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1 calizes to centrosomes and blocks centrosome reduplication.
2 CDK2 kinase inhibition also allow centrosome reduplication.
3 specifically blocks modified centrioles from reduplication.
4 mother centrioles, which prevents centriole reduplication.
5 e number and ensuring the block to centriole reduplication.
6 lecule inhibitor SU9516 suppressed centriole reduplication.
7 Mps1 mediates cyclin A-dependent centrosome reduplication.
8 roduces extra centrosomes, called centrosome reduplication.
9 to mitotic divisions without impairing endo-reduplication.
10 of Aurora A activation to prevent centrosome reduplication.
11 sible to SAS-6, correlating with a block for reduplication.
12 nabling continued proliferation after genome reduplication, a finding with implications for cancer pr
14 that myeloid alpha-defensin genes evolved by reduplication and divergence from Paneth cell defensin g
15 lls correlates with the onset of endomitotic reduplication and is associated with the loss of the abi
23 1 is a regulator of centriole and centrosome reduplication as well as the initiation of DNA replicati
28 ance as coauthor with Bateson to promote the reduplication hypothesis to explain the statistical evid
29 we describe a mechanism to prevent centriole reduplication in Drosophila melanogaster whereby the SCF
35 ppeared to be suppressed and chromosome loss/reduplication, leading to uniparental disomy (UPD), repr
36 me, while centriole disengagement provides a reduplication license to allow mother centrioles to dupl
37 of CP110, ultimately resulting in centrosome reduplication, mitotic catastrophe and abrogation of cel
40 somes where Orc1 prevents Cyclin E-dependent reduplication of both centrioles and centrosomes in a si
42 tion, but is essential to prevent subsequent reduplication of DNA and the resulting hyperdiploid stat
44 clin/cyclin-dependent kinases (CDKs) prevent reduplication of the budding yeast centrosome, called a
45 in heterozygous Men1 mice occurs by loss and reduplication of the entire mutant-bearing chromosome.
46 , gamma1 chains) revealed gaps, folding, and reduplication of the epidermo-dermal basement membrane.
47 stancing of the daughter centriole, allowing reduplication of the mother centriole even if the origin
52 human cells during G2 arrests and that this reduplication requires the activity of Polo-like kinase
57 We find that mother centrioles can undergo reduplication when original daughter centrioles are only
58 tion of Cetn2 into centrioles and centrosome reduplication, whereas depletion of Cetn3 generates extr
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