ライフサイエンスコーパス: postimplantation

1 sed HLA class I antibody response at 2 years postimplantation.

2 ested from adult rat recipients 1 to 8 weeks postimplantation.

3 arge tumors (ca. 2000 mm(3)) treated 66 days postimplantation.

4 biomicroscopy and histologically for 8 weeks postimplantation.

5 d in uncoated alginate spheres after 2 weeks postimplantation.

6 meta-analysis of up to 2 years of follow-up postimplantation.

7 ly vascularized intracutaneous site by day 7 postimplantation.

8 ze the second-generation prostheses geometry postimplantation.

9 nic cell types drives epiblast morphogenesis postimplantation.

10 ilaments penetrated through the mesh by 3 mo postimplantation.

11 1 and 6 months, and 1, 2, 3, 4, and 5 years postimplantation.

12 re scheduled at 1, 2, 3, 6, 9, and 12 months postimplantation.

13 dard parameters during the first five months postimplantation.

14 and was not associated with excess bleeding postimplantation; 8 of the 9 treated livers were free of

15 nse and seamless interface with brain tissue postimplantation achieved by ultraflexible open mesh ele

16 ser refractive surgery, LAL implantation and postimplantation adjustment provide a precise refractive

17 outcomes included heart transplantation and postimplantation adverse event rates.

18 other atrial tachyarrhythmias (AF/AT), or if postimplantation AF/AT modulate the benefits of CRT-D, r

19 ntation Apnea-Hypopnea Index (AHI) score and postimplantation AHI of less than 15 events per hour.

20 Together, immediate postimplantation allograft Prevotella/Streptococcus rati

21 Catheters were removed at 7 and 14 days postimplantation and analyzed for hydroxyproline (OHP, n

22 Corresponding image slices on postimplantation and follow-up IVUS studies of 11 malapp

23 re TGF-beta family members that regulate the postimplantation and midgestation stages of pregnancy.

24 f the defect sites were harvested at week 16 postimplantation and processed for histometric analysis

25 ear singularly in some of the cysts by day 8 postimplantation and were observed in approximately 85%

26 ICP (39+/-4 vs. 19+/-5 cm H2O at seven days postimplantation) and corresponding accelerated neurolog

27 designed algorithm based on timing (pre- and postimplantation) and location (central or peripheral) o

28 mbryonic and extraembryonic tissues at early postimplantation (approximately E5.5-6.5), coincident wi

29 e suture contamination and biofilm formation postimplantation are warranted.

30 Postimplantation bacterial meningitis was strongly assoc

31 ged with magnetic resonance (MR; 3.0 T) 11 d postimplantation before and after intravenous administra

32 ion development, but become fully methylated postimplantation by de novo methylation of the paternal

33 With the aim of improving postimplantation cell survival and pulp tissue regenerat

34 nant, and engineered grafts continue to face postimplantation challenges.

35 Baseline and postimplantation clinical correlates of stroke events we

36 r soon after implantation may help to reduce postimplantation clinical risks.

37 A major postimplantation complication is cerebrovascular vascula

38 on of support per patient has increased, the postimplantation complications have become more apparent

39 tocyst axis of symmetry into the axes of the postimplantation conceptus involves asymmetric visceral

40 Postimplantation, CoreValve was associated with a larger

41 At postimplantation day 12, the recipients were evaluated f

42 r infiltration of the graft when examined at postimplantation day 12.

43 weighted and T1-weighted postcontrast MRI by postimplantation day 40.

44 g/day, respectively, for 5 days beginning on postimplantation day 7.

45 Implanted EVPOMEs' histology on the seventh postimplantation day was used to correlate outcomes of g

46 sive mutation, 94-A/K, that results in early postimplantation death of the embryos, and we have mappe

47 Monitoring graft-host interactions postimplantation demonstrated that the 14-d in vitro-cul

48 Computed tomography angiograms at 12 months postimplantation demonstrated the stent:transverse arch

49 on of Fgf4, which plays an important role in postimplantation development and growth and patterning o

50 is globally expressed at high levels during postimplantation development and its conditional ablatio

51 methylation of the mouse genome during early postimplantation development and of maternally imprinted

52 It follows that FGFR2 is required for early postimplantation development between implantation and th

53 Mettl14 is required for mouse postimplantation development by facilitating epiblast ma

54 Most advances in early human postimplantation development depend on animal studies an

55 ernal-fetal interface is essential for early postimplantation development in mice.

56 c growth through a surge of VIP during early postimplantation development in the rodent.

57 etic events during preimplantation and early postimplantation development in vitro.

58 Postimplantation development is characterized by stage-

59 The transition from preimplantation to postimplantation development leads to the initiation of

60 In a model for postimplantation development, addition of FGF-4 to blast

61 PGCs are specified during early mammalian postimplantation development, and are uniquely programme

62 -wide accumulation of H3K9me2 is crucial for postimplantation development, and coincides with redistr

63 ities in both late preimplantation and early postimplantation development.

64 rtilized mouse eggs disturbed their pre- and postimplantation development.

65 r, less is known about the role of NO during postimplantation development.

66 of DNA methylation patterns during pre- and postimplantation development.

67 the earliest differentiation events of human postimplantation development.

68 le in all adult somatic tissues and in early postimplantation development.

69 maternal-fetal interface of mice throughout postimplantation development.

70 ice and may exert a critical function during postimplantation development.

71 ic and extraembryonic tissue lineages during postimplantation development.

72 bit a high frequency of failure in peri- and postimplantation development.

73 d shape were found throughout pre- and early postimplantation development.

74 enesis and leading to differentiation during postimplantation development.

75 o be visualized in situ to examine the early postimplantation distribution of clones obtained by tran

76 d 5 years as assessed by preimplantation and postimplantation Doppler echocardiography and 12-month c

77 Primate ESCs correspond to the postimplantation embryo and fail to resume development i

78 ognize imprinted genes but are absent in the postimplantation embryo and in ES cells.

79 of cells in the extraembryonic region of the postimplantation embryo and in trophoblast stem cells.

80 We discuss that although polarity of the postimplantation embryo can be traced back to the 8-cell

81 on modes and highlights the need to optimise postimplantation embryo culture protocols.

82 iblast cells and thus the development of the postimplantation embryo in mice.

83 the dynamics of metabolic regulation in the postimplantation embryo in vivo have remained elusive du

84 he blastocyst, stem cell populations and the postimplantation embryo provides new insights into early

85 y all trophectoderm descendants in the early postimplantation embryo through E8.5, then disappears ex

86 ld provide cues that predict the axes of the postimplantation embryo, we have used the strategy of in

87 late with the anterior-posterior axis of the postimplantation embryo.

88 nt trophoblast cells that surround the early postimplantation embryo.

89 n of these cells to distinct lineages of the postimplantation embryo.

90 mplantation structure to directly assemble a postimplantation embryo.

91 n in the blastocyst are also utilized in the postimplantation embryo.

92 Mbd3 is known to be essential for postimplantation embryogenesis in mice, but the function

93 ere report that METTL14 is indispensable for postimplantation embryonic development by facilitating t

94 l peptide, a neuropeptide regulator of early postimplantation embryonic growth, and the neuroprotecti

95 PECAM expression is next documented in the postimplantation embryonic yolk sac, where clumps of mes

96 Igf2 monoallelic expression is initiated in postimplantation embryos and that the single remaining C

97 nt epiblast stem cells (EpiSCs) derived from postimplantation embryos exhibit properties that are cha

98 sts derived from medulloblastoma nuclei form postimplantation embryos with typical cell layers.

99 DeltaDMD and H19Delta3.8kb-5'H19 in pre- and postimplantation embryos, we show that the DMD exhibits

100 methylation in embryonic stem (ES) cells and postimplantation embryos.

101 germ cell, in a few epiblast cells of early postimplantation embryos.

102 l myostatin deficiency were conferred by the postimplantation environment.

103 onship between sister cells in non-chimaeric postimplantation epiblast by ionophoretic injection of a

104 of investigation because PGCs originate from postimplantation epiblast cells in vivo.

105 cell fate decisions in rapidly proliferating postimplantation epiblast cells.

106 le with Prdm14 during PGC specification from postimplantation epiblast cells.

107 r the derivation and maintenance of ESCs and postimplantation epiblast stem cells (epiSCs).

108 itated hPSCs are transcriptionally closer to postimplantation epiblast than conventional hPSCs.

109 c stem cell lines (ES cells), as well as the postimplantation epiblast, which gives rise to epiblast

110 development, despite being expressed in the postimplantation epiblast.

111 ing pluripotent cell lines equivalent to the postimplantation epiblast.

112 ression of SOX15 promotes the reversion of a postimplantation, epiblast stem cell state back to a pre

113 c and distinct enhancer elements that govern postimplantation expression in the somitic myotomes and

114 occurs towards the region where the earlier postimplantation expression of Cer1 was strongest.

115 naive pluripotency factors are exchanged for postimplantation factors, but competent cells remain dev

116 8 children, 136 of whom completed the wave 3 postimplantation follow-up visits (77 [55%] female) with

117 the secondary end point of mortality during postimplantation follow-up were compared in PFO versus n

118 ptide (VIP) has been shown to regulate early postimplantation growth in rodents through central nervo

119 onality was an independent associate of poor postimplantation health status for 6 of 8 of the SF-36 s

120 plantation to 5.3 (2.6-12.3) events per hour postimplantation (Hodges-Lehman difference of 23.0; 95%

121 antation to 21.8 (4.30-42.6) events per hour postimplantation (Hodges-Lehman difference of 24.6; 95%

122 In vitro models of postimplantation human development are valuable to the f

123 because of the inaccessibility of the early postimplantation human embryo for study.

124 In this study, postimplantation human epiblast and amnion development a

125 DX2(+)/p63(+) CTB subpopulation in the early postimplantation human placenta that is significantly re

126 tinue to use the HA in the contralateral ear postimplantation in order to determine whether or not th

127 gh this methylation is not maintained during postimplantation in the absence of the DMD.

128 ct of the uterine decidua and a regulator of postimplantation intrauterine events.

129 g) behind the strut, and where the immediate postimplantation IVUS revealed complete apposition of th

130 on mouse chromosome 8 associated with early postimplantation lethality in homozygotes and abnormal d

131 hatase, resulted in developmental arrest and postimplantation lethality.

132 ortion results from disrupted imprinting and postimplantation loss of mutant embryos.

133 associated with enrichment in the immediate postimplantation lung of oropharyngeal anaerobic taxa, p

134 Gastruloids, stem cell models of postimplantation mammalian development, provide a platfo

135 the successful progression of both pre- and postimplantation mammalian development.

136 tial for the establishment of pregnancy in a postimplantation mammalian embryo and indicate that impa

137 e the first cell type to be specified in the postimplantation mammalian embryo and serve highly speci

138 lar assist device (VAD), requires meticulous postimplantation management.

139 isions about MCS use (DT versus bridge), and postimplantation mortality, transplantation, rehospitali

140 anscription factor TEAD4 ensures survival of postimplantation mouse and human embryos by controlling

141 repair pathway is essential for normal early postimplantation mouse development and implicate an endo

142 he blastocyst stage and is ubiquitous during postimplantation mouse development, while the maternal E

143 rm (VE) is an epithelial tissue in the early postimplantation mouse embryo that encapsulates the plur

144 In the early postimplantation mouse embryo the ECM component laminin

145 d recapitulate many features of the pre- and postimplantation mouse embryo, including gastrulation.

146 In an early postimplantation mouse embryo, TEAD4 is selectively expr

147 the mouse, is essential for survival of the postimplantation mouse embryo.

148 n methylomes for early lineages in peri- and postimplantation mouse embryos.

149 ogenitor cells (TSPCs), and loss of Tead4 in postimplantation mouse TSPCs impairs their self-renewal,

150 brane grafting was performed in all cases of postimplantation necrosis (n = 10), but 8 eyes required

151 However, postimplantation, NMP organs had significantly shorter K

152 I) was performed in both preimplantation and postimplantation nuclear transfer embryos.

153 red healing extraction sockets 6 to 8 months postimplantation of a bioactive glass (BG) or deminerali

154 I) at day (d) 18 (preimplantation) and d 34 (postimplantation) of gestation.

155 At 6 months postimplantation, only the cell-seeded engineered uteri

156 out MCS use (DT versus bridge) but important postimplantation outcomes.

157 , vascular measurements for access planning, postimplantation paravalvular regurgitation (PVR), and t

158 focused on attitudes toward hearing aid use postimplantation, patterns of usage, and perceived bimod

159 y day 11 after pump implantation; by 25 days postimplantation, PC2(-/-) islets were indistinguishable

160 ach beneficiary's pre- (percent DAOH-BF) and postimplantation (percentage of DAOH-AF) follow-up time.

161 ls of left atrial appendage (LAA) closure, a postimplantation peridevice leak (PDL) of <=5 mm (PDL<=5

162 sion with increasing angiogenesis during the postimplantation period (days 5-8).

163 lve function was comparable to the immediate postimplantation period (mean transvalvular peak velocit

164 of major NAEs than is HVAD beyond the early postimplantation period and during the constant hazard p

165 sm by which the embryos survive at the early postimplantation period by pooling maternal blood in the

166 al and trophoblast ADA died during the early postimplantation period, whereas expression in trophobla

167 nonhuman primate embryogenesis in the early postimplantation period, with possible relevance to huma

168 s well as resorption of embryos in the early postimplantation period.

169 VR RBBB was defined as new-onset RBBB in the postimplantation period.

170 pilot study was to evaluate the findings of postimplantation PET/CT of 90Y glass microspheres.

171 ein receptor type 2 (BMPR2) is essential for postimplantation physiology and fertility.

172 timulation titration protocol for conducting postimplantation polysomnograms.

173 Postimplantation predictors were VVIR cumulative percent

174 Lymph node dissection and postimplantation prostatic biopsies were not routinely p

175 decision (odds ratio, 1.76; P = 0.017); and postimplantation pump exchange and occurrence of AEs (ha

176 After a 1-month postimplantation recovery period, unblinded FCS was acti

177 ist, and cellular distribution and viability postimplantation remain key issues.

178 Low baseline ejection fraction (EF) and postimplantation RVA-paced or spontaneous QRSd predicted

179 Echocardiographic measurements 28 days postimplantation showed significantly improved RV functi

180 oscopy of the T9/mM-CSF tumor site, 2-4 days postimplantation, showed marked infiltration by macropha

181 At 7 d postimplantation, significantly less DNA damage and high

182 of preoperative aided speech recognition and postimplantation speech recognition.

183 ine non-redundant roles for TET1 at an early postimplantation stage of the mouse embryo, when its par

184 ing mouse embryo results in lethality at the postimplantation stage, demonstrating that it is an esse

185 From the two-cell to the postimplantation stage, methylation of the paternal geno

186 errant and restricted lineage priming at the postimplantation stage, which leads to early embryonic l

187 ull embryos exhibited lethality at the early postimplantation stage.

188 nt in maintaining IAP methylation during the postimplantation stage.

189 During early postimplantation stages Ada is highly expressed in both

190 ias observed in the blastocyst persists into postimplantation stages and therefore has relevance for

191 ntation development from blastocyst to early postimplantation stages by using an in vitro coculture s

192 ransgene system for controlled expression at postimplantation stages, we found that Nanog blocks prim

193 and myometrial smooth muscle at even earlier postimplantation stages.

194 methylation during preimplantation and early postimplantation stages.

195 human development and allow access to early postimplantation stages.

196 knowledge of natural mouse embryos at early postimplantation stages.

197 do detect such enrichment in data from later postimplantation stages.

198 inactive in the extraembryonic structures at postimplantation stages.

199 Leaching potentials peak at 5-30 days postimplantation, suggesting that targeted timing of imp

200 Postimplantation survival and adverse events were compar

201 Rapid blood perfusion is critical for postimplantation survival of thick, prevascularized bioa

202 A stroke event significantly lowered 2-year postimplantation survival regardless of subtype or initi

203 e grafts increased with progressively longer postimplantation survival times.

204 The postimplantation syndrome after EVAR may delay recovery

205 Statistically significant trends in the postimplantation temporal dependence of oxygen content b

206 formation of fibrovascular tissue at 14 days postimplantation than the control or DeltavirB2-infected

207 fect, with tumor growth inhibition at day 28 postimplantation (the day control animals began to requi

208 At 1 mo postimplantation, the graft lumen was fully endotheliali

209 At 24.1 +/- 6.5 months postimplantation, the keratoprosthesis was retained in a

210 Commonly, acute, postimplantation thrombocytopenia causes significant ble

211 located away from the suture strut at a mean postimplantation time of 77.4 months (range, 33 to 132 m

212 eic VM/Dk mice, analyzing animals at various postimplantation time points using dynamic microPET imag

213 escent, and adult mice and were evaluated at postimplantation times up to 15 months.

214 The greatest increase was seen from postimplantation to 6 months.

215 Impressions were obtained pre- and postimplantation to determine changes in alveolar ridge

216 From postimplantation to follow-up, arterial curvature and an

217 mporal dynamics of brain functional networks postimplantation to identify predictors of outcomes and

218 Here, we tracked the pre- to postimplantation transition of the trophoblast lineage i

219 our data provide a comprehensive analysis of postimplantation trophoblast differentiation that can be

220 use development from the eight-cell stage to postimplantation using lineage-specific RNA sequencing.

221 n, fertilization, and implantation; however, postimplantation uterine decidual cells showed terminal

222 an average 4.5-h period showed satisfactory postimplantation valve function.

223 Baseline and postimplantation variables were used to predict HFH in t

224 he progeny of inner cell mass cells into the postimplantation visceral endoderm.

225 The main reasons for postimplantation vision loss was glaucoma (12/31, 39%),

226 h an attempted LP retrieval at least 6 weeks postimplantation were included.

227 ng rabbits were treated on days 6, 9, and 12 postimplantation with alpha(nu)beta(3)-targeted fumagill

228 is presumed that impedance fluctuates early postimplantation, with implications for variations in cu

229 tly inhibited tumor growth for up to 50 days postimplantation, with negligible animal body weight los

230 changes in impedance within the first month postimplantation, with no further variation.

231 and visual-only speech tasks at 1 mo and 1 y postimplantation, with speech understanding assessed aft