ライフサイエンスコーパス: hybrid cell

1 ly impacted by the known instability of such hybrid cells.

2 tion and in situ hybridization with those of hybrid cells.

3 inactive human X chromosomes in mouse/ human hybrid cells.

4 ted with the nontumorigenic phenotype of the hybrid cells.

5 somatic nucleus in the EG-thymic lymphocyte hybrid cells.

6 e of the major proteins secreted from EC-OSB hybrid cells.

7 phenotypes among tumor and peripheral blood hybrid cells.

8 have examined the function of the resulting hybrid cells.

9 The ectopic neurons are hybrid cells.

10 chondrial respiratory chain in complementing hybrid cells.

11 pecies of recombinant mtDNA molecules in the hybrid cells.

12 from human cells as well as monochromosomal hybrid cells.

13 t dorsal root ganglion x mouse neuroblastoma hybrid cells.

14 but rather through spontaneous generation of hybrid cells.

15 were identified as surface components of the hybrid cells.

16 effects were exacerbated for fused hMSC-hCM hybrid cells.

17 human fetal liver and mouse erythroleukemia hybrid cell (A181gamma cell) that contains a single copy

18 ranscriptomic profile, leads to emergence of hybrid cells acquiring dissemination properties.

19 The tetraploid hybrid cells allowed us to separate cis- from trans-regu

20 Hybrid cells also displayed elevated levels of phenotypi

21 Hybrid cells also expressed the mRNAs and proteins for 2

22 pristone rescue Tau pathology in cytoplasmic hybrid cells, an ex vivo Alzheimer's disease model where

23 ll dynamics and establishes a foundation for hybrid cell and gene therapies based on cell-to-cell del

24 aterial demonstrates a local cytotoxicity on hybrid cells and human fibroblasts in vitro.

25 l-specific replication program in the fusion hybrid cells and independent regulation of the nuclear l

26 l cells, flow batteries, electrolysis cells, hybrid cells, and photoelectrochemical cells.

27 ease states when a variety of hepatocyte-BEC hybrid cells appear.

28 Hybrid cells are endowed with mixed epithelial and mesen

29 These hybrid cells are functionally active and possess the ben

30 M on the upper surface of ND-7 neuroblastoma hybrid cells as an indication of receptor-cytoskeleton i

31 the observed pluripotency of the EG-somatic hybrid cells as they differentiated into a variety of ti

32 f hsp90 required to bind eNOS, using yeast 2-hybrid, cell-based coprecipitation experiments, and GST-

33 Additional hybrid cells bearing portions of human chromosome 21 wer

34 unocytochemistry, CFTR was expressed in many hybrid cells but was absent or low in others.

35 Here, we identify epithelial-mesenchymal hybrid cells, capable of long-term expansion in vitro, a

36 mic specialization (ES) is a testis-specific hybrid cell/cell actin-based adherens junction and cell/

37 Interestingly, the majority of circulating hybrid cell (CHC) subpopulations were not identified in

38 l tumor-derived cell population, circulating hybrid cells (CHCs), harboring attributes from both macr

39 plications of inducing and/or utilizing such hybrid cells clinically.

40 cell-mediated chromosome transfer to isolate hybrid cell clones that retain chromosome 3 homologues w

41 Significance: Hybrid cells co-featuring epithelial and mesenchymal tra

42 on, with intermediate points represented by "hybrid" cells coexpressing phenotypic markers of more th

43 An optical fiber-based 3D hybrid cell consisting of a coaxially structured dye-sen

44 A triboelectric-pyroelectric-piezoelectric hybrid cell, consisting of a triboelectric nanogenerator

45 In addition, the hybrid cells contain porcine endogenous retroviral DNA s

46 he human HPRT gene, we treated human/hamster hybrid cells containing an inactive human X chromosome w

47 Finally, experiments in murine hybrid cells containing either the maternal or paternal

48 s with human cyclin T1 to give active TAK in hybrid cells containing human chromosome 12.

49 We also showed that hybrid cells containing two defective mtDNA haplotypes t

50 n the microcell-mediated chromosome transfer hybrid cells containing whole human chromosome 16 were i

51 my was quantitated in individual cytoplasmic hybrid cells (cybrids), containing a large mtDNA deletio

52 The hybrid cell-cycle simulation implementation is inherentl

53 Using F(1)-hybrid cells derived from crosses between distantly rela

54 phenomenon whereby medium from human-hamster hybrid cells displaying radiation-induced chromosomal in

55 These hybrid cells divide, express human and porcine proteins,

56 ons performed with human chromosome 2/rodent hybrid cell DNA as template sublocalized SULT1C1 to a re

57 The excellent performance of the hybrid cell enhances the energy-harvesting efficiency si

58 lls to evade phagocytosis, and the resultant hybrid cells exhibited increased migration, tumorigenesi

59 The resulting hybrid cells express markers of both neutrophils (Ly6G,

60 Here we report that hybrid cells expressing surface markers of neutrophils (

61 on is to promote the formation of metastatic hybrid cells following fusion between mobile leucocytes

62 We screened a panel of feline-mouse hybrid cells for susceptibility to FPV infection and fou

63 herent in cloning, meiotic recombination, or hybrid cell formation.

64 In addition, hybrid cells formed by the fusion of hMSCs with immortal

65 These hybrid cell-free biosensors have a fast response time, s

66 Hybrid cells generated by fusing dendritic cells with tu

67 Further, we demonstrate that in vivo-derived hybrid cells harbor tumor-initiating capacity in murine

68 HeLa X human skin fibroblast hybrid cells have been developed into a model for radiat

69 To define these hybrid cells (HCs), which fire single, short action pote

70 In tetraploid hybrid cells, however, normal IGF2 imprinting was perman

71 The results showed abundant hybrid cells in portal bile duct BEC, canals of Hering,

72 Differentiation of hybrid cells in vitro and in vivo yielded cell types fro

73 phosphate (cAMP)-differentiated motor neuron hybrid cells in vitro, and anti-oxidants prevented this

74 und that conditioned medium (CM) from EC-OSB hybrid cells increases the migration, invasion, and surv

75 pon cell fusion, respiration is recovered in hybrids cells, indicating that mitochondria fuse and exc

76 m approximately 8q22 to 8q24 and includes 10 hybrid cell intervals, 89 polymorphic STSs, 118 ESTs, an

77 All three types of hybrid cells investigated, F1(DU145 x PC3), F1(JCA1 x PC

78 Instead, the Th1/Th2 hybrid cell is a robust new type with properties of both

79 The output of the hybrid cell is about 7.65 muA current and 3.3 V voltage,

80 The current output of the hybrid cell is dominated by the DSSC, and the voltage ou

81 The high storage impact of the hybrid cell is investigated by its promising conversion

82 One hybrid cell line (F2.1D1) containing a number of human c

83 ed previously that in a neuroblastoma-glioma hybrid cell line (NG108-15), the heterotrimeric G-protei

84 vely nonchimeric clones from a human-hamster hybrid cell line as well as clones isolated from total g

85 onstrated with DNA isolated from a radiation hybrid cell line containing only 5 Mb of human DNA.

86 tructed with DNA isolated from a mouse/human hybrid cell line designated A15, which was previously ch

87 cation product from both total human DNA and hybrid cell line DNA containing only human chromosome 5.

88 PCR analysis of human/rodent hybrid cell line DNA samples showed that the polymorphic

89 ing flow-sorted DNA from the monochromosomal hybrid cell line GM10826.

90 cific PAC library was also produced from the hybrid cell line GM10826.

91 transcription in the neuroblastoma X glioma hybrid cell line NG108-15, a cell line expressing the en

92 screening of the G3 human-hamster radiation hybrid cell line panel and confirmed the localization by

93 solateral uptake of [3H]TC in WIF-B cells, a hybrid cell line stably exhibiting in vitro the structur

94 DNA from the hybrid cell line was cloned, and the human chromosome 2-

95 With a second hybrid cell line we obtained a single hygromycin-resista

96 ND7/23-Nav1.8 rat DRG x mouse neuroblastoma hybrid cell line which showed constitutive expression of

97 05 cells (a neuroblastoma x glioma mouse/rat hybrid cell line) and F98 (a glioma cell line).

98 ventral spinal motoneuron and neuroblastoma hybrid cell line.

99 N gene in NSC-34 cells, a mouse motor neuron hybrid cell line.

100 ni-chromosome within a human-Chinese hamster hybrid cell line.

101 utgrowth in the F11 neuroblastoma/dorsal DRG hybrid cell line.

102 However, further studies with other somatic hybrid cell lines (Bios Laboratory) localized the TnTf g

103 sing the G3 panel of human/hamster radiation hybrid cell lines and >15,000 unique human genetic marke

104 enome was assembled using 92 horse x hamster hybrid cell lines and 730 equine markers.

105 to human chromosome 1 on a panel of somatic hybrid cell lines and to 1p31.3-p31.2 by fluorescence in

106 or which a full genome sequence or radiation hybrid cell lines are unavailable.

107 cted a collection of canine-rodent microcell hybrid cell lines by fusion of canine fibroblast microce

108 with psoriasin cDNA, as did genomic DNA from hybrid cell lines containing all or part of chromosome 1

109 es of genomic DNAs from rodent/human somatic hybrid cell lines containing human chromosome 1 or the p

110 ial chromosomes (YACs) from two rodent/human hybrid cell lines containing human chromosomes 5 and 16.

111 Monoclonal hybrid cell lines derived from either mesencephalic or s

112 Hamster-human somatic hybrid cell lines from a patient with der(22) syndrome a

113 mong the VCFS patients, we developed somatic hybrid cell lines from a set of VCFS patients.

114 pothesis, we developed hamster-human somatic hybrid cell lines from VCFS/DGS patients with all three

115 A panel of 128 WG-RH hybrid cell lines generated by X-irradiation and fusion

116 the hPTTG gene using DNA from humanxhamster hybrid cell lines in PCR.

117 ion on DNA from several of the sheep-hamster hybrid cell lines suggests that loci containing multiple

118 s mapped using monochromosomal and radiation hybrid cell lines to chromosomal region 14q11.

119 have used phenotypic screening of radiation hybrid cell lines to identify the candidate lung cancer

120 We assayed the susceptibility of each of the hybrid cell lines to transduction by retroviral vectors

121 Characterization of the hybrid cell lines using a combination of fluorescence in

122 PCR amplification of rodent/human hybrid cell lines using these same primers confirms the

123 A dominant proteomic feature of aggressive hybrid cell lines was upregulation of cytoskeletal and a

124 Canine-rodent hybrid cell lines were analyzed to detect canine APOH.

125 was restored by transfection or creation of hybrid cell lines with complementing deficiencies in exp

126 is issue we have fused two human cytoplasmic hybrid cell lines, each containing a distinct pathogenic

127 In addition, a panel of 30 sheep-hamster hybrid cell lines, each of which carries one or more she

128 ation (FISH) studies and analysis of somatic hybrid cell lines, the chromosomal location of p40-phox

129 Based upon PCR analysis in hybrid cell lines, the gene for GPCR-Br (HGMW-approved s

130 ons in four of the noncomplemented microcell hybrid cell lines.

131 ual human chromosomes by typing human-rodent hybrid cell lines.

132 isolation of human DNA from the rodent/human hybrid cell lines.

133 is of genomic DNAs from rodent/human somatic hybrid cell lines.

134 rated copies of chromosome 22 in the somatic hybrid cell lines.

135 es of genomic DNAs from rodent-human somatic hybrid cell lines.

136 human DNAs from monochromosomal human-rodent hybrid cell lines.

137 ents from a panel of mouse-hamster radiation hybrid cell lines.

138 ntified by comparing sequences of 48 haploid hybrid cell lines.

139 mosomes by PCR with a panel of sheep-hamster hybrid cell lines.

140 lls and in two HeLa cell derived tumorigenic hybrid cell lines.

141 NA in YACs from monochromosomal human/rodent hybrid cells lines and radiation hybrids can be accompli

142 f coding sequences were supported by somatic hybrid cell mapping to markers on BTA18.

143 Here, we report that hybrid cell membrane nanovesicles (known as hNVs) displa

144 nd cholinergic neurons, gliomaxneuroblastoma hybrid cells (NG108-15) were used to create nerve-muscle

145 human acrocentric chromosomes associate with hybrid cell nucleoli.

146 mouse NORs are equally likely to be within a hybrid cell nucleolus.

147 , whereas B16 melanoma cells and the somatic hybrid cells of B16 x K-1735 melanoma cells produce meta

148 ilver-impregnated collagen cuff material and hybrid cells or human fibroblasts showed a marked local

149 rescence in situ hybridization and radiation hybrid cell panel analyses.

150 pectively, by using a cattle-hamster somatic hybrid cell panel and a 5,000 rad whole-genome radiation

151 This hybrid cell panel was able to localize the STSs to 1 of

152 A whole genome cattle-hamster radiation hybrid cell panel was used to construct a map of 54 mark

153 alized by breakpoint analysis using a set of hybrid cell panels consisting of natural deletions or tr

154 pecific backcross and whole-genome radiation hybrid cell panels.

155 and a neurogenic trajectory depart from the hybrid cell population.

156 These hybrid cells possess mixed carcinoma epithelial and mese

157 Hybrid cells produced by fusing BHKXpr1 or BHKPiT1 to XM

158 receptor in NG108-15 neuroblastoma X glioma hybrid cells results in a transient increase at the intr

159 ing of the FHIT/FRA3B locus in the resultant hybrid cells revealed a complex pattern of instability w

160 ltiple types of energies using an integrated hybrid cell so that the energy resources can be effectiv

161 reventing rod-fated cells diversion toward a hybrid cell state may explain the occurrence of hybrid r

162 ify discrete cell identity and intermediate "hybrid" cell states, supporting a metric to quantify cel

163 rigenic and nontumorigenic HeLa x fibroblast hybrid cells, subtractive suppression hybridization (SSH

164 dization was performed between GBM cells and hybrid cells suppressed for tumorigenicity following mic

165 is Cu-S cathode is further demonstrated in a hybrid cell that employs an Zn metal anode and an anion-

166 We report a hybrid cell that is intended for simultaneously harvesti

167 polymorphonuclear neutrophil-dendritic cell hybrid cells that develop in Th2 conditions and demonstr

168 e fused with human fibroblasts, resulting in hybrid cells that maintain a stable tetraploid DNA conte

169 of the entrapped cells and subsequent tumor hybrid cell (THC) formation.

170 In LEC11A x LEC11B hybrid cells, the cgFUT6A gene was predominantly express

171 lele-specific expression in human-chimpanzee hybrid cells-the product of fusing induced pluripotent s

172 by exposing human-mouse chromosome 3 somatic hybrid cells to aphidicolin-mediated replication stress.

173 cell growth in vitro, and the ability of the hybrid cells to form tumors in animals was suppressed.

174 lasts and in NG108-15 neuroblastoma x glioma hybrid cells treated with BMP-7, an inducer of L1 and ne

175 coincides with the appearance of a nonfused, hybrid cell type that shares the morphology, antigenicit

176 erivascular resident macrophages (PVM/Ms), a hybrid cell type with characteristics of both macrophage

177 D-line was fused to an A-line, the resulting hybrid cells underwent apoptosis in response to p53, ind

178 ieved the power conversion efficiency of the hybrid cells up to 2 %; and demonstrated that most of th

179 We validate hybrid cells using experimental lineage tracing data to

180 report, we describe a new method to generate hybrid cell vaccines, based on gene transfer of a viral

181 human ALS, and in differentiated motoneuron hybrid cells [ventral spinal cord (VSC 4.1 cells)] that

182 Although <3% of the DNA content in the hybrid cells was human, as many as 75% of the transforma

183 Although < 2% of the DNA in the hybrid cells was human, as much as 80% of transformants

184 The lifespan of these hybrid cells was longer than that of the hybrids in whic

185 puts of these complex cells and existing two-hybrid cells, we can make inferences about the topology

186 egulation of human globin genes in the LxMEL hybrid cells, we transfected the YAC into L-cells by lip

187 In culture flasks, hybrid cells were exposed to silver-impregnated collagen

188 Recombinant mtDNA molecules in the hybrid cells were identified using three independent exp

189 WIF-B rat hepatoma hybrid cells were incubated with either CM or UM or trea

190 a species-specific monoclonal antibody, the hybrid cells were shown to synthesize human neurofilamen

191 These studies used GM10115 human-hamster hybrid cells, which contain one copy of human chromosome

192 in NG108-15 mouse neuroblastoma x rat glioma hybrid cells, which express predominantly LVA currents w

193 rise to a subpopulation of skeletal-cardiac hybrid cells with a currently unknown phenotype.

194 wed by RT-PCR analysis using monochromosomal hybrid cells with a human chromosome 6 of defined parent

195 r to target cells ex vivo as well as to form hybrid cells with limited cell sources.

196 ng was used to analyze the transcriptomes of hybrid cells with respect to the human and mouse genomes

197 classic" apoptotic and necrotic neurons and "hybrid" cells with intermediate characteristics.