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1 ia inducible factor (HIF)-alpha subunits for ubiquitin dependent proteolysis.
2               Many proteins are regulated by ubiquitin-dependent proteolysis.
3 d negatively regulates Ira2 by promoting its ubiquitin-dependent proteolysis.
4 s an E3 RING domain and targets proteins for 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 rogression and postmitotic processes through ubiquitin-dependent proteolysis.
11 by the ubiquitin E3 ligase SCF(SKP2) through ubiquitin-dependent proteolysis.
12 vel regulatory mechanism of hematopoiesis by ubiquitin-dependent proteolysis.
13  Cdk-dependent G1 phosphorylation leading to ubiquitin-dependent proteolysis.
14 way that regulates the entry into mitosis by ubiquitin-dependent proteolysis.
15  processing of damaged and toxic proteins by ubiquitin-dependent proteolysis.
16 lar levels of many proteins are regulated by ubiquitin-dependent proteolysis.
17 processes by marking regulatory proteins for ubiquitin-dependent proteolysis.
18 n potential yet simultaneously target Mi for ubiquitin-dependent proteolysis.
19 ess increases phytosphingosine and activates ubiquitin-dependent proteolysis.
20 uman papillomaviruses (HPVs) targets p53 for ubiquitin-dependent proteolysis.
21  complexes that target specific proteins for ubiquitin-dependent proteolysis.
22  short-lived proteins that are controlled by ubiquitin-dependent proteolysis.
23 on was not affected in mutants defective for ubiquitin-dependent proteolysis.
24 tin chains, which correlates with defects in ubiquitin-dependent proteolysis.
25 owth, and they have at most minor effects on ubiquitin-dependent proteolysis.
26 the fat facets gene and is thus regulated by ubiquitin-dependent proteolysis.
27 xperiments identifying Gt as a substrate for ubiquitin-dependent proteolysis.
28 ulators, such as cyclins, for destruction by ubiquitin-dependent proteolysis.
29 g proteostasis, especially those involved in ubiquitin-dependent proteolysis.
30 se, the SCF(SKP2) complex, that mediates p27 ubiquitin-dependent proteolysis [5-7].
31 n, in concert with control of transcription, ubiquitin-dependent proteolysis and cytoskeletal polarit
32 ons or structurally related determinants for ubiquitin-dependent proteolysis and perhaps other proces
33 tes, stabilization of typical substrates for ubiquitin-dependent proteolysis, and enhanced susceptibi
34 etwork of proteins that function together in ubiquitin-dependent proteolysis, and the UBL method offe
35           The flexibility and specificity of ubiquitin-dependent proteolysis are mediated, in part, b
36 ver, Lys(6)-biotinylated ubiquitin inhibited ubiquitin-dependent proteolysis, as conjugates formed wi
37 esponse to DNA damage, iron ion homeostasis, ubiquitin dependent proteolysis, autophagy and regulatio
38 pass the arrest that results from inhibiting ubiquitin-dependent proteolysis because cdc16-1 cdc55::L
39 a short half-life in yeast, being subject to ubiquitin-dependent proteolysis, but we find that it is
40  the data suggest that Int6 depletion blocks ubiquitin-dependent proteolysis by decreasing both ubiqu
41 everal lines of evidence that c-Myc promotes ubiquitin-dependent proteolysis by directly activating e
42 g enzyme, Doa4, that plays a central role in ubiquitin-dependent proteolysis by the proteasome.
43                                              Ubiquitin-dependent proteolysis can initiate at ribosome
44 ns with expanded polyglutamine tracts impair ubiquitin-dependent proteolysis due to their propensity
45 s also demonstrate that KLF4 is targeted for ubiquitin-dependent proteolysis during cell cycle progre
46 vator that targets many mitotic proteins for ubiquitin-dependent proteolysis during late mitosis and
47                 These mutants cannot sustain ubiquitin-dependent proteolysis even though neither moti
48                             In recent years, ubiquitin-dependent proteolysis has been demonstrated to
49 g hypoxia-inducible factor-alpha subunits to ubiquitin-dependent proteolysis has been well documented
50  suggesting that E7 is also regulated by the ubiquitin-dependent proteolysis in cervical cancer cells
51     The proteasome, the primary protease for ubiquitin-dependent proteolysis in eukaryotes, is usuall
52               Because of the central role of ubiquitin-dependent proteolysis in regulating fundamenta
53     Our observations account for the reduced ubiquitin-dependent proteolysis in sug1 mutants and sugg
54 sment by western blotting, and evaluation of ubiquitin-dependent proteolysis in the LV by immunopreci
55             Previous studies have implicated ubiquitin-dependent proteolysis in the turnover of wild-
56 97 is also involved in pathways that lead to ubiquitin-dependent proteolysis, including ER-associated
57 le without showing obvious signs of impaired ubiquitin-dependent proteolysis, indicating that other d
58                                              Ubiquitin-dependent proteolysis is an important mechanis
59                    Our results indicate that ubiquitin-dependent proteolysis is an important mediator
60                                              Ubiquitin-dependent proteolysis is catalyzed by the 26S
61 roteins and previous studies have shown that ubiquitin-dependent proteolysis is implicated in the tur
62            Destruction of mitotic cyclins by ubiquitin-dependent proteolysis is required for cells to
63  to the nucleus in G(1) phase, but undergoes ubiquitin-dependent proteolysis later in cell cycle.
64 t in a protein that escapes the mechanism of ubiquitin-dependent proteolysis, leading to protein stab
65                                              Ubiquitin-dependent proteolysis makes a major contributi
66 ce appears to be a result of deregulation of ubiquitin-dependent proteolysis mediated by the anaphase
67                                  Strikingly, ubiquitin-dependent proteolysis of alpha2 is required fo
68 oting Complex/Cyclosome (APC/C) mediates the ubiquitin-dependent proteolysis of alphaKNL2 during mito
69 been postulated to be controlled through the ubiquitin-dependent proteolysis of an unknown inhibitor.
70 oting complex/cyclosome, which catalyzes the ubiquitin-dependent proteolysis of cell cycle regulatory
71 ciated links between fatty acid synthase and ubiquitin-dependent proteolysis of cell-cycle regulatory
72 Promoting Complex, which is required for the ubiquitin-dependent proteolysis of certain proteins duri
73                                              Ubiquitin-dependent proteolysis of cyclin B and securin
74                                              Ubiquitin-dependent proteolysis of cyclin D1 is associat
75 we characterized the enzymes involved in the ubiquitin-dependent proteolysis of E7.
76 multiprotein E3 ubiquitin ligase involved in ubiquitin-dependent proteolysis of key cell cycle regula
77 -promoting complex (APC), which triggers the ubiquitin-dependent proteolysis of key regulatory protei
78        The SCF ubiquitin E3 ligase regulates ubiquitin-dependent proteolysis of many regulatory prote
79 t that the oncogenic E6 proteins enhance the ubiquitin-dependent proteolysis of MGMT.
80                                          The ubiquitin-dependent proteolysis of mitotic cyclin B, whi
81 ng complex/cyclosome pathway responsible for ubiquitin-dependent proteolysis of mitotic cyclins, indi
82                                              Ubiquitin-dependent proteolysis of p27(kip1) is growth a
83 nset of anaphase, presumably by blocking the ubiquitin-dependent proteolysis of proteins responsible
84 , also known as the cyclosome) regulates the ubiquitin-dependent proteolysis of specific cell-cycle p
85                                              Ubiquitin-dependent proteolysis of the mitotic cyclins A
86       By triggering the appropriately timed, ubiquitin-dependent proteolysis of the mitotic regulator
87 -based E3 ubiquitin ligase that promotes the ubiquitin-dependent proteolysis of various substrates im
88 tes cellular growth by modulating either the ubiquitin-dependent proteolysis or the ubiquitination st
89 viously uncharacterized, Fbx29-mediated, and ubiquitin-dependent proteolysis pathway.
90                                              Ubiquitin-dependent proteolysis plays a critical role in
91 l as gamma-irradiated cells, indicating that ubiquitin-dependent proteolysis plays a role in the norm
92                                              Ubiquitin-dependent proteolysis plays an important role
93                                              Ubiquitin-dependent proteolysis plays an important role
94 s to evaluate the intensity of autophagy and ubiquitin-dependent proteolysis processes occurring in m
95                                              Ubiquitin-dependent proteolysis regulates diverse cellul
96                                              Ubiquitin-dependent proteolysis regulates gene expressio
97 odified proteins and that failure to execute ubiquitin-dependent proteolysis renders various cell typ
98 ntial susceptibility of the catalytic LCs to ubiquitin-dependent proteolysis therefore might explain
99 n the established role of the RUB pathway in ubiquitin-dependent proteolysis, these data suggest that
100 ns are found in several proteins involved in ubiquitin-dependent proteolysis, though no function has
101  level of E7 in cancer cells is regulated by ubiquitin-dependent proteolysis through the 26S proteaso
102        As such, TRF1 levels are regulated by ubiquitin-dependent proteolysis via an SCF E3 ligase whe
103 mediates heat stress signaling and activates ubiquitin-dependent proteolysis via the endocytosis vacu
104 checkpoint regulation of mitosis, depends on ubiquitin-dependent proteolysis, we propose that the UBA

 
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