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1 pterobranchs) and the echinoderms (including starfish).
2 antagonists that we call shallow, deep, and starfish.
3 hat accompanies cytokinesis in both frog and starfish.
4 ived from these two PP/OK-type precursors in starfish.
5 embryos of a distantly related echinoderm, a starfish.
6 orylating the serine-209 residue of eIF4E in starfish.
7 ctivation or subsequent oocyte maturation in starfish.
8 rger sea urchins were consumed only by large starfishes.
9 To address this knowledge gap, we developed starfish, a computational workflow for high-throughput e
10 ion is found in almost identical form in the starfish: a detailed element of GRN architecture has bee
11 igh densities of coral-predatory Acanthaster starfish, across the tropical north Pacific Ocean since
12 est this concept, we coexpressed G(qi) and a starfish adenosine receptor in frog oocytes and showed t
13 CCK1 acts as an autotomy-promoting factor in starfish and as such it is the first neuropeptide to be
14 susceptible to outbreaks of crown-of-thorns starfish and coral disease-with a net negative impact on
18 r disturbances (outbreaks of crown-of-thorns starfish and sedimentation), will constrain recovery cap
20 n of oocyte maturation by 1-methyladenine in starfish, and by a steroid in frogs, has been proposed t
21 in numerous bilaterian animals (e.g., worms, starfish, and vertebrates) and are closely related to AM
22 been found for them, but now it appears that starfish are able to use them to navigate to the edges o
25 s of the ASTC-type neuropeptide ArSS1 in the starfish Asterias rubens revealed that it causes muscle
26 ysis of transcriptome sequence data from the starfish Asterias rubens revealed two PP/OK-type precurs
27 tokinin-type neuropeptide (ArSK/CCK1) in the starfish Asterias rubens,(5)(,)(6) we observed that this
31 et of regulatory genes was isolated from the starfish Asterina miniata, their expression patterns det
35 two peptides (S1 and S2) were isolated from starfish but now we find that in P. miniata, for example
37 uch as acorn worms) and echinoderms (such as starfish) comprise the group Deuterostomia, well establi
38 cyclones, coral predation by crown-of-thorns starfish (COTS), and coral bleaching accounted for 48%,
39 utbreaks of the coral-eating crown-of-thorns starfish (COTS), losing much of its coral cover in the p
40 lation irruptions of Pacific crown-of-thorns starfish (CoTS, Acanthaster cf. solaris) are among the f
41 onents within the of Pacific crown-of-thorns starfish (COTS; Acanthaster sp.), a well-known coral pre
43 We previously reported that human, frog, and starfish DGCR8 bind heme when expressed in Escherichia c
44 mics and force generation on the membrane of starfish egg cells, undergo spontaneous braiding dynamic
45 These results indicate that an endogenous starfish egg PLC-gamma interacts with an egg SFK and med
46 e lumen of the endoplasmic reticulum (ER) of starfish eggs by injecting mRNA coding for a chimeric pr
47 now show that injection of Src protein into starfish eggs initiates Ca(2+) release and DNA synthesis
48 of PLC-gamma SH2 domain fusion proteins into starfish eggs specifically inhibits the initiation of ca
49 ine in more detail the endogenous factors in starfish eggs that are required for Ca2+ release at fert
50 ich is activated by a G protein, we injected starfish eggs with a PLCgamma SH2 domain fusion protein
51 ction of kinases in this family, we injected starfish eggs with the SH2 domains of Src and Fyn kinase
53 esults indicate that during fertilization of starfish eggs, activation of phospholipase Cgamma by an
60 l excitability."(3-7) In developing frog and starfish embryos, cortical excitability is generated thr
62 rwater adhesive inspired by the tube feet of starfish enables functionality in underwater robotics an
63 te portions of the arms of Archaster typicus starfish, extract and separate the active biomaterials,
65 that acts as an autotomy-promoting factor in starfish has been reported.(4) While investigating in vi
68 MCT) of echinoderms (e.g., sea cucumbers and starfish) is a remarkable example of a biological materi
69 ally, inspired by the feeding mechanism of a starfish larva, we demonstrate an analogous microparticl
72 igits leading to autoamputation, distinctive starfish-like acral keratoses and moderate degrees of de
74 rfish's pentaradial symmetry, we introduce a starfish-like wearable bioelectronic system designed for
78 several neuropeptides (e.g., bombyxin-type, starfish myorelaxant peptide, secretogranin 7B2-like, Ap
80 mides have been identified: L-type (e.g. the starfish neuropeptides S1 and S2) with the C-terminal mo
83 The resumption of meiosis in the developing starfish oocyte is the result of intracellular signaling
84 eIF4E, and the eIF4E binding protein during starfish oocyte maturation, while PI3 kinase activates t
87 yclin B is present in aggregates in immature starfish oocytes and becomes disaggregated at the time o
88 Validated for use in C. elegans embryos, starfish oocytes and fission yeast, SAIBR is ideal for s
90 work helps to tear down the large nucleus of starfish oocytes and to prevent chromosome loss in meios
93 mother centrioles need to be eliminated from starfish oocytes by extrusion into the polar bodies for
95 nase activities during meiotic maturation of starfish oocytes is a protein kinase C or PKC-like activ
96 we show that NE fragmentation during NEBD in starfish oocytes is driven by an Arp2/3 complex-nucleate
99 ed by an Arp2/3-nucleated F-actin 'shell' in starfish oocytes, in contrast to microtubule-driven tear
100 ns centromeres during prophase I in worm and starfish oocytes,(2)(,)(3) suggesting that a similar pro
106 kinin-type neuropeptide promotes autotomy in starfish, opening a new route to understanding this fasc
110 entified as a PP/OK-type neuropeptide in the starfish Patiria pectinifera (phylum Echinodermata).
113 In North-eastern Pacific kelp forests, the starfish Pycnopodia helianthoides is known to be an impo
114 nomes of 1 649 fungal species and found that starfish recovers known Starships with 95% combined prec
117 hese findings support the conclusion that in starfish, sperm-egg interaction causes egg activation by
118 e find structures including: individual HAs, starfish structures with up to 12 HA molecules, and nove
121 ment step of collagen extraction from common starfish to reduce chemical use and time consumption.
122 different contexts, from traveling waves in starfish to transient pulses in Caenorhabditis elegans.
123 for macrofauna and shell-hash content whilst starfish were counted and the shell-hash cover estimated
125 istinct sets of observed feeding scars where starfish were not detected) increased from 4.90 ha(-1) (
126 a urchin is used entirely differently in the starfish, where it responds to endomesodermal inputs tha
127 as inhibitory neuromuscular transmitters in starfish, which contrasts with the myoexcitatory actions
128 , which is inspired by animals (e.g., squid, starfish, worms) that do not have hard internal skeleton