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1 the first verified protein target of the EBV deubiquitinating enzyme.
2 lso requires the action of CYLD, a RIPK1 K63 deubiquitinating enzyme.
3 two different mutations in a gene encoding a deubiquitinating enzyme.
4 ssemble substrates, shuttling factors, and a deubiquitinating enzyme.
5 ations in USP9X, encoding a highly conserved deubiquitinating enzyme.
6 by the enzymatic activity of the EBV-encoded deubiquitinating enzyme.
7 eins, IKK, NF-kappaB, ubiquitin ligases, and deubiquitinating enzymes.
8 ng a short hairpin RNA library against known deubiquitinating enzymes.
9 tin and Uch37, one of the proteasome's three deubiquitinating enzymes.
10 umor (OTU) domain class of cysteine protease deubiquitinating enzymes.
11 tor protein may regulate a subclass of human deubiquitinating enzymes.
12 g process that is mediated by p97-associated deubiquitinating enzymes.
13 eins and recruits both ubiquitin ligases and deubiquitinating enzymes.
14 iquitin ligase BRAP2/IMP, and a subfamily of deubiquitinating enzymes.
15 ding member of a previously unknown class of deubiquitinating enzymes.
16  and is distinct from that observed in other deubiquitinating enzymes.
17 jugation is a reversible process mediated by deubiquitinating enzymes.
18 opts a fold closely resembling that of known deubiquitinating enzymes.
19 asome and one of three proteasome-associated deubiquitinating enzymes.
20       These include E3 ubiquitin ligases and deubiquitinating enzymes.
21  ubiquitin ligases (E3s) and removed through deubiquitinating enzymes.
22 n tumor domain (OTU)-containing subfamily of deubiquitinating enzymes.
23  alpha-helical hairpin that is unusual among deubiquitinating enzymes.
24                                              Deubiquitinating enzyme A (DUBA), an ovarian tumor domai
25                                              Deubiquitinating enzyme A (DUBA), which selectively clea
26                                              Deubiquitinating enzymes, a class of proteases capable o
27 s 63-linked ubiquitination of TRAF6, and the deubiquitinating enzyme A20 was found to be significantl
28 dislocation of MHCI heavy chains did require deubiquitinating enzyme activity and rapid proteasome-me
29              In vitro reconstitution of USP1 deubiquitinating enzyme activity, using either ubiquitin
30                                          The deubiquitinating enzyme AMSH has been implicated in the
31 n of receptors and was also regulated by two deubiquitinating enzymes, AMSH and UBPY, which localized
32 trate that USP53 is a catalytically inactive deubiquitinating enzyme and a novel component of tight j
33                      Itch interacts with the deubiquitinating enzyme and is required for deubiquitina
34 , we performed a siRNA screening to identify deubiquitinating enzymes and found that USP36 acts as an
35  and ENY2 orchestrate activities of multiple deubiquitinating enzymes and that imbalances in these ac
36  spatial arrangement of ubiquitin receptors, deubiquitinating enzymes and the protein unfolding machi
37 ins may also form complexes with other human deubiquitinating enzymes and thereby regulate their acti
38 perativity between an ubiquitin ligase and a deubiquitinating enzyme, and establish a role for USP7 i
39          We previously identified PfUCHL3, a deubiquitinating enzyme, and here we characterize its ac
40 ical analysis showed that AMSH1 is an active deubiquitinating enzyme, and that AMSH1 specifically cle
41 ncluding the Stk11 protein kinase, the Usp9x deubiquitinating enzyme, and their substrate kinase MARK
42 n ubiquitin ligases, of JAMM- and USP-domain-deubiquitinating enzymes, and of numerous ubiquitin-bind
43 ubiquitination processes involving the AMSH1 deubiquitinating enzyme are thus involved in both infect
44                                      Because deubiquitinating enzymes are components of the ubiquitin
45                                              Deubiquitinating enzymes are essential to the ubiquitin
46                                              Deubiquitinating enzymes are proteases that reverse this
47  Sem1p and its interacting partner, Ubp6p (a deubiquitinating enzyme), are essential to maintain telo
48       Collectively these results implicate a deubiquitinating enzyme as a regulator of the UPR.
49                     Here, we report USP15, a deubiquitinating enzyme, as a regulator of protein-prote
50                                          The deubiquitinating enzyme associated molecule with the SH3
51  ubiquitin-ligase interacts with ataxin-3, a deubiquitinating enzyme associated with Machado-Joseph d
52                      One such protein is the deubiquitinating enzyme ataxin 3, which is widely expres
53 cysteine protease domain found in four human deubiquitinating enzymes: ataxin-3, the ataxin-3-like pr
54 ic deficiency of Cyld, a recently identified deubiquitinating enzyme, attenuates the early wave of ge
55                    The identification of the deubiquitinating enzyme BAP1 as a tumor suppressor may l
56                                         This deubiquitinating enzyme binds BoNT/A light chain directl
57 u tumor suppressor (VHL) protein-interacting deubiquitinating enzyme, binds to the Robo1 receptor, an
58                                          The deubiquitinating enzyme BRCA1-associated protein 1 (BAP1
59 hibition of RNF168 at telomeres involves the deubiquitinating enzyme BRCC3 and the ubiquitin ligase U
60                      We further identify the deubiquitinating enzyme, BRCC3, as a critical regulator
61 ed-coil domain protein CCDC98/Abraxas, and a deubiquitinating enzyme BRCC36.
62  More interestingly, Mib1 is associated with deubiquitinating enzymes, BRCC36 and the mammalian ortho
63 me can be antagonized by proteasome-residing deubiquitinating enzymes, by the binding of polyubiquiti
64  we show that USP14, a proteasome-associated deubiquitinating enzyme, can inhibit the degradation of
65            Here, we show that the chlamydial deubiquitinating enzyme (Cdu) 1 localizes in the inclusi
66 nd Hse1 that recruit ubiquitinated cargo and deubiquitinating enzymes close to each other.
67 )-UAF1 (USP1-associated factor 1) complex, a deubiquitinating enzyme complex for PCNA and FANCD2.
68 sent the isolation of two novel multisubunit deubiquitinating enzyme complexes containing USP12 and U
69 teins that interact with the USP12 and USP46 deubiquitinating enzyme complexes.
70                            Incubation with a deubiquitinating enzyme converted the p110:p107 PEPC het
71                                       Hence, deubiquitinating enzymes could offer novel therapeutic t
72 n-induced and NF-kappaB-driven expression of deubiquitinating enzyme CSN5 leads to PD-L1 stabilizatio
73                                          The deubiquitinating enzyme CYLD has recently been implicate
74 stigated the role of the recently identified deubiquitinating enzyme CYLD in osteoclastogenesis and f
75                                              Deubiquitinating enzyme CYLD inhibits NEMO linear ubiqui
76                                          The deubiquitinating enzyme CYLD is a tumor suppressor prote
77 f Cancer Cell, Nikolaou et al. show that the deubiquitinating enzyme CYLD is critical for controlling
78         Despite recent studies that identify deubiquitinating enzyme cylindromatosis (CYLD) as a key
79 last precursors, Itch bound to TRAF6 and the deubiquitinating enzyme cylindromatosis.
80 ction was replaced by the recruitment of the deubiquitinating enzyme, cylindromatosis, an inhibitor o
81                              Determining how deubiquitinating enzymes discriminate between ubiquitin-
82 ry proteins such as Bro1, which recruits the deubiquitinating enzyme Doa4 to remove ubiquitin from ca
83 ion of the protein Rfu1, an inhibitor of the deubiquitinating enzyme Doa4.
84 s together with serial mutagenesis defined a deubiquitinating enzyme domain and a ubiquitin associati
85 mbrane and faces the cytosol with the active deubiquitinating enzyme domain.
86 omain, lysine 63-ubiquitin (K63-Ub)-specific deubiquitinating enzyme (DUB) and a member of two protei
87  MERS-CoV PL(pro) was recently shown to be a deubiquitinating enzyme (DUB) and to possess deISGylatin
88 ted ring domain protein 1) E3 ligase and the deubiquitinating enzyme (DUB) BRCC36 to MDC1-gammaH2AX-d
89                 An in-depth understanding of deubiquitinating enzyme (DUB) catalysis, particularly th
90      While the N-terminal domain of A20 is a deubiquitinating enzyme (DUB) for Lys63-linked polyubiqu
91                                       BRCC36-deubiquitinating enzyme (DUB) forms two different comple
92           A newly discovered virally encoded deubiquitinating enzyme (DUB) is strictly conserved acro
93                 BRCC36 is a Zn(2+)-dependent deubiquitinating enzyme (DUB) that hydrolyzes lysine-63-
94 le with the SH3 domain of STAM3 (AMSH3) is a deubiquitinating enzyme (DUB) that interacts with endoso
95 hus, our results demonstrate that USP25 is a deubiquitinating enzyme (DUB) that negatively regulates
96   These findings establish CYLD as a pivotal deubiquitinating enzyme (DUB) that regulates germ cell a
97 tein BRCA1 along with Abraxas and the BRCC36 deubiquitinating enzyme (DUB) to polyubiquitin structure
98 apid dephosphorylation and activation of the deubiquitinating enzyme (DUB) USP8.
99 the initiator E2, Ube2w, and the specialized deubiquitinating enzyme (DUB), ataxin-3, participate in
100  activity of the TRAF6-interacting the Lys63-deubiquitinating enzyme (DUB), cylindromatosis tumor sup
101                 Here, we have identified the deubiquitinating enzyme (DUB), ubiquitin-specific protea
102 ubiquitination is well studied; however, the deubiquitinating enzyme (DUB), which regulates TRAF2 sta
103                                              Deubiquitinating enzymes (DUB) form a family of cysteine
104 he Hippo pathway via ubiquitination, yet few deubiquitinating enzymes (DUB) have been implicated.
105 port that BITC and PEITC effectively inhibit deubiquitinating enzymes (DUB), including the enzymes US
106                                              Deubiquitinating enzymes (DUBs) act on ubiquitinated sub
107 ecycle at the apical membranes of CCD cells, deubiquitinating enzymes (DUBs) are likely involved in r
108 ytosed CFTR for degradation in the lysosome, deubiquitinating enzymes (DUBs) are likely to facilitate
109                                              Deubiquitinating enzymes (DUBs) are negative regulators
110                                              Deubiquitinating enzymes (DUBs) are proteases that can a
111                                              Deubiquitinating enzymes (DUBs) are proteases that proce
112                    Ubiquitinating as well as deubiquitinating enzymes (DUBs) can regulate these proce
113                                              Deubiquitinating enzymes (DUBs) control the ubiquitinati
114                                              Deubiquitinating enzymes (DUBs) function in a variety of
115                                              Deubiquitinating enzymes (Dubs) function to remove coval
116                                              Deubiquitinating enzymes (DUBs) have emerged as essentia
117                                              Deubiquitinating enzymes (DUBs) have emerged as key play
118        By countering protein ubiquitination, deubiquitinating enzymes (DUBs) help control neuronal fa
119  the dynamic removal of this modification by deubiquitinating enzymes (DUBs) impacts genome maintenan
120 are treated with a panel of linkage-specific deubiquitinating enzymes (DUBs) in parallel reactions, f
121                            To search for the deubiquitinating enzymes (DUBs) involved in the antivira
122                  The functional diversity of deubiquitinating enzymes (DUBs) is not well understood.
123                                              Deubiquitinating enzymes (DUbs) play important roles in
124            There are approximately 79 active deubiquitinating enzymes (DUBs) predicted in the human g
125                                              Deubiquitinating enzymes (DUBs) recognize and cleave lin
126                                              Deubiquitinating enzymes (DUBs) regulate various cellula
127                                              Deubiquitinating enzymes (DUBs) remove ubiquitin (Ub) fr
128            The discovery of viruses encoding deubiquitinating enzymes (DUBs) suggests they remove ubi
129        However, the proteasome also contains deubiquitinating enzymes (DUBs) that can remove ubiquiti
130 ed proteins is effected by a large number of deubiquitinating enzymes (DUBs) that function as cystein
131                                          The deubiquitinating enzymes (DUBs) that function in the ner
132 at the stability of ARTs is regulated by the deubiquitinating enzymes (DUBs) Ubp2 and Ubp15.
133 ells is likely regulated by a diverse set of deubiquitinating enzymes (DUBs) with distinct ubiquitin
134 the coronaviral enzyme over homologous human deubiquitinating enzymes (DUBs), and no significant cyto
135          Uch37 is one of the three principal deubiquitinating enzymes (DUBs), and the only ubiquitin
136 biquitin-vinylsulfone inhibitor specific for deubiquitinating enzymes (DUBs), we confirmed that, like
137 arian tumor domain-containing superfamily of deubiquitinating enzymes (DUBs), which is capable of inh
138                                              Deubiquitinating enzymes (DUBs), which reverse the proce
139  Lys(48)-linked chains are resistant to many deubiquitinating enzymes (DUBs).
140 teins, and these are countered by an army of deubiquitinating enzymes (DUBs).
141 ubiquitin chain and binds to 26 S-associated deubiquitinating enzymes (DUBs): in yeast to Ubp6, which
142 lf, the ubiquitin conjugation machinery, and deubiquitinating enzymes enable activity and regulation
143 used by a mutation in Usp53, a member of the deubiquitinating enzyme family.
144  (Slimb), whose action is antagonized by the deubiquitinating enzyme fat facets.
145 entify UCH37 as the first, to our knowledge, deubiquitinating enzyme for E2F1.
146 indicate that UCHL1 promotes metastases as a deubiquitinating enzyme for HIF-1alpha, which justifies
147 quitin specific protease 7 (USP7) is a known deubiquitinating enzyme for tumor suppressor p53 and its
148    Ubiquitin-specific protease 7 (USP7) is a deubiquitinating enzyme found in all eukaryotes that cat
149  polycomb repressor complex 1 (PRC1) and H2A-deubiquitinating enzymes (H2A-DUBs).
150 g that hRpn13 interaction may stabilize this deubiquitinating enzyme in human cells.
151                   Here we identify the first deubiquitinating enzyme in P. falciparum, PfUCH54, by it
152 ly binding the promoter region of Tnfaip3, a deubiquitinating enzyme in TLR signaling.
153 but the identities and specific functions of deubiquitinating enzymes in the nervous system are lacki
154 f c-IAPs is inhibited by USP19 and implicate deubiquitinating enzymes in the regulation of IAP stabil
155 get the MM cell in its microenvironment (eg, deubiquitinating enzyme inhibitors; chymotryptic [carfil
156 ted molecule of SH3 domain of STAM (AMSH), a deubiquitinating enzyme, interact with each other in cel
157                        These data show how a deubiquitinating enzyme-interacting protein dictates the
158          These results indicate that the EBV deubiquitinating enzyme interacts with, deubiquitinates,
159                 Here we report that USP19, a deubiquitinating enzyme, interacts with cellular IAP 1 (
160 dentified that USP2a, a circadian-controlled deubiquitinating enzyme, interacts with CRY1 and enhance
161                  Here, we show that the USP7 deubiquitinating enzyme is an integral component of the
162                                  Ataxin-3, a deubiquitinating enzyme, is the disease protein in spino
163  ubiquitin binding domain (ZnF UBP) from the deubiquitinating enzyme isopeptidase T (IsoT, or USP5) a
164             TRAF6 activity can be impeded by deubiquitinating enzymes like ubiquitin-specific proteas
165         Finally, pharmacologic inhibition of deubiquitinating enzymes markedly enhances sterol-depend
166 d by the opposition of ubiquitin ligases and deubiquitinating enzymes mediates endocytic trafficking
167                                    The USP19 deubiquitinating enzyme modulates the expression of myog
168 o involves ataxin-3 (atx3), a p97-associated deubiquitinating enzyme mutated in type-3 spinocerebella
169       Here we report the identification of a deubiquitinating enzyme, named ubiquitin-specific protea
170             We report here that USP8/UBPY, a deubiquitinating enzyme not previously implicated in mit
171 th ubiquitin-specific protease 10 (USP10), a deubiquitinating enzyme of p53.
172                   YOD1 is a highly conserved deubiquitinating enzyme of the ovarian tumor (otubain) f
173         BRCA1-associated protein-1 (BAP1), a deubiquitinating enzyme of unknown cellular function, is
174                                              Deubiquitinating enzymes of the ovarian tumour (OTU) fam
175 ellular processes and pathways, and specific deubiquitinating enzymes often play the decisive role of
176                         The diverse roles of deubiquitinating enzymes, or DUBs, in determining the fa
177 Finally, ubiquitin chains are trimmed by the deubiquitinating enzyme Otu1p, which is recruited and ac
178 s regulated in a non-canonical manner by the deubiquitinating enzyme, OTUB1 (OTU domain-containing ub
179 onjugating enzyme in the regulation of an E3/deubiquitinating enzyme pair, with important implication
180 -linked ubiquitin chains via the proteasomal deubiquitinating enzyme Poh1.
181 further show that ataxin-3, a p97-associated deubiquitinating enzyme previously implicated in ER-asso
182 chanisms, including ubiquitin E3 ligases and deubiquitinating enzymes, provide great opportunities fo
183       We focus on two of these proteins, the deubiquitinating enzyme Psmd14 and the E3 ligase Fbxw7,
184 ell as the large number and diversity of the deubiquitinating enzymes raise the possibility that sign
185                                              Deubiquitinating enzymes regulate essential cellular pro
186 he catalytic activity of this disease-linked deubiquitinating enzyme regulates several of its cellula
187 c peptidase 8 (USP8), an endosome-associated deubiquitinating enzyme, regulates the ubiquitination, t
188 unknown interplay between an E3 ligase and a deubiquitinating enzyme regulating TBP levels during cel
189 97/p47 complex-interacting protein, p135), a deubiquitinating enzyme required for p97/p47-mediated po
190 ate binding, preventative modifications, and deubiquitinating enzyme reversal of ubiquitination.
191                                        Three deubiquitinating enzymes-Rpn11, Usp14, and Uch37-are ass
192 ling pathways might be modulated by specific deubiquitinating enzyme(s).
193        In this report, we find that Usp9x, a deubiquitinating enzyme, stably associates with the SMN
194 The ubiquitination process is reversible via deubiquitinating enzymes, such as ubiquitin-specific pep
195 the most widely studied among the nearly 100 deubiquitinating enzymes, supports cancer by positively
196                        The CYLD protein is a deubiquitinating enzyme that acts as a negative regulato
197 a transcriptional co-repressor, as well as a deubiquitinating enzyme that appears to function in cell
198 eoxygenation can be influenced by Cezanne, a deubiquitinating enzyme that cleaves ubiquitin from spec
199 l of aggresomes requires Poh1, a proteasomal deubiquitinating enzyme that cleaves ubiquitinated prote
200                 We show that dCYLD encodes a deubiquitinating enzyme that deubiquitinates dTRAF2 and
201 biquitin C-terminal hydrolase L1 (UCH-L1), a deubiquitinating enzyme that functions to regulate cellu
202 e fertility genes include USP8, an essential deubiquitinating enzyme that has a role in acrosome asse
203  USP28 (ubiquitin-specific protease 28) is a deubiquitinating enzyme that has been implicated in the
204                          CYLD is a lysine 63-deubiquitinating enzyme that inhibits NF-kappaB and JNK
205 entrosome duplication that requires USP33, a deubiquitinating enzyme that is able to regulate CP110 l
206                  Cylindromatosis (CYLD) is a deubiquitinating enzyme that is altered in patients with
207             Rpn11 is a proteasome-associated deubiquitinating enzyme that is essential for viability.
208 quitin C-terminal hydrolase L1 (UCH-L1) is a deubiquitinating enzyme that is highly expressed in neur
209              Isopeptidase T (IsoT/USP5) is a deubiquitinating enzyme that is largely responsible for
210 quitin C-terminal hydrolase L1 (UCH-L1) is a deubiquitinating enzyme that is selectively and abundant
211 an ubiquitin-specific protease 7 (USP7) is a deubiquitinating enzyme that prevents protein degradatio
212                  USP14 is a proteasome-bound deubiquitinating enzyme that recycles ubiquitin and regu
213 dentification of OTUB1 as a c-IAP-associated deubiquitinating enzyme that regulates c-IAP1 stability.
214                      The CYLD gene encodes a deubiquitinating enzyme that removes Lys-63-linked ubiqu
215                                 It encodes a deubiquitinating enzyme that removes Lys63- or linear-li
216 fic proteases (UBPs) are one large family of deubiquitinating enzymes that bear signature cysteine an
217  target them for proteosomal degradation and deubiquitinating enzymes that promote their stabilizatio
218     We performed an siRNA screen to identify deubiquitinating enzymes that regulate AR; in that scree
219            Less is known, however, about the deubiquitinating enzymes that regulate T cell proliferat
220  remodeling to generate a Poh1-dependent K63-deubiquitinating enzyme to facilitate protein aggregate
221 vities of the ubiquitination machinery and a deubiquitinating enzyme to maintain and modulate the dyn
222 sing a proteomic approach, we identified the deubiquitinating enzyme ubiquitin-specific protease 11 (
223 ionally, an opioid-mediated induction of the deubiquitinating enzyme ubiquitin-specific protease 15 w
224     Employing this method, we identified the deubiquitinating enzyme ubiquitin-specific protease 22 (
225          We previously demonstrated that the deubiquitinating enzyme ubiquitin-specific protease 2a (
226         We now report the discovery that the deubiquitinating enzyme ubiquitin-specific protease 33 (
227                                          The deubiquitinating enzyme ubiquitin-specific protease 8 (U
228                       Here, we show that the deubiquitinating enzyme ubiquitin-specific protease-46 (
229                               We show that a deubiquitinating enzyme, ubiquitin C-terminal hydrolase-
230  that this ubiquitination is reversed by two deubiquitinating enzymes, ubiquitin-specific proteases (
231                Here, we characterize a yeast deubiquitinating enzyme, Ubp10, that possesses IDRs flan
232 romyces cerevisiae, Cdh1 associates with the deubiquitinating enzyme Ubp15, but the significance of t
233 iochemical characterization of a multidomain deubiquitinating enzyme, Ubp15, from Saccharomyces cerev
234 ved in numerous processes, and an associated deubiquitinating enzyme, Ubp2, modulates its activity.
235  a core particle (CP) subunit depends on the deubiquitinating enzyme Ubp3, although a regulatory part
236 all integrity is negatively regulated by the deubiquitinating enzyme Ubp3.
237 s/PKA signaling is negatively regulated by a deubiquitinating enzyme, Ubp3.
238 f-function mutation in the gene encoding the deubiquitinating enzyme Ubp6 improves growth rates in fo
239                    The proteasome-associated deubiquitinating enzyme Ubp6, which spares ubiquitin fro
240 tin chain disassembly, by binding the UBL of deubiquitinating enzyme Ubp6.
241 subject to disassembly by a proteasome-bound deubiquitinating enzyme, Ubp6.
242                Yeast proteasomes contain two deubiquitinating enzymes, Ubp6 and Rpn11.
243 3 associates with EGFR and combines with the deubiquitinating enzyme UBPY/USP8 to transfer EGFR from
244 at Smo ubiquitination is counteracted by the deubiquitinating enzyme UBPY/USP8.
245 hosphorylated neurofilament H (pNFH) and the deubiquitinating enzyme UCH-L1 in lumbar CSF samples fro
246 m1 and S5a, the ATPase subunit Rpt5, and the deubiquitinating enzyme Uch37 are ubiquitinated in situ
247 5),report crystal structures that define how deubiquitinating enzyme UCH37 is switched on or off by p
248 e cap-associated protein, which recruits the deubiquitinating enzyme UCH37 to the 26S proteasome.
249 inase adaptor (DEUBAD) domain that binds the deubiquitinating enzyme Uch37.
250 in receptor hRpn13/Adrm1 binds and activates deubiquitinating enzyme Uch37/UCHL5 and is targeted by b
251 thermore, BDNF increased the activity of the deubiquitinating enzyme UchL1 in synaptoneurosomes and u
252 r the transcriptional repression of the USP1 deubiquitinating enzyme upon exposure to DNA-damaging ag
253                                          The deubiquitinating enzyme USP1 (ubiquitin-specific proteas
254                                          The deubiquitinating enzyme USP1 controls the cellular level
255                             We show that the deubiquitinating enzyme USP1 promotes ID protein stabili
256 ns on histones, is actively destroyed by the deubiquitinating enzyme USP1.
257 ts describe a mechanism of regulation of the deubiquitinating enzyme, USP1, and of DNA repair.
258 factor 1) protein binds and stimulates three deubiquitinating enzymes: USP1, USP12, and USP46.
259   Mechanistically, nuclear Ufd1 recruits the deubiquitinating enzyme USP13 to counteract APC/C(Cdh1)-
260 e that Siah2 is subject to regulation by the deubiquitinating enzyme USP13.
261 ch resulted in a decreased expression of the deubiquitinating enzyme USP14 and several presynaptic pr
262 nction mutation in the proteasome-associated deubiquitinating enzyme Usp14, which is required for rec
263                    The proteasome-associated deubiquitinating enzyme Usp14/Ubp6 inhibits protein degr
264 0-20% in our preparations) also contains the deubiquitinating enzyme Usp14/Ubp6, which regulates prot
265 roteasome function through inhibition of the deubiquitinating enzymes USP14 and UCHL5.
266                      Here we report that the deubiquitinating enzyme, USP15, specifically deubiquitin
267 r direct effectors of ubH2B, we identified a deubiquitinating enzyme, Usp15, through affinity purific
268 removal of ubiquitin from this lysine by the deubiquitinating enzyme USP19.
269                 A previously uncharacterized deubiquitinating enzyme, USP29 binds to, cleaves poly-ub
270                        Our data identify the deubiquitinating enzyme USP2a as a novel regulator of th
271 eptide that bears sequence similarity to the deubiquitinating enzyme USP2a.
272                            We found that the deubiquitinating enzyme USP33 interacts with the Robo1 r
273                                  Because the deubiquitinating enzyme USP33 is involved in several imp
274 me pathway in human cells, we identified the deubiquitinating enzyme USP44 (ubiquitin-specific protea
275 ng et al. examine mice and cells lacking the deubiquitinating enzyme USP44.
276                                          The deubiquitinating enzyme USP48 stabilizes TRAF2 and reduc
277                We show that knockdown of the deubiquitinating enzyme USP5 (isopeptidase T) results in
278 x and leads to interaction between FoxM1 and deubiquitinating enzyme USP5, thereby deubiquitination a
279 me in a substoichiometric fashion, e.g., the deubiquitinating enzymes USP5/isopeptidase T and USP7/HA
280 interactions between a 100 kDa, multi-domain deubiquitinating enzyme, USP5 and a diubiquitin substrat
281 w role for vIRF1 through deregulation of the deubiquitinating enzyme USP7 to inhibit p53-mediated ant
282 rence in the expression level of the claspin deubiquitinating enzyme USP7 was detected.
283                         Knockdown of the p53 deubiquitinating enzyme USP7/HAUSP also reverses the sup
284 oordinated action of UBE4B, ESCRT-0, and the deubiquitinating enzyme USP8 enable the endosomal sortin
285 B3 ligand neuregulin-1 (NRG1) stabilizes the deubiquitinating enzyme USP8, which in turn stabilizes N
286 ains on the substrate in the presence of the deubiquitinating enzyme USP8.
287   Here we show that in vivo knockdown of the deubiquitinating enzyme USP9X attenuates T-cell prolifer
288  E3 ubiquitin ligase c-Cbl and also with the deubiquitinating enzyme USP9x; moreover, siRNA downregul
289 t that Ets-1 destruction is regulated by the deubiquitinating enzyme, Usp9x, and has major impact on
290 omal degradation by the dominant effect of a deubiquitinating enzyme, VCIP135/VCPIP1.
291 e disassembly of these heterodimers by major deubiquitinating enzymes was examined and it was discove
292 A (DUBA), an ovarian tumor domain-containing deubiquitinating enzyme, was discovered in a small inter
293 encoding the P. falciparum orthologue of the deubiquitinating enzyme were observed.
294           We recently reported that the USP1 deubiquitinating enzyme, which regulates the Fanconi ane
295                                 However, the deubiquitinating enzymes, which regulate MSH2 remain unk
296 dge, we have identified the first centriolar deubiquitinating enzyme whose expression regulates centr
297 ases (USPs) constitute the largest family of deubiquitinating enzymes, whose catalytic competency is
298  with specificity directed toward pathogenic deubiquitinating enzymes without inhibiting host DUBs.
299                      Here, we identified the deubiquitinating enzyme YOD1 (OTUD2) as a novel interact
300  of cofactors including UBXD1, PLAA, and the deubiquitinating enzyme YOD1, which we term ELDR compone

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