ライフサイエンスコーパス: early developmental stage

1 ing expression of the expanded CGG RNA at an early developmental stage.

2 fied pigment cell precursors at a relatively early developmental stage.

3 n a block to lymphomyeloid development at an early developmental stage.

4 of L1-80 contribute to brain development at early developmental stages.

5 a free form up to 9.85mg/g dry matter at the early developmental stages.

6 pecific gene expression events at these very early developmental stages.

7 e survival requirements for neurotrophins at early developmental stages.

8 s, even more simple versions are used during early developmental stages.

9 tes local oxygen to below baseline levels at early developmental stages.

10 ting only transiently, as cells pass through early developmental stages.

11 polarity by inhibiting dendrite outgrowth at early developmental stages.

12 ession and function of guidance molecules at early developmental stages.

13 es of polycomb repressive complexes (PRC) in early developmental stages.

14 gammadelta-transgenic mice at two sequential early developmental stages.

15 SI), the damage being most severe during the early developmental stages.

16 y gland sensory innervation of both sexes at early developmental stages.

17 etween two regulators are overrepresented in early developmental stages.

18 , leaves are not positioned at random during early developmental stages.

19 xhibit distinct molecular characteristics at early developmental stages.

20 aevis, a vertebrate well suited for study of early developmental stages.

21 ner cell mass and the epiblast of embryos at early developmental stages.

22 lis expressed sequence tags (ESTs) from four early developmental stages.

23 tners for nutrient supply, especially during early developmental stages.

24 oduction, in that the ONL appeared normal in early developmental stages.

25 propriate cDNA collections, particularly for early developmental stages.

26 d to suppress beta-globin gene expression at early developmental stages.

27 been shown to cause cardiac toxicity during early developmental stages across fishes.

28 At early developmental stages, alpha4 protein and mRNA were

29 ignaling promotes cardiac differentiation at early developmental stages and inhibits it later.

30 eavily expressed in neuronal growth cones at early developmental stages and its activation engages sm

31 n manipulated MITF RNA and protein levels at early developmental stages and observed decreased expres

32 We isolated thymocytes from early developmental stages and observed that suspensions

33 anatomy and molecular studies to clarify the early developmental stages and position of corona initia

34 le of these transcription factors beyond the early developmental stages and provide mechanistic links

35 All these features are more severe in early developmental stages and show substantial recovery

36 Annual plants grow vegetatively at early developmental stages and then transition to the re

37 in-12 in AC/VU cell fate specification at an early developmental stage, and functions downstream of f

38 olution, particularly for genes expressed at early developmental stages, and resulting in high specia

39 x1, expressed in the presumptive midbrain at early developmental stages, and the hindbrain at later s

40 Early developmental stages are highly sensitive to stres

41 Early developmental stages are ideal targets for amphibi

42 significant decrease in etsrp expression at early developmental stages as measured by quantitative r

43 al immunoblots of total proteins at selected early developmental stages, as well as EMSA of egg and 1

44 ived from ESCs correspond consistently to an early developmental stage at which the yolk sac and feta

45 alpha-1 was broadly expressed in the gut at early developmental stages, at which times soluble GFR a

46 nown whether these channels are expressed at early developmental stages, before gliogenesis or angiog

47 Xenopus can normally regenerate its limbs at early developmental stages but loses the ability during

48 ozygous matings produced Xrcc1-/- embryos at early developmental stages, but not Xrcc1-/- late-stage

49 Many TDMRs are methylated at early developmental stages, but unmethylated later, sugg

50 -reducing root nodules, may be favored at an early developmental stage by lumichrome, a previously un

51 lial cells regulate the number of neurons at early developmental stages by dynamically influencing ne

52 at broad ectopic activation of Notch at very early developmental stages causes induction of prosensor

53 sion of lamp in limbic regions, beginning in early developmental stages, combined with the results of

54 ttranscriptional control, MB neurons born at early developmental stages contain more abundant Chinmo

55 d BEST1 expression in the periphery, from an early developmental stage, could provide a mechanism tha

56 At early developmental stages (E10.5, E15.5), FgfrL1-defici

57 tral domains of the neuroepithelial layer at early developmental stages (E2.5-E4).

58 In early developmental stage (EDS) cells (from 7+3d to 7+5d

59 promelas) exposed to CAFO ditchwater during early developmental stages exhibited significantly skewe

60 cusing on the immunostimulation of different early developmental stages for gaining a more comprehens

61 , the increase was smaller and restricted to early developmental stages for rats.

62 At early developmental stages, glutamatergic synapses are s

63 liferative effects only on cardiomyocytes in early developmental stages, glycogen synthase kinase-3 a

64 pulating endosperm proliferation at a rather early developmental stage in crops.

65 phosphorylation of tau at tyr18 occurred at early developmental stages in mouse but was absent in th

66 These genes are expressed at early developmental stages in the embryonic nervous syst

67 at the extensive abnormalities formed during early developmental stages in the peripheral nervous sys

68 t plants became hypersensitive to ABA in the early developmental stages, including seed germination a

69 Parasites blocked at an early developmental stage inside hepatocytes elicit a pr

70 echanism by which endoglin functions at this early developmental stage is currently unknown.

71 quantification of the mutant viruses at the early developmental stage is even more challenging, as t

72 t its function in bone formation beyond this early developmental stage is unknown.

73 here that the level of VRN-1 transcripts in early developmental stages is critical for flowering ini

74 p63-deficient mice does not progress past an early developmental stage: it lacks stratification and d

75 We hypothesized that plasma of an early developmental stage, namely umbilical cord plasma,

76 contributing cells to the arterial valves at early developmental stages, NCC persistence in the valve

77 acquisition of stimulus-evoked exocytosis at early developmental stages occurs independent of both po

78 Such 3-D hECTs recapitulate an early developmental stage of human myocardium and promis

79 suggest that MFO activity is an index of an early developmental stage of the respiratory system.

80 istinguish the effects of stressors on three early developmental stages of each of three species: (i)

81 ial distribution and speciation of Se in the early developmental stages of fish, which provide import

82 ntrinsically hindered the transition between early developmental stages of NK cells, whereas overexpr

83 nt implications for the understanding of the early developmental stages of self-awareness, self-regul

84 and generation of L1-80 coincide in time at early developmental stages of the cerebral cortex.

85 oblotting assays to characterise PABP in the early developmental stages of the clam Spisula solidissi

86 ransactivator (tTA) that causes lethality in early developmental stages of the heterozygous progeny b

87 uring development and provide little hint at early developmental stages of the rich functional divers

88 ffect the internal concentrations already in early developmental stages of the ZFE.

89 They also show that the early developmental stages of these T cells are not gove

90 culties in histologically defining nuclei at early developmental stages, our understanding of the mec

91 At early developmental stages, physiologically high PI3K-Ak

92 Thus, pnr has dual function, during early developmental stages pnr is involved in axial patt

93 This indicates that, at early developmental stages, Ptch2 functions to suppress

94 eover, though the block of Shh signalling at early developmental stages results in the loss of chick

95 The transcript was widely detected in early developmental stages, showing the highest expressi

96 At early developmental stages somatostatin receptors couple

97 From early developmental stages, sonic hedgehog (Shh) and ind

98 e competitive advantage of the gamma gene at early developmental stages, stable transgenic mouse line

99 und that ciliary assembly occurs only during early developmental stages, supporting the idea that mat

100 We found that promoters that are active in early developmental stages tend to be CG rich and mainly

101 We show that during early developmental stages the strong expression of endo

102 vasculature scaffold in the RMS and, during early developmental stages, the RMS contains only a few

103 equence evolution, especially for genes from early developmental stages, thereby leading to animal sp

104 romoter 1 of the KOR gene and expressed from early developmental stages through adult life.

105 LEC1 gene and showed that it functions at an early developmental stage to maintain embryonic cell fat

106 ial subpallium-derived amygdalar nuclei from early developmental stages to adult.

107 shows how cells can become committed during early developmental stages to execute a specific fate mu

108 sympathetic neuron development; Fz3 acts at early developmental stages to maintain a pool of dividin

109 terenol, forskolin, and 8-bromo-cAMP in very early developmental stage (VEDS) cardiomyocytes (from 7+

110 ions between sensory axons and skin cells at early developmental stages, we conducted a detailed anal

111 When CCR7 was studied at early developmental stages, we detected a progressive in

112 At early developmental stages when GABAergic inputs dominat

113 aving localized NT-3 and trk C expression at early developmental stages when retinal neuroepithelial

114 , exon 18b is predominantly expressed during early developmental stages, while exon 18a is prevalent

115 However, null mutant mice die at an early developmental stage with severe malformations, and