ライフサイエンスコーパス: Xenopus tropicalis

1 ved in a distantly related anuran amphibian (Xenopus tropicalis).

2 EP1 and tHEP2) from the Western clawed frog (Xenopus tropicalis).

3 odal signaling during early embryogenesis in Xenopus tropicalis.

4 plays important roles in eye development in Xenopus tropicalis.

5 nteracting transcriptome of the related frog Xenopus tropicalis.

6 upts this gene ablates forelimb formation in Xenopus tropicalis.

7 urons in the dorsal embryonic spinal cord of Xenopus tropicalis.

8 germline and soma of the African clawed frog Xenopus tropicalis.

9 laevis and genome-wide sequence analysis in Xenopus tropicalis.

10 of the NTPDase family in Xenopus laevis and Xenopus tropicalis.

11 onists, chordin, noggin, and follistatin, in Xenopus tropicalis.

12 lowing importation of the West African frog, Xenopus tropicalis.

13 components of the only diploid Xenopus frog, Xenopus tropicalis.

14 N) nuclease to knockdown endogenous Dot1L in Xenopus tropicalis, a diploid species highly related to

15 amination, we studied the oocyte of the frog Xenopus tropicalis, a giant cell with an equally giant n

16 This difficulty exists in Xenopus tropicalis, an anuran quickly becoming a relevan

17 R6, and GPR12; GPRx orthologs are present in Xenopus tropicalis and Danio rerio, but apparently not i

18 nto the underlying deep mesenchymal layer in Xenopus tropicalis and extend our previous findings for

19 ethylation profiles in developing zebrafish, Xenopus tropicalis and mice and suggests roles for Tet p

20 s during the phylotypic period in zebrafish, Xenopus tropicalis and mouse.

21 Tg coding sequence from western clawed frog (Xenopus tropicalis) and zebrafish (Danio rerio).

22 rc in the early development of the amphibian Xenopus tropicalis, and found that n1-src expression is

23 in this system, including the development of Xenopus tropicalis as a genetically tractable complement

24 Using the T3-dependent metamorphosis in Xenopus tropicalis as a model, we show here that high le

25 pseudo-tetraploid Xenopus laevis and diploid Xenopus tropicalis, as a model for postembryonic develop

26 elas, Takifugu rubripes, Xenopus laevis, and Xenopus tropicalis, as well as subpockets involved in pr

27 show that interaction of FoxG1 with TLE2, a Xenopus tropicalis co-repressor of the Groucho/TLE famil

28 We present a genetic map for Xenopus tropicalis, consisting of 2886 Simple Sequence L

29 Xenopus tropicalis dril1 morphants also exhibit impaired

30 D heavy (H) chain (delta) from the amphibian Xenopus tropicalis during examination of the IgH locus.

31 c potential of MMI and PTU using a validated Xenopus tropicalis embryo model.

32 n of the Na(+), K(+)-ATPase beta3 subunit in Xenopus tropicalis embryos and show that its levels are

33 evelopmental Cell, Akkers et al. report that Xenopus tropicalis embryos transition through early deve

34 Superficially, Xenopus tropicalis embryos with reduced levels of XEgr-1

35 strulation, and Nodal signal transduction in Xenopus tropicalis embryos.

36 ral breeding' strategy for the collection of Xenopus tropicalis embryos.

37 The recent sequencing of a large number of Xenopus tropicalis expressed sequences has allowed devel

38 g the predicted transcription start sites in Xenopus tropicalis for genome wide identification of TR

39 we employ ChIP-seq and RNA-seq approaches in Xenopus tropicalis gastrulae and find that occupancy of

40 ase include the Xenopus laevis genome, a new Xenopus tropicalis genome build, epigenomic data, collec

41 t only aid in completing the assembly of the Xenopus tropicalis genome but will also serve as a valua

42 With the advent of the Xenopus tropicalis genome project, we analyzed scaffolds

43 ndant piRNAs and large piRNA clusters in the Xenopus tropicalis genome, some of which resemble the Dr

44 Here we use a library of Xenopus tropicalis genomic sequences in bacterial artifi

45 rapidly developing aquatic species, such as Xenopus tropicalis, goldfish, and zebrafish, and in Arab

46 screen of N-ethyl-N-nitrosourea mutagenized Xenopus tropicalis has identified an inner ear mutant na

47 Forward genetic screens in Xenopus tropicalis have identified more than 80 mutation

48 c sequence RNAs (sisRNAs) have been found in Xenopus tropicalis, human cell lines, and Epstein-Barr v

49 ng (RNA-seq) to explore the transcriptome of Xenopus tropicalis in 23 distinct developmental stages.

50 ZFNs directed against an eGFP transgene in Xenopus tropicalis induced mutations consistent with non

51 The western clawed frog Xenopus tropicalis is an important model for vertebrate

52 Xenopus, and in particular the diploid Xenopus tropicalis, is also ideal for functional genomic

53 Analysis of Xenopus tropicalis miRNA genes revealed a predominate po

54 sequences, more than 300 genes encoding 142 Xenopus tropicalis miRNAs were identified.

55 BD8)) as an essential regulator of human and Xenopus tropicalis neural crest specification.

56 Oocytes of Xenopus tropicalis offer several practical advantages ov

57 tially localizing RNAs in Xenopus laevis and Xenopus tropicalis oocytes, revealing a surprisingly wea

58 Approximately 30% (in Xenopus tropicalis) or 20% (in Xenopus laevis) of inject

59 vis XNC10 gene and its unequivocal Silurana (Xenopus) tropicalis orthologue, SNC10.

60 We describe here a Xenopus tropicalis rax mutant, the first mutant analyzed

61 Resumption of meiosis in oocytes of Xenopus tropicalis required translation but not transcri

62 Small Xenopus tropicalis spindles resisted inhibition of two f

63 e we describe the expression and activity of Xenopus tropicalis Sulf2 (XtSulf2), which like XtSulf1,

64 t superior cervical ganglion and the tail of Xenopus tropicalis tadpoles are remodeled.

65 sults was supported by injecting the tail of Xenopus tropicalis tadpoles with peptide 4.2, a 20-aa se

66 ent with heterotaxy, and now demonstrate, in Xenopus tropicalis, that galnt11 activates Notch signall

67 reespine stickleback and fugu, the amphibian Xenopus tropicalis, the monotreme platypus and the marsu

68 We show that in Xenopus tropicalis, these processes are connected to the

69 s (MOs) to knockdown expression of xtBcor in Xenopus tropicalis, thus creating an animal model for OF

70 between different vertebrates, ranging from Xenopus tropicalis to Homo sapiens, demonstrating that t

71 Xenopus tropicalis was used to make GFP reporter lines w

72 ino-mediated knockdown in Xenopus laevis and Xenopus tropicalis we show that Nkx6.1 knockdown results

73 Using Xenopus tropicalis, we have undertaken the first analysi

74 Tested using Xenopus tropicalis, we show that founders containing tra

75 Using morpholino oligonucleotides in Xenopus tropicalis, we show that reducing tsg gene produ

76 tion and early nervous system development in Xenopus tropicalis, where ZIP12 antisense morpholino kno

77 sue explant-based protocols, and the diploid Xenopus tropicalis which is used for genetics and gene t

78 opus laevis and its smaller diploid relative Xenopus tropicalis, which contains smaller cells and nuc

79 Xenopus tropicalis, which is a small, faster-breeding re

80 Here, we coupled the frog Xenopus tropicalis with Optical Coherence Tomography (OC

81 n-uniformly in embryos of Xenopus laevis and Xenopus tropicalis, with prominent expression in the not

82 We have identified a 7.28 kb Xenopus tropicalis Xmyf-5 (Xtmyf-5) genomic DNA fragment

83 ation, purification, and characterization of Xenopus tropicalis (Xt) allurin, a homologous protein in

84 We identified two genes for each family in Xenopus tropicalis: Xtsprouty1, Xtsprouty2, Xtspred1, an