ライフサイエンスコーパス: fruitfly

1 f a specific region of the head of the adult fruitfly.

2 x cascade which results in a fully developed fruitfly.

3 emporal regulation of adult emergence in the fruitfly.

4 s have also been seen in bacteria, fungi and fruitflies.

5 ted behaviour and rewarding reinforcement in fruitflies.

6 hermore, human alphaII-spectrin is closer to fruitfly alpha-spectrin than to human alphaI-spectrin, c

7 Fruitflies and houseflies have an open rhabdom system, i

8 norhabditis elegans, Drosophila melanogaster fruitflies and mice.

9 use of genetically tractable organisms (i.e. fruitflies and nematode worms) that exhibit a full range

10 ates and the principal model invertebrates - fruitflies and nematodes - is unclear.

11 fying genes responsible for axon guidance in fruitflies and nematodes.

12 reasing as they grow to adulthood, and adult fruitflies and rats die if they are forcibly deprived of

13 Sik3 orthologues also regulate sleep in fruitflies and roundworms.

14 een obligatorily outbreeding species such as fruitflies and self-fertilizing species such as the plan

15 able at: http://www.cs.niu.edu/~jzhou/papers/fruitfly and http://research.janelia.org/peng/proj/fly_e

16 imulated data as well as real data sets from fruitfly and human.

17 gton's-disease-relevant phenotypes in yeast, fruitfly and mouse models, as well as in a mouse model o

18 of three principal organisms--the nematode, fruitfly and mouse--indicate that cell suicide is implem

19 atically studied 5'-isomiRs in human, mouse, fruitfly and worm by analysing a large collection of sma

20 thologs from human, mouse, wallaby, chicken, fruitfly, and nematode, underscoring the age and conserv

21 including human, mouse, rat, pig, zebrafish, fruitfly, and nematode.

22 idization data in mouse, frog, zebrafish and fruitfly are integrated with chicken genomic and express

23 Initially identified in the fruitfly, balancer chromosomes are valuable genetic tool

24 itize the morphology of a single neuron in a fruitfly brain in minutes, with about a 17-fold improvem

25 a 3D digital atlas of neurite tracts in the fruitfly brain.

26 popular genomes are included: human, mouse, fruitfly, Caenorhabditis elegans worm, Saccharomyces yea

27 In meiosis in male fruitflies, chromosome pairing events do not facilitate

28 the first time that Drosophila melanogaster fruitflies could be mutated to obtain animals with insom

29 beta-catenin and its fruitfly counterpart Armadillo act as a coactivator in t

30 Fruitflies derived from a wild population vary in their

31 the embryonic hole during dorsal closure in fruitfly development.

32 ion and analysis of 3D images for roundworm, fruitfly, dragonfly, mouse, rat and human.

33 Many species of the fruitfly Drosophila are either sexually dimorphic for ab

34 Paradoxically, in the fruitfly Drosophila bifurca sperm competition is rife bu

35 Recent studies have shown that the fruitfly Drosophila exhibits behavioral sensitization in

36 udies in the worm Caenorhabditis elegans and fruitfly Drosophila have revealed the essential role int

37 of the two approaches to populations of the fruitfly Drosophila in order to estimate some important

38 In dipterans such as the fruitfly Drosophila melanogaster (D. mel.) and the mosqu

39 The genetic techniques available in the fruitfly Drosophila melanogaster allow analysis of the b

40 oderm in two highly divergent dipterans, the fruitfly Drosophila melanogaster and the mosquito Anophe

41 The fruitfly Drosophila melanogaster exhibits a robust and i

42 ily is large and functionally redundant, the fruitfly Drosophila melanogaster has only two MMPs, both

43 The mushroom body in the fruitfly Drosophila melanogaster is an associative brain

44 evel of the sole K+/Cl- cotransporter in the fruitfly Drosophila melanogaster render flies susceptibl

45 The fruitfly Drosophila melanogaster senses day-night cycles

46 Although the fruitfly Drosophila melanogaster tastes sugars, salts an

47 we show that during gonad development in the fruitfly Drosophila melanogaster the proliferation of pr

48 tion of many regulatory proteins and, in the fruitfly Drosophila melanogaster, buffers genetic variat

49 n homologue of the ether-a-go-go gene of the fruitfly Drosophila melanogaster, encodes a protein that

50 In the fruitfly Drosophila melanogaster, for example, the midli

51 In the fruitfly Drosophila melanogaster, the four male specific

52 of the circadian pacemaker machinery of the fruitfly Drosophila melanogaster.

53 ribe the first example of RNA editing in the fruitfly Drosophila melanogaster.

54 ingle-gene mutant studies of behavior in the fruitfly Drosophila melanogaster.

55 mplest olfactory system studied--that of the fruitfly Drosophila melanogaster.

56 s pombe and only about 25% fewer than in the fruitfly Drosophila melanogaster.

57 the nucleoporin 160kDa (Nup160) gene of the fruitfly Drosophila simulans is incompatible with one or

58 proper relay of olfactory information in the fruitfly Drosophila, axons of approximately 50 classes o

59 In the fruitfly Drosophila, circadian oscillations in per expre

60 In the fruitfly Drosophila, studies on identifiable neurons can

61 Arabidopsis with those among species of the fruitfly Drosophila, we find evidence for predominantly

62 tly in the melanogaster species group of the fruitfly Drosophila.

63 n species including zebrafish (Danio rerio), fruitflies (Drosophila melanogaster) and roundworms (Cae

64 rhabditis elegans), zebrafish (Danio rerio), fruitfly (Drosophila melanogaster) and mouse (Mus muscul

65 essed during the human (Homo sapiens) and/or fruitfly (Drosophila melanogaster) immune responses.

66 Fruitfly (Drosophila melanogaster) males exposed to riva

67 his circuit originally developed to describe fruitfly (Drosophila melanogaster) olfactory association

68 ae), nematode worm (Caenorhabditis elegans), fruitfly (Drosophila melanogaster), and human (Homo sapi

69 ngle X-ray diffraction patterns from relaxed fruitfly (Drosophila) flight muscle recorded on the BioC

70 In the fruitfly, Drosophila melanogaster, differences between t

71 The fruitfly, Drosophila melanogaster, exhibits many of the

72 The fruitfly, Drosophila melanogaster, has become a critical

73 The fruitfly, Drosophila melanogaster, has been of central i

74 pulation of olfactory sensory neurons in the fruitfly, Drosophila melanogaster, that are highly selec

75 y exploiting the genetic tractability of the fruitfly, Drosophila melanogaster, which exhibits the ha

76 netic analysis of learning and memory in the fruitfly, Drosophila melanogaster.

77 ows was applied to developing embryos of the fruitfly, Drosophila melanogaster.

78 e antennae of the more genetically tractable fruitfly, Drosophila melanogaster.

79 ome annotation of DNase I footprints for the fruitfly, Drosophila melanogaster.

80 ages has been examined in three insects: the fruitfly, Drosophila melanogaster; the milkweed bug, Onc

81 A new study shows that female fruitflies eat more after mating, and that a multi-funct

82 Drosophila embryo, is stably anchored in the fruitfly eggshell; an as yet unidentified factor is requ

83 atory modules involved in development of the fruitfly embryo, to elicit known and novel motifs.

84 ith a key role in anterior patterning of the fruitfly embryo.

85 ively characterize the regulatory network of fruitfly embryonic development and show that the accurac

86 In animals such as the fruitfly, even minor deviations in environmental tempera

87 uplication of intron-containing genes in the fruitfly genome.

88 Even the simple fruitfly has around 50 classes of olfactory receptor neu

89 n of these genes in the morphogenesis of the fruitfly head suggests that the regulation of head forma

90 nvertebrates, including yeast, nematodes and fruitflies; however, whether inhibition of mTOR signalli

91 between two host-specific animals (tephritid fruitflies) is clearly associated with the shift to a ne

92 ed as regulators of development in worms and fruitflies, microRNAs are emerging as pivotal modulators

93 Recent technological innovations in the fruitfly model system have allowed observations which su

94 e alteration approaches, particularly in the fruitfly model system, Drosophila melanogaster, should p

95 biology approach that employs a Drosophila (fruitfly) model of AD in which the flies overexpress the

96 ion has been shown to drive tumorigenesis in fruitfly models, definitive evidence for functional coop

97 e, mouse, pufferfish, zebrafish, sea squirt, fruitfly, mosquito, and nematode) to do this and general

98 Fruitflies, mosquitoes and butterflies possess shared an

99 cinal, to precisely map the ends of numerous fruitfly, mouse and human ncRNAs.

100 ukaryotic species (yeast, rice, arabidopsis, fruitfly, mouse, and human) through the analysis of more

101 However, fruitflies need to overcome this avoidance response in s

102 his report, we identify and characterize the fruitfly ortholog of the DEAD box protein, Gemin3.

103 Pigmentation in fruitflies presents an attractive opportunity to explore

104 gulation between the brains of silkmoths and fruitflies provide insights into the mechanisms of clock

105 develop a system to automatically annotate a fruitfly's embryonic tissue in which a gene has expressi

106 le in determining the sexual identity of the fruitfly's nervous system, but new results show that dou

107 Fruitflies show robust attraction to food odours, which

108 hosphor degron embedded within the human and fruitfly SMN YG-box oligomerization domains.

109 anization of Hox and Hox-derived genes in 13 fruitfly species and the mosquito Anopheles gambiae.

110 We have studied the evolution of Gpdh in 18 fruitfly species by sequencing 1,077 nucleotides per spe

111 epistatic inviability in hybrids between two fruitfly species, Drosophila melanogaster and D. simulan

112 n of the gene Dopa decarboxylase (Ddc) in 24 fruitfly species.

113 t in the Drosophila brain, and Tet-deficient fruitflies suffer impaired brain development, accompanie

114 We analyse the whole genome of true fruitflies (Tephritidae), flesh flies (Sarcophagidae) an

115 appear to be highly conserved from worms and fruitflies to mice and humans.

116 Y279C and T468M), we generated LS transgenic fruitflies using corkscrew (csw), the Drosophila ortholo

117 g how individual Acps regulate egg-laying in fruitflies will help provide a full molecular picture of

118 ated PTPN11 alleles, we generated transgenic fruitflies with GAL4-inducible expression of wild-type o

119 assays and verified this regulatory loop in fruitfly, zebrafish, and humans.