ライフサイエンスコーパス: bass

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

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

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

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

5 ratory populations of Atlantic Coast striped bass.

6 ratures impair growth opportunities in young bass.

7 gilthead and red sea breams and European sea bass.

8 usters of zebrafish, pufferfish, and striped bass.

9 hey induced mortality in juvenile largemouth bass.

10 NA and genomic DNA were determined for white bass.

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

12 (1978, 2003) on transformational leadership, Bass (1997) and House & Shamir (1993) on charismatic and

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

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

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

16 number of lakes suitable for high largemouth bass abundance.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

31 gement unit encompassing a panmictic striped bass breeding population.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

51 icrobial peptide constitutively expressed in bass gill tissue.

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

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

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

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

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

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

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

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

60 Bass hepcidin was purified from the gill of hybrid strip

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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