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1                         We found that early (morula, 8-14 hpf) and late (blastula-to-mid-gastrula) ce
2                These phenotypes suggest that morula acts to block mitosis-promoting activity in both
3 e behavior of Gsc-null cells was examined in morula aggregation chimeras.
4 d early embryos at the two-cell, eight-cell, morula and blastocyst stages, and revealed four modes of
5 eaving embryos but restored again in compact morula and blastocyst stages.
6  stage but dramatically increased during the morula and blastocyst stages.
7 lastomere, polyploid blastomere, compaction, morula and blastocyst-like stages by light, scanning ele
8 e, two-cell, four-cell, eight-cell, 16-cell, morula and blastocyst.
9 on of IRE-1 and CHOP at the 8-cell, 16-cell, morula, and blastocyst stages.
10 os (1-cell, 2-cell, 4-cell, 8-cell, 16-cell, morula, and blastocyst).
11            Human trophoblasts arise from the morula as trophectoderm (TE), which, after implantation,
12     Nurse cells in female-sterile alleles of morula begin to become polyploid but revert to a mitotic
13  gene expression blocking development at the morula-blastocyst transition.
14 ere defects at 3.5 d.p.c. (days post-coitus) morula/blastocyst stage and lethality before 8.5 d.p.c.
15 onstructed oocytes developed in vitro to the morula/blastocyst stage, and 8% of these embryos develop
16 ear localization of activated MAPK occurs in morula/blastula stage embryo animal and marginal zones c
17 is involved in blastocyst formation from the morula by regulating accumulation of fluid and different
18  chimeric partner elimination is a cytotoxic morula cell (MC).
19            The first branching region, where morula cells become specified for inner cell mass or tro
20                                 We show that morula compaction and ICM formation depend on PC7 and th
21 ranes of the 8-cell-stage embryo just before morula compaction.
22  male embryos were able to progress from the morula/early blastocyst stage to more advanced stages of
23                 Blastomeres are removed from morula (eight-cell)-stage embryos and cultured until the
24           When injected into an 8-cell-stage morula, embryonic stem cells (ESCs; derived from pre-imp
25  I hypersensitive sites in mouse zygotes and morula embryos, and investigate the epigenetic mechanism
26           Cyclin E protein levels decline in morula embryos, while cyclin E mRNA levels remain high.
27 ensis but was notably found on extracellular morula fibers in morulae containing dense-cored organism
28 lls, and it was found extracellularly in the morula fibrillar matrix and associated with the morula m
29 pherules demonstrating segmentation mimicked morula forms of Prototheca spp.
30   In addition to its role in the endo cycle, morula function is necessary for dividing cells to exit
31                  We show that the Drosophila morula gene is essential to maintain the absence of mito
32            Transcriptomic analysis in single morula identified novel Notch targets, such as early nai
33 t the in vitro generation of mouse transient morula-like cells (MLCs) via the manipulation of signali
34  of mouse chimeras using traditional diploid morula<-->diploid embryonic stem (ES) cell aggregations.
35 ialized tetraploid chimeras using tetraploid morula<-->diploid ES cell aggregations.
36         These regions (e.g. amphibian dorsal morula, mammalian anterior visceral endoderm) require st
37                                    Since the morula membrane is the interface between the ehrlichial
38 trated that MmpA was localized mainly on the morula membrane of E. canis.
39        A gene encoding a 23.5-kDa ehrlichial morula membrane protein designated MmpA was cloned by sc
40 the fibrillar matrix and associated with the morula membrane, the host cell cytoplasm, and the nucleu
41 ula fibrillar matrix and associated with the morula membrane.
42                               The Drosophila morula (mr) gene regulates variant cell cycles, because
43 n B protein to be inappropriately present in morula mutant nurse cells.
44  are both arrested in metaphase in different morula mutants.
45                                         Thus morula serves a dual function as a cell cycle regulator
46 owth of bacteria, concomitant with increased morula size.
47 thality, with embryos dying at or before the morula stage after only two to four cell division cycles
48 one modifications between blastomeres at the morula stage and cell sub-populations in blastocysts, di
49 suggesting ectopic Tspo silencing before the morula stage and demonstrating elevated embryonic lethal
50                    Early stages, such as the morula stage comprised transcripts mainly involved in en
51  that Rpl13a-/- embryos were arrested at the morula stage during preimplantation development.
52 yst homogenates but not those of two-cell or morula stage embryos.
53  from the wild-type paternal alleles: at the morula stage in embryos lacking maternal E-cadherin, and
54 3Galbeta1,R), which causes compaction in the morula stage of the preimplantation mouse embryo, as wel
55 for the correct specification of TE from the morula stage onwards and that both maternal and zygotic
56 fection of murine preimplantation embryos at morula stage with lentiviral vectors resulted in stable
57 tification of early-stage embryos (2-cell to morula stage).
58 mally if compaction does not occur until the morula stage, and that the zona pellucida suffices to ma
59 on caused a total loss of methylation by the morula stage, but by the epiblast stage, the repeats wer
60 cripts were first detected in embryos at the morula stage, close to the time of blastocoele formation
61                                       At the morula stage, outer cells acquire an apical-basal cell p
62                                       At the morula stage, rafts were also apically enriched in each
63  lineage differentiation event occurs at the morula stage, with outer cells initiating a trophectoder
64 mbryos systematically from the 1-cell to the morula stage.
65 mouse preimplantation embryos from 1-cell to morula stage.
66 failure of TE specification, starting at the morula stage.
67 s that BMPs regulate cell cleavage up to the morula stage.
68 l stage or lineage gene transcription at the morula stage.
69 zygotes leads to developmental arrest at the morula stage.
70 leavage stages, but then arrested before the morula stage.
71 otein depletion impairs TE initiation at the morula stage.
72 sts in zygotes and early embryos through the morula stage.
73 the cell surface from the 1-cell through the morula stage.
74 ed each cell with a zonular belt by the late morula stage.
75 betaine; Bhmt mRNA is first expressed at the morula stage; BHMT is abundant at the blastocyst stage b
76                                      We used morula-stage aggregation as a strategy to further clarif
77             Chimerism with 3F-iPS derived by morula-stage diploid aggregation was sustained during pr
78                    Production of chimeras by morula-stage embryo aggregation is an effective way to u
79  protein was isolated from 8- to 16-cell and morula-stage embryonic libraries of two distantly relate
80 he intracellular Ca2+ concentration in mouse morula-stage embryos, providing evidence for the existen
81 n mouse embryos lacking pescadillo arrest at morula stages of development, the nucleoli fail to diffe
82 ed human embryos develop beyond cleavage and morula stages to form a blastocyst in vitro.
83 toplasm and nucleus between the two-cell and morula stages.
84          In strong, larval lethal alleles of morula, the polytene ring gland cells also inappropriate
85 embryos, where it blocks the transition from morula to blastocyst during embryonic development.
86 bryo during day 5 to 7.5 of development (the morula to blastocyst stage) to promote embryonic elongat
87 orphological and functional changes from the morula to blastocyst stage.
88 ing data from 74 human embryos, spanning the morula to blastocyst stages.
89 e and protein expressions, but also inhibits morula to blastocyst transformation in a concentration-d
90 t tight junction formation plays any role in morula to blastocyst transformation that is associated w
91  key genes in TE lineage, and is involved in morula to blastocyst transformation.
92 embryos reduces Cdx2 expression and inhibits morula to blastocyst transformation.
93 sure of embryos to DKK1 during the period of morula to blastocyst transition (between d 5 and 8 of de
94          Induced deletion of Oct4 during the morula to blastocyst transition disrupts the ability of
95 the state of glucose metabolism to drive the morula to blastocyst transition.
96 ortion of trophectoderm cells and delays the morula to blastocyst transition.
97 arance of ZO-1 suggests its participation in morula to blastocyst transition.
98 provide markers for staging progression from morula to blastocyst.
99 of the development of mouse embryos from the morula to early blastocyst stage, based on 4D confocal i
100 monstrated in embryos as they developed from morula to hatched blastocysts by a progressive increase
101 deficient embryos failed to proceed from the morula to the blastocyst stage because of defects in the
102 n contrast, genic silencing initiates at the morula-to-blastocyst stage and absolutely requires Xist.
103           In conclusion, DKK1 can act on the morula-to-blastocyst stage embryo to modify subsequent t
104 ected by RT-PCR, greatly increase during the morula-to-blastocyst transition and seven of the eight k
105 ally expressed miRNAs but also inhibited the morula-to-blastocyst transition.
106 o approach revealed a role for miRNAs in the morula-to-blastocyst transition.
107 t repression of p21 transcription during the morula-to-blastocyst transition.
108 OCK1 and ROCK2 activity during the 8-cell to morula transition phenocopied TFAP2C knockdown, triggeri
109                         During the 8-cell to morula transition TFAP2C potentiates cell polarity to su
110 neously assimilate into preimplantation host morula via diploid aggregation, unique to bona fide plur

 
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