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 bitory receptors that has been identified in bony fish.

3 letal morphology considered primitive to all bony fish.

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

5 been described previously in two lineages of bony fish.

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

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

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

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

10 tail likely reflects the ancestral state for bony fishes.

11 fied by extinct and extant cartilaginous and bony fishes.

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

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

14 ancestrally lateral line placode-derived in bony fishes.

15 escribe the mechanics of feeding behavior in bony fishes.

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

17 lved in calcium and phosphate homeostasis in bony fishes.

18 duplication event early in the evolution of bony fishes.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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