ライフサイエンスコーパス: catfish

1 roduct PCBs, including PCB11, in tilapia and catfish.

2 rgy underwent skin prick tests to salmon and catfish.

3 novel communication channel among synodontid catfish.

4 ctive effects against E. ictaluri in striped catfish.

5 organs and tissues from the same individual catfish.

6 one vertebrate ancient (VA) opsin gene from catfish.

7 r large-scale comparative genome analysis in catfish.

8 not yet available for many species including catfish.

9 approximately the genome size of the channel catfish.

10 mpare all IgE-binding proteins in salmon and catfish.

11 regions of the forebrain (FB) in the channel catfish.

12 L5 cDNAs, L5a and L5b, were found in channel catfish.

13 SC) and columnaris disease, respectively, in catfish.

14 7, for which two cDNAs were found in channel catfish.

15 y of selective breeding programs for channel catfish.

16 divergence of oocyte TFIIIA from the channel catfish.

17 ounts for the evolutionary loss of scales in catfish.

18 esce in the same manner as the affected blue catfish.

19 the intestinal mucosal immune system of the catfish.

20 he intestinal epithelia of orally inoculated catfish.

21 s that had not been previously identified in catfish.

22 in sex determination and differentiation in catfish.

23 ibiotics (sulfonamides and tetracyclines) in catfish.

24 micry in a species-rich group of neotropical catfishes.

25 consumption intensity per species group was: catfish, 157 mg kg(-1) (UI 9-2751); trout, 103 mg kg(-1)

26 n identified in Ictalurus punctatus (channel catfish), a well characterized immunological model syste

27 rginine (L-Arg), a potent taste stimulus for catfish, activated a nonselective cation conductance in

28 ed as Bacillus CFU/g of intestinal tissue of catfish after feeding Bacillus spore-supplemented feed f

29 ied out to estimate the istihalah period for catfish after feeding with pig offal, based on the absen

30 ed and registered with the WHO/IUIS while no catfish allergens have been described so far.

31 Two types of catfish alloantigen-dependent cytotoxic T cells were clo

32 e resource of ESTs is to become available in catfish allowing identification of large number of SNPs,

33 The channel catfish alpha-actin gene is associated with two distinct

34 ors, which are found in most teleost fishes, catfish also possess a total of over 4000 electrorecepti

35 Amino acid conservation in catfish, amphibian, and human TFIIIA zinc fingers allows

36 Subsequent catFISH analyses revealed that in the DH, cells were pre

37 Replicate analysis of catfish and chicken eggs by the QISTMS method produced c

38 QISTMS distinguished between catfish and chicken eggs with elevated TCDD levels from

39 CC41 to monitor viral cytotoxic responses in catfish and determine that CC41 binds to a subset of LIT

40 e, acutely dissociated horizontal cells from catfish and goldfish.

41 approach may produce growth-enhanced channel catfish and increase productivity.

42 SPR/Cas9 HDR for gene integration in channel catfish and may contribute to the generation of a more e

43 r motifs, and activate transcription in both catfish and murine cells.

44 cient system for precise gene integration in catfish and other aquaculture species, and the developme

45 This opsin, identified in channel catfish and termed parapinopsin, defines a new gene fami

46 served syntenies identified here between the catfish and the three model fish species should facilita

47 Catfish TFIIIA was able to bind the catfish and Xenopus 5S RNA genes but did not efficiently

48 s is not fully understood, but evidence from catfish and zebrafish indicates major roles for octamer-

49 n similarities in the FBA sequences with the catfish and zebrafish NCCRP-1 peptides.

50 Putative conserved syntenies between catfish and zebrafish, medaka, and Tetraodon were establ

51 like fish), Gadiformes (cods), Siluriformes (catfish), and Salmoniformes (salmonids).

52 ary in the alpha subunits of the bovine rod, catfish, and rat olfactory channels.

53 ease control as probiotic feed additives for catfish aquaculture.

54 Most ribosomal protein mRNAs in channel catfish are highly similar to their mammalian counterpar

55 Most 40S RPs in channel catfish are highly similar to their orthologues in mamma

56 Peripheral waves (PWs) in the channel catfish are odorant-induced neural oscillations of synch

57 W analyses showed that mutational targets in catfish are restricted when compared with the spectrum o

58 ndent invasions of freshwaters by marine Sea Catfishes (Ariidae), rates of both morphological dispari

59 d from peripheral blood cells of the channel catfish, as well as on lymphocyte-like cells, but not on

60 found in mince of Nile tilapia and broadhead catfish at levels of 1.5 and 3.2mug/kg, respectively.

61 c helix-loop-helix family were cloned from a catfish B cell cDNA library in this study, and homologs

62 (alpha and beta) were cloned by screening a catfish B cell cDNA library.

63 this study, IgM(+)/IgD(+) and IgM(-)/IgD(+) catfish B cell populations were identified through the u

64 In catfish B cells, CFEB1 and -2 also activated transcripti

65 certain octamer sites, destroyed function in catfish B cells.

66 the activation and proliferation of channel catfish B cells.

67 rations of four species of Amazonian goliath catfishes (Brachyplatystoma rousseauxii, B. platynemum,

68 h genome database, cBARBEL (abbreviated from catfish Breeder And Researcher Bioinformatics Entry Loca

69 nce study, LSU-E2 was able to invade channel catfish by the immersion route and persist in internal o

70 The catfish CB genes are approximately 36% identical at the

71 anscription of the Cec B promoter in channel catfish cells exhibited an inducible pattern and could b

72 ct2 activated transcription in mouse but not catfish cells.

73 food items: beef steak, butter, canned tuna, catfish, cheese, eggs, french fries, fried chicken, grou

74 In catfish, ciliated ORNs express OR-type receptors and Gal

75 d social air-breathing in African sharptooth catfish Clarias gariepinus, to determine whether individ

76 African catfish (Clarias gariepinus) are commonly consumed in Ma

77 ytic activity of viscera extract from hybrid catfish (Clarias macrocephalus x Clarias gariepinus) was

78 Frigate mackerel (Auxis thazard) and catfish (Clarias macrocephalus) can be used as alternati

79 ctivity was investigated in the brain of the catfish, Clarias batrachus.

80 ypophysiotropic dopamine (DA) neurons in the catfish, Clarias batrachus.

81 analyzed, of these eight were used by the 11 catfish clonal alloantigen-dependent T cell lines.

82 Importantly, transfection of catfish clonal B cells demonstrated that this leader med

83 binds to a subset of LITRs on the surface of catfish clonal CTLs.

84 levels of IpFcRI expression were detected in catfish clonal leukocyte cell lines.

85 the phenotypes of cytotoxic cells in channel catfish, clonal alloantigen-dependent leukocyte lines we

86 oth cAMP and cGMP derived from the BD of the catfish CNGA4 olfactory modulatory subunit (fCNGA4).

87 ed by visceral alkaline-proteases from Giant catfish, commercial trypsin, and Izyme AL(R).

88 s (common barbel, Pontic shad, European wels catfish, common bleak) was evaluated by thermal methods.

89 ation of an ionotropic glutamate receptor on catfish cone horizontal cells is linked to calcium relea

90 ctivation of ionotropic kainate receptors on catfish cone horizontal cells triggered CICR from ryanod

91 We found that light induced a response in catfish cone horizontal cells, but not rod horizontal ce

92 Outbred populations of channel catfish contained an average of eight alleles per locus

93 ch in protein (93.1-93.8%), whilst broadhead catfish contained protein (55.2-59.5%) and lipid (36.6-4

94 The visceral peptidase from farmed giant catfish could be an alternative protease for generating

95 ore, PI from both Nile tilapia and broadhead catfish could serve as the promising proteinaceous mater

96 Both types of catfish CTL form conjugates with and kill targets by apo

97 These results suggest that catfish CTL show heterogeneity with respect to target re

98 sh NCCRP-1 antigen-binding domain inhibited (catfish) cytotoxicity toward conventional tumor target c

99 Thus, catfish deltam transcripts appear to originate from IGHD

100 Coding region motifs of catfish DH segments are phylogenetically conserved in so

101 Raw and heated extracts from catfish displayed a higher frequency of IgE-binding comp

102 of other fluorescent compounds isolated from catfish eggs and ovaries.

103 Blue catfish eggs are normally cream to light yellow.

104 variant, ATGtAAAT, which occurs twice in the catfish enhancer.

105 he causative agents of enteric septicemia of catfish (ESC) and motile aeromonad septicaemia (MAS), re

106 ish linkage, physical and integrated maps, a catfish EST contig viewer with SNP information overlay,

107 ue genes matched previously reported channel catfish ESTs while 847 (44.4%) ESTs representing 261 uni

108 Mining of the catfish expressed sequence tag databases using mammalian

109 mated that the minimum quarantine period for catfish fed with pig offal is 1.5days.

110 gut and to suggest the quarantine period in catfish fed with pig offal.

111 hybrid catfish produced by crossing channel catfish females with blue catfish males exhibit a number

112 Channel catfish skin is a by-product from catfish fillet production.

113 t a dose of 8x10(7) CFU/g and fed to channel catfish for 14 days before they were challenged by E. ic

114 stitute the preferred codon usage of channel catfish for the native sequences of the genes.

115 ty using fluorescence in situ hybridization (catFISH) for Arc mRNA.

116 ons is difficult in nonmodel species such as catfish, functional genome analysis will have to rely he

117 Peruvian sea catfish (Galeichthys peruvianus) sagittal otoliths prese

118 Identification of the catfish gene as delta is based on the following properti

119 crosatellite loci were identified in channel catfish gene sequences or random clones from a small ins

120 Functional categorization of the channel catfish genes indicated that the largest group was ribos

121 ly should facilitate functional inference of catfish genes.

122 ome, and opens ways for facilitating channel catfish genetic enhancement and functional genomics.

123 ive, integrative platform for all aspects of catfish genetics, genomics and related data resources.

124 A genetic linkage map of the channel catfish genome (N = 29) was constructed from two referen

125 A genetic linkage map of the channel catfish genome (N=29) was constructed using EST-based mi

126 The catfish genome database, cBARBEL (abbreviated from catfi

127 As catfish genome sequencing proceeds and ongoing quantitat

128 ighly efficient tool for editing the channel catfish genome, and opens ways for facilitating channel

129 nd Merman elements exist per haploid channel catfish genome, respectively.

130 n overlay, and GBrowse-based organization of catfish genomic data based on sequence similarity with z

131 hyrotropin-releasing hormone receptor or the catfish GnRH-R are also phosphorylated in an agonist-dep

132 n-releasing hormone receptor and the African catfish GnRH-R, both of which have a C-terminal tail, ar

133 that codes for a granzyme homologue, channel catfish granzyme-1 (CFGR-1), from nonspecific cytotoxic

134 Ictalurus punctatus (channel catfish) granzyme cDNA encodes a protein with approximat

135 ig offal, based on the absence of pig DNA in catfish gut and to suggest the quarantine period in catf

136 Among predators, adult Blue Catfish had low MC concentrations, whereas Blue Crabs ex

137 Catfish has a male-heterogametic (XY) sex determination

138 octamer motifs in the Emu3' enhancer of the catfish has been shown to be particularly important in d

139 DNA derived from the spleen of an individual catfish has shown that somatic mutation occurs within bo

140 For example, some catfish have <5% IgM(-)/IgD(+) B cells in their PBLs, wh

141 h protein isolates (FPI) were recovered from catfish heads and frames by alkaline extraction (AE) and

142 Ictalurid herpesvirus 1 (channel catfish herpesvirus [CCV]) is economically very importan

143 Channel catfish Ictalurus punctatus express two Ig isotypes: IgM

144 The primary olfactory projections of channel catfish Ictalurus punctatus have been examined with post

145 red eggs in the ovaries of adult female blue catfish (Ictalurus furcatus) from the northern arm of Eu

146 aluri, a host-restricted pathogen of channel catfish (Ictalurus punctatus) and the main pathogen of t

147 into a targeted non-coding region of channel catfish (Ictalurus punctatus) chromosome 1 using two dif

148 AC) contig-based physical map of the channel catfish (Ictalurus punctatus) genome was generated using

149 The Ig heavy chain enhancer of the channel catfish (Ictalurus punctatus) has an unusual position an

150 ster of H chain gene segments in the channel catfish (Ictalurus punctatus) has been determined.

151 revious molecular genetic studies on channel catfish (Ictalurus punctatus) have focused on limited nu

152 However, catfish (Ictalurus punctatus) is the only species of fis

153 Catfish (Ictalurus punctatus) retinal cone horizontal ce

154 The alpha-actin gene of channel catfish (Ictalurus punctatus) was cloned and sequenced.

155 ved from external taste epithelia of channel catfish (Ictalurus punctatus) were incorporated into lip

156 ultiple CK isoenzymes in the diploid channel catfish (Ictalurus punctatus) with one unusual cathodic

157 S RP complementary DNAs (cDNAs) from channel catfish (Ictalurus punctatus), making them one of the mo

158 47 60S ribosomal protein cDNAs from channel catfish (Ictalurus punctatus), of which 43 included the

159 quality reference genome sequence of channel catfish (Ictalurus punctatus), the major aquaculture spe

160 ne protective in zebrafish (Danio rerio) and catfish (Ictalurus punctatus), triggering systemic immun

161 rtebrate, has been identified in the channel catfish (Ictalurus punctatus).

162 library made from the brain mRNA of channel catfish (Ictalurus punctatus).

163 tein (gfp) as a reporter in cells of channel catfish (Ictalurus punctatus).

164 ly that causes enteric septicemia in channel catfish (Ictalurus punctatus).

165 ess database for genome biology of ictalurid catfish (Ictalurus spp.).

166 e describe, from a teleost fish (the channel catfish, Ictalurus punctatus), a novel complex chimeric

167 s were dissociated from the gills of channel catfish, Ictalurus punctatus, and cultured.

168 ncer (Emu3') of the IgH locus of the channel catfish, Ictalurus punctatus, differs from enhancers of

169 Channel catfish, Ictalurus punctatus, leukocyte immune type rece

170 utilized to successfully target the channel catfish, Ictalurus punctatus, muscle suppressor gene MST

171 er (E(mu)3') of the IgH locus of the channel catfish, Ictalurus punctatus, shows strong B cell-specif

172 In recent studies in channel catfish, Ictalurus punctatus, we identified 26 distinct

173 d amino acids were identified in the channel catfish, Ictalurus punctatus.

174 n response to certain pathogens and that the catfish IgD Fc-region, as has been suggested for human I

175 The delta-chain of catfish IgD was initially characterized as a unique chim

176 ed transcription from the core region of the catfish IgH enhancer (Emu3') in a manner dependent on th

177 )/IgD(+) B cells can express any of the four catfish IgL isotypes.

178 Recombinant IpFcRI binds catfish IgM as assessed by both coimmunoprecipation and

179 Although catfish IgM has been extensively studied at the function

180 Catfish IgM(+)/IgD(+) B cells are small and agranular.

181 Together, these findings imply that catfish IgM(-)/IgD(+) B cells likely expand in response

182 evident differences in rabbit ileal loop and catfish ileal loop responses to E. ictaluri and S. Typhi

183 will allow for more effective monitoring of catfish immune responses to pathogens.

184 We studied 11 groups of four catfish in a laboratory arena and recorded air-breathing

185 one of the most diverse groups of freshwater catfishes in South and Central America with eight subfam

186 rtalities and economic losses to the channel catfish industry of the southeast United States.

187 mponent of an immersion-oral vaccine for the catfish industry.

188 te and tactile fibers in the facial nerve of catfish innervate extraoral taste buds and terminate som

189 . ictaluri O-PS LPS mutants by using a novel catfish intestinal loop model and compare it to the rabb

190 cillus strains isolated from soil or channel catfish intestine were screened for their antagonism aga

191 To introduce desirable genes from blue catfish into channel catfish through introgression, a ge

192 Taste bud formation in channel catfish is first seen to occur in stage 39 embryos, when

193 The lateral line system of the channel catfish is formed by mechanoreceptive neuromasts located

194 Catfish is the major aquaculture species in the United S

195 Zebrafish and catfish ISG15 genes were subsequently identified by sequ

196 ely related species or a sequenced genome in catfish, it was difficult to make inferences as to the o

197 All 29 catfish JB gene segments appear functional.

198 Catfish L-lactate dehydrogenase, glyceraldehyde-3-phosph

199 Earlier studies distinguished two classes of catfish light (L) chain (designated F and G).

200 specific search functions, visualization of catfish linkage, physical and integrated maps, a catfish

201 es under positive selection in high-altitude catfishes, located at opposite ends of the RH1 intramole

202 nes encode the multiple forms of the channel catfish M-CK cDNAs.

203 rophages, a cDNA library from LPS-stimulated catfish macrophages was screened by subtractive hybridiz

204 differentially expressed genes from channel catfish macrophages, a cDNA library from LPS-stimulated

205 y crossing channel catfish females with blue catfish males exhibit a number of desirable production t

206 tions and other methods to establish goliath catfish migratory routes, their seasonal timing and poss

207 Broadhead catfish mince had 2-MIB at level of 0.8mug/kg, but no 2-

208 ns conferred significant benefit in reducing catfish mortality (P<0.05).

209 r contents of myofibrillar proteins than had catfish muscle (p<0.05).

210 Lipids from striped catfish muscle were extracted with the aid of crude prot

211 mutations, was not a significant target for catfish mutations.

212 ebrafish 17-mer peptide corresponding to the catfish NCCRP-1 antigen-binding domain inhibited (catfis

213 characterizes a zebrafish orthologue of the catfish NCCRP-1.

214 The catfish nonspecific cytotoxic cell receptor protein (NCC

215 Catfish Oct2 a and beta are tissue restricted, bind both

216 Catfish Oct2 alpha and beta isoforms are derived by alte

217 Catfish Oct2 beta is a more potent transcriptional activ

218 In transient expression assays, catfish Oct2 beta showed a marked preference for the oct

219 t analysis competition assays indicated that catfish Oct2 binds the consensus octamer motif with an a

220 To test this hypothesis, two catfish Oct2 cDNAs (alpha and beta) were cloned by scree

221 In comparisons with mammalian Oct2, the catfish Oct2 isoforms show high sequence conservation in

222 While catfish Oct2 was shown to be capable of binding PORE and

223 Catfish Oct2, when bound in this monomeric conformation,

224 Mochokid catfish offer a distinct opportunity to study a communic

225 s weakly activated by N(1)-oxide cAMP, and a catfish olfactory-like bovine rod mutant lost activation

226 p-cGMPS, which activates bovine rod, but not catfish, olfactory channels.

227 Catfish oocyte TFIIIA was identified by its association

228 loning of partial cDNAs encoding the channel catfish orthologues of rhodopsin and the red cone pigmen

229 greater content of sodium chloride than had catfish (p<0.05).

230 cDNA clones encoding portions of a putative catfish parathyroid hormone (PTH) 2 receptor (PTH2R) led

231 hould greatly enhance genome research in the catfish, particularly aiding in the identification of ge

232 Catfish, particularly ordinary muscle, was composed of h

233 induces in vitro proliferative responses of catfish PBL that were synergistically enhanced by the ad

234 e native IpFcRI glycoprotein was detected in catfish plasma using a polyclonal Ab.

235 We report that the Japanese sea catfish Plotosus japonicus senses local pH-associated in

236 The hybrid catfish produced by crossing channel catfish females wit

237 In 2008, freshwater-cultured catfish production surpassed that of salmon, the globall

238 r and sediment samples from a high-intensity catfish production system and its original water reservo

239 and sulfadiazine (SDZ) in imported Pangasius catfish products in Thailand.

240 Therefore, antibiotic residues in Pangasius catfish products should be continually regulated and mon

241 enome sequences and transcriptomes of scaled catfishes, provide crucial resources for evolutionary an

242 e populations of a North American freshwater catfish, Pylodictis olivaris, and the important role of

243 The channel catfish reference genome sequence, along with two additi

244 Catfish represent 12% of teleost or 6.3% of all vertebra

245 A total of 330 individuals of flathead catfish, representing 34 drainages throughout the specie

246 ata integration and dissemination within the catfish research community and to interested stakeholder

247 We determined that catfish respond to E. ictaluri LPS but not to S. Typhimu

248 as expressed in the horizontal-cell layer of catfish retina.

249 nd immunohistochemical (IHC) analyses of the catfish retina.

250 Muller glial cells and neurons of the distal catfish retina.

251 nt T cell lines established from the channel catfish revealed distinctly different TCR beta rearrange

252 hat an IGHD3-encoded protein is expressed in catfish serum.

253 atty acid composition of the roe of European catfish (Silurus glanis) wild specimens captured in the

254 ing material was naturally contaminated Wels catfish (Silurus glanis), caught in the Ebro River (Spai

255 Channel catfish skin collagens were typical type I collagens and

256 Channel catfish skin is a by-product from catfish fillet product

257 Collagens were extracted from catfish skins by: (1) acid; (2) homogenization-aided; an

258 t the main spawning regions of these goliath catfish species are in the western Amazon; (ii) at least

259 hodic CK isoform existed only in the channel catfish stomach, ovary, and spleen, but not in any other

260 the Japanese medaka (Oryzias latipes) and a catfish (Synodontis multipunctatus) suggests that expres

261 and a weakly electric species of synodontid catfish, Synodontis grandiops, and Synodontis nigriventr

262 of rhodopsin function in an Andean mountain catfish system spanning a range of elevations.

263 analyses showed that CF-TRX is expressed in catfish T and macrophage cell lines, but weakly in B cel

264 by the addition of culture supernatants from catfish T cell lines.

265 ange necessary to elicit neural responses in catfish taste fibers.

266 h that in mammals, genomic sequencing of the catfish TCR DB-JB-CB region reveals a unique locus conta

267 To verify this, we used the Arc CatFISH technique to show that the OUL update session re

268 he first transcriptome-level analysis of the catfish testis.

269 Two alternatively spliced forms of catfish TF12 (termed CFEB1 and -2) were identified and c

270 The N-terminal region of catfish TFIIIA contains the oocyte-specific initiating M

271 Catfish TFIIIA lacks the conserved transcription activat

272 Catfish TFIIIA was able to bind the catfish and Xenopus

273 and L29 are significantly shorter in channel catfish than in mammals due to deletions in the 3' end o

274 Channel catfish that were vaccinated with a single immersion dos

275 rly gene-based brain-imaging method (Arc/H1a catFISH) that allows comparisons of neuronal ensembles a

276 the most striking physical characteristic of catfish, the evolutionary loss of scales and provide evi

277 In catfish, the facial nerve innervates taste buds distribu

278 s screening yielded a 552-bp cDNA coding for catfish thioredoxin (CF-TRX).

279 sirable genes from blue catfish into channel catfish through introgression, a genetic linkage map is

280 le approach to determine 19 PCB congeners in catfish tissue was presented.

281 As part of our transcriptome analysis in catfish to develop molecular reagents for comparative fu

282 s indicating that taste responses of channel catfish to L-Arg are mediated by high-affinity receptors

283 ption by fluorescence in situ hybridization (catFISH) to locate populations of neurons in the mammali

284 8.0%, 5.3%, 5.1%, 2.6% and 8.0% for tilapia, catfish, trout, salmon, hybrid striped bass and yellow p

285 quence was delivered by lipofection to three catfish types: fibroblast and leukocyte cell lines, and

286 differential temporal regulation of channel catfish virus (CCV) genes, the transcriptional kinetics

287 alHV-1 shares at least 18 genes with channel catfish virus (CCV), a fish herpesvirus whose complete s

288 ogenetic catfish were immunized with channel catfish virus (CCV)-infected MHC-matched clonal T cells

289 ipts from the terminal repeat of the channel catfish virus (CCV; also known as ictalurid herpesvirus

290 equine herpesvirus 1 (EHV-1), and of channel catfish virus, an evolutionarily remote herpesvirus.

291 ponyfish muscle hydrolysis were 3.5% hybrid catfish viscera extract, 15 min reaction time and fish m

292 Creatine kinase from salmon and catfish was detected by IgE from 14% and 10% of patients

293 the 21 Bacillus strains in the intestine of catfish was determined as Bacillus CFU/g of intestinal t

294 e peptidase from the viscera of farmed giant catfish was used for producing gelatin hydrolysates (HG)

295 When viscera extract from hybrid catfish was used for the production of protein hydrolysa

296 derived from lymphocytes of juvenile channel catfish, was used to construct lambda libraries that wer

297 art of our transcriptome analysis of channel catfish, we have analyzed 1909 expressed sequence tags (

298 entral muscles of Nile tilapia and broadhead catfish were comparatively studied.

299 Homozygous gynogenetic catfish were immunized with channel catfish virus (CCV)-

300 hia coli, mammalian COS-7 cells, and channel catfish where it elicited antigen-specific immune respon