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1 izing newly deposited plasma membrane during cellularization.
2 ons in syncytial embryos, and the subsequent cellularization.
3 oordinate membrane invagination during early cellularization.
4 sure of the cells does not occur during late cellularization.
5 larized growth of the plasma membrane during cellularization.
6 ation when ectopically expressed during late cellularization.
7 g epithelial basement membranes and germline cellularization.
8  smaller yolk stalk diameters and more rapid cellularization.
9 ale pattern in the actin/myosin array during cellularization.
10 e dynamics of marked membrane regions during cellularization.
11 s required for its formation at the onset of cellularization.
12 bitor of membrane trafficking, also inhibits cellularization.
13  MMAP, Lava Lamp (Lva), is also required for cellularization.
14   This patterning cascade takes place before cellularization.
15 ups in which many segments emerge only after cellularization.
16 required for the formation of furrows during cellularization.
17 cheme of polarized membrane insertion during cellularization.
18  development such as polar nuclei fusion and cellularization.
19 yncytial divisions and is not observed after cellularization.
20  during a critical syncytial stage, prior to cellularization.
21 rotein is localized at cell membranes during cellularization.
22 differently from those that are formed after cellularization.
23 rial that appears on the cell surface during cellularization.
24 metric challenges associated with aphrogenic cellularization.
25 knockout mutants showed precocious endosperm cellularization.
26 r inhibiting actomyosin contractility during cellularization.
27 cl-NAC is safe and supports host-mediated re-cellularization.
28 esis on macroscopic scales in the absence of cellularization.
29 g and ciliogenesis but are not essential for cellularization.
30 AF, inhibits actomyosin contractility during cellularization.
31 with the reestablishment of normal endosperm cellularization.
32 ization is enriched during the fast phase of cellularization.
33 l force opens the ring channels and prevents cellularization.
34 junction gene Innexin 7, leads to failure of cellularization.
35 fferentiated epithelial cells but not during cellularization.
36 e progressively along the cell length during cellularization.
37 , in which all segments are patterned before cellularization.
38 e remainder of the embryo is generated after cellularization.
39 d reduced seed size and exhibited precocious cellularization.
40 he initial polarity cue as cells form during cellularization.
41 alazal endosperm of wild-type seeds prior to cellularization.
42  clustered mitochondria on the basal side in cellularization.
43 min before mitotic cycle 14 to 15 min during cellularization.
44 fic translational regulator, is required for cellularization.
45 ycle and polygonal territories emerge during cellularization.
46 through a special form of cytokinesis termed cellularization.
47  whether the exocyst complex is required for cellularization.
48 d rates of cytoplasmic streaming and delayed cellularization.
49 n-dependent cytoplasmic streaming and oocyte cellularization.
50 ial for furrow stabilization at the onset of cellularization.
51 cle arrest did not advance or delay onset of cellularization.
52 phase and then declines abruptly just before cellularization.
53 sands of syncytial nuclei in preparation for cellularization.
54 d in plasma membrane in the process known as cellularization.
55 bryo patterning, endosperm nuclear size, and cellularization, a phenotype that is variable between su
56 ns in the cytoskeleton during the process of cellularization, a specialized form of cytokinesis.
57         The DAH phosphorylation peaks during cellularization, a stage at which DAH function is critic
58        The absence of Bottleneck during late cellularization allows src64-dependent microfilament rin
59 nt yolk stalk diameters as well as depths of cellularization along the AP axis.
60        These mutations also strongly perturb cellularization, altering the timing and rate of furrow
61                                   Drosophila cellularization and animal cell cytokinesis rely on the
62  are remarkable for their ability to undergo cellularization and cell-cycle re-entry during regenerat
63 are equivalently partitioned among nuclei at cellularization and could play an important role in the
64         To identify new proteins involved in cellularization and cytokinesis, we have conducted a bio
65 a phase of free nuclear division followed by cellularization and differentiation of cell types.
66                        These embryos halt in cellularization and do not proceed to gastrulation.
67 arazu and huckebein, which are essential for cellularization and embryonic patterning.
68   The Drosophila MBT is marked by blastoderm cellularization and follows 13 cleavage-stage divisions.
69 ogenesis: formation of the metaphase furrow, cellularization and formation of the pole cells.
70 ygotically regulated post-MBT events such as cellularization and gastrulation movements occurred in t
71 ll cycle delays, zygotic gene transcription, cellularization and gastrulation.
72 l H3K9me3 enrichment is established prior to cellularization and matures into stable and broad hetero
73                    Because the completion of cellularization and other aspects of early development s
74  Processes under microRNA regulation include cellularization and patterning in the blastoderm, morpho
75      nuf also disrupts the initial stages of cellularization and produces disruptions in cellularizat
76 s identified several known genes controlling cellularization and proliferation as well as novel genes
77       Upon in vivo delivery, bFGF induced re-cellularization and re-vascularization in endodontically
78 in extensive endosperm proliferation without cellularization and seed abortion.
79 ink between cytoskeletal organization during cellularization and subsequent morphogenetic processes o
80 ogenous application of ABA-induced endosperm cellularization and suppressed embryo growth arrest.
81      We show that ZA formation begins during cellularization and that the basolateral membrane domain
82 ts ability to provide a durable scaffold for cellularization and tissue remodeling.
83                           Embryo development cellularization and vitellin yolk protein degradation, p
84 aging agents induce a mnk-dependent block to cellularization and zygotic gene expression.
85 ed; seven have been previously implicated in cellularization and/or cytokinesis, including KLP3A, Ani
86 lishment of a functional cytoskeleton during cellularization, and exhibit a pair-rule segmentation ph
87 widely expressed with roles in segmentation, cellularization, and gastrulation during early embryogen
88 lays, DNA replication checkpoint activation, cellularization, and high-level zygotic expression of pr
89 trol 3D spatial patterning, ECM composition, cellularization, and material properties to create a glu
90 lopmental induction during the slow phase of cellularization, and Slam protein localizes to the furro
91             However, cleavage furrows during cellularization are totally disorganized, and no embryos
92                                       Before cellularization, astral microtubules determine metaphase
93 m vulgare) grain development, from endosperm cellularization at 3 d after pollination (DAP) through d
94 ed how cyclin knockdown affects the onset of cellularization at the midblastula transition and found
95 ithelial polarity that is established during cellularization: at the onset of cellularization, the Dr
96 of spatially regulated autophagy during late cellularization, autophagy was not required for initiati
97                         As cells form during cellularization, basally localized Bazooka undergoes bas
98 Spizellomyces punctatus to show that chytrid cellularization begins with migration of nuclei and thei
99              The patches do not appear until cellularization begins, and the process fails entirely w
100 >3)-beta-D-Glucan appears transiently during cellularization but reappears in patches in the subaleur
101  a shallow gradient of weak responses at mid-cellularization changes to a step gradient of stronger r
102 o, while late expression, which occurs after cellularization, consists of narrow stripes with sharp a
103 inc-finger transcription factor expressed at cellularization, controls the transition of genes from p
104             The mitochondrial morphology and cellularization defects in Drp1 mutants are suppressed b
105                           It is required for cellularization during early embryogenesis and normal de
106 le fission of some green algae and bacteria; cellularization during embryogenesis of plants and insec
107  effects could lead to precocious or delayed cellularization during endosperm development.
108  nuclear migration, pole cell formation, and cellularization during the early stages of embryonic dev
109 er, these data suggest that AGL62 suppresses cellularization during the syncytial phase of endosperm
110 ng that AGL62 is required for suppression of cellularization during the syncytial phase.
111 ernal-excess crosses (2 x 4) delay endosperm cellularization (EC) and produce larger seeds, whereas m
112 e that the mechanisms that control endosperm cellularization, embryo growth, and embryo maturation ac
113 craps gene, identified as a gene involved in cellularization, encodes Anillin.
114                                    Endosperm cellularization failure in both hybridization directions
115            The reason for embryo arrest upon cellularization failure remains unclear.
116 inesis before a modified cytokinesis, called cellularization, finally divides the syncytium into indi
117 eycomb of polyhedral membrane compartments-a cellularization foam-each with a nucleus and cilium.
118 s showed that Sep1 was not detectable at the cellularization front in the Pnut-deficient embryos, whe
119 e organization and initial ingression of the cellularization furrow even in the absence of Pnut and S
120 o not organize properly to the metaphase and cellularization furrows and the actin ring is absent fro
121 ical divisions the actin-based metaphase and cellularization furrows do not form properly, and the nu
122  cellularization and produces disruptions in cellularization furrows similar to those observed in the
123 s anticipated to form, to the growing tip of cellularization furrows, and to contractile rings.
124 Knockdown of PAR-1 sporadically destabilizes cellularization furrows, but basolateral displacement of
125 xpansion from the base of pseudocleavage and cellularization furrows, closely mimicking Steppke loss-
126 e actin is assembled into pseudocleavage and cellularization furrows.
127 /or rearrangement, such as the metaphase and cellularization furrows.
128  the initial formation of both metaphase and cellularization furrows.
129 t: the actomyosin cytoskeleton is disrupted, cellularization halts, and embryogenesis arrests.
130 develop at a slower pace, or where endosperm cellularization happens too early, too late, or not at a
131                                              Cellularization has been extensively studied in Drosophi
132                  During Drosophila embryonic cellularization, heterochromatin rapidly appears over re
133                    We show that early during cellularization, hexagonally arrayed actomyosin fibers a
134 separation of pole cells with less effect on cellularization, highlighting mechanistic differences be
135                                           At cellularization, however, cleavage furrows do not invagi
136 pporting the morphogenetic events that drive cellularization in Drosophila embryos.
137                 Yolk catabolism initiates at cellularization in Drosophila melanogaster embryos.
138  we describe several striking differences to cellularization in Drosophila, including the formation o
139  model for studying a more ancestral mode of cellularization in insects.
140 before and after the transition to endosperm cellularization in order to investigate the involvement
141             Here, we focus on the process of cellularization in the anterior pole of the early Drosop
142             We therefore set out to describe cellularization in the beetle Tribolium castaneum, the e
143 1 is also expressed in the embryo sac before cellularization, in the egg cell after cellularization,
144 efore cellularization, in the egg cell after cellularization, in the zygote/embryo immediately after
145                      Initiation of endosperm cellularization is a critical developmental transition r
146 -embryo signals are not known, but endosperm cellularization is a key event for embryos to form shoot
147 n-based hexagonal array normally seen during cellularization is disrupted in a dose-dependent fashion
148           Our functional analysis shows that cellularization is dramatically inhibited upon injecting
149 nogaster setting the standard, initiation of cellularization is faster in D. simulans by 15 min, 42 s
150                              This process of cellularization is frequently disrupted in hybrid seeds
151  in contrast with previous models, endosperm cellularization is not required for the onset of maturat
152  results together, we propose that endosperm cellularization is required to establish dehydration tol
153 the pair-rule gene even-skipped (eve) during cellularization is robust to genetic variation in embryo
154  of endosperm development and that endosperm cellularization is triggered via direct or indirect AGL6
155 nsect species reveals that Fog's role during cellularization is widely conserved and therefore might
156 basal junctions fail to form at the onset of cellularization, leading to the failure of cleavage furr
157 esis, including syncitial nuclear divisions, cellularization, nuclear migration and fusion, and cell
158 or-beta (TGFbeta)-mediated EMT that leads to cellularization of developing cardiac valvular primordia
159 n to a distinct cell biological process: the cellularization of early embryos.
160 stration of germ plasm during the precocious cellularization of PGCs in NC10.
161                                        After cellularization of the AV cushion at ED 10.5, myocardial
162  nuclei at the embryo cortex are crucial for cellularization of the blastoderm embryo.
163 enesis, specific degradation is activated at cellularization of the blastoderm.
164                                              Cellularization of the Drosophila embryo is a specialize
165                                              Cellularization of the Drosophila embryo is a specialize
166                                              Cellularization of the Drosophila embryo is the process
167                                              Cellularization of the Drosophila embryo results in the
168 pleted early syncytial development and began cellularization of the embryo normally.
169          The onset of maturation follows the cellularization of the endosperm, and it has been propos
170 hat membrane trafficking is required for the cellularization of the syncytial blastoderm.
171 ted in cytokinesis in several systems and in cellularization of the syncytial Drosophila embryo.
172 like other proteins previously implicated in cellularization or cytokinesis, it is Golgi associated.
173 cleate stage followed by tubulin-independent cellularization, orchestrated by active membrane tension
174 with replacement by bone demonstrating graft cellularization over time.
175                   We characterize defects in cellularization, pole cell formation and cytokinesis in
176 n addition, Fog signaling affects blastoderm cellularization, primordial germ cell positioning, and c
177                                The endosperm cellularization process begins at the late globular embr
178 tes the need for a bioreactor-based scaffold cellularization process.
179 , they differ in their response to the novel cellularization protein Nullo.
180 d electrocytes) revealed no fragmentation or cellularization proximal to the amputation plane.
181   Suppression of these AGL's expression upon cellularization required PRC.
182  tissue response occurring during Drosophila cellularization, resulting from a softening of the blast
183 he monolayered epithelium is disrupted after cellularization, resulting in formation of a multilayere
184 base of invaginating membranes in Drosophila cellularization, Rho inhibition by RhoGTPase-activating
185                                       During cellularization, Sec5 becomes concentrated at the apical
186 nd fail to activate many genes essential for cellularization, sex determination and pattern formation
187 l height and larger contractile ring area in cellularization similar to that in myosin II mutants.
188 oderm and in the cleavage furrows during the cellularization stage.
189 ily activity affects the cytoskeleton during cellularization stages, embryos were microinjected with
190 hich we show is transiently transcribed when cellularization starts and functions to maintain cortica
191 ences chromatin accessibility genome-wide at cellularization, suggesting both are pioneer factors wit
192 ion of Nuf to centrosomal regions throughout cellularization suggests that it plays a similar role in
193                                       During cellularization, the actomyosin cytoskeleton forms a hex
194 shed during cellularization: at the onset of cellularization, the Drosophila beta-catenin homologue A
195                                       During cellularization, the Drosophila embryo undergoes a large
196                                       During cellularization, the Drosophila melanogaster embryo unde
197                                  Here we use cellularization, the first complete cytokinetic event in
198                                       During cellularization, the first cytokinesis in Drosophila emb
199          However, during the later stages of cellularization, the organization of the actin cytoskele
200                                       Before cellularization, the PM is polarized into discrete domai
201                                        After cellularization, tissue junction elasticity becomes akin
202 of synchronous nuclear division, followed by cellularization, to create and release many daughter 'zo
203  ring closure during Drosophila melanogaster cellularization uses two steps, only one of which involv
204 ive healing response, characterized by rapid cellularization, vascularization, and progressive breast
205    Here, dcl-NAC safety and host-mediated re-cellularization was assessed in a 6-week study in rhesus
206                 Polarity is initiated during cellularization, when cell-cell adherens junctions are p
207 lling in the Drosophila embryo occurs during cellularization, when lateral cell membranes and adheren
208 entional cytokinesis or Drosophila monolayer cellularization, where nuclei are organized in linear or
209 fungi provide a model for studying foam-like cellularization, where nuclei that are dispersed through
210 heat stress resulted in precocious endosperm cellularization, whereas severe heat-stressed seeds fail
211 llen donors resulted in failure of endosperm cellularization, whereas the endosperm of reciprocal hyb
212 force allows premature ring constriction and cellularization, whereas the experimental depletion of N
213 rolled by cell cycle progression, whereas at cellularization, which occurs in a prolonged interphase,
214 expressed for only a short time during early cellularization, which we show regulates actin bundling.
215 DS78 and MADS 79 exhibited delayed endosperm cellularization, while CRISPR-Cas9-mediated single knock
216  by other insects, we examined the timing of cellularization with respect to blastoderm formation in

 
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