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1  initial phases of sea urchin embryogenesis (Strongylocentrotus purpuratus).
2 skii and Ptychodera flava and the sea urchin Strongylocentrotus purpuratus).
3 lone (Haliotis rufescens) and purple urchin (Strongylocentrotus purpuratus).
4  The test was carried out on the otx gene of Strongylocentrotus purpuratus.
5  We have cloned cyclin E from the sea urchin Strongylocentrotus purpuratus.
6 al and environmental biology, the sea urchin Strongylocentrotus purpuratus.
7 ed and sequenced from the purple sea urchin, Strongylocentrotus purpuratus.
8 yte cDNA library from the purple sea urchin, Strongylocentrotus purpuratus.
9 atial patterns in the pregastrular embryo of Strongylocentrotus purpuratus.
10 e layer complex of the egg of the sea urchin Strongylocentrotus purpuratus.
11    SpHox8 is the paralog group 8 Hox gene of Strongylocentrotus purpuratus.
12 f the kirrelL gene of the purple sea urchin, Strongylocentrotus purpuratus.
13 ent of the larval skeleton in the sea urchin Strongylocentrotus purpuratus.
14 aster, Daphnia pulex, Ciona intestinalis and Strongylocentrotus purpuratus.
15 onsiderable extent in the purple sea urchin, Strongylocentrotus purpuratus.
16  important predator of the purple sea urchin Strongylocentrotus purpuratus.
17 arly embryogenesis of the purple sea urchin, Strongylocentrotus purpuratus.
18 3- transporter from sperm of the sea urchin, Strongylocentrotus purpuratus.
19 enes present in the genome of the echinoderm Strongylocentrotus purpuratus.
20 exceptional detail in the purple sea urchin, Strongylocentrotus purpuratus.
21 in-1, has been described from the sea urchin Strongylocentrotus purpuratus, a basal invertebrate deut
22 tiple biological processes in the sea urchin Strongylocentrotus purpuratus, a key grazer in Californi
23                                              Strongylocentrotus purpuratus, a major research model in
24                                In embryos of Strongylocentrotus purpuratus, a redox gradient establis
25                       The species chosen was Strongylocentrotus purpuratus, a research model of major
26 alifornia purple sea urchin larval spicules, Strongylocentrotus purpuratus) ACC were studied using is
27  are present in the genome of the sea urchin Strongylocentrotus purpuratus, all of which are expresse
28              The completion of the genome of Strongylocentrotus purpuratus allows a comprehensive sur
29  of pigmented cells in the purple sea urchin Strongylocentrotus purpuratus, an emerging model for div
30                           In the sea urchin, Strongylocentrotus purpuratus, an orthodenticle-related
31    This gene was originally characterized in Strongylocentrotus purpuratus and encodes an imperfect t
32 t genomic sequence of the purple sea urchin, Strongylocentrotus purpuratus and includes sequence data
33 s containing the otx gene were isolated from Strongylocentrotus purpuratus and Lytechinus variegatus
34                                              Strongylocentrotus purpuratus and Lytechinus variegatus
35 two distantly related species of sea urchin, Strongylocentrotus purpuratus and Lytechinus variegatus,
36 were identified from two sea urchin species, Strongylocentrotus purpuratus and Lytechinus variegatus,
37 that these two genes are highly conserved in Strongylocentrotus purpuratus and Lytechinus variegatus,
38 icted from cDNAs of two sea urchins species, Strongylocentrotus purpuratus and Lytechinus variegatus.
39 reviously known only in vertebrates, in both Strongylocentrotus purpuratus and Nematostella vectensis
40 ad been purified from eggs of the sea urchin Strongylocentrotus purpuratus and the gene was cloned by
41 tory control of otxbeta1/2 in the sea urchin Strongylocentrotus purpuratus and the sea star Asterina
42 erm regulatory state during specification in Strongylocentrotus purpuratus, and show how their spatia
43 cally distributed in the unfertilized egg of Strongylocentrotus purpuratus, and that the polarity of
44                                spec genes in Strongylocentrotus purpuratus are invariably associated
45                          Purple sea urchins (Strongylocentrotus purpuratus) are among the best studie
46 rse of accumulation of these two proteins in Strongylocentrotus purpuratus, both in the intact embryo
47                                        Eight Strongylocentrotus purpuratus cis-regulatory modules, in
48                            In the sea urchin Strongylocentrotus purpuratus (class Echinoidea) there a
49 85/333 gene family in the purple sea urchin, Strongylocentrotus purpuratus, consists of an estimated
50               The single Hox gene complex of Strongylocentrotus purpuratus contains 10 genes, and exp
51                  In contrast, the echinoderm Strongylocentrotus purpuratus contains a 588 kb cluster
52 genome-wide selection in purple sea urchins (Strongylocentrotus purpuratus) cultured under different
53                                          The Strongylocentrotus purpuratus cyclophilin1 gene (Sp-cyp1
54       A deuterostome Grl from the sea urchin Strongylocentrotus purpuratus displays similar patterns
55 urchins from the polymorphism of a sample of Strongylocentrotus purpuratus DNA (R(u) = 3-4).
56  been identified in the cortical granules of Strongylocentrotus purpuratus eggs, and here we examined
57 esin-II holoenzyme purified from sea urchin (Strongylocentrotus purpuratus) eggs is assembled from tw
58 elopment the veg1 tier of the sixth cleavage Strongylocentrotus purpuratus embryo contributes progeny
59                            A comparison with Strongylocentrotus purpuratus embryo single-cell transcr
60  comprise the integral spicule matrix of the Strongylocentrotus purpuratus embryo.
61  endomesoderm gene regulatory network in the Strongylocentrotus purpuratus embryo.
62 ll endomesoderm specification network of the Strongylocentrotus purpuratus embryo.
63                                       During Strongylocentrotus purpuratus embryogenesis, aboral ecto
64 llular matrix layers in the blastula wall of Strongylocentrotus purpuratus embryos at the mesenchyme
65 of the sixth-cleavage veg1 and veg2 tiers of Strongylocentrotus purpuratus embryos were labeled with
66                 The first two blastomeres of Strongylocentrotus purpuratus embryos were separated and
67                           The endo16 gene of Strongylocentrotus purpuratus encodes a secreted protein
68 f the process used to build our model of the Strongylocentrotus purpuratus endomesoderm gene network.
69                        Here, we identify the Strongylocentrotus purpuratus enzymes responsible for th
70      We find that the PGCs of the sea urchin Strongylocentrotus purpuratus exhibit broad transcriptio
71 a choanoflagellate and the purple sea urchin Strongylocentrotus purpuratus exhibit striking structura
72             Larvae of the purple sea urchin (Strongylocentrotus purpuratus) exhibit dramatic enhancem
73 the egg receptor for sperm of the sea urchin Strongylocentrotus purpuratus exhibits several character
74                       The purple sea urchin, Strongylocentrotus purpuratus, expresses a diverse immun
75 o survey the genome of the purple sea urchin Strongylocentrotus purpuratus for gene products involved
76 h a fundamental change in purple sea urchin (Strongylocentrotus purpuratus) foraging behavior and con
77                      The blimp1/krox gene of Strongylocentrotus purpuratus, formerly krox1, encodes z
78      We tested eight developmental stages in Strongylocentrotus purpuratus, from the eight-cell stage
79 e identified and annotated in the sea urchin Strongylocentrotus purpuratus genome and the embryonic e
80  an analysis of gene models derived from the Strongylocentrotus purpuratus genome assembly and have g
81 ther smaller families were identified in the Strongylocentrotus purpuratus genome by means of a permi
82                                          The Strongylocentrotus purpuratus genome contains a single t
83                   We surveyed the sea urchin Strongylocentrotus purpuratus genome for homologs of gen
84 lasses identified in vertebrate genomes, the Strongylocentrotus purpuratus genome has orthologues of
85                              Analysis of the Strongylocentrotus purpuratus genome has revealed approx
86                          The sequence of the Strongylocentrotus purpuratus genome offers unique oppor
87                            Annotation of the Strongylocentrotus purpuratus genome sequence led to the
88 embryo was carried out in the context of the Strongylocentrotus purpuratus genome sequencing project,
89  transcription factors was identified in the Strongylocentrotus purpuratus genome using permissive bl
90 rine-threonine (ser-thr) phosphatases in the Strongylocentrotus purpuratus genome, 179 annotated sequ
91 ate all transcription factors encoded in the Strongylocentrotus purpuratus genome, we identified the
92 e in silico several GTPase families from the Strongylocentrotus purpuratus genome: the monomeric Ras
93 e Meisetz are present within the sea urchin (Strongylocentrotus purpuratus) genome.
94  annotations with respect to the Sea Urchin (Strongylocentrotus purpuratus) genome.
95                                          The Strongylocentrotus purpuratus hnf6 (Sphnf6) gene encodes
96 ey ecosystem engineer, the purple sea urchin Strongylocentrotus purpuratus, in experimental mesocosms
97 has been performed on protein-coding RNAs of Strongylocentrotus purpuratus, including 10 different em
98                               The sea urchin Strongylocentrotus purpuratus is a model organism for st
99   Embryonic expression of the Endo16 gene of Strongylocentrotus purpuratus is controlled by interacti
100                           The Endo16 gene of Strongylocentrotus purpuratus is expressed at the blastu
101        The CyIIIa cytoskeletal actin gene of Strongylocentrotus purpuratus is expressed specifically
102 sing (gcm) regulatory gene of the sea urchin Strongylocentrotus purpuratus is first expressed in veg2
103                            The gatae gene of Strongylocentrotus purpuratus is orthologous to vertebra
104 eletogenesis in the embryo of the sea urchin Strongylocentrotus purpuratus is restricted to the large
105          Now that the genome of the echinoid Strongylocentrotus purpuratus is sequenced, the operatio
106            Now, the genome of the sea urchin Strongylocentrotus purpuratus is the first echinoderm ge
107                     The CyIIIa actin gene of Strongylocentrotus purpuratus is transcribed exclusively
108  germ cells (PGCs) of the sea urchin embryo (Strongylocentrotus purpuratus) is quiescent.
109 kinesin-C (SpKinC) isolated from sea urchin (Strongylocentrotus purpuratus) is the only reported kine
110          CyIIa, a cytoskeletal actin gene of Strongylocentrotus purpuratus, is expressed specifically
111 arly embryogenesis of the purple sea urchin, Strongylocentrotus purpuratus, is well described and can
112   This gene encodes a TGFbeta ligand, and in Strongylocentrotus purpuratus its transcription is activ
113 ng the complete protein was recovered from a Strongylocentrotus purpuratus library, and sequence comp
114                                              Strongylocentrotus purpuratus Otx (SpOtx) is required si
115 this finding to identify a cDNA clone from a Strongylocentrotus purpuratus ovary cDNA library that en
116 dentification of a 4.75-kb cDNA clone from a Strongylocentrotus purpuratus ovary cDNA library that en
117 th the discovery of a gene in the sea urchin Strongylocentrotus purpuratus (phylum Echinodermata) enc
118                                          The Strongylocentrotus purpuratus polyketide synthase gene (
119 The genome sequence of the purple sea urchin Strongylocentrotus purpuratus recently became available.
120            Brachyury expression patterns for Strongylocentrotus purpuratus reported in this paper are
121                                          The Strongylocentrotus purpuratus sea urchin egg receptor fo
122    A reexamination of the cDNA clones of the Strongylocentrotus purpuratus sea urchin egg receptor fo
123  receptors (RyRs) from Lytechinus pictus and Strongylocentrotus purpuratus sea urchin eggs.
124 re we examine forming spicules in embryos of Strongylocentrotus purpuratus sea urchins, and observe a
125                             The echinoderms, Strongylocentrotus purpuratus (sea urchin) and Patiria m
126 oxycoumarin]) inhibits the first cleavage of Strongylocentrotus purpuratus (sea urchin) embryos in a
127 haracterized cis-regulatory modules from the Strongylocentrotus purpuratus (sea urchin) genome and ob
128 ected the performance of purple sea urchins (Strongylocentrotus purpuratus) sourced from rapidly-decl
129  our detailed cis-regulatory analysis of the Strongylocentrotus purpuratus (Sp) endo16 gene was that
130  are present in the genome of the sea urchin Strongylocentrotus purpuratus (Sp), and each nanos mRNA
131 s of Sp-PMCA and Sp-SERCA in the sea urchin, Strongylocentrotus purpuratus (Sp), have been published.
132 enesis in a euechinoid, the well-known model Strongylocentrotus purpuratus (Sp), vs. the cidaroid Euc
133 orted speract-activated signaling pathway in Strongylocentrotus purpuratus (speract being a sperm-act
134 orms, we demonstrate for the first time that Strongylocentrotus purpuratus sperm are chemotactic and
135          The interaction between recombinant Strongylocentrotus purpuratus sperm bindin and a recombi
136 nd B (approximately 51 kDa) from sea urchin (Strongylocentrotus purpuratus) sperm flagellar microtubu
137   The glial cells missing regulatory gene of Strongylocentrotus purpuratus (spgcm) was proposed earli
138 ors during the development of the sea urchin Strongylocentrotus purpuratus: SpNot, the orthologue of
139 y and characterize a SFK from the sea urchin Strongylocentrotus purpuratus, SpSFK1.
140            Here we examine regulation of the Strongylocentrotus purpuratus tbrain gene, a required ac
141  on the surface of the egg of the sea urchin Strongylocentrotus purpuratus that mediates species-spec
142 ng the early embryogenesis of the sea urchin Strongylocentrotus purpuratus, these technologies can be
143 the ecologically important purple sea urchin Strongylocentrotus purpuratus to adapt to OA, using a br
144  of germ line determinants in the sea urchin Strongylocentrotus purpuratus to examine its mechanism o
145  have utilized the newly sequenced genome of Strongylocentrotus purpuratus to identify genes that hel
146                                  Spfkh1 is a Strongylocentrotus purpuratus transcription factor that
147 ions in the tooth of the purple sea urchin ( Strongylocentrotus purpuratus ), using high-resolution X
148 ring embryonic development of the sea urchin Strongylocentrotus purpuratus, Vasa protein is enriched
149 ar cis-regulatory system of the wnt8 gene of Strongylocentrotus purpuratus was characterized function
150                  EJ from individual females (Strongylocentrotus purpuratus) was analyzed on SDS-PAGE
151 ecifies micromeres and skeletogenic cells in Strongylocentrotus purpuratus We have determined that th
152 nesis of a model echinoderm: the sea urchin, Strongylocentrotus purpuratus We identified more than 18
153 IIa cytoplasmic actin gene of the sea urchin Strongylocentrotus purpuratus were determined and compar
154 s with previous findings from the sea urchin Strongylocentrotus purpuratus where L-type and F-type SA
155 at an abrupt outbreak of purple sea urchins (Strongylocentrotus purpuratus), which occurred in 2014 i
156  cis-regulatory elements of the SpHE gene of Strongylocentrotus purpuratus, which is asymmetrically e
157 scription factor, SpNK2.1, in the sea urchin Strongylocentrotus purpuratus whose transcripts are init
158 ing of a genomic library from the sea urchin Strongylocentrotus purpuratus with a human COUP-TF I cDN
159 from an invertebrate, the purple sea urchin (Strongylocentrotus purpuratus) with similarity in both s

 
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