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1 pointing lateral lobes, indicating body and segment polarity.
2 and nerves is perturbed, indicating loss of segment polarity.
3 opus development and establishing Drosophila segment polarity.
4 s (fss), because its paraxial mesoderm lacks segment polarity.
5 ream of Hh signaling in the establishment of segment polarity.
6 The mutants also display evidence of segment polarity.
7 that oro functions in determining embryonic segment polarity.
8 ecursor has a distinct identity conferred by segment polarity and dorso-ventral patterning genes that
12 ophila Chibby by RNA interference results in segment polarity defects that mimick a wingless gain-of-
14 recently published Boolean network model of segment polarity development in Drosophila melanogaster.
19 (Dvl2) gene is an ortholog of the Drosophila segment polarity gene Dishevelled, a member of the highl
20 ne of three mouse homologs of the Drosophila segment polarity gene Dishevelled, were created by gene
22 characterizing the expression pattern of the segment polarity gene engrailed (en) in a basal annelid,
23 es En-1 and En-2, homologs of the Drosophila segment polarity gene engrailed, in regulating the devel
27 and stripe-specific defects in pair-rule and segment polarity gene expression.fish mutant embryos als
29 en the embryos, a hierarchy of gap/pair-rule/segment polarity gene function may be a shared and ances
30 growth factors); Wnt 7a and Shh (Drosophila segment polarity gene homologs); Msx-1 and Msx-2 (Msx cl
32 a hierarchy of maternal, gap, pair-rule, and segment polarity gene interactions regulates virtually s
34 n somite is repressed in mice mutant for the segment polarity gene Mesp2 and expanded in Splotch muta
37 Drosophila melanogaster, was identified as a segment polarity gene necessary for the transduction of
38 portant insights into the functioning of the segment polarity gene network, such as the crucial role
40 esent genetic evidence showing that lines, a segment polarity gene of Drosophila, is required for the
42 the human homologue (PTCH) of the Drosophila segment polarity gene patched have been identified in NB
43 of the mammalian homologue of the Drosophila segment polarity gene patched, is a receptor for hedgeho
49 Dvl genes are homologs of the Drosophila dsh segment polarity gene, and are involved in the Wnt/wingl
50 others have recently characterized a second segment polarity gene, dTCF or pan, 12 kb upstream of ci
51 lving mammalian homologues of the Drosophila segment polarity gene, patched (ptc) and its ligand, son
52 luding the human homologue of the Drosophila segment polarity gene, patched (PTCH), the adenomatous p
57 tern resembles the expression stripes of the segment-polarity gene engrailed, which has a key role in
59 h), a vertebrate homologue of the Drosophila segment-polarity gene hedgehog, has been reported to pla
62 show that naked cuticle (nkd), a Drosophila segment-polarity gene, encodes an inducible antagonist f
65 Along the anterior-posterior axis, several segment polarity genes (wingless, engrailed, hedgehog, a
66 parallel: a cell fate programme mediated by segment polarity genes and a boundary/epithelial integri
67 omologues may not control segmentation, some segment polarity genes and their interactions are conser
69 In the trunk of the Drosophila embryo, the segment polarity genes are initially activated by the pa
71 ng computer simulations, that the Drosophila segment polarity genes constitute such a module, and tha
72 ectly control the periodic expression of the segment polarity genes engrailed (en) and wingless (wg)
73 tory effects of otd on the expression of the segment polarity genes engrailed (en) and wingless (wg).
74 l expression of orthologues of the arthropod segment polarity genes engrailed (en), hedgehog (hh), an
75 e mutants fail to maintain expression of the segment polarity genes engrailed (en), wingless (wg), an
77 roduction of secreted signals encoded by the segment polarity genes hedgehog (hh) and wingless (wg) a
80 secondary pair-rule genes directly regulate segment polarity genes in Drosophila, we analyzed Tc-prd
83 rovided by its genetic interactions with the segment polarity genes patched (ptc) and fused (fu).
85 segments and segments, via the regulation of segment polarity genes such as gooseberry, which in turn
87 s required for the correct expression of the segment polarity genes wingless, engrailed and gooseberr
88 ir-rule gene products subsequently 'imprint' segment polarity genes with reiterated patterns, thus de
89 the expression of the gap, segmentation and segment polarity genes, as well as changes in early morp
90 e epidermal pattern in each segment, several segment polarity genes, including gooseberry (gsb), spec
91 our methods to the regulatory network of the segment polarity genes, thus gaining novel insights into
96 dulates the Runt-dependent regulation of the segment-polarity genes wingless (wg) and engrailed (en).
98 lishing stripes of expression of several key segment-polarity genes, one stripe for each parasegment,
99 nvey positional information to pair-rule and segment-polarity genes, the latter forming a segmental p
102 presentatives of coordinate, gap, pair-rule, segment polarity, homeotic, and Polycomb group functions
103 the leech primary blast cell clones acquire segment polarity - i.e. a fixed sequence of positional v
104 results demonstrate the molecular basis for segment polarity in a non-bilaterian animal, suggesting
106 s study by showing that the establishment of segment polarity in the leech ectoderm is largely indepe
107 gs gave rise to a model for the formation of segment polarity in the zebrafish in which caudal is the
111 at these genes function at the pair-rule and segment polarity levels to establish the spacing and pol
112 even pair-rule stripes, but later exhibits a segment polarity-like pattern for which no phenotypic co
113 ular mechanisms underlying somite formation, segment polarity, maintenance of segment borders, and th
115 We showed previously that a model of the segment polarity network in Drosophila is robust to para
116 three models of biochemical regulation: the segment polarity network in Drosophila melanogaster, the
119 omparable to the highly conserved ectodermal segment polarity pattern observed in arthropods at any l
121 expression, and how this is converted into a segment-polarity pattern by 'timing factor' wavefronts a
122 encing of dally-like, but not dally, gives a segment polarity phenotype identical to that of null mut
124 es of this gene, mutant embryos develop with segment polarity phenotypes reminiscent to loss of eithe
125 y late morphogenetic role for this and other segment polarity proteins, mainly oriented at lobule jun
126 led expression play an important role in the segment polarity specification of the Drosophila embryo,
127 owever, while we observe nmr1 transcripts in segment polarity stripes and specific neural precursors
128 otein are expressed in identical patterns of segment polarity stripes, defined sets of neuroblasts, m
129 omplications for dissecting the pair-rule to segment-polarity transition are the regulatory interacti