ライフサイエンスコーパス: starfish

1 nload at http://cbcb.umd.edu/kingsford-group/starfish.

2 embryos of a distantly related echinoderm, a starfish.

3 orylating the serine-209 residue of eIF4E in starfish.

4 ived from these two PP/OK-type precursors in starfish.

5 ctivation or subsequent oocyte maturation in starfish.

6 rger sea urchins were consumed only by large starfishes.

7 ion is found in almost identical form in the starfish: a detailed element of GRN architecture has bee

8 est this concept, we coexpressed G(qi) and a starfish adenosine receptor in frog oocytes and showed t

9 mammalian G(i)- and G(z)-linked receptors in starfish and frog oocytes.

10 fied only in echinoderms such as sea urchin, starfish and sand dollar.

11 ids, including new data from a hemichordate, starfish and Xenoturbella.

12 n of oocyte maturation by 1-methyladenine in starfish, and by a steroid in frogs, has been proposed t

13 been found for them, but now it appears that starfish are able to use them to navigate to the edges o

14 ysis of transcriptome sequence data from the starfish Asterias rubens revealed two PP/OK-type precurs

15 e neuropeptide precursor 1; ArPPLNP1) in the starfish Asterias rubens.

16 ng systems in a deuterostome-the echinoderm (starfish) Asterias rubens.

17 et of regulatory genes was isolated from the starfish Asterina miniata, their expression patterns det

18 DNA encoding PLC-gamma was isolated from the starfish Asterina miniata.

19 ing agonists caused meiosis to resume in the starfish but not the frog oocytes.

20 two peptides (S1 and S2) were isolated from starfish but now we find that in P. miniata, for example

21 A 3.5-kb eIF4E clone isolated from starfish cDNA is 57% identical to human eIF4E and contai

22 uch as acorn worms) and echinoderms (such as starfish) comprise the group Deuterostomia, well establi

23 cyclones, coral predation by crown-of-thorns starfish (COTS), and coral bleaching accounted for 48%,

24 utbreaks of the coral-eating crown-of-thorns starfish (COTS), losing much of its coral cover in the p

25 Starfish density varied considerably between sites but,

26 We previously reported that human, frog, and starfish DGCR8 bind heme when expressed in Escherichia c

27 These results indicate that an endogenous starfish egg PLC-gamma interacts with an egg SFK and med

28 e lumen of the endoplasmic reticulum (ER) of starfish eggs by injecting mRNA coding for a chimeric pr

29 now show that injection of Src protein into starfish eggs initiates Ca(2+) release and DNA synthesis

30 of PLC-gamma SH2 domain fusion proteins into starfish eggs specifically inhibits the initiation of ca

31 ine in more detail the endogenous factors in starfish eggs that are required for Ca2+ release at fert

32 ich is activated by a G protein, we injected starfish eggs with a PLCgamma SH2 domain fusion protein

33 ction of kinases in this family, we injected starfish eggs with the SH2 domains of Src and Fyn kinase

34 Injecting starfish eggs with the tandem SH2 domains of AmPLC-gamma

35 esults indicate that during fertilization of starfish eggs, activation of phospholipase Cgamma by an

36 In starfish eggs, studies using inhibitors designed against

37 nitiating Ca(2+) release at fertilization in starfish eggs.

38 -mediated Ca(2+) release at fertilization in starfish eggs.

39 regulator of PLC-gamma in the activation of starfish eggs.

40 A starfish eIF4E fusion protein (GST-4E) was phosphorylate

41 imensional structures such as sea urchin and starfish embryos.

42 te portions of the arms of Archaster typicus starfish, extract and separate the active biomaterials,

43 Starfish have small compound eyes at the ends of their a

44 MCT) of echinoderms (e.g., sea cucumbers and starfish) is a remarkable example of a biological materi

45 ces a prominent skeleton lacking entirely in starfish larvae.

46 igits leading to autoamputation, distinctive starfish-like acral keratoses and moderate degrees of de

47 By contrast, in starfish, MAPK is activated after GVBD.

48 ribbons with linear and circular topologies, starfish membranes, and double and triple helices.

49 Recently, starfish myorelaxant peptide (SMP) was identified as a P

50 Furthermore, a PP/OK-type neuropeptide (starfish myorelaxant peptide, SMP) was recently identifi

51 mides have been identified: L-type (e.g. the starfish neuropeptides S1 and S2) with the C-terminal mo

52 The starfish nucleus collapsed approximately 1 h after wound

53 ological and mechanical changes occur in the starfish oocyte during maturation.

54 The resumption of meiosis in the developing starfish oocyte is the result of intracellular signaling

55 eIF4E, and the eIF4E binding protein during starfish oocyte maturation, while PI3 kinase activates t

56 F4E is required for protein synthesis during starfish oocyte maturation.

57 ere we show that PI-3 kinase is required for starfish oocyte maturation.

58 yclin B is present in aggregates in immature starfish oocytes and becomes disaggregated at the time o

59 We found that starfish oocytes and sea urchin eggs rapidly reseal much

60 work helps to tear down the large nucleus of starfish oocytes and to prevent chromosome loss in meios

61 Starfish oocytes are arrested at the G2/M-phase border o

62 mother centrioles need to be eliminated from starfish oocytes by extrusion into the polar bodies for

63 nase activities during meiotic maturation of starfish oocytes is a protein kinase C or PKC-like activ

64 we show that NE fragmentation during NEBD in starfish oocytes is driven by an Arp2/3 complex-nucleate

65 In starfish oocytes, Cdc2-cyclin B begins to be activated a

66 For starfish oocytes, however, our results support the concl

67 alize the entire elimination process live in starfish oocytes.

68 the plasma membrane and nuclear envelope in starfish oocytes.

69 as investigated during meiotic maturation of starfish oocytes.

70 opus japonicus (class Holothuroidea) and the starfish Patiria miniata (class Asteroidea).

71 entified as a PP/OK-type neuropeptide in the starfish Patiria pectinifera (phylum Echinodermata).

72 ently identified as a muscle relaxant in the starfish Patiria pectinifera.

73 In North-eastern Pacific kelp forests, the starfish Pycnopodia helianthoides is known to be an impo

74 roteins have been identified in sea urchins, starfish, sanddollars, and humans.

75 hese findings support the conclusion that in starfish, sperm-egg interaction causes egg activation by

76 mainly in the animal lineage, which includes starfish to humans in the deuterostome lineage.

77 for macrofauna and shell-hash content whilst starfish were counted and the shell-hash cover estimated

78 There was no evidence that starfish were more abundant in the presence of shell-has

79 a urchin is used entirely differently in the starfish, where it responds to endomesodermal inputs tha

80 as inhibitory neuromuscular transmitters in starfish, which contrasts with the myoexcitatory actions

81 , which is inspired by animals (e.g., squid, starfish, worms) that do not have hard internal skeleton