コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 he Ubx gene is repressed (first thoracic leg imaginal disc).
2 ferentially expressed in the Drosophila wing imaginal disc.
3 nit (RnrL) reduce compensatory growth in the imaginal disc.
4 elopment of the Drosophila melanogaster wing imaginal disc.
5 C1 double null clones in the Drosophila wing imaginal disc.
6 ly enhance robustness in the Drosophila wing imaginal disc.
7 lium is essential for patterning of the wing imaginal disc.
8 Branchless FGF-expressing cells in the wing imaginal disc.
9 itted progenitor cells of the Drosophila eye imaginal disc.
10 ence that the DVM FCs may arise from the leg imaginal disc.
11 s enriched in the dorsal portion of the wing imaginal disc.
12 crete subpopulation of cells within the wing imaginal disc.
13 ling the formation of SOPs in the adult wing imaginal disc.
14 e embryonic head and developing eye-antennal imaginal disc.
15 expression of brm(K804R) in the eye-antennal imaginal disc.
16 proliferative program and growth of the eye imaginal disc.
17 dorsoventral boundary in the Drosophila wing imaginal disc.
18 al timer coordinating development within the imaginal disc.
19 oximodistal (PD) axis of the Drosophila wing imaginal disc.
20 tic pathway elucidated in the Drosophila eye imaginal disc.
21 tations that impair regeneration in the wing imaginal disc.
22 rogenitor cells develop together in the wing imaginal disc.
23 ol of epithelial integrity in the Drosophila imaginal disc.
24 regulates folds within the third instar wing imaginal disc.
25 r/posterior compartment boundary of the wing imaginal disc.
26 the progression of S phase in Drosophila eye imaginal discs.
27 texts; for example, in the wing, leg and eye imaginal discs.
28 cell proliferation and promotes apoptosis in imaginal discs.
29 ession domain of homothorax (hth) in the leg imaginal discs.
30 leg regeneration in fragments of Drosophila imaginal discs.
31 -induced p53-independent apoptosis in larval imaginal discs.
32 nt Crumbs (Crb) affects growth in Drosophila imaginal discs.
33 ss of Crb similarly results in overgrowth of imaginal discs.
34 phila Schneider line 2 (S2) cells and larval imaginal discs.
35 dispensable in primary epithelia such as the imaginal discs.
36 direct targets of PcG-mediated repression in imaginal discs.
37 rior compartment boundary of Drosophila wing imaginal discs.
38 it was rescued by expression of nito in wing imaginal discs.
39 the Ultrabithorax (Ubx) gene in larval wing imaginal discs.
40 e mutants and disproportionate growth of the imaginal discs.
41 d/or Phol for binding to the bxd PRE in wing imaginal discs.
42 is deregulated in rbf mutant cells in larval imaginal discs.
43 eded to limit IR-induced apoptosis in larval imaginal discs.
44 arge cohort of miRNAs expressed primarily in imaginal discs.
45 the pathway by which Ras regulates growth in imaginal discs.
46 entially expressed genes in wing and haltere imaginal discs.
47 en signaling in Drosophila melanogaster wing imaginal discs.
48 on and hyperplastic overgrowth of Drosophila imaginal discs.
49 ila, and fat mutants have severely overgrown imaginal discs.
50 NA-mediated translational repression in wing imaginal discs.
51 gene expression, cell affinity and growth in imaginal discs.
52 uses abnormal epithelial cysts in Drosophila imaginal discs.
53 led2 leads to Wingless stabilization in wing imaginal discs.
54 se early larval lethality and the absence of imaginal discs.
55 capacity to regulate cell differentiation in imaginal discs.
56 daries and the compartment boundaries in the imaginal discs.
57 l septate junctions and causes overgrowth of imaginal discs.
58 h for mRNAs misregulated in pacman null wing imaginal discs.
59 n the epithelia of the foregut, hindgut, and imaginal discs.
60 ved in the cytoplasmic retention of Ci155 in imaginal discs.
61 r regions of the Drosophila Ubx gene in wing imaginal discs.
62 in G1/G0-arrested, uncommitted cells in eye imaginal discs.
63 n long-range Hh signaling in Drosophila wing imaginal discs.
64 postembryonic morphogenesis of leg and wing imaginal discs.
65 Wingless signaling in the eye, wing and leg imaginal discs.
66 for PHO in repressing transcription in wing imaginal discs.
67 he transcription activation by Trl in larval imaginal discs.
68 apoptosis in surface epithelia of Drosophila imaginal discs.
69 in, in contrast to epithelial tissues of the imaginal discs.
70 al size or the state of development of their imaginal discs.
71 hough more restricted, results in the larval imaginal discs.
72 (SAC) genes and preventing apoptosis in wing imaginal discs.
73 silencing, some PcG mutants also have small imaginal discs.
74 ibble (scrib) are eliminated from Drosophila imaginal discs.
75 in every segment boundary within the larval imaginal discs.
76 een reported to be a survival factor in wing imaginal discs.
77 t translational repression in developing eye imaginal discs; (2) in dendritic elaboration of larval s
78 ssues [5, 6] or transplantation of a damaged imaginal disc [7, 8] delays the onset of metamorphosis.
79 logous Drosophila genes that specify the eye imaginal disc, a finding that is consistent with the ide
80 la, null mutations in pacman result in small imaginal discs, a delay in onset of pupariation and leth
81 n ligase, cause dramatic loss of polarity in imaginal discs accompanied by tumorous proliferation def
82 both cases, the epidermal tissue of the wing imaginal disc acts as a niche expressing the ligands Ser
84 ligands, Gbb and Dpp, to patterning the wing imaginal disc along its A/P axis, change as a function o
86 To study this question the Drosophila wing imaginal disc, an epithelial primordial organ that later
87 onditionally ablate patches of tissue in the imaginal disc and assess the ability of the surviving si
88 other developing epithelia, such as the wing imaginal disc and the embryonic germband in Drosophila,
89 hogenetic furrow, that sweeps across the eye imaginal disc and transforms thousands of undifferentiat
90 h factor (FGF) proteins produced by the wing imaginal disc and transported by cytonemes to the air sa
92 1 and okra, show progressive degeneration of imaginal discs and die as pupae, while other genotypes s
94 ling pathway functions to suppress growth in imaginal discs and has been suggested to control organ s
95 rs, including the histone demethylase little imaginal discs and histone-interacting protein p55, that
96 derably reduces toxic mHtt aggregates in eye imaginal discs and partially restores rhabdomere morphol
98 le that is expressed in all cells of the eye imaginal discs and, unlike many other Egfr inhibitors, d
99 itates with Egfr from cultured cells and eye imaginal discs, and Egfr activity promotes tyrosine phos
100 teristic of Hh signaling loss in embryos and imaginal discs, and epistasis analysis places ihog actio
101 modulator of Hippo pathway activity in wing imaginal discs, and implicate Yorkie activation in compe
102 in has a graded distribution in eye and wing imaginal discs, and is largely localised to the Golgi in
103 ua (Cic) restricts cell growth in Drosophila imaginal discs, and its levels are, in turn, downregulat
104 posterior compartments in the embryo and in imaginal discs, and posterior to the morphogenetic furro
105 osophila tumor suppressor lethal(2) tumorous imaginal discs, and showed that hTid-1L promoted while h
107 Hippo pathway components in Drosophila wing imaginal discs are organized into distinct junctional co
108 ate that the developing adult organs, called imaginal discs, are a regulator of critical size in larv
111 However, the development of appendages from imaginal discs as in Drosophila is a derived state, whil
112 replication and proliferation in brains and imaginal discs, as well as for gene amplification in ova
113 t specifically reduced misfolded Rh-1 in the imaginal disc assay also delayed age-related retinal deg
114 regulates Dpp and Notch signaling in larval imaginal discs, at least partially via regulation of thi
115 d-type Rh-1 were overexpressed in developing imaginal discs beyond the ER protein folding capacity of
116 in damaged and regenerating Drosophila wing imaginal discs but that is dispensable for these fates i
117 sues where Ubx is active (third thoracic leg imaginal disc) but is not bound in tissues where the Ubx
118 d activate transcription in embryos and wing imaginal discs, but it is no longer processed into the r
120 ed a glycolytic tumor in the Drosophila wing imaginal disc by activating the oncogene PDGF/VEGF-recep
121 antiproliferative action of DNOS1 in the eye imaginal disc by impacting the retinoblastoma-dependent
122 We propose that p53 maintains plasticity of imaginal discs by co-regulating the maintenance of genom
123 patterns the embryonic epidermis and larval imaginal discs by regulating the transcription factor, C
125 , many cells in the posterior regions of eye imaginal discs carrying a double knockdown of Mcm10 and
127 larity gene scribble in clones of Drosophila imaginal disc cells can cooperate with Ras signaling to
135 We find that after IR, p53 is required for imaginal disc cells to repair DNA, and in its absence th
137 14 kb upstream of the bantam hairpin in eye imaginal disc cells, arguing that this regulation is dir
140 tion is dramatically increased in lgl larval imaginal discs compared to both wild type and brat mutan
141 ental checkpoint extends larval growth after imaginal disc damage by inhibiting the transcription of
143 sine-specific demethylase 1) and Lid (little imaginal discs), demethylate histone H3 at Lys 4 (H3K4),
147 Fas2 is expressed in dynamic patterns during imaginal disc development, and in the eye we have shown
148 l genes and genetic pathways involved in leg imaginal disc development, we employed a Genome Wide Ass
154 etic furrow sweeps anteriorly across the eye imaginal disc, driven by Hedgehog secretion from photore
155 f adult structures through expression in all imaginal discs, driven by enhancers from the 3' cis-regu
156 of founder cells that give rise to the wing-imaginal disc during normal development and following co
157 essive cell death restricted to the antennal imaginal disc during the middle third instar larval stag
160 (5) mutants of the Broad-Complex (BR-C), and imaginal disc elongation and eversion is abolished in br
164 -suppressor genes (nTSGs) in Drosophila wing imaginal disc epithelia that tumor initiation depends on
172 inal discs in mid-third instar larvae, since imaginal discs from larvae with reduced or no ecdysone s
173 tep in the development of these late-forming imaginal discs from the imaginal primordia appears to be
174 lesser extent, Ds suppress overgrowth of the imaginal discs from which appendages develop and regulat
176 t Drosophila melanogaster body develops from imaginal discs, groups of cells set-aside during embryog
177 chanism of growth control is not specific to imaginal disc growth and could be of general relevance.
178 d downstream of fat, both for its effects on imaginal disc growth and for the expression of Wingless
180 ess of EpiTools by analyzing Drosophila wing imaginal disc growth, revealing previously overlooked pr
184 Specification and development of Drosophila imaginal discs have been studied for many years as model
186 ila larvae by inducing apoptosis in the wing imaginal disc in a spatially and temporally regulated ma
187 KA-RII is uniformly overproduced in the wing imaginal disc in Cos1(A1) mutants, but only certain cell
188 ining olfactory sensory cells) from a common imaginal disc in Drosophila, we investigated whether the
189 onset of metamorphosis are regulated by the imaginal discs in Drosophila, and suggest that the termi
191 s of GFP-expressing salivary glands and wing imaginal discs in living Drosophila melanogaster pupae i
193 we show that ecdysone promotes the growth of imaginal discs in mid-third instar larvae, since imagina
194 uction is essential for proliferation of the imaginal discs, in part, by regulating JAK/STAT signalin
195 tion needed to transform a relatively simple imaginal disc into a more complex and three-dimensional
197 Following segregation of the Drosophila wing imaginal disc into dorsal (D) and ventral (V) compartmen
202 upation phenotype seen when a single pair of imaginal discs is homozygous for a neoplastic TSG mutati
203 t the initial ato transcription in different imaginal discs is regulated by distinct 3' cis-regulator
205 Car for late endosome-to-lysosome fusion in imaginal discs is specific as early endosomes are unaffe
206 show that damage to, or slow growth of, the imaginal discs is sufficient to retard metamorphosis bot
207 t the normal role of this exoribonuclease in imaginal discs is to suppress the expression of transcri
208 t expressed until differentiation in the eye imaginal disc it was more easily trans-inactivated than
209 sophila tumor suppressor lethal (2) tumorous imaginal discs (l(2)tid) gene, hTID1, encodes two protei
212 dentified the Trithorax group protein Little imaginal discs (Lid) as a regulator of dMyc-induced cell
215 topic expression of DIP1 in wing and haltere imaginal discs malforms the adult structures and enhance
218 input derived from the transplanted antennal imaginal disc, most antennal lobe projection neurons (29
221 ne expression analyses of the larval genital imaginal disc of D. mauritiana, D. sechellia, and two D.
223 hat IR-induced apoptosis still occurs in the imaginal discs of chk2 and p53 mutant larvae, albeit wit
229 compartment borders that subdivide the wing imaginal discs of Drosophila third instar larvae are eac
231 anscriptional profiling of dissected genital imaginal discs of each sex at three time points during e
232 la melanogaster, IR induces apoptosis in the imaginal discs of larvae, typically assayed at 4-6 hr af
233 he exception of the wing imaginal discs, the imaginal discs of Manduca sexta are not formed until ear
235 that Rig protein is present in the brain and imaginal discs of second and third instar larvae, where
237 ytoneme modulation was recapitulated in wing imaginal discs of transgenic Drosophila, providing evide
240 Drosophila, including controlling growth of imaginal discs, planar cell polarity (PCP) and the proxi
243 The study of regeneration in Drosophila imaginal discs provides an opportunity to use powerful g
244 gaster Live imaging of single DSBs in larval imaginal discs recapitulates the spatio-temporal dynamic
249 of aveugle mutant cells in the eye and wing imaginal discs resemble those caused by reduction of EGF
250 cumulation of cyclin B in the developing eye imaginal disc, resulting in additional mitotic cycles an
251 -epsilon or sgg/gsk3beta in Drosophila wing imaginal discs results in the accumulation of dMyc prote
254 etic circuits tumors depend on because their imaginal discs, simple epithelia present in the larva, c
255 Thor gene in E(z) mutants partially restores imaginal disc size toward wild-type and results in an in
257 nduction of apoptosis in the Drosophila wing imaginal disc stimulates activation of the Hippo pathway
258 nonoverlapping patterns in both embryos and imaginal discs, suggesting that transcription of these n
259 re types of filopodia in the Drosophila wing imaginal disc that are proposed to serve as conduits in
260 ecified during embryogenesis and, unlike the imaginal discs that make up the thoracic and head segmen
266 2 mutants show impaired development of their imaginal discs, the primordial tissues that form the adu
269 ous, induced strong overgrowth in Drosophila imaginal discs through modulating the activity of the Hi
270 brid screens to identify a protein, tumorous imaginal discs (Tid1), that binds to the cytoplasmic dom
273 at a subset of peripodial cells in different imaginal discs undergo a cuboidal-to-squamous cell shape
276 val is accompanied by compensatory growth of imaginal discs via increased nutritional uptake and cell
278 , ecdysone appears to regulate the growth of imaginal discs via Thor/4E-BP, a negative growth regulat
281 nder cells specified in the mesothoracic leg imaginal disc, we also demonstrate that the TGFbeta path
282 /N-deacetylase-sulphotransferase in the wing imaginal disc, we find that lack of Heparan Sulfate (HS)
283 m, the embryonic nervous system and the wing imaginal disc, we show that Flybow in conjunction with s
284 mitotic cell junction dynamics in Drosophila imaginal discs, we mathematically predict the convergenc
285 eceptor development begins in the larval eye imaginal disc, where eight distinct photoreceptor cells
286 esses gene expression in the Drosophila wing imaginal disc, where it is expressed in symmetrical late
287 stat92E is active ubiquitously in early wing imaginal discs, where it acts to inhibit the induction o
288 required for development of the wing and leg imaginal discs, whereas cleavage at the S1 site is suffi
289 eveloping and intact epithelium ( Drosophila imaginal discs), wherein cell-cell adhesion properties a
290 ferentially expressed in the Drosophila wing imaginal disc, which gives rise to two distinct adult st
292 Drosophila adult structures derive from imaginal discs, which are sacs with apposed epithelial s
293 sophila melanogaster are derived from larval imaginal discs, which originate as clusters of cells wit
294 or the observed uniformity of growth in wing imaginal discs, which persists in the presence of gradie
295 including upregulation of the same genes in imaginal discs, which suggests that Sbb cooperates with
296 sophila, the adult wing is derived from wing imaginal discs, which undergo a period of growth and pro
297 ation along the basal surface of larval wing imaginal discs, which was restored with wild type pgant3
WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。