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1 with the reestablishment of normal endosperm cellularization.
2 l force opens the ring channels and prevents cellularization.
3 g epithelial basement membranes and germline cellularization.
4  smaller yolk stalk diameters and more rapid cellularization.
5 ale pattern in the actin/myosin array during cellularization.
6 e dynamics of marked membrane regions during cellularization.
7 s required for its formation at the onset of cellularization.
8 bitor of membrane trafficking, also inhibits cellularization.
9  MMAP, Lava Lamp (Lva), is also required for cellularization.
10 junction gene Innexin 7, leads to failure of cellularization.
11   This patterning cascade takes place before cellularization.
12 ups in which many segments emerge only after cellularization.
13 required for the formation of furrows during cellularization.
14 cheme of polarized membrane insertion during cellularization.
15  development such as polar nuclei fusion and cellularization.
16 yncytial divisions and is not observed after cellularization.
17 fferentiated epithelial cells but not during cellularization.
18  during a critical syncytial stage, prior to cellularization.
19 rotein is localized at cell membranes during cellularization.
20 differently from those that are formed after cellularization.
21 rial that appears on the cell surface during cellularization.
22 , in which all segments are patterned before cellularization.
23 e remainder of the embryo is generated after cellularization.
24 d reduced seed size and exhibited precocious cellularization.
25 he initial polarity cue as cells form during cellularization.
26 alazal endosperm of wild-type seeds prior to cellularization.
27 min before mitotic cycle 14 to 15 min during cellularization.
28 fic translational regulator, is required for cellularization.
29 through a special form of cytokinesis termed cellularization.
30  whether the exocyst complex is required for cellularization.
31 d rates of cytoplasmic streaming and delayed cellularization.
32 n-dependent cytoplasmic streaming and oocyte cellularization.
33 ial for furrow stabilization at the onset of cellularization.
34 cle arrest did not advance or delay onset of cellularization.
35 phase and then declines abruptly just before cellularization.
36 sands of syncytial nuclei in preparation for cellularization.
37 d in plasma membrane in the process known as cellularization.
38 ization is enriched during the fast phase of cellularization.
39 izing newly deposited plasma membrane during cellularization.
40 ons in syncytial embryos, and the subsequent cellularization.
41 oordinate membrane invagination during early cellularization.
42 sure of the cells does not occur during late cellularization.
43 larized growth of the plasma membrane during cellularization.
44 ation when ectopically expressed during late cellularization.
45 bryo patterning, endosperm nuclear size, and cellularization, a phenotype that is variable between su
46 ns in the cytoskeleton during the process of cellularization, a specialized form of cytokinesis.
47         The DAH phosphorylation peaks during cellularization, a stage at which DAH function is critic
48        The absence of Bottleneck during late cellularization allows src64-dependent microfilament rin
49 nt yolk stalk diameters as well as depths of cellularization along the AP axis.
50        These mutations also strongly perturb cellularization, altering the timing and rate of furrow
51                                   Drosophila cellularization and animal cell cytokinesis rely on the
52  are remarkable for their ability to undergo cellularization and cell-cycle re-entry during regenerat
53 are equivalently partitioned among nuclei at cellularization and could play an important role in the
54         To identify new proteins involved in cellularization and cytokinesis, we have conducted a bio
55 a phase of free nuclear division followed by cellularization and differentiation of cell types.
56                        These embryos halt in cellularization and do not proceed to gastrulation.
57 arazu and huckebein, which are essential for cellularization and embryonic patterning.
58   The Drosophila MBT is marked by blastoderm cellularization and follows 13 cleavage-stage divisions.
59 ogenesis: formation of the metaphase furrow, cellularization and formation of the pole cells.
60 ll cycle delays, zygotic gene transcription, cellularization and gastrulation.
61                    Because the completion of cellularization and other aspects of early development s
62  Processes under microRNA regulation include cellularization and patterning in the blastoderm, morpho
63      nuf also disrupts the initial stages of cellularization and produces disruptions in cellularizat
64 s identified several known genes controlling cellularization and proliferation as well as novel genes
65       Upon in vivo delivery, bFGF induced re-cellularization and re-vascularization in endodontically
66 ink between cytoskeletal organization during cellularization and subsequent morphogenetic processes o
67      We show that ZA formation begins during cellularization and that the basolateral membrane domain
68 ts ability to provide a durable scaffold for cellularization and tissue remodeling.
69                           Embryo development cellularization and vitellin yolk protein degradation, p
70 aging agents induce a mnk-dependent block to cellularization and zygotic gene expression.
71 ed; seven have been previously implicated in cellularization and/or cytokinesis, including KLP3A, Ani
72 lishment of a functional cytoskeleton during cellularization, and exhibit a pair-rule segmentation ph
73 widely expressed with roles in segmentation, cellularization, and gastrulation during early embryogen
74 lays, DNA replication checkpoint activation, cellularization, and high-level zygotic expression of pr
75 lopmental induction during the slow phase of cellularization, and Slam protein localizes to the furro
76             However, cleavage furrows during cellularization are totally disorganized, and no embryos
77                                       Before cellularization, astral microtubules determine metaphase
78 m vulgare) grain development, from endosperm cellularization at 3 d after pollination (DAP) through d
79 ed how cyclin knockdown affects the onset of cellularization at the midblastula transition and found
80 ithelial polarity that is established during cellularization: at the onset of cellularization, the Dr
81 of spatially regulated autophagy during late cellularization, autophagy was not required for initiati
82                         As cells form during cellularization, basally localized Bazooka undergoes bas
83              The patches do not appear until cellularization begins, and the process fails entirely w
84 >3)-beta-D-Glucan appears transiently during cellularization but reappears in patches in the subaleur
85  a shallow gradient of weak responses at mid-cellularization changes to a step gradient of stronger r
86 o, while late expression, which occurs after cellularization, consists of narrow stripes with sharp a
87                           It is required for cellularization during early embryogenesis and normal de
88  effects could lead to precocious or delayed cellularization during endosperm development.
89  nuclear migration, pole cell formation, and cellularization during the early stages of embryonic dev
90 er, these data suggest that AGL62 suppresses cellularization during the syncytial phase of endosperm
91 ng that AGL62 is required for suppression of cellularization during the syncytial phase.
92 ernal-excess crosses (2 x 4) delay endosperm cellularization (EC) and produce larger seeds, whereas m
93 craps gene, identified as a gene involved in cellularization, encodes Anillin.
94                                    Endosperm cellularization failure in both hybridization directions
95 inesis before a modified cytokinesis, called cellularization, finally divides the syncytium into indi
96 s showed that Sep1 was not detectable at the cellularization front in the Pnut-deficient embryos, whe
97 e organization and initial ingression of the cellularization furrow even in the absence of Pnut and S
98 o not organize properly to the metaphase and cellularization furrows and the actin ring is absent fro
99 ical divisions the actin-based metaphase and cellularization furrows do not form properly, and the nu
100  cellularization and produces disruptions in cellularization furrows similar to those observed in the
101 s anticipated to form, to the growing tip of cellularization furrows, and to contractile rings.
102 Knockdown of PAR-1 sporadically destabilizes cellularization furrows, but basolateral displacement of
103 xpansion from the base of pseudocleavage and cellularization furrows, closely mimicking Steppke loss-
104 /or rearrangement, such as the metaphase and cellularization furrows.
105  the initial formation of both metaphase and cellularization furrows.
106 e actin is assembled into pseudocleavage and cellularization furrows.
107 t: the actomyosin cytoskeleton is disrupted, cellularization halts, and embryogenesis arrests.
108                                              Cellularization has been extensively studied in Drosophi
109 separation of pole cells with less effect on cellularization, highlighting mechanistic differences be
110                                           At cellularization, however, cleavage furrows do not invagi
111                 Yolk catabolism initiates at cellularization in Drosophila melanogaster embryos.
112  we describe several striking differences to cellularization in Drosophila, including the formation o
113  model for studying a more ancestral mode of cellularization in insects.
114             Here, we focus on the process of cellularization in the anterior pole of the early Drosop
115             We therefore set out to describe cellularization in the beetle Tribolium castaneum, the e
116 1 is also expressed in the embryo sac before cellularization, in the egg cell after cellularization,
117 efore cellularization, in the egg cell after cellularization, in the zygote/embryo immediately after
118                      Initiation of endosperm cellularization is a critical developmental transition r
119 -embryo signals are not known, but endosperm cellularization is a key event for embryos to form shoot
120 n-based hexagonal array normally seen during cellularization is disrupted in a dose-dependent fashion
121           Our functional analysis shows that cellularization is dramatically inhibited upon injecting
122 nogaster setting the standard, initiation of cellularization is faster in D. simulans by 15 min, 42 s
123 the pair-rule gene even-skipped (eve) during cellularization is robust to genetic variation in embryo
124  of endosperm development and that endosperm cellularization is triggered via direct or indirect AGL6
125 basal junctions fail to form at the onset of cellularization, leading to the failure of cleavage furr
126 esis, including syncitial nuclear divisions, cellularization, nuclear migration and fusion, and cell
127 or-beta (TGFbeta)-mediated EMT that leads to cellularization of developing cardiac valvular primordia
128 n to a distinct cell biological process: the cellularization of early embryos.
129                                        After cellularization of the AV cushion at ED 10.5, myocardial
130  nuclei at the embryo cortex are crucial for cellularization of the blastoderm embryo.
131 enesis, specific degradation is activated at cellularization of the blastoderm.
132                                              Cellularization of the Drosophila embryo is a specialize
133                                              Cellularization of the Drosophila embryo is a specialize
134                                              Cellularization of the Drosophila embryo is the process
135                                              Cellularization of the Drosophila embryo results in the
136 pleted early syncytial development and began cellularization of the embryo normally.
137 hat membrane trafficking is required for the cellularization of the syncytial blastoderm.
138 ted in cytokinesis in several systems and in cellularization of the syncytial Drosophila embryo.
139 like other proteins previously implicated in cellularization or cytokinesis, it is Golgi associated.
140                   We characterize defects in cellularization, pole cell formation and cytokinesis in
141                                The endosperm cellularization process begins at the late globular embr
142 tes the need for a bioreactor-based scaffold cellularization process.
143 , they differ in their response to the novel cellularization protein Nullo.
144 d electrocytes) revealed no fragmentation or cellularization proximal to the amputation plane.
145   Suppression of these AGL's expression upon cellularization required PRC.
146 he monolayered epithelium is disrupted after cellularization, resulting in formation of a multilayere
147                                       During cellularization, Sec5 becomes concentrated at the apical
148 nd fail to activate many genes essential for cellularization, sex determination and pattern formation
149 oderm and in the cleavage furrows during the cellularization stage.
150 ily activity affects the cytoskeleton during cellularization stages, embryos were microinjected with
151 hich we show is transiently transcribed when cellularization starts and functions to maintain cortica
152 ion of Nuf to centrosomal regions throughout cellularization suggests that it plays a similar role in
153                                       During cellularization, the actomyosin cytoskeleton forms a hex
154 shed during cellularization: at the onset of cellularization, the Drosophila beta-catenin homologue A
155                                       During cellularization, the Drosophila embryo undergoes a large
156                                       During cellularization, the Drosophila melanogaster embryo unde
157                                  Here we use cellularization, the first complete cytokinetic event in
158                                       During cellularization, the first cytokinesis in Drosophila emb
159          However, during the later stages of cellularization, the organization of the actin cytoskele
160                                       Before cellularization, the PM is polarized into discrete domai
161  ring closure during Drosophila melanogaster cellularization uses two steps, only one of which involv
162 heat stress resulted in precocious endosperm cellularization, whereas severe heat-stressed seeds fail
163 llen donors resulted in failure of endosperm cellularization, whereas the endosperm of reciprocal hyb
164 force allows premature ring constriction and cellularization, whereas the experimental depletion of N
165 rolled by cell cycle progression, whereas at cellularization, which occurs in a prolonged interphase,
166  by other insects, we examined the timing of cellularization with respect to blastoderm formation in

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