ライフサイエンスコーパス: fetal tissue

1 logy, were not found within the transplanted fetal tissue.

2 gs on chimeric maternal cells that reside in fetal tissue.

3 at myelin disorders is limited at present to fetal tissue.

4 ocortex in paraformaldehyde-fixed postmortem fetal tissue.

5 fection in lymphocytes, placenta, and bovine fetal tissue.

6 in response to increased invasiveness of ape fetal tissue.

7 variants of at least 500 kb in placental or fetal tissue.

8 own's syndrome and control post-mortem human fetal tissue.

9 uman neoplasms because they are derived from fetal tissue.

10 nd mTORC2 signaling in multiple maternal and fetal tissues.

11 blood leukocytes, placenta, lung, aorta, and fetal tissues.

12 f mRNA transcripts in a variety of adult and fetal tissues.

13 tantial reactions were also found in certain fetal tissues.

14 observed in lung, pancreas and spleen and in fetal tissues.

15 ripts by northern-blot analysis of adult and fetal tissues.

16 han those seen in first and second trimester fetal tissues.

17 ceeded those observed in the placenta and in fetal tissues.

18 LCK isoform(s) in both human adult and human fetal tissues.

19 w splice variants of Bright were observed in fetal tissues.

20 is ubiquitously expressed in both adult and fetal tissues.

21 subunit, was investigated in human adult and fetal tissues.

22 ntion of a maternal immune attack on foreign fetal tissues.

23 and dentate gyrus in the adult brain and to fetal tissues.

24 xpression and is greatly enhanced in various fetal tissues.

25 ze all-trans-retinol and steroid alcohols in fetal tissues.

26 ent of these cells in second trimester human fetal tissues.

27 els of viral RNA in maternal, placental, and fetal tissues.

28 ity and increases infection of placental and fetal tissues.

29 r ACD cells, contribute to the allantois and fetal tissues.

30 the control of metabolism and maturation of fetal tissues.

31 t for BH(4) compared with maternal and other fetal tissues.

32 dinated interactions between endometrial and fetal tissues.

33 es the loss of Rb in both extraembryonic and fetal tissues.

34 d more rapid uptake and clearance than other fetal tissues.

35 d on embryonic stem cells derived from human fetal tissues.

36 r mechanisms of the immune response to human fetal tissues.

37 and has a tendency for higher expression in fetal tissues.

38 region that is differentially methylated in fetal tissues.

39 delicate balance of active hormone levels in fetal tissues?

40 the fetoplacental interface and in numerous fetal tissues, 2) ex vivo, the placenta released high am

41 is, VHL mRNA was reverse transcribed from 13 fetal tissues (8-10 weeks gestation).

42 It is widely expressed in fetal tissues, abundantly expressed in adult thymus, bon

43 7me3) was lower in the Zfp423 promoter of OB fetal tissue, accompanied by reduced binding of enhancer

44 was found predominant in a variety of human fetal tissue, adult tissues, and several carcinomas.

45 y contribute to oxidative damage observed in fetal tissues after in utero ethanol exposure.

46 A number of exploratory studies using human fetal tissue allografts have suggested that transplantat

47 f-1L have similar distributions in adult and fetal tissues, although apaf-1L transcripts are more abu

48 gnant women may result in acute infection of fetal tissue and brain tissue, causing microcephaly and

49 ry cilium in developing podocytes from human fetal tissue and in undifferentiated cultured podocytes.

50 in adult skeletal muscle but very low in the fetal tissue and in undifferentiated skeletal muscle cel

51 human samples, including 17 adult tissues, 7 fetal tissues and 6 purified primary haematopoietic cell

52 Abundantly expressed in fetal tissues and adult muscle, the developmentally regu

53 Amounts of gadolinium chelate in the fetal tissues and amniotic fluid were minimal compared w

54 ntigen-presenting cells can be identified in fetal tissues and are related to adult populations of an

55 and KCNQ1OT1, with monoallelic expression in fetal tissues and biallelic expression in adult samples.

56 Immunohistochemistry studies of human fetal tissues and bioinformatics analysis of a microarra

57 is expressed in proliferating cells such as fetal tissues and cancers.

58 d widespread beta-gal expression in multiple fetal tissues and cell types.

59 P-C in reproductive, placental, and selected fetal tissues and fetal fluid, PrP-Sc was detected only

60 Sc) in reproductive, placental, and selected fetal tissues and fetal fluids in sheep.

61 was present in reproductive, placental, and fetal tissues and fetal fluids.

62 ion is based upon histopathologic changes in fetal tissues and identification of tissue parasites by

63 methylation of 56 CpG sites was observed in fetal tissues and in adult blood DNA.

64 ase isozyme M2 (hPKM2) is expressed in early fetal tissues and is progressively replaced by the other

65 can penetrate the placental barrier to enter fetal tissues and is safe for use in pregnant mice.

66 endogenous CEA promoter; CEA is expressed in fetal tissues and normal gastrointestinal tissues, and C

67 ion of PCOLCE RNA in various human adult and fetal tissues and of Pcolce RNA at various stages of mou

68 Informative fetal tissues and PGL tumors demonstrate maternal alleli

69 tic domains, are expressed in neoplastic and fetal tissues and potentially have a role in embryonic d

70 The even distribution of PDE7A mRNA among fetal tissues and the relative abundance of its two mRNA

71 that appears to be primarily associated with fetal tissues and tumors.

72 decidual T cells proliferated in response to fetal tissue, and depletion of T regulatory cells led to

73 L. monocytogenes was isolated from fetal tissue, and the pathology was consistent with L. m

74 Gadolinium chelate levels in the placenta, fetal tissues, and amniotic fluid were obtained by using

75 ived neural progenitors and brain organoids, fetal tissues, and animal models.

76 gans, endothelial lining of the vasculature, fetal tissues, and carcinomas.

77 n thymus, bone marrow, fetal liver and other fetal tissues, and in all proliferating cell lines teste

78 Nox3 is expressed primarily in fetal tissues, and Nox4 is expressed in not only fetal t

79 tors, diminished ZIKV burden in maternal and fetal tissues, and protected against fetal demise.

80 eptor are widely expressed in both adult and fetal tissues, and recent gene-targeting and disruption

81 progenitor B (pro-B), pre-B, and B cells in fetal tissues, and thus supports the idea of a multifoca

82 transcripts were detected in human adult and fetal tissues, and very high transcript levels were foun

83 Despite profound placental abnormalities, fetal tissues appeared remarkably normal, suggesting tha

84 Although embryonic and fetal tissue are frequently envisaged as providing suffi

85 Epitheliasin transcripts in fetal tissues are observed only in kidney and lung.

86 Nox5 is expressed in a variety of fetal tissues as well as in adult spleen and uterus.

87 Expression of human TBX1 in adult and fetal tissues, as determined by Northern blot analysis,

88 for the first time its distribution in human fetal tissues, as well as its expression in adult kidney

89 sion of prolactin receptors (PRLRs) in human fetal tissues at 7.5-14 wk of gestation and in tissues o

90 nscription was detected in a wide variety of fetal tissues at both 8 and 14 weeks.

91 c expression patterns; they are expressed in fetal tissues, breast, and prostate, and in many cancers

92 n mRNA-binding protein that is abundant in a fetal tissue but either absent from or scarce in adult t

93 l tissues, and Nox4 is expressed in not only fetal tissues, but also kidney, placenta and glioblastom

94 ts are expressed in brain and lung tumor and fetal tissues, but are generally absent from normal adul

95 It is widely expressed, including in fetal tissues, but is most highly expressed in lymphoid

96 ocytosed nonspecifically and then carried to fetal tissues by a pH gradient from acidic endosomes to

97 By contrast, early in gestation, injured fetal tissues can be completely recreated, without fibro

98 Blood, highly perfused, and fetal tissues contained the highest levels of HPCs.

99 d CCR5 on T cells and their progenitors from fetal tissue, cord blood, SCID-hu Thy/Liv mice, and adul

100 roducts were observed in matching normal and fetal tissues; deleted cDNA sequence revealed canonical

101 nt mice and ICP-MS analyses of placental and fetal tissue demonstrated undetectably low transplacenta

102 s higher than that previously observed using fetal-tissue-derived OPCs, and no tumors from these graf

103 story of parasite development and associated fetal tissue destruction.

104 s is developmentally lethal, indicating that fetal tissue development is tightly controlled by miRNAs

105 Although fetal tissue did not appear to rescue a significant numb

106 Fetal tissue Doppler and spectral Doppler imaging are po

107 spite intimate juxtaposition of maternal and fetal tissues during mammalian pregnancy, reciprocal mig

108 of mothers to tolerate genetically different fetal tissues during pregnancy.

109 HsPMP20 mRNA expression was low in human fetal tissues, especially in the brain.

110 family members, ADAMTS9 is expressed in all fetal tissues examined as well as some adult tissues.

111 ed several different Tnk1 transcripts in all fetal tissues examined.

112 In human, the gene is imprinted in most fetal tissues except the heart, and KVLQT1 is part of a

113 Fetal tissues exhibiting the highest viral tropism were

114 Although other fetal tissues express 52beta, there may be differences i

115 ts of three alpha-1 chains, is only found in fetal tissues, fibrosis, and cancer in humans.

116 The homotrimers occur in fetal tissues, fibrosis, and cancer, where their collage

117 However, the use of human fetal tissue for research and transplantation is controv

118 ed because it might be more practicable than fetal tissue for the purpose of transplantation to prima

119 neural stem cells (NSCs) as alternatives to fetal tissues for cell replacement.

120 Explants of fetal tissue from malaria-positive placentas also secret

121 hich implies tolerance mechanisms protecting fetal tissues from maternal immune attack.

122 of PCR in detecting N. caninum infection in fetal tissues from spontaneous bovine abortion.

123 udy, time-dependent (3 h-11 days) changes in fetal tissue gene expression in a rat model of in utero

124 within the female reproductive tract and in fetal tissues harvested from CWD experimentally and natu

125 isease and the difficulty in obtaining human fetal tissue has generated interest in finding correspon

126 cultures of NPCs derived from human iPSCs or fetal tissue have similar characteristics, although they

127 e in a neonatal spinal environment or within fetal tissue implants, especially because previous work

128 o the DC projection, in all groups receiving fetal tissue implants.

129 d the technical outlook for the use of human fetal tissue in clinical transplantation.

130 rectly measure transcripts from a variety of fetal tissues in the maternal blood sample.

131 the virus to specifically target developing fetal tissues in utero.

132 , and message was detected in most adult and fetal tissues including the epidermis.

133 cript of PKDL is expressed at high levels in fetal tissues, including kidney and liver, and down-regu

134 n of survivin in several apoptosis-regulated fetal tissues, including the stem cell layer of stratifi

135 ndings were obtained in 12- to 18-week human fetal tissue, indicating a highly restricted pattern of

136 The SCID-hu mouse implanted with human fetal tissue is a novel model for investigating human vi

137 Fetal tissue is considered to be immune privileged and i

138 Deriving NPCs from human fetal tissue is feasible, although problematic issues in

139 ic expression in female hybrid placental and fetal tissues is negatively correlated with the other X-

140 NMHC II-A and II-B, the mRNA level in human fetal tissues is substantially lower than in adult tissu

141 be ubiquitously expressed in human adult and fetal tissues, is highly related to the DRPLA gene, in w

142 As the assay involves the use of fetal tissues, it is possible to follow new blood vessel

143 the most primitive hematopoietic cells from fetal tissues lack the expression of CD38.

144 med expression in both human adult and human fetal tissues (lung, liver, brain, and kidney) and in hu

145 aternal unresponsiveness to HLA-G-expressing fetal tissues may be shaped in the thymus by a previousl

146 cell polarity (PCP) pathway is required for fetal tissue morphogenesis as well as for maintenance of

147 Analysis of human and fetal tissue mRNAs confirmed that mElf-1 is expressed in

148 In fetal tissue (n = 10), ductal plate cells, primitive bil

149 Fetal tissues, normal adult tissues, and breast carcinom

150 mprinting tumors was also observed in normal fetal tissues of 6 12 weeks gestation, suggesting a simi

151 n = 2; mid third trimester), with harvest of fetal tissues on GD 80, 100, 130, or 145.

152 olated from the placenta, amniotic fluid, or fetal tissues only from rats infected prior to breeding

153 n embryos (human embryonic stem cells), from fetal tissue or from adult sources (bone marrow, fat, sk

154 t occur, this has not been evident in normal fetal tissues or WTs.

155 n embryos (human embryonic stem cells), from fetal tissue, or from adult sources (bone marrow, fat, s

156 certain extrahepatic tissues (in addition to fetal tissues), our data raise the possibility that CYP3

157 on analysis revealed two active promoters in fetal tissues, P2 and P3, whereas P3 was the only promot

158 human CSF-1 concentrations were measured in fetal tissue, placenta, and fetal/maternal sera.

159 ive CSF-1 crossed the placenta and peaked in fetal tissue, placenta, and serum 10 minutes after injec

160 Gene array techniques applied to fetal tissues present additional confounding pitfalls.

161 In fetal tissues, PTPRO expression was observed in the brai

162 ve tract and target Neu5Gc-positive sperm or fetal tissues, reducing reproductive compatibility.

163 quantitative distribution of VHL mRNA within fetal tissues reflected that seen by in situ hybridizati

164 iptional regulatory genes that might mediate fetal tissue regeneration, we surveyed homeobox gene exp

165 HOXB13 expression was decreased in wounded fetal tissue relative to unwounded fetal controls or wou

166 Use of the HDBR and other fetal tissue resources discussed here will contribute to

167 Northern blotting of adult and fetal tissues revealed low and restricted expression of

168 hern hybridization analysis revealed that in fetal tissue RTVP-1 RNA was detected only in the kidney,

169 amples, 188 chorionic villus samples, and 37 fetal tissue samples were tested; the amplification fail

170 titutively in extrahepatic organs, including fetal tissue samples, and is highly inducible in various

171 eir expression, with exception of testis and fetal tissues, seems to be restricted to tumor cells onl

172 Although present in human fetal tissues, shortly after birth telomerase activity i

173 Northern blots of 13 human fetal tissues show antiquitin to be highly expressed in

174 Analysis of human fetal tissue showed that dysferlin was expressed at the

175 mRNA broadly distributed in normal adult and fetal tissues, structurally distinct from the 1.9-kb Sur

176 uitous expression pattern in human adult and fetal tissues suggest a critical role for TMCO1.

177 both IGF2 and H19 was observed in all other fetal tissues, suggesting a tissue-specific LOI in the c

178 on in carcinomas as well as normal adult and fetal tissues suggests an important functional role for

179 All other fetal tissues tested showed equal expression from both a

180 on of the sedlin gene in all human adult and fetal tissues tested, with the highest levels in kidney,

181 MAGE-F1, which is expressed in all adult and fetal tissues tested.

182 ot or only at very low levels in most of the fetal tissues tested.

183 4.0- and 3.0-kb transcripts in all adult and fetal tissues tested.

184 tected an approximately 6-kb mRNA in several fetal tissues tested.

185 ies of mRNA were seen in all human adult and fetal tissues tested.

186 ng LCM of epithelial cells from fresh frozen fetal tissue that enables quantitative analyses of micro

187 ressed ubiquitously in the limited number of fetal tissues that were tested, but is selectively expre

188 In fetal tissue the AR-Ser(P)-213 antigen was present in ep

189 t epithelial (RPE) cells isolated from human fetal tissue, three separate studies failed with various

190 its transcription persists in placental and fetal tissues, throughout embryogenesis.

191 els in the general population, children, and fetal tissue to establish background levels and the risk

192 programs remarkably similar to those of the fetal tissue to organize into cerebral cortex-like regio

193 es conducted directly in human embryonic and fetal tissue to provide an overview of what is known abo

194 he greater sensitivity of rapidly developing fetal tissues to ionizing radiation.

195 rovide evidence for the ability of different fetal tissues to support the development of gammadelta T

196 Because of limitations associated with fetal tissue transplants, a clone (1RB3AN27) of simian v

197 genes that are unmethylated in 11 different fetal tissue types, we show that increases in DNA methyl

198 Fetal tissue was harvested at embryonic day 14.5 (E14.5)

199 FIV sequestration in fetal tissues was common without detectable virus in blo

200 Moreover, Akt activity in various fetal tissues was unchanged compared with that observed

201 The engrafted fetal tissues were also stained positive for alpha-actin

202 e maternal plasma samples and homogenates of fetal tissues were determined by high-performance liquid

203 opism towards reproductive and embryonic and fetal tissues where exposure to a single alpha particle

204 wed monoallelic expression in both adult and fetal tissue, whereas PHLDA2, SLC22A18, and SLC22A18AS w

205 erfamily are expressed in tumors, testis and fetal tissues, which has been described as a cancer/test

206 els of viral RNA in maternal, placental, and fetal tissues, which resulted in protection against plac

207 have now extended these studies by replacing fetal tissue with neonatal pig thymic and hematopoietic

208 ed in a variety of human and mouse adult and fetal tissues with substantial expression levels in the

209 ely abundant 8kb transcript in all adult and fetal tissues with the exception of adult thymus.

210 hest expression levels of FBN3 were found in fetal tissues, with only low levels in postnatal tissues

211 nces in transcript abundance among adult and fetal tissues, with predominant expression in liver, kid