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1 h a wound-closure assay in the presence of a mitotic inhibitor.
2  B protein levels in response to colcemid, a mitotic inhibitor.
3 otypes suggest a possible role for Skb1 as a mitotic inhibitor.
4 ibed role for PAK-related protein kinases as mitotic inhibitors.
5 in response to treatment with epirubicin and mitotic inhibitors.
6 complex/cyclosome (APC/C), such as the early mitotic inhibitor 1 (Emi1) and spindle checkpoint protei
7 otic checkpoint complex and interphase early mitotic inhibitor 1 (Emi1) ensures the correct order and
8                   In vertebrate cells, early mitotic inhibitor 1 (Emi1) has been proposed as an impor
9                          Disruption of early mitotic inhibitor 1 (Emi1) interferes with normal cell c
10 rowing body of evidence indicates that early mitotic inhibitor 1 (Emi1) is essential for genomic stab
11                      The APC inhibitor early mitotic inhibitor 1 (Emi1) was recently found to be requ
12   We identify the mutation as being in early mitotic inhibitor 1 (emi1), a negative regulator of the
13         In mouse oocytes, we find that early mitotic inhibitor 1 (Emi1), an inhibitor of the anaphase
14 attenuated by high levels of the Emi1 (early mitotic inhibitor-1) protein.
15                 In mouse, we find that early mitotic inhibitor 2 (Emi2), which is an anaphase-promoti
16 t rather the relative abundance of the Swe1p mitotic inhibitor and the mitosis-promoting cyclins.
17 ompounds 8, 9a, 18 and 19a are highly potent mitotic inhibitors and selectively cytotoxic to cancer c
18 ization to other tyrosine kinase inhibitors, mitotic inhibitors, and platinum-based therapy, there is
19 AdBDNF, and intraventricular infusion of the mitotic inhibitor Ara-C completely blocked the performan
20 dicate that MCAK affects cell sensitivity to mitotic inhibitors by modulating the frequency of microt
21  can protect normal proliferating cells from mitotic inhibitors by preventing their entry into mitosi
22 bly checkpoint complex, Mad2B, and the early mitotic inhibitor Emi1.
23                  We have discovered an early mitotic inhibitor, Emi1, which regulates mitosis by inhi
24           MK-1775 (also known as AZD1775), a mitotic inhibitor, has been demonstrated to enhance the
25 s to evaluate the activity of ON 01910.Na, a mitotic inhibitor, in in vitro and in vivo models of pan
26                                  Emi1 (early mitotic inhibitor) inhibits APC/C (anaphase-promoting co
27      Targeting AKT in combination with WEE1 (mitotic inhibitor kinase) seems to have potential to mak
28                                      WEE1, a mitotic inhibitor kinase, regulates the DNA damage repai
29 entry and exit and allow the suggestion that mitotic inhibitors may have selective effects in tumors
30                  Groups A and B received the mitotic inhibitor monocrotaline, followed by male F344 (
31 is lower than on hard even in the absence of mitotic inhibitors normally used to temper the astrocyte
32 kpoint proteins, formation of interphase and mitotic inhibitors of Cdc20, and correction of faulty mi
33                                    The novel mitotic inhibitor, ON 01910.Na, showed activity in precl
34 inoblastoma, and decreased expression of the mitotic inhibitor p21.
35 nt kinase (Cdk)-2 and -4, high levels of the mitotic inhibitors, p21Waf1 and p27Kipl, and decreased c
36 -like growth factor-I receptor (IGF-IR), and mitotic inhibitors, respectively, clustered with others
37  Finally, cells chronically treated with the mitotic inhibitor retinoic acid displayed a selective do
38                                          The mitotic inhibitor Skb1 localizes to a set of cortical no
39 mergence is essential for degradation of the mitotic inhibitor, Swe1.
40 d size would cause G2 arrest enforced by the mitotic inhibitor Swe1p, explaining previous findings th
41      Mitotic delay is due to the Wee1 family mitotic inhibitor Swe1p, whose degradation is linked to
42                     Here we describe a novel mitotic inhibitor that acts during Drosophila gastrulati
43  enabling them to survive in the presence of mitotic inhibitors, which is a characteristic of mature
44 ere discovered as proapoptotic molecules and mitotic inhibitors with potencies at low nanomolar conce

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