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1 ia inducible factor (HIF)-alpha subunits for ubiquitin dependent proteolysis.
2 rogression and postmitotic processes through ubiquitin-dependent proteolysis.
3 Many proteins are regulated by ubiquitin-dependent proteolysis.
4 d negatively regulates Ira2 by promoting its ubiquitin-dependent proteolysis.
5 h F-box-binding protein beta-TrCP, undergoes ubiquitin-dependent proteolysis.
6 criptional activity and targets ER alpha for ubiquitin-dependent proteolysis.
7 dulate multiple biological processes through ubiquitin-dependent proteolysis.
8 due to accelerated protein breakdown through ubiquitin-dependent proteolysis.
9 transcription factors, is regulated through ubiquitin-dependent proteolysis.
10 by the ubiquitin E3 ligase SCF(SKP2) through ubiquitin-dependent proteolysis.
11 vel regulatory mechanism of hematopoiesis by ubiquitin-dependent proteolysis.
12 Cdk-dependent G1 phosphorylation leading to ubiquitin-dependent proteolysis.
13 way that regulates the entry into mitosis by ubiquitin-dependent proteolysis.
14 processing of damaged and toxic proteins by ubiquitin-dependent proteolysis.
15 lar levels of many proteins are regulated by ubiquitin-dependent proteolysis.
16 processes by marking regulatory proteins for ubiquitin-dependent proteolysis.
17 n potential yet simultaneously target Mi for ubiquitin-dependent proteolysis.
18 ess increases phytosphingosine and activates ubiquitin-dependent proteolysis.
19 uman papillomaviruses (HPVs) targets p53 for ubiquitin-dependent proteolysis.
20 complexes that target specific proteins for ubiquitin-dependent proteolysis.
21 short-lived proteins that are controlled by ubiquitin-dependent proteolysis.
22 on was not affected in mutants defective for ubiquitin-dependent proteolysis.
23 tin chains, which correlates with defects in ubiquitin-dependent proteolysis.
24 owth, and they have at most minor effects on ubiquitin-dependent proteolysis.
25 the fat facets gene and is thus regulated by ubiquitin-dependent proteolysis.
26 xperiments identifying Gt as a substrate for ubiquitin-dependent proteolysis.
27 ulators, such as cyclins, for destruction by ubiquitin-dependent proteolysis.
29 n, in concert with control of transcription, ubiquitin-dependent proteolysis and cytoskeletal polarit
30 ons or structurally related determinants for ubiquitin-dependent proteolysis and perhaps other proces
31 tes, stabilization of typical substrates for ubiquitin-dependent proteolysis, and enhanced susceptibi
32 etwork of proteins that function together in ubiquitin-dependent proteolysis, and the UBL method offe
34 ver, Lys(6)-biotinylated ubiquitin inhibited ubiquitin-dependent proteolysis, as conjugates formed wi
35 pass the arrest that results from inhibiting ubiquitin-dependent proteolysis because cdc16-1 cdc55::L
36 a short half-life in yeast, being subject to ubiquitin-dependent proteolysis, but we find that it is
37 the data suggest that Int6 depletion blocks ubiquitin-dependent proteolysis by decreasing both ubiqu
38 everal lines of evidence that c-Myc promotes ubiquitin-dependent proteolysis by directly activating e
41 ns with expanded polyglutamine tracts impair ubiquitin-dependent proteolysis due to their propensity
42 s also demonstrate that KLF4 is targeted for ubiquitin-dependent proteolysis during cell cycle progre
43 vator that targets many mitotic proteins for ubiquitin-dependent proteolysis during late mitosis and
46 g hypoxia-inducible factor-alpha subunits to ubiquitin-dependent proteolysis has been well documented
47 suggesting that E7 is also regulated by the ubiquitin-dependent proteolysis in cervical cancer cells
49 Our observations account for the reduced ubiquitin-dependent proteolysis in sug1 mutants and sugg
51 97 is also involved in pathways that lead to ubiquitin-dependent proteolysis, including ER-associated
52 le without showing obvious signs of impaired ubiquitin-dependent proteolysis, indicating that other d
56 roteins and previous studies have shown that ubiquitin-dependent proteolysis is implicated in the tur
60 ce appears to be a result of deregulation of ubiquitin-dependent proteolysis mediated by the anaphase
62 been postulated to be controlled through the ubiquitin-dependent proteolysis of an unknown inhibitor.
63 oting complex/cyclosome, which catalyzes the ubiquitin-dependent proteolysis of cell cycle regulatory
64 ciated links between fatty acid synthase and ubiquitin-dependent proteolysis of cell-cycle regulatory
65 Promoting Complex, which is required for the ubiquitin-dependent proteolysis of certain proteins duri
68 multiprotein E3 ubiquitin ligase involved in ubiquitin-dependent proteolysis of key cell cycle regula
69 -promoting complex (APC), which triggers the ubiquitin-dependent proteolysis of key regulatory protei
73 ng complex/cyclosome pathway responsible for ubiquitin-dependent proteolysis of mitotic cyclins, indi
75 nset of anaphase, presumably by blocking the ubiquitin-dependent proteolysis of proteins responsible
76 , also known as the cyclosome) regulates the ubiquitin-dependent proteolysis of specific cell-cycle p
79 -based E3 ubiquitin ligase that promotes the ubiquitin-dependent proteolysis of various substrates im
80 tes cellular growth by modulating either the ubiquitin-dependent proteolysis or the ubiquitination st
83 l as gamma-irradiated cells, indicating that ubiquitin-dependent proteolysis plays a role in the norm
87 odified proteins and that failure to execute ubiquitin-dependent proteolysis renders various cell typ
88 ntial susceptibility of the catalytic LCs to ubiquitin-dependent proteolysis therefore might explain
89 n the established role of the RUB pathway in ubiquitin-dependent proteolysis, these data suggest that
90 ns are found in several proteins involved in ubiquitin-dependent proteolysis, though no function has
91 level of E7 in cancer cells is regulated by ubiquitin-dependent proteolysis through the 26S proteaso
93 mediates heat stress signaling and activates ubiquitin-dependent proteolysis via the endocytosis vacu
94 checkpoint regulation of mitosis, depends on ubiquitin-dependent proteolysis, we propose that the UBA
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