ライフサイエンスコーパス: bony fish

1 t S100 family members are found in teleosts (bony fish).

2 an ancient origin and had already emerged in bony fish.

3 bitory receptors that has been identified in bony fish.

4 letal morphology considered primitive to all bony fish.

5 eins have been identified mostly in mice and bony fish.

6 been described previously in two lineages of bony fish.

7 in vertebrate phylogeny at the level of the bony fish.

8 m a very highly ordered vertebrate muscle in bony fish.

9 s were evident for amphibians, reptiles, and bony fishes.

10 atures, most likely present in the ancestral bony fishes.

11 tail likely reflects the ancestral state for bony fishes.

12 fied by extinct and extant cartilaginous and bony fishes.

13 unting by both cartilaginous and non-teleost bony fishes.

14 cent common ancestor (MRCA) of tetrapods and bony fishes.

15 ancestrally lateral line placode-derived in bony fishes.

16 escribe the mechanics of feeding behavior in bony fishes.

17 lved in calcium and phosphate homeostasis in bony fishes.

18 duplication event early in the evolution of bony fishes.

19 uring the initial evolutionary radiations of bony fishes.

20 nonlinear (74%), followed by mammals (58%), bony fish (49%) and birds (35%).

21 to multimeric forms of parvalbumins for most bony fish, a complete loss of reactivity was observed fo

22 e the diversification of lower jaws in early bony fishes, a major contributor to this initial radiati

23 heir embryonic origins remain controversial: bony fish ampullary organs are derived from lateral line

24 ired to complete the life cycle of a typical bony fish and a salamander at the same developmental sta

25 ns are actually major myelin constituents in bony fish and amphibia, and so are coexpressed with P0.

26 of the herpesviruses that occur primarily in bony fish and amphibians.

27 n a tetrapod species, so far known only from bony fish and basal sarcopterygians.

28 experienced a vigorous rearrangement in the bony fish and bird lineages, and a translocation and exp

29 ago in the common ancestor of tetrapods and bony fish and diversified as multigene families independ

30 tebrate species, including cartilaginous and bony fish and marine reptiles, from northern Gulf of Mex

31 originated in the ancestors of Teleostei or bony fish and of the Tetrapoda or amphibians, reptiles,

32 ion occurred prior to the divergence between bony fish and tetrapods around 400 million years ago.

33 of this superfamily before the divergence of bony fish and tetrapods, approximately 360-450 million y

34 four clusters of Hox genes characteristic of bony fish and tetrapods.

35 s represent an ancient lineage in ray-finned bony fishes and hence in jawed vertebrates.

36 strates the role of jaws in the evolution of bony fishes and highlights patterns of diversity that st

37 ns (cartilaginous fishes) and osteichthyans (bony fishes and tetrapods) have contrasting skeletal ana

38 obranchs (shark and rays) and osteichthyans (bony fishes and tetrapods).

39 ns (cartilaginous fishes) and osteichthyans (bony fishes and tetrapods).

40 omprising more than 60,000 living species of bony fishes and tetrapods.

41 s a deeply embedded developmental program in bony fishes and that tuning of this trade-off can genera

42 major groupings of fish, the Actinopterygii (bony fish) and Elasmobranchii (sharks, skates and rays).

43 It is absent in cartilaginous and bony fish, and it is common to all tetrapods.

44 lary organs in cartilaginous and non-teleost bony fishes, and indicate that jawed vertebrates primiti

45 ieved to be basal to other living ray-finned bony fishes, and they may be useful for providing inform

46 as also been identified in cartilaginous and bony fishes, and we report in this study a BAFF-like gen

47 In contrast, bony fish are capable of both repair, and de novo produc

48 rt the hypothesis that the distal radials of bony fish are homologous to the wrist and/or digits of t

49 ry of an isotype with similarities to IgD in bony fish are perplexing.

50 Polypterid bony fishes are believed to be basal to other living ray

51 a representative of the lobe-finned clade of bony fishes) are lateral line placode-derived, non-placo

52 ion by Nrps is conserved between mammals and bony fish, as we show that morpholinos targeting the Nrp

53 ostomes (jawed vertebrates-cartilaginous and bony fishes), based on their distinct embryonic origins:

54 range of other vertebrate orders, including bony fish, birds, amphibians, and mammals.

55 a subunits, KCNQ2, and KCNQ3 (including from bony fish, birds, and mammals) all possess the motif.

56 , we report foraminifer, metazoan (mollusks, bony fish, bryozoans, decapods, and sharks among others)

57 macula, resembling the macula lagena of some bony fishes but not of tetrapods.

58 s identified orthologs for P19 and NEEP21 in bony fish, but not urochordate or invertebrate phyla.

59 ved tooth resorption, a primitive feature in bony fishes, but absent in sharks and their relatives.

60 ally symmetrical tail structure common among bony fishes, but the hydrodynamic purpose of this asymme

61 pparently appeared with the radiation of the bony fish clade Euteleostei, whereas the second extensio

62 tion in jaws during the earliest interval of bony fish evolutionary history (423-359 Ma).

63 Using preparations of intact, relaxed, bony fish fin muscles and the ID-02 low-angle X-ray came

64 This tuna is unique among bony fish for maintaining elevated body temperatures (21

65 of other incompletely known Siluro-Devonian 'bony fishes' for reconstructing patterns of trait evolut

66 reexisting gene from the kidney and liver of bony fishes, for a novel role in the brood pouch of preg

67 e report several new examples of these giant bony fishes from Asia, Europe, and North America.

68 ources connect developmental evolution among bony fishes, further highlighting the bowfin's importanc

69 Ancient bony fishes had heterocercal tails, like modern sharks a

70 findings pertaining to immunity in teleost (bony) fish have led to major new insights about mammalia

71 Most bony fish, however, have only 2 types of B lymphocytes,

72 Long-lived bony fish (i.e., Class Osteichthyes) are a particularly

73 Heretofore, bony fish IgM was the one exception with IgM mRNA splice

74 ter the divergence of cartilaginous fish and bony fish, implying that early vertebrate mineralization

75 In the bony fishes it is unclear what proprioceptive feedback i

76 We show that a common ancestor of bony fishes likely had a thin retina without additional

77 ocrania are incompletely preserved for early bony fishes, limiting a detailed understanding of comple

78 l system that represents a third independent bony fish lineage.

79 despite the divergence of cartilaginous and bony fish lineages or the transition of the primary jaw

80 ated - the neoselachian sharks, neopterygian bony fishes, lissamphibians, turtles, lepidosaurs, croco

81 re arrayed around the actin filaments in the bony fish muscle A-band cell unit.

82 ", low-angle diffraction X-ray patterns from bony fish muscle, indicating that they all arise from th

83 of ancestral CHIA predate the divergence of bony fishes, one leading to a newly identified paralogou

84 udes observations of neofunctionalization in bony fishes or crustaceans, and the involvement of ILPs

85 ds, and APRIL is not identifiable in several bony fishes or in birds, the latter of which also lack a

86 Chimeric TCRs containing amphibian, bony fish, or cartilaginous fish Vbetas can recognize an

87 ichirs as possibly the most primitive living bony fish (Osteichthyes) made knowledge about their mito

88 rates of shark dermal denticles (scales) and bony fish otoliths (ear stones) in reef sediments, we as

89 In bony fishes, patterning of the vertebral column, or spin

90 sunfish (Mola mola) is the world's heaviest bony fish reaching a body mass of up to 2.3 tonnes.

91 Most bony fishes rely on suction mechanisms to capture and tr

92 Bony fish represent the most basal vertebrate branch wit

93 lly all jawed vertebrates, including sharks, bony fishes, reptiles, and birds.

94 mbly with other high-quality assemblies from bony fishes revealed few inter-chromosomal but frequent

95 o show that diverse marine predators-sharks, bony fishes, sea turtles and penguins-exhibit Levy-walk-

96 Selected teleostean (bony) fish species of the family Batrachoididae (toadfis

97 e further duplicated in teleosts through the bony-fish specific WGD, while only kank1 and kank4 dupli

98 Sea lamprey (jawless fish) and zebrafish (bony fish) support the unbranched axon concept, with 94%

99 her subsets of ligands are shared with basal bony fish T2Rs indicating an astonishing degree of funct

100 tes), which represents a sister clade to all bony fish T2Rs.

101 However, in many aquatic animals like bony fishes, teeth and taste buds are colocalized one ne

102 te extensive evolutionary divergence between bony fish (teleosts) and mammals, the molecular pathways

103 D), an enzyme expressed in cartilaginous and bony fish that is also required for somatic hypermutatio

104 A recent study with the world's largest bony fish, the ocean sunfish (Mola mola), is highlighted

105 biogeochemical function sustained by marine bony fishes: the excretion of intestinal carbonates.

106 described divergent isotype is restricted to bony fish, thus we have named this isotype "IgT" (tau) f

107 outside the MHC in all examined species from bony fish to mammals, but it is assumed to have transloc

108 Comparison of bony fish versus amphibian and mammalian AIDs suggests e

109 the presence of a single large gill cover in bony fishes versus separate covers for each gill chamber

110 uring the emergence of land vertebrates from bony fish, which only display SHM.

111 is seems to be true for dolphins, sharks and bony fish, which swim at 0.2 < St < 0.4.

112 igin of C-cells is conserved in a ray-finned bony fish (zebrafish) and a cartilaginous fish (the litt