ライフサイエンスコーパス: rainbow trout

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

2 y got subsequently lost in Euteleostei (e.g. rainbow trout).

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

4 h in vivo exposure experiment with juvenile rainbow trout.

5 d significantly attenuated virulence against rainbow trout.

6 he transcriptomes of several clonal lines of rainbow trout.

7 biomagnify from dietary exposure in juvenile rainbow trout.

8 f IHNV genotypes that differ in virulence in rainbow trout.

9 with particularly negative consequences for rainbow trout.

10 , liver, gill, testis and ovary samples from rainbow trout.

11 form, ERalpha2 (i.e., NR3A1b), exists in the rainbow trout.

12 within the 12 beta2m genes of an individual rainbow trout.

13 rtant role in regulating IL-18 activities in rainbow trout.

14 ave been compared with their counterparts in rainbow trout.

15 ydroxylated metabolites (alkyl-OH-6PPD-Q) in rainbow trout.

16 ronic toxicity of 6PPD-Q in early life stage rainbow trout.

17 o biotransformation rates, BCFs, and BMFs in rainbow trout.

18 ad seabream compared to European seabass and rainbow trout.

19 y was lower in all sole extracts compared to rainbow trout.

20 and detection of low drug concentrations in rainbow trout.

21 stic pathogen with moderate pathogenicity in rainbow trout.

22 metabolites formed in the liver microsome of rainbow trout.

23 ne disrupting potential exerted by HF-FPW in rainbow trout.

24 with regards to estrogenicity in humans and rainbow trout.

25 al changes in gonadotropins and estradiol in rainbow trout.

26 t significantly lower rates in comparison to rainbow trout.

27 nvolved in spontaneous maleness of XX-female rainbow trout.

28 arctic fish were significantly lower than in rainbow trout.

29 s of aTFM substantially higher than those of rainbow trout.

30 mpacting the stress and feeding responses in rainbow trout.

31 ified samples of farmed Atlantic salmons and rainbow trouts.

32 alamin-binding protein was identified in the rainbow trout, a protein that structurally behaves like

33 , we have cloned and characterized a C5aR in rainbow trout, a teleost fish.

34 Rainbow Trout accumulated intracellular and extracellula

35 ed fish rhabdoviruses were used to vaccinate rainbow trout against a lethal challenge with infectious

36 ression and visual pigment absorbance in the rainbow trout alevin but only visual pigment absorbance

37 posure in the single cones of small juvenile rainbow trout (alevin), opsin expression in large juveni

38 Rainbow trout alevins were exposed from hatch until 28 d

39 of the classical and alternative pathways in rainbow trout, an evolutionarily relevant teleost specie

40 al administration of 80 mg kg(-1) day(-1) in rainbow trout and assess its biosafety at concentration

41 and OmpF.2, were associated with pathogenic rainbow trout and Atlantic salmon isolates, respectively

42 s representing typical pathogenic strains in rainbow trout and Atlantic salmon, respectively.

43 Rainbow trout and brown trout have been introduced globa

44 lyzed the expression of all six subgroups in rainbow trout and brown trout Salmo trutta.

45 Here, we investigated whether diploid rainbow trout and diploid and triploid brown trout diffe

46 nge test confirmed moderate pathogenicity in rainbow trout and established Koch's postulates.

47 eshwater organisms, including Daphnia magna, rainbow trout and juvenile crayfish, and is able to capt

48 trogressive hybridization between introduced rainbow trout and native cutthroat trout in western Nort

49 ously published in vivo and in vitro data in rainbow trout and new data on the synthesis of gonadotro

50 vidence about the process of VE formation in rainbow trout and other non-cyprinoid fish and allow com

51 ls as well as the content of contaminants of rainbow trout and sole side streams (head, skin and visc

52 We find that NALT is present in rainbow trout and that it resembles other teleost mucosa

53 d had a higher functional response than both rainbow trout and triploid brown trout.

54 and on the absorbance of visual pigments in rainbow trout and zebrafish.

55 port fish (predominantly largemouth bass and rainbow trout), and 505 prey fish (14 species) at 25 lak

56 hicken), reptiles (turtle), fish (salmon and rainbow trout), and amphibians (frog), were isolated.

57 with orthologous regions in Atlantic salmon, rainbow trout, and Arctic char also revealed extensive c

58 Odorous molecules in earthen-ponds rainbow trout aquaculture farming in Germany were invest

59 d for the first time in German earthen-ponds rainbow trout aquaculture water including, amongst other

60 Evidence suggests that dab and rainbow trout are able to quickly adjust their food inta

61 Rainbow trout are particularly susceptible and may suffe

62 These studies indicate that early life stage rainbow trout are sensitive to subchronic 6PPD-Q exposur

63 nts of host jumps and increased virulence in rainbow trout are unknown for any fish rhabdovirus.

64 chlorodibenzo-p-dioxin (TCDD), dimerize with rainbow trout ARNTb (rtARNTb), and recognize dioxin resp

65 stigate this hypothesis, we used the teleost rainbow trout as a model system.

66 Using rainbow trout as a model we characterized responses to t

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

68 clonal structure of the systemic and mucosal rainbow trout B cell repertoire.

69 nd cloning strategy, followed by screening a rainbow trout BAC library yielded a unique DNA sequence

70 vide useful information for the selection of rainbow trout based on the seasons and locations in term

71 clones from the same fish now shows that the rainbow trout beta2m locus consists of two expressed gen

72 s we conclude that blastomeres isolated from rainbow trout blastulae will incorporate and continue to

73 Herein, as part of a rainbow trout broodstock improvement program, we evaluat

74 show aTFM concentrations similar to those of rainbow trout but not with sea lamprey.

75 ed the bioconcentration of PFASs in juvenile rainbow trout by exposing the fish in separate tanks und

76 Caligus rogercresseyi in Atlantic salmon and rainbow trout by performing single-step Genome-Wide Asso

77 like cathepsin Ds in other species, however, rainbow trout cathepsin D appears to have only one putat

78 From our experiments, rainbow trout cell lines appear as a suitable conservati

79 University (OSU) and the Swanson (SW) River rainbow trout clonal lines.

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

81 e, 3442 chicken, 7451 pigs, 753 sheep and 88 rainbow trout data points in the database, and at least

82 ee levels of inclusion (60%, 75% and 90%) in rainbow trout diets.

83 These results suggest that rainbow trout do not manage their energy budgets effecti

84 ifying properties of lecithins isolated from rainbow trout egg (RL) and trout processing discard (WL)

85 The rainbow trout egg vitelline envelope (VE) is constructed

86 was employed with VE proteins isolated from rainbow trout eggs in a peptidomics-based approach to de

87 est relative to rainbow trout ERalpha2 being rainbow trout ERalpha1, suggesting a recent, unique dupl

88 subtype clade, with the closest relative to rainbow trout ERalpha2 being rainbow trout ERalpha1, sug

89 Both the rainbow trout ERbeta subtypes, ERbeta1 [NR3A2a] and ERbe

90 The rainbow trout ERbeta1 and ERbeta2 are not closely associ

91 esence of both transcripts in all individual rainbow trout examined suggest that the two forms of rtA

92 ally regulated mRNAs and lncRNAs in juvenile rainbow trout exposed to E2.

93 in vitro findings were confirmed in vivo in rainbow trout exposed to LPS and OSPW for 48 h, which re

94 this end we conducted genome scans of seven rainbow trout families from a single broodstock populati

95 ing was initiated using a large outbred F(2) rainbow trout family (n=480) and results were confirmed

96 host component from rainbow trout.IMPORTANCE Rainbow trout farming is a major food source industry wo

97 e investigated restoration of EPA and DHA in rainbow trout fed a FOFD preceded by a grow-out period o

98 The C50QRA indicator was used for monitoring rainbow trout fillet spoilage and revealed a visually-de

99 ties, protein denaturation, and structure of rainbow trout fillet was studied and compared with refri

100 nfluence of feeding regime on composition of rainbow trout fillets, as well as on lipid and protein o

101 oxidative stress and oxidative stability of rainbow trout fillets.

102 balustinum were characterized from diseased rainbow trout fingerlings.

103 bed for the first time in German aquaculture rainbow trout fish, including, amongst others, (E,Z,Z)-2

104 group of dab and individuals and a group of rainbow trout for analysis.

105 we recorded the phenotypic sex of 20,210 XX-rainbow trout from a French farm population at 10 and 15

106 llow-up acute study with exogenously feeding rainbow trout fry revealed a 96-h LC(50) of 0.47 mug/L.

107 ini [EPC] fish cell line) and in vivo (using rainbow trout fry) in a dose-dependent and time-dependen

108 The rainbow trout genetic linkage groups have been assigned

109 The status of rainbow trout genetic maps has progressed significantly

110 maps, identifying paralogous regions of the rainbow trout genome arising from the evolutionarily rec

111 Due to an additional round of WGD, the rainbow trout genome offers a unique opportunity to inve

112 identified 180 duplicated regions within the rainbow trout genome.

113 etic basis of whirling disease resistance in rainbow trout, genome-wide mapping was initiated using a

114 Here, the inflammation of the rainbow trout gill cell line RTgill-W1 was induced via e

115 ished an in vitro screening method using the rainbow trout gill cell line, RTgill-W1, to investigate

116 ld-coated iron oxide NPs were incubated with rainbow trout gill cell total protein extracts and mass

117 ly characterize copper and silver binding to rainbow trout gill cells, either as cultured reconstruct

118 ow to reconstruct and culture the freshwater rainbow trout gill epithelium on flat permeable membrane

119 ator (ARNT) protein were isolated from RTG-2 rainbow trout gonad cells.

120 11 strongly inhibits the growth of different rainbow trout Gram-positive and Gram-negative bacteria,

121 where lens tumors were induced in zebrafish, rainbow trout, hamsters, and mice by carcinogenic agents

122 Rainbow trout has a male heterogametic (XY) sex determin

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

124 er characterized by in vitro bioassays using rainbow trout hepatocytes (Oncorhynchus mykiss) and in v

125 W1 (rainbow trout normal liver), and primary rainbow trout hepatocytes exposed to model chemotherapeu

126 NV elicited an innate immune response in the rainbow trout host, making LJ001 potentially useful for

127 association between activity and boldness in rainbow trout, however, there was in both brown trout ty

128 multi-scale mathematical model of the female rainbow trout hypothalamus-pituitary-ovary-liver axis to

129 this study, we undertook the analysis of the rainbow trout IgHmu repertoire in this critical tissue f

130 We detected responses of rainbow trout IgT to an intestinal parasite only in the

131 cient interaction with a host component from rainbow trout.IMPORTANCE Rainbow trout farming is a majo

132 ork, we investigate the swimming dynamics of rainbow trout in the wake of a thrust-producing oscillat

133 nces are also present in both pufferfish and rainbow trout, indicating the likely presence of a solub

134 coding RNAs (lncRNAs), in skeletal muscle of rainbow trout injected with E2.

135 The rainbow trout interleukin (IL)-1 beta gene consists of s

136 -vasotocin isolated from the pineal gland of rainbow trout is detected, demonstrating the ability of

137 suggests that pathogenic Atlantic salmon and rainbow trout isolates represent distinct host-specific

138 change involving certain Atlantic salmon and rainbow trout isolates.

139 (-10 degrees C) were evaluated using farmed rainbow trout killed by asphyxia in air or percussion.

140 The double haploid rainbow trout lines and linkage map present a foundation

141 ctive transport assay based on the permanent rainbow trout liver cell line RTL-W1 was used to qualita

142 intrinsic clearance (CL(IN VITRO,INT)) from rainbow trout liver S9 fractions (RT-S9) can be applied

143 ghly volatile linear and cyclic siloxanes in rainbow trout liver S9 subcellular fractions and the ext

144 s of clearance measured in isolated perfused rainbow trout livers, and the importance of active trans

145 n addition, the lower functional response of rainbow trout may explain why they are implicated in few

146 The increased activity and aggression of rainbow trout may reflect an increased stress response t

147 ely correlated (p<0.01 and r=0.451) with the rainbow trout muscle Sigma18PCBs.

148 at reagent was found to react with all three rainbow trout Mx proteins.

149 The method was applied to Nile tilapia and rainbow trout (n=29) and 14% of them contained enrofloxa

150 topminnow hepatocellular carcinoma), RTL-W1 (rainbow trout normal liver), and primary rainbow trout h

151 microsomal but not in cytosolic fractions of rainbow trout (O. mykiss) liver S9.

152 formis), coho salmon (Oncorhynchus kisutch), rainbow trout (O. mykiss), Chinook salmon (O. tshawytsch

153 fect of seasonal and regional differences of rainbow trout on its aroma and aroma-active profile was

154 chus labrax); turbot (Scophthalmus maximus); rainbow trout (Onchorynchus mykiss); and salmon (Salmo s

155 In rainbow trout (Onchoryncus mykiss), proliferative cells

156 ered two further subgroups (IFN-e and -f) in rainbow trout Oncorhynchus mykiss and analyzed the expre

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

158 n IFN-gamma homologue has been identified in rainbow trout Oncorhynchus mykiss, and its biological ac

159 se shark (Ginglymostoma cirratum (Gici)) and rainbow trout (Oncorhynchus mykiss (Onmy)).

160 Exposed juvenile rainbow trout (Oncorhynchus mykiss) accumulated surfacta

161 e and absence of widely introduced salmonids rainbow trout (Oncorhynchus mykiss) and brook trout (Sal

162 Rainbow trout (Oncorhynchus mykiss) and brown trout (Sal

163 Rainbow trout (Oncorhynchus mykiss) and brown trout (Sal

164 nt a chromosome-anchored genome assembly for rainbow trout (Oncorhynchus mykiss) and characterize a 5

165 on data collected in two previous studies of rainbow trout (Oncorhynchus mykiss) and common carp (Cyp

166 ns of organic chemicals in two fish species: rainbow trout (Oncorhynchus mykiss) and fathead minnow (

167 salmonids, including two sensitive species, rainbow trout (Oncorhynchus mykiss) and lake trout (Salv

168 terize the cobalamin-binding proteins of the rainbow trout (Oncorhynchus mykiss) and to compare their

169 nent of total gangliosides found in sperm of rainbow trout (Oncorhynchus mykiss) and was shown to be

170 In this regard, rainbow trout (Oncorhynchus mykiss) appeared unusual: tr

171 e for off-odour development in earthen-ponds rainbow trout (Oncorhynchus mykiss) aquaculture farming

172 Atlantic salmon (Salmo salar) and rainbow trout (Oncorhynchus mykiss) are two of the most

173 st time, to our knowledge, in teleosts using rainbow trout (Oncorhynchus mykiss) as a model.

174 CK11 is a rainbow trout (Oncorhynchus mykiss) CC chemokine phyloge

175 isolation and functional characterization of rainbow trout (Oncorhynchus mykiss) CD4-1(+) T cells and

176 ellular coat, or vitelline envelope (VE), of rainbow trout (Oncorhynchus mykiss) eggs consists of thr

177 Ig superfamily members within the available rainbow trout (Oncorhynchus mykiss) EST gene index, we i

178 omic analysis to examine stress responses in rainbow trout (Oncorhynchus mykiss) exposed to five dist

179 from a cDNA library prepared from 3-week-old rainbow trout (Oncorhynchus mykiss) eyed embryos.

180 ing and film on the rancidity development in rainbow trout (Oncorhynchus mykiss) fillets during refri

181 ntent in the muscle and edible skin parts of rainbow trout (Oncorhynchus mykiss) fillets, sampled at

182 ticals in fish bile samples was validated in rainbow trout (Oncorhynchus mykiss) following short-term

183 al fluids (SF(INTESTINAL)) designed to mimic rainbow trout (Oncorhynchus mykiss) gastrointestinal con

184 A rainbow trout (Oncorhynchus mykiss) gene for tumor necro

185 Mx1 gene expression was studied in the rainbow trout (Oncorhynchus mykiss) gonad (RTG) (fibrobl

186 shelf life of vacuum packaged low processed rainbow trout (Oncorhynchus mykiss) gravad during storag

187 shelf life of vacuum packaged low processed rainbow trout (Oncorhynchus mykiss) gravad during storag

188 as complex mixtures in a primary culture of rainbow trout (Oncorhynchus mykiss) hepatocytes.

189 bes the discovery and sequence analysis of a rainbow trout (Oncorhynchus mykiss) IL-17A/F2 molecule a

190 ng the epithelial barrier model built on the rainbow trout (Oncorhynchus mykiss) intestinal cell line

191 RTgutGC cells, derived from rainbow trout (Oncorhynchus mykiss) intestine, were used

192 In this study, PFAS exposure on rainbow trout (Oncorhynchus mykiss) is examined at the m

193 Two rainbow trout (Oncorhynchus mykiss) Mx cDNAs were cloned

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

195 etomidate, but not benzocaine or MS-222; and rainbow trout (Oncorhynchus mykiss) showed no avoidance

196 a molecular mass<30kDa (PF30) isolated from rainbow trout (Oncorhynchus mykiss) skin gelatin hydroly

197 the trigeminal nerve of a teleost fish, the rainbow trout (Oncorhynchus mykiss) to determine what ty

198 we performed transcriptomics on the CNSS of rainbow trout (Oncorhynchus mykiss) to establish: (1) ho

199 Our studies have revealed that rainbow trout (Oncorhynchus mykiss) use a novel strategy

200 e processing on the shelf-life of fillets of rainbow trout (Oncorhynchus mykiss) were examined.

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

202 Rainbow trout (Oncorhynchus mykiss) were exposed to wate

203 of organisms in aquatic ecosystems, juvenile rainbow trout (Oncorhynchus mykiss) were separately expo

204 To address this, adult and juvenile Rainbow Trout (Oncorhynchus mykiss) were, respectively,

205 determine whether blastomeres isolated from rainbow trout (Oncorhynchus mykiss) will incorporate and

206 Rainbow trout (Oncorhynchus mykiss), a model aquaculture

207 In rainbow trout (Oncorhynchus mykiss), a nasopharynx-assoc

208 monstrate that BPA deposition in the eggs of rainbow trout (Oncorhynchus mykiss), an ecologically and

209 ae, including Atlantic salmon (Salmo salar), rainbow trout (Oncorhynchus mykiss), and Arctic char (Sa

210 one that negatively affects muscle growth in rainbow trout (Oncorhynchus mykiss), but the mechanisms

211 We find that beta2m of a salmonid fish, the rainbow trout (Oncorhynchus mykiss), does not conform to

212 ommon ancestor of salmonid fishes, including rainbow trout (Oncorhynchus mykiss), experienced a whole

213 European seabass (Dicentrarchus labrax) and rainbow trout (Oncorhynchus mykiss), fed diets at 25%, 5

214 3 genes from other vertebrate taxa including rainbow trout (Oncorhynchus mykiss), frog (Xenopus laevi

215 uced during early life stages of ammonotelic rainbow trout (Oncorhynchus mykiss), suggesting that the

216 h), brook trout (Salvelinus fontinalis), and rainbow trout (Oncorhynchus mykiss), suggesting that tol

217 In the rainbow trout (Oncorhynchus mykiss), the only ER describ

218 y, lake sturgeon (Acipenser fulvescens), and rainbow trout (Oncorhynchus mykiss), were selected to ev

219 might have added to the controversy is that rainbow trout (Oncorhynchus mykiss), which have served a

220 netic subgroup have gained high virulence in rainbow trout (Oncorhynchus mykiss).

221 and rtAHR2beta) have been identified in the rainbow trout (Oncorhynchus mykiss).

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

223 rt the first detailed genetic linkage map of rainbow trout (Oncorhynchus mykiss).

224 that produces an acute, lethal infection in rainbow trout (Oncorhynchus mykiss).

225 r structure-related toxicities in vivo using rainbow trout (Oncorhynchus mykiss).

226 o additive mixtures on the fillet quality of rainbow trout (Oncorhynchus mykiss).

227 (the "alkaline tide") and growth in juvenile rainbow trout (Oncorhynchus mykiss).

228 e kidneys of Chinook salmon or in tissues of rainbow trout (Oncorhynchus mykiss).

229 that return to the surface, was examined in rainbow trout (Oncorhynchus mykiss).

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

231 ed batch of liver S9 fractions isolated from rainbow trout (Oncorhynchus mykiss).

232 ves in the gill and skin mucosal surfaces of rainbow trout (Oncorhynchus mykiss).

233 itism on bioaccumulation of selenium (Se) in rainbow trout (Oncorhynchus mykiss).

234 have recently reported a homolog to CCR7 in rainbow trout (Oncorhynchus mykiss).

235 st fish, we generated recombinant C5a of the rainbow trout, Oncorhynchus mykiss (tC5a), and used fluo

236 investigated whether a relevant model fish (rainbow trout, Oncorhynchus mykiss) could detect OSPW us

237 as ligand, RANKL, TRAIL-like, and TNF-New in rainbow trout, Oncorhynchus mykiss, immune and nonimmune

238 Habitat for rainbow trout, Oncorhynchus mykiss, is projected to decl

239 es of somatosensory receptors on the head of rainbow trout, Oncorhynchus mykiss, using extracellular

240 e of interleukin 18 has been identified from rainbow trout, Oncorhynchus mykiss.

241 and subsequently during embryogenesis in the rainbow trout, Oncorhynchus mykiss.

242 The deduced sequence of rainbow trout ovarian cathepsin D shows significant homo

243 timicrobial activity against a wide range of rainbow trout pathogens.

244 Rainbow trout pIgR is known to transport IgT and IgM acr

245 Rainbow trout possess one membrane-bound and two soluble

246 lysis was performed using 76 doubled haploid rainbow trout produced by androgenesis from a hybrid bet

247 As a rainbow trout producer, Italy is accounted as fifth in t

248 o historical stocking locations with greater rainbow trout propagule pressure, warmer water temperatu

249 The cellular localization of the rainbow trout proteins was determined by transient expre

250 gnificant and ubiquitous distribution in the rainbow trout providing the potential for complex intera

251 erm exposure study with early life stages of rainbow trout (RBT; Oncorhynchus mykiss) using benzo[a]p

252 in fat and defatted (protein) fillet of 130 rainbow trout, reared with feed incorporating a high or

253 essential endocrine components of the female rainbow trout reproductive axis.

254 types of Onchorhynchus mykiss (steelhead and rainbow trout, respectively), we have dissected the gene

255 ted with lice density in Atlantic salmon and rainbow trout, respectively.

256 nificantly in seabream, European seabass and rainbow trout, respectively.

257 onal species (chick, Spanish ribbed newt and rainbow trout) reveals significant sequence identity, wi

258 rtAhR2alpha and rtAhR2beta, were cloned from rainbow trout (rt) cDNA libraries.

259 have cloned and functionally characterized a rainbow trout (rt) molecule (rtCD80/86) that shows the h

260 t, three type I IFN genes were identified in rainbow trout (rt) Oncorhynchus mykiss and are classifie

261 In rainbow trout RTG-2 and RTS-11 cells, polyinosinic-polyc

262 forms of functional C3 occur not only in the rainbow trout (Salmo gairdneri), a quasi-tetraploid old

263 s can infect aquatic animals, such as farmed rainbow trout, sea trout, sea bass, and sea bream, by ca

264 SV) by intraperitoneal injection in juvenile rainbow trout showed that exchanges of the viral P or M

265 g, Fe, Zn, Se and P (K(PLE) > 1) contents of rainbow trout side streams, Zn (K(PLE)5.97) and Fe (K(PL

266 es insights into mRNA and lncRNA networks in rainbow trout skeletal muscle and their regulation by E2

267 (alevin), opsin expression in large juvenile rainbow trout (smolt), zebrafish, or killifish remained

268 s maintained in the presence of cells from a rainbow trout spleen cell line (RTS34st) are able to pro

269 A rainbow trout strain selected for high performance on a

270 resistant Hofer and susceptible Trout Lodge rainbow trout strains following pathogen exposure with t

271 osure for both the resistant and susceptible rainbow trout strains.

272 In rainbow trout such lines have existed for decades and ha

273 length polymorphism pattern is observed with rainbow trout, suggesting multiple beta2m genes in the g

274 Two different genes were identified in rainbow trout that resemble mammalian CD4.

275 cute mortality was only observed in juvenile rainbow trout that were exposed to oxidized 6PPD, sugges

276 (Bf-1 and Bf-2) in another teleost fish (the rainbow trout) that are about 9% more similar to mammali

277 between native cutthroat trout and invasive rainbow trout, the world's most widely introduced invasi

278 s on the health status of aquaculture reared rainbow trout through the investigation of clinical chem

279 underlying immune response and resistance of rainbow trout to the whirling disease parasite.

280 ctor RUNX1 is enriched in the fetal ovary in rainbow trout, turtle, mouse, goat, and human.

281 In rainbow trout, two TNF-alpha molecules were described pr

282 dynamics of Ichthyophthirius multifiliis in rainbow trout using a simple macroparasite model by incl

283 structed a second generation genetic map for rainbow trout using microsatellite markers to facilitate

284 ypes revealed that IgT utilizes the standard rainbow trout V(H) families, but surprisingly, the IgT i

285 r weight proteins (HMWPs; M(r) > 110 kDa) of rainbow trout VEs that are heterodimers of individual VE

286 g in vivo models of systemic inflammation in rainbow trout, we find canonical pyrogenic cytokine resp

287 minism underlying spontaneous maleness in XX-rainbow trout, we recorded the phenotypic sex of 20,210

288 In small groups, however, rainbow trout were bolder than both types of brown trout

289 A total of 2626 Atlantic salmon and 2643 rainbow trout were challenged and genotyped with 50 K an

290 mic environment (MCE) on development rate in rainbow trout were evaluated within a quantitative trait

291 Juvenile rainbow trout were exposed to 1.0 mg l(-1) citrate-cappe

292 Rainbow trout were fed six different diets, which differ

293 Bioconcentration factors (BCFs) in rainbow trout were measured for 10 anionic surfactants w

294 Rainbow trout were more active and aggressive but less b

295 To determine the vulnerable life stage, rainbow trout were placed in cages in three lakes contai

296 Rainbow trout were simultaneously exposed to 11 chemical

297 Growing rainbow trout with diets where FO was replaced by either

298 atural vertebrate host, Oncorhynchus mykiss (rainbow trout), with variants of a coevolved viral patho

299 y-four of these genes were conserved ISGs in rainbow trout, zebrafish, and human.

300 on single-cone opsin expression in juvenile rainbow trout, zebrafish, and killifish and on the absor