ライフサイエンスコーパス: gastrulate

1 , many of which were not known previously to gastrulate.

2 s mutants entirely lack mesoderm and fail to gastrulate.

3 form an abnormal egg cylinder which does not gastrulate.

4 en they became growth-arrested and failed to gastrulate.

5 wall when most of the embryos have begun to gastrulate.

6 and fail to grow, to become patterned or to gastrulate.

7 In mouse, Smad4-null embryos do not gastrulate, a phenotype consistent with loss of other TG

8 These embryos gastrulate abnormally and develop with excessive notocho

9 Western analysis, resulted in the failure to gastrulate, absence of the gut and an animalized phenoty

10 cation-checkpoint defective but cellularize, gastrulate and activate high levels of zygotic gene expr

11 nic tissue allows the double null embryos to gastrulate and begin organogenesis, suggesting that extr

12 s of SRF(LacZ/)(+) "knock-in" mice failed to gastrulate and form mesoderm, similar to the findings of

13 EXT1 homozygous mutants fail to gastrulate and generally lack organized mesoderm and ext

14 Upon fus knockdown, embryos fail to gastrulate and show mesodermal differentiation defects t

15 nsistent developmental defects, a failure to gastrulate, and embryonic lethality, including changes i

16 Unlike Bmpr1a-null embryos, which fail to gastrulate, Bmpr-MORE embryos initiate gastrulation, but

17 velopment reveals that C5a knockdown embryos gastrulate, but approximately 90% develop a prolapse of

18 end on common actomyosin-based mechanisms to gastrulate, but different cell fate regulators, and, sur

19 duplications, and its embryos are small and gastrulate by simple invagination.

20 , like sea urchins, has an early embryo that gastrulates by invagination, but like vertebrates, has a

21 evelopment involves the aggregation of newly gastrulated cells into epithelial fields, as a prelude t

22 g this process remain unclear, as numbers of gastrulating cells are very limited.

23 d, targeting genes likely to be expressed in gastrulating cells or their neighbors.

24 he stalk of cytoplasm that normally connects gastrulating cells to the yolk mass.

25 g the cell shape or directional migration of gastrulating cells.

26 e mesendoderm cells were injected into early gastrulating chick embryos, which revealed that they int

27 transverse blastoderm isolates obtained from gastrulating chick embryos.

28 re of the colony, reminiscent of generalized gastrulating chordate embryos.

29 Mouse embryos lacking Bmpr1a fail to gastrulate, complicating studies on the requirements for

30 ryos homozygous for gammaGCS-HS(tm1) fail to gastrulate, do not form mesoderm, develop distal apoptos

31 gination of the mesodermal primordium in the gastrulating Drosophila embryo, the internalized cells m

32 Damaged DNA in syncytial and gastrulating Drosophila embryos delays the metaphase/ana

33 re we apply particle tracking velocimetry in gastrulating Drosophila embryos to measure the movement

34 lor imaging of fast cellular dynamics across gastrulating Drosophila embryos.

35 Embryos lacking DRhoGEF2 fail to gastrulate due to a defect in cell shape changes require

36 ated functions for the AVE in organizing the gastrulating embryo and indicate that visceral endoderm-

37 Fate allocation in the gastrulating embryo is spatially organized as cells diff

38 The organizer is a unique region in the gastrulating embryo that induces and patterns the body a

39 e derives from a small group of cells in the gastrulating embryo, known as "the organizer" in recogni

40 that patterns it into a tissue resembling a gastrulating embryo.

41 al cell intercalation and axial extension in gastrulating embryos and explants.

42 In gastrulating embryos, FOXF1 marks most extra-embryonic m

43 Compared with wild-type ES cells and gastrulating embryos, Oct4 repression is lost and its pr

44 tiating embryonic stem cells, and in vivo in gastrulating embryos, the lineage specification of early

45 re detected in the nascent mesoderm of early gastrulating embryos.

46 miR-17-5p expression within the mesoderm of gastrulating embryos.

47 rmal gene expression by TGFbeta signaling in gastrulating embryos.

48 is specifically expressed in the mesoderm of gastrulating embryos.

49 of gene expression in the dorsal ectoderm of gastrulating embryos.

50 th the embryonic germ layers, reminiscent of gastrulating embryos.

51 arrow domain in the ventral marginal zone of gastrulating embryos.

52 rom eggs depleted of xSmad8(11) mRNA fail to gastrulate; instead, at the time of gastrulation, they i

53 w that the Wnt-11 gene is expressed by newly gastrulated mesoderm cells within avian embryos.

54 l genetic fate mapping, that Mesp1+ cells in gastrulating mesoderm are rapidly specified into committ

55 y, Axial Protocadherin (AXPC), it subdivides gastrulating mesoderm into paraxial and axial domains.

56 that oriented tissue strain generated by the gastrulating mesoderm plays a major role in determining

57 aused an increase in the population of newly gastrulated mesodermal (NGM) cells that express the tran

58 establish the anterior-posterior axis of the gastrulating mouse embryo and is necessary later for mes

59 is expressed in the primitive streak of the gastrulating mouse embryo and is required for paraxial m

60 y in development, to define its roles in the gastrulating mouse embryo.

61 tegration of human NC cells (hNCCs) into the gastrulating mouse embryo.

62 e coexpressed in the primitive streak of the gastrulating mouse embryo.

63 mitive streak is the defining feature of the gastrulating mouse embryo.

64 This cell population is also present in gastrulating mouse embryos and generates haematopoietic

65 the epiblast and nascent Flk1(+) mesoderm of gastrulating mouse embryos using single-cell RNA sequenc

66 ng haematopoietic and vascular potential) in gastrulating mouse embryos.

67 essed in embryonic organizing centers of the gastrulating mouse, frog, fish, and chick.

68 DNA synthesis, initiated transcription, and gastrulated normally.

69 heckpoint defective and fail to cellularize, gastrulate or to initiate high-level zygotic transcripti

70 As an embryo gastrulates or makes neural tissue it shortens across th

71 en they became growth arrested and failed to gastrulate, pointing to the early essential role for hep

72 Because ventralized embryos still gastrulate, producing a mechanical force that strains th

73 e Wnt and Bmp signaling pathways pattern the gastrulating vertebrate embryo using a network of secret

74 t proteins stimulate TCF3 phosphorylation in gastrulating Xenopus embryos and mammalian cells.

75 ) and triggers rapid apoptotic cell death in gastrulating Xenopus embryos.

76 dergoing convergent extension in explants of gastrulating Xenopus embryos.

77 ogs scn5Laa and scn5Lab were detected in the gastrulating zebrafish embryo and subsequently in the em

78 age Caenorhabditis elegans embryo and in the gastrulating zebrafish embryo.

79 other transcription factors in real-time in gastrulating zebrafish embryos.