ライフサイエンスコーパス: morula

1 These phenotypes suggest that morula acts to block mitosis-promoting activity in both

2 e behavior of Gsc-null cells was examined in morula aggregation chimeras.

3 eaving embryos but restored again in compact morula and blastocyst stages.

4 lastomere, polyploid blastomere, compaction, morula and blastocyst-like stages by light, scanning ele

5 e, two-cell, four-cell, eight-cell, 16-cell, morula and blastocyst.

6 Nurse cells in female-sterile alleles of morula begin to become polyploid but revert to a mitotic

7 gene expression blocking development at the morula-blastocyst transition.

8 ere defects at 3.5 d.p.c. (days post-coitus) morula/blastocyst stage and lethality before 8.5 d.p.c.

9 onstructed oocytes developed in vitro to the morula/blastocyst stage, and 8% of these embryos develop

10 ear localization of activated MAPK occurs in morula/blastula stage embryo animal and marginal zones c

11 is involved in blastocyst formation from the morula by regulating accumulation of fluid and different

12 chimeric partner elimination is a cytotoxic morula cell (MC).

13 We show that morula compaction and ICM formation depend on PC7 and th

14 ranes of the 8-cell-stage embryo just before morula compaction.

15 male embryos were able to progress from the morula/early blastocyst stage to more advanced stages of

16 Blastomeres are removed from morula (eight-cell)-stage embryos and cultured until the

17 I hypersensitive sites in mouse zygotes and morula embryos, and investigate the epigenetic mechanism

18 Cyclin E protein levels decline in morula embryos, while cyclin E mRNA levels remain high.

19 ensis but was notably found on extracellular morula fibers in morulae containing dense-cored organism

20 lls, and it was found extracellularly in the morula fibrillar matrix and associated with the morula m

21 pherules demonstrating segmentation mimicked morula forms of Prototheca spp.

22 In addition to its role in the endo cycle, morula function is necessary for dividing cells to exit

23 We show that the Drosophila morula gene is essential to maintain the absence of mito

24 of mouse chimeras using traditional diploid morula<-->diploid embryonic stem (ES) cell aggregations.

25 ialized tetraploid chimeras using tetraploid morula<-->diploid ES cell aggregations.

26 Since the morula membrane is the interface between the ehrlichial

27 trated that MmpA was localized mainly on the morula membrane of E. canis.

28 A gene encoding a 23.5-kDa ehrlichial morula membrane protein designated MmpA was cloned by sc

29 the fibrillar matrix and associated with the morula membrane, the host cell cytoplasm, and the nucleu

30 ula fibrillar matrix and associated with the morula membrane.

31 The Drosophila morula (mr) gene regulates variant cell cycles, because

32 n B protein to be inappropriately present in morula mutant nurse cells.

33 are both arrested in metaphase in different morula mutants.

34 Thus morula serves a dual function as a cell cycle regulator

35 owth of bacteria, concomitant with increased morula size.

36 thality, with embryos dying at or before the morula stage after only two to four cell division cycles

37 one modifications between blastomeres at the morula stage and cell sub-populations in blastocysts, di

38 suggesting ectopic Tspo silencing before the morula stage and demonstrating elevated embryonic lethal

39 yst homogenates but not those of two-cell or morula stage embryos.

40 from the wild-type paternal alleles: at the morula stage in embryos lacking maternal E-cadherin, and

41 3Galbeta1,R), which causes compaction in the morula stage of the preimplantation mouse embryo, as wel

42 for the correct specification of TE from the morula stage onwards and that both maternal and zygotic

43 fection of murine preimplantation embryos at morula stage with lentiviral vectors resulted in stable

44 mally if compaction does not occur until the morula stage, and that the zona pellucida suffices to ma

45 on caused a total loss of methylation by the morula stage, but by the epiblast stage, the repeats wer

46 cripts were first detected in embryos at the morula stage, close to the time of blastocoele formation

47 At the morula stage, rafts were also apically enriched in each

48 failure of TE specification, starting at the morula stage.

49 s that BMPs regulate cell cleavage up to the morula stage.

50 l stage or lineage gene transcription at the morula stage.

51 zygotes leads to developmental arrest at the morula stage.

52 leavage stages, but then arrested before the morula stage.

53 sts in zygotes and early embryos through the morula stage.

54 the cell surface from the 1-cell through the morula stage.

55 mouse preimplantation embryos from 1-cell to morula stage.

56 ed each cell with a zonular belt by the late morula stage.

57 betaine; Bhmt mRNA is first expressed at the morula stage; BHMT is abundant at the blastocyst stage b

58 We used morula-stage aggregation as a strategy to further clarif

59 Chimerism with 3F-iPS derived by morula-stage diploid aggregation was sustained during pr

60 Production of chimeras by morula-stage embryo aggregation is an effective way to u

61 protein was isolated from 8- to 16-cell and morula-stage embryonic libraries of two distantly relate

62 he intracellular Ca2+ concentration in mouse morula-stage embryos, providing evidence for the existen

63 n mouse embryos lacking pescadillo arrest at morula stages of development, the nucleoli fail to diffe

64 ed human embryos develop beyond cleavage and morula stages to form a blastocyst in vitro.

65 In strong, larval lethal alleles of morula, the polytene ring gland cells also inappropriate

66 embryos, where it blocks the transition from morula to blastocyst during embryonic development.

67 orphological and functional changes from the morula to blastocyst stage.

68 e and protein expressions, but also inhibits morula to blastocyst transformation in a concentration-d

69 t tight junction formation plays any role in morula to blastocyst transformation that is associated w

70 key genes in TE lineage, and is involved in morula to blastocyst transformation.

71 embryos reduces Cdx2 expression and inhibits morula to blastocyst transformation.

72 sure of embryos to DKK1 during the period of morula to blastocyst transition (between d 5 and 8 of de

73 Induced deletion of Oct4 during the morula to blastocyst transition disrupts the ability of

74 arance of ZO-1 suggests its participation in morula to blastocyst transition.

75 of the development of mouse embryos from the morula to early blastocyst stage, based on 4D confocal i

76 deficient embryos failed to proceed from the morula to the blastocyst stage because of defects in the

77 n contrast, genic silencing initiates at the morula-to-blastocyst stage and absolutely requires Xist.

78 ected by RT-PCR, greatly increase during the morula-to-blastocyst transition and seven of the eight k

79 t repression of p21 transcription during the morula-to-blastocyst transition.

80 OCK1 and ROCK2 activity during the 8-cell to morula transition phenocopied TFAP2C knockdown, triggeri

81 During the 8-cell to morula transition TFAP2C potentiates cell polarity to su

82 neously assimilate into preimplantation host morula via diploid aggregation, unique to bona fide plur