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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                            A comparison with Strongylocentrotus purpuratus embryo single-cell transcr
45 ll endomesoderm specification network of the Strongylocentrotus purpuratus embryo.
46  comprise the integral spicule matrix of the Strongylocentrotus purpuratus embryo.
47  endomesoderm gene regulatory network in the Strongylocentrotus purpuratus embryo.
48                                       During Strongylocentrotus purpuratus embryogenesis, aboral ecto
49 llular matrix layers in the blastula wall of Strongylocentrotus purpuratus embryos at the mesenchyme
50 of the sixth-cleavage veg1 and veg2 tiers of Strongylocentrotus purpuratus embryos were labeled with
51                 The first two blastomeres of Strongylocentrotus purpuratus embryos were separated and
52                           The endo16 gene of Strongylocentrotus purpuratus encodes a secreted protein
53 f the process used to build our model of the Strongylocentrotus purpuratus endomesoderm gene network.
54                        Here, we identify the Strongylocentrotus purpuratus enzymes responsible for th
55      We find that the PGCs of the sea urchin Strongylocentrotus purpuratus exhibit broad transcriptio
56 a choanoflagellate and the purple sea urchin Strongylocentrotus purpuratus exhibit striking structura
57 the egg receptor for sperm of the sea urchin Strongylocentrotus purpuratus exhibits several character
58 o survey the genome of the purple sea urchin Strongylocentrotus purpuratus for gene products involved
59 e identified and annotated in the sea urchin Strongylocentrotus purpuratus genome and the embryonic e
60  an analysis of gene models derived from the Strongylocentrotus purpuratus genome assembly and have g
61 ther smaller families were identified in the Strongylocentrotus purpuratus genome by means of a permi
62                                          The Strongylocentrotus purpuratus genome contains a single t
63                   We surveyed the sea urchin Strongylocentrotus purpuratus genome for homologs of gen
64 lasses identified in vertebrate genomes, the Strongylocentrotus purpuratus genome has orthologues of
65                              Analysis of the Strongylocentrotus purpuratus genome has revealed approx
66                          The sequence of the Strongylocentrotus purpuratus genome offers unique oppor
67                            Annotation of the Strongylocentrotus purpuratus genome sequence led to the
68 embryo was carried out in the context of the Strongylocentrotus purpuratus genome sequencing project,
69  transcription factors was identified in the Strongylocentrotus purpuratus genome using permissive bl
70 rine-threonine (ser-thr) phosphatases in the Strongylocentrotus purpuratus genome, 179 annotated sequ
71 ate all transcription factors encoded in the Strongylocentrotus purpuratus genome, we identified the
72 e in silico several GTPase families from the Strongylocentrotus purpuratus genome: the monomeric Ras
73                                          The Strongylocentrotus purpuratus hnf6 (Sphnf6) gene encodes
74                               The sea urchin Strongylocentrotus purpuratus is a model organism for st
75   Embryonic expression of the Endo16 gene of Strongylocentrotus purpuratus is controlled by interacti
76                           The Endo16 gene of Strongylocentrotus purpuratus is expressed at the blastu
77        The CyIIIa cytoskeletal actin gene of Strongylocentrotus purpuratus is expressed specifically
78 sing (gcm) regulatory gene of the sea urchin Strongylocentrotus purpuratus is first expressed in veg2
79                            The gatae gene of Strongylocentrotus purpuratus is orthologous to vertebra
80 eletogenesis in the embryo of the sea urchin Strongylocentrotus purpuratus is restricted to the large
81          Now that the genome of the echinoid Strongylocentrotus purpuratus is sequenced, the operatio
82            Now, the genome of the sea urchin Strongylocentrotus purpuratus is the first echinoderm ge
83                     The CyIIIa actin gene of Strongylocentrotus purpuratus is transcribed exclusively
84   This gene encodes a TGFbeta ligand, and in Strongylocentrotus purpuratus its transcription is activ
85 ng the complete protein was recovered from a Strongylocentrotus purpuratus library, and sequence comp
86                                              Strongylocentrotus purpuratus Otx (SpOtx) is required si
87 this finding to identify a cDNA clone from a Strongylocentrotus purpuratus ovary cDNA library that en
88 dentification of a 4.75-kb cDNA clone from a Strongylocentrotus purpuratus ovary cDNA library that en
89                                          The Strongylocentrotus purpuratus polyketide synthase gene (
90 The genome sequence of the purple sea urchin Strongylocentrotus purpuratus recently became available.
91            Brachyury expression patterns for Strongylocentrotus purpuratus reported in this paper are
92                                          The Strongylocentrotus purpuratus sea urchin egg receptor fo
93    A reexamination of the cDNA clones of the Strongylocentrotus purpuratus sea urchin egg receptor fo
94  receptors (RyRs) from Lytechinus pictus and Strongylocentrotus purpuratus sea urchin eggs.
95 re we examine forming spicules in embryos of Strongylocentrotus purpuratus sea urchins, and observe a
96 orms, we demonstrate for the first time that Strongylocentrotus purpuratus sperm are chemotactic and
97          The interaction between recombinant Strongylocentrotus purpuratus sperm bindin and a recombi
98            Here we examine regulation of the Strongylocentrotus purpuratus tbrain gene, a required ac
99  on the surface of the egg of the sea urchin Strongylocentrotus purpuratus that mediates species-spec
100 the ecologically important purple sea urchin Strongylocentrotus purpuratus to adapt to OA, using a br
101  of germ line determinants in the sea urchin Strongylocentrotus purpuratus to examine its mechanism o
102  have utilized the newly sequenced genome of Strongylocentrotus purpuratus to identify genes that hel
103                                  Spfkh1 is a Strongylocentrotus purpuratus transcription factor that
104 ar cis-regulatory system of the wnt8 gene of Strongylocentrotus purpuratus was characterized function
105 ecifies micromeres and skeletogenic cells in Strongylocentrotus purpuratus We have determined that th
106 nesis of a model echinoderm: the sea urchin, Strongylocentrotus purpuratus We identified more than 18
107 IIa cytoplasmic actin gene of the sea urchin Strongylocentrotus purpuratus were determined and compar
108 s with previous findings from the sea urchin Strongylocentrotus purpuratus where L-type and F-type SA
109 scription factor, SpNK2.1, in the sea urchin Strongylocentrotus purpuratus whose transcripts are init
110 ing of a genomic library from the sea urchin Strongylocentrotus purpuratus with a human COUP-TF I cDN
111 alifornia purple sea urchin larval spicules, Strongylocentrotus purpuratus) ACC were studied using is
112                          Purple sea urchins (Strongylocentrotus purpuratus) are among the best studie
113 genome-wide selection in purple sea urchins (Strongylocentrotus purpuratus) cultured under different
114 esin-II holoenzyme purified from sea urchin (Strongylocentrotus purpuratus) eggs is assembled from tw
115             Larvae of the purple sea urchin (Strongylocentrotus purpuratus) exhibit dramatic enhancem
116 h a fundamental change in purple sea urchin (Strongylocentrotus purpuratus) foraging behavior and con
117 e Meisetz are present within the sea urchin (Strongylocentrotus purpuratus) genome.
118  annotations with respect to the Sea Urchin (Strongylocentrotus purpuratus) genome.
119  germ cells (PGCs) of the sea urchin embryo (Strongylocentrotus purpuratus) is quiescent.
120 kinesin-C (SpKinC) isolated from sea urchin (Strongylocentrotus purpuratus) is the only reported kine
121 ected the performance of purple sea urchins (Strongylocentrotus purpuratus) sourced from rapidly-decl
122 nd B (approximately 51 kDa) from sea urchin (Strongylocentrotus purpuratus) sperm flagellar microtubu
123                  EJ from individual females (Strongylocentrotus purpuratus) was analyzed on SDS-PAGE
124 from an invertebrate, the purple sea urchin (Strongylocentrotus purpuratus) with similarity in both s
125 at an abrupt outbreak of purple sea urchins (Strongylocentrotus purpuratus), which occurred in 2014 i
126  initial phases of sea urchin embryogenesis (Strongylocentrotus purpuratus).
127 skii and Ptychodera flava and the sea urchin Strongylocentrotus purpuratus).
128 lone (Haliotis rufescens) and purple urchin (Strongylocentrotus purpuratus).
129 in-1, has been described from the sea urchin Strongylocentrotus purpuratus, a basal invertebrate deut
130 tiple biological processes in the sea urchin Strongylocentrotus purpuratus, a key grazer in Californi
131                                              Strongylocentrotus purpuratus, a major research model in
132                                In embryos of Strongylocentrotus purpuratus, a redox gradient establis
133                       The species chosen was Strongylocentrotus purpuratus, a research model of major
134  are present in the genome of the sea urchin Strongylocentrotus purpuratus, all of which are expresse
135  of pigmented cells in the purple sea urchin Strongylocentrotus purpuratus, an emerging model for div
136                           In the sea urchin, Strongylocentrotus purpuratus, an orthodenticle-related
137 erm regulatory state during specification in Strongylocentrotus purpuratus, and show how their spatia
138 cally distributed in the unfertilized egg of Strongylocentrotus purpuratus, and that the polarity of
139 rse of accumulation of these two proteins in Strongylocentrotus purpuratus, both in the intact embryo
140 85/333 gene family in the purple sea urchin, Strongylocentrotus purpuratus, consists of an estimated
141                       The purple sea urchin, Strongylocentrotus purpuratus, expresses a diverse immun
142                      The blimp1/krox gene of Strongylocentrotus purpuratus, formerly krox1, encodes z
143      We tested eight developmental stages in Strongylocentrotus purpuratus, from the eight-cell stage
144 ey ecosystem engineer, the purple sea urchin Strongylocentrotus purpuratus, in experimental mesocosms
145 has been performed on protein-coding RNAs of Strongylocentrotus purpuratus, including 10 different em
146          CyIIa, a cytoskeletal actin gene of Strongylocentrotus purpuratus, is expressed specifically
147 arly embryogenesis of the purple sea urchin, Strongylocentrotus purpuratus, is well described and can
148 y and characterize a SFK from the sea urchin Strongylocentrotus purpuratus, SpSFK1.
149 ng the early embryogenesis of the sea urchin Strongylocentrotus purpuratus, these technologies can be
150 ring embryonic development of the sea urchin Strongylocentrotus purpuratus, Vasa protein is enriched
151  cis-regulatory elements of the SpHE gene of Strongylocentrotus purpuratus, which is asymmetrically e
152 exceptional detail in the purple sea urchin, Strongylocentrotus purpuratus.
153  The test was carried out on the otx gene of Strongylocentrotus purpuratus.
154  We have cloned cyclin E from the sea urchin Strongylocentrotus purpuratus.
155 al and environmental biology, the sea urchin Strongylocentrotus purpuratus.
156 ed and sequenced from the purple sea urchin, Strongylocentrotus purpuratus.
157 yte cDNA library from the purple sea urchin, Strongylocentrotus purpuratus.
158 atial patterns in the pregastrular embryo of Strongylocentrotus purpuratus.
159 e layer complex of the egg of the sea urchin Strongylocentrotus purpuratus.
160    SpHox8 is the paralog group 8 Hox gene of Strongylocentrotus purpuratus.
161 f the kirrelL gene of the purple sea urchin, Strongylocentrotus purpuratus.
162 ent of the larval skeleton in the sea urchin Strongylocentrotus purpuratus.
163 aster, Daphnia pulex, Ciona intestinalis and Strongylocentrotus purpuratus.
164 onsiderable extent in the purple sea urchin, Strongylocentrotus purpuratus.
165  important predator of the purple sea urchin Strongylocentrotus purpuratus.
166 arly embryogenesis of the purple sea urchin, Strongylocentrotus purpuratus.
167 3- transporter from sperm of the sea urchin, Strongylocentrotus purpuratus.
168 enes present in the genome of the echinoderm Strongylocentrotus purpuratus.
169 ors during the development of the sea urchin Strongylocentrotus purpuratus: SpNot, the orthologue of
170 erage intrageneric sequence divergence among Strongylocentrotus species.

 
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