemolymph.
5  and can diffuse into the pupal wing via the hemolymph.
6 cumulation of soluble yolk precursors in the hemolymph.
7  through the cuticle and proliferates in the hemolymph.
8 om anterior ganglia or reach the STG via the hemolymph.
9 h that of jhamt and matched JH levels in the hemolymph.
10 ciated with the accessory salivary glands or hemolymph.
11           This glucanase was not detected in hemolymph.
12 gh the Golgi organelle and are secreted into hemolymph.
13 sed within 20 min of the pathogen contacting hemolymph.
14 o B. thuringiensis, which appeared to die in hemolymph.
15 e proteins (DAFPs), four of which are in the hemolymph.
16  the regulation of immune proteinases in the hemolymph.
17 to the inhibitory regulation of PAP-3 in the hemolymph.
18 teinase cascades and regulated by serpins in hemolymph.
19 ly remove growth-promoting activity from the hemolymph.
20 , and elevated carbohydrate levels in larval hemolymph.
21 n heart and release neuromodulators into the hemolymph.
22 ared with lysozyme activity of immune larval hemolymph.
23 vely expressed in fat body and secreted into hemolymph.
24 esent in nephrocytes, which filter the fly's hemolymph.
25 unction in taking up waste material from the hemolymph.
26 times greater in pupal than in larval immune hemolymph.
27 moral roles of 5-HT, we measured 5-HT in the hemolymph.
28 ntration similar to that found in the insect hemolymph.
29 CABs) and increase glucose content in larval hemolymph.
30 rood chamber, mimic aphids suck on ant larva hemolymph.
31 tes sugar transport from the midgut lumen to hemolymph.
32 ough the midgut, or by transport through the hemolymph.
33 cotine or in the exhalation of nicotine from hemolymph.
34 reduced level of TEP1-LRIM1-APL1C complex in hemolymph.
35 he endoplasmic reticulum (ER) to cytosol and hemolymph.
36 secretion of antimicrobial peptides into the hemolymph [1] [2].
37 we show that corazonin concentrations in the hemolymph 20 min before natural preecdysis onset range f
38 fore, the persistent increase of 5-HT in the hemolymph 24 hr after sensitization training indicates t
39 higher in the lumen, 58.1 +/- 7.34, than the hemolymph, 3.96 +/- 2.89.
40                   Chloride was higher in the hemolymph, 57.6 +/- 7.84, than in the lumen, 3.51 +/- 2.
41  diffusion of paracrine 5-HT through the fly hemolymph [8] and by activation of the contralaterally p
42 , and promoted clearance of glucose from the hemolymph, a hallmark of bona fide insulin action.
43 a of the renal system and gut participate in hemolymph acid-base regulation by varying acid-base tran
44 olated by immunoaffinity chromatography from hemolymph activated by treatment with Micrococcus luteus
45 t-1), which was previously identified in the hemolymph-activated transcriptome of the entomopathogeni
46                                        Also, hemolymph AFPs and those associated with the layer of ep
47 droides canadensis, and demonstrate that the hemolymph AFPs are crucial for inhibiting trehalose crys
48            Lysozyme activity of immune pupal hemolymph against Micrococcus lysodeikticus was 11 times
49        The results from protein profiling of hemolymph, analyzed by surface-enhanced laser desorption
50 e in flies, namely, iron withdrawal from the hemolymph and accumulation in the fat body.
51             Previous metabolite profiling of hemolymph and bacteriocyte, alongside metabolic pathway
52 etory cells is secreted into the circulating hemolymph and binds to metabotropic GABAB receptors expr
53 PGRPs activate antimicrobial pathways in the hemolymph and cells, or are peptidoglycan (PGN)-lytic am
54   opnS was expressed during growth in insect hemolymph and expression was elevated as the cell densit
55                                         Both hemolymph and fat body in honey bees were marked with fl
56 he beetle Dendroides canadensis, AFPs in the hemolymph and gut inhibit ice nucleators.
57                      Acid-base status in the hemolymph and gut lumen of insects is generally well reg
58  body, the tissue producing most of mosquito hemolymph and immune proteins.
59 ted from the central nervous system into the hemolymph and initiates cuticle tanning.
60           Based on the levels of 5-HT in the hemolymph and its regulation by environmental events, we
61 om experimentally infected cattle and within hemolymph and larvae derived from acquisition-fed female
62 rast them to previous analyses of Drosophila hemolymph and mammalian blood plasma.
63 ides are highly stable in the insect gut and hemolymph and many of them are orally active.
64 ied glycated proteins in human serum, insect hemolymph and mouse brain homogenates, confirming this t
65 e HPT into the peripheral circulation in the hemolymph and strongly reduces aggressive behavior in cr
66 opose that MCO1 oxidizes ferrous iron in the hemolymph and that the resulting ferric iron is bound by
67 ups, one of which releases bursicon into the hemolymph and the other of which regulates its release.
68 t proteins present in the bristle, tegument, hemolymph, and "cryosecretion".
69 larvae, could not replicate in G. mellonella hemolymph, and also had a growth defect in human serum.
70 ade the tick midgut, disseminate through the hemolymph, and are transmitted to the vertebrate host vi
71 otein isoforms of Dscam were detected in the hemolymph, and hemocyte-specific loss of Dscam impaired
72  efficiently blocks pro-PO activation in the hemolymph, and it forms SDS-stable acyl-enzyme complexes
73 Here we used X-ray imaging, radio-tracing of hemolymph, and micropressure measurements in the America
74 ased as an exosomal cargo in the circulating hemolymph, and such glial-specific expression resets nor
75       Upon mating, 20HE titer in ovaries and hemolymph are increased and act on nearby midgut progeni
76 nfections, LRIM1 and APL1C, circulate in the hemolymph as a high-molecular-weight complex held togeth
77 274 is secreted from glia to the circulating hemolymph as an exosomal cargo, a process requiring ESCR
78 rk shows that this parasite is not consuming hemolymph, as has been the accepted view, but damages ho
79  sexta serpin-3 is constitutively present in hemolymph at a low concentration of 5-12 microg/ml and i
80  larvae develop many melanotic tumors in the hemolymph at the third instar stage.
81       As ecdysone is first secreted into the hemolymph before reaching the CNS [3], our finding raise
82 protein (betaGRP), a soluble receptor in the hemolymph, binds to the surfaces of bacteria and fungi a
83 nd potential immunodeficiency, as a range of hemolymph biochemistry parameters were altered and the d
84                                              Hemolymph (blood analog) physiology showed a compromised
85 lymph glands (larval hematopoietic organ) or hemolymph (blood equivalent).
86 ere used to analyze polar metabolites in the hemolymph (blood) extracted from larvae of the very smal
87 ed growth of the bacterium in the Drosophila hemolymph (blood) or overt damage to Drosophila tissues.
88 y the impact of host dietary protein on host hemolymph (blood) osmolality (i.e., its concentration of
89 irst step in determining the roles played by hemolymph-borne agents in the crab Cancer productus, we
90 together with the wild-type strain in insect hemolymph but not in defined culture medium.
91 istributing ingested nicotine from midgut to hemolymph, but not in the clearing of hemolymph nicotine
92 sly characterized lepidopteran betaGRPs from hemolymph, but unlike these it is secreted into the larv
93 sealed from high ionic concentrations of the hemolymph by a barrier to allow phototransduction.
94 d and insulate it against the potassium-rich hemolymph by forming intercellular septate junctions.
95 ent complex of serpin-6 and PAP-3 in induced hemolymph by immunoaffinity chromatography and mass spec
96                Trehalose enters the mosquito hemolymph by the trehalose transporter AgTreT1.
97 t contribute to detoxification of the insect hemolymph by uptake of molecules through an SD-like neph
98 s associated with inappropriate responses of hemolymph carbohydrate concentration to insulin and with
99 er Ogt(sxc) or Oga in the IPCs increased the hemolymph carbohydrate concentration.
100 ize lipid in their muscles, twofold-elevated hemolymph carbohydrate concentrations, and they accumula
101  geometry of surrounding structures like the hemolymph channel and the acoustic trachea as well as th
102 chnique results in an ability to distinguish hemolymph chemical variations with developmental stage,
103                           Body movements and hemolymph circulation cannot account for these cycles; t
104 ure that are produced through body motion or hemolymph circulation.
105  these and other neuropeptides in crustacean hemolymph, complementing current tissue-based studies an
106 ted is the means for two-point monitoring of hemolymph composition for individual flies.
107 all amount of this protein into the female's hemolymph could contribute to the cost of mating.
108 wo-hybrid screen was performed using certain hemolymph DAFPs as "bait" in an effort to identify endog
109 that may be either proteins (including other hemolymph DAFPs) or low-molecular mass enhancers such as
110  Benton et al. (2014) show that in crayfish, hemolymph-derived cells enter a neurogenic niche to repl
111 sma proliferation specifically depletes host hemolymph diacylglyceride, the major lipid class transpo
112 SDRNFLRFa, and TNRNFLRFa were sequenced from hemolymph dialysates.
113                       The periodic change in hemolymph direction is referred to as cardiac reversal.
114        Shaken bees also have lower levels of hemolymph dopamine, octopamine, and serotonin.
115 ternal O2 transport: flows of gut fluids and hemolymph driven by peristaltic contractions of a space-
116 ignificantly increased levels of 5-HT in the hemolymph during training, 1.5 hr after training, and 24
117 t evidence that dPrx4, on secretion into the hemolymph, elicits a JAK/STAT-mediated response.
118             The concentration of 5-HT in the hemolymph expressed a diurnal rhythm.
119 n); (b) how the concentrations of 20E in the hemolymph feed back on the prothoracic gland to decrease
120  an open hemocoel, in which the mechanism of hemolymph flow control is ambiguous.
121 lizing the body, which could explain complex hemolymph flows.
122 he developed technique that samples only the hemolymph fluid is efficient and enables accurate organi
123 tivation and melanization of bacteria in the hemolymph following microbial challenge.
124                                   We sampled hemolymph from five snails from six different laboratory
125  technique capable of obtaining 50-300 nL of hemolymph from individual Drosophila larvae.
126   Mass spectroscopic analysis of extracts of hemolymph from mated and virgin 7-day-old males resulted
127 low valves (ostia) that allow the pumping of hemolymph from posterior toward the anterior.
128                          Here we report that hemolymph from the silkmoth, Bombyx mori, rapidly melani
129 squito midgut wall and are released into the hemolymph, from where they invade the salivary glands an
130 %) of ingested nicotine from the midgut into hemolymph, from which nicotine is exhaled through the sp
131 in neurons function as a nutrient sensor for hemolymph fructose and assign opposing valence to feedin
132 3a is both necessary and sufficient to sense hemolymph fructose and promote feeding in hungry flies b
133                               Interestingly, hemolymph fructose levels are tightly linked to feeding
134 a, which was recently shown to function as a hemolymph fructose sensor in adult flies [17], as the ma
135 own that a high sugar diet leads to elevated hemolymph glucose and systemic insulin resistance in dev
136 eprived of food, and injections of AI reduce hemolymph glucose levels, suggesting that the function o
137  neuropeptides involved in the regulation of hemolymph glucose.
138 ish in scotophase and monitored activity and hemolymph glucose/lactate over 24 h in early spring.
139 lls, but dye perfusion experiments show that hemolymph has no access to the interior of the clump of
140              Our focus on proteins of insect hemolymph has provided valuable insights into insect bio
141 eing slower in protein-rich, high-osmolality hemolymphs, highlighting a novel "bottom-up" mechanism b
142         Like the HP21 products purified from hemolymph, HP21 that was activated by HP14 in the in vit
143 y and abundance of microorganisms within the hemolymph (i.e. blood) of Biomphalaria snails, the inter
144 pecies and important effector protein of the hemolymph immune system, displays two distinct doubly st
145 ing electrophoresis experiments on butterfly hemolymph in his kitchen.
146 s recently shown to suppress melanization of hemolymph in Manduca sexta in part by inhibiting the enz
147 ) indicated it inhibits melanization of host hemolymph in vitro, while two predicted anti-microbial p
148 of the fly, which are in direct contact with hemolymph in vivo, but the mechanisms causing increased
149 cascade regulates the melanization of blood (hemolymph) in insects and other arthropods.
150 nterobacter sp. achieved high populations in hemolymph, in contrast to B. thuringiensis, which appear
151 e with a bacteria-binding lectin in M. sexta hemolymph, indicating that they may be important for ens
152         These data demonstrate that although hemolymph infection may be undetectable, transmission to
153 hila revealed that L-proline in the insect's hemolymph initiates a metabolic shift.
154                Here, we examined the role of hemolymph (insect blood) filtration in regulating system
155 synthesized by the fat body, secreted to the hemolymph (insect blood), and continuously incorporated
156 ed that hemocytes-by removing virus from the hemolymph instead of amplifying it and by participating
157 uttling of pre-selected metabolites from the hemolymph into defensive secretions.
158 atory system in which the heart pumps blood (hemolymph) into the body cavity, where it directly bathe
159 rom chill-coma involves a reestablishment of hemolymph ion content and volume driven by removal of Na
160 de evidence that physiological mechanisms of hemolymph ion content and volume regulation, such as ion
161                  Thus, oxygen tension of the hemolymph is an indicator of infection status, with pH a
162         The growth-promoting activity of the hemolymph is caused by a heat-stable factor that can be
163 iary in the snail-schistosome interaction as hemolymph is in very close contact with the parasite at
164 It appears that the level of bombyxin in the hemolymph is modulated by the brain in response to varia
165  Of note, mJHBP is structurally unrelated to hemolymph JHBP from lepidopteran insects.
166        A serine proteinase pathway in insect hemolymph leads to prophenoloxidase activation, an innat
167 ia glabrata produces increased quantities of hemolymph lectins, some of which are unique polypeptides
168  found that increasing levels of 5-HT in the hemolymph led to significant alterations in feeding beha
169            Addition of acetyl-SVAFS-amide to hemolymph led to unregulated proPO activation.
170 dosymbiont is limited by the availability of hemolymph lipids.
171 rating that bacterial proliferation requires hemolymph-lipids.
172        A serine proteinase cascade in insect hemolymph mediates prophenoloxidase activation, a defens
173                This analysis showed that the hemolymph metabolomes of males and females are markedly
174 ansported to the pheromone gland through the hemolymph, most probably by lipophorin.
175  they exhaled less nicotine because of lower hemolymph nicotine concentrations.
176 gut to hemolymph, but not in the clearing of hemolymph nicotine or in the exhalation of nicotine from
177 ose level (29.6 +/- 0.6 mg/mL) in the larval hemolymph of a beetle, Dendroides canadensis, and demons
178 ,3-glucan recognition protein present in the hemolymph of a pyralid moth, Plodia interpunctella.
179  parasitemic cattle and kinete levels in the hemolymph of adult female Boophilus ticks following acqu
180                  Injection of VU573 into the hemolymph of adult female mosquitoes (Ae. aegypti) disru
181                    Partial purification from hemolymph of an activator of proPAP3 resulted in an acti
182 to the cecropin family was isolated from the hemolymph of bacteria-challenged adult Aedes aegypti.
183 on and characterization of pro-HP14 from the hemolymph of bacteria-injected M. sexta larvae.
184                A surge of amino acids in the hemolymph of blood-fed female mosquitoes activates a nut
185  transgenic defensin were accumulated in the hemolymph of bloodfed female mosquitoes, persisting for
186 quired an unidentified soluble factor in the hemolymph of Bombyx morii.
187  biosynthesis, dramatically increased in the hemolymph of CLIPA14 kd mosquitoes in response to system
188 ate at the physiological pH and pO(2) of the hemolymph of control snails.
189               Serotonin (5-HT) levels in the hemolymph of crustaceans has been implied to alter aggre
190                               Examination of hemolymph of diseased clams revealed high levels of reve
191 ate at the physiological pH and pO(2) of the hemolymph of estivating snails is compared with metaboli
192 e amino acid sequence, was purified from the hemolymph of fed female Amblyomma hebraeum ticks.
193 to search for the JH homologs present in the hemolymph of fourth instar nymphs of R. prolixus.
194                       By amplifying DNA from hemolymph of infected pea aphids, we obtained a set of g
195 lites from the transport lipoproteins in the hemolymph of its host.
196 a histidine-rich glycoprotein, both from the hemolymph of M. edulis.
197 he prophenoloxidase activation system in the hemolymph of M. sexta.
198 rotease 14 (HP14), an initiating protease in hemolymph of Manduca sexta, upon the binding of beta-1,3
199 oteinases have been purified from the larval hemolymph of Manduca sexta: hemolymph proteinase 14 (HP1
200        Serpin-6 is constitutively present in hemolymph of naive larvae, and its mRNA and protein leve
201  In this study, hemocyanin purified from the hemolymph of Nephrops norvegicus displays diphenoloxidas
202 tions are lower than what are present in the hemolymph of overwintering larvae.
203 ing protein (mJHBP), which circulates in the hemolymph of pupal and adult Aedes aegypti males and fem
204 ater and from host-feeding on the water-rich hemolymph of SWD pupae.
205 ecently isolated Manduca sexta serpin-6 from hemolymph of the bacteria-challenged larvae, which selec
206 d to identify JH III from hexane extracts of hemolymph of the Caribbean fruit fly.
207 crodialysis to sample neuropeptides from the hemolymph of the crab, Cancer borealis.
208  thought to filter and detoxify the blood or hemolymph of the fly.
209 en-related proteins (FREPs) are found in the hemolymph of the freshwater snail Biomphalaria glabrata,
210 ese bees was very different from that of the hemolymph of the host bee but consistently matched the f
211                        We have purified from hemolymph of the tobacco hornworm, Manduca sexta, a new
212 dentified more than 20 serine proteinases in hemolymph of the tobacco hornworm, Manduca sexta, but fu
213 mutants due to excessive iron present in the hemolymph of these flies.
214 itional bacteria that were isolated from the hemolymph of wild-caught D. melanogaster.
215   The presence of trypanosomes either in the hemolymph or in the gut early in the infection process d
216 e insect vector, from the gut lumen into the hemolymph or other tissues and finally into the salivary
217 um, but not to the midgut surface facing the hemolymph or to ovaries.
218 ly inhibiting trehalose precipitation in the hemolymph (or blood) of overwintering beetle larvae.
219 ps in the number of parasites in the midgut, hemolymph, or eggs of replete female ticks after acquisi
220       Adult Drosophila melanogaster maintain hemolymph osmolarity within a narrow range.
221                                  The average hemolymph oxygen tension was higher in "Ca.
222                                  The average hemolymph pH was significantly higher in infected ACPs (
223                                          The hemolymph phenoloxidase (PO) activity of WSSV-infected s
224                    Ookinete melanization and hemolymph phenoloxidase activity were further increased
225 -mediated knockdown of MFS2 increases blood (hemolymph) Pi and decreases formation of Malpighian tubu
226         Many freeze-tolerant insects produce hemolymph PINs, which induce freezing at high subzero te
227 mily of fibrinogen-related proteins (FREPs), hemolymph polypeptides that consist of one or two amino-
228 mosquitoes (Ae. aegypti) is exacerbated when hemolymph potassium levels are elevated, suggesting that
229 uropeptides and fewer protein fragments than hemolymph prepared by typical analysis methods.
230 bodies reduced total RHBP circulating in the hemolymph, promoting oxidative damage to hemolymphatic p
231  in insects is the proteolytic activation of hemolymph prophenoloxidase (proPO), regulated by proteas
232 eases (IMP-1 and IMP-2) and Serpin-1 mediate hemolymph prophenoloxidase cleavage and immune response
233 he molecular basis for the autoactivation of hemolymph protease 14 (HP14), an initiating protease in
234          Covalent complexes of serpin-4 with hemolymph proteases HP-1 and HP-6 appeared in plasma act
235                   We found that CLIPA14 is a hemolymph protein that is rapidly cleaved following a sy
236             Nosema infection decreased total hemolymph protein titers in 1 and 7-day old adult bees (
237 pping lambda clones for Manduca sexta PAP-2, hemolymph proteinase 12 (HP12), and HP24.
238  from the larval hemolymph of Manduca sexta: hemolymph proteinase 14 (HP14), which autoactivates in t
239 a cDNA encoding a modular protein designated hemolymph proteinase 14 (HP14).
240  tobacco hornworm Manduca sexta, recombinant hemolymph proteinase 14 precursor (pro-HP14) interacts w
241 ta serpin-1 isoforms A, E, and J can inhibit hemolymph proteinase 8, which activates the cytokine spa
242 PO, attacin-2, and a complex of serpin-6 and hemolymph proteinase-8 were also detected in the protein
243 ions of two additional M. sexta proteinases, hemolymph proteinases 6 and 8 (HP6 and HP8).
244 an insect immune response, requires a set of hemolymph proteins including pathogen recognition protei
245 Hemocyanins are multimeric copper-containing hemolymph proteins involved in oxygen binding and transp
246 midgut cells and eliminated upon exposure to hemolymph proteins of the complement-like system.
247        Abolition of cellular accumulation of hemolymph proteins with dramatically reduced lacuna chan
248 eased endocytic activity and accumulation of hemolymph proteins, dextran particles, and silver nitrat
249  nephrocytes and then heart function and the hemolymph proteome were analyzed.
250 the fruit fly, the dorsal vessel, which is a hemolymph-pumping organ, has provided a unique model sys
251 r of females harboring kinetes detectable in hemolymph (r = 0.9).
252 he essential amino acid arginine in A. pisum hemolymph reduces the transport of the precursor glutami
253      Analysis of in vitro microdialysates of hemolymph revealed more neuropeptides and fewer protein
254  replication was not detected in the midgut, hemolymph, salivary gland, coxal gland, or reproductive
255 ated the absolute bacterial load using qPCR: hemolymph samples contained 2784 +/- 339 bacteria/mul.
256  amino acids were identified from individual hemolymph samples of both wild-type (WT) control and the
257                                              Hemolymph sampling performed under mineral oil and in ai
258 s of evaporation compared to the traditional hemolymph-sampling techniques.
259 onses of insects is mediated by a network of hemolymph serine proteases (HPs) and noncatalytic serine
260 e cleaved forms of the previously identified hemolymph serine proteinase, HP21.
261 of antimicrobial peptides are stimulated via hemolymph (serine) protease 5 (HP5) in Manduca sexta Pre
262                                 Normal pupal hemolymph showed an increase in antibacterial activity a
263                                    Mites fed hemolymph showed fitness metrics no different from the s
264 ed, with a small but significant decrease in hemolymph sodium ions and an increase in calcium ions af
265    Anti-JH antiserum specifically recognizes hemolymph-soluble Hex-1 protein, supporting that the uni
266          Toxins expressed under control of a hemolymph-specific promoter increased fungal lethality t
267 d correlates with a decrease in the two main hemolymph sugars, trehalose and glucose, and in glycogen
268 longer and produced more eggs than those fed hemolymph, suggesting that fat body is integral to their
269 lic profiles of the gut compartments and the hemolymph, suggesting that gut bacteria degrade plant po
270  The detection of these neuropeptides in the hemolymph suggests that they are functioning as hormones
271                   Both the prepatterning and hemolymph-supplied components of this system can change
272  steroid hormone 20-hydroxyecdysone and with hemolymph taken from growing larvae.
273 htly acidic pH equivalent of fed female tick hemolymph, the wild-type and the histidine-rich recombin
274  have a dorsal heart that drives O2-carrying hemolymph through peripheral vessels and an open hemocoe
275                                 Although the hemolymph titer of juvenile hormone normally decreases t
276                         At adult eclosion JH hemolymph titer was low, increased in 1-day old sugar-fe
277                            However, absolute hemolymph titers were lower than Ae. aegypti.
278 ith the transport of glutamine from A. pisum hemolymph to the bacteriocyte cytoplasm.
279 nd is necessary for iron relocation from the hemolymph to the fat body.
280 rogressive drift of Na(+) and water from the hemolymph to the gut, but the physiological mechanisms u
281 arget sporozoites as they travel through the hemolymph to the salivary glands.
282  this group blocks bursicon release into the hemolymph together with tanning and wing expansion.
283            AgTreT1 RNA silencing reduces the hemolymph trehalose concentration by 40%, and the mosqui
284  Consistent with elevated iron levels in the hemolymph, Tsf1 mutants exhibited increased susceptibili
285 ed the effects of larval worker infection on hemolymph Vg titers.
286 roduced here is a method to sample nanoliter hemolymph volumes from individual adult fruit-flies for
287  The half-life of an increase in 5-HT in the hemolymph was approximately 0.5 hr.
288                                       Immune hemolymph was collected from fifth instar larvae and 1-d
289              By deep sequencing of RNAs from hemolymph, we identified transcripts of a novel retroele
290 ting entry of Acp62F into the mated female's hemolymph, we propose that Acp62F is a candidate for a m
291 quantitative amino acid analyses of obtained hemolymph were carried out in two optimized buffer condi
292 ng to known peptides derived from FREPs from hemolymph were found in one of these genes.
293              Moreover, levels of 5-HT in the hemolymph were significantly correlated with the magnitu
294  glutamine, glutamate, and taurine in the gb hemolymph were significantly lower at 35%, 38%, and 57%
295 ilum burden increases in salivary glands and hemolymph when the JAK-STAT pathway is suppressed by RNA
296 , we predict that Sp22D is secreted into the hemolymph where it may interact with pathogen surfaces a
297  S. poulsonii resides extracellularly in the hemolymph, where it must acquire metabolites to sustain
298  These vesicles and virions circulate in the hemolymph, where they are acquired by parasitic wasps du
299 ramatic expansion of blast-like cells in the hemolymph with high mitotic index.
300                           Supplementation of hemolymph with proHP14 greatly enhanced prophenoloxidase

 
Page Top