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1 lation ensures mitotic fidelity after genome reduplication.
2 sible to SAS-6, correlating with a block for reduplication.
3 calizes to centrosomes and blocks centrosome reduplication.
4 CDK2 kinase inhibition also allow centrosome reduplication.
5 specifically blocks modified centrioles from reduplication.
6 mother centrioles, which prevents centriole reduplication.
7 e number and ensuring the block to centriole reduplication.
8 lecule inhibitor SU9516 suppressed centriole reduplication.
9 Mps1 mediates cyclin A-dependent centrosome reduplication.
10 roduces extra centrosomes, called centrosome reduplication.
11 to mitotic divisions without impairing endo-reduplication.
12 of Aurora A activation to prevent centrosome reduplication.
13 n, perivascular edema, and basement membrane reduplication.
14 ulatory mislocation (56%), followed by place reduplication (19%), and chimeric assimilation (13%).
15 nabling continued proliferation after genome reduplication, a finding with implications for cancer pr
17 that myeloid alpha-defensin genes evolved by reduplication and divergence from Paneth cell defensin g
18 lls correlates with the onset of endomitotic reduplication and is associated with the loss of the abi
26 1 is a regulator of centriole and centrosome reduplication as well as the initiation of DNA replicati
27 was dispensable in the mouse liver for endo-reduplication, but this could be explained by the ORC1 h
29 ently showed that naturally occurring genome reduplication does not alter mitotic chromosome structur
33 ance as coauthor with Bateson to promote the reduplication hypothesis to explain the statistical evid
34 we describe a mechanism to prevent centriole reduplication in Drosophila melanogaster whereby the SCF
40 layer, except for 12.5% with mild segmental reduplication involving 13.7 +/- 10.2% capillary circumf
44 ppeared to be suppressed and chromosome loss/reduplication, leading to uniparental disomy (UPD), repr
45 me, while centriole disengagement provides a reduplication license to allow mother centrioles to dupl
46 the question of how a cell undergoing genome reduplication might regulate chromosome structure to pre
47 of CP110, ultimately resulting in centrosome reduplication, mitotic catastrophe and abrogation of cel
50 somes where Orc1 prevents Cyclin E-dependent reduplication of both centrioles and centrosomes in a si
52 tion, but is essential to prevent subsequent reduplication of DNA and the resulting hyperdiploid stat
54 clin/cyclin-dependent kinases (CDKs) prevent reduplication of the budding yeast centrosome, called a
55 in heterozygous Men1 mice occurs by loss and reduplication of the entire mutant-bearing chromosome.
56 , gamma1 chains) revealed gaps, folding, and reduplication of the epidermo-dermal basement membrane.
57 stancing of the daughter centriole, allowing reduplication of the mother centriole even if the origin
62 human cells during G2 arrests and that this reduplication requires the activity of Polo-like kinase
67 We find that mother centrioles can undergo reduplication when original daughter centrioles are only
68 tion of Cetn2 into centrioles and centrosome reduplication, whereas depletion of Cetn3 generates extr
69 mosome separation failure thus causes genome reduplication, which alters mitotic chromosome structure