ライフサイエンスコーパス: mammalian embryo

1 causes regression of Mullerian ducts in the mammalian embryo.

2 hat Gdf1 provides a Vg1-like function in the mammalian embryo.

3 a pluripotent founder cell population in the mammalian embryo.

4 ion factors that are used to regionalize the mammalian embryo.

5 role for chordin during gastrulation of the mammalian embryo.

6 ripotency is manifest in the preimplantation mammalian embryo.

7 rtant roles in many organs of the developing mammalian embryo.

8 fiber cell differentiation in the developing mammalian embryo.

9 definitive erythrocytes in the liver of the mammalian embryo.

10 tween these states during development of the mammalian embryo.

11 and is the first migratory cell type in the mammalian embryo.

12 the earliest differentiated cell type of the mammalian embryo.

13 been established in either the chick or the mammalian embryo.

14 to facilitate L-R axis establishment in the mammalian embryo.

15 etermines left-right patterning in the early mammalian embryo.

16 ultiple divergent progenitor lineages of the mammalian embryo.

17 vern BMP target gene expression in the early mammalian embryo.

18 on and establishment of the body plan of the mammalian embryo.

19 first functional organ in both the avian and mammalian embryo.

20 rmally expressed in pluripotent cells of the mammalian embryo.

21 oles for Galpha13 in other cell types in the mammalian embryo.

22 p1 function in Hh-mediated patterning of the mammalian embryo.

23 nal organ that develops in both the bird and mammalian embryo.

24 tion of axons, and implantation of the early mammalian embryo.

25 -dependent local and long-range effects in a mammalian embryo.

26 maintaining cell-cell adhesions in the early mammalian embryo.

27 r the maintenance of progenitor cells in the mammalian embryo.

28 tical from early on for the viability of the mammalian embryo.

29 Sry that is critical for masculinization of mammalian embryos.

30 also required for the normal development of mammalian embryos.

31 important in the development of polarity in mammalian embryos.

32 that observed in the ganglionic eminences of mammalian embryos.

33 e in highly photosensitive specimens such as mammalian embryos.

34 rom the indifferent gonad (genital ridge) in mammalian embryos.

35 nciple source of catecholamine production in mammalian embryos.

36 eled the distribution of alpha-internexin in mammalian embryos.

37 opic X chromosome inactivation, and death of mammalian embryos.

38 the enteric and autonomic nervous systems of mammalian embryos.

39 ivered from sperm, are eliminated from early mammalian embryos.

40 n factors important for DHS establishment in mammalian embryos.

41 rogramming of epigenetic states in plant and mammalian embryos.

42 n, is required for the normal development of mammalian embryos.

43 udy gene regulation by T3 in uterus-enclosed mammalian embryos.

44 segregation and maintenance of viability in mammalian embryos.

45 of the earliest epithelial morphogenesis in mammalian embryos.

46 amming is critical for normal development of mammalian embryos.

47 ive cardiac mesoderm in amphibian, bird, and mammalian embryos.

48 YY1 is essential for the development of mammalian embryos.

49 t also originate early during development of mammalian embryos.

50 In mammalian embryos, a receptor tyrosine kinase proto-onco

51 nce a major determinant of oxygen tension in mammalian embryos after implantation is embryonic blood

52 In the mammalian embryo, an understanding of the dynamic nature

53 al output of a Shh-patterning process in the mammalian embryo and a framework for elaborating regulat

54 t mosaicism to study cell segregation in the mammalian embryo and integrate live-cell imaging to exam

55 type to be specified in the postimplantation mammalian embryo and serve highly specialized, essential

56 des a framework for quantitative analyses of mammalian embryos and establishes GATA6 as a nodal point

57 cytochrome P450 family that is expressed in mammalian embryos and in brain and is induced by RA in t

58 ells, embryoid body-derived cells (EBCs), or mammalian embryos and is a significant obstacle to stem

59 trithorax, maintains Hox gene expression in mammalian embryos and is rearranged in human leukemias r

60 l and spatial patterns of gene expression in mammalian embryos and therefore play important roles in

61 of Zic3 during left-right patterning in the mammalian embryo, and provide basis for further understa

62 t cells to differentiate from the developing mammalian embryo, and they subsequently form the blastoc

63 d extension (CE) driving axial elongation in mammalian embryos, and in particular, the cellular behav

64 symmetric position of the meiotic spindle in mammalian embryos, and the developmental potential of th

65 wn to be important for muscle development in mammalian embryos are those encoding the basic helix-loo

66 In the mammalian embryo, both sexes are initially morphological

67 iologically active factors to the developing mammalian embryo by in utero gene transfer has generated

68 Cell identity is specified in the early mammalian embryo by the generation of precursors for two

69 In vitro manipulation of preimplantation mammalian embryos can influence differentiation and grow

70 Mammalian embryos can only survive if they attach to the

71 Since the short-term, in vitro culture of mammalian embryos can result in DNA methylation changes,

72 e NC-derived RET+ population of fetal gut in mammalian embryos consists of multipotential progenitors

73 ell lineage specified in the preimplantation mammalian embryo depends on intrinsic factors for its de

74 pare this to the role of Oct4 in maintaining mammalian embryo-derived stem cells.

75 Early-stage mammalian embryos develop in a low O(2) environment (hyp

76 Mammalian embryos develop in a low oxygen environment.

77 A critical event in mammalian embryo development is construction of an inner

78 In the mammalian embryo, DLGH1 is essential for normal urogenit

79 ation of primordial germ cells (PGCs) in the mammalian embryo does not depend on maternal determinant

80 The preimplantation development of the mammalian embryo encompasses a series of critical events

81 Early mammalian embryos exhibit remarkable plasticity, as high

82 In early mammalian embryos, GATA3 is selectively expressed in the

83 e two first cell fate decisions taken in the mammalian embryo generate three distinct cell lineages:

84 of cytoplasmic flows for the development of mammalian embryos has been unknown.

85 thways that control development of the early mammalian embryo have remained poorly understood, in par

86 during the first cell-fate determination in mammalian embryos have been debated for years.

87 Cells of early mammalian embryos have the potential to develop into any

88 is the first reported use of nanocrystals in mammalian embryo imaging.

89 K cells are recruited in high numbers to the mammalian embryo implantation sites, yet remain pregnanc

90 he foregut region of late gastrula avian and mammalian embryos in a pattern that overlaps with expres

91 Preimplantation mammalian embryos in culture secrete autocrine growth fa

92 matopoiesis initiates within the yolk sac of mammalian embryos in overlapping primitive and definitiv

93 e (NT) formation in the spinal region of the mammalian embryo involves a wave of "zippering" that pas

94 The preimplantation mammalian embryo is a paradigm of tissue self-organizati

95 orta, gonad, mesonephros (AGM) region of the mammalian embryo is crucial for development of the adult

96 Development of the mammalian embryo is dependent upon temporally and spatia

97 The developing mammalian embryo is entirely dependent on the maternal c

98 ter implantation, the basic body plan of the mammalian embryo is established during gastrulation when

99 Establishment of cell polarity in the mammalian embryo is fundamental for the first cell fate

100 development, although direct evidence in the mammalian embryo is lacking.

101 raembryonic and embryonic tissues within the mammalian embryo is not as strict as believed and that a

102 The early mammalian embryo is patterned by signals emanating from

103 rigger that establishes cell polarity in the mammalian embryo is unclear.

104 In mammalian embryos, it has not been previously experiment

105 In mammalian embryos, male and female external genitalia de

106 t the role of extra-embryonic tissues in the mammalian embryo might not be to induce the axes but to

107 nd definitive (adult), was described for the mammalian embryo more than a century ago.

108 e successful development, cells of the early mammalian embryo must differentiate to either trophectod

109 During development, the mammalian embryo must integrate signals to control growt

110 In mammalian embryos, myogenic precursor cells emigrate fro

111 d and a transcriptional regulator per se The mammalian embryo obtains beta-carotene from the maternal

112 The ontogeny of the hematopoietic system in mammalian embryos occurs during the yolk sac (YS) and th

113 Transcriptional activation in mammalian embryos occurs in a stepwise manner.

114 In the developing mammalian embryo, one allele of a DMD is unmethylated, a

115 uratus) parallels nephron development in the mammalian embryo, providing a vertebrate model for kidne

116 ation of haemangioblasts, which is absent in mammalian embryos, raising the possibility that these ce

117 The mammalian embryo relies on maternal circulating retinoid

118 riation on gene regulation in the developing mammalian embryo remain largely unexplored.

119 e-specific gene expression in the developing mammalian embryo remain largely unknown.

120 nisms of lineage-specific gene regulation in mammalian embryos remain only partially defined.

121 The mammalian embryo represents a fundamental paradox in bio

122 Development of external genitalia in mammalian embryos requires tight coordination of a compl

123 The first cell differentiation in mammalian embryos segregates polarized trophectoderm cel

124 The earliest cell fate decision in the mammalian embryo separates the extra-embryonic trophobla

125 It has been generally accepted that the mammalian embryo starts its development with all cells i

126 conserved developmental domain in avian and mammalian embryos that contributes myocardium and smooth

127 In mammalian embryos, the expression of Insulin-like growth

128 c acid (atRA) can support development of the mammalian embryo to parturition in vitamin A-deficient (

129 o Schwann cell precursors, recently shown in mammalian embryos to populate post-embryonic parasympath

130 Mammalian embryos transiently exhibit aerobic glycolysis

131 e, the epithelial trophectoderm cells of the mammalian embryo undergo a phenotypic change that allows

132 is an important source of vitamin A for the mammalian embryo, which depends on its adequate supply t

133 ecification are problematic for the study of mammalian embryos, which has favored using pluripotent c

134 Two new protocols for infecting non-mammalian embryos with viruses, together with RNA inhibi

135 Growth and survival of the mammalian embryo within the uterine environment depends

136 In the early mammalian embryo, X chromosome inactivation (XCI) achiev