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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 imulated data as well as real data sets from fruitfly and human.
16 gton's-disease-relevant phenotypes in yeast, fruitfly and mouse models, as well as in a mouse model o
17  of three principal organisms--the nematode, fruitfly and mouse--indicate that cell suicide is implem
18 atically studied 5'-isomiRs in human, mouse, fruitfly and worm by analysing a large collection of sma
19 thologs from human, mouse, wallaby, chicken, fruitfly, and nematode, underscoring the age and conserv
20 including human, mouse, rat, pig, zebrafish, fruitfly, and nematode.
21 mouse, rat, cow, chicken, lizard, zebrafish, fruitfly, Arabidopsis and rice.
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  observed changes in intrinsic firing in the fruitfly dorsal fan-shaped body neuron in a model with R
33 ion and analysis of 3D images for roundworm, fruitfly, dragonfly, mouse, rat and human.
34                          Many species of the fruitfly Drosophila are either sexually dimorphic for ab
35                        Paradoxically, in the fruitfly Drosophila bifurca sperm competition is rife bu
36           Recent studies have shown that the fruitfly Drosophila exhibits behavioral sensitization in
37 udies in the worm Caenorhabditis elegans and fruitfly Drosophila have revealed the essential role int
38  of the two approaches to populations of the fruitfly Drosophila in order to estimate some important
39                     In dipterans such as the fruitfly Drosophila melanogaster (D. mel.) and the mosqu
40      The genetic techniques available in the fruitfly Drosophila melanogaster allow analysis of the b
41 oderm in two highly divergent dipterans, the fruitfly Drosophila melanogaster and the mosquito Anophe
42                                          The fruitfly Drosophila melanogaster exhibits a robust and i
43                                          The fruitfly Drosophila melanogaster has been extensively us
44 ily is large and functionally redundant, the fruitfly Drosophila melanogaster has only two MMPs, both
45                     The mushroom body in the fruitfly Drosophila melanogaster is an associative brain
46                                          The fruitfly Drosophila melanogaster provides a rapid, ethic
47 evel of the sole K+/Cl- cotransporter in the fruitfly Drosophila melanogaster render flies susceptibl
48                                          The fruitfly Drosophila melanogaster senses day-night cycles
49                                 Although the fruitfly Drosophila melanogaster tastes sugars, salts an
50 we show that during gonad development in the fruitfly Drosophila melanogaster the proliferation of pr
51 tion of many regulatory proteins and, in the fruitfly Drosophila melanogaster, buffers genetic variat
52 n homologue of the ether-a-go-go gene of the fruitfly Drosophila melanogaster, encodes a protein that
53                                       In the fruitfly Drosophila melanogaster, for example, the midli
54                                       In the fruitfly Drosophila melanogaster, the four male specific
55  of the circadian pacemaker machinery of the fruitfly Drosophila melanogaster.
56 ribe the first example of RNA editing in the fruitfly Drosophila melanogaster.
57 ingle-gene mutant studies of behavior in the fruitfly Drosophila melanogaster.
58 mplest olfactory system studied--that of the fruitfly Drosophila melanogaster.
59 s pombe and only about 25% fewer than in the fruitfly Drosophila melanogaster.
60  the nucleoporin 160kDa (Nup160) gene of the fruitfly Drosophila simulans is incompatible with one or
61               Here, we present data from the fruitfly Drosophila simulans that address these question
62                                       In the fruitfly Drosophila, about two dozen sleep-inducing neur
63 proper relay of olfactory information in the fruitfly Drosophila, axons of approximately 50 classes o
64                                       In the fruitfly Drosophila, circadian oscillations in per expre
65                                       In the fruitfly Drosophila, studies on identifiable neurons can
66  Arabidopsis with those among species of the fruitfly Drosophila, we find evidence for predominantly
67 tly in the melanogaster species group of the fruitfly Drosophila.
68 n species including zebrafish (Danio rerio), fruitflies (Drosophila melanogaster) and roundworms (Cae
69 se of non-mammalian model organisms - mainly fruitflies (Drosophila melanogaster), nematode worms (Ca
70 rhabditis elegans), zebrafish (Danio rerio), fruitfly (Drosophila melanogaster) and mouse (Mus muscul
71 essed during the human (Homo sapiens) and/or fruitfly (Drosophila melanogaster) immune responses.
72                                              Fruitfly (Drosophila melanogaster) males exposed to riva
73 his circuit originally developed to describe fruitfly (Drosophila melanogaster) olfactory association
74 ae), nematode worm (Caenorhabditis elegans), fruitfly (Drosophila melanogaster), and human (Homo sapi
75 ngle X-ray diffraction patterns from relaxed fruitfly (Drosophila) flight muscle recorded on the BioC
76                                       In the fruitfly, Drosophila melanogaster, differences between t
77                                          The fruitfly, Drosophila melanogaster, exhibits many of the
78                                          The fruitfly, Drosophila melanogaster, has become a critical
79                                          The fruitfly, Drosophila melanogaster, has been of central i
80 pulation of olfactory sensory neurons in the fruitfly, Drosophila melanogaster, that are highly selec
81 y exploiting the genetic tractability of the fruitfly, Drosophila melanogaster, which exhibits the ha
82 netic analysis of learning and memory in the fruitfly, Drosophila melanogaster.
83 ows was applied to developing embryos of the fruitfly, Drosophila melanogaster.
84 e antennae of the more genetically tractable fruitfly, Drosophila melanogaster.
85 ome annotation of DNase I footprints for the fruitfly, Drosophila melanogaster.
86 ages has been examined in three insects: the fruitfly, Drosophila melanogaster; the milkweed bug, Onc
87                A new study shows that female fruitflies eat more after mating, and that a multi-funct
88 Drosophila embryo, is stably anchored in the fruitfly eggshell; an as yet unidentified factor is requ
89 atory modules involved in development of the fruitfly embryo, to elicit known and novel motifs.
90 ith a key role in anterior patterning of the fruitfly embryo.
91 ively characterize the regulatory network of fruitfly embryonic development and show that the accurac
92                       In animals such as the fruitfly, even minor deviations in environmental tempera
93 uplication of intron-containing genes in the fruitfly genome.
94                              Even the simple fruitfly has around 50 classes of olfactory receptor neu
95 n of these genes in the morphogenesis of the fruitfly head suggests that the regulation of head forma
96 nvertebrates, including yeast, nematodes and fruitflies; however, whether inhibition of mTOR signalli
97 between two host-specific animals (tephritid fruitflies) is clearly associated with the shift to a ne
98 esses across different organisms: nematodes, fruitflies, mice, rats and humans.
99 ed as regulators of development in worms and fruitflies, microRNAs are emerging as pivotal modulators
100      Recent technological innovations in the fruitfly model system have allowed observations which su
101 e alteration approaches, particularly in the fruitfly model system, Drosophila melanogaster, should p
102  biology approach that employs a Drosophila (fruitfly) model of AD in which the flies overexpress the
103 ion has been shown to drive tumorigenesis in fruitfly models, definitive evidence for functional coop
104 e, mouse, pufferfish, zebrafish, sea squirt, fruitfly, mosquito, and nematode) to do this and general
105                                              Fruitflies, mosquitoes and butterflies possess shared an
106 cinal, to precisely map the ends of numerous fruitfly, mouse and human ncRNAs.
107 ukaryotic species (yeast, rice, arabidopsis, fruitfly, mouse, and human) through the analysis of more
108                                     However, fruitflies need to overcome this avoidance response in s
109 his report, we identify and characterize the fruitfly ortholog of the DEAD box protein, Gemin3.
110                              Pigmentation in fruitflies presents an attractive opportunity to explore
111 gulation between the brains of silkmoths and fruitflies provide insights into the mechanisms of clock
112 develop a system to automatically annotate a fruitfly's embryonic tissue in which a gene has expressi
113 le in determining the sexual identity of the fruitfly's nervous system, but new results show that dou
114                                              Fruitflies show robust attraction to food odours, which
115 hosphor degron embedded within the human and fruitfly SMN YG-box oligomerization domains.
116 anization of Hox and Hox-derived genes in 13 fruitfly species and the mosquito Anopheles gambiae.
117  We have studied the evolution of Gpdh in 18 fruitfly species by sequencing 1,077 nucleotides per spe
118 epistatic inviability in hybrids between two fruitfly species, Drosophila melanogaster and D. simulan
119 n of the gene Dopa decarboxylase (Ddc) in 24 fruitfly species.
120 t in the Drosophila brain, and Tet-deficient fruitflies suffer impaired brain development, accompanie
121          We analyse the whole genome of true fruitflies (Tephritidae), flesh flies (Sarcophagidae) an
122 appear to be highly conserved from worms and fruitflies to mice and humans.
123                                 We note that fruitflies use essentially the same strategy.
124 Y279C and T468M), we generated LS transgenic fruitflies using corkscrew (csw), the Drosophila ortholo
125 g how individual Acps regulate egg-laying in fruitflies will help provide a full molecular picture of
126 ated PTPN11 alleles, we generated transgenic fruitflies with GAL4-inducible expression of wild-type o
127  assays and verified this regulatory loop in fruitfly, zebrafish, and humans.

 
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