ライフサイエンスコーパス: Strongylocentrotus

1 , fully-ciliated mid- or late-gastrula stage Strongylocentrotus droebachiensis embryos were pulse lab

2 ntrotus pallidus but not in RSR orthologs of Strongylocentrotus droebachiensis or Hemicentrotus pulch

3 vior of a deep-sea echinoid, the sea urchin, Strongylocentrotus fragilis.

4 specific egg receptor for bindin, EBR1, from Strongylocentrotus franciscanus (Sf) and S. purpuratus (

5 l analysis to identify unique transcripts in Strongylocentrotus franciscanus that are absent or diver

6 m bindin locus in 134 adult red sea urchins (Strongylocentrotus franciscanus).

7 ial chromosome genome library of a congener, Strongylocentrotus franciscanus.

8 hat Hemicentrotus pulcherrimus fits into the Strongylocentrotus genus and examine the evolution of th

9 two exons and one intron, in the sea urchin Strongylocentrotus intermedius represented by two morpho

10 nts were found in the spec2a RSR ortholog in Strongylocentrotus pallidus but not in RSR orthologs of

11 In the sea urchin Strongylocentrotus purpuratus (class Echinoidea) there a

12 th the discovery of a gene in the sea urchin Strongylocentrotus purpuratus (phylum Echinodermata) enc

13 The echinoderms, Strongylocentrotus purpuratus (sea urchin) and Patiria m

14 oxycoumarin]) inhibits the first cleavage of Strongylocentrotus purpuratus (sea urchin) embryos in a

15 haracterized cis-regulatory modules from the Strongylocentrotus purpuratus (sea urchin) genome and ob

16 our detailed cis-regulatory analysis of the Strongylocentrotus purpuratus (Sp) endo16 gene was that

17 are present in the genome of the sea urchin Strongylocentrotus purpuratus (Sp), and each nanos mRNA

18 s of Sp-PMCA and Sp-SERCA in the sea urchin, Strongylocentrotus purpuratus (Sp), have been published.

19 enesis in a euechinoid, the well-known model Strongylocentrotus purpuratus (Sp), vs. the cidaroid Euc

20 orted speract-activated signaling pathway in Strongylocentrotus purpuratus (speract being a sperm-act

21 The glial cells missing regulatory gene of Strongylocentrotus purpuratus (spgcm) was proposed earli

22 ions in the tooth of the purple sea urchin ( Strongylocentrotus purpuratus ), using high-resolution X

23 The completion of the genome of Strongylocentrotus purpuratus allows a comprehensive sur

24 This gene was originally characterized in Strongylocentrotus purpuratus and encodes an imperfect t

25 t genomic sequence of the purple sea urchin, Strongylocentrotus purpuratus and includes sequence data

26 s containing the otx gene were isolated from Strongylocentrotus purpuratus and Lytechinus variegatus

27 Strongylocentrotus purpuratus and Lytechinus variegatus

28 two distantly related species of sea urchin, Strongylocentrotus purpuratus and Lytechinus variegatus,

29 were identified from two sea urchin species, Strongylocentrotus purpuratus and Lytechinus variegatus,

30 that these two genes are highly conserved in Strongylocentrotus purpuratus and Lytechinus variegatus,

31 icted from cDNAs of two sea urchins species, Strongylocentrotus purpuratus and Lytechinus variegatus.

32 reviously known only in vertebrates, in both Strongylocentrotus purpuratus and Nematostella vectensis

33 ad been purified from eggs of the sea urchin Strongylocentrotus purpuratus and the gene was cloned by

34 tory control of otxbeta1/2 in the sea urchin Strongylocentrotus purpuratus and the sea star Asterina

35 spec genes in Strongylocentrotus purpuratus are invariably associated

36 Eight Strongylocentrotus purpuratus cis-regulatory modules, in

37 The single Hox gene complex of Strongylocentrotus purpuratus contains 10 genes, and exp

38 In contrast, the echinoderm Strongylocentrotus purpuratus contains a 588 kb cluster

39 The Strongylocentrotus purpuratus cyclophilin1 gene (Sp-cyp1

40 A deuterostome Grl from the sea urchin Strongylocentrotus purpuratus displays similar patterns

41 urchins from the polymorphism of a sample of Strongylocentrotus purpuratus DNA (R(u) = 3-4).

42 been identified in the cortical granules of Strongylocentrotus purpuratus eggs, and here we examined

43 elopment the veg1 tier of the sixth cleavage Strongylocentrotus purpuratus embryo contributes progeny

44 ll endomesoderm specification network of the Strongylocentrotus purpuratus embryo.

45 comprise the integral spicule matrix of the Strongylocentrotus purpuratus embryo.

46 endomesoderm gene regulatory network in the Strongylocentrotus purpuratus embryo.

47 During Strongylocentrotus purpuratus embryogenesis, aboral ecto

48 llular matrix layers in the blastula wall of Strongylocentrotus purpuratus embryos at the mesenchyme

49 of the sixth-cleavage veg1 and veg2 tiers of Strongylocentrotus purpuratus embryos were labeled with

50 The first two blastomeres of Strongylocentrotus purpuratus embryos were separated and

51 The endo16 gene of Strongylocentrotus purpuratus encodes a secreted protein

52 f the process used to build our model of the Strongylocentrotus purpuratus endomesoderm gene network.

53 Here, we identify the Strongylocentrotus purpuratus enzymes responsible for th

54 We find that the PGCs of the sea urchin Strongylocentrotus purpuratus exhibit broad transcriptio

55 the egg receptor for sperm of the sea urchin Strongylocentrotus purpuratus exhibits several character

56 o survey the genome of the purple sea urchin Strongylocentrotus purpuratus for gene products involved

57 e identified and annotated in the sea urchin Strongylocentrotus purpuratus genome and the embryonic e

58 an analysis of gene models derived from the Strongylocentrotus purpuratus genome assembly and have g

59 ther smaller families were identified in the Strongylocentrotus purpuratus genome by means of a permi

60 The Strongylocentrotus purpuratus genome contains a single t

61 We surveyed the sea urchin Strongylocentrotus purpuratus genome for homologs of gen

62 lasses identified in vertebrate genomes, the Strongylocentrotus purpuratus genome has orthologues of

63 Analysis of the Strongylocentrotus purpuratus genome has revealed approx

64 The sequence of the Strongylocentrotus purpuratus genome offers unique oppor

65 Annotation of the Strongylocentrotus purpuratus genome sequence led to the

66 embryo was carried out in the context of the Strongylocentrotus purpuratus genome sequencing project,

67 transcription factors was identified in the Strongylocentrotus purpuratus genome using permissive bl

68 rine-threonine (ser-thr) phosphatases in the Strongylocentrotus purpuratus genome, 179 annotated sequ

69 ate all transcription factors encoded in the Strongylocentrotus purpuratus genome, we identified the

70 e in silico several GTPase families from the Strongylocentrotus purpuratus genome: the monomeric Ras

71 The Strongylocentrotus purpuratus hnf6 (Sphnf6) gene encodes

72 The sea urchin Strongylocentrotus purpuratus is a model organism for st

73 Embryonic expression of the Endo16 gene of Strongylocentrotus purpuratus is controlled by interacti

74 The Endo16 gene of Strongylocentrotus purpuratus is expressed at the blastu

75 The CyIIIa cytoskeletal actin gene of Strongylocentrotus purpuratus is expressed specifically

76 sing (gcm) regulatory gene of the sea urchin Strongylocentrotus purpuratus is first expressed in veg2

77 The gatae gene of Strongylocentrotus purpuratus is orthologous to vertebra

78 eletogenesis in the embryo of the sea urchin Strongylocentrotus purpuratus is restricted to the large

79 Now that the genome of the echinoid Strongylocentrotus purpuratus is sequenced, the operatio

80 Now, the genome of the sea urchin Strongylocentrotus purpuratus is the first echinoderm ge

81 The CyIIIa actin gene of Strongylocentrotus purpuratus is transcribed exclusively

82 This gene encodes a TGFbeta ligand, and in Strongylocentrotus purpuratus its transcription is activ

83 ng the complete protein was recovered from a Strongylocentrotus purpuratus library, and sequence comp

84 Strongylocentrotus purpuratus Otx (SpOtx) is required si

85 this finding to identify a cDNA clone from a Strongylocentrotus purpuratus ovary cDNA library that en

86 dentification of a 4.75-kb cDNA clone from a Strongylocentrotus purpuratus ovary cDNA library that en

87 The Strongylocentrotus purpuratus polyketide synthase gene (

88 The genome sequence of the purple sea urchin Strongylocentrotus purpuratus recently became available.

89 Brachyury expression patterns for Strongylocentrotus purpuratus reported in this paper are

90 The Strongylocentrotus purpuratus sea urchin egg receptor fo

91 A reexamination of the cDNA clones of the Strongylocentrotus purpuratus sea urchin egg receptor fo

92 receptors (RyRs) from Lytechinus pictus and Strongylocentrotus purpuratus sea urchin eggs.

93 re we examine forming spicules in embryos of Strongylocentrotus purpuratus sea urchins, and observe a

94 The interaction between recombinant Strongylocentrotus purpuratus sperm bindin and a recombi

95 Here we examine regulation of the Strongylocentrotus purpuratus tbrain gene, a required ac

96 on the surface of the egg of the sea urchin Strongylocentrotus purpuratus that mediates species-spec

97 the ecologically important purple sea urchin Strongylocentrotus purpuratus to adapt to OA, using a br

98 of germ line determinants in the sea urchin Strongylocentrotus purpuratus to examine its mechanism o

99 have utilized the newly sequenced genome of Strongylocentrotus purpuratus to identify genes that hel

100 Spfkh1 is a Strongylocentrotus purpuratus transcription factor that

101 ar cis-regulatory system of the wnt8 gene of Strongylocentrotus purpuratus was characterized function

102 ecifies micromeres and skeletogenic cells in Strongylocentrotus purpuratus We have determined that th

103 IIa cytoplasmic actin gene of the sea urchin Strongylocentrotus purpuratus were determined and compar

104 s with previous findings from the sea urchin Strongylocentrotus purpuratus where L-type and F-type SA

105 scription factor, SpNK2.1, in the sea urchin Strongylocentrotus purpuratus whose transcripts are init

106 ing of a genomic library from the sea urchin Strongylocentrotus purpuratus with a human COUP-TF I cDN

107 alifornia purple sea urchin larval spicules, Strongylocentrotus purpuratus) ACC were studied using is

108 Purple sea urchins (Strongylocentrotus purpuratus) are among the best studie

109 genome-wide selection in purple sea urchins (Strongylocentrotus purpuratus) cultured under different

110 esin-II holoenzyme purified from sea urchin (Strongylocentrotus purpuratus) eggs is assembled from tw

111 Larvae of the purple sea urchin (Strongylocentrotus purpuratus) exhibit dramatic enhancem

112 annotations with respect to the Sea Urchin (Strongylocentrotus purpuratus) genome.

113 e Meisetz are present within the sea urchin (Strongylocentrotus purpuratus) genome.

114 germ cells (PGCs) of the sea urchin embryo (Strongylocentrotus purpuratus) is quiescent.

115 kinesin-C (SpKinC) isolated from sea urchin (Strongylocentrotus purpuratus) is the only reported kine

116 nd B (approximately 51 kDa) from sea urchin (Strongylocentrotus purpuratus) sperm flagellar microtubu

117 EJ from individual females (Strongylocentrotus purpuratus) was analyzed on SDS-PAGE

118 from an invertebrate, the purple sea urchin (Strongylocentrotus purpuratus) with similarity in both s

119 skii and Ptychodera flava and the sea urchin Strongylocentrotus purpuratus).

120 initial phases of sea urchin embryogenesis (Strongylocentrotus purpuratus).

121 in-1, has been described from the sea urchin Strongylocentrotus purpuratus, a basal invertebrate deut

122 Strongylocentrotus purpuratus, a major research model in

123 In embryos of Strongylocentrotus purpuratus, a redox gradient establis

124 The species chosen was Strongylocentrotus purpuratus, a research model of major

125 are present in the genome of the sea urchin Strongylocentrotus purpuratus, all of which are expresse

126 In the sea urchin, Strongylocentrotus purpuratus, an orthodenticle-related

127 erm regulatory state during specification in Strongylocentrotus purpuratus, and show how their spatia

128 cally distributed in the unfertilized egg of Strongylocentrotus purpuratus, and that the polarity of

129 rse of accumulation of these two proteins in Strongylocentrotus purpuratus, both in the intact embryo

130 85/333 gene family in the purple sea urchin, Strongylocentrotus purpuratus, consists of an estimated

131 The purple sea urchin, Strongylocentrotus purpuratus, expresses a diverse immun

132 The blimp1/krox gene of Strongylocentrotus purpuratus, formerly krox1, encodes z

133 has been performed on protein-coding RNAs of Strongylocentrotus purpuratus, including 10 different em

134 CyIIa, a cytoskeletal actin gene of Strongylocentrotus purpuratus, is expressed specifically

135 arly embryogenesis of the purple sea urchin, Strongylocentrotus purpuratus, is well described and can

136 y and characterize a SFK from the sea urchin Strongylocentrotus purpuratus, SpSFK1.

137 ng the early embryogenesis of the sea urchin Strongylocentrotus purpuratus, these technologies can be

138 ring embryonic development of the sea urchin Strongylocentrotus purpuratus, Vasa protein is enriched

139 cis-regulatory elements of the SpHE gene of Strongylocentrotus purpuratus, which is asymmetrically e

140 atial patterns in the pregastrular embryo of Strongylocentrotus purpuratus.

141 The test was carried out on the otx gene of Strongylocentrotus purpuratus.

142 We have cloned cyclin E from the sea urchin Strongylocentrotus purpuratus.

143 ed and sequenced from the purple sea urchin, Strongylocentrotus purpuratus.

144 yte cDNA library from the purple sea urchin, Strongylocentrotus purpuratus.

145 e layer complex of the egg of the sea urchin Strongylocentrotus purpuratus.

146 SpHox8 is the paralog group 8 Hox gene of Strongylocentrotus purpuratus.

147 important predator of the purple sea urchin Strongylocentrotus purpuratus.

148 ent of the larval skeleton in the sea urchin Strongylocentrotus purpuratus.

149 aster, Daphnia pulex, Ciona intestinalis and Strongylocentrotus purpuratus.

150 onsiderable extent in the purple sea urchin, Strongylocentrotus purpuratus.

151 arly embryogenesis of the purple sea urchin, Strongylocentrotus purpuratus.

152 3- transporter from sperm of the sea urchin, Strongylocentrotus purpuratus.

153 al and environmental biology, the sea urchin Strongylocentrotus purpuratus.

154 enes present in the genome of the echinoderm Strongylocentrotus purpuratus.

155 exceptional detail in the purple sea urchin, Strongylocentrotus purpuratus.

156 ors during the development of the sea urchin Strongylocentrotus purpuratus: SpNot, the orthologue of

157 erage intrageneric sequence divergence among Strongylocentrotus species.