ライフサイエンスコーパス: Oncorhynchus

1 s of transspecies evolution within the genus Oncorhynchus.

2 of trans-species evolution within the genus Oncorhynchus.

3 The different patterns in Oncorhynchus and the other two genera could be due to hi

4 Native Colorado River cutthroat trout (CRCT; Oncorhynchus clarkii pleuriticus) are now relegated to 3

5 We project that native cutthroat trout Oncorhynchus clarkii, already excluded from much of its

6 Within Oncorhynchus, five of seven species had alleles that wer

7 first reported on juvenile wild pink salmon (Oncorhynchus gorbuscha) in 2001.

8 content of diploid and triploid pink salmon Oncorhynchus gorbuscha, reared in aquaculture in a bay o

9 ncient DNA analyses establish the species as Oncorhynchus keta (chum salmon), and stable isotope anal

10 communities of decomposing salmon carcasses (Oncorhynchus keta) compared with those of terrestrial ne

11 y-reared underyearling juvenile chum salmon (Oncorhynchus keta), thyrotropin-releasing hormone gene e

12 sealcoated asphalt on juvenile coho salmon (Oncorhynchus kisutch) and embryo-larval zebrafish (Danio

13 e-scale population structure of coho salmon (Oncorhynchus kisutch) by comparing archived (1938) and m

14 gy, and habitat models within a coho salmon (Oncorhynchus kisutch) population model to assess how pro

15 or below 1 part per billion), juvenile coho (Oncorhynchus kisutch) were exposed to a range of mixture

16 he DNA level in hatchery-reared coho salmon (Oncorhynchus kisutch) with those of their wild counterpa

17 s between such growth traits in coho salmon (Oncorhynchus kisutch), an important fish species distrib

18 efish (Coregonus clupeaformis), coho salmon (Oncorhynchus kisutch), rainbow trout (O. mykiss), Chinoo

19 ymostoma cirratum (Gici)) and rainbow trout (Oncorhynchus mykiss (Onmy)).

20 ial infections of a natural vertebrate host, Oncorhynchus mykiss (rainbow trout), with variants of a

21 erated recombinant C5a of the rainbow trout, Oncorhynchus mykiss (tC5a), and used fluoresceinated tC5

22 er subgroups (IFN-e and -f) in rainbow trout Oncorhynchus mykiss and analyzed the expression of all s

23 genes were identified in rainbow trout (rt) Oncorhynchus mykiss and are classified into two groups b

24 ampsocephalus gunnari, and the rainbow trout Oncorhynchus mykiss as a reference.

25 ted by our simulations and the reanalysis of Oncorhynchus mykiss experimental data.

26 Exposed juvenile rainbow trout (Oncorhynchus mykiss) accumulated surfactants, naphthols,

27 f widely introduced salmonids rainbow trout (Oncorhynchus mykiss) and brook trout (Salvelinus fontina

28 Rainbow trout (Oncorhynchus mykiss) and brown trout (Salmo trutta) repr

29 ed in two previous studies of rainbow trout (Oncorhynchus mykiss) and common carp (Cyprinus carpio).

30 hemicals in two fish species: rainbow trout (Oncorhynchus mykiss) and fathead minnow (Pimephales prom

31 out-migration success in juvenile steelhead (Oncorhynchus mykiss) and focuses on the application of m

32 o bioassays using rainbow trout hepatocytes (Oncorhynchus mykiss) and in vivo studies with Japanese m

33 isulfide polymerization of IgM in the trout (Oncorhynchus mykiss) and its effect on its half-life wer

34 lamin-binding proteins of the rainbow trout (Oncorhynchus mykiss) and to compare their properties wit

35 angliosides found in sperm of rainbow trout (Oncorhynchus mykiss) and was shown to be present promine

36 In this regard, rainbow trout (Oncorhynchus mykiss) appeared unusual: trout beta2m gene

37 development in earthen-ponds rainbow trout (Oncorhynchus mykiss) aquaculture farming in Germany.

38 ocal anadromous (ocean-run) steelhead trout (Oncorhynchus mykiss) by blocking their migration route a

39 cts of gamma irradiation on the DNA of fish (Oncorhynchus mykiss) by real-time PCR were studied.

40 unctional characterization of rainbow trout (Oncorhynchus mykiss) CD4-1(+) T cells and the establishm

41 hether a relevant model fish (rainbow trout, Oncorhynchus mykiss) could detect OSPW using its olfacto

42 r vitelline envelope (VE), of rainbow trout (Oncorhynchus mykiss) eggs consists of three proteins, ca

43 members within the available rainbow trout (Oncorhynchus mykiss) EST gene index, we identified a uni

44 rary prepared from 3-week-old rainbow trout (Oncorhynchus mykiss) eyed embryos.

45 the rancidity development in rainbow trout (Oncorhynchus mykiss) fillets during refrigerated storage

46 scle and edible skin parts of rainbow trout (Oncorhynchus mykiss) fillets, sampled at two growth stag

47 bile samples was validated in rainbow trout (Oncorhynchus mykiss) following short-term laboratory exp

48 mentation on a wild population of steelhead (Oncorhynchus mykiss) from the Hood River, Oregon, by mat

49 Juvenile steelhead (Oncorhynchus mykiss) from two different hatcheries were

50 A rainbow trout (Oncorhynchus mykiss) gene for tumor necrosis factor (TNF

51 expression was studied in the rainbow trout (Oncorhynchus mykiss) gonad (RTG) (fibroblast) cell line.

52 tures in a primary culture of rainbow trout (Oncorhynchus mykiss) hepatocytes.

53 ry and sequence analysis of a rainbow trout (Oncorhynchus mykiss) IL-17A/F2 molecule and an IL-17RA r

54 th of the young of the year steelhead trout (Oncorhynchus mykiss) in the recipient tributary over the

55 Two rainbow trout (Oncorhynchus mykiss) Mx cDNAs were cloned by using RACE

56 e of CD8alpha(+) cells in the rainbow trout (Oncorhynchus mykiss) nasal epithelium.

57 n of plasmablasts and plasma cells in trout (Oncorhynchus mykiss) peripheral blood and splenic and an

58 d first-generation hatchery steelhead trout (Oncorhynchus mykiss) reared in a common environment.

59 not benzocaine or MS-222; and rainbow trout (Oncorhynchus mykiss) showed no avoidance to the three ag

60 ss<30kDa (PF30) isolated from rainbow trout (Oncorhynchus mykiss) skin gelatin hydrolysates was encap

61 nerve of a teleost fish, the rainbow trout (Oncorhynchus mykiss) to determine what types of somatose

62 ur studies have revealed that rainbow trout (Oncorhynchus mykiss) use a novel strategy for the genera

63 the shelf-life of fillets of rainbow trout (Oncorhynchus mykiss) were examined.

64 the shelf-life of fillets of rainbow trout (Oncorhynchus mykiss) were examined.

65 Rainbow trout (Oncorhynchus mykiss) were exposed to waterborne venlafax

66 aquatic ecosystems, juvenile rainbow trout (Oncorhynchus mykiss) were separately exposed to a mixtur

67 her blastomeres isolated from rainbow trout (Oncorhynchus mykiss) will incorporate and continue to de

68 BPA deposition in the eggs of rainbow trout (Oncorhynchus mykiss), an ecologically and economically i

69 tlantic salmon (Salmo salar), rainbow trout (Oncorhynchus mykiss), and Arctic char (Salvelinus alpinu

70 hic invertebrates, juvenile steelhead trout (Oncorhynchus mykiss), and water striders (Gerris remigis

71 vely affects muscle growth in rainbow trout (Oncorhynchus mykiss), but the mechanisms directing with

72 eta2m of a salmonid fish, the rainbow trout (Oncorhynchus mykiss), does not conform to the mammalian

73 of salmonid fishes, including rainbow trout (Oncorhynchus mykiss), experienced a whole genome duplica

74 her vertebrate taxa including rainbow trout (Oncorhynchus mykiss), frog (Xenopus laevis), chicken (Ga

75 ly life stages of ammonotelic rainbow trout (Oncorhynchus mykiss), suggesting that the urea cycle may

76 In the rainbow trout (Oncorhynchus mykiss), the only ER described is an isofor

77 n (Acipenser fulvescens), and rainbow trout (Oncorhynchus mykiss), were selected to evaluate TFM redu

78 ed to the controversy is that rainbow trout (Oncorhynchus mykiss), which have served as the primary m

79 the surface, was examined in rainbow trout (Oncorhynchus mykiss).

80 ) have been identified in the rainbow trout (Oncorhynchus mykiss).

81 SalHV-1) is a pathogen of the rainbow trout (Oncorhynchus mykiss).

82 tailed genetic linkage map of rainbow trout (Oncorhynchus mykiss).

83 an acute, lethal infection in rainbow trout (Oncorhynchus mykiss).

84 (HR) and low-responsive (LR) rainbow trout (Oncorhynchus mykiss).

85 ects the freshwater production of steelhead (Oncorhynchus mykiss).

86 er S9 fractions isolated from rainbow trout (Oncorhynchus mykiss).

87 and skin mucosal surfaces of rainbow trout (Oncorhynchus mykiss).

88 umulation of selenium (Se) in rainbow trout (Oncorhynchus mykiss).

89 reported a homolog to CCR7 in rainbow trout (Oncorhynchus mykiss).

90 mologue has been identified in rainbow trout Oncorhynchus mykiss, and its biological activities have

91 L, TRAIL-like, and TNF-New in rainbow trout, Oncorhynchus mykiss, immune and nonimmune tissues.

92 Habitat for rainbow trout, Oncorhynchus mykiss, is projected to decline the least (

93 sory receptors on the head of rainbow trout, Oncorhynchus mykiss, using extracellular recording from

94 n 18 has been identified from rainbow trout, Oncorhynchus mykiss.

95 y during embryogenesis in the rainbow trout, Oncorhynchus mykiss.

96 Here we use five decades of data from Oncorhynchus nerka (sockeye salmon) in Bristol Bay, Alas

97 rain of semelparous spawning kokanee salmon (Oncorhynchus nerka kennerlyi).

98 s primary trophic resources, sockeye salmon (Oncorhynchus nerka) and red elderberry (Sambucus racemos

99 roductive behaviour of adult sockeye salmon (Oncorhynchus nerka) and the activity of their principal

100 e series from nine stocks of sockeye salmon (Oncorhynchus nerka) from the Fraser River system in Brit

101 ream-spawning populations of sockeye salmon (Oncorhynchus nerka) had similar reproductive success to

102 beach and creek ecotypes of sockeye salmon (Oncorhynchus nerka) in Little Togiak Lake, Alaska, to ex

103 us arctos) predation in wild sockeye salmon (Oncorhynchus nerka) populations spawning in pristine hab

104 was extremely high [during a sockeye salmon (Oncorhynchus nerka) smolt outmigration and at a counting

105 tching in two populations of sockeye salmon (Oncorhynchus nerka) that overlap in timing of spawning b

106 ted for 11 species in three salmonid genera, Oncorhynchus, Salmo, and Salvelinus.

107 ted for 11 species in three salmonid genera: Oncorhynchus, Salmo, and Salvelinus.

108 and endangered Pacific salmon and steelhead (Oncorhynchus sp.).

109 fic allelic lineages observed in five of the Oncorhynchus species.

110 n the passage of juvenile Pacific salmonids (Oncorhynchus spp.) at seven dams in the Columbia/Snake R

111 Pacific salmon (Oncorhynchus spp.) can transport bioaccumulated organic

112 the Great Lakes, introduced Pacific salmon (Oncorhynchus spp.) can transport persistent organic poll

113 Pacific salmon (Oncorhynchus spp.) navigate towards spawning grounds usi

114 conomically important group, Pacific salmon (Oncorhynchus spp.), experience site-specific thermal reg

115 tion or abundance for populations of salmon (Oncorhynchus spp.), groundfish, herring (Clupea pallasii

116 iverse and strong effects in Pacific salmon (Oncorhynchus spp.).

117 bioamplification of POPs in Chinook salmon ( Oncorhynchus tshawytscha ) eggs and larvae.

118 on the early life growth of Chinook salmon (Oncorhynchus tshawytscha) and steelhead (O. mykiss) in w

119 ol of locomotor activity in juvenile salmon (Oncorhynchus tshawytscha) by manipulating 3 neurotransmi

120 ler whales (Orcinus orca) on Chinook salmon (Oncorhynchus tshawytscha) has changed since the 1970s al

121 t age and age at maturity in Chinook salmon (Oncorhynchus tshawytscha) populations introduced to New

122 ly demonstrate that juvenile Chinook salmon (Oncorhynchus tshawytscha) respond to magnetic fields lik

123 I ask whether fluctuation in Chinook salmon (Oncorhynchus tshawytscha) spawner population size throug

124 ilised digestive lipase from Chinook salmon (Oncorhynchus tshawytscha) to generate flavour compounds

125 ally distinct populations of Chinook salmon (Oncorhynchus tshawytscha) within a single metapopulation

126 %, Snake River spring/summer chinook salmon (Oncorhynchus tshawytscha) would probably continue to dec

127 externally fertilising fish, chinook salmon (Oncorhynchus tshawytscha), and find that in less than 48

128 EPB-1 locus is sex-linked in chinook salmon (Oncorhynchus tshawytscha).