ライフサイエンスコーパス: rainbow trout

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

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

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

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

5 with particularly negative consequences for rainbow trout.

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

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

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

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

10 ave been compared with their counterparts in rainbow trout.

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

12 al changes in gonadotropins and estradiol in rainbow trout.

13 t significantly lower rates in comparison to rainbow trout.

14 arctic fish were significantly lower than in rainbow trout.

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

16 mpacting the stress and feeding responses in rainbow trout.

17 d significantly attenuated virulence against rainbow trout.

18 he transcriptomes of several clonal lines of rainbow trout.

19 biomagnify from dietary exposure in juvenile rainbow trout.

20 ified samples of farmed Atlantic salmons and rainbow trouts.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

40 Rainbow trout are particularly susceptible and may suffe

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

60 The rainbow trout ERbeta1 and ERbeta2 are not closely associ

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

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

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

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

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

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

67 oxidative stress and oxidative stability of rainbow trout fillets.

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

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

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

71 The rainbow trout genetic linkage groups have been assigned

72 The status of rainbow trout genetic maps has progressed significantly

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

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

75 identified 180 duplicated regions within the rainbow trout genome.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

91 (-10 degrees C) were evaluated using farmed rainbow trout killed by asphyxia in air or percussion.

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

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

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

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

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

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

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

99 In rainbow trout (Onchoryncus mykiss), proliferative cells

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

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

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

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

104 Exposed juvenile rainbow trout (Oncorhynchus mykiss) accumulated surfacta

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

132 Rainbow trout (Oncorhynchus mykiss) were exposed to wate

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

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

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

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

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

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

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

140 3 genes from other vertebrate taxa including rainbow trout (Oncorhynchus mykiss), frog (Xenopus laevi

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

164 Rainbow trout possess one membrane-bound and two soluble

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

195 Rainbow trout were fed six different diets, which differ

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

197 Rainbow trout were simultaneously exposed to 11 chemical

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

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

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