ライフサイエンスコーパス: embryonic stage

1 elanogaster's ventral nerve cord at the late embryonic stage.

2 ints such as part of the male or part at the embryonic stage.

3 sential for the viability of plants from the embryonic stage.

4 ral patterning in a representative amphioxus embryonic stage.

5 T-1(-/-) mice to die of anemia during a late embryonic stage.

6 d cardiomyocyte contribution irrespective of embryonic stage.

7 he patterning of the neural tube at the same embryonic stage.

8 the murine homologue of APE1 die at an early embryonic stage.

9 e culture colony-forming unit (CFU-C) at the embryonic stage.

10 blocks lymphocyte differentiation at a late embryonic stage.

11 DNMT1 DNA methyltransferase die at an early embryonic stage.

12 neurons in ontogenetic radial clones at the embryonic stage.

13 urs when thalamic Tsc1 is deleted at a later embryonic stage.

14 (O-Ab) axis first develops during the early embryonic stage.

15 ic development of steroidogenic cells at the embryonic stage.

16 mined the onset of the glomerulopathy in the embryonic stage.

17 e the mammalian spinal cord (SC) at an early embryonic stage.

18 the musculature at the postmetamorphic E80% embryonic stage.

19 eled and 5-HTLIR axon profiles from the E80% embryonic stage.

20 significantly in post-natal lens compared to embryonic stages.

21 s, but no gross morphological defects during embryonic stages.

22 modeling of the craniofacial skeleton beyond embryonic stages.

23 promote distal epithelial maturation during embryonic stages.

24 cell fate in the dorsal spinal cord at early embryonic stages.

25 genesis and Fkh is required only during late embryonic stages.

26 gration showed no obvious abnormality during embryonic stages.

27 established sequentially and not until late embryonic stages.

28 dy to identify genes involved in these early embryonic stages.

29 ation are likely to function at the earliest embryonic stages.

30 l genes, leading to abnormalities at various embryonic stages.

31 with liver-selective expression of NPC1 from embryonic stages.

32 eine equivalent to 2-4 cups of coffee at two embryonic stages.

33 these predicted genes are expressed only in embryonic stages.

34 y and follow its morphogenesis through later embryonic stages.

35 ) that expressed ChAT transiently during the embryonic stages.

36 ed twists and breaks of cardioblasts at late embryonic stages.

37 y neurons expressing pacemaker properties at embryonic stages.

38 agile eggs that fail to develop beyond early embryonic stages.

39 x1 in the pancreatic exocrine lineage during embryonic stages.

40 adult CNS, few data are available concerning embryonic stages.

41 ges arising in the mouse spinal cord at late embryonic stages.

42 RMs) than the coactivator p300, during early embryonic stages.

43 ages as well as the survival of RGCs at late embryonic stages.

44 xed ancestry of these brain regions at early embryonic stages.

45 conditionally induced in smn mutants during embryonic stages.

46 out the possible actions of NGF during early embryonic stages.

47 l divergence between alpha- and gamma-MNs at embryonic stages.

48 kA(+)/TrkC(+) double positive cells at early embryonic stages.

49 ole in microglial establishment during early embryonic stages.

50 population here identified is restricted to embryonic stages.

51 the main olfactory epithelium starting from embryonic stage 11.5 through adulthood.

52 ndgut curvature that normally occurs between embryonic stage 12 and 15 to generate the characteristic

53 ells led to embryonic lethality around mouse embryonic stage 13.5, likely as a consequence of fetal a

54 Results from embryonic stages 24-46 are presented.

55 rior recess and posterior tubercle nuclei at embryonic stage 26, and dorsomedial hypothalamus at stag

56 issociated chick ciliary ganglion neurons at embryonic stages 34, 37, and 40.

57 n to erupt as mature taste buds (stage 4) by embryonic stage 48.

58 e only the rt transcript is present at early embryonic stages (5 and 6), suggesting its maternal orig

59 thelium of the tongue primordium at an early embryonic stage, acquire epithelial cell phenotypes, and

60 as well as representative samples from post-embryonic stages across the life cycle.

61 synapses in zebrafish spinal cord at both an embryonic stage and a larval stage.

62 In late embryonic stage and adult mice, both genes are expressed

63 nrich neural progenitor cells from different embryonic stages and adult and compared their gene expre

64 pproximately 450-kDa form expressed in early embryonic stages and an approximately 350-kDa form obser

65 to implement cartilage size and shape across embryonic stages and between species simultaneously, pro

66 tants, we examined GATA-1 expression at late embryonic stages and found some blood cell differentiati

67 f 5 kb pairs was detected for D-AKAP2 in all embryonic stages and in all adult tissues tested.

68 e Drosophila Nidogen (Ndg) gene at different embryonic stages and in four mesodermal cell types is go

69 lobase pairs was detected for D-AKAP1 in all embryonic stages and in most adult tissues, cDNA cloning

70 arker of arterial endothelial cells (ECs) at embryonic stages and is essential for cardiovascular dev

71 ntral nervous system (CNS) beginning at late embryonic stages and its levels remain high in the adult

72 lates homeobox Pax6 gene expression in early embryonic stages and plays a dominant role in eye develo

73 om brain and eye tissues obtained at several embryonic stages and postnatal days.

74 its boundary to the embryonic body at early embryonic stages and the fate of cells constituting this

75 Mice mutant for PTEN die at early embryonic stages and the mutant embryonic fibroblasts di

76 Mouse cerebellar development occurs at late embryonic stages and through the first few weeks of post

77 h quickly fuse to the medial elements at the embryonic stage, and that the postparietals are homologo

78 ubiquitously in adult tissues and at various embryonic stages, and expression in adult testis is high

79 nicotine exposed during the vulnerable post-embryonic stages, and identified new biomarkers for nico

80 ouse, Cfh expression was observed from early embryonic stages, and in the eye its expression increase

81 KLF6 transcript level in eyes enucleated at embryonic stages, and the corneas and lenses isolated at

82 , ovary, testes, embryonic stem cells, three embryonic stages, and whole newborns.

83 becoming apparent at the four- to eight-cell embryonic stage; and (3) may play a key role in the cont

84 ve) progenitors in the limb buds at the late embryonic stage ( approximately E12), a significant numb

85 tudy tissue-specific gene expression in post-embryonic stages are challenging.

86 c receptors, however, at both early and late embryonic stages are those having high affinity for alph

87 n various developmental processes during the embryonic stage as well as in regulating tissue homeosta

88 anglion of the chick differentiates at early embryonic stages as VIIIth nerve axons enter the brainst

89 to regulate the generation of RGCs at early embryonic stages as well as the survival of RGCs at late

90 ining mammalian LHRH mRNA arises at an early embryonic stage before the migration of bona fide LHRH n

91 s can be observed occurring independently in embryonic stages before becoming coordinated at hatching

92 g late fetal development, whereas at earlier embryonic stages (before day E15), rolling and adhesion

93 Thin spongy myocardium is critical at early embryonic stage [before embryonic day (E) 13.5 in mice]

94 In the lens epithelium, it was high during embryonic stages but decreased with development.

95 hroughout the endodermal epithelium at early embryonic stages but excluded from the region that will

96 dc1 and nadc2 genes are not expressed at the embryonic stage, but the expression is detectable all th

97 NA is sufficient for progression through the embryonic stages, but larval organs show asynchronous an

98 ail body axis of vertebrates is elongated in embryonic stages by "convergent extension" tissue moveme

99 expression from the ovary and several early embryonic stages by deep sequencing followed by computat

100 ssion in mouse for several adult tissues and embryonic stages by Northern blot analysis and in situ h

101 tion but disruption of the STAT3 gene during embryonic stages causes lethality.

102 ine-binding receptors at both early and late embryonic stages contain alpha4 and beta2 subunits, repr

103 The data show that, even at late embryonic stages, corneal keratocytes are not terminally

104 We conclude that flow-sorted embryonic-stage Crx-positive donor cells have the potent

105 Only the embryonic-stage Crx-positive donor cells integrated with

106 differentiation was observed throughout the embryonic stages, defining decreased differentiation as

107 ical analysis of BMPER(-/-) embryos at early embryonic stages demonstrates that commencement of coron

108 In syncytial embryos, Piwi displays an embryonic stage-dependent localization pattern.

109 10-fold higher number of rods compared with embryonic-stage donors.

110 c-78 and aipl-1 arrested development at late embryonic stages due to severe disorganization of sarcom

111 wever, comparative studies focusing on early/embryonic stages during insect development are limited t

112 ing the major period of neurogenesis between embryonic stages (E) 10.5 and E13.5.

113 At late embryonic stages (e.g., 5-7 days after fertilization), r

114 g wild-type and Dlx5 null otic vesicles from embryonic stages E10 and E10.5.

115 Ca2+ channel current (ICa) density in early embryonic stages (E11-13) of beta2-AR transgenic positiv

116 following in utero electroporation (IUEP) at embryonic stage E14.

117 tive lesions in cardiac myocytes at the late embryonic stage (E16.5-E18.5), leading to approximately

118 protocol can be applied to aortic rings from embryonic stage E18 through to adulthood and can incorpo

119 ce homozygous for Gpx4_U46S died at the same embryonic stage (E7.5) as Gpx4(-/-) embryos as expected.

120 In embryonic stages, E9-12, anti-ELF localized to the prima

121 At early embryonic stages (embryonic day [E] 12-13) pre-tongue ex

122 Two embryonic stages, embryonic day 13 (E13) and E15-16, and

123 RNA and maternal GNE protein at the earliest embryonic stage, emphasizing the critical role of gne in

124 vity is lacking in the nuclear extract of an embryonic-stage erythroid line expressing zeta-globin.

125 ortical neurons was markedly impaired at the embryonic stage, even though hyperphosphorylation of tau

126 eginning at E12.5, persisting throughout all embryonic stages examined although in older embryos and

127 s observed in all muscle lineages and at all embryonic stages examined.

128 ler transcript (4.5 kb) was seen at the four embryonic stages examined.

129 ity phenotypes similar to Vangl2 KOs at late embryonic stages except that Vangl2 CKO mice are viable

130 At early embryonic stages, expression of Sim2 is immediately down

131 dence of thermal local adaptation during the embryonic stage for developmental rate or survival.

132 along the developing axon tracts and by late embryonic stages form a sheath around all neuropile comp

133 on of Scr-RNAi at both of the final two post-embryonic stages (fourth and fifth) did result in format

134 eflect their genetic profile rather than the embryonic stage from which they were derived.

135 s studied in ascidian muscle cells at twelve embryonic stages from gastrulation to the mature cell, a

136 re, conditionally deleting Gbx2 at different embryonic stages has revealed a sustained role of Gbx2 i

137 At early embryonic stages, high Ctbp2 levels sustain Notch signal

138 At late embryonic stages, however, dramatic neurodegeneration le

139 Axon removal during late embryonic stages, however, elicits an increase in prolif

140 ion and Purkinje cell topography during late embryonic stages; however, this phenotype was Shh indepe

141 From early embryonic stages, immune cells are faced with a barrage

142 ration program, being activated at different embryonic stages in different plant species.

143 hybridization studies during mid-late human embryonic stages in normal tissue showed restricted FRMD

144 ved in positional identity regulation at key embryonic stages in other animals display persisting reg

145 of retinoic acid (RA) across a wide range of embryonic stages in the chick embryo.

146 Examination of different embryonic stages in the mutants revealed that the mispos

147 In contrast, M6b was expressed at early embryonic stages in the ventricular zone of the spinal c

148 ck cranial ganglia were evaluated at various embryonic stages in vitro and related to its receptor ex

149 Zebrafish dscam is also present at early embryonic stages including blastulation and gastrulation

150 ernal product and peak ESC expression during embryonic stages indicate that ESC is most critical duri

151 Examination of earlier embryonic stages indicates that the association of macro

152 d in cerebellar Purkinje cells from the late embryonic stage into adulthood.

153 rm at mesenchyme blastula stage and at later embryonic stages is refined to just the stomodael openin

154 s expressed very transiently during an early embryonic stage, it has been difficult to determine whet

155 ited to the ovary, oocyte, egg and the early embryonic stages leading up to the mid-blastula transiti

156 Downregulation of FGFR2b signaling during embryonic stages led to abnormal development of the labi

157 ion patterns of Tcf/Lef factors during these embryonic stages led us to examine whether different Tcf

158 s undergo segment-specific apoptosis at late embryonic stages, long after they have extended their ax

159 g in the distal limb primes the ZRS at early embryonic stages maintaining a poised, but inactive stat

160 oli cells can be traced back to neonatal and embryonic stages, making this the earliest known molecul

161 by immunohistochemistry in newborn and late embryonic stage mice.

162 matopoietic tissues at embryonic day 9.5, an embryonic stage not previously described to harbor HSCs.

163 tested one of these relationships using the embryonic stage of a Chinook salmon population.

164 of the gamma-gene remained restricted to the embryonic stage of development, whereas in humans, expre

165 use developing central nervous system during embryonic stages of active axonogenesis.

166 Although morphological changes during embryonic stages of anuran development have been well do

167 on a role for ephrin-B2 during the earliest embryonic stages of arterial/venous determination, our c

168 Sp1(-/-) cells progress through most embryonic stages of blood cell development but cannot co

169 ns in the brain during NP-C disease, even at embryonic stages of development prior to the onset of ph

170 3 protein is present in brain cells in early embryonic stages of development, and in cultured neural

171 During the embryonic stages of development, when both p27(Kip1) and

172 hereas comparative transcriptomic studies of embryonic stages of hemimetabolous insects are completel

173 is expressed selectively but transiently at embryonic stages of myogenesis in the developing myotome

174 d with the calyceal processes from the early embryonic stages of outer segment growth onwards.

175 sed on tumour and host tissue are now in the embryonic stages of trying to identify genes which may h

176 ed at the dorsal margin of the eye disc from embryonic stages on, acts upstream of wingless to contro

177 in the regulation of cell proliferation from embryonic stages onward, through the function of the cen

178 both are essential for plant viability from embryonic stages onward.

179 rulation, and has not been observed in later embryonic stages or in adult tissues.

180 Neurog3 in insulin-expressing beta cells at embryonic stages or in Pdx1-expressing islet cells in ad

181 Moreover, the vascular pattern at each embryonic stage prefigured the mineral distribution patt

182 Thus, from the earliest embryonic stages, progenitors of the retina are a dynami

183 ions exhibit immature properties of an early embryonic stage, raising concerns about their ability to

184 s was markedly prolonged in cells from early embryonic stages relative to later stages of development

185 Full maintenance at late embryonic stages requires additional sequences adjacent

186 onditional ablation of COUP-TFII at an early embryonic stage resulted in failed formation of pre-lymp

187 Removal of the beta1 integrins at an embryonic stage resulted in severe cortical lamination d

188 (1)/S transition, especially during the late embryonic stages, resulting in a reduced progenitor pool

189 by conditional deletion of Smad4 at the late embryonic stage, results in the formation of abnormal ba

190 lysis of RARalpha beta2(-) mutant kidneys at embryonic stages revealed that nephrons were formed and

191 PMC transplantations at late embryonic stages revealed that these cells remain fusion

192 s of pigeon and chicken retinas at different embryonic stages reveals that the genetic programmes und

193 During late embryonic stages, Sema 1a expression in the mushroom bod

194 nt a cell lineage of the early embryo and an embryonic staging series.

195 centrotus purpuratus, including 10 different embryonic stages, six feeding larval and metamorphosed j

196 screen for proteins that are degraded in an embryonic stage-specific manner.

197 stages of heart development and during later embryonic stages, suggestive of a specialized role for T

198 This is a much earlier embryonic stage than previously described for centipedes

199 er, many studies are conducted on a range of embryonic stages that are not fully represented in the b

200 This approach was performed at three embryonic stages that are prior to, or coincident with,

201 nt fraction of total Dlx5 transcripts at all embryonic stages that were examined.

202 L-/R-symmetry-breaking event at a very early embryonic stage, the six-cell stage, which also establis

203 At early embryonic stages, the neural tube contains multipotentia

204 At early embryonic stages, the SMP is bilateral, surrounding the

205 ervous system and skeletal muscle from early embryonic stages through adulthood.

206 epigenetically poised (bivalent) state from embryonic stages through the end of meiosis.

207 lation of Mfsd2a results in a leaky BBB from embryonic stages through to adulthood, but the normal pa

208 pithelial cells of the middle ears from late embryonic stages through to day 13 of postnatal life.

209 nervous system, changing over time from the embryonic stage to the adult stage.

210 pressed in postmitotic cortical neurons from embryonic stages to adulthood and in the proliferative r

211 In retina, RHBDD2 is expressed from embryonic stages to adulthood, and its levels show age-d

212 e gland, HOXB13 is highly expressed from the embryonic stages to adulthood.

213 aracterized its neuroanatomical profile from embryonic stages to adulthood.

214 forelimb and hindlimb autopods at sequential embryonic stages to decipher the molecular events that u

215 lanocyte differentiation, rather than during embryonic stages to establish their stem cell precursors

216 pathetic neurons die by apoptosis from early embryonic stages to perinatal stages.

217 tracts that once formed normally during the embryonic stages underwent dramatic degeneration postnat

218 a and DeltaCm increased with maturation from embryonic stages until postnatal day 6 (P6).

219 ensity of labeled cells continued during the embryonic stages, until around birth.

220 fate control and pattern formation at later embryonic stages using a combination of laser microsurge

221 The frequency of GnRH release in the late embryonic stage was surprisingly high, reaching a maximu

222 At the embryonic stage, we found that PSD-95 puncta outnumber g

223 t-negative form of a Bmp receptor at various embryonic stages, we determined when Bmp signaling was r

224 hedgehog (Shh) and Gli1 lineages at varying embryonic stages, we performed a quantitative and qualit

225 omain that were positive for GABA markers at embryonic stages were also positive for GLYT2, suggestin

226 the skeletal abnormalities observed at later embryonic stages were caused by delayed or defective pre

227 nuclear layer (ONL) were ChAT-IR during the embryonic stages, were less immunoreactive during the po

228 blastocyst stage of a ball of cells and the embryonic stage when almost all organ systems begin to d

229 ssed manyfold higher in desiccation-tolerant embryonic stages when compared with intolerant nauplius

230 no indication of any of these phenotypes at embryonic stages when heads perceive no significant mech

231 ribution directly by the rhombic lip at late embryonic stages when hRPe is no longer present; indeed,

232 n of these elements is maintained during the embryonic stages when the bulk of the genome is being de

233 re" set of 6,794 transcripts - shared by all embryonic stages - which are mainly involved in anatomic

234 of Nav1.2, Nav1.3, Nav1.6 and beta3 mRNA at embryonic stages whilst Nabeta1.1 and Nabeta2.1 mRNA was

235 Rnd3-null mice died at the embryonic stage with fetal arrhythmias.

236 nerated from MLC2a-Cre (CFKO-2a) died in the embryonic stage with thin ventricular wall and ventricul

237 t IGF2 expression varied significantly among embryonic stages with expression being 50% higher in ear

238 ation of melanophores that differentiated at embryonic stages, with a diminished contribution from me

239 and analyze key morphogenetic events during embryonic stages X to 11.