ライフサイエンスコーパス: killifish

1 the teleost Fundulus heteroclitus (Atlantic killifish).

2 the naturally short-lived African turquoise killifish.

3 vo-morpholino knock down technique for adult killifish.

4 pothalamic sexual dimorphism is conserved in killifish.

5 Killifish AHRR encodes a 680-residue protein with a pred

6 gene under control of AHR response elements, killifish AHRR inhibited the TCDD-dependent transactivat

7 pressed AHRR proteins from human, mouse, and killifish all fail to bind [(3)H]TCDD or [(3)H]beta-naph

8 Recently, we observed in the gill of killifish, an environmental model organism, that arsenic

9 Two distantly related fish species, bluefin killifish and black bream, express these old paralogs di

10 rates in the upstream reach containing only killifish and crabs.

11 port of the use of vivo-morpholinos in adult killifish and demonstrates that vivo-morpholinos are a v

12 Toxicity reduction, which was dramatic in killifish and duckweed even for low extents of sulfidati

13 on in juvenile rainbow trout, zebrafish, and killifish and on the absorbance of visual pigments in ra

14 Adult killifish and sediments were collected from seven sites

15 Eiders have similar Delta(199)Hg as killifish but much higher delta(202)Hg, suggesting that

16 and associated consequences in PAH-resistant killifish by integrating genomic, physiological, and mod

17 io rerio (zebrafish), Fundulus heteroclitus (killifish), Caenorhabditis elegans (nematode worm), and

18 The euryhaline killifish CFTR coding sequence is highly homologous to t

19 Killifish collected from Grande Terre had divergent gene

20 dues (Ala127, Thr233, Asn317, and Tyr386) of killifish CYP1A to the corresponding residues of human C

21 0G enabled TCB to dock closer to the heme in killifish CYP1A.

22 in ensembles of rat or human CYP1A1 than of killifish CYP1A.

23 ns are due primarily to Leu387 and Val230 in killifish CYP1A.

24 multiple models of rat, human, scup, and/or killifish CYP1As, based on multiple templates, retaining

25 pine densities in the hypothalamus than male killifish (densities of 0.34+/-0.06 microm-1 and 0.25+/-

26 nating oil across space and time in resident killifish during the first 4 mo of the spill event.

27 stuarine organisms (green crab, blue mussel, killifish, eider) to investigate methylmercury (MMHg) so

28 ntal features of the non-conventional annual killifish embryo to study the principles underlying tiss

29 properties of adjacent tissues in the early killifish embryo.

30 ne turnover in the EVL cells of post-epiboly killifish embryos is accelerated at cell-cell contacts,

31 Furthermore, laboratory exposures of Gulf killifish embryos to field-collected sediments from Gran

32 Gulf killifish embryos were exposed to dissolved Cu and CuO N

33 genome for the short-lived African turquoise killifish, establishing its role as a vertebrate system

34 a wider range in laboratory experiments with killifish exposed to MeHg enriched food.

35 h using a natural temperature gradient where killifish fed on natural food sources.

36 During embryogenesis, the killifish Fundulus heteroclitus forms a monolayered tigh

37 sequences were identified in a teleost (the killifish Fundulus heteroclitus), two elasmobranch speci

38 of Deepwater Horizon crude oil on fish, Gulf killifish ( Fundulus grandis ) were collected from an oi

39 cles (NPs) and their bioavailability to Gulf killifish (Fundulus grandis) embryos, with the aim of qu

40 ate CYP3 diversity better, we determined the killifish (Fundulus heteroclitus) CYP3A30 and CYP3A56 an

41 the neuroarchitecture of the male and female killifish (Fundulus heteroclitus) hypothalamus to evalua

42 l variation patterns across the range of the killifish (Fundulus heteroclitus) in 310 loci, including

43 Atlantic killifish (Fundulus heteroclitus) inhabiting the Atlanti

44 The Atlantic killifish (Fundulus heteroclitus) is an environmental se

45 as many fish species, including the Atlantic killifish (Fundulus heteroclitus) possess two distinct A

46 However, in Atlantic killifish (Fundulus heteroclitus), a population genetic

47 under varying temperature regimes using the killifish, Fundulus heteroclitus.

48 Through analysis of 384 whole killifish genome sequences and comparative transcriptomi

49 lease (CRISPR/Cas9) system and the turquoise killifish genome, this platform enables the generation o

50 h as the use of the very short-lived African killifish (Harel et al.), are bridging the translational

51 ammalian studies, we found that adult female killifish have 25% greater dendritic spine densities in

52 In killifish, high nucleotide diversity has likely been a c

53 The mangrove killifish (Kryptolebias marmoratus) is the only vertebra

54 We found that, in wild-caught bluefin killifish Lucania goodei (Fundulidae) and wild-caught ze

55 SWS1, SWS2-A, and SWS2-B pigments of bluefin killifish (Lucania goodei) have the wavelengths of maxim

56 Here, using the African turquoise killifish (Nothobranchius furzeri), a naturally short-li

57 genome engineering in the African turquoise killifish (Nothobranchius furzeri), which is the shortes

58 Atlantic killifish populations have rapidly adapted to normally l

59 nal") genetic architecture characteristic of killifish populations previously studied in Florida, whe

60 the naturally short-lived African turquoise killifish, providing a unique resource for comparative a

61 cking of TCDD to sets of consensus models of killifish, rat, and human CYP1As showed species differen

62 uvenile rainbow trout (smolt), zebrafish, or killifish remained unchanged.

63 mmon large consumers-primarily insectivorous killifish (Rivulus hartii), omnivorous guppies (Poecilia

64 ompared life history traits in a Trinidadian killifish, Rivulus hartii, from fish communities that di

65 and field mesocosms, MeHg concentrations in killifish significantly increased at elevated temperatur

66 of polymorphic inserts in the genomes of the killifish species, Fundulus heteroclitus.

67 ause of the fast life cycle of the turquoise killifish, stable lines can be generated as rapidly as 2

68 fespan differences between various turquoise killifish strains.

69 y suppression, and contaminant resistance in killifish subpopulations from sites throughout the estua

70 results show that contaminants have affected killifish subpopulations throughout the estuary, even in

71 exhibited by laboratory-spawned embryos from killifish subpopulations throughout the estuary.

72 thesis in several subpopulations of Atlantic killifish that have evolved a gradation of resistance to

73 AHRR mRNA is widely expressed in killifish tissues and is inducible by TCDD or polychlori

74 boratory has shown that rapid acclimation of killifish to seawater is mediated by trafficking of CFTR