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1 flava and the sea urchin Strongylocentrotus purpuratus).
2 sea urchin embryogenesis (Strongylocentrotus purpuratus).
3 in the purple sea urchin, Strongylocentrotus purpuratus.
4 l biology, the sea urchin Strongylocentrotus purpuratus.
5 ed out on the otx gene of Strongylocentrotus purpuratus.
6 lin E from the sea urchin Strongylocentrotus purpuratus.
7 ogastrulation in both S. franciscanus and S. purpuratus.
8 divergent from a closely related species, S. purpuratus.
9 he pregastrular embryo of Strongylocentrotus purpuratus.
10 orphism is decreased with respect to wild S. purpuratus.
11 effector domain of rab3 in Stronglocentrotus purpuratus.
12 om the purple sea urchin, Strongylocentrotus purpuratus.
13 om the purple sea urchin, Strongylocentrotus purpuratus.
14 the egg of the sea urchin Strongylocentrotus purpuratus.
15 s only one Hox gene cluster per genome in S. purpuratus.
16 ralog group 8 Hox gene of Strongylocentrotus purpuratus.
17 keleton in the sea urchin Strongylocentrotus purpuratus.
18 arly embryonic gene regulatory network in S. purpuratus.
19 of the purple sea urchin Strongylocentrotus purpuratus.
20 x, Ciona intestinalis and Strongylocentrotus purpuratus.
21 in the purple sea urchin, Strongylocentrotus purpuratus.
22 ve selection along the lineage leading to S. purpuratus.
23 of the purple sea urchin, Strongylocentrotus purpuratus.
24 sperm of the sea urchin, Strongylocentrotus purpuratus.
25 genome of the echinoderm Strongylocentrotus purpuratus.
29 The species chosen was Strongylocentrotus purpuratus, a research model of major importance in deve
32 a urchin larval spicules, Strongylocentrotus purpuratus) ACC were studied using isothermal acid solut
33 genome of the sea urchin Strongylocentrotus purpuratus, all of which are expressed with different ti
34 mpletion of the genome of Strongylocentrotus purpuratus allows a comprehensive survey of the compleme
36 iginally characterized in Strongylocentrotus purpuratus and encodes an imperfect tandem repeat of six
37 of the purple sea urchin, Strongylocentrotus purpuratus and includes sequence data and genomic resour
38 a similar pattern of Endo16 expression in S. purpuratus and L. variegatus, despite dramatic divergenc
40 x gene were isolated from Strongylocentrotus purpuratus and Lytechinus variegatus libraries, and the
41 m two sea urchin species, Strongylocentrotus purpuratus and Lytechinus variegatus, by screening expre
43 s are highly conserved in Strongylocentrotus purpuratus and Lytechinus variegatus, two sea urchin spe
45 y in vertebrates, in both Strongylocentrotus purpuratus and Nematostella vectensis suggests that this
46 om eggs of the sea urchin Strongylocentrotus purpuratus and the gene was cloned by PCR using oligonuc
47 beta1/2 in the sea urchin Strongylocentrotus purpuratus and the sea star Asterina miniata provides an
48 247 amino acids, binds both the sperm of S. purpuratus and the sperm of another genus of sea urchin,
49 e during specification in Strongylocentrotus purpuratus, and show how their spatial expression change
50 n the unfertilized egg of Strongylocentrotus purpuratus, and that the polarity of the maternal asymme
53 gg membrane-associated protein in eggs of S. purpuratus as well as another sea urchin Lytechinus vari
54 -regulatory region from 15 individuals of S. purpuratus as well as seven closely related species in t
55 base pairs long, were amplified from the S. purpuratus BAC DNA by PCR, inserted in an expression vec
56 of these two proteins in Strongylocentrotus purpuratus, both in the intact embryo and in micromere c
59 in the purple sea urchin, Strongylocentrotus purpuratus, consists of an estimated 50 (+/-10) members
60 ingle Hox gene complex of Strongylocentrotus purpuratus contains 10 genes, and expression of eight of
61 contrast, the echinoderm Strongylocentrotus purpuratus contains a 588 kb cluster of 11 orthologs of
62 cluster of the sea urchin Strongylocentrous purpuratus contains ten genes in a 500 kb span of the ge
65 e Grl from the sea urchin Strongylocentrotus purpuratus displays similar patterns of developmental ex
67 oligosialic acid chains derived from the S. purpuratus egg cell surface complex inhibited fertilizat
68 ection of an antibody against SpSFK1 into S. purpuratus eggs also causes a small increase in the dela
69 the cortical granules of Strongylocentrotus purpuratus eggs, and here we examined the regulation of
70 in lysates of L. variegatus eggs, but not S. purpuratus eggs, the antibody stimulates SFK activity.
72 purified from sea urchin (Strongylocentrotus purpuratus) eggs is assembled from two heterodimerized k
73 ier of the sixth cleavage Strongylocentrotus purpuratus embryo contributes progeny to both ectodermal
74 lete repertoire of genes expressed in the S. purpuratus embryo, up to late gastrula stage, by means o
79 s sea urchin genomic fragment as probe, a S. purpuratus embryonic cDNA library was screened and two d
80 s in the blastula wall of Strongylocentrotus purpuratus embryos at the mesenchyme blastula stage.
81 ge veg1 and veg2 tiers of Strongylocentrotus purpuratus embryos were labeled with DiI lineage tracer,
82 first two blastomeres of Strongylocentrotus purpuratus embryos were separated and the resulting twin
85 Here, we identify the Strongylocentrotus purpuratus enzymes responsible for the formation of epsi
86 he PGCs of the sea urchin Strongylocentrotus purpuratus exhibit broad transcriptional repression, yet
87 of the purple sea urchin (Strongylocentrotus purpuratus) exhibit dramatic enhancement in settlement f
88 r sperm of the sea urchin Strongylocentrotus purpuratus exhibits several characteristics that are con
89 The purple sea urchin, Strongylocentrotus purpuratus, expresses a diverse immune response protein
90 e temporal and quantitative features, the S. purpuratus expression construct is expressed accurately
91 lysis of the S. purpuratus pks and of one S. purpuratus fmo was carried out using antisense technolog
92 of the purple sea urchin Strongylocentrotus purpuratus for gene products involved in biomineralizati
93 The blimp1/krox gene of Strongylocentrotus purpuratus, formerly krox1, encodes zinc finger transcri
94 Phylogenetic analysis suggests that one S. purpuratus fox gene is equally related to foxA and foxB
96 tissue stereom, can be identified in the S. purpuratus genome and are likely to be the same genes th
97 notated in the sea urchin Strongylocentrotus purpuratus genome and the embryonic expression of key co
98 Like all of us, I am excited to see the S. purpuratus genome appear and heartily congratulate, by w
99 e models derived from the Strongylocentrotus purpuratus genome assembly and have gathered strong evid
100 es were identified in the Strongylocentrotus purpuratus genome by means of a permissive blast search
102 e surveyed the sea urchin Strongylocentrotus purpuratus genome for homologs of gene families thought
103 rse organisms was assembled to search the S. purpuratus genome for homologs, and the expression patte
104 n vertebrate genomes, the Strongylocentrotus purpuratus genome has orthologues of all but four (E, H,
108 out in the context of the Strongylocentrotus purpuratus genome sequencing project, and results from s
109 ors was identified in the Strongylocentrotus purpuratus genome using permissive blast searches with a
110 -thr) phosphatases in the Strongylocentrotus purpuratus genome, 179 annotated sequences were studied
111 on factors encoded in the Strongylocentrotus purpuratus genome, we identified the C2H2 zinc finger ge
114 GTPase families from the Strongylocentrotus purpuratus genome: the monomeric Ras superfamily, the he
118 on protein-coding RNAs of Strongylocentrotus purpuratus, including 10 different embryonic stages, six
120 binant EGF4 from both S. franciscanus and S. purpuratus induces exogastrula in a species-specific man
122 w the feeding rate of P. helianthoides on S. purpuratus is affected by temperature in laboratory test
123 ion of the Endo16 gene of Strongylocentrotus purpuratus is controlled by interactions with at least 1
125 ytoskeletal actin gene of Strongylocentrotus purpuratus is expressed specifically in the aboral ectod
126 ry gene of the sea urchin Strongylocentrotus purpuratus is first expressed in veg2 daughter cells as
128 embryo of the sea urchin Strongylocentrotus purpuratus is restricted to the large micromere lineage
129 he genome of the echinoid Strongylocentrotus purpuratus is sequenced, the operation of its genes can
130 te that the effect of P. helianthoides on S. purpuratus is strongly mediated by temperature, and that
131 genome of the sea urchin Strongylocentrotus purpuratus is the first echinoderm genome to be sequence
132 The CyIIIa actin gene of Strongylocentrotus purpuratus is transcribed exclusively in the embryonic a
134 isolated from sea urchin (Strongylocentrotus purpuratus) is the only reported kinesin with a CBD.
135 ytoskeletal actin gene of Strongylocentrotus purpuratus, is expressed specifically though transiently
136 of the purple sea urchin, Strongylocentrotus purpuratus, is well described and can serve as an excell
137 a TGFbeta ligand, and in Strongylocentrotus purpuratus its transcription is activated in the presump
138 tein was recovered from a Strongylocentrotus purpuratus library, and sequence comparisons demonstrate
139 used to obtain cDNA clones of SpMyb, the S. purpuratus member of the myb family of transcription fac
141 4.75-kb cDNA clone from a Strongylocentrotus purpuratus ovary cDNA library that encodes a 160-kDa pro
142 ntify a cDNA clone from a Strongylocentrotus purpuratus ovary cDNA library that encodes a 581-amino-a
143 a gene in the sea urchin Strongylocentrotus purpuratus (phylum Echinodermata) encoding a precursor p
149 y expression patterns for Strongylocentrotus purpuratus reported in this paper are entirely consisten
151 of the cDNA clones of the Strongylocentrotus purpuratus sea urchin egg receptor for sperm resulted in
153 ng spicules in embryos of Strongylocentrotus purpuratus sea urchins, and observe a sequence of three
155 its the first cleavage of Strongylocentrotus purpuratus (sea urchin) embryos in a concentration-depen
156 gulatory modules from the Strongylocentrotus purpuratus (sea urchin) genome and obtained orthologous
157 functionally characterized Stronglycentrotus purpuratus (Sp) ATP-binding cassette (ABC) transporters.
158 egulatory analysis of the Strongylocentrotus purpuratus (Sp) endo16 gene was that the later expressio
160 genome of the sea urchin Strongylocentrotus purpuratus (Sp), and each nanos mRNA accumulates specifi
162 oid, the well-known model Strongylocentrotus purpuratus (Sp), vs. the cidaroid Eucidaris tribuloides
164 hologous to the previously reported genes S. purpuratus SpEGF-II and Anthocidaris crassispina AcEGF-I
165 ated signaling pathway in Strongylocentrotus purpuratus (speract being a sperm-activating peptide spe
166 ction between recombinant Strongylocentrotus purpuratus sperm bindin and a recombinant fragment of th
167 51 kDa) from sea urchin (Strongylocentrotus purpuratus) sperm flagellar microtubules, and compared t
168 issing regulatory gene of Strongylocentrotus purpuratus (spgcm) was proposed earlier to be the genomi
169 lopment of the sea urchin Strongylocentrotus purpuratus: SpNot, the orthologue of the vertebrate Not
172 examine regulation of the Strongylocentrotus purpuratus tbrain gene, a required activator of the skel
173 the egg of the sea urchin Strongylocentrotus purpuratus that mediates species-specific binding of spe
174 genesis of the sea urchin Strongylocentrotus purpuratus, these technologies can be applied generally.
175 portant purple sea urchin Strongylocentrotus purpuratus to adapt to OA, using a breeding experiment t
176 minants in the sea urchin Strongylocentrotus purpuratus to examine its mechanism of germ line determi
177 newly sequenced genome of Strongylocentrotus purpuratus to identify genes that help the oocyte accomp
179 f the purple sea urchin ( Strongylocentrotus purpuratus ), using high-resolution X-ray photoelectron
180 lopment of the sea urchin Strongylocentrotus purpuratus, Vasa protein is enriched in the small microm
181 ystem of the wnt8 gene of Strongylocentrotus purpuratus was characterized functionally, and shown to
182 degrees C, P. helianthoides were common, S. purpuratus was rare and kelp was persistent, whereas whe
184 and skeletogenic cells in Strongylocentrotus purpuratus We have determined that the DNG has likely be
185 in gene of the sea urchin Strongylocentrotus purpuratus were determined and compared to the genomical
186 odifiers predicted from the annotation of S. purpuratus, were compared against cnidarians, arthropods
187 dings from the sea urchin Strongylocentrotus purpuratus where L-type and F-type SALMFamides are encod
188 ments of the SpHE gene of Strongylocentrotus purpuratus, which is asymmetrically expressed along this
189 pNK2.1, in the sea urchin Strongylocentrotus purpuratus whose transcripts are initially detected with
190 brary from the sea urchin Strongylocentrotus purpuratus with a human COUP-TF I cDNA probe revealed th
191 e, the purple sea urchin (Strongylocentrotus purpuratus) with similarity in both sequence and genomic
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