ライフサイエンスコーパス: sea anemone

1 desktop and bench-top studies of the starlet sea anemone.

2 inase 1 (PMP1) of jellyfish and in toxins of sea anemone.

3 volutionarily related to peptide toxins from sea anemones.

4 he cnidarian Nematostella vectensis (starlet sea anemone), a close relative to the Bilateria, possess

5 natoxin II (EqtII), a protein toxin from the sea anemone Actinia equina, readily creates pores in sph

6 pore-forming protein toxin isolated from the sea anemone Actinia equina.

7 toxic polypeptides secreted in the venom of sea anemones, actinoporins are the pore-forming toxins w

8 nthozoan species, and show that in the model sea anemone Aiptasia pallida the TSR domain promotes col

9 mic changes associated with symbiosis in the sea anemone Aiptasia pallida, an important model system

10 The small sea anemone Aiptasia provides a tractable laboratory mod

11 then applied to identify fatty acids from a sea anemone, Aiptasia pulchella, and dinoflagellate symb

12 f several fungal species than to that of the sea anemone (although the insertion site differs in the

13 g early-branching animals such as amphioxus, sea anemone, amoebas and Trichoplax, and in plants and a

14 ing site conservation identifies new ATLs in sea anemone and ancestral archaea, indicating that ATL i

15 proteins found in nematocysts of jellyfish, sea anemones and Hydra, but have lost the most important

16 spiders, mites, scorpions), Cnidaria (Hydra, sea anemones), and Mollusca (oysters) but not in most ot

17 Cnidarians (corals, sea anemones, and "jellyfish") diverged from other anima

18 zed the proteomes of cilia from sea urchins, sea anemones, and choanoflagellates.

19 animals, such as snakes, spiders, scorpions, sea anemones, and cone snails, produce a variety of high

20 Increased growth (abundance and size) of the sea anemone (Anemonia viridis) population was observed a

21 eurin B (ApB) isolated from the venom of the sea anemone Anthopleura xanthogrammica is one of a famil

22 ino acid polypeptide toxins from the Pacific sea anemone Anthopleura xanthogrammica that interfere wi

23 nthopleurin B (ApB), a toxin produced by the sea anemone Anthopleura xanthogrammica, is the most pote

24 Examples include the homology between a sea anemone antihypertensive/antiviral protein and a sea

25 -NF-kappaB alleles in natural populations of sea anemones are discussed.

26 Sea anemones are seemingly primitive animals that, along

27 dinium and its cnidarian hosts (e.g. corals, sea anemones) are the foundation of coral-reef ecosystem

28 Feeney and Brooker introduce sea-anemone associated fish.

29 e detected in the COI and ND5 genes of other sea anemones, but not in the COI and ND5 genes of other

30 Several polypeptide toxins from sea anemones caused delayed inactivation of mammalian vo

31 The phylum Cnidaria (sea anemones, corals, hydras and jellyfish) is the likel

32 However, the coral and sea anemone cox1 group I introns differed in several asp

33 ild-type red fluorescent progenitor eqFP578 (sea anemone Entacmaea quadricolor), is monomeric and cha

34 Symbiont-free individuals of the sea anemone Exaiptasia pallida (commonly referred to as

35 s (both ITS2-type A4) were isolated from the sea anemone Exaiptasia pallida and placed into unialgal

36 y scale we have characterized NF-kappaB in a sea anemone (Exaiptasia pallida; called Aiptasia herein)

37 The sea anemone genome is complex, with a gene repertoire, e

38 Cnidarians (corals, sea anemones, hydroids, and jellyfish) are a basal taxon

39 nel gene families are highly expanded in the sea anemone, including three subfamilies of the Shaker K

40 ium) and their cnidarian hosts (e.g. corals, sea anemones) is the foundation of coral reef ecosystems

41 ), including 14 874 predicted genes from the sea anemone itself.

42 th cnidarians, a group that includes corals, sea anemones, jellyfish, and hydroids, is supported by s

43 Hox and TALE proteins interact in a sea anemone, just as they do in flies and mice, indicati

44 nd NADH dehydrogenase subunit 5 (ND5) of the sea anemone Metridium senile (phylum Cnidaria) each cont

45 ents of TRPA1 was isolated from the venom of sea anemone Metridium senile.

46 reported for the cox1 group I intron in the sea anemone Metridium senile.

47 -pair mitochondrial (mt) DNA molecule of the sea anemone, Metridium senile (class Anthozoa, phylum Cn

48 This suggests that the sea anemone mitochondrial introns may have been acquired

49 We used both the sea anemone model system Aiptasia and several species of

50 s, including entamoeba, soybean rust, hydra, sea anemone, nematodes, fruit flies, beetle, sea urchin,

51 The sea anemone Nematostella is a non-bilaterian animal, a m

52 The sea anemone Nematostella vectensis (Nv) is a leading mod

53 Among the basal animals, the starlet sea anemone Nematostella vectensis (phylum Cnidaria) has

54 Among marine invertebrates, the starlet sea anemone Nematostella vectensis has emerged as an imp

55 tic analysis of the Talpid3 homolog from the sea anemone Nematostella vectensis identified a highly c

56 The sea anemone Nematostella vectensis is a useful cnidarian

57 The sea anemone Nematostella vectensis is the leading develo

58 The starlet sea anemone Nematostella vectensis serves as a cnidarian

59 n-bilaterian phylum Cnidaria, embryos of the sea anemone Nematostella vectensis undergo rapid synchro

60 A simple NF-kappaB pathway is present in the sea anemone Nematostella vectensis, an important model o

61 Bilateria, some representatives, such as the sea anemone Nematostella vectensis, exhibit bilateral sy

62 s recombination-mediated transgenesis in the sea anemone Nematostella vectensis.

63 nd characterized Erg channel paralogs in the sea anemone Nematostella vectensis.

64 cular composition of the apical organ of the sea anemone Nematostella vectensis.

65 velopment of a basal metazoan, the cnidarian sea anemone Nematostella vectensis.

66 of an emerging cnidarian model, the starlet sea anemone Nematostella vectensis.

67 t the onset of gastrulation in the anthozoan sea anemone Nematostella vectensis.

68 proteins derived from human and the starlet sea anemone (Nematostella vectensis) in 1) a high-throug

69 ined how the axial properties of the starlet sea anemone, Nematostella vectensis (Anthozoa, Cnidaria)

70 Over the past 20 years, the starlet sea anemone, Nematostella vectensis, a small estuarine a

71 The starlet sea anemone, Nematostella vectensis, is a basal metazoan

72 for an emerging model system, the cnidarian sea anemone, Nematostella vectensis.

73 lly during bilaterian embryogenesis from the sea anemone, Nematostella vectensis.

74 onents of the circadian clock in the starlet sea anemone, Nematostella vectensis: a model cnidarian w

75 Anthopleurin B (ApB) is a high-affinity sea anemone neurotoxin that interacts with voltage-sensi

76 one antihypertensive/antiviral protein and a sea anemone neurotoxin, and the homology between tick an

77 ite of APETx1, a peptide toxin purified from sea anemone, on the human ether-a-go-go-related gene (hE

78 or, alternatively, large cnidarians such as sea anemones or sea pens.

79 The sea anemone peptide APETx2 is a potent and selective blo

80 The structurally defined sea anemone peptide toxins ShK and BgK potently block th

81 1) according to a structure similar to other sea anemone peptides belonging to structural group 9a.

82 s, with a primary structure similar to other sea anemone peptides belonging to structural group 9a.

83 he cnidarian Nematostella vectensis (starlet sea anemone) provides a molecular genetic view into the

84 ucturally defined polypeptide, ShK, from the sea anemone Stichodactyla helianthus inhibited Kv1.3 pot

85 ShK toxin from the sea anemone Stichodactyla helianthus is a 35-residue pro

86 ) T(EM) cells, and the potent Kv1.3-blocking sea anemone Stichodactyla helianthus peptide (ShK) suppr

87 y analoging to ShK, a peptide toxin from the sea anemone Stichodactyla helianthus that inhibits the v

88 versatile serine protease inhibitor from the sea anemone Stichodactyla helianthus with high biomedica

89 toxin, a potassium channel blocker from the sea anemone Stichodactyla helianthus, is a 35 residue po

90 cholysins I and II (StnI and StnII) from the sea anemone Stichodactyla helianthus, it is shown that a

91 I, a pore-forming protein from the Caribbean Sea anemone Stichodactyla helianthus, was encapsulated w

92 protein ion-channel ligand isolated from the sea anemone Stichodactyla helianthus.

93 natoxin II (EqtII) is a model alpha-PFT from sea anemone that oligomerizes and forms pores in sphingo

94 d a Kv1.3 blocker peptide (ShK) derived from sea anemone to generate a subtype-selective Kv1.3 blocke

95 In the presence of sea anemone toxin (ATX-II; 20 nmol/L), an increase in pa

96 The sea anemone toxin anthopleurin B, which impairs open-cha

97 ashion at the transcriptional level, and the sea anemone toxin BDS-I is shown to protect against Abet

98 loop participate in alpha-scorpion toxin and sea anemone toxin binding to overlapping sites and that

99 mined the ability of anthopleurin B (ApB), a sea anemone toxin that selectively modifies inactivation

100 Anthopleurin B (ApB) is a type 1 sea anemone toxin, which binds to voltage-sensitive sodi

101 ffects on binding of alpha-scorpion toxin or sea anemone toxin.

102 xD) shows close structural similarity to the sea anemone toxins BgK and ShK.

103 alpha-Scorpion toxins and sea anemone toxins bind to a common extracellular site o

104 fold lower affinities for alpha-scorpion and sea anemone toxins, respectively.

105 of proteins that contain domains related to sea anemone toxins.

106 mol), a residue that is conserved among many sea anemone toxins.

107 fabricated on the scaffold present in ShK, a sea anemone type I (SAK1) toxin stabilized by three disu

108 peptides were isolated from the venom of the sea anemone Urticina grebelnyi.

109 Scorpion and sea anemone venoms contain several polypeptides that del