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1 rsally towards, and occasionally beyond, the blastopore.
2 ed ectopically, extending posteriorly to the blastopore.
3 eously by the lateral closure of a slit-like blastopore.
4 ally regarding the embryological fate of the blastopore.
5 "bilateral primitive streak" just inside the blastopore.
6 doderm and lies circumferentially around the blastopore.
7 which involute over the posterior lip of the blastopore.
8 confirms surface localization in C. albicans blastopores.
9   Gastrulation is heralded by formation of a blastopore, an opening in the blastula.
10 e apical constriction of bottle cells at the blastopore and ectopic constriction of ectoderm cells tr
11  to the development of forces that close the blastopore and elongate the body axis, to examine the ro
12 nserved "cassette" of genes expressed in the blastopore and later in the gut, involved in posterior p
13 5 and Wnt11 ligands are expressed around the blastopore and play an important role in regulating cell
14 age in a ring of mesendoderm just inside the blastopore and subsequently in the posterior mesoderm, n
15  gastrulation cell movements relative to the blastopore and the organizer are similar from fish to ma
16 oderm formation, as well as the formation of blastopores and the wild-type body axis.
17  the hindgut, but rather through the closing blastopore; and that the cells undergo a long-range migr
18 sing from the dorsal and ventral lips of the blastopore are able to spread and migrate on fibronectin
19 n contrast, cells lateral and ventral to the blastopore are less polarized and have tortuous cell bou
20 ngeal endoderm sits at the dorsal lip of the blastopore at the onset of gastrulation, and because thi
21 on, endoderm and mesoderm cells move via the blastopore beneath the ectoderm.
22  primitive streak evolved from the ancestral blastopore by acquisition of an additional medio-lateral
23 e scales and in different regions around the blastopore by characterizing large scale tissue deformat
24  show that their early expression around the blastopore can subsequently be traced into the tail bud;
25 ent of the progress of convergent extension, blastopore closure and archenteron formation in a single
26 n, we demonstrate a distinct role for Fry in blastopore closure and dorsal axis elongation.
27                 We describe the mechanics of blastopore closure at multiple scales and in different r
28 curred earlier relative to the time point of blastopore closure in comparison with slowly developing
29                                              Blastopore closure in the amphibian embryo involves larg
30    CT occurs without CE and drives symmetric blastopore closure in ventralized embryos.
31 vergence force generation in explants and of blastopore closure in whole embryos.
32  of Profilin1 in vivo specifically inhibited blastopore closure in Xenopus but did not affect converg
33 These forces are tuned to generate sustained blastopore closure throughout the course of gastrulation
34 rsal mesoderm and interferes with the normal blastopore closure, a defect that can be rescued by a do
35 trix adhesion, and dose-dependent failure of blastopore closure, arguably because of failure to devel
36 ling disrupted both convergent extension and blastopore closure, mesendoderm internalization proceede
37                                              Blastopore closure, notochord formation, somite developm
38 e have previously shown XProfilin1 regulates blastopore closure, overexpression or depletion of XProf
39         Kif2a depletion generates defects in blastopore closure.
40 eby generating tensile force contributing to blastopore closure.
41 e production and structural stiffness of the blastopore during gastrulation.
42 ion for the various characteristic shapes of blastopore-equivalents in different organisms and a fram
43             Wnt target expression around the blastopore falls into two main categories: a horseshoe s
44 able pattern of spindle orientation into the blastopore, followed by invagination.
45  the blastopore lip, and it functions during blastopore formation and closure.
46 he region of the dorsal marginal zone before blastopore formation and persists in this region during
47  RNA was sufficient to partly restore normal blastopore formation in Vangl2-deficient embryos.
48  can generate the force required for initial blastopore formation.
49 Rab11 to regulate apical constriction during blastopore formation.
50 pithelial sheets of cells through a circular blastopore in amphibians to ingression of mesenchymal ce
51         Consequently, in Wnt1 morphants, the blastopore is located at the border of the re-specified
52                        The axial side of the blastopore is marked by the organizer, a signaling cente
53  the primitive streak, the equivalent of the blastopore, is a critical step during the early developm
54 ains for Wnt3, Wnt5, and Wnt6 genes from the blastopore lip (or its equivalent) to the tail bud.
55 et of gastrulation on the dorsal side of the blastopore lip and, subsequently, in the prospective neu
56 entral mesoderm, that precedes and parallels blastopore lip formation at the border between the mesod
57 e partial dependence of Xombi expression and blastopore lip formation on fibroblast growth factor (FG
58 o posterior truncation, including defects in blastopore lip formation, gastrulation and neural tube c
59 F-actin was consistently oriented toward the blastopore lip in dorsal and lateral cells, but oriented
60 ected at the apical surfaces of cells at the blastopore lip, and it functions during blastopore forma
61                                       At the blastopore lip, Vangl2 is required for the apical accumu
62 logies especially pronounced adjacent to the blastopore lip.
63 ends the tissue and creates a crevice at the blastopore lip.
64 ene expression expanded away from the dorsal blastopore lip.
65 ctoderm of Xenopus embryos that resemble the blastopore lip.
66 ryology, the idea that the dorsal lip of the blastopore ;organized' the early patterning of the embry
67    Its expression is later restricted to the blastopore region and the posterior of the invaginating
68 derm, directed by signals emanating from the blastopore region.
69 te over the anterior and lateral lips of the blastopore, respectively.
70 and lateral epithelial cells proximal to the blastopore reveals changing patterns of strain rate thro
71 s marginal zone cells involuting through the blastopore, somitogenic mesoderm during somite formation
72 e find that the germ cells accumulate at the blastopore; that the cells do not internalize through th
73  major goals of gastrulation: closure of the blastopore to bring the endoderm and mesoderm fully insi
74                        Cells surrounding the blastopore undergo rapid cell state changes that include
75                          Cells dorsal to the blastopore, which are fated to become neural plate ectod
76 echanical environments in regions around the blastopore, which was reflected by the strain rate maps.