ライフサイエンスコーパス: Ciona intestinalis

1 e larva of a sibling chordate, the ascidian, Ciona intestinalis.

2 al tube closure in the invertebrate chordate Ciona intestinalis.

3 ng dynamics using the invertebrate chordate, Ciona intestinalis.

4 mechanism for zippering in a basal chordate, Ciona intestinalis.

5 n the CNS of a simple chordate, the ascidian Ciona intestinalis.

6 anded breaks in the genome of the sea squirt Ciona intestinalis.

7 PNS development of the invertebrate chordate Ciona intestinalis.

8 ence to investigate cilia in the urochordate Ciona intestinalis.

9 ervous system of the ascidian tadpole larva, Ciona intestinalis.

10 latory network in the invertebrate chordate, Ciona intestinalis.

11 or of ectodermal development in the ascidian Ciona intestinalis.

12 -bp notochord-specific CRM from the ascidian Ciona intestinalis.

13 expression patterns of NCLC in the ascidian Ciona intestinalis.

14 alyze cardiac cell migration in the ascidian Ciona intestinalis.

15 C. savignyi to its divergent sister species, Ciona intestinalis.

16 es was performed by using the basal chordate Ciona intestinalis.

17 fied in the genome sequences of the ascidian Ciona intestinalis.

18 regions in the ascidians Ciona savignyi and Ciona intestinalis.

19 or tissue-specific enhancers in the ascidian Ciona intestinalis.

20 of the genome of the most studied ascidian, Ciona intestinalis.

21 mbe, Drosophila melanogaster, zebrafish, and Ciona intestinalis.

22 gene, CiVegTR, was isolated in the ascidian Ciona intestinalis.

23 -3beta and snail homologues in the ascidian, Ciona intestinalis, a member of the subphylum Urochordat

24 We have examined ASICs from the ascidian Ciona intestinalis, a simple chordate organism whose ner

25 eart progenitor cells of the simple chordate Ciona intestinalis also generate precursors of the atria

26 ting the ARNTL gene family in the genomes of Ciona intestinalis, amphioxus, zebrafish, and human.

27 the zebrafish (Danio rerio) and the ascidian Ciona intestinalis, an invertebrate chordate belonging t

28 enic regulatory factor (MRF) of the ascidian Ciona intestinalis, an invertebrate chordate.

29 rization of TERT genes from two sea squirts, Ciona intestinalis and Ciona savignyi.

30 D family gene was identified in the ascidian Ciona intestinalis and designated CiMDF (Ciona intestina

31 lated organisms that make cellulose, such as Ciona intestinalis and Dictyostelium discoideum, reveale

32 sms, Drosophila melanogaster, Daphnia pulex, Ciona intestinalis and Strongylocentrotus purpuratus.

33 macaque and Opossum, the chordate genome of Ciona intestinalis and the import and integration of the

34 t absent from the genomes of the urochordate Ciona intestinalis and the lower eukaryotes D. melanogas

35 using a simple method to introduce DNA into Ciona intestinalis and the several available tissue-spec

36 We identified putative MBL homologs in Ciona intestinalis and Trichoplax adhaerens, and investi

37 g the notochord of the invertebrate chordate Ciona intestinalis as a model.

38 Using Ciona intestinalis as a simple chordate model, we show t

39 ique phylogenetic position of the sea squirt Ciona intestinalis as part of the sister group to the ve

40 nderlying basis of enhancer activity for the Ciona intestinalis betagamma-crystallin gene, which driv

41 In ascidians, such as Ciona intestinalis, Brachyury is expressed exclusively i

42 subsequently identified in human, mouse, and Ciona intestinalis, but their existence in dinoflagellat

43 mo sapiens, Mus musculus, Takifugu rubripes, Ciona intestinalis, Caenorhabditis elegans, Drosophila m

44 ses fewer substitutions than the sea squirt (Ciona intestinalis) CB1 sequence.

45 Caenorhabditis elegans (Ce), the sea squirt Ciona intestinalis (Ci) and amphioxus Branchiostoma flor

46 single MRF gene of the invertebrate chordate Ciona intestinalis (Ci-MRF).

47 he voltage sensor of the prototypic VSP from Ciona intestinalis, Ci-VSP, we generated chimeric protei

48 s was recently identified in the urochordate Ciona intestinalis (CiCBR).

49 A chordate ortholog of UNC-3, Ciona intestinalis COE, was also both required and suffi

50 The ascidian Ciona intestinalis, commonly known as a 'sea squirt', ha

51 Here we show that the gut mucosa of Ciona intestinalis contains an extensive matrix of chiti

52 the genome of a urochordate, the sea squirt, Ciona intestinalis, did not turn up any genuine ortholog

53 sed to improve and enrich the description of Ciona intestinalis embryonic development, based on an im

54 Comprehensive gene networks in Ciona intestinalis embryos provide a foundation for char

55 revised cell lineage of the pigment cells in Ciona intestinalis embryos.

56 Here we show that the tunicate Ciona intestinalis exhibits a proto-placodal ectoderm (P

57 POUIV gene families to examine the tunicate Ciona intestinalis for evidence of structures homologous

58 s, making for a direct orthology between the Ciona intestinalis gene CiPax6 and Pax6 in mammals.

59 d the distribution of DNA methylation in the Ciona intestinalis genome.

60 we estimated that the invertebrate chordate Ciona intestinalis has 15,500 protein-coding genes (+/-3

61 The ascidian Ciona intestinalis has a monolobal transferrin (nicatran

62 A forward genetic screen in the ascidian Ciona intestinalis identified a mutant line (frimousse)

63 uccess of an introduced marine invertebrate (Ciona intestinalis) in Northern California.

64 The invertebrate chordate Ciona intestinalis is a widely used model organism in bi

65 t specification in the invertebrate chordate Ciona intestinalis is similar to that of vertebrates but

66 nt evidence that the embryo of the ascidian, Ciona intestinalis, is an easily manipulated system for

67 In Ciona intestinalis, leprecan was identified as a target

68 e demonstrate that, in the chordate ascidian Ciona intestinalis, miR-124 plays an extensive role in p

69 ian Ciona intestinalis and designated CiMDF (Ciona intestinalis Muscle Determination Factor).

70 y through mediation of Ca(2+) transients, in Ciona intestinalis neural induction.

71 Here we show that the tunicate Ciona intestinalis possesses a cephalic melanocyte linea

72 estigate this process in the simple chordate Ciona intestinalis Previous studies have implicated Noda

73 s trunk ventral cells, TVCs) of the ascidian Ciona intestinalis provide a simple chordate model with

74 the CNS of the tadpole larva of the ascidian Ciona intestinalis provides us with a chordate nervous s

75 of the gene for the FlgCK from the tunicate Ciona intestinalis, providing support for the linkage of

76 ans and even a highly divergent invertebrate Ciona intestinalis qualitatively and quantitatively supp

77 rithm on simulated next-generation data from Ciona intestinalis, real next-generation data from Droso

78 motivated by our experiments in the ascidian Ciona intestinalis showing that the peripheral sensory n

79 In the ascidian, Ciona intestinalis, snail (Ci-sna) is expressed at the 3

80 stinct moto- and interneuron subtypes in the Ciona intestinalis tadpole larva.

81 ntrols the rhythmic swimming behavior of the Ciona intestinalis tadpole.

82 ed several cDNAs derived from the sea squirt Ciona intestinalis that encode vitamin K-dependent prote

83 -induced short-tailed mutant in the ascidian Ciona intestinalis that is the product of a premature st

84 identified in the primitive ascidian species Ciona intestinalis that possesses the characteristic fea

85 euterostomian invertebrate - the urochordate Ciona intestinalis - that is orthologous to vertebrate c

86 ll type in the tadpole larva of the tunicate Ciona intestinalis, the bipolar tail neuron, shares a se

87 In the simple chordate Ciona intestinalis, the notochord plate consists of just

88 In Ciona intestinalis, the palps consist of three conical p

89 Here, we employ the invertebrate chordate Ciona intestinalis to delineate an essential in vivo rol

90 rphological simplicity of the basal chordate Ciona intestinalis to elucidate Mesp regulation and func

91 loit wild populations of the marine chordate Ciona intestinalis to show that levels of buffering are

92 tic manipulability, we chose the sea squirt, Ciona intestinalis, to explore intraspecies sequence com

93 tion and streamlined genome of the ascidian, Ciona intestinalis, to investigate heart development in

94 invasive tunicates, Ciona robusta (formerly Ciona intestinalis type A) and C. intestinalis (formerly

95 inalis type A) and C. intestinalis (formerly Ciona intestinalis type B), globally distributed and sym

96 results suggest that the native S4 from the Ciona intestinalis voltage-sensitive phosphatase (Ci-VSP

97 The Ciona intestinalis voltage-sensitive phosphatase (Ci-VSP

98 ht consists of the voltage-sensing domain of Ciona intestinalis voltage-sensitive phosphatase and sup

99 2 K(+) channel and the voltage sensor of the Ciona intestinalis voltage-sensitive phosphatase, agains

100 rents are significantly faster than those of Ciona intestinalis voltage-sensitive phosphatase.

101 The genome of the invertebrate chordate Ciona intestinalis was found to be a stable mosaic of me

102 on pattern of CiMDF, the MyoD-family gene of Ciona intestinalis, was analyzed in unmanipulated and mi

103 The draft genome of the primitive chordate, Ciona intestinalis, was published three years ago.

104 ge-gated proton channels in humans, mice and Ciona intestinalis were discovered.

105 ogs transcribed in eggs of Xenopus laevis or Ciona intestinalis were found, pinpointing evolutionary

106 Eggs of the ascidian Ciona intestinalis were injected with the Src-homology 2

107 anogaster and in the non-vertebrate chordate Ciona intestinalis, which each have only one talin gene,

108 We show that the urochordate Ciona intestinalis, which split from the vertebrate line

109 identified ABC proteins from the sea squirt (Ciona intestinalis), zebrafish (Danio rerio), and chicke