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1 rganisms such as zebrafish (Danio rerio) and clawed African frog (Xenopus laevis).
2 ad subfamily with highest homology scored to clawed African frog and human Smad2.
3 laeobiology of Megaraptora, a group of large-clawed carnivorous theropod dinosaurs known from Cretace
4 ts lowermost third receives the axons of the clawed class II Kenyon cells, which are the first to dif
5 dinosaurs that includes birds and the sickle-clawed Dromaeosauridae, has hitherto been largely restri
6 Mangold Organizer (SMO) in the South African Clawed Frog (X. laevis), a popular model of development,
7 gments between the violet pigment of African clawed frog (Xenopus laevis) and its ancestral UV pigmen
8 es from 16-cell embryos of the South African clawed frog (Xenopus laevis) and microextraction of thei
9   We address this question using the African clawed frog (Xenopus laevis) as a model.
10 vealed that expressing HvSWEET11b in African clawed frog (Xenopus laevis) oocytes facilitated the bid
11          Here, we show that AID from African clawed frog (Xenopus laevis), but not pufferfish (Takifu
12  the bull frog (Rana catesbeiana) and in the clawed frog (Xenopus laevis), which demonstrates that th
13 dothelin signaling components in the African clawed frog (Xenopus laevis).
14  a full-size Tg coding sequence from western clawed frog (Xenopus tropicalis) and zebrafish (Danio re
15                     Here we show, by using a clawed frog (Xenopus tropicalis), that GRP is not a mamm
16 hepcidins (tHEP1 and tHEP2) from the Western clawed frog (Xenopus tropicalis).
17 vertebrates, such as mouse, chicken, western clawed frog and zebrafish, are widely used in toxicity t
18 ith their human, mouse, chicken, and western clawed frog orthologs, resulting in 366 alignments.
19 ass II beta chains, more similar to HLA-DRB, clawed frog Xela-F3, and nurse shark Gici-B.
20 ight into embryonic nutrition in the African clawed frog Xenopus laevis by studying YPs.
21                  We have determined that the clawed frog Xenopus laevis contains twice the number of
22                                  The African clawed frog Xenopus laevis has been instrumental to inve
23                                  The African clawed frog Xenopus laevis is an important model organis
24 ral tube closure in mouse and in the African Clawed Frog Xenopus laevis to elucidate the etiology of
25 bines experimental advantages of the African clawed frog Xenopus laevis with more tractable genetics.
26 amphibian epidermis derived from the African clawed frog Xenopus laevis, and imaged calcium activity
27                                       In the clawed frog Xenopus laevis, neural crest induction depen
28 clamp recordings on oocytes from the African clawed frog Xenopus laevis, which endogenously express T
29  recent work on vocalizations of the African clawed frog Xenopus laevis.
30 nous ALF and TFIIA activities in the African clawed frog Xenopus laevis.
31 in the retinal photoreceptors of the African clawed frog Xenopus laevis.
32 ix separating these epithelia in the African clawed frog Xenopus laevis.
33  method using oocytes from the South African clawed frog Xenopus laevis.
34                                  The western clawed frog Xenopus tropicalis is an important model for
35 ions in the germline and soma of the African clawed frog Xenopus tropicalis.
36 erio (zebrafish) and Xenopus laevis (African clawed frog) embryos, zygotic irf6 transcripts are prese
37 6-, 32-, and 50-cell Xenopus laevis (African clawed frog) embryos.
38 tudy gastrulation in Xenopus laevis (African clawed frog) embryos.
39 s and to classic model organisms (zebrafish, clawed frog) in one- and two-protein imaging experiments
40       Larvae of Silurana tropicalis (Western clawed frog) were exposed to DY7-contaminated water (0 t
41 ammalian tetrapods (anole lizard and African clawed frog).
42 d consequences of tetraploidy in the African clawed frog, we sequenced the Xenopus laevis genome and
43          We show here that the South African clawed frog, Xenopus laevis, is a suitable model for inv
44  roles in vocal communication in the African clawed frog, Xenopus laevis.
45 or: the courtship songs of the South African clawed frog, Xenopus laevis.
46 ty reference genome sequence for the western clawed frog, Xenopus tropicalis, along with draft chromo
47                                  The African clawed frog, Xenopus, is a widely used comparative model
48                   Vocal behaviors of African clawed frogs (Xenopus laevis) are produced by a single p
49                      Male and female African clawed frogs (Xenopus laevis) produce rhythmic, sexually
50                      Male and female African clawed frogs (Xenopus laevis) produce sexually dimorphic
51  affect the development of testes in African clawed frogs (Xenopus laevis), but little is known about
52 ular basis of temporal complexity of African clawed frogs (Xenopus laevis).
53 of atrazine on sexual development in African clawed frogs (Xenopus laevis).
54 istence of Dracunculus infections in African clawed frogs (Xenopus laevis).
55                 MicroRNAs from the testes of clawed frogs (Xenopus) were extracted and the expression
56 rt1-paralogue (dm-w) of female-heterogametic clawed frogs (Xenopus; ZW /ZZ ), is known across >8740 s
57 viposition is imminent, female South African clawed frogs swim to an advertising male and produce an
58 . medinensis L3s were recovered from African clawed frogs tissues up to 58 days post-infection, and D
59 ds isolated from cane toads Bufo marinus and clawed frogs Xenopus laevis.
60 hich occurs naturally on the skin of African clawed frogs--was immobilized on gold microelectrodes vi
61 us laevis) and Western (Silurana tropicalis) clawed frogs.
62            A swimming microrobot design with clawed geometry, a red blood cell (RBC) membrane-camoufl
63 ndritic morphologies reminiscent of class II clawed Kenyon cells that supply the gamma lobes in other
64 d by a special class of intrinsic neuron-the clawed Kenyon cells-that are the first to differentiate
65 osophila melanogaster, Class II (also called clawed) Kenyon cells are well known for their extensive
66 st naturally-occurring virus reported in any clawed lobster species.
67 rus clarkii and Orconectes rusticus, and the clawed lobster, Homarus americanus.
68  ventrosum is closer to that of Nephropidae (clawed lobsters) than Astacidae (freshwater crayfish), t
69 aracterized by an extensive size range, with clawed NWMs (subfamily Callitrichinae, or callitrichines
70      Hemigrapsus takanoi, the Japanese brush-clawed shore crab, is a highly successful invader in Eur
71 human (Homo sapiens), murine (Mus musculus), clawed toad (Xenopus laevis) and the yeasts Schizosaccha
72 (Ambystoma mexicanum), and the South African clawed toad (Xenopus laevis), we traced the origins of f
73 hanol and a salinity of 5); (ii) the African clawed toad Xenopus laevis (stages 24, 32 and 34 exposed
74 yte nuclear envelopes (NEs) from the African clawed toad Xenopus laevis, immunogold labeling of compo
75 gs and sperm chromatin, respectively, of the clawed toad Xenopus laevis.
76 a simple vertebrate model, the embryo of the clawed toad, Xenopus laevis, in which a known GABAergic
77  of the jelly coating from the South African clawed toad, Xenopus laevis.
78 tern characterized by forelimb hyperflexure, clawed toes of all limbs, and a kinked tail.