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1 inding sites conserved between zebrafish and pufferfish.
2 ree additional species: mouse, zebrafish and pufferfish.
3 es conservation of linkage between human and pufferfish.
4 gan (VNO) of mammals and also in the nose of pufferfish.
5 vely processed in humans, are absent in both pufferfish.
6 tive, and cost-effective detection of TTX in pufferfish.
7 iggerfishes, boxfishes, ocean sunfishes, and pufferfishes.
8 s, bottom-dwelling flatfishes, seahorses and pufferfishes.
9 ments of DNA spanning the mouse, chicken and pufferfish alpha globin gene clusters and compared them
10 marine alkaloid, first isolated in 1909 from pufferfish and named after the biological order tetraodo
11 d genomic sequences are also present in both pufferfish and rainbow trout, indicating the likely pres
12 larities of gene expression profiles between pufferfish and zebrafish during maternal to zygotic tran
16 cross the vertebrates studied (human, mouse, pufferfish, and zebrafish), and exonic splicing enhancer
19 ly derived morphological structures like the pufferfish beak form via a conserved developmental baupl
20 a suggest that dental novelties, such as the pufferfish beak, can develop later in ontogeny through m
21 rule out the hypothesis that the simplified pufferfish body plan is due to reduction in Hox cluster
23 t 4679 sequences conserved between human and pufferfish coincide with histone acetylation islands, an
24 rimary sequence of prepro-osteocalcin from 2 pufferfish compared with carp shows that there are many
25 sumption of contaminated marine species like pufferfish due to its expansion to nonendemic areas has
26 ully applied to the quantification of TTX in pufferfish extracts, and the results obtained correlated
29 ure and cDNA sequence of the APP gene in the pufferfish Fugu rubripes and Tetraodon fluviatilis, resp
30 the SART1 gene in the compact genomes of the pufferfish Fugu rubripes and Tetraodon nigroviridis.
31 rresponding to the wnt1 gene of the Japanese pufferfish Fugu rubripes confirms the compact structure
34 two snail genes in the compact genome of the pufferfish Fugu rubripes, and examine the phylogenetic r
35 ity of GCAPs in more detail, we searched the pufferfish (Fugu rubripes) and zebrafish (Danio rerio) g
36 lone from the compact genome of the Japanese pufferfish (Fugu rubripes) containing portions of three
40 losa), the lamprey (Petromyzon marinus), the pufferfish (Fugu rubripes), and the frog (Xenopus laevis
41 ion maps of this locus between human, mouse, pufferfish (Fugu rubripes), and, in part, zebrafish (Dan
43 rthologues of human, chimpanzee, mouse, rat, pufferfish (Fugu) and zebrafish demonstrates that these
46 e cloning and characterization of a Japanese pufferfish, Fugu rubripes achaete-scute homolog 1, Fash1
55 quence from the mouse, rat, dog, chicken and pufferfish genomes revealed a strongly statistically sig
57 complete Hox gene complement of the Japanese pufferfish has now been determined, together with the ge
58 undance of repetitive DNA, the genome of the pufferfish has shown to be ideal for comparative genomic
59 tionarily distant genomes, such as human and pufferfish, have identified specific sets of 'ultraconse
61 proteins had highly diverged from or had no pufferfish homologs, highlighting the extent of protein
63 Consequently, it can be dangerous to consume pufferfish, including the edible muscle, from the Easter
65 st lethal Nav channel toxins (snakes, newts, pufferfish, insects), and in specialized habitats (naked
66 rst-generation teeth that line the embryonic pufferfish jaw, with timing of development and gene expr
68 s, followed by loss of a Hoxc cluster in the pufferfish lineage and loss of a Hoxd cluster in the zeb
70 plication before divergence of zebrafish and pufferfish lineages, followed by loss of a Hoxc cluster
71 Our results show that CNEs identified in pufferfish-mammal whole-genome comparisons are crucial d
72 ypothesized that this secondarily simplified pufferfish morphology is due to reduced complexity of th
73 4 DNA elements from four species (zebrafish, pufferfish, mouse, and rat), that included 21 genes with
75 enes as the earliest developmental defect in pufferfish pelvic fin loss and suggest that altered Hoxd
76 nopterygii, Teleostei) such as zebrafish and pufferfish possess duplicated Hox clusters that have und
82 ic structure of Hox clusters in the Southern pufferfish Spheroides nephelus and interrogated genomic
83 y, we employ a genomic approach by using the pufferfish (Spheroides nephelus) to characterize a nonre
86 ptide data set and the human, zebrafish, and pufferfishes (T. nigroviridis and Takifugu rubripes) pro
87 asis for the evolution of pelvis loss in the pufferfish Takifugu rubripes (fugu), we isolated fugu or
89 sequences upstream of the mespb gene in the pufferfish Takifugu rubripes (Tr-mespb) are able to driv
90 sequence comparisons among human, mouse, and pufferfish (Takifugu rubripes (Fugu)) have revealed a se
91 frican clawed frog (Xenopus laevis), but not pufferfish (Takifugu rubripes), can induce CSR in AID-de
93 the human genome that are conserved in human-pufferfish, Takifugu (Fugu) rubripes, or ultraconserved
94 A more distant outgroup comparison with the pufferfish Tetraodon nigroviridis reveals ALG2/GGAZ/HSAX
99 rt the cryo-electron microscopy structure of pufferfish TMEM206, which forms a trimeric channel, with
100 -Gln-Cys-Gln-Cys-Ala-Cys638-, conserved from pufferfish to humans far removed from the MRE-binding zi
101 and mouse urocortin III are 76% identical to pufferfish urocortin-related peptide and more distantly
102 1 x-ray crystal structures of human VKOR and pufferfish VKOR-like, with substrates and antagonists in
106 genome sequences (human, chimpanzee, mouse, pufferfish, zebrafish, sea squirt, fruitfly, mosquito, a