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1 ogue of the Drosophila planar cell or tissue polarity gene.
2  identified rasp, a novel Drosophila segment polarity gene.
3 nt action of the gap, pair-rule, and segment polarity genes.
4 e eye, likewise dependent on the planar cell polarity genes.
5 nes into the segmental expression of segment polarity genes.
6 n and growth of lateral organ primordia, and polarity genes.
7  has not been defined for any of the segment-polarity genes.
8 maternal effect, gap, pair-rule, and segment polarity genes.
9 ith pod-1, defines a new class of C. elegans polarity genes.
10             Mutation of different apicobasal polarity genes activates c-Jun N-terminal kinase (JNK) s
11 l: a cell fate programme mediated by segment polarity genes and a boundary/epithelial integrity progr
12 ty are largely independent of other stomatal polarity genes and of the brassinosteroid signaling comp
13 These findings provide insight into how cell polarity genes and receptor tyrosine kinase signaling in
14 s may not control segmentation, some segment polarity genes and their interactions are conserved.
15 s are homologs of the Drosophila dsh segment polarity gene, and are involved in the Wnt/wingless sign
16 suggest it requires cytoplasmic dynein, cell polarity genes, and microtubule-associated proteins that
17 anogaster cells with mutations in epithelial polarity genes, and wild-type cells exposed to 'super-co
18 on is directed by the activity of the planar polarity genes, and, in particular, higher activity of t
19                                          Key polarity genes aPKC, par6, vang, pk, and fmi are upregul
20                      The crumbs (crb) apical polarity genes are essential for the development and fun
21                                These segment polarity genes are expressed in some, but not all of the
22  trunk of the Drosophila embryo, the segment polarity genes are initially activated by the pair-rule
23              To understand how these segment polarity genes are regulated, we examined the results of
24         These findings show that planar cell polarity genes are required for responses to cell death.
25 ression of the gap, segmentation and segment polarity genes, as well as changes in early morphologica
26 ressor function, consistent with the loss of polarity genes associated with hyperproliferation in Dro
27 e for 1000 generations without the important polarity gene BEM1.
28                   Inactivation of these cell polarity genes cannot drive metastatic behavior alone or
29 ter simulations, that the Drosophila segment polarity genes constitute such a module, and that this m
30                              Mutation of the polarity gene Crumbs homolog 1 (CRB1) is responsible for
31                       The Drosophila segment polarity gene cubitus interruptus (ci) encodes a zinc fi
32                                  The segment polarity gene cubitus interruptus (ci) maps to the most
33  signaling is thought to involve the segment polarity gene cubitus interruptus (ci).
34 , the human homologue of the Drosophila cell polarity gene dachsous (ds), that segregates with MVP in
35  reoriented mitosis required the planar cell polarity genes dachsous, fat, and atrophin.
36 ene is an ortholog of the Drosophila segment polarity gene Dishevelled, a member of the highly conser
37 ree mouse homologs of the Drosophila segment polarity gene Dishevelled, were created by gene targetin
38 have recently characterized a second segment polarity gene, dTCF or pan, 12 kb upstream of ci, in a h
39 key to the coordinated regulation of segment-polarity genes during embryogenesis.
40  of rin are similar to those of RhoA and the polarity genes, e.g. fz and dsh.
41 la, members of the frizzled family of tissue-polarity genes encode proteins that are likely to functi
42 at naked cuticle (nkd), a Drosophila segment-polarity gene, encodes an inducible antagonist for the W
43        The expression domains of the segment polarity gene engrailed (en) allow one to subdivide the
44 rizing the expression pattern of the segment polarity gene engrailed (en) in a basal annelid, the pol
45                                  The segment-polarity gene Engrailed and the homeotic genes Ultrabith
46 and En-2, homologs of the Drosophila segment polarity gene engrailed, in regulating the development o
47 One example is the expression of the segment polarity gene engrailed, which at embryonic and early po
48 embles the expression stripes of the segment-polarity gene engrailed, which has a key role in establi
49 e in repressing transcription of the segment-polarity gene engrailed.
50 ntrol the periodic expression of the segment polarity genes engrailed (en) and wingless (wg) via regu
51 ects of otd on the expression of the segment polarity genes engrailed (en) and wingless (wg).
52 sion of orthologues of the arthropod segment polarity genes engrailed (en), hedgehog (hh), and wingle
53 s fail to maintain expression of the segment polarity genes engrailed (en), wingless (wg), and hedgeh
54               We report that primary segment polarity genes (engrailed, hedgehog and wingless) are no
55                 To determine whether segment polarity gene expression is established differently outs
56              These results show that segment polarity gene expression is necessary for the survival o
57 pe-specific defects in pair-rule and segment polarity gene expression.fish mutant embryos also exhibi
58 oskeleton, but in addition they control cell polarity, gene expression, microtubule dynamics and vesi
59 Fmi2, homologs of the Drosophila planar cell polarity gene, flamingo; hFat2, a homolog of the Drosoph
60 y phenotype by mutations in two other tissue polarity genes, flamingo and prickle.
61 tion, highlighting the importance of "planar polarity" genes for defining the shape of a neuron in al
62  mammalian homologs of the Drosophila tissue polarity gene frizzled.
63                                We study four polarity genes, frizzled (fz), prickle (pk), Van gogh/st
64                  Previous studies of segment polarity gene function largely focused on neuroblasts th
65 mbryos, a hierarchy of gap/pair-rule/segment polarity gene function may be a shared and ancestral fea
66                                   The tissue polarity gene fuzzy (fy) has two roles in the developmen
67 ds to the promoter region of the planar cell polarity gene Fuzzy to regulate its transcription.
68    We also provide evidence that the segment-polarity gene, gooseberry (gsb), controls expression of
69 he Drosophila wing, a "core" group of planar polarity genes has been identified which acts downstream
70                                      Segment polarity genes have a dual function in early neurogenesi
71 picardial lineage only and finally, the cell polarity genes heart and soul and nagie oko are required
72 rtebrate homologue of the Drosophila segment-polarity gene hedgehog, has been reported to play an imp
73 n of secreted signals encoded by the segment polarity genes hedgehog (hh) and wingless (wg) and are i
74                     We show that the segment polarity genes hedgehog and wingless specify the identit
75 factors); Wnt 7a and Shh (Drosophila segment polarity gene homologs); Msx-1 and Msx-2 (Msx class home
76                                  The segment polarity gene homologues have a conserved role in the sp
77           Here, we describe a new C. elegans polarity gene identified during screens for conditional
78 Lethal giant larvae (Lgl) is an apical-basal polarity gene identified in Drosophila, where it functio
79 asolateral, recycling, implicating this cell polarity gene in assembly or maintenance of the apical e
80 n vivo invasion model via knocking down cell polarity gene in Drosophila wing discs, and identify Rho
81 ed recently to represent Stardust, a crucial polarity gene in Drosophila.
82 rosophila melanogaster pair rule and segment polarity genes in a range of arthropods.
83 ry pair-rule genes directly regulate segment polarity genes in Drosophila, we analyzed Tc-prd and Tc-
84 ferentiation by transcriptionally repressing polarity genes in neuronal progenitors.
85 -2 genes appear to act downstream of the par polarity genes in the one- and two-cell stages and downs
86 mal pattern in each segment, several segment polarity genes, including gooseberry (gsb), specify cell
87 al apicobasal polarity is controlled by many polarity genes, including the crb genes.
88 chy of maternal, gap, pair-rule, and segment polarity gene interactions regulates virtually simultane
89 segment exhibits a unique network of segment polarity gene interactions.
90         Expression of the Drosophila segment polarity genes is initiated by a pre-pattern of pair-rul
91                  Here we tested whether cell polarity genes, known to regulate embryonic neuroblast a
92 encing of Drosophila ovaries, where inducing polarity-gene l(2)gl-knockdown (Lgl-KD) causes invasive
93 boring T2D-associated variants regulate cell polarity genes LAMA1 and CRB2.
94  a mammalian ortholog of the Drosophila cell polarity gene lgl, exhibit MCCs resembling severe perive
95  is repressed in mice mutant for the segment polarity gene Mesp2 and expanded in Splotch mutants.
96                Here we show that the segment polarity gene midline is required for neuroblast formati
97                           Hence, the segment polarity genes midline and H15 play an important role in
98 n Drosophila, hedgehog is one of the segment-polarity genes, mutations of which disrupt the pattern a
99                       The Drosophila segment polarity gene naked cuticle (nkd) encodes an EF hand pro
100 la melanogaster, was identified as a segment polarity gene necessary for the transduction of wingless
101          We anticipate that co-option of the polarity gene network is a fundamental mechanism shaping
102 e show that co-option of the abaxial-adaxial polarity gene network plays a role in the evolution of s
103 ed to a Drosophila melanogaster segmentation polarity gene network to identify regulatory function pe
104 insights into the functioning of the segment polarity gene network, such as the crucial role of the w
105 that, in sporadic CRCs of both species, cell polarity genes not only contribute in preventing cancer
106               Here we describe a new segment polarity gene of Drosophila melanogaster, oroshigane (or
107 netic evidence showing that lines, a segment polarity gene of Drosophila, is required for the functio
108 stripes of expression of several key segment-polarity genes, one stripe for each parasegment, in the
109 d-type worms in histology, expression of key polarity genes, or neoblast distribution.
110 ules, as well as decreased expression of the polarity gene Par3 (pard3).
111 ecently discovered that the loss of the cell polarity gene PARD6B selectively diminishes apical endos
112  the human homolog of the drosophila segment polarity gene patched (ptc).
113 n homologue (PTCH) of the Drosophila segment polarity gene patched have been identified in NBCCS pati
114 ammalian homologue of the Drosophila segment polarity gene patched, is a receptor for hedgehog (HH) a
115 tein kinase A and the product of the segment polarity gene patched.
116 by its genetic interactions with the segment polarity genes patched (ptc) and fused (fu).
117 mmalian homologues of the Drosophila segment polarity gene, patched (ptc) and its ligand, sonic hedge
118 he human homologue of the Drosophila segment polarity gene, patched (PTCH), the adenomatous polyposis
119  the hereditary basal cell carcinoma/segment polarity gene, patched.
120 th strong homology to the Drosophila segment polarity gene, patched.
121                 Here we show that the tissue polarity gene prickle (pk) encodes a protein with a trip
122 dy shows that, in ascidians, the planar cell polarity gene prickle regulates sequential establishment
123 ns closely related to the Drosophila segment polarity gene product armadillo.
124 he transcription factor TBX5 and planar cell polarity gene PTK7, respectively, the encoded proteins o
125 lanar polarity and for the novel planar cell polarity gene, Ptk7, as essential regulators of mediolat
126 ir-rule transcription factor Runt in segment-polarity gene regulation.
127              Drosophila patched is a segment polarity gene required for the correct patterning of lar
128 b(ponli) (ponli) and crumbs2b (crb2b) apical polarity genes' restrictive transcription in the red, gr
129 ns in the Arabidopsis KANADI (KAN) and YABBY polarity genes result in amorphous or arrested integumen
130     We show that MDCK cells silenced for the polarity gene scribble (scrib(KD)) are hypersensitive to
131                       Loss of the epithelial polarity gene scribble in clones of Drosophila imaginal
132  two of these: a mutation in the planar cell polarity gene scribbled homolog (Drosophila) (Scrib) and
133                Here we show that the segment-polarity gene smoothened is required for the response of
134                            We found that the polarity genes SPA2, PEA2, BUD6, and BNI1 participate in
135 sophila Crumbs also interacts with two other polarity genes, Stardust and Discs Lost.
136 enopus homolog of the Drosophila planar cell polarity gene strabismus (stbm) participates in the regu
137     While the expression patterns of segment polarity genes such as engrailed have been shown to be s
138  and segments, via the regulation of segment polarity genes such as gooseberry, which in turn regulat
139 itional information to pair-rule and segment-polarity genes, the latter forming a segmental pre-patte
140 ods to the regulatory network of the segment polarity genes, thus gaining novel insights into the dev
141 d interacts genetically with all of the core polarity genes to influence the specification of the R3
142            Mutations in the core planar cell polarity gene Van Gogh-like 2 (Vangl2) result in hair ce
143 ined with a mutant allele of the planar cell polarity gene Vangl2 (Vangl2(Lp)), Fz1 and/or Fz2 mutati
144  matrix, epithelial cilia or the planar cell polarity genes Vangl2 and Ptk7 In wild-type mice, collag
145 o in vivo screen on a subcohort of candidate polarity genes, which revealed 6 novel positive regulato
146                We have expressed the segment polarity gene wingless (wg) ectopically in imaginal disc
147                       The Drosophila segment polarity gene wingless (wg) is essential for cell fate d
148 the Runt-dependent regulation of the segment-polarity genes wingless (wg) and engrailed (en).
149       The expression patterns of the segment polarity genes wingless and engrailed are conserved duri
150 ed for the correct expression of the segment polarity genes wingless, engrailed and gooseberry.
151 the anterior-posterior axis, several segment polarity genes (wingless, engrailed, hedgehog, and patch
152 gene products subsequently 'imprint' segment polarity genes with reiterated patterns, thus defining t

 
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