戻る
「早戻しボタン」を押すと検索画面に戻ります。

今後説明を表示しない

[OK]

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             Mesoderm induction begins during gastrulation.
2 ity and cell blebbing, eventually abrogating gastrulation.
3 niche, and germ line commitment occurs after gastrulation.
4 rocess of apical constriction during Xenopus gastrulation.
5 in convergent extension movements in Xenopus gastrulation.
6  blastopore closure throughout the course of gastrulation.
7 ndent epiblast populations, specified before gastrulation.
8  constriction during Drosophila melanogaster gastrulation.
9 ession of individual cells start well before gastrulation.
10 y modulation and tissue morphogenesis during gastrulation.
11  (YSL) secretes a ventralizing signal during gastrulation.
12 stic and can form multiple individuals until gastrulation.
13 er emerging from the primitive streak during gastrulation.
14 rs of endoderm, mesoderm and ectoderm during gastrulation.
15 TGFbeta) signal expressed posteriorly before gastrulation.
16 s required for Wnt5b/Vangl2 signaling during gastrulation.
17 ment of mesendodermal cells during zebrafish gastrulation.
18 d more recently in cell intercalation during gastrulation.
19 tical role in C&E movements during zebrafish gastrulation.
20 ts, specified in the primitive streak during gastrulation.
21 organization of germ layers during mammalian gastrulation.
22 ed cell migration and cell morphology during gastrulation.
23 nt5b/Vangl2/Ror2 signaling during vertebrate gastrulation.
24 properties of the cellular blastoderm during gastrulation.
25 tructural stiffness of the blastopore during gastrulation.
26  particularly during the early stages before gastrulation.
27 formation dynamics diverge near the onset of gastrulation.
28 rning of DV tissues along the AP axis during gastrulation.
29 of approximately 1,000 mesoderm cells during gastrulation.
30 tion of a three-dimensional body plan during gastrulation.
31  of the ectoderm persists throughout much of gastrulation.
32 ts, and the Wnt antagonist iCRT14, following gastrulation.
33 the dynamic cellular events occurring during gastrulation.
34 onvergent and extension cell movement during gastrulation.
35  and protein are expressed from oogenesis to gastrulation.
36 to during the formation of mesoderm layer in gastrulation.
37 ipotent states, before lineage commitment at gastrulation.
38 ocytes, and to a developmental arrest during gastrulation.
39 this process, but is known to act only after gastrulation.
40 tion on expression levels of 205 genes up to gastrulation.
41 rvive through implantation but fail prior to gastrulation.
42 an inhibitor of Rho-kinase activity, prevent gastrulation.
43 eral displacement of Bazooka still occurs by gastrulation.
44 oposterior axis but fail to progress through gastrulation.
45 ed, basolateral displacement still occurs by gastrulation.
46 g convergent extension during Xenopus laevis gastrulation.
47 and mesodermal cell behaviors during Xenopus gastrulation.
48  cell movements and lineage induction during gastrulation.
49 tory genes during early frog development and gastrulation.
50  points to a simplified model for Drosophila gastrulation.
51 to the formation of the primitive streak and gastrulation.
52 r axial elongation of the mouse embryo after gastrulation.
53  against being caught up in the movements of gastrulation.
54  the embryo is severely altered during early gastrulation.
55 ryos null for Rala and Ralb do not live past gastrulation.
56 sults in embryonic lethality with failure of gastrulation.
57 ess than half of the genomes needed to reach gastrulation.
58 invagination of the mesoderm at the onset of gastrulation.
59 tes mesendoderm development during zebrafish gastrulation.
60  h post-fertilization, immediately following gastrulation.
61 of early mesoderm formation during mammalian gastrulation.
62  postpone EMT during Drosophila melanogaster gastrulation.
63 iated with pattern formation at the onset of gastrulation.
64 or Wnt signaling activation during embryonic gastrulation.
65 non-canonical Wnt pathways during vertebrate gastrulation.
66 d evolution of similar transitions in animal gastrulation.
67 hogenesis and papc expression during Xenopus gastrulation.
68  pluripotency protein Ventx2 at the onset of gastrulation.
69 arise from basal posterior progenitors after gastrulation.
70  spatiotemporal pattern starting during late gastrulation.
71 that drive initial cell shape changes during gastrulation.
72  the conditions for successful pregnancy and gastrulation.
73 internalization of the ventral furrow during gastrulation.
74 l, whose function is required for vertebrate gastrulation.
75 in pigment cells, and its inhibition impairs gastrulation.
76  during germ layer formation at the onset of gastrulation.
77  several aspects of embryogenesis, including gastrulation.
78 enous strain during a critical period around gastrulation.
79 f Smad2/3 binding and gene expression during gastrulation.
80 vergence and extension cell behaviors during gastrulation.
81 ibits the repression of lambda-olt 2-1 after gastrulation.
82 to a diploblastic epithelial body plan after gastrulation [2, 3].
83 ene regulatory network (GRN) at the onset of gastrulation (24 h postfertilization) in N. vectensis Su
84  individual regulatory genes each hour up to gastrulation (30 h) in four different spatial domains of
85                            During vertebrate gastrulation, a complex set of mass cellular rearrangeme
86                            During Drosophila gastrulation, a higher number of cells undergo invaginat
87 utant embryos that fail to form cells before gastrulation ('acellular' embryos), such that the global
88 ation and t48, which in the evolution of fly gastrulation acted as a likely switch from an ingression
89                            During Drosophila gastrulation, actomyosin contraction in ventral cells ge
90 of dorsal transverse folds during Drosophila gastrulation, adherens junctions shift basally in the in
91 ry mesenchyme cells (PMCs) during sea urchin gastrulation, although the relative contributions of the
92 out how changes in cell behavior might drive gastrulation among arthropods.
93 tors resulted in developmental arrest before gastrulation and a failure to activate >75% of zygotic g
94 fically in the epiblast are able to initiate gastrulation and advance to late primitive streak stages
95 mit CM number in zebrafish embryos: prior to gastrulation and after the initial wave of CM differenti
96 ed cell movements are crucial for vertebrate gastrulation and are controlled by multiple signals.
97 Basic body plans are organized by the end of gastrulation and are refined as limbs, organs, and nervo
98            In zebrafish, ZGA is required for gastrulation and clearance of maternal messenger RNAs, w
99 remain receptive to extracellular cues after gastrulation and continue to make basic germ layer decis
100 by morpholino injection causes arrest before gastrulation and early embryonic death.
101 ot required for force production during late gastrulation and early neurulation.
102                                       During gastrulation and immediately after, Xtgfbi is expressed
103 s TRPM6 (XTRPM6) is elevated at the onset of gastrulation and is concentrated in the lateral mesoderm
104 the prospective neural crest epiblast during gastrulation and is unlikely to operate through mesoderm
105 yury (T, BRA) is one of the first markers of gastrulation and lineage specification in vertebrates.
106                                          The gastrulation and mitotic phenotypes can be rescued by ei
107                      Loss of XTRPM6 produced gastrulation and neural tube closure defects.
108 at drives key morphogenetic events including gastrulation and neural tube formation.
109 phic imaging with a typical duration of 2 h (gastrulation and neurulation stages), intricacies of ima
110 pathway in endomesoderm specification during gastrulation and overall animal-vegetal patterning at ea
111 pp-a, one of the two paralogs, begins during gastrulation and persists throughout the first week of d
112 al or cellular defects, including failure of gastrulation and problems with placement and function of
113 of inductive interactions that begins before gastrulation and progressively divide embryonic ectoderm
114               Both changes set the stage for gastrulation and require downregulation of Cdc25 phospha
115 ol of cell adhesion and morphogenesis during gastrulation and segmentation stages.
116 and in vivo imaging of SHG nanoprobes during gastrulation and segmentation.
117 roles played by growth factors in sea urchin gastrulation and skeletogenesis.
118           Here we identify two genes, folded gastrulation and t48, which in the evolution of fly gast
119  in ventral-posterior germ layer patterning, gastrulation and tadpole morphology.
120 he formation of the three germ layers during gastrulation and the differentiation of adult stem cells
121  delamination of mesendodermal precursors at gastrulation and the proper specification of the neural
122 epression of endogenous Bmp signaling during gastrulation and this enables mesodermal progenitors to
123 ers epithelial cell shape changes that drive gastrulation and tissue folding and is one of the most e
124                    They are activated during gastrulation and undergo a dynamic shift from a transcri
125  However, this strong coupling diminished at gastrulation and was absent in non-embryonic samples, in
126 derm-endoderm boundary is established before gastrulation, and ectodermal cells at the boundary are t
127 ion of the transcription factor Gata2 during gastrulation, and Gata2 is required in both ectodermal a
128 sed cell rearrangements in processes such as gastrulation, and has also been implicated in regulation
129     PTU is teratogenic during late blastula, gastrulation, and neurulation; whereas MMI is not.
130  are expressed in a localized fashion by mid-gastrulation, and which thus provide spatial regulatory
131 r in many developmental processes, including gastrulation, anterior-posterior axis specification, org
132 different progenitor cell populations during gastrulation are poorly understood.
133 a signaling pathway active during Drosophila gastrulation as a model system to study Ric-8/Galpha int
134             Knockout embryos did not undergo gastrulation, as demonstrated by the absence of mesoderm
135 time is highest immediately before and after gastrulation, as well early in the segmentation period.
136 emerge as the cell cycle slows just prior to gastrulation at a major embryonic transition known as th
137                        NC cells arise during gastrulation at the neural plate border (NPB), which is
138                            During vertebrate gastrulation, axial mesendoderm migrates in a group, the
139 itially arises in the developing skin during gastrulation, based on the appearance of polarized apica
140                   Treatment with SB43 during gastrulation blocks anterior PMC positioning and the for
141 quires an inhibition of Wnt signals prior to gastrulation, but becomes insensitive during early gastr
142 tively along a fibronectin (FN) substrate at gastrulation, but how the adhesive and mechanical forces
143  epithelial-mesenchymal transition (EMT) and gastrulation, but its role in self-renewal, pluripotency
144 tinuing roles in Bazooka localization during gastrulation, but other polarity cues partially restore
145 els in cell aggregates and during vertebrate gastrulation, but the role of differential Cdh activity
146 ansfated from notochord to somite fate after gastrulation by ectopic expression of msgn1, a master re
147  cells and the elongating archenteron during gastrulation; Cadherin (G form) has an important role in
148                                Shortly after gastrulation, canonical Wnts promote the recruitment of
149                                    Zebrafish gastrulation cell movements occur in the context of dyna
150 fects on ECM organization underlying PCP and gastrulation cell movements.
151 oderm undergo morphogenetic movements during gastrulation, cells in both germ layers read their posit
152                                 During mouse gastrulation, cells in the primitive streak undergo epit
153 ctions with the extracellular proteins Short gastrulation/Chordin (Chd) and Twisted gastrulation (Tsg
154 xes, is required for normal morphogenesis at gastrulation, closure of the anterior neural tube, axial
155  Zic3 demonstrates an early role for Zic3 in gastrulation, CNS, cardiac and left-right axial developm
156 nt of left-right (LR) asymmetry occurs after gastrulation commences and utilizes a conserved cascade
157 anterior and visceral mesoderm precursors as gastrulation commences, and find that both Cytochalasin
158  three populations acts independently during gastrulation, confirming previous hypotheses that cell b
159                                              Gastrulation constitutes a fundamental yet diverse morph
160 ing, required for hypochord induction during gastrulation, continues to act in the tailbud to specify
161             As the primary driving forces of gastrulation, convergence and extension (C&E) movements
162                            During vertebrate gastrulation, convergence and extension movements elonga
163 tion events occurring prior to completion of gastrulation coordinate the morphogenetic movements unde
164 cipates in noncanonical Wnt signaling during gastrulation, Daam2 function remains completely uncharac
165 s embryos was sufficient to fully rescue the gastrulation defect caused by loss of hepatocystin.
166                                              Gastrulation Defective (GD) cleaves and activates Snake
167                                              Gastrulation defects are not rescued by a Kif2a mutated
168 ltaN) mice were not viable, and several post-gastrulation defects revealed the first in vivo function
169                Ric-8 mutants exhibit similar gastrulation defects to Cta mutants.
170 man heterotaxy phenotype but also have early gastrulation defects, axial patterning defects and neura
171 -1; miR-9a double mutant revealed defects in gastrulation, demonstrating the importance of co-activat
172 n and monkey in vitro models simulating peri-gastrulation development to show the conserved principle
173  inhibition of jagn just before the start of gastrulation disrupts this asymmetric division of the ER
174 he resultant directed fluid flow during late gastrulation/early neurulation.
175 m-like properties of the epiblast of the pre-gastrulation embryo and for cellular and physiological h
176                      After the initiation of gastrulation, embryos that lack Pten in the epiblast sho
177                             During zebrafish gastrulation, endodermal cells sequentially exhibit firs
178                                       During gastrulation, epiblast cells are pluripotent and their f
179 c processes, including the cell movements of gastrulation, epiboly and dorsal convergence.
180 disrupts migration of the mesoderm after the gastrulation epithelial-to-mesenchymal transition (EMT).
181 rate a critical role for Cripto during mouse gastrulation, especially in mesoderm and endoderm format
182 fish tailbud is not a simple continuation of gastrulation events.
183 y to trigger actomyosin contractility during gastrulation events.
184 s a model, we show that regulation of folded gastrulation expression by the Fork head transcription f
185 eractive Nodal signalling contributes to the gastrulation failure of Tet mutants.
186 sh ybx1 lead to deregulated Nodal signaling, gastrulation failure, and embryonic lethality.
187                 Loss of Zfp568, which causes gastrulation failure, or mutation of the ZFP568-binding
188 ssion in dorsal posterior cells during early gastrulation, focusing Wnt1 signaling to the posterior-v
189 three signaling pathways are required during gastrulation for the proper expression of pax3a and zic3
190 vely regulate each other's expression during gastrulation, forming a self-sustaining network that ope
191   Altogether, our data establish that during gastrulation, FOXF1 marks all posterior primitive streak
192                                              Gastrulation generates three layers of cells (ectoderm,
193    Historically, the position of the site of gastrulation has been used to understand the development
194 stically reducing the level of FGF8 later in gastrulation has no apparent effect on somitogenesis or
195 nd spreading of the animal hemisphere during gastrulation, here we provide evidence that radial inter
196               PZR was required for zebrafish gastrulation in a manner dependent upon PZR tyrosyl phos
197 mplex epithelium in planula stages following gastrulation in addition to previously described roles f
198 ing critical morphogenetic events, including gastrulation in diverse organisms and neural tube closur
199                           Around the time of gastrulation in higher vertebrate embryos, inductive int
200       This protocol describes how to observe gastrulation in living mouse embryos by using light-shee
201 vide essential cues to mesoderm cells during gastrulation in many metazoans.
202 static and developmental contexts, including gastrulation in many organisms and neural tube formation
203 ates that mesoderm induction continues after gastrulation in neuromesodermal progenitors (NMPs) withi
204 progression from preimplantation epiblast to gastrulation in rodents.
205 ions that form two aggregations during early gastrulation in the crustacean Parhyale hawaiensis.
206  with the elongation of the notochord during gastrulation in the rapidly developing species.
207 f a reprogramming capability occurs at early gastrulation in the sea urchin embryo and requires activ
208 rs systemically must be established prior to gastrulation in the very early embryo and, because it is
209 rotocol for applying this technique to study gastrulation in Xenopus laevis (African clawed frog) emb
210 rax transcription is initiated at the end of gastrulation in Xenopus, and is a key part of the regula
211 e that Uhrf1 phosphorylation is required for gastrulation in zebrafish.
212 ulates CE, and Wnts regulate many aspects of gastrulation including CE and EMT.
213 imelines and summarizes key stages following gastrulation, including endoderm patterning, organ speci
214 igration away from the primitive streak when gastrulation initiates, but previous studies have shown
215                                           At gastrulation, interactions between the pair-rule genes l
216                  Germ-layer formation during gastrulation is both a fundamental step of development a
217 enetically proving that Tcf3 function during gastrulation is independent of beta-catenin interaction.
218 ism in the early Drosophila embryo, in which gastrulation is preceded by 13 sequential nuclear cleava
219 a demonstrate that Alk4/5/7 signaling during gastrulation is required to direct PMCs to the oral hood
220 and ECM assembly/remodeling during zebrafish gastrulation is unclear.
221 d that cell organization in the embryo until gastrulation is well described by a purely mechanical mo
222               Isolated skin explanted before gastrulation lacks strain and fails to acquire a global
223    Conditional inactivation of Cripto during gastrulation leads to varied defects in mesoderm and end
224 als its abnormal development at the onset of gastrulation, many hours before changes are obvious to t
225 te the position of the head and the onset of gastrulation, marked by T/Brachyury (T/Bra) at the poste
226                            During Drosophila gastrulation, mitosis is associated with the transcripti
227 s, demonstrating that in the early stages of gastrulation most subapical clusters in mesoderm not onl
228                                        While gastrulation movements offer mechanistic paradigms for h
229                                              Gastrulation movements place endodermal precursors, meso
230 he source of this extrinsic force, we mapped gastrulation movements temporally using light sheet micr
231 he cytoplasmic tyrosine kinase Arg modulates gastrulation movements through control of actin remodeli
232 r of APJ/Apelin receptor signaling, promotes gastrulation movements, and might be the first in a seri
233 nimal caps are not compliant enough to allow gastrulation movements.
234 and body plan evolution despite variation in gastrulation movements.
235 d convergence and extension movements during gastrulation, neurulation and epidermis defects and enha
236                   We conclude that perturbed gastrulation not only explains the neurulation defects,
237                                              Gastrulation of the Drosophila embryo is one of the most
238 lls gained the ability to reprogram early in gastrulation only after extended contact with the vegeta
239  in mice, required for embryonic growth from gastrulation onward.
240 layers that provide the structural basis for gastrulation or subsequent developmental events [1].
241                        The Drosophila Folded gastrulation pathway triggers epithelial cell shape chan
242 rations provide only weak rescue of an early gastrulation phenotype induced by Megf8 knockdown.
243 eletion of Igf2 can completely rescue Zfp568 gastrulation phenotypes through late gestation.
244 tion of all three Tet genes in mice leads to gastrulation phenotypes, including primitive streak patt
245                             During amphibian gastrulation, presumptive endoderm is internalised as pa
246                     It has been considered a gastrulation process unique to amphibians, but we show t
247 rk recapitulates these variable and bistable gastrulation profiles and emphasizes the importance of t
248                                     Modes of gastrulation range from stochastic translocation of indi
249 hich is distinct from PCP signaling or other gastrulation regulators, including BMP and Nodals.
250 ypotheses that cell behavior during Parhyale gastrulation relies on intrinsic signals instead of an i
251  regulated switch to late replication during gastrulation, reminiscent of mammalian X Chromosome inac
252 ergent extension movements during vertebrate gastrulation require a balanced activity of non-canonica
253 t and its conditional ablation, beginning at gastrulation, results in increased apoptosis, growth ret
254 bition renders the concentration of dNTPs at gastrulation robust, with respect to large variations in
255                           To assess the post-gastrulation role of YY1, a conditional knock-out (cKO)
256 ulate cell polarity and intercalation during gastrulation, signaling molecules acting in other pathwa
257 , using enhancers of brinker (brk) and short gastrulation (sog), both of which are directly activated
258                                Later, during gastrulation, Sox32 restricts Pou5f3-Nanog complexes to
259             Strikingly, mouse EpiSCs express gastrulation stage regional markers in self-renewing con
260 t1 in mouse embryos causes death at the post-gastrulation stage; however, the functions of Dnmt1 and
261                          PTU exposure during gastrulation (stage 8-12.5) was identified as the critic
262 d mesodermal cells during cleavage and early gastrulation stages.
263 , suggesting that they might use alternative gastrulation strategies.
264 ntration caused changes in cell movements at gastrulation that also altered the tissue fates of these
265 nase MRCK-1 as a key regulator of C. elegans gastrulation that integrates spatial and developmental p
266 te embryos undergo dramatic shape changes at gastrulation that require locally produced and anisotrop
267 ed population of cells emerges at the end of gastrulation that, under the influence of Wnt and FGF si
268                                           By gastrulation the ectodermal territories of the sea urchi
269                                       During gastrulation, the animal and marginal regions dissociate
270                            Immediately after gastrulation, the CB consists of four separate regulator
271                              At the start of gastrulation, the ER divides asymmetrically into a popul
272                                  Around late gastrulation, the PPE forms at the border surrounding th
273                                       During gastrulation, the primary morphogenetic event of early d
274                            During Drosophila gastrulation, the ventral mesodermal cells constrict the
275 d CaN signaling opposes BMP signaling during gastrulation, thereby promoting neural induction and the
276 we examined whether C5a could be involved in gastrulation through cAMP transport.
277 ng is required for mesoderm induction during gastrulation through positive transcriptional regulation
278 els in the embryo blocks force generation at gastrulation through two distinct mechanisms: destabiliz
279 entiation to mimic lineage commitment during gastrulation to ectoderm (early switch) or mesoderm/endo
280 ailbud that make a germ layer decision after gastrulation to form spinal cord and mesoderm.
281 r of left-right (L-R) information from early gastrulation to morphogenesis.
282 F-beta-receptor signaling is required during gastrulation to pattern the anterior skeleton.
283 Short gastrulation/Chordin (Chd) and Twisted gastrulation (Tsg).
284                                      Twisted gastrulation (TWSG1) is a secreted BMP binding protein t
285                                              Gastrulation was arguably the key evolutionary innovatio
286 n and random motility exhibited during early gastrulation were dependent on both Nodal and Rac1 signa
287           In the sea urchin embryo, cells at gastrulation were found to reprogram and replace missing
288 milar in both species until the beginning of gastrulation, when BMP signaling broadens and intensifie
289 of the three major germ layers occurs during gastrulation, when cells ingressing through the primitiv
290 ter is expressed throughout the embryo until gastrulation, when it becomes specifically expressed in
291 ipts differentially expressed by PMCs during gastrulation, when these cells undergo a striking sequen
292       These progenitors are specified during gastrulation, when they transiently express Foxa2, a gen
293 h changes broadly regulate translation until gastrulation, when this coupling disappears.
294 t activation induces the neural crest during gastrulation, whereas activation of both pathways mainta
295  genes is also upregulated in males prior to gastrulation; whether it results in functional dosage co
296 Dynamic local methylation was evident during gastrulation, which enabled the identification of putati
297 ) axis elongation are fundamental aspects of gastrulation, which is initiated by formation of the pri
298 mits the developmental rate beginning during gastrulation without affecting the normal patterning of
299 ation (Tcf3(DeltaN/DeltaN)) progress through gastrulation without apparent defects, thus genetically
300                            During vertebrate gastrulation, Wnt/planar cell polarity (PCP) signaling o

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。
 
Page Top