ライフサイエンスコーパス: salmonid

1 , Siluriformes (catfish), and Salmoniformes (salmonids).

2 onova shasta, which causes lethal disease in salmonids.

3 the global and long history introductions of salmonids.

4 presence of CD4-1(+)CD3epsilon(+) T cells in salmonids.

5 re based on studies of embryo-lethality with salmonids.

6 d the AhRs of sturgeons differ from those of salmonids.

7 e resource for functional genome research in salmonids.

8 ain critical instream habitat for ESA-listed salmonids.

9 of carotenoids (red-pink pigments) in farmed salmonids.

10 tion and treatment of infections in cultured salmonids.

11 linked to the sex determining locus (sdY) of salmonids.

12 Pancreas disease (PD), caused by a salmonid alphavirus (SAV), has a large negative economic

13 Due to the marked heterochiasmy in salmonids, an efficient two-stage mapping approach was a

14 lder' ohnologues that began diverging in the salmonid ancestor.

15 Our results demonstrate that salmonid and freshwater resources were more important fo

16 is important for development and survival of salmonids and crustaceans and has been shown to reduce c

17 uate downstream passage behavior of juvenile salmonids and dam approach behavior of upstream migratin

18 ines, felines, equids, ovids, suids, bovins, salmonids and murids.

19 ghly fatal hemorrhagic septicemic disease in salmonids and other fishes, leading to epizootics throug

20 tially impacting both economically-important salmonids and their associated river food web.

21 Sturgeons are evolutionarily distinct from salmonids, and the AhRs of sturgeons differ from those o

22 In salmonid aquaculture, a variety of technologies have bee

23 ae virus associated with high mortalities in salmonid aquaculture.

24 ng freshwater bryozoans as primary hosts and salmonids as secondary hosts.

25 the Northern Rocky Mountains for two native salmonids-bull trout (BT) and cutthroat trout (CT).

26 rom vegetable sources in the diets of farmed salmonids, but the consequences for the oxidative stabil

27 e model can be used to support management of salmonids by predicting population responses to predicte

28 e health condition of out-migrating juvenile salmonids can influence migration success.

29 Salmonid CCL19-like genes all contain the DCCL-conserved

30 ), spreads easily throughout farmed and wild salmonids, constituting a significant economic burden.

31 e the human Alu sequence, the SINEs found in salmonids could provide useful genetic markers and prime

32 nant contribution of algal-derived energy to salmonid diets in manipulated reaches.

33 , we demonstrate the major impact of LORe on salmonid evolution.

34 fp, which causes enteric redmouth disease in salmonid fish species.

35 eat to healthy and sustainable production of salmonid fish worldwide.

36 We find that beta2m of a salmonid fish, the rainbow trout (Oncorhynchus mykiss),

37 Salmonid fish, whose ancestor underwent WGD by autotetra

38 g of resistance to this important disease of salmonid fish.

39 In the embryos and young juveniles of salmonid fishes and rodents, TH induces switches in opsi

40 responsible for bacterial kidney disease in salmonid fishes world-wide.

41 Six cyprinid and salmonid fishes, including an asymptomatic carrier, were

42 The common ancestor of salmonid fishes, including rainbow trout (Oncorhynchus m

43 rently related to the tetraploid ancestry of salmonid fishes, was detected at one simple sequence rep

44 ed DNA fingerprint patterns in 14 species of salmonid fishes.

45 ned ecological and phenotypic variability of salmonid fishes.

46 cates efforts to detect allelic variation in salmonid fishes.

47 er certain conditions, mortality of juvenile salmonid fishes.

48 n the diversity of life histories within the salmonid fishes.

49 ication of QTL for important traits in other salmonid fishes.

50 MDH-B, duplicated by ancestral polyploidy in salmonid fishes.

51 a reference sequence for the study of other salmonids for a range of purposes.

52 While whole salmonid fry showed a small upregulation of IGF-IR expre

53 and brown trout (Salmo trutta) represent two salmonid genera separated for 15--20 million years.

54 C gene was generated for 11 species in three salmonid genera, Oncorhynchus, Salmo, and Salvelinus.

55 gene were generated for 11 species in three salmonid genera: Oncorhynchus, Salmo, and Salvelinus.

56 One-quarter of each salmonid genome, harbouring at least 4550 ohnologues, ha

57 ach the immunological function of the ILT in salmonid gills.

58 In salmonids, growth and development are important fitness

59 revious evidence for the portfolio effect in salmonids has arisen from examinations of time series of

60 Wild stocks of Pacific salmonids have experienced sharp declines in abundance o

61 of a recent whole genome-duplication event, salmonids have four: MSTN-1 (-1a and -1b) and MSTN-2 (-2

62 Salmonid herpesvirus 1 (SalHV-1) is a pathogen of the ra

63 into the molecular mechanisms implicated in salmonid immune response and resistance to whirling dise

64 enthic algae, most insect taxa, and juvenile salmonids increased in manipulated areas.

65 r histocompatibility class (MHC) IIB gene of salmonids is analyzed for patterns indicative of natural

66 e results demonstrate that the IFN system of salmonids is far more complex than previously realized,

67 nism for evolving new MHC class I alleles in salmonids is recombination in intron II that shuffles al

68 lymphoid tissues in mammals, diversified in salmonids leading to the presence of six CCL19-like gene

69 The striking difference in salmonid MHC class I and class II evolution contrasts wi

70 The difference may arise because salmonid MHC class I and II genes are not linked, wherea

71 s an opportunity to explore the evolution of salmonid miRNAs following the relatively recent whole ge

72 l to data on the passage of juvenile Pacific salmonids (Oncorhynchus spp.) at seven dams in the Colum

73 e (PKD) is a major threat to wild and farmed salmonid populations because of its lethal effect at hig

74 of allele frequencies at duplicated loci in salmonid populations.

75 Salmonids possess all four subgroups, whereas other tele

76 he presence and absence of widely introduced salmonids rainbow trout (Oncorhynchus mykiss) and brook

77 As previously observed in other salmonids, recombination rates showed large sex differen

78 needs of Endangered Species Act (ESA)-listed salmonids relative to climate change in the central Colu

79 d phylogenetic approaches, we establish that salmonids retain two IGF-IRa paralogues from ssWGD and a

80 This review will focus primarily on farmed salmonids (salmon and trout) within a comparative contex

81 million years ago of the common ancestor of salmonids (salmonid-specific fourth vertebrate whole-gen

82 robes homologous to two previously described salmonid short interspersed nuclear elements (SINEs) det

83 for the biological limit governing suitable salmonid spawning and egg incubation conditions.

84 velinus namaycush) and among several related salmonid species (lake trout; brook trout, Salvelinus fo

85 ely recent whole genome duplication event in salmonid species and to investigate the role of miRNAs i

86 ction on the class IIB gene in all 11 of the salmonid species for both the ABS and the non-ABS codons

87 mpacted the propagation and survival of many salmonid species over six continents, with particularly

88 cal adaptations that potentially facilitated salmonid species radiation.

89 we used genomic DNA sequence data from nine salmonid species to compare nucleotide identities for or

90 Across salmonid species, life-history strategies range from who

91 apping approach within and across a range of salmonid species.

92 hogen Myxobolus cerebralis, afflicts several salmonid species.

93 (IPNVs) exhibit a wide range of virulence in salmonid species.

94 s, homologous sequences are present in other salmonid species.

95 ars ago of the common ancestor of salmonids (salmonid-specific fourth vertebrate whole-genome duplica

96 ing probes homologous to the 5' or 3' end of salmonid-specific small interspersed nuclear elements.

97 However, while a salmonid-specific whole genome duplication (ssWGD) is kn

98 management approaches for restoring depleted salmonid stocks.

99 onstrates that riparian management targeting salmonids strongly affects river food webs via changes i

100 sensus sequence of a transposase gene of the salmonid subfamily of elements was engineered by elimina

101 serve the out-migratory behavior of juvenile salmonids tagged by surgical implantation of acoustic mi

102 ative homeologous regions inherited from the salmonid tetraploid ancestor were identified for 10 pair

103 of the two genes expected from the ancestral salmonid tetraploidy.

104 transposase binds to the inverted repeats of salmonid transposons in a substrate-specific manner, and

105 ury conditions, by mid-21st century juvenile salmonids' weights are expected to be lower in the Colum