ライフサイエンスコーパス: pufferfish

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 iggerfishes, boxfishes, ocean sunfishes, and pufferfishes.

7 ments of DNA spanning the mouse, chicken and pufferfish alpha globin gene clusters and compared them

8 d genomic sequences are also present in both pufferfish and rainbow trout, indicating the likely pres

9 larities of gene expression profiles between pufferfish and zebrafish during maternal to zygotic tran

10 g of ADAR2 genes from human, mouse, chicken, pufferfish and zebrafish.

11 the protein sequences of DRADA from mammals, pufferfish and zebrafish.

12 oxAalpha and HoxAbeta clusters of zebrafish, pufferfish, and striped bass.

13 cross the vertebrates studied (human, mouse, pufferfish, and zebrafish), and exonic splicing enhancer

14 sequence conservation between human, mouse, pufferfish, and zebrafish.

15 e, and rat and 22% for targets identified in pufferfish as well as mammals.

16 ly derived morphological structures like the pufferfish beak form via a conserved developmental baupl

17 a suggest that dental novelties, such as the pufferfish beak, can develop later in ontogeny through m

18 rule out the hypothesis that the simplified pufferfish body plan is due to reduction in Hox cluster

19 t 4679 sequences conserved between human and pufferfish coincide with histone acetylation islands, an

20 rimary sequence of prepro-osteocalcin from 2 pufferfish compared with carp shows that there are many

21 fied from the genome sequences of zebrafish, pufferfish, frogs, chickens, humans, and mice.

22 Given that spiny pufferfish from the sister family Diodontidae and a fish

23 ure and cDNA sequence of the APP gene in the pufferfish Fugu rubripes and Tetraodon fluviatilis, resp

24 the SART1 gene in the compact genomes of the pufferfish Fugu rubripes and Tetraodon nigroviridis.

25 rresponding to the wnt1 gene of the Japanese pufferfish Fugu rubripes confirms the compact structure

26 For example, genes from the pufferfish Fugu rubripes generally contain one or more i

27 The Japanese pufferfish Fugu rubripes has a 400 Mb genome with high g

28 two snail genes in the compact genome of the pufferfish Fugu rubripes, and examine the phylogenetic r

29 ity of GCAPs in more detail, we searched the pufferfish (Fugu rubripes) and zebrafish (Danio rerio) g

30 lone from the compact genome of the Japanese pufferfish (Fugu rubripes) containing portions of three

31 en the human 7q36 chromosomal region and the pufferfish (Fugu rubripes) genome.

32 We then compared mouse, human, and pufferfish (Fugu rubripes) genomic sequences, and identi

33 we have cloned and sequenced 60 kb from the pufferfish (Fugu rubripes) lck locus.

34 losa), the lamprey (Petromyzon marinus), the pufferfish (Fugu rubripes), and the frog (Xenopus laevis

35 ion maps of this locus between human, mouse, pufferfish (Fugu rubripes), and, in part, zebrafish (Dan

36 located downstream of the wnt-1 gene in the pufferfish (Fugu rubripes).

37 rthologues of human, chimpanzee, mouse, rat, pufferfish (Fugu) and zebrafish demonstrates that these

38 Analysis of the genome database for the pufferfish, Fugu rubrides, identified a goldfish ISG15 (

39 The genome of the pufferfish, Fugu rubripes (Fugu) is compact.

40 e cloning and characterization of a Japanese pufferfish, Fugu rubripes achaete-scute homolog 1, Fash1

41 The compact genome of the pufferfish, Fugu rubripes, has proven a valuable tool in

42 gene family from the reference genome of the pufferfish, Fugu rubripes.

43 nd characterisation of two top1 genes in the pufferfish, Fugu rubripes.

44 isolated homologous genes from the Japanese pufferfish, Fugu rubripes.

45 ntaining 43kb of genomic DNA of the Japanese pufferfish, Fugu rubripes.

46 Ralpha) gene from the genome of the Japanese pufferfish, Fugu rubripes.

47 e analysis of the TSC2 gene in human and the pufferfish, Fugu rubripes.

48 and MCH receptors in both zebrafish and the pufferfish, Fugu.

49 quence from the mouse, rat, dog, chicken and pufferfish genomes revealed a strongly statistically sig

50 milies from the sequenced fugu and Tetraodon pufferfish genomes.

51 complete Hox gene complement of the Japanese pufferfish has now been determined, together with the ge

52 undance of repetitive DNA, the genome of the pufferfish has shown to be ideal for comparative genomic

53 tionarily distant genomes, such as human and pufferfish, have identified specific sets of 'ultraconse

54 The zebrafish and pufferfish homologs share high similarity to mammalian s

55 proteins had highly diverged from or had no pufferfish homologs, highlighting the extent of protein

56 rphology is due to reduced complexity of the pufferfish Hox complexes.

57 Consequently, it can be dangerous to consume pufferfish, including the edible muscle, from the Easter

58 st lethal Nav channel toxins (snakes, newts, pufferfish, insects), and in specialized habitats (naked

59 rst-generation teeth that line the embryonic pufferfish jaw, with timing of development and gene expr

60 The toxicity of tetrodotoxin (TTX) in pufferfish (Lagocephalus sceleratus) from Mersin Bay in

61 s, followed by loss of a Hoxc cluster in the pufferfish lineage and loss of a Hoxd cluster in the zeb

62 RH2 or "green-sensitive" opsin gene in both pufferfish lineages, designated RH2-2.

63 plication before divergence of zebrafish and pufferfish lineages, followed by loss of a Hoxc cluster

64 Our results show that CNEs identified in pufferfish-mammal whole-genome comparisons are crucial d

65 ypothesized that this secondarily simplified pufferfish morphology is due to reduced complexity of th

66 4 DNA elements from four species (zebrafish, pufferfish, mouse, and rat), that included 21 genes with

67 Smooth pufferfish of the family Tetraodontidae have the smalles

68 enes as the earliest developmental defect in pufferfish pelvic fin loss and suggest that altered Hoxd

69 nopterygii, Teleostei) such as zebrafish and pufferfish possess duplicated Hox clusters that have und

70 The very small vertebrate genome of the pufferfish provides a simple and economical way of compa

71 In chicken and pufferfish, regions that may correspond to this element

72 used to extract TTX from Trumpet shells and pufferfish samples.

73 for comparison with mammalian, chicken, and pufferfish sequences.

74 The pufferfish skeleton lacks ribs and pelvic fins, and has

75 ic structure of Hox clusters in the Southern pufferfish Spheroides nephelus and interrogated genomic

76 y, we employ a genomic approach by using the pufferfish (Spheroides nephelus) to characterize a nonre

77 chromosome genomic library from the Southern pufferfish, Spheroides nephelus.

78 Pufferfish such as fugu and tetraodon carry the smallest

79 ptide data set and the human, zebrafish, and pufferfishes (T. nigroviridis and Takifugu rubripes) pro

80 asis for the evolution of pelvis loss in the pufferfish Takifugu rubripes (fugu), we isolated fugu or

81 errogated genomic databases for the Japanese pufferfish Takifugu rubripes (fugu).

82 sequences upstream of the mespb gene in the pufferfish Takifugu rubripes (Tr-mespb) are able to driv

83 sequence comparisons among human, mouse, and pufferfish (Takifugu rubripes (Fugu)) have revealed a se

84 frican clawed frog (Xenopus laevis), but not pufferfish (Takifugu rubripes), can induce CSR in AID-de

85 anscripts of a myoD paralogue from the tiger pufferfish (Takifugu rubripes).

86 the human genome that are conserved in human-pufferfish, Takifugu (Fugu) rubripes, or ultraconserved

87 A more distant outgroup comparison with the pufferfish Tetraodon nigroviridis reveals ALG2/GGAZ/HSAX

88 ied orthologs in the genome database for the pufferfish Tetraodon nigroviridis.

89 As were isolated from zebrafish and a second pufferfish, Tetraodon fluviatilis.

90 Adult pufferfishes (Tetraodontidae) exhibit a distinctive parr

91 -Gln-Cys-Gln-Cys-Ala-Cys638-, conserved from pufferfish to humans far removed from the MRE-binding zi

92 and mouse urocortin III are 76% identical to pufferfish urocortin-related peptide and more distantly

93 However, no clear bias towards the pufferfishes was observed, suggesting significant sequen

94 Pufferfish were caught by trawl fishing, longlining and

95 We demonstrate that a pufferfish WT1 transgene can be expressed and spliced ap

96 genome sequences (human, chimpanzee, mouse, pufferfish, zebrafish, sea squirt, fruitfly, mosquito, a