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1 ved in a distantly related anuran amphibian (Xenopus tropicalis).
2 s musculus), and 2 frogs (Xenopus laevis and Xenopus tropicalis).
3 EP1 and tHEP2) from the Western clawed frog (Xenopus tropicalis).
4 sorder-associated IMPDH2 mutant, S160del, in Xenopus tropicalis.
5 ebrafish, and microphthalmia and coloboma in Xenopus tropicalis.
6 in to specify initial competence in the frog Xenopus tropicalis.
7 odal signaling during early embryogenesis in Xenopus tropicalis.
8  plays important roles in eye development in Xenopus tropicalis.
9 nteracting transcriptome of the related frog Xenopus tropicalis.
10 upts this gene ablates forelimb formation in Xenopus tropicalis.
11 urons in the dorsal embryonic spinal cord of Xenopus tropicalis.
12 germline and soma of the African clawed frog Xenopus tropicalis.
13  laevis and genome-wide sequence analysis in Xenopus tropicalis.
14  of the NTPDase family in Xenopus laevis and Xenopus tropicalis.
15 onists, chordin, noggin, and follistatin, in Xenopus tropicalis.
16 lowing importation of the West African frog, Xenopus tropicalis.
17 components of the only diploid Xenopus frog, Xenopus tropicalis.
18 N) nuclease to knockdown endogenous Dot1L in Xenopus tropicalis, a diploid species highly related to
19 amination, we studied the oocyte of the frog Xenopus tropicalis, a giant cell with an equally giant n
20                   We generated zebrafish and Xenopus tropicalis acbd6 knockouts by CRISPR/Cas9 and ch
21 genome sequence for the western clawed frog, Xenopus tropicalis, along with draft chromosome-scale se
22                    This difficulty exists in Xenopus tropicalis, an anuran quickly becoming a relevan
23 ebrates, with two members in elephant shark, Xenopus tropicalis and Anolis lizard and three members i
24 R6, and GPR12; GPRx orthologs are present in Xenopus tropicalis and Danio rerio, but apparently not i
25 nto the underlying deep mesenchymal layer in Xenopus tropicalis and extend our previous findings for
26 ethylation profiles in developing zebrafish, Xenopus tropicalis and mice and suggests roles for Tet p
27 s during the phylotypic period in zebrafish, Xenopus tropicalis and mouse.
28 d Flt3lg homoeologs with the related diploid Xenopus tropicalis and with humans indicated a higher co
29 Tg coding sequence from western clawed frog (Xenopus tropicalis) and zebrafish (Danio rerio).
30 rc in the early development of the amphibian Xenopus tropicalis, and found that n1-src expression is
31 in this system, including the development of Xenopus tropicalis as a genetically tractable complement
32      Using the T3-dependent metamorphosis in Xenopus tropicalis as a model, we show here that high le
33                                        Using Xenopus tropicalis as a model, we show that DDX3 is requ
34 pseudo-tetraploid Xenopus laevis and diploid Xenopus tropicalis, as a model for postembryonic develop
35 elas, Takifugu rubripes, Xenopus laevis, and Xenopus tropicalis, as well as subpockets involved in pr
36  show that interaction of FoxG1 with TLE2, a Xenopus tropicalis co-repressor of the Groucho/TLE famil
37                 We present a genetic map for Xenopus tropicalis, consisting of 2886 Simple Sequence L
38 loped fast, efficient, and penetrant genetic Xenopus tropicalis desmoid tumor models to identify and
39                                              Xenopus tropicalis dril1 morphants also exhibit impaired
40 D heavy (H) chain (delta) from the amphibian Xenopus tropicalis during examination of the IgH locus.
41 c potential of MMI and PTU using a validated Xenopus tropicalis embryo model.
42 n of the Na(+), K(+)-ATPase beta3 subunit in Xenopus tropicalis embryos and show that its levels are
43 evelopmental Cell, Akkers et al. report that Xenopus tropicalis embryos transition through early deve
44                               Superficially, Xenopus tropicalis embryos with reduced levels of XEgr-1
45 strulation, and Nodal signal transduction in Xenopus tropicalis embryos.
46 ral breeding' strategy for the collection of Xenopus tropicalis embryos.
47 nic effects of aquatic exposure of Silurana (Xenopus) tropicalis embryos to commercial NA extracts an
48   The recent sequencing of a large number of Xenopus tropicalis expressed sequences has allowed devel
49 g the predicted transcription start sites in Xenopus tropicalis for genome wide identification of TR
50 hizosaccharomyces pombe, Xenopus laevis, and Xenopus tropicalis formed stable homotetramers, the mtSS
51 ablished models for skeletal ciliopathies in Xenopus tropicalis Froglets exhibited severe limb deform
52 we employ ChIP-seq and RNA-seq approaches in Xenopus tropicalis gastrulae and find that occupancy of
53 ase include the Xenopus laevis genome, a new Xenopus tropicalis genome build, epigenomic data, collec
54 t only aid in completing the assembly of the Xenopus tropicalis genome but will also serve as a valua
55                       With the advent of the Xenopus tropicalis genome project, we analyzed scaffolds
56 ndant piRNAs and large piRNA clusters in the Xenopus tropicalis genome, some of which resemble the Dr
57                     Here we use a library of Xenopus tropicalis genomic sequences in bacterial artifi
58  rapidly developing aquatic species, such as Xenopus tropicalis, goldfish, and zebrafish, and in Arab
59  screen of N-ethyl-N-nitrosourea mutagenized Xenopus tropicalis has identified an inner ear mutant na
60 the egg cytoplasm between Xenopus laevis and Xenopus tropicalis have been shown to account for spindl
61                   Forward genetic screens in Xenopus tropicalis have identified more than 80 mutation
62 wo closely related frogs, Xenopus laevis and Xenopus tropicalis, have surprisingly different microtub
63  rod photoreceptors in retinas of developing Xenopus tropicalis heterozygous, but not homozygous muta
64 c sequence RNAs (sisRNAs) have been found in Xenopus tropicalis, human cell lines, and Epstein-Barr v
65 ng (RNA-seq) to explore the transcriptome of Xenopus tropicalis in 23 distinct developmental stages.
66   ZFNs directed against an eGFP transgene in Xenopus tropicalis induced mutations consistent with non
67                      The western clawed frog Xenopus tropicalis is an important model for vertebrate
68       Xenopus, and in particular the diploid Xenopus tropicalis, is also ideal for functional genomic
69                                  Analysis of Xenopus tropicalis miRNA genes revealed a predominate po
70  sequences, more than 300 genes encoding 142 Xenopus tropicalis miRNAs were identified.
71 s the impact of Smarcc1 depletion in a novel Xenopus tropicalis model of congenital hydrocephalus.
72 BD8)) as an essential regulator of human and Xenopus tropicalis neural crest specification.
73                                   Oocytes of Xenopus tropicalis offer several practical advantages ov
74 tially localizing RNAs in Xenopus laevis and Xenopus tropicalis oocytes, revealing a surprisingly wea
75                        Approximately 30% (in Xenopus tropicalis) or 20% (in Xenopus laevis) of inject
76 vis XNC10 gene and its unequivocal Silurana (Xenopus) tropicalis orthologue, SNC10.
77  we show that the genetically tractable frog Xenopus tropicalis, paired with optical coherence tomogr
78                           We describe here a Xenopus tropicalis rax mutant, the first mutant analyzed
79               Targeted disruption of CE14 in Xenopus tropicalis recapitulates an ocular coloboma phen
80          Resumption of meiosis in oocytes of Xenopus tropicalis required translation but not transcri
81            In vivo investigation of TAOK1 in Xenopus tropicalis reveals a role in motile cilia format
82                                        Small Xenopus tropicalis spindles resisted inhibition of two f
83 e we describe the expression and activity of Xenopus tropicalis Sulf2 (XtSulf2), which like XtSulf1,
84 t superior cervical ganglion and the tail of Xenopus tropicalis tadpoles are remodeled.
85 sults was supported by injecting the tail of Xenopus tropicalis tadpoles with peptide 4.2, a 20-aa se
86 6-expressing NPCs isolated from regenerating Xenopus tropicalis tails.
87        Here we show, by using a clawed frog (Xenopus tropicalis), that GRP is not a mammalian counter
88 ent with heterotaxy, and now demonstrate, in Xenopus tropicalis, that galnt11 activates Notch signall
89 reespine stickleback and fugu, the amphibian Xenopus tropicalis, the monotreme platypus and the marsu
90                              We show that in Xenopus tropicalis, these processes are connected to the
91 s (MOs) to knockdown expression of xtBcor in Xenopus tropicalis, thus creating an animal model for OF
92                                We found that Xenopus tropicalis Tmem16a is present at the apical memb
93  between different vertebrates, ranging from Xenopus tropicalis to Homo sapiens, demonstrating that t
94                             Here we leverage Xenopus tropicalis to study in vivo ten genes with the s
95                                              Xenopus tropicalis was used to make GFP reporter lines w
96 ction of this gene, we used the diploid frog Xenopus tropicalis We discover that Dyrk1a is expressed
97 ino-mediated knockdown in Xenopus laevis and Xenopus tropicalis we show that Nkx6.1 knockdown results
98                                        Using Xenopus tropicalis, we have undertaken the first analysi
99                                        Using Xenopus tropicalis, we individually target five of these
100                                 Tested using Xenopus tropicalis, we show that founders containing tra
101         Using morpholino oligonucleotides in Xenopus tropicalis, we show that reducing tsg gene produ
102 dx17 crispants and heterozygous knockouts in Xenopus tropicalis were generated for assessment of morp
103 tion and early nervous system development in Xenopus tropicalis, where ZIP12 antisense morpholino kno
104 sue explant-based protocols, and the diploid Xenopus tropicalis which is used for genetics and gene t
105 opus laevis and its smaller diploid relative Xenopus tropicalis, which contains smaller cells and nuc
106                                              Xenopus tropicalis, which is a small, faster-breeding re
107                    Here, we coupled the frog Xenopus tropicalis with Optical Coherence Tomography (OC
108 n-uniformly in embryos of Xenopus laevis and Xenopus tropicalis, with prominent expression in the not
109 orecast CRISPR/Cas9 gene editing outcomes in Xenopus tropicalis, Xenopus laevis, and zebrafish.
110                 We have identified a 7.28 kb Xenopus tropicalis Xmyf-5 (Xtmyf-5) genomic DNA fragment
111 ation, purification, and characterization of Xenopus tropicalis (Xt) allurin, a homologous protein in
112  present the cryo-EM structure of OTOP3 from Xenopus tropicalis (XtOTOP3) along with functional chara
113   We identified two genes for each family in Xenopus tropicalis: Xtsprouty1, Xtsprouty2, Xtspred1, an

 
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