ライフサイエンスコーパス: bass

1 s of silanols and fewer Bronsted acid sites (BASs).

2 part of the China Benzene and Sperm Study (C-BASS).

3 gilthead and red sea breams and European sea bass.

4 usters of zebrafish, pufferfish, and striped bass.

5 hey induced mortality in juvenile largemouth bass.

6 NA and genomic DNA were determined for white bass.

7 ed from the skin and gills of hybrid striped bass.

8 in, from the skin and gill of hybrid striped bass.

9 dal dosage and the state of satiation of the bass.

10 ratory populations of Atlantic Coast striped bass.

11 omposite climatic trends influencing Striped bass.

12 aryngeal teeth in the stomachs of largemouth bass.

13 ture genetic breeding programs in largemouth bass.

14 is elevated from synonymy for the Largemouth Bass.

15 ratures impair growth opportunities in young bass.

16 dos os Santos Bay, Brazil was also analysed: bass (0.169-0.195 mug g(-)(1)), mullet (0.043-0.361 mug

17 (1978, 2003) on transformational leadership, Bass (1997) and House & Shamir (1993) on charismatic and

18 the role of kisspeptins in the European sea bass, a perciform fish, we studied the distribution of k

19 uccess was negatively related and largemouth bass abundance was positively related to water temperatu

20 ssful walleye recruitment and low largemouth bass abundance was predicted to decline from 9% of lakes

21 number of lakes suitable for high largemouth bass abundance.

22 Consumption and growth in older bass (age 3-4) was far less sensitive to temperature.

23 The substantial power gain brought by BASS allows us to reveal accurate transcriptomic and cel

24 t for 12-90% of MeHg observed in YOY striped bass and 6-22% of MeHg in YOY summer flounder.

25 Until the recent report by Bass and co-workers, no true antagonists had been discov

26 Until the recent report by Bass and co-workers, no true antagonists of somatostatin

27 required for suction expansion in largemouth bass and compared it to the power capacities of the axia

28 horn shark, zebrafish (Aa, Ab), and striped bass and found extensive conservation of noncoding seque

29 D3 bioaccessibility in salmon, sardine, sea bass and hake.

30 nt relationship between length of largemouth bass and length of silver carp consumed (p < 0.001, F =

31 a relationship between length of largemouth bass and length of silver carp consumed.

32 pterus salmoides is retained for the Florida Bass and Micropterus nigricans is elevated from synonymy

33 binding to the purified lipid was stable to bass and neuraminidase treatment, labile to acid treatme

34 oural adaptions to weather events by striped bass and other coastal fishes will depend on maintenance

35 itment within wild populations of largemouth bass and possibly other exploited species in which behav

36 gs, 230 sport fish (predominantly largemouth bass and rainbow trout), and 505 prey fish (14 species)

37 a key role in the antimicrobial defenses of bass and that its functions are potentially conserved be

38 apia, catfish, trout, salmon, hybrid striped bass and yellow perch, respectively.

39 zheimer's disease, contains a tyrosine-based BaSS, and mutation of the tyrosine residue results in no

40 on rate of 100% for both wild and farmed sea bass, and of 67%, 80%, 100% for extensively, semi-intens

41 such as farmed rainbow trout, sea trout, sea bass, and sea bream, by causing disease or stress reacti

42 well-known Altamaha, Bartram's, and Choctaw basses, and two additional undescribed species currently

43 pyridine, which shows that up to 77% of the BASs are accessible (remarkable for a zeolite that has a

44 ionship warrants investigation as largemouth bass are large-gaped predators capable of exhibiting top

45 upstream gradient, food consumption in age 0 bass becomes increasingly constrained, and as a result,

46 ow how a staggered antiparallel coiled-coil 'BASS' (bipolar assembly) domain directs the assembly of

47 gement unit encompassing a panmictic striped bass breeding population.

48 ith APP tail 1), that interacts with the APP-BaSS but binds poorly when the critical tyrosine is muta

49 es capable of supporting abundant largemouth bass but failed walleye recruitment was predicted to inc

50 BASS can be easily incorporated into the pipelines of ex

51 species analyzed such as tilapia, smallmouth bass, chicken, or rat.

52 ylogenetic analysis also shows that the sand bass cofactor protein SBP1 and cofactor related protein

53 ed delimitation of species in the Largemouth Bass complex that necessitates a change in scientific no

54 e found that two connexins were expressed in bass cone photoreceptors.

55 In striped bass cones, this calcium feedback includes direct modula

56 we suggest that temperature-sensitive age 0 bass constrain the upstream distribution limits of bass

57 f this study were to determine if largemouth bass consume juvenile silver carp, and if there was a re

58 Bass describes the fascinating life history, behavior, a

59 ibility to rapidly authenticate European sea bass (Dicentrarchus labrax L.) according to production m

60 e IL-4/13 isoforms found in the European sea bass (Dicentrarchus labrax L.).

61 racterized several genes in the European sea bass (Dicentrarchus labrax) and evaluated variations in

62 We used the European sea bass (Dicentrarchus labrax) as a model and combined geno

63 between fresh skinless and frozen-thawed sea bass (Dicentrarchus labrax) fillets using the two-dimens

64 ove immunity and performance in European sea bass (Dicentrarchus labrax) yolk-sac larvae was explored

65 turally characterise the polar lipids of sea bass (Dicentrarchus labrax), fed with an experimental di

66 O(2) on responses to hypoxia in European sea bass (Dicentrarchus labrax).

67 y the lipids of farmed and wild European sea bass (Dicentrarchus labrax).

68 ope: gilthead sea bream (Sparus aurata); sea bass (Dicentrarchus labrax); turbot (Scophthalmus maximu

69 ding an LPXRFa precursor in the European sea bass, Dicentrarchus labrax.

70 The spreading process is modelled within the Bass diffusion framework that enables us to compare the

71 he atomic structure of the bipolar assembly (BASS) domain that directs four Kinesin-5 subunits to for

72 ly adding piscivorous bass, whereas a nearby bass-dominated lake remained unmanipulated and served as

73 Atlantic Coast striped bass exhibit exceptionally low levels of genetic variati

74 Sea bass exhibited greater hypoxia tolerance (~20% reduced O

75 When applied to navigating larval zebrafish, BASS extracts a dictionary of remarkably long, non-Marko

76 lications, not only for ASBT(NM) but for the BASS family as a whole and indeed other transporters tha

77 The BASS family is characterised by two helices that cross-o

78 The bile acid sodium symporter (BASS) family transports a wide array of molecules across

79 proving the growth performance of largemouth bass fed with a SBM-based diet.

80 reasonably higher in farmed than in wild sea bass fillets, due to the higher total lipid content of t

81 ntiation between fresh and frozen-thawed sea bass fillets.

82 ataset of soaring gliders climbing thermals, BASS finds the spiraling patterns characteristic of soar

83 y eggs, mullet fish (Mugil Cephalus) and sea bass fish (Dicentrarchus Labrax) samples.

84 Using a case of striped bass fisheries in Massachusetts, we pool the local knowl

85 icrobial peptide constitutively expressed in bass gill tissue.

86 However, black sea bass given access to freely swimming squid oriented towa

87 RASP was compared to BASS, GraphST, SEDR, SpatialPCA, STAGATE, and CellCharte

88 e (SNP) on the electrical synapses of hybrid bass H2-type horizontal cells.

89 MERGANSER predicted that 32-cm smallmouth bass had a median Hg concentration of 0.53 mug g(-1) (ro

90 ows: (1) the result of Fst showed largemouth bass had high genetic differentiation, and the gene flow

91 riation in migration timing of adult Striped bass has implications for predation risk on the seaward-

92 The striped bass has two retina-expressed class III myosin genes, ea

93 hat rapid evolution of introduced smallmouth bass has undermined a 20-y manual suppression effort in

94 P1), isolated from the mast cells of striped bass, has potent activities against bacteria, viruses, f

95 nvestigation into recent declines in striped bass health in the Chesapeake Bay in Maryland resulted i

96 Strikingly, N-terminal BASS helices bend as they emerge from the central bundle

97 To gain insight into potential role(s) of bass hepcidin in innate immunity in fish, we synthesized

98 Synthetic bass hepcidin was active in vitro against Gram-negative

99 Bass hepcidin was purified from the gill of hybrid strip

100 isolation of a novel antimicrobial peptide, bass hepcidin, from the gill of hybrid striped bass, whi

101 A novel antimicrobial peptide from the gill, bass hepcidin, is predominantly expressed in the liver a

102 igh-throughput screening in a hybrid striped bass (HSB) model of meningoencephalitis identified atten

103 min) than the time (1.3 min) invested by the bass in flushing a D. hornii before rejecting the beetle

104 and haemoglobin-O(2) binding affinity of sea bass in hypoxic conditions with ambient (~650 muatm) or

105 tions by otherwise resident riverine striped bass in the Hudson River Estuary, New York, USA, caused

106 ccurring in the early life stages of striped bass in the San Francisco Estuary, a population in conti

107 and their adverse effects on larval striped bass in this estuary.

108 he presence of a basolateral sorting signal (BaSS) in their cytoplasmic domain.

109 ighly attenuated in vivo in a hybrid striped bass infection challenge despite being more adherent and

110 migration timing of non-native adult Striped bass influenced by estuary outflow and sea surface tempe

111 tends to have more low frequency sound, and bass instruments typically provide the musical pulse tha

112 We propose that BASS is a mechanically stable, plectonemically-coiled ju

113 BASS is a novel 26-nm four-helix bundle, consisting of t

114 BASS is applicable when Cartesian fully-sampled k-space

115 Sufficient first summer growth of age 0 bass is essential for overwinter survival because young

116 Placement of spawning nests by adult bass is likely subject to strong evolutionary selection

117 ch, named bias-accelerated subset selection (BASS), is proposed for learning efficacious sampling pat

118 , Decatur, Lower Tuscaloosa, Weyburn-Midale, Bass Islands, and Grand Ronde carbon sequestration geolo

119 a great deal of detailed information on sea bass lipids composition and, once the spectra signals ha

120 For the same season wild sea bass lipids contain not only higher molar percentages of

121 hes for quantitative characterization of sea bass lipids were developed.

122 Hepcidin gene expression in bass liver increased significantly within hours of infec

123 In white bass liver, hepcidin gene expression was induced 4500-fo

124 re monitored from 1999 to 2011 in largemouth bass (LMB) and yellow perch (YP) in 23 lakes in Massachu

125 d metabolism, and organ growth of largemouth bass (LMB; Micropterus salmoides) fed high-and low-fishm

126 In contrast to other teleosts, the sea bass LPXRFa precursor contains only two putative RFamide

127 d species currently classified as Smallmouth Bass (M. dolomieu).

128 bass, white bass (Morone chrysops) x striped bass (M. saxatilis).

129 Does low frequency sound (bass) make people dance more?

130 Although largemouth bass Micropterus salmoides has shown its extremely econo

131 total Hg (THg) concentrations of Smallmouth Bass (Micropterus dolomieu) collected from reservoir, ta

132 m extent of the aquatic ectotherm smallmouth bass (Micropterus dolomieu) in two headwater rivers.

133 Although they co-occur with largemouth bass (Micropterus nigricans), an abundant native predato

134 cus) and two non-native fish, the largemouth bass (Micropterus salmoides) and Mississippi silverside

135 le free amino acid composition in largemouth bass (Micropterus salmoides) during its later life stage

136 esponse were examined in juvenile largemouth bass (Micropterus salmoides) exposed to a potent synthet

137 Captive largemouth bass (Micropterus salmoides) reject the gyrinid beetle,

138 Using males from two lines of largemouth bass (Micropterus salmoides) selectively bred over three

139 and average Hg concentrations in largemouth bass (Micropterus salmoides)-equivalent fish (LMBE) in 1

140 nd warmwater fish species such as largemouth bass (Micropterus salmoides).

141 The Black Basses (Micropterus) are an iconic lineage of freshwater

142 Bluegill, Lepomis macrochirus and Smallmouth Bass, Micropterus dolomieu).

143 Striped bass migrated later in years when Delta outflow was grea

144 The plasma of the striped bass Morone saxatilis contains a fucose-specific lectin

145 was purified from the gill of hybrid striped bass (Morone chrysops x Morone saxatilis) based on antim

146 re derived from each parental species, white bass (Morone chrysops) and striped bass (Morone saxatili

147 from the gill of hybrid striped bass, white bass (Morone chrysops) x striped bass (M. saxatilis).

148 Using striped bass (Morone saxatilis) and six multiplexed microsatelli

149 Striped bass (Morone saxatilis) are long-lived, highly migratory

150 ing the empirical example of coastal Striped Bass (Morone saxatilis) during their seasonal feeding mi

151 Striped bass (Morone saxatilis) exhibit striking variation in mi

152 Chesapeake Bay striped bass (Morone saxatilis) is currently experiencing an epi

153 MsaFBP32) isolated from serum of the striped bass (Morone saxatilis), composed of two tandem domains

154 es, white bass (Morone chrysops) and striped bass (Morone saxatilis).

155 e channels in cone photoreceptors of striped bass (Morone saxatilis).

156 inal pigment epithelium (RPE) of the striped bass, Morone saxatilus.

157 The synthetic, amidated white bass moronecidin exhibited broad spectrum antimicrobial

158 Striped bass moved out of the estuary, exhibiting novel migratio

159 Reanalysis of Chesapeake Bay striped bass mtDNA data from two previous studies estimated popu

160 Native peptides from sea bass muscle were analyzed by two different approaches: m

161 ential for overwinter survival because young bass must persist from energy reserves accumulated durin

162 Bass Myo3A, a class III myosin, was expressed in HeLa ce

163 The striped bass Nramp gene (MsNramp) and a 554-amino-acid sequence

164 ich cleaves DNA between the first and second bass of the recognition sequence (A/CGT), Tsp49I hydroly

165 uth bass originated from northern largemouth bass of USA.

166 The bass' oral tolerance of gyrinidal varies broadly as a fu

167 data for fast authentication of European sea bass origin.

168 oss of genetic diversity; China's largemouth bass originated from northern largemouth bass of USA.

169 dy the related proteins from the barred sand bass (P. nebulifer) and the nematode C. elegans.

170 BASS performs cell type clustering at the single-cell sc

171 intensive control program produced a larger bass population dominated by young and early-maturing fi

172 populations; (3) The majority of largemouth bass populations had a significant heterozygosity excess

173 declining walleye and increasing largemouth bass populations have raised questions regarding the fut

174 ts indicate enhancement of native largemouth bass populations is unlikely to substantially reduce sil

175 ated in both study streams and explained why bass positioned nests twice as far upstream in the warm

176 weaker than previously demonstrated for sea bass post-larvae.

177 BASS produces a sequence of SPs with the aim of finding

178 n compared to control), being salmon and sea bass proteolysis extent (40 and 33%, respectively) the m

179 f alternative adrenergic receptors including BasS, QseE and CpxA and their associated signalling casc

180 pread musical practice of carrying rhythm in bass-ranged instruments and complements previously estab

181 Compared with greedy approaches, BASS rapidly learns effective SPs for various reconstruc

182 n tends to occur at the Bronsted acid sites (BASs) rather than the Cu(II) sites.

183 temporary walleye recruitment and largemouth bass relative abundance to modeled water temperature, la

184 eld data reveal the upstream extent of adult bass reproduction corresponds to a point in the downstre

185 rior led to increased targeting by black sea bass, resulting in decreased survival of the squid in a

186 n the myosin PCR screen of cDNA from striped bass retina and striped bass RPE, we amplified 17 distin

187 tion of the PL-type calcium channel of white bass retinal horizontal cells was studied in isolated, c

188 of zebrafish and the HoxA cluster of striped bass revealed a striking loss of conservation of these p

189 of cDNA from striped bass retina and striped bass RPE, we amplified 17 distinct myosins from eight my

190 trading seabass species, including the chalk bass, Serranus tortugarum, switch mating roles repeatedl

191 HC from defatted Asian sea bass skin at different levels (0.25%-2%, w/v) were loade

192 lutionary selection in temperate systems: if bass spawn too far upstream, their young are unlikely to

193 We identified that the Bass Strait Islands are highly suitable for BNWs and pre

194 We use two paleoecological records from the Bass Strait islands to identify the initiation of anthro

195 t risk of disease occurrence, including some Bass Strait islands where BNW translocations are propose

196 forager on the shallow continental shelf of Bass Strait, and represents the greatest biomass of mari

197 t via two main routes: (i) directly east via Bass Strait, or (ii) south-east around Tasmania, which i

198 foraging distribution largely restricted to Bass Strait, the shallow (max.

199 trations and sea-surface height anomalies in Bass Strait.

200 In both cases, BASS succeeds in identifying rare action sequences in th

201 [COG]) received instructions on the modified Bass technique (MBT) after their toothbrushing performan

202 up); 2) F (Fones technique group); and 3) B (Bass technique group).

203 different brushing techniques (Fones versus Bass technique in their common modifications).

204 al CBT of the modified Fones or the modified Bass technique, respectively.

205 rp was present in 18% of diets of largemouth bass that consumed fish.

206 and were recovered from diets of largemouth bass that were 94-262 mm total length.

207 Here, we present a computational method, BASS, that enables multi-scale and multi-sample analysis

208 included bovine, chicken, bullfrog, striped bass, thresher shark, and Pacific hagfish.

209 We illustrate the benefits of BASS through comprehensive simulations and applications

210 ted the aroma transformation of Japanese sea bass through enzymatic incubation by controlling attache

211 ing the springtime provide a cue for Striped bass to initiate migration, but sea surface temperature

212 e designed an unsupervised algorithm called "BASS" to efficiently identify and segment recurring beha

213 Applied to a novel chemotaxis assay, BASS uncovers chemotactic strategies deployed by zebrafi

214 Mercury concentrations in piscivorous adult bass varied little over the course of the study.

215 North American warm-water fishes, largemouth bass virus (LMBV).

216 omposition and on the infectivity of striped bass virus, an aquareovirus, were examined.

217 75 min, 10.0 mL/min) was used to defeat sea bass viscera to facilitate the fermentation process.

218 Sea bass was aquacultured using either FO or OP diet.

219 BASS was tested with five reconstruction methods for par

220 rase activities from the gut of European sea bass, we have obtained isolates with high probiotic pote

221 In the retina of white bass, we identified a class of bistratified, wide-field

222 Largemouth bass were collected from the La Grange Pool of the Illin

223 est and we observed a mismatch between where bass were present and the highest densities of prey acro

224 Here, 196 young-of-the-year (YOY) striped bass were sampled from Maryland's Choptank, Potomac and

225 -dominated lake by slowly adding piscivorous bass, whereas a nearby bass-dominated lake remained unma

226 ss hepcidin, from the gill of hybrid striped bass, white bass (Morone chrysops) x striped bass (M. sa

227 sity, distribution, and systematics of Black Basses will serve as important basis for the management

228 ne expression in vivo following infection of bass with the fish pathogens, Streptococcus iniae or Aer

229 onstrain the upstream distribution limits of bass within temperate streams.