ライフサイエンスコーパス: mammalian embryo

1 rmally expressed in pluripotent cells of the mammalian embryo.

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

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

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

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

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

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

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

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

10 causes regression of Mullerian ducts in the mammalian embryo.

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

12 a pluripotent founder cell population in the mammalian embryo.

13 egulatory networks in the sparsely available mammalian embryo.

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

15 role for chordin during gastrulation of the mammalian embryo.

16 the structure responsible for implanting the mammalian embryo.

17 in morphogenesis and patterning of the early mammalian embryo.

18 al inputs necessary to pattern and shape the mammalian embryo.

19 from individual self-organizing units in the mammalian embryo.

20 es behind the regulative nature of the early mammalian embryo.

21 tween these states during development of the mammalian embryo.

22 etrically inherited fate determinants in the mammalian embryo.

23 ) cells located in the major arteries of the mammalian embryo.

24 ripotency is manifest in the preimplantation mammalian embryo.

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

26 formation and subsequent gastrulation in the mammalian embryo.

27 fiber cell differentiation in the developing mammalian embryo.

28 definitive erythrocytes in the liver of the mammalian embryo.

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

30 the earliest differentiated cell type of the mammalian embryo.

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

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

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

34 ultiple divergent progenitor lineages of the mammalian embryo.

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

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

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

38 amming is critical for normal development of mammalian embryos.

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

40 YY1 is essential for the development of mammalian embryos.

41 t also originate early during development of mammalian embryos.

42 Sry that is critical for masculinization of mammalian embryos.

43 also required for the normal development of mammalian embryos.

44 important in the development of polarity in mammalian embryos.

45 that observed in the ganglionic eminences of mammalian embryos.

46 e in highly photosensitive specimens such as mammalian embryos.

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

48 nciple source of catecholamine production in mammalian embryos.

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

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

51 the enteric and autonomic nervous systems of mammalian embryos.

52 d, partly due to the in utero development of mammalian embryos.

53 to the process of hair follicle formation in mammalian embryos.

54 anslated to ensure successful development of mammalian embryos.

55 s found in pre-, peri- and post-implantation mammalian embryos.

56 common inner cell mass (ICM) progenitors in mammalian embryos.

57 NA orchestrate the growth and development of mammalian embryos.

58 tage in response to physiological demands in mammalian embryos.

59 aplotype-resolved approach by applying it to mammalian embryos.

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

61 n factors important for DHS establishment in mammalian embryos.

62 rogramming of epigenetic states in plant and mammalian embryos.

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

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

65 segregation and maintenance of viability in mammalian embryos.

66 of the earliest epithelial morphogenesis in mammalian embryos.

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

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

69 me number, or aneuploidy, is common in early mammalian embryos, although the underlying cell biologic

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

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

72 les that cell competition plays in the early mammalian embryo and how they contribute to ensure norma

73 blishment of pregnancy in a postimplantation mammalian embryo and indicate that impairment of the Hip

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

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

76 re limited by the difficulty of working with mammalian embryos and by the relative scarcity of active

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

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

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

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

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

82 s during the key events that shape the early mammalian embryo, and discuss how they work together to

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

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

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

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

87 f their effects on HH-dependent processes in mammalian embryos, and their mechanism of action is uncl

88 nisms that explain how plasticity is lost in mammalian embryos are highlighted and crystallize a prop

89 ring maternal-to-zygotic transition (MZT) in mammalian embryos are not well-studied.

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

91 Cell fate decisions in early mammalian embryos are tightly regulated processes crucia

92 Polarization of the mammalian embryo at the right developmental time is crit

93 In the mammalian embryo, both sexes are initially morphological

94 During the trunk to tail transition the mammalian embryo builds the outlets for the intestinal a

95 cellular drivers of upper lip fusion in the mammalian embryo by establishing a live-imaging modality

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

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

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

99 Mammalian embryos can only survive if they attach to the

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

101 Mammalian embryos change shape dramatically upon implant

102 Yet, in mammalian embryos, concentrations change rapidly compare

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

104 Thus, mammalian embryos coordinate cellular- and tissue-level

105 W) culture system is a platform for in-vitro mammalian embryo culture that has been shown to enhance

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

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

108 How a mammalian embryo determines and arrives at its attachmen

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

110 Mammalian embryos develop in a low oxygen environment.

111 Although mammalian embryo development depends on critical protein

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

113 During early mammalian embryo development, a small number of cells ma

114 iption of zygotic genes and is essential for mammalian embryo development.

115 ed to ensure the developmental plasticity of mammalian embryo development.

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

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

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

119 Early mammalian embryos exhibit remarkable plasticity, as high

120 The mammalian embryo exhibits a remarkable plasticity that a

121 To implant in the uterus, the mammalian embryo first specifies two cell lineages: the

122 To implant in the uterus, mammalian embryos form blastocysts comprising trophectod

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

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

125 The caudal lateral epiblast of mammalian embryos harbours bipotent progenitors that con

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

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

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

129 date, single-cell RNA-sequencing studies of mammalian embryos have focused exclusively on eutherian

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

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

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

133 ast lineages occurs during maturation of the mammalian embryo in an ERK signal-dependent manner.

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

135 Preimplantation mammalian embryos in culture secrete autocrine growth fa

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

137 e our knowledge of DNA replication stress in mammalian embryos, in programming, and in reprogramming,

138 n period and determine that cells within the mammalian embryo initiate growth phase only at the time

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

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

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

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

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

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

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

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

147 The anterior-posterior axis of the mammalian embryo is laid down by the anterior visceral e

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

149 The early mammalian embryo is patterned by signals emanating from

150 The body plan of the mammalian embryo is shaped through the process of gastru

151 ic information modules pattern and shape the mammalian embryo is still lacking, mostly owing to the i

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

153 The amnion, an extra-embryonic tissue in mammalian embryos, is thought to provide crucial signali

154 In mammalian embryos, it has not been previously experiment

155 However, early mammalian embryos lack efficient spindle assembly mechan

156 In mammalian embryos, male and female external genitalia de

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

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

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

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

161 The first mitosis of the mammalian embryo must partition the parental genomes con

162 Upon fertilization, the mammalian embryo must switch from dependence on maternal

163 In mammalian embryos, myogenic precursor cells emigrate fro

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

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

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

167 While non-mammalian embryos often rely on spatial pre-patterning,

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

169 In mammalian embryos, proper zygotic genome activation (ZGA

170 ell open chromatin maps, representative of a mammalian embryo, provide access to the regulatory bluep

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

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

173 The mammalian embryo relies on maternal circulating retinoid

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

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

176 hat drive essential patterning events in the mammalian embryo remain poorly understood.

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

178 r programmes to shape the in vivo developing mammalian embryo remains unknown.

179 The mammalian embryo represents a fundamental paradox in bio

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

181 The mammalian embryo's caudal lateral epiblast (CLE) harbour

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

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

184 Mammalian embryos sequentially differentiate into trophe

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

186 ther, embryoids provide an in vitro model of mammalian embryo that displays extensive development of

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

188 In the mammalian embryo, the potential for self-organization is

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

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

191 ild a multiscale three-dimensional model for mammalian embryo to recapitulate the observed patterning

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

193 Dynamic metabolism is exhibited by early mammalian embryos to support changing cell fates during

194 pluripotency is required for cells in early mammalian embryos to transition away from heightened sel

195 Mammalian embryos transiently exhibit aerobic glycolysis

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

197 Pluripotent cells of the mammalian embryo undergo extensive chromatin rewiring to

198 Pluripotent cells in the mammalian embryo undergo state transitions marked by cha

199 is for the regulative abilities of the early mammalian embryo whereby fate decisions are coordinated

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

201 However, in mammalian embryos, which develop inside the mother, earl

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

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

204 pre-patterning triggered by fertilization in mammalian embryos, with important implications for under

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

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