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1 etely fertile and the resulting oocytes were euploid.
2 other regenerative adult tissues are largely euploid.
3 full-blown clonal adenomas remain remarkably euploid.
4 feration of wild-type aneuploids compared to euploids.
5 ysts with parental DNA (n = 2,277), 71% were euploid, 27% were meiotic aneuploid, and 2% were mitotic
6 birth rates and miscarriage rates across 484 euploid, 282 low-grade mosaic, and 131 medium-grade mosa
7                        The cells also remain euploid after at least 12 passages.
8 esult in decreased fitness compared with the euploid ancestor in rich media.
9 ngs suggest that the fitness ranking between euploid and aneuploid cells is dependent on context and
10 uman pre-implantation embryos are mosaics of euploid and aneuploid cells, yet those with a low propor
11 uman pre-implantation embryos are mosaics of euploid and aneuploid cells.
12 enomic(1) and transcriptomic(6) data for 796 euploid and aneuploid natural isolates.
13 ly, an unblinded clinical evaluation of 1269 euploid and aneuploid samples utilizing this high-throug
14                  The combined results of the euploid and aneuploid studies suggest that aneuploid eff
15 s produced by maize rad51 double mutants are euploid and exhibit near-normal rates of meiotic crossov
16                                              Euploid and T21 cardiac endothelial cells coexpressed SO
17 ee weeks resulted in growth deficits in both euploid and trisomic mice.
18 omy 7 or 13 (DLD1+7 and DLD1+13), as well as euploid and trisomy 13 amniocytes (AF and AF+13).
19  a similar extent, in cortical cultures from euploid and trisomy 16 mice.
20 tly reduced incidence compared with control (euploid) animals that did not have trisomy.
21 ded personalized embryo transfer (pET) using euploid blastocyst in patients with one or more previous
22                                   Those with euploid blastocyst(s) and an informative receptivity res
23 ts for whom in vitro fertilization yielded a euploid blastocyst, the use of receptivity testing to gu
24 ryos likely to develop into high-quality and euploid blastocysts.
25 ibute to divergence between the trisomic and euploid brains.
26          The majority of meiotic progeny are euploid, but approximately one-third are diploid/aneuplo
27                                           In euploid, but not trisomic cortical cultures, kainic acid
28  young adults with Down syndrome compared to euploid cases (13-25 years, Down syndrome n = 6, control
29                   When exponentially growing euploid cells are used in gene-expression comparisons wi
30    In one gastric cancer, both aneuploid and euploid cells contained large numbers of likely clonal i
31 ely proliferating aneuploid cells to that of euploid cells grown into stationary phase.
32 1 inhibition and increased the proportion of euploid cells in mosaic epiblast.
33 rwent apoptosis at rates similar to those of euploid cells in vitro.
34                 Third, a small percentage of euploid cells rescues embryonic tissue in mosaic gastrul
35 ploid cells was masked when stationary phase euploid cells were used for normalization in transcripto
36  potential, provided they contain sufficient euploid cells, a finding of significance for the assessm
37  essential for proper proteasome function in euploid cells, and deletion of this deubiquitinase leads
38 n chimeric embryos, containing aneuploid and euploid cells, reveal that the fate of aneuploid cells d
39 and NFkappaB signaling both in aneuploid and euploid cells, suggesting a non-cell autonomous response
40 adulthood in trisomic mice are equivalent to euploid cells, we used microarrays to assess the trisomi
41 t to increase chemotherapeutic resistance in euploid cells.
42 oint (SAC), is crucial for the production of euploid cells.
43 eased load of protein aggregates compared to euploid cells.
44  xenografts, relative to genetically matched euploid cells.
45  forming mosaics of intermixed aneuploid and euploid cells.
46 s to test genotype-phenotype correlations in euploid cells.
47 s that cause lethality in aneuploid, but not euploid, cells could therefore provide new cancer therap
48  used microarrays to assess the trisomic and euploid cerebella.
49 ssues from 49 patients with T21 and 226 with euploid CHD (eCHD).
50  the probability of successful delivery of a euploid chromosome set to each daughter cell.
51  their interactions with other proteins from euploid chromosomes.
52 tic, 43 prodromal AD, 83 AD dementia) and 44 euploid cognitively normal controls.
53    Moreover, nearly all LKO hepatocytes were euploid compared with control hepatocytes, suggesting po
54 ulti-region transcriptome analysis of DS and euploid control brains spanning from mid-fetal developme
55 alin-preserved fetuses (eight trisomy 21, 10 euploid control fetuses), and the pelvic bone anatomy wa
56 d progenitor cell compartments compared with euploid control littermates.
57 n, and contrast threshold, compared with the euploid control mice.
58 inal physiology in Ts65Dn mice compared with euploid control mice.
59 ploid strains grew significantly better than euploid control strains under conditions suboptimal for
60 ed growth and oxidative balances relative to euploid control strains.
61                          Cognitively healthy euploid controls aged up to 75 years who had no biomarke
62                 One hundred and thirty-eight euploid controls and 259 adults with Down syndrome under
63 ally aneuploid isolates compared to isogenic euploid controls and found that 10-30% of amplified gene
64 ic interactions in those with DS compared to euploid controls by genes in interferon response, heme m
65 id progeny of aneuploid parent(s) but not in euploid controls from diploid lineages.
66  cells (hiPSCs) alongside otherwise isogenic euploid controls from male and female mosaic samples.
67 cells (iPSCs) alongside, otherwise, isogenic euploid controls from mosaic DS fibroblasts and equipped
68 arcelona Neuroimaging Initiative (DABNI) and euploid controls from the Sant Pau Initiative on Neurode
69 fetuses with trisomy 21, age and sex-matched euploid controls, and embryonic day 15.5 forebrains from
70 ther NCC-specific genes relative to isogenic euploid controls.
71 during GI colonization, relative to isogenic euploid controls.
72 ] with Alzheimer's disease dementia) and 242 euploid controls.
73 e model) overexpress APP protein relative to euploid controls.
74 in thymus samples from 19 DS subjects and 21 euploid controls.
75  and decreased NFAT activation compared with euploid controls.
76 erations that were largely absent from their euploid counterparts and that correlated with improved f
77 chromosome mis-segregation compared to their euploid counterparts.
78  variation and improved fitness over that of euploid counterparts.
79 ntent was higher in trisomy 16 compared with euploid cultures.
80 nce in the Morris water maze is identical to euploid, demonstrating that this region is necessary for
81  of DNA synthesis and mitosis that maintains euploid DNA content during proliferation.
82 ction of Stat3 gene copy number in targeted, euploid E14 clones resulted in dose-dependent losses of
83 from chromosomes, and promotes production of euploid eggs.
84 ough AURKA, a function crucial to generating euploid eggs.
85 f the first mitotic phase when compared with euploid embryos (n=28).
86 ntation potential directly using a set of 97 euploid embryos capable of implantation outperformed 15
87 ll cycle parameter timing is observed in all euploid embryos to the four-cell stage, whereas only 30%
88 apabilities somewhat equivalent to uniformly euploid embryos, and they have comparable clinical outco
89  and trisomy 21 embryos develop similarly to euploid embryos, monosomy 21 embryos exhibit high rates
90 ht to be more likely to develop into healthy euploid embryos.
91 an develop to term at rates similar to fully euploid embryos.
92 st for identifying and selecting IVF-derived euploid embryos.
93 lial cells expressed 6.9-fold more SOST than euploid endothelial cells (P = 2.7 x 10-27).
94 ce images of 131 individuals with DS and 216 euploid (EU) adult controls, including AD and OSA cases.
95  on most X-chromosome markers, compared with euploid female reference DNA.
96 ave a significantly greater iliac angle than euploid fetuses have.
97 ween second trimester Down syndrome (DS) and euploid fetuses, we used Affymetrix microarrays to compa
98 lanced chromosome segregation, production of euploid gametes and fertility.
99 s us to generate, for the first time, viable euploid gametes containing recombinant hybrid genomes fr
100 mplexes are regulated to ensure formation of euploid gametes.
101 g microtubule dynamics and for maintaining a euploid genome.
102                          Here we report that euploid human cells do not die in the absence of survivi
103  development, we turned to 45,X and isogenic euploid human induced pluripotent stem cells (hiPSCs) fr
104 ith DS and periodontal disease (group 1), 20 euploid individuals with periodontal disease (group 2; p
105 patients was significantly lower compared to euploid individuals with periodontal disease, whereas IL
106  disease (group 2; positive control), and 12 euploid individuals without periodontal disease (group 3
107 s small and hypocellular compared to that of euploid individuals.
108       A panel of genomically diverse T21 and euploid induced pluripotent stem cells (iPSCs) were crea
109 rized a panel of genomically diverse T21 and euploid induced pluripotent stem cells (iPSCs).
110 lso applies to other chromosomes, generating euploid iPSCs from cells of a Down syndrome mouse model.
111                           It can also create euploid iPSCs from human trisomic patient fibroblasts.
112 AB compared to those differentiated from the euploid iPSCs.
113  pluripotent stem cells (iPSCs) and isogenic euploid iPSCs.
114 s) promoting efficient chromosome sorting in euploids is adjusted to promote crossover formation betw
115 ell lines derived from ST zygotes had normal euploid karyotypes and contained exclusively donor mtDNA
116 measured in 52 middle-trimester fetuses with euploid karyotypes and in 52 fetuses with Down syndrome.
117 day 18.5 Ts66Yah and Ts65Dn mice, along with euploid littermate controls, were used for gene expressi
118 separately from Ts16 mouse fetuses and their euploid littermates, were cultured in various combinatio
119 ertheless extended host survival relative to euploid littermates.
120 ewer granule cells in dentate gyrus than did euploid littermates.
121  cortex from fetal trisomy 16 mice and their euploid littermates.
122  genes that are expressed from two copies in euploid males and females alike and qualify as candidate
123                        Memory performance in euploid mice correlated strongly with functional connect
124 ed facial dysmorphology in both trisomic and euploid mice.
125 ignificantly higher in trisomic mice than in euploid mice.
126 c VHL functions with missense mutations in a euploid model offers a novel opportunity to elucidate th
127 ne dosage between children with DS and their euploid mothers.
128 ogenous truncated trkB expression in normal, euploid neurons reproduced the Ts16 BDNF signaling failu
129 APP fragments from highly compartmentalized, euploid neurons that express APP and processing enzymes
130 , as well as numerous subchromosomal CNVs in euploid neurons.
131  equivalent developmental potential as fully euploid ones.
132 ut concentrations and simulated fractions of euploid or trisomy-21 "fetal" DNA is analyzed using both
133                       Similarly, compared to euploid, P6 trisomic mice showed an 18% reduction in mit
134                     Importantly, analysis in euploid placentas from first trimester pregnancy loss re
135  of meiosis in near isogenic allohaploid and euploid plants showed that the mechanism(s) promoting ef
136 m the estimated gestational age (EGA) in the euploid population with the quadratic equation FTD = -0.
137 ention-deficit/hyperactivity disorder in the euploid population, this has not been studied in down sy
138 ccurring conditions at higher rates than the euploid population.
139 esize that a threshold exists in both DS and euploid populations for the number of genetic perturbati
140    Remarkably, inducing ribosome stalling in euploids produces similar aging phenotypes, while up-reg
141 ation was found to be longer in Ts16 than in euploid progenitors, the Ts16 growth fraction was reduce
142 enitors exit the cell cycle than do control, euploid progenitors.
143                      Consequently, the term 'euploid' refers to a chromosome complement that is an ex
144 nase C (AURKC) is essential for formation of euploid sperm in humans because mutations in AURKC are c
145            Moreover, the reliance on viable (euploid) spores has the potential to introduce selection
146 erage protein levels are shifted towards the euploid state chromosome-wide.
147                    There are various natural euploid states with some organisms existing as haploids
148                         M1 was more fit than euploid strain M2 during DC and mouse gastrointestinal c
149 % of patient M's baseline BC population, but euploid strains were 98% of the population after 3d of e
150 Findings suggest that echinocandin tolerant, euploid strains were a subpopulation to more fit Tri7 st
151 hibited a general fitness defect relative to euploid strains when grown under replete conditions.
152                                 Trisomic and euploid transcriptomes were robustly distinguished.
153 many more L1 insertions in aneuploid than in euploid tumor cells.
154                                              Euploid types that have more than two sets of chromosome
155  tetraploids and function as bridges between euploid types.
156 euploid UPR-deficient cells grew better than euploid UPR-deficient cells but exhibited heightened gen
157 at hepatocytes in the stage of promotion are euploid, whereas those in the stage of progression exhib
158             Thus, the egg genotype is either euploid with R2d2 or aneuploid with both homologs of chr
159 l varieties revealed that all varieties were euploid, with significantly fewer CNVs, indicating that
160                                    Resulting euploid XY iPSCs can be differentiated into the male ger

 
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