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1  and fail to grow, to become patterned or to gastrulate.
2 , many of which were not known previously to gastrulate.
3 s mutants entirely lack mesoderm and fail to gastrulate.
4 form an abnormal egg cylinder which does not gastrulate.
5 en they became growth-arrested and failed to gastrulate.
6  wall when most of the embryos have begun to gastrulate.
7 ckout of these ligands leads to a failure to gastrulate.
8 ortantly, embryos depleted for NCAM2 fail to gastrulate.
9          In mouse, Smad4-null embryos do not gastrulate, a phenotype consistent with loss of other TG
10                                These embryos gastrulate abnormally and develop with excessive notocho
11 Western analysis, resulted in the failure to gastrulate, absence of the gut and an animalized phenoty
12 cation-checkpoint defective but cellularize, gastrulate and activate high levels of zygotic gene expr
13 nic tissue allows the double null embryos to gastrulate and begin organogenesis, suggesting that extr
14 s of SRF(LacZ/)(+) "knock-in" mice failed to gastrulate and form mesoderm, similar to the findings of
15              EXT1 homozygous mutants fail to gastrulate and generally lack organized mesoderm and ext
16          Upon fus knockdown, embryos fail to gastrulate and show mesodermal differentiation defects t
17 nd that it can be clearly distinguished from gastrulating and extraembryonic cell populations in the
18 nsistent developmental defects, a failure to gastrulate, and embryonic lethality, including changes i
19    Unlike Bmpr1a-null embryos, which fail to gastrulate, Bmpr-MORE embryos initiate gastrulation, but
20 velopment reveals that C5a knockdown embryos gastrulate, but approximately 90% develop a prolapse of
21 end on common actomyosin-based mechanisms to gastrulate, but different cell fate regulators, and, sur
22  duplications, and its embryos are small and gastrulate by simple invagination.
23 , like sea urchins, has an early embryo that gastrulates by invagination, but like vertebrates, has a
24  epiblast-like cells into multiple key human gastrulating cell types, collectively called human gastr
25 evelopment involves the aggregation of newly gastrulated cells into epithelial fields, as a prelude t
26 d specification of primordial germ cells and gastrulating cells (or mesendoderm cells), can be robust
27 g this process remain unclear, as numbers of gastrulating cells are very limited.
28 d, targeting genes likely to be expressed in gastrulating cells or their neighbors.
29 he stalk of cytoplasm that normally connects gastrulating cells to the yolk mass.
30 g the cell shape or directional migration of gastrulating cells.
31 e mesendoderm cells were injected into early gastrulating chick embryos, which revealed that they int
32 transverse blastoderm isolates obtained from gastrulating chick embryos.
33 re of the colony, reminiscent of generalized gastrulating chordate embryos.
34 d increased chromosome segregation errors in gastrulating CI-derived embryos that had avoided the fir
35         Mouse embryos lacking Bmpr1a fail to gastrulate, complicating studies on the requirements for
36 ryos homozygous for gammaGCS-HS(tm1) fail to gastrulate, do not form mesoderm, develop distal apoptos
37 gination of the mesodermal primordium in the gastrulating Drosophila embryo, the internalized cells m
38                 Damaged DNA in syncytial and gastrulating Drosophila embryos delays the metaphase/ana
39 re we apply particle tracking velocimetry in gastrulating Drosophila embryos to measure the movement
40 lor imaging of fast cellular dynamics across gastrulating Drosophila embryos.
41 recently obtained time-lapse imaging data of gastrulating Drosophila embryos.
42             Embryos lacking DRhoGEF2 fail to gastrulate due to a defect in cell shape changes require
43               Despite the diversity of (pre-)gastrulating embryo and adult body shapes across the ani
44 ated functions for the AVE in organizing the gastrulating embryo and indicate that visceral endoderm-
45                       Fate allocation in the gastrulating embryo is spatially organized as cells diff
46      The organizer is a unique region in the gastrulating embryo that induces and patterns the body a
47 e derives from a small group of cells in the gastrulating embryo, known as "the organizer" in recogni
48  Nanog blocks primitive hematopoiesis in the gastrulating embryo, resulting in a loss of red blood ce
49  that patterns it into a tissue resembling a gastrulating embryo.
50 which is supplemented with mesoderm from the gastrulating embryo.
51 al cell intercalation and axial extension in gastrulating embryos and explants.
52  cells of the germline, are specified in pre-gastrulating embryos in mammals, and subsequently migrat
53 olved in gene repression by ERK signaling in gastrulating embryos of a simple proto-vertebrate (Ciona
54                                           In gastrulating embryos, FOXF1 marks most extra-embryonic m
55         Compared with wild-type ES cells and gastrulating embryos, Oct4 repression is lost and its pr
56 tiating embryonic stem cells, and in vivo in gastrulating embryos, the lineage specification of early
57 th the embryonic germ layers, reminiscent of gastrulating embryos.
58 re detected in the nascent mesoderm of early gastrulating embryos.
59  miR-17-5p expression within the mesoderm of gastrulating embryos.
60 rmal gene expression by TGFbeta signaling in gastrulating embryos.
61 is specifically expressed in the mesoderm of gastrulating embryos.
62 of gene expression in the dorsal ectoderm of gastrulating embryos.
63 arrow domain in the ventral marginal zone of gastrulating embryos.
64 low ES cells resemble the post-implantation, gastrulating epiblast.
65                    Furthermore, iETX embryos gastrulate generating embryonic and extra-embryonic meso
66 early all model organisms, a fate map of the gastrulating human embryo remains elusive.
67 le-cell transcriptional profile of an entire gastrulating human embryo, staged to be between 16 and 1
68 tomic characteristics with amnion cells of a gastrulating human embryo.
69 rom eggs depleted of xSmad8(11) mRNA fail to gastrulate; instead, at the time of gastrulation, they i
70 w that the Wnt-11 gene is expressed by newly gastrulated mesoderm cells within avian embryos.
71 l genetic fate mapping, that Mesp1+ cells in gastrulating mesoderm are rapidly specified into committ
72 y, Axial Protocadherin (AXPC), it subdivides gastrulating mesoderm into paraxial and axial domains.
73 that oriented tissue strain generated by the gastrulating mesoderm plays a major role in determining
74 aused an increase in the population of newly gastrulated mesodermal (NGM) cells that express the tran
75 establish the anterior-posterior axis of the gastrulating mouse embryo and is necessary later for mes
76  is expressed in the primitive streak of the gastrulating mouse embryo and is required for paraxial m
77 tegration of human NC cells (hNCCs) into the gastrulating mouse embryo.
78 y in development, to define its roles in the gastrulating mouse embryo.
79 e coexpressed in the primitive streak of the gastrulating mouse embryo.
80 mitive streak is the defining feature of the gastrulating mouse embryo.
81      This cell population is also present in gastrulating mouse embryos and generates haematopoietic
82 ivided into distinct pools of progenitors in gastrulating mouse embryos at earlier stages than previo
83                     3D time-lapse imaging of gastrulating mouse embryos combined with cell and tissue
84 the epiblast and nascent Flk1(+) mesoderm of gastrulating mouse embryos using single-cell RNA sequenc
85 carrying NB relevant oncogenes in utero into gastrulating mouse embryos.
86 ng haematopoietic and vascular potential) in gastrulating mouse embryos.
87 onal and architectural features of the early gastrulating mouse epiblast.
88 essed in embryonic organizing centers of the gastrulating mouse, frog, fish, and chick.
89  DNA synthesis, initiated transcription, and gastrulated normally.
90 heckpoint defective and fail to cellularize, gastrulate or to initiate high-level zygotic transcripti
91                                 As an embryo gastrulates or makes neural tissue it shortens across th
92 ecapitulates most developmental landmarks of gastrulating ovine embryos: trophoblast maturation, hypo
93 en they became growth arrested and failed to gastrulate, pointing to the early essential role for hep
94            Because ventralized embryos still gastrulate, producing a mechanical force that strains th
95 lating cell types, collectively called human gastrulating stem cells (hGaSCs).
96                         In many embryos, the gastrulating tissue is surrounded by a rigid protective
97 e Wnt and Bmp signaling pathways pattern the gastrulating vertebrate embryo using a network of secret
98 t proteins stimulate TCF3 phosphorylation in gastrulating Xenopus embryos and mammalian cells.
99 ) and triggers rapid apoptotic cell death in gastrulating Xenopus embryos.
100 dergoing convergent extension in explants of gastrulating Xenopus embryos.
101 ogs scn5Laa and scn5Lab were detected in the gastrulating zebrafish embryo and subsequently in the em
102 age Caenorhabditis elegans embryo and in the gastrulating zebrafish embryo.
103 L) and the yolk syncytial layer (YSL) in the gastrulating zebrafish embryo.
104  other transcription factors in real-time in gastrulating zebrafish embryos.

 
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