ライフサイエンスコーパス: somite stage

1 imately at 24 hr of development around the 3-somite stage).

2 tectable in host embryos before stage 12 (16-somite stage).

3 omozygous embryos is arrested prior to the 8-somite stage.

4 Pea3 and Er81) from early blastula to the 10 somite stage.

5 d causes developmental arrest before the one somite stage.

6 y in the neural crest, beginning at the five-somite stage.

7 gratory neural crest cells occur at the five-somite stage.

8 entral portion of the MHB beginning at the 8-somite stage.

9 ing by the anterior neural ridge at the five-somite stage.

10 cells to the placode at least until the four-somite stage.

11 ta1 expression is partly inhibited at the 10-somite stage.

12 eclining rapidly in donors older than the 10-somite stage.

13 ain and repression of Otx2 as early as the 7-somite stage.

14 as disrupted normal development at the early somite stage.

15 o arise every 5-10 min up to at least the 16-somite stage.

16 eart development, if performed before the 18-somite stage.

17 first Pax-3-positive cells begins at the 13-somite stage.

18 e presumptive posterior hindbrain at the 6-8 somite stage.

19 in and the rostral hindbrain at the 8- to 10-somite stage.

20 DFC migration or cohesion in the tailbud at somite stages.

21 haryngeal endoderm at the crescent and early somite stages.

22 ll death in the mes/met between the 7 and 30 somite stages.

23 bryonic hematopoiesis) between the 21- to 26-somite stages.

24 or expansion of the Otx2 domain during early somite stages.

25 regional domains of gene expression at early somite stages.

26 STARS) first occurs in the somites by the 16 somite stage [17 hours post fertilization (hpf)].

27 to 13-somite stages (beating begins at the 9-somite stage), a time span of about 23 h.

28 terior to posterior progression until the 22 somite stage, after which time QmyoD is activated in som

29 col14a1a expression peaked between 18-somite stage and 24 hours postfertilization (hpf), where

30 tube if the ablation is done prior to the 5-somite stage and no regeneration after the 6-somite stag

31 between the one-somite and the six- to eight-somite stages and is solely dependent on Wnt1 function i

32 ulation valley at approximately the 16-to 18-somite stage, and at 24 hours postfertilization (hpf), a

33 f17, Fgf18, and Gbx2 in the mes/met at early somite stages, and in the absence of the midbrain and ce

34 at lead to convergent extension during early somite stages, and that these cell rearrangements fail i

35 -) embryos, the mes/met is deleted by the 30 somite stage ( approximately E10).

36 then was eliminated in the mes/met by the 10 somite stage ( approximately E8.75).

37 right asymmetry (L/R), are observed at early somite stages ( approximately E8.5) [1, 2].

38 pancreatic mesenchyme between the 26 and 27 somite stages (approximately 10.0 dpc) and became interm

39 ow-tract smooth muscle cells) through the 14-somite stage at approximately 8.75 days after fertilizat

40 Hand1-null mice survived to the nine somite stage at which time they succumbed to numerous de

41 ly heart forming regions in situ at 2- to 13-somite stages (beating begins at the 9-somite stage), a

42 ardium in mice at embryonic day (ED) 8.5 (12 somite stage) before the onset of AV mesenchymal cell fo

43 on of the first somite and occurs at the 4-6 somite stage, before neural tube closure.

44 acodal invagination continues through the 35-somite stage, by which time condensation of the trigemin

45 he notochord tip between the 4-somite and 12-somite stage causes posterior expansion of the Nkx2.5-ex

46 In addition, early somite stage chimeras generated by injecting Lim1(-)(/)(

47 umptive opV placode ectoderm occurs by the 8-somite stage, concomitant with robust Pax-3 expression.

48 sion in the early embryo up to the 30- to 35-somite stage, declining from Incubation Day 4 on and bec

49 lemented with retinoic acid until only the 6-somite stage, demonstrating that retinoic acid is only n

50 rentiated myocytes, however, appeared in two somite-stage-dependent phases.

51 In our model, specification occurs during somite stages due to varying Hedgehog protein levels, wh

52 ur period from mid-primitive streak to early somite stages (E7.25 to E8.5), when the conceptus underg

53 Rather, HPP-CFC were detected first at early somite stages (E8.25), exclusively in the yolk sac.

54 By early somite stages (E8.5), GATA-2 mRNA expression is downregu

55 When BMP-2 protein was added to the 16-18 somite stage (ED 9.25) AV endocardial endothelium in cul

56 ain is present in virtually all BLs of early somite stage embryos and then becomes restricted to spec

57 shown by the intermediate sensitivity of 4-5 somite stage embryos bearing only a single effective p53

58 is gene, dissections were performed on early somite stage embryos during an eight-hour time window of

59 In somite stage embryos, Cerr1 expression is restricted to

60 We screened for genes expressed in early somite-stage embryos that respond oppositely to treatmen

61 In late somite-stage embryos, lft1 and lft2 are expressed asymme

62 data, and in situ hybridization analysis of somite-stage embryos, we carried out comparative analyse

63 At early somite stages, endodermal cells located at least two cel

64 During head-fold and somite stages, expression was restricted to vascular end

65 alogous ablations are performed at the 10-12 somite stage, however, a marked increase in the numbers

66 halmic placode is observed as early as the 4-somite stage in a narrow band of ectoderm contiguous to

67 During somite stages in no tail embryos, connexin43.4 expressio

68 Gene expression analysis during early somite stages indicates that spc4 is genetically upstrea

69 ized to the hindbrain neural crest at the 15-somite stage, indicating a critical role for foxd3 in th

70 At late somite stages, left-sided southpaw expression transientl

71 ween the opV and mmV placodes even at the 16-somite stage, long after neurogenesis has begun in the o

72 bel exposed anterior endoderm cells of early somite stage mouse embryos, cultured the embryos into th

73 ession pattern in the presomitic mesoderm of somite stage mouse embryos.

74 ns of the diencephalon and midbrain in early somite-stage mouse embryos.

75 At the six- to eight-somite stage nodal is expressed transiently in the left

76 mlin RNA expression is upregulated at the 35 somite stage of development.

77 est adjacent to somites 3-6, prior to the 13-somite stage of development.

78 At the 4/5 somite stage of HH8, when retinoid signaling is initiate

79 ulation, which is initiated during the early somite stages of development when the embryo begins to e

80 ing such that during late gastrula and early somite stages of embryogenesis, Wnt activity must be sup

81 From the 8-somite stage onwards, significant numbers of cells are c

82 sue, which is evident at the presomite-early somite stage prior to the onset of Fgf8 neuroectodermal

83 ablation of dorsal r5 and r6 prior to the 10 somite stage, r4 neural crest cells migrate along normal

84 of retinoids to VAD embryos prior to the six-somite stage rescues the expression of nodal, cSnR, and

85 oic acid to VAD embryos at or before the 4/5 somite stage rescues the expression of RARalpha2 and RAR

86 expressed in placodal ectoderm from the 4-5 somite stage (ss) onwards, well before the otic placode

87 ax3(+/+) littermates (embryonic day 10.0; 30 somite stage), suggesting that Pax3 regulation of TGFbet

88 We have now determined that at the 15- to 17-somite stage, the prospective diencephalon is the most-a

89 , the brain caudalizes, and at the 22- to 24-somite stage, the prospective thalamic territory is the

90 At the 3-somite stage, the whole head ectoderm rostral to the fir

91 ted PE specification role for Tbx5a at early somite stages; this role occurs earlier than, and appear

92 ethality of the Disp1(C829F) allele at early somite stages through the supply of non-cholesterol modi

93 ryos show that Cubn is required during early somite stages to convey survival signals in the developi

94 eural keel and cranial mesoderm during early somite stages to promote first pouch formation.

95 ls, labeled by lipophilic dye at the 4- to 6-somite stage, to regions of the heart at 20 to 25 somite

96 found that grafted sclerotome fragments from somite stages V-XX were capable of giving rise to integr

97 At early somite stages, VAD embryos have increased cell death in

98 nner cells (DFCs) from gastrulation to early somite stages when these cells form a ciliated Kupffer's

99 detected) and in the heart at the 14- to 18-somite stage (when only HGF ligand can be detected).

100 At the most advanced somite stages, when completion of spinal closure is immi

101 e endocardial progenitors as early as the 10-somite stage which suggests that Hh signaling is require

102 left wall of the KV between the six- and 12-somite stages, which is coincident with known left-sided

103 somite stage and no regeneration after the 6-somite stage with either ablation procedure.

104 enotypes: embryos fail to turn, arresting at somite stages with a small, linear heart tube, an open g

105 on in forebrain pattern is evident by the 12-somite stage, with most neuraxes lacking telencephalon a

106 We show that in gastrula and early-somite stage Xenopus embryos, Wnt/beta-catenin activity

107 the second phase, dorsomedial quadrants from somite stages XI-XIII consistently form morphologically

108 ed to the cartilage fate do not appear until somite stage XII, but that not all sclerotome cells are

109 Presomite whole embryos and somite-staged yolk sac and embryo proper cells were plat