ライフサイエンスコーパス: Atlantic salmon

1 ish poxvirus, which was isolated from farmed Atlantic salmon.

2 complete FO replacement in diets for farmed Atlantic salmon.

3 other species, this is not yet the case for Atlantic salmon.

4 SNPs were discovered in the MSTN-1b gene of Atlantic salmon.

5 ted with the genetic regulation of growth in Atlantic salmon.

6 or SNP markers in a commercial population of Atlantic salmon.

7 ining IFNb and IFNc in antiviral immunity of Atlantic salmon.

8 MH-linked markers in natural populations of Atlantic salmon.

9 or as a whole but remains as high as 5.0 for Atlantic salmon.

10 negative impact on the global aquaculture of Atlantic salmon.

11 trains were tested for virulence in juvenile Atlantic salmon.

12 ak of leiomyosarcoma in the swim bladders of Atlantic salmon.

13 onasal receptor (SVR) partial sequences from Atlantic salmon.

14 mportance of olfaction in the biology of the Atlantic salmon.

15 Thus, Atlantic salmon adjust lipid metabolism in response to d

16 oung-of-the-year (YOY) and one-year-old (1+) Atlantic salmon and brown trout in response to flow chan

17 on-fortified and fortified samples of farmed Atlantic salmons and rainbow trouts.

18 re perhaps the most important problem facing Atlantic Salmon aquaculture after feed sustainability.

19 lesh color are of economic importance to the Atlantic salmon aquaculture industry.

20 gative economic and animal welfare impact on Atlantic salmon aquaculture.

21 by this microbe, has a substantial impact on Atlantic salmon aquaculture.

22 Farmed Atlantic salmon are a global commodity and, as an oily f

23 Finally, we demonstrate that the Atlantic salmon assembly can serve as a reference sequen

24 The species analysed were: Atlantic salmon, Australian sardine, prawn (six species)

25 ere each year, hundreds of thousands of farm Atlantic salmon escape from fish farms.

26 atty acid composition of over 3,000 Scottish Atlantic salmon farmed between 2006 and 2015, we find th

27 revalent inflammatory diseases in commercial Atlantic salmon farms in Norway.

28 Atlantic salmon fertilize externally, and we were theref

29 lted in lower connective tissue stability of Atlantic salmon fillets.

30 icrobiota harboured in the distal digesta of Atlantic salmon freshwater fish (FW) kept in a commercia

31 ses induced significantly lower mortality in Atlantic salmon fry than the parent strains did in in vi

32 ated and induced 15% cumulative mortality in Atlantic salmon fry, compared to 68% mortality induced b

33 Thus, the tetraploid Atlantic salmon genome appears to contain at least two p

34 troviruses by not harboring sequences in the Atlantic salmon genome.

35 equences of the 13 protein-coding genes from Atlantic salmon have been compared with their counterpar

36 and reintroduce a sustainable population of Atlantic Salmon have focused on determining whether Lake

37 scle and brain of alevin and adult stages of Atlantic salmon, identifying 10 variants categorised as

38 nd high mortalities in stocks of Chinook and Atlantic salmon in the USA.

39 This study examined the glacial history of Atlantic salmon in western Europe using two independent

40 with 10% CM, in a 16 week feeding trial with Atlantic salmon (initial weight 240 g fish(-1)).

41 nd RtxA each have cytotoxic activity against Atlantic salmon kidney (ASK) cells.

42 died among selected (FP) and unselected (WP) Atlantic salmon lines that were reared together to avoid

43 To utilize the large difference between Atlantic salmon male and female recombination rates, a t

44 diagnostics for the salmon gill poxvirus in Atlantic salmon may help curb this disease and provide c

45 nalysis indicates that consumption of farmed Atlantic salmon may pose health risks that detract from

46 The Atlantic salmon miRNAs experimentally identified in this

47 collected from two unrelated populations of Atlantic salmon; one challenged with SAV as fry in fresh

48 markers and eight microsatellite loci in two Atlantic salmon populations in Ireland on two temporal s

49 variation over five decades in four marginal Atlantic salmon populations located at the southern limi

50 The major declines in Atlantic salmon populations occurred against a backdrop

51 abundance and productivity of North American Atlantic salmon populations.

52 availability, which are ultimately linked to Atlantic salmon populations.

53 productivity and recovery of North American Atlantic salmon populations.

54 levels (11% and 5.5% of diet) was tested in Atlantic salmon post-smolts compared to fish fed a FO di

55 nt ingredients in the diets, cause losses in Atlantic salmon production.

56 Map alignments with orthologous regions in Atlantic salmon, rainbow trout, and Arctic char also rev

57 copy number of the miRNA genes in the draft Atlantic salmon reference genome sequence.

58 ion (HSMI), recently associated with a novel Atlantic salmon reovirus (ASRV), is currently one of the

59 territoriality and growth rates of yearling Atlantic salmon Salmo salar were examined in relation to

60 In this work the drying kinetics of Atlantic salmon (Salmo salar L.) fillets and the influen

61 role of collagen in texture variations among Atlantic salmon (Salmo salar L.) grown under commercial

62 essing survival, growth rate and movement of Atlantic salmon (Salmo salar L.) juveniles from 10 famil

63 here, there are concerns that escaped farmed Atlantic salmon (Salmo salar L.) may impact on wild salm

64 of seven quinolone antibiotics in tissue of Atlantic salmon (Salmo salar L.) was developed.

65 ffect on flesh quality of pre-rigor filleted Atlantic salmon (Salmo salar L.) was investigated.

66 Atlantic salmon (Salmo salar L.), a member of the family

67 rees C) affect the flesh quality of triploid Atlantic salmon (Salmo salar L., 1.6+/-0.3kg).

68 ms of this study were to identify lncRNAs in Atlantic salmon (Salmo salar) and evaluate their transcr

69 surmuletus), Bluefish (Pomatamus saltatrix), Atlantic salmon (Salmo salar) and flying gurnard (Trigla

70 O-acetylated N-glycans from fish serum of Atlantic salmon (Salmo salar) are characterized by capil

71 nd textural changes during frozen storage of Atlantic salmon (Salmo salar) fillets at four temperatur

72 e activities in ice-stored and super-chilled Atlantic salmon (Salmo salar) fillets, and the effect on

73 The Atlantic salmon (Salmo salar) has been widely used as a

74 Actually, Atlantic salmon (Salmo salar) is the species most transf

75 The complete sequence of the Atlantic salmon (Salmo salar) mitochondrial genome has b

76 e show that nutrient pulses from decomposing Atlantic salmon (Salmo salar) parents alter selection pr

77 investigated the dio gene family in juvenile Atlantic salmon (Salmo salar) parr, which prepare for se

78 North American Atlantic salmon (Salmo salar) populations experienced su

79 ke Ontario once supported a large complex of Atlantic Salmon (Salmo salar) populations that became ex

80 free proteomics were combined to investigate Atlantic salmon (Salmo salar) sampled from three differe

81 Exposure to sea lice from farmed Atlantic salmon (Salmo salar) was thought to be the caus

82 variation in spermatozoal traits among wild Atlantic salmon (Salmo salar), a species naturally adapt

83 he identification of six melanopsin genes of Atlantic salmon (Salmo salar), a valuable teleost model

84 effect locus controlling age at maturity in Atlantic salmon (Salmo salar), an important fitness trai

85 O. mykiss), Chinook salmon (O. tshawytscha), Atlantic salmon (Salmo salar), and Arctic charr (Salveli

86 e present a high-quality genome assembly for Atlantic salmon (Salmo salar), and show that large genom

87 ia associated with epitheliocystis in farmed Atlantic salmon (Salmo salar), gills with proliferative

88 ive fish in the family Salmonidae, including Atlantic salmon (Salmo salar), rainbow trout (Oncorhynch

89 inter flounder (Pleuronectes americanus) and Atlantic salmon (Salmo salar), reveals a similar pattern

90 able oil (VO) has little effect on growth in Atlantic salmon (Salmo salar), several studies have show

91 pid composition and growth was determined in Atlantic salmon (Salmo salar), using a combination of cD

92 died for their effects on lipid oxidation in Atlantic salmon (Salmo salar).

93 liver and white muscle metabolic profile of Atlantic salmon (Salmo salar).

94 fontinalis; Arctic char, Salvelinus alpinus; Atlantic salmon, Salmo salar; and brown trout, Salmo tru

95 senting a major problem in the production of Atlantic salmon (Salmon salar).

96 The gut microbiota of Atlantic salmon showed similarities with that of mammals

97 Atlantic salmon sperm can be considered to enter a compe

98 osons were also isolated from the genomes of Atlantic salmon (SSTN, Salmo salar) and frog (RTTN, Rana

99 Matrilineal phylogenetic divergence among Atlantic salmon stocks of the Bay of Fundy in south east

100 a standard commercial reference feed (ST) in Atlantic salmon subjected to an ASRV challenge.

101 ed as a nutritionally regulated gene from an Atlantic salmon subtractive hybridization library with h

102 The complete nucleotide sequence of the Atlantic salmon swim bladder sarcoma virus (SSSV) provir

103 tected in diseased farmed koi carp, ayu, and Atlantic salmon, their genetic relationships to poxvirus

104 is study, we examined the immune response of Atlantic salmon to S. parasitica infection and to its ce

105 4-72 hr after transfer of freshwater-adapted Atlantic salmon to seawater, there are increases in thei

106 Atlantic salmon undergo dramatic physiological changes a

107 btained in CHSE-214 cells, and virulence for Atlantic salmon was retained.

108 To identify miRNAs from Atlantic salmon, we constructed whole fish miRNA librari

109 Pre-rigour fillets of Atlantic salmon were either super-chilled to a core temp

110 epitheliocystis from proliferative gills of Atlantic salmon, which exhibits developmental stages dif

111 ononuclear cells in the fast muscle of adult Atlantic salmon, while quantitative real-time PCR showed