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 to observations of Coastal Cutthroat Trout (Oncorhynchus clarkii clarkii) occurrence and variables r

5 Q exposure on coastal cutthroat trout (CCT) (Oncorhynchus clarkii clarkii), a species sympatric with

6 in median length of Coastal Cutthroat Trout Oncorhynchus clarkii clarkii, but a coexisting species,

7 tion of threatened Lahontan cutthroat trout (Oncorhynchus clarkii henshawi).

8 hus tshawytscha), westslope cutthroat trout (Oncorhynchus clarkii lewisi), and nonfry life stages of

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

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

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

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

13 reas the unique life history of pink salmon (Oncorhynchus gorbuscha) presents an opportunity to do so

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

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

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

17 the distributional responses of chum salmon (Oncorhynchus keta), a keystone species, to the recent cl

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

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

20 nts over a six-week peak run of Coho salmon (Oncorhynchus kisutch) at a local spawning stream.

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

22 of concern owing to its role in coho salmon (Oncorhynchus kisutch) deaths via urban runoff mortality

23 the upper thermal tolerance of coho salmon (Oncorhynchus kisutch) during sustained swimming and acut

24 hwest, acute mortality of adult coho salmon (Oncorhynchus kisutch) follows rain events and is correla

25 l, we studied immune-stimulated coho salmon (Oncorhynchus kisutch) from three experiment groups shari

26 Klamath River and Trinity River coho salmon (Oncorhynchus kisutch) in 2021.

27 sh representing nine cohorts of coho salmon (Oncorhynchus kisutch) in California, we show that bimoda

28 anchors of biological decline: coho salmon (Oncorhynchus kisutch) mortality risk (p < 0.001) and los

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

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

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

32 lop and apply this framework to coho salmon (Oncorhynchus kisutch), a highly migratory and culturally

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

34 in sensitive species, including coho salmon (Oncorhynchus kisutch), brook trout (Salvelinus fontinali

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

36 In U.S. Pacific Northwest coho salmon (Oncorhynchus kisutch), stormwater exposure annually caus

37 none) causes acute mortality in coho salmon (Oncorhynchus kisutch), yet its mechanisms of toxicity re

38 to cause the acute mortality of coho salmon (Oncorhynchus kisutch).

39 red to cause acute mortality in coho salmon (Oncorhynchus kisutch).

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

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

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

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

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

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

46 tracting sulfated polysaccharides (SPs) from Oncorhynchus mykiss byproducts using alkaline/acid solub

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

48 thermal tolerance of two populations of wild Oncorhynchus mykiss near the species' southern range lim

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

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

51 Rainbow trout (Oncorhynchus mykiss) and brown trout (Salmo trutta fario

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

53 -anchored genome assembly for rainbow trout (Oncorhynchus mykiss) and characterize a 55-Mb double-inv

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

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

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

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

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

59 luding two sensitive species, rainbow trout (Oncorhynchus mykiss) and lake trout (Salvelinus namaycus

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

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

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

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

64 ntic salmon (Salmo salar) and rainbow trout (Oncorhynchus mykiss) are two of the most susceptible sal

65 knowledge, in teleosts using rainbow trout (Oncorhynchus mykiss) as a model.

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

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

68 CK11 is a rainbow trout (Oncorhynchus mykiss) CC chemokine phylogenetically relat

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

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

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

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

73 o examine stress responses in rainbow trout (Oncorhynchus mykiss) exposed to five distinct environmen

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

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

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

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

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

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

80 NTESTINAL)) designed to mimic rainbow trout (Oncorhynchus mykiss) gastrointestinal conditions.

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

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

83 vacuum packaged low processed rainbow trout (Oncorhynchus mykiss) gravad during storage at 7 +/- 1 de

84 vacuum packaged low processed rainbow trout (Oncorhynchus mykiss) gravad during storage at 7 1 C for

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

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

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

88 al barrier model built on the rainbow trout (Oncorhynchus mykiss) intestinal cell line, RTgutGC and t

89 RTgutGC cells, derived from rainbow trout (Oncorhynchus mykiss) intestine, were used to evaluate th

90 this study, PFAS exposure on rainbow trout (Oncorhynchus mykiss) is examined at the molecular level,

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

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

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

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

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

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

97 ark dose (BMD) assay for rainbow trout (RBT; Oncorhynchus mykiss) to derive transcriptomic points-of-

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

99 ranscriptomics on the CNSS of rainbow trout (Oncorhynchus mykiss) to establish: (1) how the CNSS resp

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

101 ith early life stages of rainbow trout (RBT; Oncorhynchus mykiss) using benzo[a]pyrene (B[a]P) as the

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

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

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

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

106 ress this, adult and juvenile Rainbow Trout (Oncorhynchus mykiss) were, respectively, exposed for 96

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

108 Rainbow trout (Oncorhynchus mykiss), a model aquaculture fish, was expo

109 In rainbow trout (Oncorhynchus mykiss), a nasopharynx-associated lymphoid

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

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

112 tion mixtures in coho salmon, rainbow trout (Oncorhynchus mykiss), and fathead minnow (Pimephales pro

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

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

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

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

117 ss (Dicentrarchus labrax) and rainbow trout (Oncorhynchus mykiss), fed diets at 25%, 50% and 60% inse

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

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

120 (Salvelinus fontinalis), and rainbow trout (Oncorhynchus mykiss), suggesting that tolerant species m

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

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

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

124 inook salmon or in tissues of rainbow trout (Oncorhynchus mykiss).

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

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

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

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

129 ated toxicities in vivo using rainbow trout (Oncorhynchus mykiss).

130 ures on the fillet quality of rainbow trout (Oncorhynchus mykiss).

131 tide") and growth in juvenile rainbow trout (Oncorhynchus mykiss).

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

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

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

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

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

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

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

139 have gained high virulence in rainbow trout (Oncorhynchus mykiss).

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

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

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

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

144 ntic salmon (Salmo salar) and rainbow trout (Oncorhynchus mykiss, Walbaum).

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

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

147 s using an in vitro digestion model based on Oncorhynchus mykiss.

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

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

150 ieved in distinguishing wild Salmo salar and Oncorhynchus nerka samples.

151 of iconic, keystone populations of sockeye (Oncorhynchus nerka) and Chinook (Oncorhynchus tshawytsch

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

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

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

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

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

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

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

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

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

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

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

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

164 The ecosystems supporting Pacific salmon (Oncorhynchus spp.) are changing rapidly as a result of c

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

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

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

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

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

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

171 For anadromous Pacific salmon (Oncorhynchus spp.), juveniles from thousands of locally

172 One example is Pacific salmon (Oncorhynchus spp.), supporting subsistence harvests, and

173 ly and ecologically critical Pacific salmon (Oncorhynchus spp.).

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

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

176 mineralogical compositions of Chinook salmon Oncorhynchus tshawytscha otolith pairs.

177 seasonal changes in juvenile Chinook Salmon Oncorhynchus tshawytscha size, growth and production ove

178 Chinook salmon Oncorhynchus tshawytscha stocks distribute across the No

179 havioural assay with juvenile Chinook salmon Oncorhynchus tshawytscha that varied in their past preda

180 ar (YOY) growth potential of Chinook salmon (Oncorhynchus tshawytscha) and Dolly Varden (Salvelinus m

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

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

183 on and knockout studies in a Chinook salmon (Oncorhynchus tshawytscha) cell line were conducted to as

184 We isolated a Chinook salmon (Oncorhynchus tshawytscha) cell line, GS2, with a stat2 g

185 While Chinook (Oncorhynchus tshawytscha) experienced a down-river range

186 fish was made from moribund Chinook salmon (Oncorhynchus tshawytscha) from the Eel River, California

187 In 2020, newly hatched Chinook salmon (Oncorhynchus tshawytscha) fry in California's Central Va

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

189 shing on the survival of the Chinook salmon (Oncorhynchus tshawytscha) in the Sandy River (OR, USA),

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

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

192 of sockeye (Oncorhynchus nerka) and Chinook (Oncorhynchus tshawytscha) salmon in the Northeast Pacifi

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

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

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

196 %, Snake River spring/summer chinook salmon (Oncorhynchus tshawytscha) would probably continue to dec

197 sonal migration patterns) of Chinook salmon (Oncorhynchus tshawytscha), a phenotypically diverse anad

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

199 In Chinook salmon (Oncorhynchus tshawytscha), exposure to a high but enviro

200 n (Acipenser transmontanus), chinook salmon (Oncorhynchus tshawytscha), westslope cutthroat trout (On

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