ライフサイエンスコーパス: trout

1 zed a novel GHR from a teleost fish (rainbow trout).

2 bsequently lost in Euteleostei (e.g. rainbow trout).

3 es (lake whitefish, coho salmon, and rainbow trout).

4 icantly lower rates in comparison to rainbow trout.

5 ish were significantly lower than in rainbow trout.

6 M substantially higher than those of rainbow trout.

7 the stress and feeding responses in rainbow trout.

8 CD diastereomers during biotransformation in trout.

9 ction involves abnormal monoamine content in trout.

10 nsporter type 2 in distinct brain regions of trout.

11 icantly attenuated virulence against rainbow trout.

12 criptomes of several clonal lines of rainbow trout.

13 ficant predictors of plasma TH levels in the trout.

14 fy from dietary exposure in juvenile rainbow trout.

15 brominated PBDEs is occurring in Great Lakes trout.

16 pting potential exerted by HF-FPW in rainbow trout.

17 es in gonadotropins and estradiol in rainbow trout.

18 mples of farmed Atlantic salmons and rainbow trouts.

19 ta) (TMF(-SMELT) = 1.62, CI: 0.96-2.72; TMF(-TROUT) = 3.58, CI: 1.82-7.03).

20 Steelhead trout (52 individual fishes) have MeHg of predominantly

21 gh its stimulation of Tnfalpha production in trout, a primitive teleost fish.

22 inding protein was identified in the rainbow trout, a protein that structurally behaves like an inter

23 Simulations show that trout abundance could be greatly reduced under constant

24 The data were a 15-year record of brook trout abundance from 72 sites distributed across a 170-k

25 t contaminant trends due to significant lake trout age structure changes.

26 to mitigate the effect of a fluctuating lake trout age structure to directly improve the log-linear r

27 and visual pigment absorbance in the rainbow trout alevin but only visual pigment absorbance in the s

28 n the single cones of small juvenile rainbow trout (alevin), opsin expression in large juvenile rainb

29 nce, biomass, growth rate, and production of trout all increased with stream temperature.

30 analysis to trace the geographical origin of trout, also according to the type of feed.

31 tions are generally declining in Great Lakes trout, although there are clear exceptions to this trend

32 g(-)(1)ww in barbel, 9.2-97.0 ng g(-1)ww in trout and 9.0-239.5 ng g(-1)ww in eel.

33 nvestigated the presence of NDL PCBs in eel, trout and barbel from the River Roya.

34 e expression of all six subgroups in rainbow trout and brown trout Salmo trutta.

35 Hg concentrations in lake trout and burbot increased significantly over the early

36 oral variations in Hg concentrations in lake trout and burbot were similar with respect to timing of

37 AEs and 869 BMFs from 19 species (primarily trout and carp) was developed from the literature.

38 cs of hybridization between native cutthroat trout and invasive rainbow trout, the world's most widel

39 organisms, including Daphnia magna, rainbow trout and juvenile crayfish, and is able to capture the

40 rook trout and salmon, suggesting that brook trout and mottled sculpin either use salmon tissue to di

41 ive hybridization between introduced rainbow trout and native cutthroat trout in western North Americ

42 blished in vivo and in vitro data in rainbow trout and new data on the synthesis of gonadotropins in

43 Phylogenetic tree and synteny analyses of trout and other fish species suggest that two types (nam

44 important conservation implications for bull trout and other imperiled species.

45 e study lakes were exceeded, impacting brown trout and perch populations.

46 mottled sculpin differed from those of brook trout and salmon, suggesting that brook trout and mottle

47 e three inland, freshwater datasets are ELA, TROUT and SWAT.

48 We find that NALT is present in rainbow trout and that it resembles other teleost mucosa-associa

49 Lake trout and walleye composites were collected between 2004

50 entrations and age-corrected trends for lake trout and walleye in the Great Lakes over the 2004-2014

51 of TEQ associated with all Great Lakes lake trout and walleye samples is due to the nonortho CP-PCBs

52 elines for wildlife protection based on lake trout and walleye total TEQ were uniformly exceeded in a

53 centration trends in top predator fish (lake trout and walleye) of the Great Lakes (GL) from 2004 to

54 in the Great Lakes' top predator fish (lake trout and walleye) was assembled by integrating previous

55 Component B (Dec604 CB), was present in lake trout and whitefish at concentrations of 10-60 ng/g lipi

56 h, gummy shark, oyster (four species), ocean trout and yellowtail kingfish.

57 the absorbance of visual pigments in rainbow trout and zebrafish.

58 h (predominantly largemouth bass and rainbow trout), and 505 prey fish (14 species) at 25 lakes throu

59 lt, but nonracemic in the top predator, lake trout, and all invertebrate species.

60 Michigan, Huron, Ontario, and Superior lake trout, and Lake Erie walleye, respectively.

61 d caloric turnover rates for Lake Huron lake trout, and reveal how these processes are regulated by b

62 Odorous molecules in earthen-ponds rainbow trout aquaculture farming in Germany were investigated w

63 e first time in German earthen-ponds rainbow trout aquaculture water including, amongst others, 4-hyd

64 Brown trout are at the northern limit of their geographic dist

65 Using rainbow trout as a model we characterized responses to two natur

66 dictions to investigate the success of brown trout as top predators across a stream temperature gradi

67 regulation of B cell populations in rainbow trout, as well as an essential role for sphingolipids in

68 Consumption by bull trout at other settings were lower and more variable, bu

69 both young-of-the-year (YOY) and adult brown trout attained 100% at the end of summer, while seasonal

70 sms that contributed to these responses: (1) trout became more selective in their diet as stream temp

71 ocky Mountains for two native salmonids-bull trout (BT) and cutthroat trout (CT).

72 f head kidney leukocytes from Ag-experienced trout but not naive controls, yet it does not confer pro

73 M concentrations similar to those of rainbow trout but not with sea lamprey.

74 rements of heavier PAHs (>/=5 rings) in lake trout, but lighter PAHs (</=4 rings) were overpredicted,

75 ioconcentration of PFASs in juvenile rainbow trout by exposing the fish in separate tanks under flow-

76 Trout by-product hydrolysates, generated using trout pep

77 und between local escapes and subsequent sea trout catch.

78 Recombinant His-tagged trout CK12a (rCK12a) is not chemotactic in vitro but it

79 ogical active hormone, T3, in the Lake Mjosa trout co-occurred with their low Se:Hg molar ratios.

80 The trout cobalamin-binding protein was glycosylated and dis

81 Like haptocorrin and transcobalamin, the trout cobalamin-binding protein was present in plasma an

82 The trout cobalamin-binding protein was purified from roe fl

83 Like haptocorrin, the trout cobalamin-binding protein was stable at low pH and

84 In vitro, tSC present in mucus coats trout commensal isolates such as Microbacterium sp., Sta

85 Metal concentrations in the Hayle trout, compared to fish from a relatively unimpacted riv

86 Studies in rats and rainbow trout confirmed that DHA biosynthesis proceeds through t

87 We also simulated bull trout consumption and growth during salmon smolt outmigr

88 Native Colorado River cutthroat trout (CRCT; Oncorhynchus clarkii pleuriticus) are now r

89 tive salmonids-bull trout (BT) and cutthroat trout (CT).

90 Once validated, Lake Michigan trout data files were analyzed for polyfluoroalkyl acids

91 chicken, 7451 pigs, 753 sheep and 88 rainbow trout data points in the database, and at least 290 publ

92 and temperature had strong effects on brook trout demography.

93 s of inclusion (60%, 75% and 90%) in rainbow trout diets.

94 One-day consumption by laboratory-held bull trout during the first day of feeding experiments after

95 he delta(202)Hg and Delta(199)Hg of the lake trout equaled the isotopic composition of the bloater af

96 ranscriptional response of mature male brown trout exposed for 4 days to 1.7, 15.3, and 225.9 mug/L l

97 Furthermore, GST and SOD activities of trout exposed to both Se-Met and parasites were generall

98 ulated mRNAs and lncRNAs in juvenile rainbow trout exposed to E2.

99 single-cell CLEM to magnetic cells from the trout failed to identify any intracellular structures co

100 d we conducted genome scans of seven rainbow trout families from a single broodstock population to id

101 igated restoration of EPA and DHA in rainbow trout fed a FOFD preceded by a grow-out period on 50% or

102 shows effectively that quality and safety of trout feeds has greatly improved during the last years a

103 of feeding regime on composition of rainbow trout fillets, as well as on lipid and protein oxidation

104 ve stress and oxidative stability of rainbow trout fillets.

105 alysis of MG in different types of water and trout fish samples.

106 the first time in German aquaculture rainbow trout fish, including, amongst others, (E,Z,Z)-2,4,7-tri

107 e efficient than the synthetic feed to color trout flesh (up to twofold increase in the retention of

108 variation in prey abundance influenced lake trout foraging tactics (i.e., the balance of the number

109 ntain fish as the apex predator; a cutthroat trout from the experiment, the only fish species in the

110 were much lower than those reported for lake trout from the more urbanized and industrialized Laurent

111 y trends in Walleye, Northern Pike, and Lake Trout from the Province of Ontario, Canada, which contai

112 ] fish cell line) and in vivo (using rainbow trout fry) in a dose-dependent and time-dependent manner

113 We then determined whether bull trout genetic diversity was related to climate vulnerabi

114 e to an additional round of WGD, the rainbow trout genome offers a unique opportunity to investigate

115 e duplicated genes have been retained in the trout genome.

116 cterize copper and silver binding to rainbow trout gill cells, either as cultured reconstructed epith

117 construct and culture the freshwater rainbow trout gill epithelium on flat permeable membrane support

118 Lake trout greatly reduced their use of littoral habitat and

119 young growing fish, slow growing, older lake trout (>5 yr) recycled an average of 482 Tonnes.yr(-1) o

120 ith shorter springs and longer summers, lake trout had reduced access to littoral habitat and assimil

121 The methodology was validated in trout, hake and Atlantic horse mackerel and was used to

122 ns tumors were induced in zebrafish, rainbow trout, hamsters, and mice by carcinogenic agents (methyl

123 ed a lymphoid cell line derived from rainbow trout head kidney cells.

124 Lipid profiles of fish oil extracted from trout heads, spines and viscera using supercritical carb

125 sic clearance determined using cryopreserved trout hepatocytes can be extrapolated to the whole anima

126 of this study demonstrate that cryopreserved trout hepatocytes can be used to reliably obtain in vitr

127 ate depletion experiments with cryopreserved trout hepatocytes from a single source.

128 , a significant decreasing trend in the lake trout Hg concentrations was found between 2004 and 2015

129 he proportion of IgT(+) to IgM(+) B cells in trout HK.

130 Furthermore, we identified trout homologs for CD141 and CD103 and demonstrated that

131 ted an innate immune response in the rainbow trout host, making LJ001 potentially useful for future v

132 ale mathematical model of the female rainbow trout hypothalamus-pituitary-ovary-liver axis to use as

133 sis revealed high constitutive expression of trout IL-17A/F2 in mucosal tissues from healthy fish, su

134 In addition, the bioactivity of the trout IL-17A/F2 is investigated for the first time in an

135 xpression and bioactivity results imply that trout IL-17A/F2 plays an important role in promoting inf

136 ased MHC-II surface expression that point to trout IL-6 as a differentiation factor for IgM antibody-

137 e present study was to establish the role of trout IL-6 on B cells, comparing its effects to those in

138 Our results reveal that, in trout, IL-6 is a differentiation factor for B cells, sti

139 apture-mark-recapture study of eastern brook trout in four streams in Western Massachusetts, USA to p

140 one-year-old (1+) Atlantic salmon and brown trout in response to flow change during summer.

141 ed that salmon are a source of POPs to brook trout in stream reaches receiving salmon spawners from L

142 The degree of binge-feeding by bull trout in the field was slightly reduced but largely in a

143 ntroduced rainbow trout and native cutthroat trout in western North America will lead to genomic exti

144 NAs (lncRNAs), in skeletal muscle of rainbow trout injected with E2.

145 ason for this paradox is that past nonnative trout invasions and habitat loss have restricted most CR

146 olorado River Basin, owing to past nonnative trout invasions and habitat loss.

147 metabolic rate (RMR) in juvenile salmon and trout is positively related to dominance status and abil

148 grees C) were evaluated using farmed rainbow trout killed by asphyxia in air or percussion.

149 ks were largely maintained throughout marble trout lifetime in both populations.

150 ne fragrance ingredients were measured using trout liver S9 fractions and used as inputs to a recentl

151 o biotransformation experiments with rat and trout liver S9 fractions for different incubation times

152 rthern Pike (NP), and 70% to 76-92% for Lake Trout (LT).

153 utively expressed at high levels in all four trout MALT.

154 although concentrations in Lake Ontario Lake Trout may have stopped increasing in response to volunta

155 irmed that trout MRAP interacts with the two trout MC1R variants and MC2R, but failed to detect regul

156 , regardless of the climate data set or bull trout model employed.

157 ndex improved explanatory power for the lake trout model suggesting that trends may have been affecte

158 lpha3) that has only low identities to known trout molecules.

159 xperiments in mammalian cells confirmed that trout MRAP interacts with the two trout MC1R variants an

160 ll as an essential role for sphingolipids in trout mucosal homeostasis.

161 that the majority of tSC is in free form in trout mucus and free tSC is able to directly bind bacter

162 results showed that the presence of PCBs in trout muscle is directly linked to the chemical quality

163 elated (p<0.01 and r=0.451) with the rainbow trout muscle Sigma18PCBs.

164 thod was applied to Nile tilapia and rainbow trout (n=29) and 14% of them contained enrofloxacin at l

165 The predominant B-cell subset found in trout NALT are IgT(+) B cells, similar to skin and gut.

166 Trout NALT consists of diffuse lymphoid cells and lacks

167 Trout NALT is capable of mounting strong anti-viral immu

168 of CK12 (but not CK10 or CK13) expression in trout nasopharynx-associated lymphoid tissue.

169 uleatus), 41 +/- 38 (char), and 9.9 +/- 5.9 (trout) ng g(-1) wet weight.

170 coho salmon (Oncorhynchus kisutch), rainbow trout (O. mykiss), Chinook salmon (O. tshawytscha), Atla

171 As a tissue of choice, we selected trout olfactory epithelium that has been previously sugg

172 The trout olfactory organ is colonized by abundant symbiotic

173 rax); turbot (Scophthalmus maximus); rainbow trout (Onchorynchus mykiss); and salmon (Salmo salar), i

174 further subgroups (IFN-e and -f) in rainbow trout Oncorhynchus mykiss and analyzed the expression of

175 and Champsocephalus gunnari, and the rainbow trout Oncorhynchus mykiss as a reference.

176 Exposed juvenile rainbow trout (Oncorhynchus mykiss) accumulated surfactants, nap

177 collected in two previous studies of rainbow trout (Oncorhynchus mykiss) and common carp (Cyprinus ca

178 ganic chemicals in two fish species: rainbow trout (Oncorhynchus mykiss) and fathead minnow (Pimephal

179 he cobalamin-binding proteins of the rainbow trout (Oncorhynchus mykiss) and to compare their propert

180 f-odour development in earthen-ponds rainbow trout (Oncorhynchus mykiss) aquaculture farming in Germa

181 n and functional characterization of rainbow trout (Oncorhynchus mykiss) CD4-1(+) T cells and the est

182 film on the rancidity development in rainbow trout (Oncorhynchus mykiss) fillets during refrigerated

183 the muscle and edible skin parts of rainbow trout (Oncorhynchus mykiss) fillets, sampled at two grow

184 lex mixtures in a primary culture of rainbow trout (Oncorhynchus mykiss) hepatocytes.

185 discovery and sequence analysis of a rainbow trout (Oncorhynchus mykiss) IL-17A/F2 molecule and an IL

186 he growth of the young of the year steelhead trout (Oncorhynchus mykiss) in the recipient tributary o

187 presence of CD8alpha(+) cells in the rainbow trout (Oncorhynchus mykiss) nasal epithelium.

188 wild and first-generation hatchery steelhead trout (Oncorhynchus mykiss) reared in a common environme

189 e, but not benzocaine or MS-222; and rainbow trout (Oncorhynchus mykiss) showed no avoidance to the t

190 ular mass<30kDa (PF30) isolated from rainbow trout (Oncorhynchus mykiss) skin gelatin hydrolysates wa

191 sing on the shelf-life of fillets of rainbow trout (Oncorhynchus mykiss) were examined.

192 tion on the shelf-life of fillets of rainbow trout (Oncorhynchus mykiss) were examined.

193 Rainbow trout (Oncorhynchus mykiss) were exposed to waterborne v

194 isms in aquatic ecosystems, juvenile rainbow trout (Oncorhynchus mykiss) were separately exposed to a

195 e that BPA deposition in the eggs of rainbow trout (Oncorhynchus mykiss), an ecologically and economi

196 in benthic invertebrates, juvenile steelhead trout (Oncorhynchus mykiss), and water striders (Gerris

197 negatively affects muscle growth in rainbow trout (Oncorhynchus mykiss), but the mechanisms directin

198 cestor of salmonid fishes, including rainbow trout (Oncorhynchus mykiss), experienced a whole genome

199 sturgeon (Acipenser fulvescens), and rainbow trout (Oncorhynchus mykiss), were selected to evaluate T

200 ave added to the controversy is that rainbow trout (Oncorhynchus mykiss), which have served as the pr

201 bioaccumulation of selenium (Se) in rainbow trout (Oncorhynchus mykiss).

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

203 turn to the surface, was examined in rainbow trout (Oncorhynchus mykiss).

204 n high- (HR) and low-responsive (LR) rainbow trout (Oncorhynchus mykiss).

205 of liver S9 fractions isolated from rainbow trout (Oncorhynchus mykiss).

206 he gill and skin mucosal surfaces of rainbow trout (Oncorhynchus mykiss).

207 gated whether a relevant model fish (rainbow trout, Oncorhynchus mykiss) could detect OSPW using its

208 out by-product hydrolysates, generated using trout pepsin, were characterized and studied in terms of

209 Rainbow trout pIgR is known to transport IgT and IgM across epit

210 However, other biological functions for trout pIgR or trout secretory component (tSC) remain unk

211 Indo-west Pacific, the large predatory coral trout Plectropomus leopardus (Serranidae), can behaviour

212 ectropomus pessuliferus marisrubri and coral trout Plectropomus leopardus, use to indicate hidden pre

213 Here, we show that a fish--the coral trout Plectropomus leopardus--has partner-choice abiliti

214 ommercially-important marine fish, the coral trout Plectropomus leopardus.

215 The visual stimulus of a top predator (coral trout, Plectropomus leopardus) restricted the foraging a

216 cenarios, refugia with high probabilities of trout population occupancy (>0.9) were predicted to exis

217 strong gradient in genetic diversity in bull trout populations across the Columbia River Basin, where

218 Furthermore, the majority of brook trout populations are projected to persist if high winte

219 inear mixed models, allelic richness in bull trout populations was positively related to habitat patc

220 egion, had the strongest negative effects on trout populations.

221 and GHR2b, the two type 2 GHRs isolated from trout previously.

222 As a rainbow trout producer, Italy is accounted as fifth in the world

223 ical stocking locations with greater rainbow trout propagule pressure, warmer water temperatures, and

224 and defatted (protein) fillet of 130 rainbow trout, reared with feed incorporating a high or low fish

225 ologically relevant to trout, we showed that trout recruit a moray collaborator more often when the s

226 tellite genotypes, we document in situ brook trout reproduction, which is the initial phase in the re

227 l endocrine components of the female rainbow trout reproductive axis.

228 ormation (t0.5 = 6.4 and 38.1 min in rat and trout, respectively), alpha-HBCD appears the most resist

229 and 0.419 after 60 min incubation in rat and trout, respectively).

230 TCDD raw concentrations in Lake Ontario lake trout revealed decreases of 94% and 96%, respectively.

231 In rainbow trout RTG-2 and RTS-11 cells, polyinosinic-polycytidylic

232 terestingly, delta-HBCD was detected only in trout S9 fraction assays indicating metabolic interconve

233 ethod, we consider two populations of marble trout Salmo marmoratus living in Slovenian streams, wher

234 studies of oxidative stress using the brown trout Salmo trutta as model.

235 occur where an important predator, the brown trout Salmo trutta, is also small.

236 all six subgroups in rainbow trout and brown trout Salmo trutta.

237 This procedure was tested in brown trout ( Salmo trutta ) kept in captivity.

238 almon (classified as wild or farmed) and sea trout (Salmo trutta L.).

239 excluding smelt (Osmerus eperlanus) or brown trout (Salmo trutta) (TMF(-SMELT) = 1.62, CI: 0.96-2.72;

240 an lakes (Mjosa, Randsfjorden), and in brown trout (Salmo trutta) and Arctic char (Salvelinus alpinus

241 ly contaminated with metals, including brown trout (Salmo trutta) inhabiting the River Hayle in South

242 n Arctic char (Salvelinus alpinus) and brown trout (Salmo trutta) when the benthic link was included

243 quences for somatic growth in juvenile brown trout (Salmo trutta).

244 h the insertion of a silicone tag into brown trout (Salmo trutta).

245 ffect plasma TH levels in free-ranging brown trout, Salmo trutta , from Lake Mjosa (a Se-deprived lak

246 or stream fishes and cold-water species like trout, salmon, and char that are already constrained to

247 %, 5.1%, 2.6% and 8.0% for tilapia, catfish, trout, salmon, hybrid striped bass and yellow perch, res

248 hod by forecasting suitable habitat for bull trout (Salvelinus confluentus) in the Interior Columbia

249 c variation and habitat features in 130 bull trout (Salvelinus confluentus) populations from 24 water

250 rvations with laboratory experiments of bull trout (Salvelinus confluentus), a large freshwater pisci

251 ity decline and loss of an established brook trout (Salvelinus fontinalis [Mitchill]) population in B

252 spring) on survival and recruitment of brook trout (Salvelinus fontinalis) at a broad spatial scale u

253 agged, sampled seasonally) data set of brook trout (Salvelinus fontinalis) from four sites in a strea

254 ion size and mean body size in eastern brook trout (Salvelinus fontinalis).

255 In lake trout (Salvelinus namaycush) from northern Canada (e.g.,

256 In experiment 2, lake trout (Salvelinus namaycush) were raised in captivity on

257 ture dataset to test if a population of lake trout (Salvelinus namaycush), a cold-water stenotherm, a

258 rends in mercury (Hg) concentrations in lake trout (Salvelinus namaycush), burbot (Lota lota), and no

259 es Basin), and species identity (i.e., brook trout [Salvelinus fontinalis] or mottled sculpin [Cottus

260 (PFCs) were determined in Lake Ontario Lake Trout sampled annually between 1997 and 2008 in order to

261 other biological functions for trout pIgR or trout secretory component (tSC) remain unknown.

262 The trout secretory delta transcript is produced via a run-o

263 dant symbiotic bacteria, which are coated by trout secretory immunoglobulin.

264 as low relative to its host, and parasitized trout showed slowed Se accumulation in the muscle as com

265 consequence, also the PCBs values in muscle trout, showed a decreasing trend.

266 e levels of the eighteen PCBs in feed and in trout, showed a statistical significant difference (p<0.

267 hts into mRNA and lncRNA networks in rainbow trout skeletal muscle and their regulation by E2 while u

268 Our results show that the majority of trout skin and gut bacteria are coated in vivo by tSC.

269 , opsin expression in large juvenile rainbow trout (smolt), zebrafish, or killifish remained unchange

270 nd (2) how can the paradoxical loss of PS in trout smolts be reconciled?

271 n lakes with pH > 6.5 that were stocked with trout species.

272 High cobalamin-binding capacity was found in trout stomach (210 pmol/g), roe (400 pmol/g), roe fluid

273 el memIgD(+)memIgM(-) B lymphocyte subset in trout that expresses memCCR7 and responds to viral infec

274 and Randsfjorden) had cVMS concentrations in trout that were up to 2 orders of magnitude higher than

275 native cutthroat trout and invasive rainbow trout, the world's most widely introduced invasive fish,

276 or CD141 and CD103 and demonstrated that, in trout, this skin CD8(+) DC-like subpopulation expresses

277 n this study we show that collagen activates trout thrombocytes in whole blood and under flow conditi

278 The constitutive expression of trout TNF-alpha3 was generally lower than the other two

279 Recombinant trout Tnfalpha (rTnfalpha) and PGF2alpha recapitulate th

280 mechanisms employed by the River Hayle brown trout to tolerate high metal concentrations.

281 . major sphingolipids modulate the growth of trout total skin and gill symbiotic bacteria.

282 sequenced, assembled and annotated the brown trout transcriptome using a de novo approach.

283 In rainbow trout, two TNF-alpha molecules were described previously

284 enrichment of (-)-alpha-HBCD in rat than in trout underlines the species-specific differences in HBC

285 ivergent HEV-like virus from fish (cutthroat trout virus) representing a second genus.

286 The biotransformation rate in trout was slower than in rat.

287 but modified to be ecologically relevant to trout, we showed that trout recruit a moray collaborator

288 Finally, when trout were bath challenged with viral hemorrhagic septic

289 Juvenile rainbow trout were exposed to 1.0 mg l(-1) citrate-capped Ag NPs

290 Rainbow trout were fed six different diets, which differed in th

291 Trout were injected with three different Ba137/Ba135 iso

292 Candidate species identified in lake trout were qualified using theoretical isotopic profile

293 Rainbow trout were simultaneously exposed to 11 chemicals.

294 Growing rainbow trout with diets where FO was replaced by either 50% or

295 Infection of brown trout with hemorrhagic septicemia virus resulted in earl

296 ld play a more important role in the diet of trout with increasing stream temperature.

297 ertebrate host, Oncorhynchus mykiss (rainbow trout), with variants of a coevolved viral pathogen, inf

298 us primarily on farmed salmonids (salmon and trout) within a comparative context and will give an ove

299 persistence of native Yellowstone cutthroat trout (YCT) and competing invasive species.

300 le-cone opsin expression in juvenile rainbow trout, zebrafish, and killifish and on the absorbance of