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1 igned along the short axis of the elliptical egg cylinder.
2 etween implantation and the formation of the egg cylinder.
3 f visceral endoderm at the distal tip of the egg cylinder.
4 ogical transition from the blastocyst to the egg cylinder.
5 ero-like transition of the blastocyst to the egg cylinder.
6  undergoes a dramatic transformation into an egg cylinder.
7 imaging of the transition from blastocyst to egg cylinder.
8 represent a realistic geometry for the mouse egg-cylinder.
9 uctures, they fail to differentiate and form egg cylinders.
10 can attach to the substrate and develop into egg cylinders after 5 d, and the second starts with late
11 ous mutant embryos fail to form an organized egg cylinder and lack mesoderm, like mutant mice lacking
12 ls, lacked the extraembryonic portion of the egg cylinder, and appeared strikingly similar to E6.5 sm
13 ly concentrated in the lateral region of the egg cylinder, and is later found circumferentially in th
14 etic fates begins in proximal regions of the egg cylinder at the mid-primitive streak stage (E7.0) wi
15 n disruption and developmental arrest of the egg cylinder before gastrulation.
16                Wnt3-/- mice develop a normal egg cylinder but do not form a primitive streak, mesoder
17 mbryos revealed that they had a disorganized egg cylinder by E5.5, which degenerated by E6.5.
18            The axis of the post-implantation egg cylinder can be traced back to organization of the p
19 evels of unrepaired DNA strand breaks in the egg cylinder compared with normal embryos.
20 tocyst-derived embryonic stem (ES) cells and egg cylinder-derived epiblast stem cells (EpiSCs).
21 no visceral endoderm formed, and finally the egg cylinder disintegrated.
22 sults demonstrate that smad2 is required for egg cylinder elongation, gastrulation, and mesoderm indu
23 h the onset of RA synthesis, being absent in egg cylinder embryos but present in the posterior mesode
24 r' and 'younger' AVE domains coalesce as the egg cylinder emerges from the blastocyst structure.
25 als are required for epiblast proliferation, egg cylinder formation, and mesoderm induction.
26 dy reported for laminin) die at the onset of egg cylinder formation, support the view that hensin and
27 dhesion-mediated tension release facilitates egg cylinder formation.
28 h MRP results in successful implantation and egg-cylinder formation, followed by severe developmental
29  of symmetry) generally became distal as the egg cylinder formed, while those that originated opposit
30 ng murine peri-implantation development, the egg cylinder forms from a solid cell mass by the apoptot
31 ive streak forms on the opposite side of the egg cylinder from this anterior Hex expression domain ap
32 ects of early mouse development, such as its egg-cylinder gastrulation and method of implantation, di
33 t type II activin receptors are required for egg cylinder growth, primitive streak formation, and ros
34  cells are present in the deformed primitive egg cylinder; however, the visceral endoderm cells are n
35 n dissection of the mural trophectoderm form egg cylinders in only 3 d.
36 ransition from the pre- to post-implantation egg cylinder morphology in vitro.
37 lls to mediate signals that are required for egg cylinder organization and gastrulation.
38 tions in the future posterior portion of the egg cylinder rather than regionalization of a radial pat
39  for DVE formation, as well as the elongated egg cylinder shape, without affecting embryo-intrinsic t
40 t embryos developed normally until the early egg cylinder stage (embryonic day 6.0), when they became
41 us mutant embryos fail to develop beyond the egg cylinder stage and are resorbed by 10.5 days of gest
42 ceptor mutations were growth arrested at the egg cylinder stage and did not form mesoderm.
43 tant embryos progressed normally to the late egg cylinder stage at approximately 6.5 days post coitus
44                       RA was not detected in egg cylinder stage embryos but was detected in late prim
45 erformed in implanting blastocysts and early egg cylinder stage embryos developed in culture.
46 gation in the extraembryonic portion of late egg cylinder stage embryos.
47 ed in apposition to this structure in normal egg cylinder stage embryos.
48                                       By the egg cylinder stage of development, at which point the ep
49 e and disappearance of columnar cells at the egg cylinder stage of the embryo.
50 Although haploid cells have been observed in egg cylinder stage parthenogenetic mouse embryos, most c
51                                 At the early egg cylinder stage, continued expression of ER was obser
52    Hence, ALK3 is essential, beyond just the egg cylinder stage, for myocyte-dependent functions and
53                                       At the egg cylinder stage, the distal visceral endoderm is colu
54 epithelium that forms the outer layer of the egg-cylinder stage mouse embryo.
55 cies chimeras cultured in vitro to the early egg-cylinder stage.
56 ved and were integrated into the epiblast of egg-cylinder-stage embryos.
57 , they never integrated into the epiblast of egg-cylinder-stage embryos.
58 gastrulation in the proximal epiblast of the egg cylinder, then is restricted to the posterior proxim
59              Mutant embryos form an abnormal egg cylinder which does not gastrulate.
60 menogenesis and forms the primed pluripotent egg cylinder, which is able to generate the embryonic ti